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Open Access 01-04-2025

Blood ammonia and eye-hand coordination negatively affect health-related quality of life in women with minimal hepatic encephalopathy

Auteurs: Daniela Batallas, Juan José Gallego, Franc Casanova-Ferrer, Alessandra Fiorillo, Pablo Rivas-Diaz, Adrià López-Gramaje, Yaiza M. Arenas, Luis Aparicio, Desamparados Escudero-García, Lucía Durbán, María-Pilar Rios, Salvador Benlloch, Amparo Urios, Vanesa Hidalgo, Carmina Montoliu, Alicia Salvador

Gepubliceerd in: Quality of Life Research

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Abstract

Purpose

Minimal hepatic encephalopathy (MHE) is common in cirrhosis, leading to cognitive impairment and eye-hand coordination (EHC) alterations. Hyperammonemia plays a key role in MHE, contributing to motor and cognitive deficits. Elevated blood ammonia levels and impaired EHC correlate with neuropsychiatric dysfunction, yet their direct impact on health-related quality of life (HRQoL) is complex. This study examines the associations between blood ammonia, EHC, and HRQoL, and the moderating influence of sex on these associations.

Methods

Eighty-seven cirrhotic patients (67 male) and 23 healthy volunteers (11 male), aged 44–80 years, performed the Psychometric Hepatic Encephalopathy Score (PHES) for MHE diagnosis, the Vienna Test System, bimanual and visuomotor tests, and completed the SF-36 questionnaire to measure HRQoL. Blood samples were taken to test ammonia levels.

Results

Results indicated a significant association between elevated blood ammonia and impaired EHC among cirrhotic patients. However, increased blood ammonia and EHC did not directly predict HRQoL. Moderated moderation analysis revealed that women with MHE showed greater sensitivity to hyperammonemia and EHC deficits in tasks requiring fine motor control and stability skills (aiming, tapping, and bimanual coordination), which were linked to lower HRQoL in both physical and mental domains. In women without MHE, alterations in linear tracking were linked to worse HRQoL. These effects were not observed in men.

Conclusions

The findings underscore the sex-specific impacts of MHE, with women disproportionately affected by ammonia-related motor impairments and their subsequent influence on HRQoL. These results could contribute to developing targeted strategies to improve outcomes in this vulnerable population.
Opmerkingen

Supplementary Information

The online version contains supplementary material available at https://​doi.​org/​10.​1007/​s11136-025-03920-3.
Daniela Batallas and Juan José Gallego these two authors have contributed equally.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Plain English Summary

This study examines how minimal hepatic encephalopathy (MHE), a common condition in patients with cirrhosis, affects thinking and coordination. High ammonia levels in the blood are linked to cognitive issues and coordination problems, which may impact patients' health-related quality of life (HRQoL). We studied 87 cirrhotic patients and 23 healthy volunteers, who completed tests to measure MHE, coordination, and HRQoL, along with blood tests for ammonia levels.
The results showed an association between higher ammonia levels and worse coordination in cirrhotic patients. However, these factors did not directly predict HRQoL. Interestingly, the study found that for women with MHE, high ammonia and poor coordination significantly affected their HRQoL, while this was not the case for men. These findings suggest that considering sex differences is crucial in understanding the way MHE impacts patients, which could improve diagnosis and treatment strategies.

Introduction

Cirrhosis, a chronic liver disease that compromises liver function, poses a challenge to patient wellness and daily functioning [1], and could lead to hepatic encephalopathy (HE), a neuropsychiatric syndrome with symptoms ranging from cognitive and motor dysfunctions to severe coma [2, 3]. Around 30–50% of patients with liver cirrhosis show minimal hepatic encephalopathy (MHE), which represents the initial stage of HE [2, 3]. Although devoid of overt HE symptoms, these individuals exhibit subtle cognitive and motor deficits [410]. MHE generally does not interfere with basic daily activities such as dressing or eating [11], but is strongly associated with difficulties in executive function, eye-hand coordination (EHC), psychomotor speed, and sustained attention [710]. These deficits compromise the ability to perform more demanding tasks, such as managing finances, maintaining work performance, planning, and driving, which collectively have a detrimental impact on health-related quality of life (HRQoL) [1216].
The adverse effects of MHE on quality of life are well-documented, particularly with respect to its association with reduced quality of life and increased work-related disability [11, 16, 17]. Previous studies have consistently reported lower scores across multiple HRQoL domains in patients with cirrhosis [18, 19]. Moreover, increasing severity of liver cirrhosis, or the presence of MHE, is closely linked to a decline in several components of HRQoL [15, 20]. Physical health is the most severely affected domain, underscoring the significant physical challenges faced by these patients [14, 2123].
One key aspect of these physical limitations is the substantial impairment in eye-hand coordination (EHC) observed in patients with MHE [9, 10, 24]. EHC refers to the coordinated use of vision and hand movements to perform physical tasks, relying on the dynamic integration of multiple sensorimotor systems, including visual processing, attention, central neural processing, and motor function [2527]. In MHE, these systems are significantly disrupted [10, 2830], resulting in reduced functional independence. This impairment not only compromises the ability to perform daily tasks but also contributes to heightened frustration and diminished self-confidence, compounding the overall burden of MHE and further reducing HRQoL.
Beyond the physical impact, MHE also imposes a substantial mental and emotional toll. Psychiatric symptoms, including anxiety and depression, are well-documented comorbidities in patients with cirrhosis and contribute to a substantial decline in HRQoL [6, 11, 31]. These symptoms particularly impair emotional well-being and social functioning, and can intensify the physical limitations caused by cirrhosis complications, such as ascites or bleeding episodes, further compromising daily functioning [14, 32, 33].
Despite the established link between psychiatric symptoms and the broader context of cirrhosis, variability in study findings suggests underlying complexities that remain poorly understood. Emerging research indicates a potential correlation between HE and mood/anxiety disorders; however, current evidence is insufficient to draw definitive conclusions [34]. This indicates a critical knowledge gap and highlights the need for targeted interventions to address the unique challenges faced by this patient population.
Furthermore, hyperammonemia plays a crucial role in the pathogenesis of MHE, as ammonia is neurotoxic and readily crosses the blood–brain barrier [3537]. Some studies show the synergistic effect of elevated serum ammonia levels and inflammation on neurological alterations in MHE patients [38, 39]. It is well-established that ammonia-mediated astrocyte dysfunction, neurotransmitter imbalances, and neuroinflammation collectively contribute to both motor and cognitive impairments associated with MHE [40, 41]. As mentioned, despite the link between MHE and a higher prevalence of neuropsychiatric symptoms such as depression, anxiety, and cognitive disorders [6, 11, 31], the mechanisms by which MHE contributes to subjective health outcomes of their emotional and physical well-being are not fully understood. While depression and anxiety are common in patients with cirrhosis, the specific ways in which MHE-related factors, such as hyperammonemia or motor coordination impairments, exacerbate these subjective experiences remain unclear. Addressing this gap is crucial for understanding the full impact of MHE on HRQoL.
Moreover, it is essential to assess sex disparities in this context. Specifically, chronic conditions like cirrhosis often exhibit differing epidemiology, natural progression, and treatment responses based on sex [42]. Examining potential sex-related distinctions is crucial for identifying individuals susceptible to psychological distress and cognitive decline. Prior studies have emphasized the adverse effects of chronic illnesses on HRQoL, with some findings suggesting that gender might influence perceptions of HRQoL in these conditions [43, 44]. Nevertheless, there is a paucity of literature on sex differences in cirrhosis, particularly regarding MHE. To redress this lack, therefore, this study aims to explore the potential associations between blood ammonia levels, EHC, and HRQoL as well as the moderating influence of sex on these associations in patients with and without MHE. The results of this study will enhance understanding of the negative effects of ammonia on quality of life and the influence of sex on these effects, enabling a more accurate evaluation of mental and physical health in cirrhotic patients.

Methods

Participants

This observational and cross-sectional study was reported following STROBE guidelines (Supplementary material). A total of 109 patients with liver cirrhosis were consecutively recruited from the outpatient clinics of Clínico and Arnau de Vilanova hospitals in Valencia, Spain. Diagnosis was based on clinical, biochemical, and ultrasonographic assessments. Inclusion criteria were chronic liver cirrhosis, ability to stand and walk unaided, and age over 18 years. Exclusion criteria were overt HE, recent alcohol intake (in the past six months), substance abuse history (excluding alcohol), antibiotic use, recent use of drugs affecting cognitive function (in the past 6 weeks), neurological or psychiatric disorders, and hepatocellular carcinoma.
A control group of 28 healthy volunteers was included in the study after liver disease was ruled out through clinical, analytical, and serological tests. The enrolled subjects exhibited no fever or any clinical or biological indications of recent infection.
Study participants were scheduled for two separate sessions: in the first session, blood was drawn, psychometric tests were performed to diagnose MHE, and subjects completed the SF-36 test. The coordination tests were administered during the second session held within the following three days.
Incomplete assessment in five controls and 22 patients left a final sample of 23 healthy volunteers and 87 patients (Supplementary Fig. 1).
Written informed consent was obtained from all participants before inclusion in the study. Study protocols were approved by the Research Ethics Committees of Hospital Clínico Universitario and Arnau de Vilanova Hospital of Valencia, Valencia, Spain (approval code: 2018/210; approval date: 2 March 2018) and were in accordance with the ethical guidelines of the Helsinki Declaration.

MHE diagnosis

All participants underwent the Psychometric Hepatic Encephalopathy Score (PHES), a set of five psychometric tests utilized for MHE diagnosis [3, 6]. The PHES score, adjusted for age and educational level, was calculated using Spanish normality tables (http://​www.​redeh.​org/​TEST_​phes.​htm). Cirrhotic patients were categorized as having MHE if the score was ≤ − 4 points. According to the PHES score, patients were grouped into 24 individuals with MHE (18 men and 6 women), and 63 without MHE (NMHE) (49 men and 14 women). A group of 23 healthy volunteers (11 men and 12 women) were included as controls after performing the PHES battery to rule out any cognitive impairment (Table 1).
Table 1
Clinical and demographic variables of participants
 
Controls
(N = 23)
NMHE
(N = 63)
MHE
(N = 24)
P
Effect size
Sex (m/w)
11/12
49/14
18/6
0.025
0.265b
Age (years)a
63.7 ± 7.3
62.2 ± 8.6
62.6 ± 8.1
0.741
0.006c
Educational levela
14.1 ± 0.7
11.4 ± 0.4
11.8 ± 0.7
0.005
0.096c
Etiology of cirrhosis
     
Alcohol
31
12
  
HBV/HCV
2/11
1/2
  
HCV + alcohol
0/2
1
  
MASH/MASH + alcohol
9/4
7/1
  
Other
4
   
Child–Pugh class (A/B/C)
 
50/13/0
17/6/1
  
NMHE and MHE, patients without and with minimal hepatic encephalopathy according to PHES score, m men, w women, HBV hepatitis B virus, HCV hepatitis C virus, MASH metabolic dysfunction-associated steatohepatitis, Child Pugh Scores measure the severity of chronic liver disease. Class C represents the highest classification of liver severity, while class A indicates the least severe. Reporting numbers represent the number of subjects in class A, B or C
aValues are expressed as mean ± standard deviation. Educational level is expressed as years of schooling
bValues are expressed as Cramér’s V coefficient
cValues are expressed as np2

Blood ammonia

Fasting venous blood ammonia levels were measured promptly after collection on the same day as psychometric testing using the PocketChemBA System Ammonia II Test Kit (Arkay, Inc., Kyoto, Japan) following the manufacturers’ instructions. This device employs microdiffusion technology to quantify ammonia concentrations in μM, using a 20 μL blood sample.

Short form-36 health survey (SF-36)

HRQoL was measured using the Spanish version of the SF-36 [43]. It consists of 36 items related to different physical and mental health aspects, grouped into eight subscales: physical functioning, role-physical, bodily pain, general health, vitality, social functioning, role-emotional, and mental health. For each subscale, the items were transformed into a 0–100 scale, with higher scores indicating better HRQL. Following Hidalgo et al., 2021 [45], the eight subscales were stratified into two global measures: subjective physical health (SPH), which includes physical functioning, role-physical, bodily pain, general health, and vitality scales; and subjective mental health (SMH), which includes general health, vitality, social functioning, role-emotional, and mental health scales. In the present study, Cronbach's α was 0.89, indicating high internal scale reliability.

Eye-hand coordination

Vienna test system

The Motor Performance Series (MLS) from the Vienna Test System (version 8.0; Schuhfried, Austria) was used to assess four specific motor skills: aiming, linear tracking, tremor (steadiness), and tapping (see Supplementary methods). Following Zwierko et al. [46], indices were calculated as: Aiming Index (AI) = number of accurate hits per time taken for the test (nh/t); Linear Tracking Index (LTI) = number of errors per time taken for the test (ne/t); Steadiness Index (SI) = number of errors (ne); and Tapping Index (TI) = number of accurate hits (nh).

Bimanual and visuomotor coordination tests

We conducted bimanual (BC) and visuomotor coordination (VC) tests as previously described [9]. Both tests were administered twice, without rest period, and the total time for completion was recorded in minutes [9].
Of the total participants, five (one MHE, two NMHE, and two controls) had missing data for all Vienna test outcomes (aiming, linear tracking, steadiness, and tapping), leaving 105 subjects included in these analyses, and a further 10 controls did not complete the SF-36, leaving 100 participants. For all other measures, the sample size remained at 110 participants.

Statistical analysis

Group differences in all variables were analyzed using one-way ANOVA for continuous data and Chi-square test for categorical data.
To investigate whether blood ammonia levels were associated with EHC after adjusting for covariates (age, sex, educational level), we performed logistic regression analysis, including EHC as the dependent variable, covariates in block one, and ammonia levels in block two. To determine the relationship between ammonia levels and HRQoL, we next performed hierarchical regression analysis, including HRQoL variables (SPH or SMH) as the dependent variable, covariates in block one, and ammonia levels in block two. As the following step, the association between EHC and HRQoL was analyzed by again performing hierarchical regression analysis, including SPH or SMH as the dependent variable, the covariates in block one, and the EHC indices in block two.
We analyzed the influence of sex (men and women) and group (with or without MHE) on these relationships using moderated moderation analysis tested with the Hayes’ PROCESS macro (Model 3) for SPSS, which measures whether the moderating effect of one variable (W) on the relationship between the independent variable (X) and the dependent variable (Y) is further moderated by a second variable (Model 3; see Supplementary Fig. 2). A more detailed explanation is provided in Supplementary Methods. Age and educational level were added as covariates. All p-values reported are two-tailed, and the level of significance was set at p < 0.05. Statistical analyses were performed with SPSS 26.0 (IBM Corporation, Armonk, NY, USA).
A post hoc power analysis was conducted using G*Power software (version 3.1.9.7 for Windows) to calculate statistical power. Based on a moderate effect size (f2 = 0.15) and significance level (α = 0.05), with a total sample size of n = 87, the power analysis yielded 1 − β = 0.811. See Supplementary Methods for a more detailed explanation.
To assess the potential bias introduced by missing data, we compared results with and without the excluded participants. These analyses confirmed that excluding subjects with missing data did not alter the main results of the study (Supplementary Table 4).

Results

Preliminary analyses

Descriptive statistics of each parameter and differences between MHE patients, NMHE patients and the control group are presented in Table 1.
MHE patients showed significantly higher blood ammonia levels than controls (p = 0.003) but no significant differences were found between MHE and NMHE patients (Table 2). When separating men and women within each group, overall ANOVA revealed no statistically significant sex-dependent differences in ammonia levels (p = 0.064 for men, p = 0.075 for women) (Supplementary Table 1). However, pairwise comparisons showed significantly higher blood ammonia levels in both men and women with MHE compared to their respective controls (p = 0.002 and p = 0.01, respectively).
Table 2
Blood ammonia levels, performance in eye-hand coordination tests, and SF-36 scores in the three study groups
 
Controls
(N = 23)
NMHE
(N = 63)
MHE
(N = 24)
F (df, RSE)
Global anova p
Effect size (NP2)
Blood ammonia (µM)
11.86 ± 5.8
27.85 ± 3.5
39.22 ± 5.7**
5.81 (2, 107)
0.004
0.09
Vienna Test System
      
 Aiming index (nh/t)
1.98 ± 0.1
1.66 ± 0.1**
1.18 ± 0.1*** ααα
20.61 (2, 102)
0.001
0.288
 Linear tracking index (ne/t)
0.61 ± 0.2
0.31 ± 0.1
0.55 ± 0.2
0.79 (2, 104)
0.456
0.015
 Steadiness index (ne)
9.85 ± 3.4
18.89 ± 2.0
28.52 ± 3.2*** α
8.08 (2, 102)
0.001
0.137
 Tapping index (nh)
187.9 ± 5.3
172.9 ± 3.1
148.1 ± 5.1*** ααα
15.20 (2, 102)
0.001
0.230
Coordination Tests
      
 Visuomotor coordination (min)
2.44 ± 0.14
2.80 ± 0.08
4.04 ± 0.13*** ααα
41.57 (2, 107)
0.001
0.437
 Bimanual coordination (min)
2.09 ± 0.14
2.30 ± 0.9
3.36 ± 0.14*** ααα
25.65 (2, 107)
0.001
0.324
SF-36 Test
      
 Subjective physical health
254.1 ± 39.0
315.4 ± 17.8
252.2 ± 28.9
2.27 (2, 97)
0.108
0.045
 Subjective mental health
226.8 ± 38.1
335.6 ± 17.3*
282.5 ± 28.1
3.945 (2, 97)
0.023
0.075
Values are expressed as mean ± SEM. NMHE and MHE, patients without and with minimal hepatic encephalopathy according to PHES score, df degrees of freedom, RSE residual standard error, np2 partial eta squared, t time taken for the test, ne number of errors, nh number of hits, min total minutes employed in the tests. Significant differences compared to controls are indicated by asterisks: *p < 0.05; **p < 0.01; ***p < 0.001; and from NMHE patients by α. (α: p < 0.05; ***/ααα: p < 0.001). Significant P values (p < 0.05) are in bold
Regarding the aiming index (AI) from the Vienna test, MHE patients performed poorly compared with either NMHE patients (p < 0.001) or controls (p < 0.001), and NMHE patients showed significantly worse performance than controls (p = 0.009). Similar differences were observed in SI and TI, in which MHE patients showed higher number of errors and lower hits, respectively, than either NMHE patients (p = 0.036 and p < 0.001, respectively) or controls (p < 0.001), without significant differences between NMHE and controls. Additionally, no significant between-group differences were found in LTI (Table 2).
In visuomotor and bimanual coordination tests, MHE patients also showed poor performance compared with NMHE patients (p < 0.001) and controls (p < 0.001), without significant differences between NMHE and controls (Table 2).
Regarding HRQoL, no significant between-group differences were found in SPH. In SMH, there were no significant differences between MHE patients and NMHE patients or controls, but NMHE patients reported significantly better SMH than controls (p = 0.033) (Table 2).

Relationship between ammonia levels and EHC indices

Results showed that higher ammonia levels were associated with worse AI (p = 0.003) TI (p = 0.040), and SI (p = 0.006) and longer execution time in BC (p = 0.025). However, LTI and VC were not linked with blood ammonia (Table 3).
Table 3
Relationship between blood ammonia levels and eye-hand coordination indices
 
ΔR2
B
p
Aiming index
0.165
  
Ammonia
 
− 0.296
0.003
Sex
 
− 0175
0.063
Educational level
 
0.071
0.447
Age
 
− 0.273
0.004
Linear tracking index
0.007
  
Ammonia
 
− 0.130
0.188
Sex
 
− 0.023
0.814
Educational level
 
0.102
0.301
Age
 
0.044
0.657
Steadiness index
0.052
  
Ammonia
 
0.273
0.006
Sex
 
− 0.109
0.275
Educational level
 
− 0.096
0.968
Age
 
− 0.016
0.870
Tapping index
0.157
  
Ammonia
 
− 0.190
0.040
Sex
 
0.034
0.717
Educational level
 
0.157
0.091
Age
 
− 0.343
0.001
Visuomotor coordination
0.122
  
Ammonia
 
0.114
0.217
Sex
 
0.162
0.082
Educational level
 
− 0.137
0.141
Age
 
0.290
0.002
Bimanual coordination
0.145
  
Ammonia
 
0.206
0.025
Sex
 
0.100
0.277
Educational level
 
− 0.161
0.081
Age
 
0.284
0.002
∆R2 R square change. Significant P values (p < 0.05) are in bold

Relationship between ammonia and HRQoL: the role of sex

To test associations between ammonia and both SPH and SMH, linear regression analyses were performed. In Model 1, sex was a significant predictor for both SPH (p = 0.008) and SMH (p < 0.001) (Table 4). Age and educational level showed no significant relationships with SPH or with SMH (Table 4). Model 2 incorporated blood ammonia levels, but no significant changes were observed in the explained variance for either SPH (∆R2 = 0.000) or SMH (∆R2 = 0.001). The regression coefficients for ammonia were not significant for either dimension of HRQoL (Table 4).
Table 4
Relationship between blood ammonia and subjective physical and mental health across all groups
 
Subjective Physical Health
Subjective Mental Health
 
R2
∆ R2
B
p
R2
∆ R2
B
p
Model 1
0.269
0.072**
  
0.33
0.11***
  
Age
  
0.055
0.589
  
0.132
0.183
Sex
  
0.271
0.008
  
0.337
 < 0.001
Educational level
  
− 0.003
0.977
  
− 0.088
0.366
Model 2
0.270
0.000
  
0.338
0.001
  
Ammonia
  
− 0.017
0.866
  
0.025
0.793
R2 R square, ∆R2 R square change. **p < 0.01; *** p < 0.001 Significant P values (p < 0.05) are in bold
However, the moderated moderation analysis revealed significant X × W × Z interactions between ammonia levels and SPH (p = 0.016) (Table 5; Fig. 1). Specifically, higher ammonia levels were associated with lower SPH, but this effect was only significant in women with MHE (p = 0.039). No significant association between blood ammonia levels and SPH was observed in the NMHE, regardless of sex. As regards SMH, similar X × W × Z interactions were found (p = 0.005), significant only in women with MHE (p = 0.011). No significant association was observed for SMH in the NMHE group, independently of sex (Table 5, Fig. 1 and Supplementary Table 2).
Table 5
Moderated moderation analysis between blood ammonia levels and subjective physical and mental health in MHE and NMHE groups
X variable: Ammonia levels
Y variable
effect
statistics
SPH
ΔR2 interaction = 0.058 F = 6.031, df (1,88) = 179.21 p = 0.016 LLCI = 34.19 ULCI = 324.224
 
B
SE
t
p
CI 95%
 
Interactions
      
Test of conditional ammonia X group by sex
   
 
Men
30.613
  
0.381
 
 
Women
− 148.596
  
0.023
 
Conditional effect of SPH depending on sex and group
   
Without MHE
Men
− 1.942
17.095
− 0.114
0.910
− 35.91, 32.03
Without MHE
Women
29.015
39.242
0.739
0.462
− 48.97, 107.00
MHE
Men
28.671
33.077
0.867
0.388
− 37.06, 94.40
MHE
Women
− 119.581
56.903
− 2.102
0.039
− 232.66, − 6.50
SMH
ΔR2 interaction = 0.071 F = 8.026, df (1,88) = 6.709 p = 0.005, LLCI = 2.003 ULCI = 11.415
  
B
SE
t
p
CI 95%
 
Interactions
      
Test of conditional ammonia X group by sex
    
 
Men
0.457
  
0.686
 
 
Women
− 6.252
  
0.003
 
Conditional effect of SMH depending on group and sex
  
Without MHE
Men
0.076
0.555
0.137
0.891
− 1.03, 1.18
Without MHE
Women
1.433
1.274
1.126
0.263
− 1.10, 3.96
MHE
Men
0.533
1.073
0.496
0.621
− 1.60, 2.67
MHE
Women
− 4.819
1.847
− 2.610
0.011
− 8.49, − 1.15
∆R2 R square change, HRQoL health-related quality of life, CI confidence interval, MHE minimal hepatic encephalopathy, LLCI lower limit confidence interval, ULCI upper limit confidence interval, SPH subjective physical health, SMH subjective mental health, SE standard error. Significant P values (p < 0.05) are in bold

Relationship between EHC and HRQoL in cirrhotic patients: the role of sex

Linear regression analyses showed no associations between EHC outcomes with SPH or SMH (Table 6). However, results of moderated moderation analysis revealed significant X × W × Z interactions across several motor EHC outcomes with SPH and SMH (Table 7 and Supplementary Table 3).
Table 6
Relationship between hand–eye coordination and subjective physical and mental health
 
Subjective Physical Health
Subjective Mental Health
 
R2
∆ R2
B
p
R2
∆ R2
B
p
Model 1
0.271
0.073
  
0.342
0.117
  
Age
  
− 0.039
0.713
  
0.042
0.680
Sex
  
0.271
0.009
  
0.342
0.001
Educational level
  
− 0.014
0.893
  
− 0.107
0.283
Model 2
0.305
0.093
  
0.359
0.129
  
Aiming Index
  
− 0.059
0.610
  
0.032
0.748
Linear Tracking Index
  
− 0.040
0.716
  
− 0.026
0.792
Steadiness Index
  
− 0.067
0.546
  
− 0.038
0.707
Tapping Index
  
0.004
0.971
  
− 0.018
0.858
Visuomotor coordination
  
− 0.106
0.482
  
0.012
0.904
Bimanual coordination
  
0.123
0.378
  
0.077
0.441
R2 R square, ∆R2 R square change
Table 7
Moderated moderation analysis between hand–eye coordination outcomes and subjective physical and mental health in MHE and NMHE groups
X variable: Aiming index
    
B
SE
t
p
CI 95%
SPH
ΔR2 interaction = 0.0333 F = 3.368, df (1,86) = − 10.611 p = 0.070 LLCI = − 22.103 ULCI = 0.882
Without MHE
Men
 
0.413
3.409
0.121
0.904
− 6.363, 7.189
Without MHE
Women
 
− 1.082
2.083
− 0.520
0.605
− 5.22, 3.059
MHE
Men
 
6.391
5.464
1.170
0.245
− 4.471, 17.252
MHE
Women
 
− 5.716
3.496
− 1.635
0.106
− 12.665, 1.234
SMH
ΔR2 interaction = 0.0392 F = 4,189, df (1,86) = − 11.210 p = 0.044 LLCI = − 22.096 ULCI = − 0.322
Without MHE
Men
 
− 0.048
1.9737
− 0.024
0.981
− 3.971, 3.876
Without MHE
Women
 
2.0504
3.2292
-0.635
0.527
− 4.369, 8.470
MHE
Men
 
− 4.3137
3.3117
− 1.302
0.196
− 10.987, 2.269
MHE
Women
 
8.9936
5.1760
1.737
0.086
− 1.296, 19.283
X variable: Linear tracking index
    
B
SE
t
p
CI 95%
SPH
ΔR2 interaction = 0.051 F = 5.501, df (1,89) = − 337.184 p = 0.021 LLCI = − 622.617 ULCI = − 51.750
 
Without MHE
Men
 
4.886
19.053
0.256
0.798
− 32.97, 42.74
 
Without MHE
Women
 
− 361.314
137.441
− 2.629
0.010
− 634.41, − 88.22
 
MHE
Men
 
13.659
47.606
0.287
0.775
− 80.93, 108.25
 
MHE
Women
 
− 15.357
17.354
− 0.885
0.379
− 49.84, 19.13
SMH
ΔR2 interaction = 0.050 F = 5.623, df (1,89) = − 326.73 p = 0.020 LLCI = − 600.764 ULCI = − 50.699
Without MHE
Men
 
4.528
18.292
0.248
0.805
-31.82, 40.87
Without MHE
Women
 
− 357.076
131.951
− 2.706
0.008
− 619.26,− 94.89
MHE
Men
 
24.222
45.704
0.530
0.598
− 66.59, 115.03
MHE
Women
 
− 10.651
16.661
− 0.639
0.524
− 43.76, 22.45
X variable: Steadiness index
SPH
ΔR2 interaction = 0.045 F = 4.800, df (1,84) = 8.543, p = 0.031, LLCI = 0.792 ULCI = 16.293
 
Without MHE
Men
 
0.098
1.048
0.093
0.926
-1.99, 2.18
Without MHE
Women
 
2.002
2.262
0.885
0.379
-2.49, 6.50
MHE
Men
 
− 2.050
1.743
− 1.177
0.243
− 5.52, 1.42
MHE
Women
 
− 8.689
3.265
− 2.661
0.009
− 15.18, − 2.20
SMH
ΔR2 interaction = 0.063 F = 7.294, df (1,84) = 9.833, p = 0.008, LLCI = 2.593 ULCI = 17.074
Without MHE
Men
 
0.0057
0.979
0.006
0.996
− 1.94, 1.95
Without MHE
Women
 
1.623
2.114
0.768
0.445
− 2.58, 5.83
MHE
Men
 
− 1.629
1.628
− 1.001
0.320
− 4.87, 1.61
MHE
Women
 
− 9.856
3.051
− 3.228
0.002
− 15.91, − 3.78
X variable: Tapping index
SPH
ΔR2 interaction = 0.0566 F = 6.211, df (1,84) = − 7.698, p = 0.015, LLCI = − 13.841 ULCI = − 1.556
 
Without MHE
Men
 
− 0.320
0.617
− 0.519
0.605
− 1.55, 0.91
Without MHE
Women
 
− 2.593
1.655
− 1.567
0.121
− 5.88, 0.70
MHE
Men
 
1.547
0.903
1.714
0.090
− 0.25, 3.34
MHE
Women
 
6.973
3.264
2.136
0.036
0.48, 13.46
SMH
ΔR2 interaction = 0.063 F = 7.869, df (1,87) = − 7.856, p = 0.006, LLCI = − 13.423 ULCI = − 2.290
Without MHE
Men
 
− 0.325
0.561
− 0.579
0.564
− 1.44, 0.79
Without MHE
Women
 
− 2.589
1.532
− 1.691
0.095
− 5.63, 0.46
MHE
Men
 
1.434
0.828
1.732
0.086
− 0.21, 3.08
MHE
Women
 
7.027
2.965
2.369
0.020
1.13, 12.92
X variable: Visuomotor coordination
SPH
ΔR2 interaction = 0.0312 F = 3.369, df (1,88) = -8.975 p = 0.069, LLCI = -19.814 ULCI = 1.865
 
Without MHE
Men
 
25.660
31.915
0.8040
0.423
− 37.764, 89.086
Without MHE
Women
 
108.405
58.607
18.497
0.068
− 8.065, 224.874
MHE
Men
 
− 22.821
28.416
− 0.8031
0.424
− 79.293, 33.650
MHE
Women
 
− 104.091
73.971
− 14.072
0.163
− 251.093, 42.911
SMH
ΔR2 interaction = 0.0469 F = 5.2436, df (1,88) = 195.936, p = 0.024 LLCI = 25.892 ULCI = 365.979
Without MHE
Men
 
11.576
30.560
0.379
0.706
− 49.16, 72.31
Without MHE
Women
 
91.905
56.120
1.638
0.105
− 19.62, 203.43
MHE
Men
 
− 22.437
27.211
− 0.825
0.412
− 76.51, 31.64
MHE
Women
 
− 138.044
70.832
− 1.949
0.055
− 278.81, 2.72
X variable: Bimanual coordination
  
B
SE
t
p
CI 95%
SPH
ΔR2 interaction = 0.077 F = 8.997, df (1,88) = 431.142, p = 0.004 LLCI = − 145.490 ULCI = 716.784
 
Without MHE
Men
 
90.226
38.853
2.322
0.023
13.01, 167.44
Without MHE
Women
 
177.155
85.918
2.062
0.042
6.41, 347.90
MHE
Men
 
15.475
21.263
0.728
0.469
− 26.78, 57.73
MHE
Women
 
− 328.737
128.481
− 2.559
0.012
− 584.07, − 73.41
SMH
ΔR2 interaction = 0.059 F = 7.035, df (1,88) = − 371.922 p = 0.010 LLCI = 93.212 ULCI = 650.573
 
B
SE
t
p
CI 95%
Without MHE
Men
 
81.401
37.903
2.148
0.035
6.07, 156.73
Without MHE
Women
 
146.223
83.815
1.745
0.085
− 20.34, 312.79
MHE
Men
 
5.179
20.336
0.249
0.803
− 36.04, 46.40
MHE
Women
 
− 301.921
125.336
− 2.409
0.018
− 551.00, − 52.84
R2 R square, ∆R2 R square change, SPH subjective physical health, SMH subjective mental health, AI aiming index, LTI linear tracking index, SI steadiness index, TI tapping index, VC visuomotor coordination, BC bimanual coordination, LLCI lower limit confidence interval, ULCI upper limit confidence interval. **p < 0.01; *** p < 0.001
Regarding the LTI, women without MHE exhibited pronounced negative effects (p = 0.010 for SPH; p = 0.008 for SMH), whereas there was no significant association between LTI and SPH or SMH in the MHE group, independently of sex.
For the SI, associations were significant only in women with MHE (p = 0.009 for SPH; p = 0.002 for SMH). In contrast, no significant associations were observed in the NMHE group, regardless of sex.
As regards the TI, women with MHE exhibited positive interactions (p = 0.036 for SPH; p = 0.020 for SMH). No significant associations were found in the NMHE group.
In terms of BC, the direction of the interaction changed depending on the group and sex. For SPH, the relationship was positive in men (p = 0.023) and women (p = 0.042) without MHE, but negative in women with MHE (p = 0.012). For SMH, the relationship was positive in men without MHE (p = 0.035), but negative in women with MHE (p = 0.018).
No significant associations were found for the AI or VC with SPH (Table 7). For SMH, a significant X × W × Z interaction was found (AI: p = 0.044; VC: p = 0.024). However, post hoc analyses revealed that the conditional effects of VC or AI within specific groups (MHE and without MHE) and by sex did not reach statistical significance.

Discussion

The present study was aimed at exploring the relationship between blood ammonia levels, eye-hand coordination, minimal hepatic encephalopathy, and health-related quality of life, while also investigating the moderating influence of sex on these associations.
Our study revealed a significant association between elevated blood ammonia levels and impaired EHC performance among cirrhotic patients. Specifically, higher blood ammonia concentrations correlated with worse outcomes across multiple EHC tasks, including aiming, tapping, steadiness, and bimanual coordination. Furthermore, patients with MHE exhibited notably lower performance across most EHC tasks compared to patients without MHE and the control group.
Previous studies have highlighted slowness and inaccuracy in similar tasks, underscoring the disruption of motor control preceding physical frailty and reduced coordination among MHE patients [24, 47]. Other previous research, while not focusing specifically on EHC, has demonstrated increased variability in gripping force with the right hand and lateral pinch with both hands in patients with MHE [10, 48]. Further variations in motor performance also observed include increased variability in motor reaction times among MHE patients.
Blood ammonia levels play a crucial role in liver cirrhosis, as raised levels can lead to substantial neurological difficulties including motor impairment. Prior research in animal models of HE has underscored the impact of hyperammonemia in various neuronal areas, suggesting its contribution to the decline in motor function observed in cirrhotic patients with MHE [4951]. To our best knowledge, however, this study is among the first to explore this relationship in the specific context of fine motor skills and their implications in patient-perceived quality of life.
Interestingly, no significant associations of blood ammonia levels or EHC were found with either SPH or SMH. However, a significant interaction emerged when including sex as a moderator in the analysis. These findings suggest that while blood ammonia levels and EHC may not directly influence SPH or SMH in MHE patients, underlying factors such as sex may moderate the relationship between these variables and HRQoL, indicating that this relationship may be sex-specific.
The moderated moderation analysis revealed that this relationship was significant in women with MHE. Specifically, elevated ammonia levels were associated with lower scores in the SPH and SMH dimensions. From a biological perspective, women have been documented to exhibit greater susceptibility to neurocognitive alterations and higher comorbidity rates, likely due to differences in hepatic and cerebral metabolism [52]. Estrogen and other sex hormones have been shown to influence the neuroinflammatory response and astrocyte function, exacerbating the effects of ammonia accumulation in the brain [53, 54].
In our postmenopausal sample, however, the role of these hormones likely reflects the downstream effects of reduced estrogenic signaling rather than direct hormonal activity. This impaired estrogenic signaling, compounded by the absence of other factors critical for neuronal health, may amplify vulnerability to ammonia-induced astrocyte dysfunction [55]. Such dysfunction disrupts cerebral homeostasis and appears to result in greater neuropsychiatric impairments in women than in men. These findings highlight the importance of considering estrogen not as a primary contributor but as part of a complex cascade of interrelated factors that collectively lead to the neuropsychiatric impairments observed in this demographic. Additionally, hormonal fluctuations may further exacerbate the perception of fatigue and weakness, significantly impacting subjective quality of life in women.
Women with MHE also demonstrated stronger associations between some EHC deficits and poorer HRQoL outcomes compared to men, suggesting that women may be more sensitive to motor impairments. This finding is consistent with prior research suggesting that chronic conditions have a greater impact on HRQoL in women, possibly due to hormonal, inflammatory, or psychosocial factors [5659]. However, the associations between EHC and HRQoL were not consistent across all indices. Significant relationships between certain indices (e.g., tapping, steadiness and bimanual coordination) and both dimensions of HRQoL (SPH and SMH) were observed in women with MHE but not in men or non-MHE patients, whereas other indices, such as aiming and visuomotor coordination, showed no significant associations with HRQoL in women with MHE. These inconsistencies may reflect a varying sensitivity of EHC to the motor and cognitive deficits that impact HRQoL. Steadiness, tapping, and bimanual coordination assess fine motor skills and coordination, essential for performing daily activities that require successful spatial–temporal interactions [60, 61]. In contrast, visuomotor tracking tasks, (aiming and linear tracking) involve combining visual perception with motor execution such as following a moving target. They require continuous perceptual-motor regulation, and this regulation involves prospective control of action, based on exploiting control laws that minimize the gap between the actual behavior and the desired one [6264]. For instance, tapping, steadiness and bimanual coordination may capture fine motor control and stability under high cognitive demand, which may be more directly relevant to daily functioning and perceived quality of life in women.
A number of factors may help explain our observations. Women may rely more on this kind of fine motor skills in their daily activities if performing societally assigned roles such as caregiving or household tasks. As a result, deficits in these areas might appear more pronounced or distressing in women than men, affecting both their performance and perceived quality of life. Fine motor tasks like steadiness, tapping, and bimanual coordination demand precise control, stability, and coordination, which are sensitive to the subtle motor and cognitive disruptions caused by MHE. Women with MHE may exhibit greater impairments in these tasks due to sex-specific vulnerabilities in neural processing, heightened sensitivity to inflammation, and the interaction between motor and cognitive deficits. This heightened vulnerability may stem from biological factors that also make women more responsive to the detrimental cognitive and behavioral effects of chronic inflammation [65], underscoring the importance of considering sex differences when evaluating the broader impacts of MHE.
We also found significant interaction effects for linear tracking in women without MHE, who showed pronounced negative associations between this outcome and both SPH and SMH. These findings indicate that even in the absence of MHE, motor coordination deficits such as those measured by linear tracking may affect women’s perception of their overall quality of life. It suggests that difficulties in tasks requiring precise visuomotor tracking may interfere with daily activities and psychosocial functioning.
Our results agree with previous studies showing gender disparities in the impact of chronic conditions on quality of life [5659], but the factors which may explain this relationship are yet to be pinpointed. Specifically, women with chronic health conditions seem to report and experience poorer quality of life in the physical and psychological domains compared to men with chronic health conditions. Societal and cultural factors may contribute to this gender-specific association. Women may encounter distinct psychosocial stressors or utilize coping mechanisms differently from men, potentially impacting their perception and reporting of HRQoL in the context of cirrhosis. Particularly, societal expectations concerning gender roles may heighten this difference, as women often assume caregiving and household management responsibilities, which heavily rely on fine motor skills. Lastly, differences in coping mechanisms and responses to illness between genders may further elucidate the varying impact of EHC on quality of life perception.
Finally, an unexpected finding that poorer bimanual coordination performance (indicated by longer execution times) is associated with better SPH and SMH health in men without MHE warrants careful interpretation. This counterintuitive result suggests that factors beyond motor execution directly influence men’s perceptions of their HRQoL. Men may perceive slower task completion as caused by task complexity rather than personal limitations, framing it positively as evidence of persistence and effort. This mindset, emphasizing quality over speed, may mitigate negative emotional impacts and reinforce a sense of control. Additionally, slower coordination may not meaningfully affect functional independence in daily life, allowing men to maintain a positive view of their health despite worse performance. Future studies should investigate how men interpret motor performance and its relevance to their daily lives. Understanding these interpretations can help clarify the mechanisms driving this paradoxical relationship.
Overall, our study is not without limitations. Firstly, the sample size of cirrhotic patients, particularly women, was somewhat reduced compared to men and healthy volunteers. This could limit the generalizability of the findings; larger and more balanced samples, particularly in terms of sex distribution among cirrhotic patients, would provide a more robust basis for drawing conclusions. Nonetheless, it is important to note that this unbalanced number of women and men reflects the different prevalence of this illness between the two sexes. Another potential drawback is the lower smaller sample size of the control group than the patient group, although control subjects were age-matched with patients. Secondly, HRQoL assessment was based solely on self-report measures using the SF-36 questionnaire. While widely used and validated, self-reported measures may be influenced by various factors such as mood, perception, and cognitive biases. Incorporating objective measures like waist circumference, HRV, blood pressure, triglyceride levels, etc., or clinician-rated assessments of HRQoL, could offer more comprehensive insight. Thirdly, the study focused on hyperammonemia and EHC as predictors of HRQoL, but other potential confounding variables, such as comorbidities, medication use, socioeconomic status, and psychological factors, were not comprehensively assessed or controlled for in the analyses. Considering these factors in future studies could provide a more nuanced understanding of the determinants of HRQoL. Finally, longitudinal measures were not included, so causality between ammonia levels, motor dysfunction, and HRQoL cannot be established. Future research should include long-term follow-up to evaluate how fluctuations in ammonia levels affect the progression of motor symptoms and quality of life. Additionally, the inclusion of additional biomarkers such as systemic inflammation could shed more light on underlying pathophysiological mechanisms.

Conclusions

This study contributes significantly to the understanding of MHE and its impact on HRQoL in cirrhotic patients, by exploring the associations between hyperammonemia, EHC, and HRQoL while considering sex differences and MHE status. The findings of this study suggest that sex moderates the relationship between ammonia levels, EHC deficits, and HRQoL. Women with MHE are disproportionately affected, showing greater sensitivity to motor impairments and their impact on HRQoL. These impairments are evident in tasks requiring fine motor skills, such as precision, steadiness, and bimanual coordination, which are essential for daily functioning. The study underscores the importance of considering sex as a critical factor when evaluating neurological and quality-of-life outcomes in patients with MHE, highlighting the importance of considering biological, psychological, and social factors in the assessment and management of this population. Future research should address these disparities by incorporating larger, more diverse samples and exploring additional biomarkers to better understand the underlying mechanisms and inform targeted interventions. Future longitudinal studies with larger, more balanced samples are needed to confirm these findings and explore their clinical implications.

Declarations

Competing interests

The authors have no relevant financial or non-financial interests to disclose.

Ethical approval

Study protocols were approved by the Research Ethics Committees of Hospital Clinico Universitario and Arnau de Vilanova Hospital of Valencia, Valencia, Spain (approval code: 2018/210; approval date: 2 March 2018) and were in accordance with the ethical guidelines of the Helsinki Declaration.
Written informed consent was obtained from all individual participants included in the study.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://​creativecommons.​org/​licenses/​by/​4.​0/​.

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Literatuur
2.
go back to reference American Association for the Study of Liver Diseases and others. (2014). Hepatic encephalopathy in chronic liver disease: 2014 practice guideline by the European association for the study of the liver and the American association for the study of liver diseases. Journal of Hepatology, 61(3), 642–659. https://doi.org/10.1016/j.jhep.2014.05.042 American Association for the Study of Liver Diseases and others. (2014). Hepatic encephalopathy in chronic liver disease: 2014 practice guideline by the European association for the study of the liver and the American association for the study of liver diseases. Journal of Hepatology, 61(3), 642–659. https://​doi.​org/​10.​1016/​j.​jhep.​2014.​05.​042
3.
go back to reference Ferenci, P., Lockwood, A., Mullen, K., Tarter, R., Weissenborn, K., & Blei, A. T. (2002). Hepatic encephalopathy—definition, nomenclature, diagnosis, and quantification: Final report of the working party at the 11th World congresses of gastroenterology, Vienna, 1998. Hepatology, 35(3), 716–721.PubMed Ferenci, P., Lockwood, A., Mullen, K., Tarter, R., Weissenborn, K., & Blei, A. T. (2002). Hepatic encephalopathy—definition, nomenclature, diagnosis, and quantification: Final report of the working party at the 11th World congresses of gastroenterology, Vienna, 1998. Hepatology, 35(3), 716–721.PubMed
5.
go back to reference Nardone, R., Taylor, A. C., Höller, Y., Brigo, F., Lochner, P., & Trinka, E. (2016). Minimal hepatic encephalopathy: A review. Neuroscience research, 111, 1–12.PubMed Nardone, R., Taylor, A. C., Höller, Y., Brigo, F., Lochner, P., & Trinka, E. (2016). Minimal hepatic encephalopathy: A review. Neuroscience research, 111, 1–12.PubMed
9.
go back to reference Felipo, V., Ordoño, J. F., Urios, A., El Mlili, N., Giménez-Garzó, C., Aguado, C., González-Lopez, O., Giner-Duran, R., Serra, M. A., Wassel, A., Rodrigo, J. M., Salazar, J., & Montoliu, C. (2012). Patients with minimal hepatic encephalopathy show impaired mismatch negativity correlating with reduced performance in attention tests. Hepatology, 55(2), 530–539.PubMed Felipo, V., Ordoño, J. F., Urios, A., El Mlili, N., Giménez-Garzó, C., Aguado, C., González-Lopez, O., Giner-Duran, R., Serra, M. A., Wassel, A., Rodrigo, J. M., Salazar, J., & Montoliu, C. (2012). Patients with minimal hepatic encephalopathy show impaired mismatch negativity correlating with reduced performance in attention tests. Hepatology, 55(2), 530–539.PubMed
10.
go back to reference San Martín-Valenzuela, C., Borras-Barrachina, A., Gallego, J. J., Urios, A., Mestre-Salvador, V., Correa-Ghisays, P., Ballester, M. P., Escudero-García, D., Tosca, J., Montón, C., & Ríos, M. P. (2020). Motor and cognitive performance in patients with liver cirrhosis with minimal hepatic encephalopathy. Journal of Clinical Medicine, 9(7), 2154.PubMedPubMedCentral San Martín-Valenzuela, C., Borras-Barrachina, A., Gallego, J. J., Urios, A., Mestre-Salvador, V., Correa-Ghisays, P., Ballester, M. P., Escudero-García, D., Tosca, J., Montón, C., & Ríos, M. P. (2020). Motor and cognitive performance in patients with liver cirrhosis with minimal hepatic encephalopathy. Journal of Clinical Medicine, 9(7), 2154.PubMedPubMedCentral
11.
go back to reference Prasad, S., Dhiman, R. K., Duseja, A., Chawla, Y. K., Sharma, A., & Agarwal, R. (2007). Lactulose improves cognitive functions and health-related quality of life in patients with cirrhosis who have minimal hepatic encephalopathy. Hepatology, 45(3), 549–559.PubMed Prasad, S., Dhiman, R. K., Duseja, A., Chawla, Y. K., Sharma, A., & Agarwal, R. (2007). Lactulose improves cognitive functions and health-related quality of life in patients with cirrhosis who have minimal hepatic encephalopathy. Hepatology, 45(3), 549–559.PubMed
14.
go back to reference Groeneweg, M., Quero, J. C., De Bruijn, I., Hartmann, I. J., Essink-bot, M. L., Hop, W. C., & Schalm, S. W. (1998). Subclinical hepatic encephalopathy impairs daily functioning. Hepatology, 28(1), 45–49.PubMed Groeneweg, M., Quero, J. C., De Bruijn, I., Hartmann, I. J., Essink-bot, M. L., Hop, W. C., & Schalm, S. W. (1998). Subclinical hepatic encephalopathy impairs daily functioning. Hepatology, 28(1), 45–49.PubMed
16.
go back to reference Rabiee, A., Ximenes, R. O., Nikayin, S., Hickner, A., Juthani, P., Rosen, R. H., & Garcia-Tsao, G. (2021). Factors associated with health-related quality of life in patients with cirrhosis: A systematic review. Liver International, 41(1), 6–15.PubMed Rabiee, A., Ximenes, R. O., Nikayin, S., Hickner, A., Juthani, P., Rosen, R. H., & Garcia-Tsao, G. (2021). Factors associated with health-related quality of life in patients with cirrhosis: A systematic review. Liver International, 41(1), 6–15.PubMed
19.
go back to reference Les, I., Doval, E., Flavià, M., Jacas, C., Cárdenas, G., Esteban, R., Guardia, J., & Córdoba, J. (2010). Quality of life in cirrhosis is related to potentially treatable factors. European Journal of Gastroenterology & Hepatology, 22(2), 221–227. Les, I., Doval, E., Flavià, M., Jacas, C., Cárdenas, G., Esteban, R., Guardia, J., & Córdoba, J. (2010). Quality of life in cirrhosis is related to potentially treatable factors. European Journal of Gastroenterology & Hepatology, 22(2), 221–227.
20.
go back to reference Bao, Z. J., Qiu, D. K., Ma, X., Fan, Z. P., Zhang, G. S., Huang, Y. Q., Yu, X. F., & Zeng, M. D. (2007). Assessment of health-related quality of life in Chinese patients with minimal hepatic encephalopathy. World Journal of Gastroenterology: WJG, 13(21), 3003–3008.PubMedPubMedCentral Bao, Z. J., Qiu, D. K., Ma, X., Fan, Z. P., Zhang, G. S., Huang, Y. Q., Yu, X. F., & Zeng, M. D. (2007). Assessment of health-related quality of life in Chinese patients with minimal hepatic encephalopathy. World Journal of Gastroenterology: WJG, 13(21), 3003–3008.PubMedPubMedCentral
21.
go back to reference Marchesini, G., Bianchi, G., Amodio, P., Salerno, F., Merli, M., Panella, C., Loguercio, C., Apolone, G., Niero, M., Abbiati, R., Italian Study Group for Quality of Life in Cirrhosis. (2001). Factors associated with poor health-related quality of life of patients with cirrhosis. Gastroenterology, 120, 170–178.PubMed Marchesini, G., Bianchi, G., Amodio, P., Salerno, F., Merli, M., Panella, C., Loguercio, C., Apolone, G., Niero, M., Abbiati, R., Italian Study Group for Quality of Life in Cirrhosis. (2001). Factors associated with poor health-related quality of life of patients with cirrhosis. Gastroenterology, 120, 170–178.PubMed
23.
go back to reference Román, E., Córdoba, J., Torrens, M., Torras, X., Villanueva, C., Vargas, V., Guarner, C., & Soriano, G. (2011). Minimal hepatic encephalopathy is associated with falls. Official Journal of the American College of Gastroenterology ACG, 106, 476–482. Román, E., Córdoba, J., Torrens, M., Torras, X., Villanueva, C., Vargas, V., Guarner, C., & Soriano, G. (2011). Minimal hepatic encephalopathy is associated with falls. Official Journal of the American College of Gastroenterology ACG, 106, 476–482.
24.
go back to reference Felipo, V., Urios, A., Giménez-Garzó, C., Cauli, O., Andrés-Costa, M. J., González, O., Serra, M. A., Sánchez-González, J., Aliaga, R., Giner-Durán, R., & Belloch, V. (2014). Non invasive blood flow measurement in cerebellum detects minimal hepatic encephalopathy earlier than psychometric tests. World Journal of Gastroenterology, 20(33), 11815–11825.PubMedPubMedCentral Felipo, V., Urios, A., Giménez-Garzó, C., Cauli, O., Andrés-Costa, M. J., González, O., Serra, M. A., Sánchez-González, J., Aliaga, R., Giner-Durán, R., & Belloch, V. (2014). Non invasive blood flow measurement in cerebellum detects minimal hepatic encephalopathy earlier than psychometric tests. World Journal of Gastroenterology, 20(33), 11815–11825.PubMedPubMedCentral
26.
go back to reference Bard, C., Fleury, M., & Hay, L. (1990). Development of eye-hand coordination across the life span. Bard, C., Fleury, M., & Hay, L. (1990). Development of eye-hand coordination across the life span.
28.
go back to reference Casanova-Ferrer, F., García-Cena, C. E., Gallego, J. J., Fiorillo, A., Urios, A., Calvo-Córdoba, A., Ballester, M. P., Ríos, M. P., Durbán, L., Hidalgo, M. R., & García, F. (2022). Minimal hepatic encephalopathy is associated to alterations in eye movements. Scientific Reports, 12(1), 16837.PubMedPubMedCentral Casanova-Ferrer, F., García-Cena, C. E., Gallego, J. J., Fiorillo, A., Urios, A., Calvo-Córdoba, A., Ballester, M. P., Ríos, M. P., Durbán, L., Hidalgo, M. R., & García, F. (2022). Minimal hepatic encephalopathy is associated to alterations in eye movements. Scientific Reports, 12(1), 16837.PubMedPubMedCentral
29.
go back to reference Rega, D., Aiko, M., Peñaranda, N., Urios, A., Gallego, J. J., Giménez-Garzó, C., Casanova, F., Fiorillo, A., Cabrera-Pastor, A., San-Miguel, T., & Ipiens, C. (2021). Patients with minimal hepatic encephalopathy show altered thermal sensitivity and autonomic function. Journal of Clinical Medicine, 10(2), 1–8. Rega, D., Aiko, M., Peñaranda, N., Urios, A., Gallego, J. J., Giménez-Garzó, C., Casanova, F., Fiorillo, A., Cabrera-Pastor, A., San-Miguel, T., & Ipiens, C. (2021). Patients with minimal hepatic encephalopathy show altered thermal sensitivity and autonomic function. Journal of Clinical Medicine, 10(2), 1–8.
30.
go back to reference Urios, A., Mangas-Losada, A., Gimenez-Garzó, C., González-López, O., Giner-Durán, R., Serra, M. A., Noe, E., Felipo, V., & Montoliu, C. (2017). Altered postural control and stability in cirrhotic patients with minimal hepatic encephalopathy correlate with cognitive deficits. Liver International, 37(7), 1013–1022.PubMed Urios, A., Mangas-Losada, A., Gimenez-Garzó, C., González-López, O., Giner-Durán, R., Serra, M. A., Noe, E., Felipo, V., & Montoliu, C. (2017). Altered postural control and stability in cirrhotic patients with minimal hepatic encephalopathy correlate with cognitive deficits. Liver International, 37(7), 1013–1022.PubMed
31.
go back to reference Nardelli, S., Pentassuglio, I., Pasquale, C., Ridola, L., Moscucci, F., Merli, M., Mina, C., Marianetti, M., Fratino, M., Izzo, C., & Merkel, C. (2013). Depression, anxiety and alexithymia symptoms are major determinants of health related quality of life (HRQoL) in cirrhotic patients. Metabolic Brain Disease, 28, 239–243.PubMed Nardelli, S., Pentassuglio, I., Pasquale, C., Ridola, L., Moscucci, F., Merli, M., Mina, C., Marianetti, M., Fratino, M., Izzo, C., & Merkel, C. (2013). Depression, anxiety and alexithymia symptoms are major determinants of health related quality of life (HRQoL) in cirrhotic patients. Metabolic Brain Disease, 28, 239–243.PubMed
34.
go back to reference Eftekar, M. (2020). The association between hepatic encephalopathy/minimal hepatic encephalopathy and depressive and anxiety disorders: A systematic review. Australasian Psychiatry, 28(1), 61–65.PubMed Eftekar, M. (2020). The association between hepatic encephalopathy/minimal hepatic encephalopathy and depressive and anxiety disorders: A systematic review. Australasian Psychiatry, 28(1), 61–65.PubMed
36.
go back to reference Cauli, O., Rodrigo, R., Llansola, M., Montoliu, C., Monfort, P., Piedrafita, B., El Mlili, N., Boix, J., Agustí, A., & Felipo, V. (2009). Glutamatergic and gabaergic neurotransmission and neuronal circuits in hepatic encephalopathy. Metabolic Brain Disease, 24, 69–80.PubMed Cauli, O., Rodrigo, R., Llansola, M., Montoliu, C., Monfort, P., Piedrafita, B., El Mlili, N., Boix, J., Agustí, A., & Felipo, V. (2009). Glutamatergic and gabaergic neurotransmission and neuronal circuits in hepatic encephalopathy. Metabolic Brain Disease, 24, 69–80.PubMed
37.
go back to reference Laubenberger, J., Haussinger, D., Bayer, S., Gufler, H., Hennig, J., & Langer, M. (1997). Proton magnetic resonance spectroscopy of the brain in symptomatic and asymptomatic patients with liver cirrhosis. Gastroenterology, 112(5), 1610–1616.PubMed Laubenberger, J., Haussinger, D., Bayer, S., Gufler, H., Hennig, J., & Langer, M. (1997). Proton magnetic resonance spectroscopy of the brain in symptomatic and asymptomatic patients with liver cirrhosis. Gastroenterology, 112(5), 1610–1616.PubMed
39.
go back to reference Felipo, V., Urios, A., Montesinos, E., Molina, I., Garcia-Torres, M. L., Civera, M., Del Olmo, J. A., Ortega, J., Martinez-Valls, J., Serra, M. A., & Cassinello, N. (2012). Contribution of hyperammonemia and inflammatory factors to cognitive impairment in minimal hepatic encephalopathy. Metabolic Brain Disease, 27(1), 51–58.PubMed Felipo, V., Urios, A., Montesinos, E., Molina, I., Garcia-Torres, M. L., Civera, M., Del Olmo, J. A., Ortega, J., Martinez-Valls, J., Serra, M. A., & Cassinello, N. (2012). Contribution of hyperammonemia and inflammatory factors to cognitive impairment in minimal hepatic encephalopathy. Metabolic Brain Disease, 27(1), 51–58.PubMed
43.
go back to reference Alonso, J., Prieto, L., & Anto, J. M. (1995). La version espanola del SF-36 Health Survey (Cuestionario de Salud SF-36): Un instrumento para la medida de los resultados clínicos. Medicina Clínica (Barcelona), 104, 771–776. Alonso, J., Prieto, L., & Anto, J. M. (1995). La version espanola del SF-36 Health Survey (Cuestionario de Salud SF-36): Un instrumento para la medida de los resultados clínicos. Medicina Clínica (Barcelona), 104, 771–776.
46.
go back to reference Zwierko, T., Jedziniak, W., Lesiakowski, P., Śliwiak, M., Kirkiewicz, M., & Lubiński, W. (2019). Eye-hand coordination impairment in glaucoma patients. International Journal of Environmental Research and Public Health, 16(22), 4332.PubMedPubMedCentral Zwierko, T., Jedziniak, W., Lesiakowski, P., Śliwiak, M., Kirkiewicz, M., & Lubiński, W. (2019). Eye-hand coordination impairment in glaucoma patients. International Journal of Environmental Research and Public Health, 16(22), 4332.PubMedPubMedCentral
47.
go back to reference Mechtcheriakov, S., Graziadei, I. W., Kugener, A., Schuster, I., Mueller, J., Hinterhuber, H., Vogel, W., & Marksteiner, J. (2006). Motor dysfunction in patients with liver cirrhosis: Impairment of handwriting. Journal of Neurology, 253, 349–356.PubMed Mechtcheriakov, S., Graziadei, I. W., Kugener, A., Schuster, I., Mueller, J., Hinterhuber, H., Vogel, W., & Marksteiner, J. (2006). Motor dysfunction in patients with liver cirrhosis: Impairment of handwriting. Journal of Neurology, 253, 349–356.PubMed
50.
go back to reference Llansola, M., Arenas, Y. M., Sancho-Alonso, M., Mincheva, G., Palomares-Rodriguez, A., Doverskog, M., Izquierdo-Altarejos, P., & Felipo, V. (2024). Neuroinflammation alters GABAergic neurotransmission in hyperammonemia and hepatic encephalopathy, leading to motor incoordination. Mechanisms and therapeutic implications. Frontiers in Pharmacology, 15, 1358323.PubMedPubMedCentral Llansola, M., Arenas, Y. M., Sancho-Alonso, M., Mincheva, G., Palomares-Rodriguez, A., Doverskog, M., Izquierdo-Altarejos, P., & Felipo, V. (2024). Neuroinflammation alters GABAergic neurotransmission in hyperammonemia and hepatic encephalopathy, leading to motor incoordination. Mechanisms and therapeutic implications. Frontiers in Pharmacology, 15, 1358323.PubMedPubMedCentral
51.
go back to reference Ong, J. P., Aggarwal, A., Krieger, D., Easley, K. A., Karafa, M. T., Van Lente, F., Arroliga, A. C., & Mullen, K. D. (2003). Correlation between ammonia levels and the severity of hepatic encephalopathy. The American Journal of Medicine, 114(3), 188–193.PubMed Ong, J. P., Aggarwal, A., Krieger, D., Easley, K. A., Karafa, M. T., Van Lente, F., Arroliga, A. C., & Mullen, K. D. (2003). Correlation between ammonia levels and the severity of hepatic encephalopathy. The American Journal of Medicine, 114(3), 188–193.PubMed
52.
go back to reference Pemmasani, G., Tremaine, W. J., Kumar, V. C. S., Aswath, G., Sapkota, B., Karagozian, R., & John, S. (2023). Sex differences in clinical characteristics and outcomes associated with alcoholic hepatitis. European Journal of Gastroenterology & Hepatology, 35(10), 1192–1196. Pemmasani, G., Tremaine, W. J., Kumar, V. C. S., Aswath, G., Sapkota, B., Karagozian, R., & John, S. (2023). Sex differences in clinical characteristics and outcomes associated with alcoholic hepatitis. European Journal of Gastroenterology & Hepatology, 35(10), 1192–1196.
54.
go back to reference Macedo de Oliveira, M., Monnet-Aimard, A., Bosoi, C. R., Tremblay, M., & Rose, C. F. (2022). Sex is associated with differences in oxidative stress and susceptibility to severe hepatic encephalopathy in bile-duct ligated rats. Journal of Neurochemistry, 2022(162), 337–351. https://doi.org/10.1111/jnc.15661 Macedo de Oliveira, M., Monnet-Aimard, A., Bosoi, C. R., Tremblay, M., & Rose, C. F. (2022). Sex is associated with differences in oxidative stress and susceptibility to severe hepatic encephalopathy in bile-duct ligated rats. Journal of Neurochemistry, 2022(162), 337–351. https://​doi.​org/​10.​1111/​jnc.​15661
55.
go back to reference Brown, C. M., Choi, E., Xu, Q., Vitek, M. P., & Colton, C. A. (2008). The APOE4 genotype alters the response of microglia and macrophages to 17β-estradiol. Neurobiology of Aging, 29(12), 1783–1794.PubMed Brown, C. M., Choi, E., Xu, Q., Vitek, M. P., & Colton, C. A. (2008). The APOE4 genotype alters the response of microglia and macrophages to 17β-estradiol. Neurobiology of Aging, 29(12), 1783–1794.PubMed
58.
go back to reference Orfila, F., Ferrer, M., Lamarca, R., Tebe, C., Domingo-Salvany, A., & Alonso, J. (2006). Gender differences in health-related quality of life among the elderly: The role of objective functional capacity and chronic conditions. Social Science & Medicine, 63(9), 2367–2380. Orfila, F., Ferrer, M., Lamarca, R., Tebe, C., Domingo-Salvany, A., & Alonso, J. (2006). Gender differences in health-related quality of life among the elderly: The role of objective functional capacity and chronic conditions. Social Science & Medicine, 63(9), 2367–2380.
62.
go back to reference Gibson, J. J. (1979). The ecological approach to visual perception, the ecological approach to visual perception. Houghton Mifflin and Company. Gibson, J. J. (1979). The ecological approach to visual perception, the ecological approach to visual perception. Houghton Mifflin and Company.
Metagegevens
Titel
Blood ammonia and eye-hand coordination negatively affect health-related quality of life in women with minimal hepatic encephalopathy
Auteurs
Daniela Batallas
Juan José Gallego
Franc Casanova-Ferrer
Alessandra Fiorillo
Pablo Rivas-Diaz
Adrià López-Gramaje
Yaiza M. Arenas
Luis Aparicio
Desamparados Escudero-García
Lucía Durbán
María-Pilar Rios
Salvador Benlloch
Amparo Urios
Vanesa Hidalgo
Carmina Montoliu
Alicia Salvador
Publicatiedatum
01-04-2025
Uitgeverij
Springer New York
Gepubliceerd in
Quality of Life Research
Print ISSN: 0962-9343
Elektronisch ISSN: 1573-2649
DOI
https://doi.org/10.1007/s11136-025-03920-3