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Record W7117321800 · doi:10.30978/mg-2025-4-107

Cognitive impairment in patients with moderate and advanced liver fibrosis in the background of metabolic dysfunction-associated steatotic liver disease

2025· article· W7117321800 on OpenAlexaboutno aff
I. Y. Hospodarskyy, S. I. Hospodarska

Bibliographic record

VenueModern Gastroenterology · 2025
Typearticle
Language
FieldMedicine
TopicLiver Disease Diagnosis and Treatment
Canadian institutionsnot available
Fundersnot available
KeywordsMontreal Cognitive AssessmentPhysical examinationCognitionLiver diseaseLiver fibrosisCognitive impairmentFatty liverDisease

Abstract

fetched live from OpenAlex

Objective — to study cognitive impairment in patients with moderate and advanced liver fibrosis due to metabolically associated steatotic liver disease (MASLD) using various cognitive tests, as well as to investigate possible ways to correct such disorders. Materials and methods. A total of 86 patients (43 men and 43 women aged 24 to 55 years) were examined, in whom the diagnosis of MASLD with fibrosis of the 2nd (46 people) and 3rd (40 people) degrees was confirmed. Patients underwent an initial (screening) clinical, psychometric and laboratory examination before the start of treatment, as well as a repeat examination after 1 month. At the beginning of the observation, these patients were randomized into 2 groups, matched by age, gender and severity of clinical manifestations. 43 patients in group 1 received standard recommendations for patients with MASLD, which included advice on lifestyle changes (diet and physical activity). Patients in group 2 (43 people) additionally received Hepamerz (L-ornithine-L-aspartate) 1 sachet (3 g) 2 times a day with meals for 1 month. Non-invasive psychometric tests were used during the study. Each patient underwent standardized tests for objective assessment of cognitive functions. The tests were selected in collaboration with a clinical psychologist. Each participant underwent evaluation in a separate, quiet examination room with a qualified research assistant. The assessment was carried out in the following order: Mini-Mental State Examination (MMSE), Montreal Cognitive Assessment (MoCA), 10-point clock drawing test. Statistical analysis was performed using Statistica software. Results. The vast majority of them did not have characteristic complaints from the digestive system, most of them actively complained only about physical weakness and fatigue. As for cognitive changes and decreased mental performance, most of them associated this group of symptoms with such causes as stress, lack of sleep, prolonged overload. Patients reported such changes mostly only when actively questioned by the doctor. Changes in laboratory liver tests were also mild and uncharacteristic in such patients. The use of standard cognitive tests revealed mild cognitive impairment even in patients with moderate liver fibrosis. The most sensitive for their detection was the 10-point clock test, the MoCA test was less effective. The standard MMSE test was practically uninformative for detecting minimal cognitive impairment. We conducted these tests again after the patient read the text aloud for 15 minutes. This modification allowed us to objectively detect the phenomenon of rapid cognitive fatigue. In healthy volunteers, such cognitive load had practically no effect on the performance of all three tests. In contrast, patients with moderate liver fibrosis showed a sharp decrease in the performance of all three tests (p < 0.05). In patients with advanced liver fibrosis (F3), the performance of cognitive tests was reduced to a much greater extent than in F2. At the screening stage, all results were significantly lower compared to the data of the control group (p < 0.05). These indicators were even lower when conducting cognitive tests after 15-minute reading aloud of the text by the patient (p < 0.05). The use of L-ornithine-L-aspartate 1 sachet (3 g) 2 times a day during meals for 1 month contributed to a significant improvement in cognitive performance in patients with MASLD. The indicated therapeutic effect was faster in patients with moderately severe liver fibrosis, indicating the potential advantage of earlier prescription of the drug. Conclusions. The presence of MASLD is accompanied by mild cognitive impairment even in the presence of moderately severe fibrotic changes in the liver (F2). The 10-point clock test turned out to be the most sensitive for their detection. Patients with moderately expressed fibrotic changes in the liver (F2) show rapid cognitive fatigue, which can be effectively detected by using the above-mentioned cognitive tests after 15-minute reading of the text. Such changes can significantly affect the working capacity of patients, especially in the case of intellectual activities or professions that require constant attention and concentration. In the case of advanced liver fibrosis (F3), almost all examined patients showed not only rapid cognitive fatigue, but also a significant decrease in the results of all cognitive tests we used. The changes we detected corresponded to the stage of moderate cognitive impairment, which can disrupt not only professional activities, but also everyday life and social adaptation of such patients. The use of L-ornithine-L-aspartate for 1 month significantly improved cognitive performance in patients with MASLD. The therapeutic effect was more rapid in patients with moderate liver fibrosis.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.005

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0020.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.008
GPT teacher head0.229
Teacher spread0.220 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2025
Admission routes1
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