Prevalence of polypharmacy and associated side effects in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD): a systematic review and meta-analysis

Objectives Metabolic dysfunction-associated steatotic liver disease (MASLD) is a prevalent chronic condition often accompanied by multiple comorbidities requiring complex pharmacological management. This review aims to examine the prevalence of polypharmacy in patients with MASLD, alongside an explo...

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Main Authors: Rajna Golubic, Peter Fitzgerald, Sumantra Ray, Sarah Armes, Jenneffer Tibaes, Ramya Rajaram, Mark W Ruddock, Mary Jo Kurth
Format: Article
Language:English
Published: BMJ Publishing Group
Series:BMJ Nutrition, Prevention & Health
Online Access:https://nutrition.bmj.com/content/early/2025/07/23/bmjnph-2025-001236.full
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author Rajna Golubic
Peter Fitzgerald
Sumantra Ray
Sarah Armes
Jenneffer Tibaes
Ramya Rajaram
Mark W Ruddock
Mary Jo Kurth
author_facet Rajna Golubic
Peter Fitzgerald
Sumantra Ray
Sarah Armes
Jenneffer Tibaes
Ramya Rajaram
Mark W Ruddock
Mary Jo Kurth
author_sort Rajna Golubic
collection DOAJ
description Objectives Metabolic dysfunction-associated steatotic liver disease (MASLD) is a prevalent chronic condition often accompanied by multiple comorbidities requiring complex pharmacological management. This review aims to examine the prevalence of polypharmacy in patients with MASLD, alongside an exploration of reported associations with side effects and observed relationships with patient-reported outcomes.Methods We conducted a systematic review using MEDLINE, CINAHL, Embase, Cochrane CENTRAL and Scopus databases, supplemented by a grey literature search, from inception to August 2024. Inclusion criteria were randomised controlled trials, cohort studies or case-control studies that evaluated the prevalence of polypharmacy and its consequences in adults with MASLD. Three reviewers independently performed study selection and data extraction. The quality of included studies was assessed using the Newcastle-Ottawa Scale. The primary outcome was the prevalence of polypharmacy, with secondary outcomes including side effects and quality of life (QoL). A meta-analysis with a random-effect model was performed.Results Six studies were included, of which three (totalling 2194 participants) were used in a meta-analysis. Polypharmacy prevalence ranged from 25% to 89%, with a pooled prevalence of 81% (95% CI 59 to 93), I²=99.5%. Adverse outcomes associated with polypharmacy included increased risk of hepatic encephalopathy-related hospitalisations, reduced QoL across physical and mental health domains, and augmented liver disease progression, particularly in individuals with advanced MASLD. Commonly used medications, such as anticholinergics and insulin, were linked to significant symptom burdens and metabolic dysregulation. Risk of bias assessments revealed that 50% of included studies had high risk due to limitations in study design, such as cross-sectional design and inconsistent definitions of polypharmacy, which reduced the certainty of evidence.Conclusions Polypharmacy is highly prevalent in MASLD and associated with poorer clinical outcomes and reduced QoL. Interventions such as deprescribing programmes and enhanced medication management strategies are needed to mitigate risks and optimise patient care.
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spelling doaj-art-c9f033602c95469286203e5fde5ddb132025-08-20T03:31:42ZengBMJ Publishing GroupBMJ Nutrition, Prevention & Health2516-554210.1136/bmjnph-2025-001236Prevalence of polypharmacy and associated side effects in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD): a systematic review and meta-analysisRajna Golubic0Peter Fitzgerald1Sumantra Ray2Sarah Armes3Jenneffer Tibaes4Ramya Rajaram5Mark W Ruddock6Mary Jo Kurth7NNEdPro Global Institute for Food Nutrition and Health, Cambridge, England, UKRandox Laboratories Ltd, Crumlin, Antrim, UK1 NNEdPro Global Institute for Food Nutrition and Health, Cambridge, UK2NNEdPro Global Institute for Food, Nutrition and Health, St John’s Innovation Centre, Cambridge, UK10NNEdPro Global Institute for Food, Nutrition and Health, Cambridge, UK2NNEdPro Global Institute for Food, Nutrition and Health, St John’s Innovation Centre, Cambridge, UKRandox Laboratories Ltd, Crumlin, Antrim, UKRandox Laboratories Ltd, Crumlin, Antrim, UKObjectives Metabolic dysfunction-associated steatotic liver disease (MASLD) is a prevalent chronic condition often accompanied by multiple comorbidities requiring complex pharmacological management. This review aims to examine the prevalence of polypharmacy in patients with MASLD, alongside an exploration of reported associations with side effects and observed relationships with patient-reported outcomes.Methods We conducted a systematic review using MEDLINE, CINAHL, Embase, Cochrane CENTRAL and Scopus databases, supplemented by a grey literature search, from inception to August 2024. Inclusion criteria were randomised controlled trials, cohort studies or case-control studies that evaluated the prevalence of polypharmacy and its consequences in adults with MASLD. Three reviewers independently performed study selection and data extraction. The quality of included studies was assessed using the Newcastle-Ottawa Scale. The primary outcome was the prevalence of polypharmacy, with secondary outcomes including side effects and quality of life (QoL). A meta-analysis with a random-effect model was performed.Results Six studies were included, of which three (totalling 2194 participants) were used in a meta-analysis. Polypharmacy prevalence ranged from 25% to 89%, with a pooled prevalence of 81% (95% CI 59 to 93), I²=99.5%. Adverse outcomes associated with polypharmacy included increased risk of hepatic encephalopathy-related hospitalisations, reduced QoL across physical and mental health domains, and augmented liver disease progression, particularly in individuals with advanced MASLD. Commonly used medications, such as anticholinergics and insulin, were linked to significant symptom burdens and metabolic dysregulation. Risk of bias assessments revealed that 50% of included studies had high risk due to limitations in study design, such as cross-sectional design and inconsistent definitions of polypharmacy, which reduced the certainty of evidence.Conclusions Polypharmacy is highly prevalent in MASLD and associated with poorer clinical outcomes and reduced QoL. Interventions such as deprescribing programmes and enhanced medication management strategies are needed to mitigate risks and optimise patient care.https://nutrition.bmj.com/content/early/2025/07/23/bmjnph-2025-001236.full
spellingShingle Rajna Golubic
Peter Fitzgerald
Sumantra Ray
Sarah Armes
Jenneffer Tibaes
Ramya Rajaram
Mark W Ruddock
Mary Jo Kurth
Prevalence of polypharmacy and associated side effects in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD): a systematic review and meta-analysis
BMJ Nutrition, Prevention & Health
title Prevalence of polypharmacy and associated side effects in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD): a systematic review and meta-analysis
title_full Prevalence of polypharmacy and associated side effects in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD): a systematic review and meta-analysis
title_fullStr Prevalence of polypharmacy and associated side effects in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD): a systematic review and meta-analysis
title_full_unstemmed Prevalence of polypharmacy and associated side effects in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD): a systematic review and meta-analysis
title_short Prevalence of polypharmacy and associated side effects in individuals with metabolic dysfunction-associated steatotic liver disease (MASLD): a systematic review and meta-analysis
title_sort prevalence of polypharmacy and associated side effects in individuals with metabolic dysfunction associated steatotic liver disease masld a systematic review and meta analysis
url https://nutrition.bmj.com/content/early/2025/07/23/bmjnph-2025-001236.full
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