Evidence map›Paper›PMID 38227760›Full record

ArticleThe journals of gerontology. Series A, Biological sciences and medical sciences2024

Late-Life Metabolic Dysfunction-Associated Steatotic Liver Disease and its Association With Physical Disability and Dementia.

Daniel Clayton-Chubb, William W Kemp, Ammar Majeed, Robyn L Woods, Joanne Ryan, Anne M Murray, Trevor T J Chong, John S Lubel, Cammie Tran, Alexander D Hodge and 3 more

Abstract read
In one paragraph

Article in The journals of gerontology. Series A, Biological sciences and medical sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Daniel Clayton-ChubbDepartment of Gastroenterology, Alfred Health, Melbourne, Victoria, Australia.ORCID 0000-0001-7479-9669
William W KempDepartment of Gastroenterology, Alfred Health, Melbourne, Victoria, Australia.
Ammar MajeedDepartment of Gastroenterology, Alfred Health, Melbourne, Victoria, Australia.
Robyn L WoodsSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.ORCID 0000-0003-1249-6149
Joanne RyanSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.ORCID 0000-0002-7039-6325
Anne M MurrayBerman Center for Outcomes and Clinical Research and Department of Medicine, Geriatrics Division, Hennepin Healthcare Research Institute, Minneapolis, Minnesota, USA.
Trevor T J ChongTurner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Melbourne, Victoria, Australia.ORCID 0000-0001-7764-3811
John S LubelDepartment of Gastroenterology, Alfred Health, Melbourne, Victoria, Australia.
Cammie TranSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
Alexander D HodgeDepartment of Medicine, Eastern Clinical School, Monash University, Melbourne, Victoria, Australia.
Hans G SchneiderSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.
John J McNeilSchool of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.ORCID 0000-0002-1049-5129
Stuart K RobertsDepartment of Gastroenterology, Alfred Health, Melbourne, Victoria, Australia.

Funding

ASPirin in Reducing Events in the ElderlyU01AG029824 · NIA · HENNEPIN HEALTHCARE RESEARCH INSTITUTE · PI MCNEIL, JOHN JAMES, MURRAY, ANNE M · 2009 to 2018
$64.6M
Main Administrative CoreU19AG062682 · NIA · HENNEPIN HEALTHCARE RESEARCH INSTITUTE · PI CHAN, ANDREW T, MCNEIL, JOHN JAMES · 2019 to 2023
$42.9M
NCI NIH HHSNCI NIH HHS 5U01AG029824-02NIA NIH HHSNIA NIH HHS U01 AG029824NIA NIH HHS U19 AG062682NIH HHS 5U01AG029824-02NIH HHS U01AG029824
6 · The paper itself

Abstract

backgroundThe burden of metabolic dysfunction-associated steatotic liver disease (MASLD) is growing rapidly, including among older adults. The number of older adults is also rising with concomitantly increasing rates of age-related physical and cognitive dysfunction. However, data on whether MASLD affects physical and cognitive function in older adults is limited. As such, we aimed to identify whether prevalent MASLD influences the risk of incident physical disability or dementia in initially healthy older adults.

methodsA post-hoc analysis of participants from the ASPREE-XT cohort study, which recruited community-dwelling older adults without a history of cardiovascular disease, dementia, or independence-limiting functional impairment. The Fatty Liver Index (to identify MASLD) was calculated in those with complete data. Cox proportional-hazards models were used to investigate the outcomes of dementia and persistent physical disability in participants with MASLD vs those without.

resultsOf the 9 097 individuals included (mean age 75.1 ± 4.2 years; 45.0% men), 341 (3.7%) developed persistent physical disability and 370 (4.1%) developed dementia over a median follow-up of 6.4 years (IQR 5.3-7.5 years). When adjusting for known contributors including age, gender, education, comorbidity, and functional measures, MASLD was associated with an increased risk of persistent physical disability (HR 1.41 [95% CI: 1.07-1.87]) and reduced risk of incident dementia (HR 0.63 [95% CI: 0.48-0.83]).

conclusionsPrevalent MASLD is associated with reduced rates of incident dementia but increased risk of persistent physical disability in initially relatively healthy older adults. Understanding the mechanisms underlying these divergent results to allow appropriate risk stratification and counseling is important.

Indexed as

Cardiovascular DiseasesDementiaFatty LiverAgedCohort StudiesFemaleHealth StatusHumansMaleAgingDisabilityEpidemiologyNonalcoholic fatty liver diseasePhysical function

Identifiers

PMID38227760
PMCPMC10923210

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.