Evidence map›Paper›PMID 38319411›Full record

ArticleAging clinical and experimental research2024

Association between inflammatory bowel disease and frailty: a two-sample Mendelian randomization study.

Jingyi Feng, Xi Chen, Wenjing Cai, Xueying Zhou, Xuefang Zhang

Abstract read
In one paragraph

Article in Aging clinical and experimental research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jingyi Feng *School of Nursing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Xi Chen *Hospital for Skin Diseases, Institute of Dermatology Chinese Academy of Medical Sciences, Peking Union Medical College, Nanjing, China.
Wenjing CaiSchool of Nursing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Xueying ZhouSchool of Nursing, Nanjing University of Chinese Medicine, Nanjing, Jiangsu, China.
Xuefang ZhangNanjing Hospital of Chinese Medicine Affiliated to Nanjing University of Chinese Medicine, Nanjing, 210022, China. 20211051@njucm.edu.cn.

Funding

Nanjing Health Science and Technology Development Special Funds Program YKK19100Postgraduate Research & Practice Innovation Program of Jiangsu Province SJCX23_0836
6 · The paper itself

Abstract

backgroundAn association has been identified between inflammatory bowel disease (IBD) and frailty; however, the causal nature of this connection remains uncertain. We consequently conducted a two-sample Mendelian randomization (MR) analysis to explore this particular association.

methodsWe acquired distinct datasets for inflammatory bowel disease (IBD), Crohn's disease (CD), ulcerative colitis (UC), and frailty from the published genome-wide association studies (GWAS) database, meticulously selecting instrumental variables (IVs). Subsequently, we employed a bidirection MR to examine the causal relationship between IBD (including CD and UC) and frailty. We utilized statistical methods, with a primary emphasis on inverse-variance weighted (IVW), accompanied by a series of sensitivity analyses to confirm heterogeneity and pleiotropy influenced the outcomes of the MR.

resultsWe found positive causal effects of genetically increased frailty risk on IBD (OR: 1.015, 95% CI 1.005-1.025, P = 0.004). Furthermore, when scrutinizing specific IBD subtypes, both Crohn's disease (CD) and ulcerative colitis (UC) demonstrated an increased predisposition to frailty (OR: 1.018, 95% CI 1.01-1.027, P < 0.05) and (OR = 1.016, 95% CI 1.005-1.027, P < 0.05). Nevertheless, despite the consistent trends observed in the weighted median and MR-Egger regression analyses for both conditions, statistical significance remained elusive. Notably, the results of the inverse MR analysis did not establish an association between frailty and an elevated risk of IBD development.

conclusionsOur research indicates that IBD, encompassing both CD and UC, may augment the propensity for frailty. Clinical practitioners must prioritize early frailty assessment in individuals afflicted with inflammatory bowel disease, inclusive of Crohn's disease and ulcerative colitis, facilitating proactive measures and timely interventions. However, our findings do not provide evidence supporting a causal effect of frailty on IBD (including CD and UC). Consequently, further studies are essential to explore the intricate mechanisms that clarify the effect of frailty on IBD.

Indexed as

Colitis, UlcerativeCrohn DiseaseFrailtyInflammatory Bowel DiseasesGenome-Wide Association StudyHumansMendelian Randomization AnalysisCausal relationshipFrailtyGenome-wide association studiesInflammatory bowel diseaseMendelian randomization

Identifiers

PMID38319411
PMCPMC10847216

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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.