Evidence mapPaperPMID 40909065Full record

ArticleCureus2025

Genetic Association and Causal Effects Between Obesity and Multiple Sclerosis: A Robust Two-Sample Mendelian Randomization Study.

Abdulaziz Almosallam

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In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Abdulaziz AlmosallamInternal Medicine, Majmaah University, Al Majma'ah, SAU.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA relationship between obesity, as measured by body mass index (BMI), and multiple sclerosis (MS) has been reported in several observational studies. This study aimed to investigate the potential causal relationship between BMI and the risk of developing MS using a Mendelian randomization (MR) approach. MATERIALS AND

methodsA two-sample MR analysis was performed using single nucleotide polymorphisms (SNPs) associated with the exposures - BMI and MS - sourced from publicly available genome-wide association studies (GWAS) at a genome-wide significance threshold of

resultsThe MR analysis revealed a causal effect of BMI on MS as indicated by IVW (odds ratio (OR) = 1.39; 95% confidence interval (CI) = 1.23, 1.58; P = 1.42e-07), IVW method with modified second-order weights (IVW (Mod.2nd)) (OR = 1.39; 95% CI = 1.28, 1.51; P = 2.31e-15), MR-Egger (OR = 1.39; 95% CI = 1.01, 1.92; P = 4.51e-02), MR-Genotype Recoding Invariance Property (MR-GRIP) (OR = 1.41; 95% CI = 1.21, 1.65; P = 1.80e-05), MR-PRESSO (OR = 1.39; 95% CI = 1.28, 1.51; P = 3.79e-14), MR-RAPS (OR = 1.39; 95% CI = 1.24, 1.56; P = 2.66e-08), and GSMR (OR = 1.38; 95% CI = 1.23, 1.55; P = 3.35e-08). No evidence of horizontal pleiotropy or heterogeneity was detected, and the findings were confirmed to be robust.

conclusionThis study provides evidence that an increase in body size (BMI) can lead to MS. Therefore, maintaining a healthy weight during early life could be a potential strategy to reduce MS risk.

Indexed as

body mass indexcausal effectsgenetic associationmendelian randomizationmultiple sclerosis

Identifiers

PMID40909065
PMCPMC12406069

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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 Socratic graph.