Evidence mapPaperPMID 42407119Full record

ArticleBriefings in bioinformatics2026

METEOR: a data-adaptive Mendelian randomization method for powerful detection of shared and specific exposures underlying multiple outcomes.

Liye Zhang, Ran Yan, Weiming Gong, Xiang Zhou, Lu Liu, Zhongshang Yuan

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2026. 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

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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

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5 · Who and what money

Authors and funding

6 authors.

Liye ZhangDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0000-0003-4207-0536
Ran YanDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.
Weiming GongDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.
Xiang ZhouDepartment of Biostatistics, University of Michigan, Ann Arbor, MI 48109, United States.
Lu LiuDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.
Zhongshang YuanDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, Jinan, Shandong 250012, China.ORCID 0000-0002-3527-4488

Funding

National Natural Science Foundation of China 82373686Natural Science Foundation of Shandong Province ZR2024JQ029Scientific Research Innovation Capability Support Project for Young Faculty SRICSPYF-ZY2025123Shandong Excellent Young Scientists Fund Program 2026HWYQ-022Taishan Scholar Project of Shandong Province tsqn202211025
6 · The paper itself

Abstract

Accurate identification of causal exposures for multimorbidity can benefit the co-prevention and co-management of multiple-related outcomes. This goal can be conceptually addressed within a multi-outcome Mendelian randomization (MR) framework. However, existing multi-outcome MR methods suffer from restrictions on format and availability of data inputs, fail to account for the potential sample overlap, rely on pre-selected independent instrumental variables (IVs), and are unable to account for horizontal pleiotropy. Here, we propose METEOR, a novel MR method that jointly models one exposure and multiple outcomes to identify both shared and outcome-specific causal exposures. METEOR accounts for sample overlap between exposure and outcomes, allows outcomes from different genome-wide association studies (GWAS) datasets, self-adaptively determines IVs from correlated single-nucleotide polymorphisms, and explicitly models horizontal pleiotropy. Using summary statistics, METEOR infers causal effects under a joint-likelihood framework with a scalable, sampling-based algorithm. Simulations show that METEOR presents well-calibrated $P$-values for both global and single-outcome tests, and achieves average power improvements of 55.33% and 56.50% over five existing MR methods in the global and single tests, respectively. In real data applications, METEOR produces the most accurate causal effect estimates in positive control analyses, reduces false positives by 18.75% in negative control analyses, and highlights that controlling BMI could benefit the co-management of multiple cardiovascular diseases (CVDs) and multiple gastrointestinal (GI) diseases, while controlling blood pressure could benefit the co-management of multimorbidity across CVDs and mental disorders (MDs), as well as across GI diseases and MDs.

Indexed as

Mendelian Randomization AnalysisAlgorithmsGenome-Wide Association StudyHumansPolymorphism, Single Nucleotidelikelihoodmultimorbiditymultiple-outcomes Mendelian randomizationself-adaptive determination of instrumental variable

Identifiers

PMID42407119
PMCPMC13336660

What Socratic holds

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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.