Evidence map›Paper›PMID 42668868›Full record

ArticleClinical, cosmetic and investigational dermatology2026

Body Mass Index and Facial Aging: Mendelian Randomization and Exploratory Target Prioritization.

Yuan Hu, Ke-Han Li, Ming-Jie He, Chun-Shui Yu, Shao-Bo Wang

Abstract read
In one paragraph

Article in Clinical, cosmetic and investigational dermatology, 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
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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

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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

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

5 authors.

Yuan Hu *Department of Dermatology, Suining Central Hospital, Suining, Sichuan, People's Republic of China.ORCID 0000-0003-2188-5920
Ke-Han Li *Department of Dermatology, Suining Central Hospital, Suining, Sichuan, People's Republic of China.
Ming-Jie HeDepartment of Dermatology, First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, People's Republic of China.ORCID 0009-0008-7803-1559
Chun-Shui YuDepartment of Dermatology, Suining Central Hospital, Suining, Sichuan, People's Republic of China.
Shao-Bo WangDepartment of Gastrointestinal Surgery, Suining Central Hospital, Suining, Sichuan, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Facial aging reflects genetic, metabolic, and environmental influences. Although obesity has been associated with older perceived facial age, the shared genetic basis and direction of the BMI-facial aging relationship remain uncertain. Objective: To evaluate genetic correlations between facial aging and 15 metabolic traits, assess bidirectional associations by Mendelian randomization (MR), and conduct exploratory locus, gene, and compound prioritization. Methods: Public genome-wide association study (GWAS) summary statistics were analyzed using linkage disequilibrium score regression (LDSC) and bidirectional MR with inverse-variance weighted (IVW), weighted median, MR-Egger, and MR-PRESSO methods. Because BMI showed the most consistent signal, related loci were evaluated by fine-mapping, colocalization, ANNOVAR, MAGMA, and GCTA-fastBAT. DGIdb screening and molecular docking were used for hypothesis generation. Results: BMI showed the strongest genetic correlation with facial aging (rg = 0.215; FDR-adjusted P = 3.94×10 Limitations: The facial-aging phenotype was perception-based, the GWAS datasets were predominantly of European ancestry and may have partially overlapping samples, and all downstream analyses were computational. Conclusion: Higher BMI may contribute to perceived facial aging, but these findings do not show that BMI reduction or any candidate compound improves facial aging. Metabolic health is the more clinically actionable implication, whereas the prioritized genes and compounds remain exploratory and require functional validation.

Indexed as

body mass indexfacial aginggene prioritizationgenetic correlationMendelian randomizationmolecular dockingobesity

Identifiers

PMID42668868
PMCPMC13525796

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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.