Infectious diseases and sarcopenia-related phenotypes: A phenome-wide Mendelian randomization study with exploratory proteomic analysis.

Authors

Ang Li, Yongqian Fan

Published in

Experimental gerontology. Pages 113341. Sep 29, 2026. Epub Sep 29, 2026.

Abstract

Sarcopenia-related traits may be associated with infection-related disease liabilities, but broad phenome-wide genetic screening remains limited. We conducted a two-sample MR-PheWAS of more than 2000 FinnGen R12 phenome-wide endpoints against appendicular lean mass (ALM) and left-hand grip strength (HGS). Multiple testing was controlled using Benjamini-Hochberg false discovery rate (BH-FDR) correction applied separately to 2317 ALM and 2307 HGS primary-estimator tests. Twenty-one ALM endpoints and two HGS endpoints were FDR-significant; the two HGS endpoints were height and weight quantitative traits, and no disease phenotype or infection-related phenotype was FDR-significant for HGS. Among the FDR-significant ALM endpoints, four were infection-related. Rickettsioses were supported by a single instrument and were reported separately, whereas three multi-instrument phenotypes were prioritized for detailed follow-up: postzoster neuralgia, tonsillitis, and sequelae of tuberculosis. On the normalized ALM scale, postzoster neuralgia was associated with higher ALM (IVW beta = 0.01217, P = 1.17 × 10^-4), whereas tonsillitis (beta = -0.02580, P = 1.91 × 10^-4) and sequelae of tuberculosis (beta = -0.01247, P = 2.15 × 10^-4) were associated with lower ALM. Candidate-specific HGS analyses and reverse MR did not show statistically significant associations for these three phenotypes. An exploratory ALM-HGS intersection identified 23 nominally associated disease phenotypes, including five infection-related phenotypes. Exploratory proteomic analyses identified candidate proteins and pathways but did not establish mediation. Overall, the findings indicate phenotype-specific heterogeneity in genetic associations with muscle-related traits and require independent replication.

PMID:
42810599
Bibliographic data and abstract were imported from PubMed on 30 Sep 2026.

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