ArticleBMC pulmonary medicine2026
The association between obstructive sleep apnea and frailty traits: a bidirectional Mendelian randomization study.
Article in BMC pulmonary medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
17 authors.
Funding
Abstract
backgroundThis study aimed to explore the causal association between obstructive sleep apnea (OSA) and frailty traits using a bidirectional two-sample Mendelian randomization (MR) analysis.
methodsSummary data from large-scale European genome-wide association studies were used to assess the genetic link between OSA and frailty traits, including frailty index, appendicular lean mass, grip strength, and walking pace. Effect estimates were primarily evaluated using inverse-variance weighted (IVW) analysis, complemented by MR-Egger, weighted median (WM), simple mode, and weighted mode analyses. Sensitivity analyses were performed to assess heterogeneity, outliers, and horizontal pleiotropy.
resultsForward MR analysis showed no significant effect of OSA on frailty traits. However, reverse MR analysis suggested that a higher frailty index was associated with an increased risk of OSA (IVW: odds ratio [OR], 1.777; 95% confidence interval [CI], 1.137–2.777; p = 0.01) based on 14 single nucleotide polymorphisms (SNPs), and a faster walking pace was identified as a protective factor against OSA (IVW: OR, 0.204; 95% CI, 0.104–0.399; p < 0.01; WM: OR, 0.368; 95% CI, 0.193–0.703; p < 0.01) based on 56 SNPs. No significant pleiotropy was detected, and sensitivity analyses confirmed the robustness of these findings.
conclusionOur MR study provided evidence that frailty traits may have a causal effect on OSA in the European ancestry population, with frailty index increasing the risk and walking pace acting as a protective factor.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.