Evidence map›Paper›PMID 39792154›Full record

ArticleJournal of bone and mineral metabolism2025

Osteoporosis and stroke: a bidirectional mendelian randomization study.

Miao He, Haochuan Yong, Zhidong Cao, Jie Li

Abstract read
In one paragraph

Article in Journal of bone and mineral metabolism, 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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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Miao HeDepartment of Orthopedic Surgery, Chongqing Emergency Medical Center (Chongqing University Central Hospital), Jiankang Road 1, Chongqing, 400010, China.
Haochuan YongDepartment of Orthopedic Surgery, Chongqing Emergency Medical Center (Chongqing University Central Hospital), Jiankang Road 1, Chongqing, 400010, China.
Zhidong CaoDepartment of Orthopedic Surgery, Chongqing Emergency Medical Center (Chongqing University Central Hospital), Jiankang Road 1, Chongqing, 400010, China.
Jie LiDepartment of Orthopedic Surgery, Chongqing Emergency Medical Center (Chongqing University Central Hospital), Jiankang Road 1, Chongqing, 400010, China. renzhitianxinglj@sina.com.ORCID http://orcid.org/0000-0002-3286-2006

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNumerous observational studies have identified a link between osteoporosis and stroke. However, the causal genetic relationship between these conditions remains unclear. This study employs a two-sample bidirectional Mendelian randomization (MR) approach to ascertain the causal relationship between osteoporosis and stroke. MATERIALS AND

methodsWe conducted a two-sample Mendelian randomization (MR) study to investigate the potential causal relationship between osteoporosis and stroke, including its subtypes. Genetic data for osteoporosis and stroke, along with their subtypes, were sourced from published genome-wide association studies (GWAS). Single nucleotide polymorphisms (SNPs) demonstrating genome-wide significance (p < 5 × 10^ - 8) and independence (r^2 < 0.001) were selected for further analysis, provided they had an F-statistic ≥ 10. The inverse-variance weighted (IVW) method was employed to evaluate causality, with results reported as odds ratios (ORs). Heterogeneity was assessed using Cochran's Q test, while pleiotropy was tested using the MR-Egger intercept test. A leave-one-out sensitivity analysis was performed to ensure the robustness of the results.

resultsEmploying the IVW method, MR Egger method, and median-weighted method, we found no significant bidirectional causal relationship between osteoporosis and stroke or its subtypes, irrespective of the inclusion of potential pleiotropic SNPs. Sensitivity analyses affirmed the reliability and stability of these findings.

conclusionOur study findings indicate that there is no direct causal relationship between osteoporosis and stroke or its subtypes in either direction. Based on our results, although no direct link was found, secondary effects do exist.

Indexed as

Mendelian Randomization AnalysisOsteoporosisStrokeGenome-Wide Association StudyHumansPolymorphism, Single NucleotideGenome-wide association studyMendelian randomizationOsteoporosisStroke

Identifiers

PMID39792154
PMCPMC12089162

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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.