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Osteoarthritis and cardiovascular disease: A Mendelian randomization study

OBJECTIVE: This Mendelian randomization (MR) study aimed to investigate the causal relationship between osteoarthritis (OA) and cardiovascular disease (CVD). METHODS: From a genome-wide association study of European ancestry, we selected single nucleotide polymorphisms for two types of OA, knee oste...

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Detalles Bibliográficos
Autores principales: Wang, Zhao, Kang, Chan, Xu, Pai, Zhang, Shuyi, Song, Jae Hwang, Wang, Dongyang, Yuan, Shuai, Lee, Hyun Jong, Zhang, Meng, Wang, Zhihui, Sun, Hao, Fan, Ruobing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9717609/
https://www.ncbi.nlm.nih.gov/pubmed/36465459
http://dx.doi.org/10.3389/fcvm.2022.1025063
Descripción
Sumario:OBJECTIVE: This Mendelian randomization (MR) study aimed to investigate the causal relationship between osteoarthritis (OA) and cardiovascular disease (CVD). METHODS: From a genome-wide association study of European ancestry, we selected single nucleotide polymorphisms for two types of OA, knee osteoarthritis (KOA) and hip osteoarthritis (HOA), as instrumental variables. We evaluated three types of CVD: coronary heart disease (CHD), heart failure (HF), and stroke. We used the traditional inverse variance weighting (IVW) method and other methods to estimate causality. Heterogeneity and sensitivity tests were also applied. Finally, we conducted a MR analysis in the opposite direction to investigate reverse causality. RESULTS: IVW analysis showed that HOA significantly affected the incidence of HF [odds ratio (OR): 1.0675; 95% confidence interval (CI): 0.0182–0.1125, P = 0.0066]. HOA significantly affected the incidence of stroke (OR: 1.1368; 95% CI: 1.0739–1.2033, P = 9.9488e-06). CHD could dramatically affect the incidence of KOA (OR: 0.9011; 95% CI: 0.8442–0.9619, P = 0.0018). The rest of the results were negative. CONCLUSIONS: Our results revealed a potential causal relationship between HOA and risk of HF, and a potential causal relationship between HOA and risk of stroke. Our findings also suggested that CHD has a significant causal relationship with the risk of KOA. This paper may provide new ideas for the treatment of OA and CVD.