Causal Relationship Between Parathyroid Hormone and the Risk of Osteoarthritis: A Mendelian Randomization Study

Background Previous studies have demonstrated an inverse association between parathyroid hormone (PTH) and the risk of osteoarthritis (OA). However, it remains unknown whether such association reflects causality. We aimed to apply a Mendelian randomization (MR) approach to investigate the causal ass...

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Published inFrontiers in genetics Vol. 12; p. 686939
Main Authors Huang, Guiwu, Zhong, Yanlin, Li, Wenchang, Liao, Weiming, Wu, Peihui
Format Journal Article
LanguageEnglish
Published Frontiers Media S.A 26.07.2021
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Summary:Background Previous studies have demonstrated an inverse association between parathyroid hormone (PTH) and the risk of osteoarthritis (OA). However, it remains unknown whether such association reflects causality. We aimed to apply a Mendelian randomization (MR) approach to investigate the causal association between PTH and OA. Materials and Methods We performed a two-sample MR analysis using summary statistics from 13 cohorts (PTH, N = 29,155) and a recent genome-wide association study meta-analysis (OA, N = 455,221) by the UK Biobank and Arthritis Research UK OA Genetics (arcOGEN). MR analyses were carried out mainly using the inverse-variance-weighted method. Sensitivity analyses were performed to test the robustness of the associations using the weighted median method, the MR–Egger method, and “leave-one-out” analysis. Analyses were performed again to test whether the associations remained statistically significant after excluding any outlier variants that were detected using the MR-PRESSO (Mendelian Randomization Pleiotropy RESidual Sum and Outlier) test. Results Five single-nucleotide polymorphisms (SNPs) were selected as instrumental variables at the genome-wide significance threshold ( p < 5 × 10 –8 ). The causal effect between PTH and OA was genetically predicted using the inverse-variance-weighted method (odds ratio = 0.67, 95% confidence interval: 0.50–0.90; p = 0.008). This result was borne out using the weighted median method (odds ratio = 0.73, 95% confidence interval: 0.60–0.90; p = 0.004). The causality remained robust after discarding the outlier variants as well as SNPs associated with confounding factors. Conclusion MR analysis supported a potential causative relationship between decreased serum circulating PTH and a higher risk of hip and knee OA.
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Reviewed by: Shuai Yuan, Karolinska Institutet (KI), Sweden; Ville Karhunen, University of Oulu, Finland
These authors have contributed equally to this work
Edited by: Dipender Gill, St George’s University of London, United Kingdom
This article was submitted to Applied Genetic Epidemiology, a section of the journal Frontiers in Genetics
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2021.686939