Benjamin G Faber, Monika Frysz, Jiayi Zheng, Huandong Lin, Kaitlyn Flynn, Raja Ebsim, Fiona R Saunders, Rhona A Beynon, Jenny S Gregory, Richard M Aspden, Nicholas C Harvey, Claudia Lindner, Tim Cootes, David Evans, George Davey Smith, Xin Gao, Sijia Wang, John Kemp, Jon Tobias
{"title":"髋部形状对髋部骨折有因果效应,但对髋部骨关节炎无因果效应:GWAS 元分析和因果分析的结果","authors":"Benjamin G Faber, Monika Frysz, Jiayi Zheng, Huandong Lin, Kaitlyn Flynn, Raja Ebsim, Fiona R Saunders, Rhona A Beynon, Jenny S Gregory, Richard M Aspden, Nicholas C Harvey, Claudia Lindner, Tim Cootes, David Evans, George Davey Smith, Xin Gao, Sijia Wang, John Kemp, Jon Tobias","doi":"10.1101/2024.01.26.24301811","DOIUrl":null,"url":null,"abstract":"Objectives\nHip shape is thought to be an important causal risk factor for hip osteoarthritis and fracture. We aimed to identify genetic determinants of hip shape and use these to assess causal relationships with hip osteoarthritis. Methods\nStatistical hip shape modelling was used to derive 10 hip shape modes (HSMs) from DXA images in UK Biobank and Shanghai Changfeng cohorts (n<sub>total</sub>=43,485). Genome-wide association study meta-analyses were conducted for each HSM. Two-sample Mendelian randomisation (MR) was used to estimate causal effects between HSM and hip osteoarthritis using hip fracture as a positive control.\nResults\nAnalysis of the first 10 HSMs identified 290 independent association signals (P<5×10<sup>-8</sup>). Hip shape SNPs were also associated (P<1.7×10<sup>-4</sup>) with hip osteoarthritis (n=29) and hip fracture (n=4). Fine mapping implicated SMAD3 and PLEC as candidate genes that may be involved in the development of hip shape and hip osteoarthritis. MR analyses suggested there was no causal effect between any HSM and hip osteoarthritis, however there was evidence that HSM2 (higher neck-shaft angle) and HSM4 (wider femoral neck) have a causal effect on hip fracture (OR<sub>IVW</sub> 1.27 [95% CI 1.12-1.44], P=1.79×10<sup>-4</sup> and OR<sub>IVW</sub> 0.74 [0.65-0.84], P=7.60×10<sup>-6</sup> respectively)\nConclusions We report the largest hip shape GWAS meta-analysis that identifies hundreds of novel loci, some of which are also associated with hip osteoarthritis and hip fracture. MR analyses suggest hip shape may not cause hip osteoarthritis but is implicated in hip fractures. Consequently, interventions aimed at modifying hip shape in older adults to prevent hip osteoarthritis may prove ineffective.","PeriodicalId":501212,"journal":{"name":"medRxiv - Rheumatology","volume":"22 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hip shape shows a causal effect on hip fracture but not hip osteoarthritis: findings from a GWAS meta-analysis and causal analyses\",\"authors\":\"Benjamin G Faber, Monika Frysz, Jiayi Zheng, Huandong Lin, Kaitlyn Flynn, Raja Ebsim, Fiona R Saunders, Rhona A Beynon, Jenny S Gregory, Richard M Aspden, Nicholas C Harvey, Claudia Lindner, Tim Cootes, David Evans, George Davey Smith, Xin Gao, Sijia Wang, John Kemp, Jon Tobias\",\"doi\":\"10.1101/2024.01.26.24301811\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objectives\\nHip shape is thought to be an important causal risk factor for hip osteoarthritis and fracture. We aimed to identify genetic determinants of hip shape and use these to assess causal relationships with hip osteoarthritis. Methods\\nStatistical hip shape modelling was used to derive 10 hip shape modes (HSMs) from DXA images in UK Biobank and Shanghai Changfeng cohorts (n<sub>total</sub>=43,485). Genome-wide association study meta-analyses were conducted for each HSM. Two-sample Mendelian randomisation (MR) was used to estimate causal effects between HSM and hip osteoarthritis using hip fracture as a positive control.\\nResults\\nAnalysis of the first 10 HSMs identified 290 independent association signals (P<5×10<sup>-8</sup>). Hip shape SNPs were also associated (P<1.7×10<sup>-4</sup>) with hip osteoarthritis (n=29) and hip fracture (n=4). Fine mapping implicated SMAD3 and PLEC as candidate genes that may be involved in the development of hip shape and hip osteoarthritis. MR analyses suggested there was no causal effect between any HSM and hip osteoarthritis, however there was evidence that HSM2 (higher neck-shaft angle) and HSM4 (wider femoral neck) have a causal effect on hip fracture (OR<sub>IVW</sub> 1.27 [95% CI 1.12-1.44], P=1.79×10<sup>-4</sup> and OR<sub>IVW</sub> 0.74 [0.65-0.84], P=7.60×10<sup>-6</sup> respectively)\\nConclusions We report the largest hip shape GWAS meta-analysis that identifies hundreds of novel loci, some of which are also associated with hip osteoarthritis and hip fracture. MR analyses suggest hip shape may not cause hip osteoarthritis but is implicated in hip fractures. Consequently, interventions aimed at modifying hip shape in older adults to prevent hip osteoarthritis may prove ineffective.\",\"PeriodicalId\":501212,\"journal\":{\"name\":\"medRxiv - Rheumatology\",\"volume\":\"22 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-01-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"medRxiv - Rheumatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2024.01.26.24301811\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv - Rheumatology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.01.26.24301811","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Hip shape shows a causal effect on hip fracture but not hip osteoarthritis: findings from a GWAS meta-analysis and causal analyses
Objectives
Hip shape is thought to be an important causal risk factor for hip osteoarthritis and fracture. We aimed to identify genetic determinants of hip shape and use these to assess causal relationships with hip osteoarthritis. Methods
Statistical hip shape modelling was used to derive 10 hip shape modes (HSMs) from DXA images in UK Biobank and Shanghai Changfeng cohorts (ntotal=43,485). Genome-wide association study meta-analyses were conducted for each HSM. Two-sample Mendelian randomisation (MR) was used to estimate causal effects between HSM and hip osteoarthritis using hip fracture as a positive control.
Results
Analysis of the first 10 HSMs identified 290 independent association signals (P<5×10-8). Hip shape SNPs were also associated (P<1.7×10-4) with hip osteoarthritis (n=29) and hip fracture (n=4). Fine mapping implicated SMAD3 and PLEC as candidate genes that may be involved in the development of hip shape and hip osteoarthritis. MR analyses suggested there was no causal effect between any HSM and hip osteoarthritis, however there was evidence that HSM2 (higher neck-shaft angle) and HSM4 (wider femoral neck) have a causal effect on hip fracture (ORIVW 1.27 [95% CI 1.12-1.44], P=1.79×10-4 and ORIVW 0.74 [0.65-0.84], P=7.60×10-6 respectively)
Conclusions We report the largest hip shape GWAS meta-analysis that identifies hundreds of novel loci, some of which are also associated with hip osteoarthritis and hip fracture. MR analyses suggest hip shape may not cause hip osteoarthritis but is implicated in hip fractures. Consequently, interventions aimed at modifying hip shape in older adults to prevent hip osteoarthritis may prove ineffective.