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A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis

BACKGROUND: Our study aims to investigate an intrinsic link underlying sex hormone-binding globulin (SHBG) and rheumatoid arthritis (RA), which remains inconclusive in observational settings. METHODS: Summary statistics were collected from the largest GWAS(s) on SHBG adjusted for BMI (SHBG(adj)BMI;...

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Autores principales: Jiang, Yuan, Liu, Qianwen, Alfredsson, Lars, Klareskog, Lars, Kockum, Ingrid, Jiang, Xia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10466838/
https://www.ncbi.nlm.nih.gov/pubmed/37644603
http://dx.doi.org/10.1186/s40246-023-00528-x
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author Jiang, Yuan
Liu, Qianwen
Alfredsson, Lars
Klareskog, Lars
Kockum, Ingrid
Jiang, Xia
author_facet Jiang, Yuan
Liu, Qianwen
Alfredsson, Lars
Klareskog, Lars
Kockum, Ingrid
Jiang, Xia
author_sort Jiang, Yuan
collection PubMed
description BACKGROUND: Our study aims to investigate an intrinsic link underlying sex hormone-binding globulin (SHBG) and rheumatoid arthritis (RA), which remains inconclusive in observational settings. METHODS: Summary statistics were collected from the largest GWAS(s) on SHBG adjusted for BMI (SHBG(adj)BMI; N(overall) = 368,929; N(men) = 180,094; N(women) = 188,908), crude SHBG (N(overall) = 370,125; N(men) = 180,726; N(women) = 189,473), and RA (N(case) = 22,350; N(control) = 74,823). A genome-wide cross-trait design was performed to quantify global and local genetic correlation, identify pleiotropic loci, and infer a causal relationship. RESULTS: Among the overall population, a significant global genetic correlation was observed for SHBG(adj)BMI and RA ([Formula: see text]  = 0.11, P = 1.0 × 10(−4)) which was further supported by local signal (1q25.2). A total of 18 independent pleiotropic SNPs were identified, of which three were highly likely causal variants and four were found to have effects on both traits through gene expression mediation. A putative causal association of SHBG(adj)BMI on RA was demonstrated (OR = 1.20, 95% CI = 1.01–1.43) without evidence of reverse causality (OR = 0.999, 95% CI = 0.997–1.000). Sex-specific analyses revealed distinct shared genetic regions (men: 1q32.1-q32.2 and 5p13.1; women: 1q25.2 and 22q11.21-q11.22) and diverse pleiotropic SNPs (16 in men and 18 in women, nearly half were sex-specific) underlying SHBG(adj)BMI and RA, demonstrating biological disparities between sexes. Replacing SHBG(adj)BMI with crude SHBG, a largely similar yet less significant pattern of results was observed. CONCLUSION: Our cross-trait analysis suggests an intrinsic, as well as a sex-specific, link underlying SHBG and RA, providing novel insights into disease etiology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40246-023-00528-x.
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spelling pubmed-104668382023-08-31 A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis Jiang, Yuan Liu, Qianwen Alfredsson, Lars Klareskog, Lars Kockum, Ingrid Jiang, Xia Hum Genomics Research BACKGROUND: Our study aims to investigate an intrinsic link underlying sex hormone-binding globulin (SHBG) and rheumatoid arthritis (RA), which remains inconclusive in observational settings. METHODS: Summary statistics were collected from the largest GWAS(s) on SHBG adjusted for BMI (SHBG(adj)BMI; N(overall) = 368,929; N(men) = 180,094; N(women) = 188,908), crude SHBG (N(overall) = 370,125; N(men) = 180,726; N(women) = 189,473), and RA (N(case) = 22,350; N(control) = 74,823). A genome-wide cross-trait design was performed to quantify global and local genetic correlation, identify pleiotropic loci, and infer a causal relationship. RESULTS: Among the overall population, a significant global genetic correlation was observed for SHBG(adj)BMI and RA ([Formula: see text]  = 0.11, P = 1.0 × 10(−4)) which was further supported by local signal (1q25.2). A total of 18 independent pleiotropic SNPs were identified, of which three were highly likely causal variants and four were found to have effects on both traits through gene expression mediation. A putative causal association of SHBG(adj)BMI on RA was demonstrated (OR = 1.20, 95% CI = 1.01–1.43) without evidence of reverse causality (OR = 0.999, 95% CI = 0.997–1.000). Sex-specific analyses revealed distinct shared genetic regions (men: 1q32.1-q32.2 and 5p13.1; women: 1q25.2 and 22q11.21-q11.22) and diverse pleiotropic SNPs (16 in men and 18 in women, nearly half were sex-specific) underlying SHBG(adj)BMI and RA, demonstrating biological disparities between sexes. Replacing SHBG(adj)BMI with crude SHBG, a largely similar yet less significant pattern of results was observed. CONCLUSION: Our cross-trait analysis suggests an intrinsic, as well as a sex-specific, link underlying SHBG and RA, providing novel insights into disease etiology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40246-023-00528-x. BioMed Central 2023-08-29 /pmc/articles/PMC10466838/ /pubmed/37644603 http://dx.doi.org/10.1186/s40246-023-00528-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Jiang, Yuan
Liu, Qianwen
Alfredsson, Lars
Klareskog, Lars
Kockum, Ingrid
Jiang, Xia
A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis
title A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis
title_full A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis
title_fullStr A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis
title_full_unstemmed A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis
title_short A genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis
title_sort genome-wide cross-trait analysis identifies genomic correlation, pleiotropic loci, and causal relationship between sex hormone-binding globulin and rheumatoid arthritis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10466838/
https://www.ncbi.nlm.nih.gov/pubmed/37644603
http://dx.doi.org/10.1186/s40246-023-00528-x
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