Modular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the Young Finns Study

Abstract We analysed whole blood genome-wide expression data to identify gene co-expression modules shared by early traits of osteoporosis and atherosclerosis. Gene expression was profiled for the Young Finns Study participants. Bone mineral density and content were measured as early traits of osteo...

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Autores principales: Binisha H. Mishra, Pashupati P. Mishra, Emma Raitoharju, Saara Marttila, Nina Mononen, Harri Sievänen, Jorma Viikari, Markus Juonala, Marika Laaksonen, Nina Hutri-Kähönen, Mika Kähönen, Olli T. Raitakari, Terho Lehtimäki
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Publicado: Nature Portfolio 2021
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spelling oai:doaj.org-article:55ba293c76de490eb8878024557d1e772021-12-02T13:26:58ZModular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the Young Finns Study10.1038/s41598-021-86536-02045-2322https://doaj.org/article/55ba293c76de490eb8878024557d1e772021-03-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-86536-0https://doaj.org/toc/2045-2322Abstract We analysed whole blood genome-wide expression data to identify gene co-expression modules shared by early traits of osteoporosis and atherosclerosis. Gene expression was profiled for the Young Finns Study participants. Bone mineral density and content were measured as early traits of osteoporosis. Carotid and bulbus intima media thickness were measured as early traits of atherosclerosis. Joint association of the modules, identified with weighted co-expression analysis, with early traits of the diseases was tested with multivariate analysis. Among the six modules significantly correlated with early traits of both the diseases, two had significant (adjusted p-values (p.adj) < 0.05) and another two had suggestively significant (p.adj < 0.25) joint association with the two diseases after adjusting for age, sex, body mass index, smoking habit, alcohol consumption, and physical activity. The three most significant member genes from the significant modules were NOSIP, GXYLT2, and TRIM63 (p.adj ≤ 0.18). Genes in the modules were enriched with biological processes that have separately been found to be involved in either bone metabolism or atherosclerosis. The gene modules and their most significant member genes identified in this study support the osteoporosis-atherosclerosis comorbidity hypothesis and can provide new joint biomarkers for both diseases and their dual prevention.Binisha H. MishraPashupati P. MishraEmma RaitoharjuSaara MarttilaNina MononenHarri SievänenJorma ViikariMarkus JuonalaMarika LaaksonenNina Hutri-KähönenMika KähönenOlli T. RaitakariTerho LehtimäkiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Binisha H. Mishra
Pashupati P. Mishra
Emma Raitoharju
Saara Marttila
Nina Mononen
Harri Sievänen
Jorma Viikari
Markus Juonala
Marika Laaksonen
Nina Hutri-Kähönen
Mika Kähönen
Olli T. Raitakari
Terho Lehtimäki
Modular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the Young Finns Study
description Abstract We analysed whole blood genome-wide expression data to identify gene co-expression modules shared by early traits of osteoporosis and atherosclerosis. Gene expression was profiled for the Young Finns Study participants. Bone mineral density and content were measured as early traits of osteoporosis. Carotid and bulbus intima media thickness were measured as early traits of atherosclerosis. Joint association of the modules, identified with weighted co-expression analysis, with early traits of the diseases was tested with multivariate analysis. Among the six modules significantly correlated with early traits of both the diseases, two had significant (adjusted p-values (p.adj) < 0.05) and another two had suggestively significant (p.adj < 0.25) joint association with the two diseases after adjusting for age, sex, body mass index, smoking habit, alcohol consumption, and physical activity. The three most significant member genes from the significant modules were NOSIP, GXYLT2, and TRIM63 (p.adj ≤ 0.18). Genes in the modules were enriched with biological processes that have separately been found to be involved in either bone metabolism or atherosclerosis. The gene modules and their most significant member genes identified in this study support the osteoporosis-atherosclerosis comorbidity hypothesis and can provide new joint biomarkers for both diseases and their dual prevention.
format article
author Binisha H. Mishra
Pashupati P. Mishra
Emma Raitoharju
Saara Marttila
Nina Mononen
Harri Sievänen
Jorma Viikari
Markus Juonala
Marika Laaksonen
Nina Hutri-Kähönen
Mika Kähönen
Olli T. Raitakari
Terho Lehtimäki
author_facet Binisha H. Mishra
Pashupati P. Mishra
Emma Raitoharju
Saara Marttila
Nina Mononen
Harri Sievänen
Jorma Viikari
Markus Juonala
Marika Laaksonen
Nina Hutri-Kähönen
Mika Kähönen
Olli T. Raitakari
Terho Lehtimäki
author_sort Binisha H. Mishra
title Modular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the Young Finns Study
title_short Modular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the Young Finns Study
title_full Modular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the Young Finns Study
title_fullStr Modular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the Young Finns Study
title_full_unstemmed Modular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the Young Finns Study
title_sort modular genome-wide gene expression architecture shared by early traits of osteoporosis and atherosclerosis in the young finns study
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/55ba293c76de490eb8878024557d1e77
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