4.6 Article

Gene set analysis of transcriptomics data identifies new biological processes associated with early markers of atherosclerosis but not with those of osteoporosis: Atherosclerosis-osteoporosis co/multimorbidity study in the Young Finns Study

期刊

ATHEROSCLEROSIS
卷 361, 期 -, 页码 1-9

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.atherosclerosis.2022.10.005

关键词

Osteoporosis; Atherosclerosis; Co; multimorbidity; Transcriptomics; Gene set analysis

资金

  1. Academy of Finland [349708, 322098, 286284, 134309, 126925, 121584, 124282, 129378, 117787, 41071, 330809, 338395]
  2. Social Insurance Institution of Finland
  3. Competitive State Research Financing of the Expert Responsibility area of Kuopio University Hospital [X51001]
  4. Competitive State Research Financing of the Expert Responsibility area of Tampere University Hospital [X51001]
  5. Competitive State Research Financing of the Expert Responsibility area of Turku University Hospital [X51001]
  6. Juho Vainio Foundation
  7. Paavo Nurmi Foundation
  8. Finnish Foundation for Cardiovascular Research
  9. Finnish Cultural Foundation
  10. Sigrid Juselius Foundation
  11. Tampere Tuberculosis Foundation
  12. Emil Aaltonen Foundation
  13. Yrjo Jahnsson Foundation
  14. Signe and Ane Gyllenberg Foundation
  15. Diabetes Research Foundation of Finnish Diabetes Association
  16. European Union's Horizon 2020 research and innovation programme [848146, 755320]
  17. European Research Council (ERC) [742927]
  18. Tampere University Hospital Supporting Foundation
  19. Finnish Society of Clinical Chemistry
  20. Laboratoriolaaketieteen Edistamissa atio Sr
  21. Ida Montinin Saatio
  22. Kalle Kaiharin saatio
  23. Finnish Cultural Foundation [50191928]
  24. Aarne Koskelonsaatio
  25. Faculty of Medicine and Health Technology, Tampere University

向作者/读者索取更多资源

This study aimed to identify the shared biological processes underlying atherosclerosis-osteoporosis co/multimorbidity. Gene set analysis was performed on whole-blood transcriptomic data, and novel biological processes associated with high carotid intima-media thickness (CIMT) were identified. However, no associations were found with reduced bone mineral density (BMD).
Aim: We aimed at identifying the shared biological processes underlying atherosclerosis-osteoporosis co/ multimorbidity. Methods: We performed gene set analysis (GSA) of whole-blood transcriptomic data to identify biological pro-cesses shared by the early markers of these two diseases. Early markers of diseases, carotid intima-media thickness (CIMT) for atherosclerosis and trabecular bone mineral density (BMD) from distal radius and tibia for osteoporosis, were used to categorize the study participants into cases and controls. Participants with high CIMT (>90th percentile) were defined as cases for subclinical atherosclerosis. Study population-based T-scores for BMD were calculated and T-score <=-1 was used for the definition of low BMD cases i.e., early indicator of osteoporosis.Results: We did not identify any gene sets jointly associated with early markers of atherosclerosis and osteopo-rosis. We identified three novel and replicated 234 gene sets significantly associated with high CIMT with false discovery rate (FDR) <= 0.01. Only two genes, both related to the immune system, were identified to be associated with high CIMT by traditional differential gene expression analysis. However, none of the studied gene sets or individual genes were significantly associated with tibial or radial BMD. The three novel CIMT associated gene sets contained genes involved in copper homeostasis, neural crest cell migration and nicotinate and nicotinamide metabolism. The 234 replicated gene sets in this study are related to the immune system, hypoxia and apoptosis, consistent with the existing literature on atherosclerosis.Conclusions: This study identified novel biological processes associated with high CIMT but not with reduced BMD.

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