Cell-Type Composition Affects Adipose Gene Expression Associations With Cardiometabolic Traits

Author:

Brotman Sarah M.1,Oravilahti Anniina2,Rosen Jonathan D.1,Alvarez Marcus3,Heinonen Sini4,van der Kolk Birgitta W.4ORCID,Fernandes Silva Lilian2,Perrin Hannah J.1,Vadlamudi Swarooparani1,Pylant Cortney5,Deochand Sonia5,Basta Patricia V.5,Valone Jordan M.16,Narain Morgan N.17,Stringham Heather M.8,Boehnke Michael8,Kuusisto Johanna29,Love Michael I.110,Pietiläinen Kirsi H.411,Pajukanta Päivi312ORCID,Laakso Markku29ORCID,Mohlke Karen L.1ORCID

Affiliation:

1. 1Department of Genetics, The University of North Carolina, Chapel Hill, NC

2. 2Institute of Clinical Medicine, Internal Medicine, University of Eastern Finland, Kuopio, Finland

3. 3Department of Human Genetics, David Geffen School of Medicine at the University of California, Los Angeles, Los Angeles, CA

4. 4Obesity Research Unit, Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Finland

5. 5Department of Epidemiology, The University of North Carolina, Chapel Hill, NC

6. 6UNC Neuroscience Center, The University of North Carolina, Chapel Hill, NC

7. 7Curriculum of Toxicology and Environmental Medicine, The University of North Carolina, Chapel Hill, NC

8. 8Department of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan, Ann Arbor, MI

9. 9Department of Medicine, Kuopio University Hospital, Kuopio, Finland

10. 10Department of Biostatistics, The University of North Carolina, Chapel Hill, NC

11. 11HealthyWeightHub, Endocrinology, Abdominal Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland

12. 12Institute for Precision Health, David Geffen School of Medicine at University of California, Los Angeles, Los Angeles, CA

Abstract

Understanding differences in adipose gene expression between individuals with different levels of clinical traits may reveal the genes and mechanisms leading to cardiometabolic diseases. However, adipose is a heterogeneous tissue. To account for cell-type heterogeneity, we estimated cell-type proportions in 859 subcutaneous adipose tissue samples with bulk RNA sequencing (RNA-seq) using a reference single-nuclear RNA-seq data set. Cell-type proportions were associated with cardiometabolic traits; for example, higher macrophage and adipocyte proportions were associated with higher and lower BMI, respectively. We evaluated cell-type proportions and BMI as covariates in tests of association between >25,000 gene expression levels and 22 cardiometabolic traits. For >95% of genes, the optimal, or best-fit, models included BMI as a covariate, and for 79% of associations, the optimal models also included cell type. After adjusting for the optimal covariates, we identified 2,664 significant associations (P ≤ 2e−6) for 1,252 genes and 14 traits. Among genes proposed to affect cardiometabolic traits based on colocalized genome-wide association study and adipose expression quantitative trait locus signals, 25 showed a corresponding association between trait and gene expression levels. Overall, these results suggest the importance of modeling cell-type proportion when identifying gene expression associations with cardiometabolic traits. Article Highlights

Funder

Finnish Foundation for Cardiovascular Research, Centre of Excellence of Cardiovascular and Metabolic Diseases

Orion Foundation

Finnish Diabetes Research Foundation

Novo Nordisk

Academy of Finland

Finnish Medical Foundation

Paulo Foundation

Helsinki University Hospital Research Funds

Paavo Nurmi Foundation

Sigrid Juselius Foundation

Gyllenberg Foundation

National Institutes of Health

Ida Montin Foundation

Government Research Funds for Helsinki University Hospital and the University of Helsinki

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3