Monocyte miRNAs Are Associated With Type 2 Diabetes

Author:

Parker Daniel C.12,Wan Ma3,Lohman Kurt3,Hou Li3,Nguyen Anh Tram3,Ding Jingzhong4,Bertoni Alain4,Shea Steve5,Burke Gregory L.4,Jacobs David R.6,Post Wendy7,Corcoran David8,Hoeschele Ina9,Parks John S.4,Liu Yongmei3ORCID

Affiliation:

1. Division of Geriatrics, Department of Medicine, Duke University School of Medicine, Durham, NC

2. Duke University Center for the Study of Aging and Human Development, Durham, NC

3. Division of Cardiology, Department of Medicine, Duke Molecular Physiology Institute, Duke University School of Medicine, Durham, NC

4. Wake Forest University School of Medicine, Winston-Salem, NC

5. Columbia University School of Medicine, New York, NY

6. University of Minnesota School of Public Health, Minneapolis, MN

7. Johns Hopkins University School of Medicine, Baltimore, MD

8. Duke Center for Genomic and Computational Biology, Duke University, Durham, NC

9. Department of Statistics and Fralin Life Sciences Institute, Virginia Tech, Blacksburg, VA

Abstract

miRNAs are small noncoding RNAs that may contribute to common diseases through epigenetic regulation of gene expression. Little is known regarding the role of miRNAs in type 2 diabetes (T2D). We performed miRNA sequencing and transcriptomic profiling of peripheral monocytes from the longitudinal Multi-Ethnic Study of Atherosclerosis (MESA) (N = 1,154). We examined associations between miRNAs and prevalent impaired fasting glucose and T2D and evaluated the T2D-associated miRNA effect on incident T2D. Of 774 detected miRNAs, 6 (miR-22-3p, miR-33a-5p, miR-181c-5p, miR-92b-3p, miR-222–3p, and miR-944) were associated with prevalent T2D. For five of the six miRNAs (all but miR-222-3p), our findings suggest a dose-response relationship with impaired fasting glucose and T2D. Two of the six miRNAs were associated with incident T2D (miR-92b-3p: hazard ratio [HR] 1.64, P = 1.30E-03; miR-222-3p: HR 1.97, P = 9.10E-03) in the highest versus lowest tertile of expression. Most of the T2D-associated miRNAs were also associated with HDL cholesterol concentrations. The genes targeted by these miRNAs belong to key nodes of a cholesterol metabolism transcriptomic network. Higher levels of miRNA expression expected to increase intracellular cholesterol accumulation in monocytes are linked to an increase in T2D risk.

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference40 articles.

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