Plasma Extracellular MicroRNAs Associated With Cardiovascular Disease Risk Factors in Middle‐Aged and Older Adults

Author:

Karlin Hannah12ORCID,Sooda Meera12ORCID,Larson Martin13ORCID,Rong Jian14,Huan Tianxiao125,Mens Michelle M. J.67,van Rooij Frank J. A.6ORCID,Ikram M. Arfan6ORCID,Courchesne Paul12ORCID,Freedman Jane E.8ORCID,Joehanes Roby12ORCID,Mueller Gregory P.9,Kavousi Maryam6ORCID,Ghanbari Mohsen6ORCID,Levy Daniel1210ORCID

Affiliation:

1. Framingham Heart Study Framingham MA USA

2. Population Sciences Branch National Heart, Lung, and Blood Institute Bethesda MD USA

3. Department of Biostatistics Boston University School of Public Health Boston MA USA

4. Department of Neurology Boston University Chobanian & Avedisian School of Medicine Boston MA USA

5. Ophthalmology and Visual Sciences University of Massachusetts Medical School Worcester MA USA

6. Department of Epidemiology Erasmus MC University Medical Center Rotterdam The Netherlands

7. Department of Social and Behavioral Sciences Harvard T.H Chan School of Public Health Boston MA USA

8. Department of Medicine, Division of Cardiovascular Medicine Vanderbilt University Medical Center Nashville TN USA

9. Department of Anatomy, Physiology, and Genetics, F. Edward Hebert School of Medicine Uniformed Services University of the Health Sciences Bethesda MD USA

10. Boston University School of Medicine Boston MA USA

Abstract

Background Extracellular microRNAs (miRNAs) are a class of noncoding RNAs that remain stable in the extracellular milieu, where they contribute to various physiological and pathological processes by facilitating intercellular signaling. Previous studies have reported associations between miRNAs and cardiovascular diseases (CVDs); however, the plasma miRNA signatures of CVD and its risk factors have not been fully elucidated at the population level. Methods and Results Plasma miRNA levels were measured in 4440 FHS (Framingham Heart Study) participants. Linear regression analyses were conducted to test the cross‐sectional associations of each miRNA with 8 CVD risk factors. Prospective analyses of the associations of miRNAs with new‐onset obesity, hypertension, type 2 diabetes, CVD, and all‐cause mortality were conducted using proportional hazards regression. Replication was carried out in 1999 RS (Rotterdam Study) participants. Pathway enrichment analyses were conducted and target genes were predicted for miRNAs associated with ≥5 risk factors in the FHS. In the FHS, 6 miRNAs (miR‐193b‐3p, miR‐122‐5p, miR‐365a‐3p, miR‐194‐5p, miR‐192‐5p, and miR‐193a‐5p) were associated with ≥5 risk factors. This miRNA signature was enriched for pathways associated with CVD and several genes annotated to these pathways were predicted targets of the identified miRNAs. Furthermore, miR‐193b‐3p, miR‐194‐5p, and miR‐193a‐5p were each associated with ≥2 risk factors in the RS. Prospective analysis revealed 8 miRNAs associated with all‐cause mortality in the FHS. Conclusions These findings highlight associations between miRNAs and CVD risk factors that may provide valuable insights into the underlying pathogenesis of CVD.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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