Coronary Artery Disease and Type 2 Diabetes: A Proteomic Study

Author:

Ferrannini Giulia12ORCID,Manca Maria Laura3,Magnoni Marco4,Andreotti Felicita5,Andreini Daniele67,Latini Roberto8,Maseri Attilio9,Maggioni Aldo P.10,Ostroff Rachel M.11,Williams Stephen A.11,Ferrannini Ele12ORCID

Affiliation:

1. Department of Medical Sciences, Postgraduate School of Internal Medicine, University of Turin, Turin, Italy

2. Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden

3. Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy

4. IRCCS Ospedale San Raffaele and Università Vita-Salute San Raffaele, Milan, Italy

5. Institute of Cardiology, FPG IRCCS, Catholic University Medical School, Rome, Italy

6. Centro Cardiologico Monzino, IRCCS, Milan, Italy

7. Cardiovascular Section, Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy

8. Mario Negri Institute of Pharmacological Research-IRCCS, Milan, Italy

9. Heart Care Foundation, Florence, Italy

10. ANMCO Research Center, Heart Care Foundation, Florence, Italy

11. Clinical Research and Development, SomaLogic Inc., Boulder, CO

12. CNR Institute of Clinical Physiology, Pisa, Italy

Abstract

OBJECTIVE Coronary artery disease (CAD) is a major challenge in patients with type 2 diabetes (T2D). Coronary computed tomography angiography (CCTA) provides a detailed anatomic map of the coronary circulation. Proteomics are increasingly used to improve diagnostic and therapeutic algorithms. We hypothesized that the protein panel is differentially associated with T2D and CAD. RESEARCH DESIGN AND METHODS In CAPIRE (Coronary Atherosclerosis in Outlier Subjects: Protective and Novel Individual Risk Factors Evaluation—a cohort of 528 individuals with no previous cardiovascular event undergoing CCTA), participants were grouped into CAD− (clean coronaries) and CAD+ (diffuse lumen narrowing or plaques). Plasma proteins were screened by aptamer analysis. Two-way partial least squares was used to simultaneously rank proteins by diabetes status and CAD. RESULTS Though CAD+ was more prevalent among participants with T2D (HbA1c 6.7 ± 1.1%) than those without diabetes (56 vs. 30%, P < 0.0001), CCTA-based atherosclerosis burden did not differ. Of the 20 top-ranking proteins, 15 were associated with both T2D and CAD, and 3 (osteomodulin, cartilage intermediate-layer protein 2, and HTRA1) were selectively associated with T2D only and 2 (epidermal growth factor receptor and contactin-1) with CAD only. Elevated renin and GDF15, and lower adiponectin, were independently associated with both T2D and CAD. In multivariate analysis adjusting for the Framingham risk panel, patients with T2D were “protected” from CAD if female (P = 0.007), younger (P = 0.021), and with lower renin levels (P = 0.02). CONCLUSIONS We concluded that 1) CAD severity and quality do not differ between participants with T2D and without diabetes; 2) renin, GDF15, and adiponectin are shared markers by T2D and CAD; 3) several proteins are specifically associated with T2D or CAD; and 4) in T2D, lower renin levels may protect against CAD.

Funder

Heart Care Foundation of the Italian Association of Hospital Cardiologists, Florence, Italy

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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