Diabetes and Risk of Arterial Stiffness: A Mendelian Randomization Analysis

Author:

Xu Min123,Huang Ya123,Xie Lan4,Peng Kui123,Ding Lin123,Lin Lin123,Wang Po123,Hao Mingli123,Chen Yuhong123,Sun Yimin45,Qi Lu6,Wang Weiqing123,Ning Guang123,Bi Yufang123

Affiliation:

1. State Key Laboratory of Medical Genomics, Key Laboratory for Endocrine and Metabolic Diseases of Ministry of Health, National Clinical Research Center for Metabolic Diseases, Collaborative Innovation Center of Systems Biomedicine, and Shanghai Clinical Center for Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China

2. Shanghai Institute of Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China

3. Department of Endocrine and Metabolic Diseases, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China

4. Department of Biomedical Engineering, Medical Systems Biology Research Center, Tsinghua University School of Medicine, Beijing, China

5. National Engineering Research Center for Beijing Biochip Technology, Beijing, China

6. Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA

Abstract

We aimed to explore the causal association between type 2 diabetes (T2D) and increased arterial stiffness. We performed a Mendelian randomization (MR) analysis in 11,385 participants from a well-defined community study in Shanghai during 2011–2013. We genotyped 34 T2D-associated common variants identified in East Asians and created a genetic risk score (GRS). We assessed arterial stiffness noninvasively with the measurement of brachial-ankle pulse wave velocity (baPWV). We used the instrumental variable (IV) estimator to qualify the causal relationship between T2D and increased arterial stiffness. We found each 1-SD increase in T2D_GRS was associated with 6% higher risk in increased arterial stiffness (95% CI 1.01, 1.12), after adjustment of other metabolic confounders. Using T2D_GRS as the IV, we demonstrated a causal relationship between T2D and arterial stiffening (odds ratio 1.24, 95% CI 1.06, 1.47; P = 0.008). When categorizing the genetic loci according to their effect on insulin secretion or resistance, we found genetically determined decrease in insulin secretion was associated with increase in baPWV (βIV = 122.3 cm/s, 95% CI 41.9, 204.6; P = 0.0005). In conclusion, our results provide evidence supporting a causal association between T2D and increased arterial stiffness in a Chinese population.

Funder

China National Clinical Research Center for Metabolic Diseases

National Basic Research Program of China 973 Program of China

National High-tech R&D Program of China

National Natural Science Foundation of China

Joint Research Program for Important Diseases of the Shanghai Municipal Commission of Health and Family Planning

Shanghai Pujiang Project

Shu Guang Project of Shanghai Municipal Education Commission and Shanghai Education Development Foundation

Gaofeng Clinical Medicine Grant Support from the Shanghai Municipal Education Commission

National High-tech R&D Program of China (863 Program)

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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