Intensive Risk Factor Management and Cardiovascular Autonomic Neuropathy in Type 2 Diabetes: The ACCORD Trial

Author:

Tang Yaling12,Shah Hetal12ORCID,Bueno Junior Carlos Roberto1,Sun Xiuqin13,Mitri Joanna12,Sambataro Maria4ORCID,Sambado Luisa4,Gerstein Hertzel C.5ORCID,Fonseca Vivian6ORCID,Doria Alessandro12ORCID,Pop-Busui Rodica7ORCID

Affiliation:

1. Research Division, Joslin Diabetes Center, Boston, MA

2. Department of Medicine, Harvard Medical School, Boston, MA

3. Department of Endocrinology and Metabolism, Anzhen Hospital Affiliated to Capital Medical University, Beijing, China

4. Endocrine, Metabolism and Nutrition Disease Unit, Internal Medicine Department, Santa Maria of Ca’ Foncello Hospital, Treviso, Italy

5. McMaster University and the Population Health Research Institute, Hamilton, Ontario, Canada

6. Section of Endocrinology, Tulane University Health Sciences Center, New Orleans, LA

7. Division of Metabolism, Endocrinology & Diabetes, Department of Internal Medicine, University of Michigan, Ann Arbor, MI

Abstract

OBJECTIVE The effects of preventive interventions on cardiovascular autonomic neuropathy (CAN) remain unclear. We examined the effect of intensively treating traditional risk factors for CAN, including hyperglycemia, hypertension, and dyslipidemia, in individuals with type 2 diabetes (T2D) and high cardiovascular risk participating in the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial. RESEARCH DESIGN AND METHODS CAN was defined as heart rate variability indices below the fifth percentile of the normal distribution. Of 10,251 ACCORD participants, 71% (n = 7,275) had a CAN evaluation at study entry and at least once after randomization. The effects of intensive interventions on CAN were analyzed among these subjects through generalized linear mixed models. RESULTS As compared with standard intervention, intensive glucose treatment reduced CAN risk by 16% (odds ratio [OR] 0.84, 95% CI 0.75–0.94, P = 0.003)—an effect driven by individuals without cardiovascular disease (CVD) at baseline (OR 0.73, 95% CI 0.63–0.85, P < 0.0001) rather than those with CVD (OR 1.10, 95% CI 0.91–1.34, P = 0.34) (Pinteraction = 0.001). Intensive blood pressure (BP) intervention decreased CAN risk by 25% (OR 0.75, 95% CI 0.63–0.89, P = 0.001), especially in patients ≥65 years old (OR 0.66, 95% CI 0.49–0.88, P = 0.005) (Pinteraction = 0.05). Fenofibrate did not have a significant effect on CAN (OR 0.91, 95% CI 0.78–1.07, P = 0.26). CONCLUSIONS These data confirm a beneficial effect of intensive glycemic therapy and demonstrate, for the first time, a similar benefit of intensive BP control on CAN in T2D. A negative CVD history identifies T2D patients who especially benefit from intensive glycemic control for CAN prevention.

Funder

Iacocca Foundation

National Institute of Diabetes and Digestive and Kidney Diseases

JDRF

National Heart, Lung, and Blood Institute

Publisher

American Diabetes Association

Subject

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

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