Influence of autonomic nervous system dysfunction on the development of type 2 diabetes - The CARDIA study

被引:136
作者
Carnethon, MR
Jacobs, DR
Sidney, S
Liu, K
机构
[1] Northwestern Univ, Dept Prevent Med, Feinberg Sch Med, Chicago, IL 60611 USA
[2] Univ Minnesota, Sch Publ Hlth, Div Epidemiol, Minneapolis, MN 55455 USA
[3] Kaiser Permanente Med Care Program, Div Res, Oakland, CA 94611 USA
关键词
D O I
10.2337/diacare.26.11.3035
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - We investigated whether autonomic nervous system dysfunction, estimated by slow heart rate recovery (HRR) following cessation of an exercise treadmill test, was associated with increases in insulin and glucose over time and the development of type 2 diabetes. RESEARCH DESIGN AND METHODS - Maximal exercise tests were performed by 3,295 healthy adults aged 18-30 years in the Coronary Artery Risk Development in Young Adults (CARDIA) study. Repeat measurements of insulin and glucose collected at 7-, 10-, and 15-year examinations were compared by quartiles of HRR (maximum heart rate minus heart rate 2 min after cessation of the test). Incident diabetes was identified at any follow-up examination as glucose greater than or equal to7 mmol/l or the use of diabetes control medication. RESULTS - Among participants who did not develop diabetes, fasting insulin concentrations increased from baseline to year 15. Following adjustment (for age, race, sex, smoking status, and BMI), participants with the slowest HRR (quartile 1) had higher fasting insulin at each examination than participants with faster HRR (e.g., year 15 examination: 88.1 vs. 81.3 pmol/l for quartile I vs. quartile 4, respectively, P = 0.05). Glucose did not differ by quartile of HRR at any examination. Among participants with poor fitness, the risk of developing diabetes (n = 98) was 3.4-fold greater (95% CI 1.5-8.0) when HRR was <42 vs. >42 bpm. This persisted following adjustment for baseline insulin. CONCLUSIONS - Autonomic dysfunction, in combination with poor physical fitness, may be a mechanism associated with early glucose dysmetabolism and the development of diabetes.
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页码:3035 / 3041
页数:7
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