3.8 Article

Exercise training-induced changes in coagulation factors in older adults

期刊

MEDICINE AND SCIENCE IN SPORTS AND EXERCISE
卷 39, 期 4, 页码 587-592

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1249/mss.0b013e31802eff4b

关键词

factor VIII; prothrombin fragment; thrombosis; physical activity

资金

  1. NIA NIH HHS [AG17474, AG15389] Funding Source: Medline

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The coagulation cascade plays a critical role in the development of cardiovascular disease (CVD). Elevated plasma prothrombin fragment 1 + 2 (F1 + 2) and factor VIII antigen (FVIII:Ag) levels have been associated with a hypercoagulable state, enhancing the risk for vascular thrombotic events. Aerobic training is known to reduce CVD risk, and an improved coagulation profile may contribute to this reduction. Purpose: To analyze the effect of 6 months of standardized aerobic exercise training on resting F1 + 2 and FVIII:Ag levels in men and postmenopausal women aged 50-75 while accounting for several possibly confounding factors. Materials and Methods: Sedentary men (N = 16) and women (N = 31) underwent supervised aerobic training 3 d(.)wk(-1) for 6 months while maintaining the American Heart Association step I diet. Baseline and final testing included measurement of F1 + 2, FVIII:Ag, plasma lipoproteinlipid levels, body composition, and VO2(max). Results: When adjusted for baseline values and changes in diastolic blood pressure with training, F1 + 2 was found to decrease significantly with exercise training from 1.493 +/- 0.058 to 1.422 +/- 0.059 nM (P = 0.014). FVHI:Ag levels were found to increase significantly with training when adjusted for baseline values, from 152.5 +/- 6.7% of standard at baseline to 156.0 +/- 6.1 % of standard at final testing (P = 0.005). Training-induced changes in coagulation markers were independent of changes in blood lipids, aerobic capacity, and body composition. Conclusions: These results indicate that endurance training has a significant impact on the coagulation cascade, reducing coagulation activity in the common pathway and thrombin formation at rest while increasing the activation potential of the intrinsic pathway.

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