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A Novel Digital Platform for a Monitored Home-based Cardiac Rehabilitation Program
Published on: April 19, 2019
Relations Between Physical Activity, Subclinical Myocardial Injury, and Cardiovascular Mortality in the General
Charles German1, Muhammad Imtiaz Ahmad2, Yabing Li3
1Department of Internal Medicine, Section on Cardiology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Abstract:
We examined the association between poor physical activity (PA) and subclinical myocardial injury (SC-MI), and how concomitant exposure to poor PA and SC-MI modifies their association with cardiovascular disease (CVD) mortality. This analysis included 6,044 participants free of CVD from the NHANES-III survey. Leisure time PA was defined as: ideal (3 to 5.99 METs and ≥5 times/week or any PA with ≥6METs and ≥3times/week), intermediate (any activity other than ideal), or poor (no activity at all). SC-MI was defined as an electrocardiographic cardiac infarction/injury score ≥10 units. CVD mortality was ascertained from the National Death Index. In multivariable logistic regression analysis, poor PA (odds ratio [OR] [95% confidence interval, CI]: 1.30 [1.10 to 1.54]) and intermediate PA (OR [95%CI]: 1.19 [1.02 to 1.38]), compared with ideal PA, were associated with an increased odds of SC-MI. During a median follow-up of 14 years, 589 CVD deaths occurred. In multivariable Cox-proportional hazard analysis, the presence (vs absence) of SC-MI was associated with a 33% increased risk of CVD mortality whereas poor (vs ideal) PA was associated with a 67% increased risk of CVD mortality (HR [95%CI]: 1.33 [1.11 to 1.58] and 1.67 [1.37 to 2.05], respectively). Additionally, the concomitant presence of both poor PA and SC-MI were associated with a higher risk of CVD mortality (HR [95%CI]: 2.25[1.68 to 3.00]) compared with ideal PA and the absence of SC-MI. In conclusion, poor PA is associated with an increased risk of SC-MI and their concomitant presence is associated with a marked increase in CVD mortality, underscoring the potential role of PA in preventing clinical and subclinical CVD outcomes.
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