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Approximately 80% of US adults and adolescents are insufficiently active. Physical activity fosters normal growth and development and can make people feel, function, and sleep better and reduce risk of many chronic diseases.
Background The relationships between physical activity (PA) and both cardiovascular disease (CVD) and type 2 diabetes mellitus (T2DM) have predominantly been estimated using categorical measures of PA, masking the shape of the dose‐response relationship. In this systematic review and meta‐analysis, for the very first time we are able to derive a single continuous PA metric to compare the association between PA and CVD/T2DM, both before and after adjustment for a measure of body weight. Methods and Results The search was applied to MEDLINE and EMBASE electronic databases for all studies published from January 1981 to March 2014. A total of 36 studies (3 439 874 participants and 179 393 events, during an average follow‐up period of 12.3 years) were included in the analysis (33 pertaining to CVD and 3 to T2DM). An increase from being inactive to achieving recommended PA levels (150 minutes of moderate‐intensity aerobic activity per week) was associated with lower risk of CVD mortality by 23%, CVD incidence by 17%, and T2DM incidence by 26% (relative risk [RR], 0.77 [0.71–0.84]), (RR, 0.83 [0.77–0.89]), and (RR, 0.74 [0.72–0.77]), respectively, after adjustment for body weight. Conclusions By using a single continuous metric for PA levels, we were able to make a comparison of the effect of PA on CVD incidence and mortality including myocardial infarct (MI), stroke, and heart failure, as well as T2DM. Effect sizes were generally similar for CVD and T2DM, and suggested that the greatest gain in health is associated with moving from inactivity to small amounts of PA.
This statement summarizes evidence that adverse pregnancy outcomes (APOs) such as hypertensive disorders of pregnancy, preterm delivery, gestational diabetes, small-for-gestational-age delivery, placental abruption, and pregnancy loss increase a woman’s risk of developing cardiovascular disease (CVD) risk factors and of developing subsequent CVD (including fatal and nonfatal coronary heart disease, stroke, peripheral vascular disease, and heart failure). This statement highlights the importance of recognizing APOs when CVD risk is evaluated in women, although their value in reclassifying risk may not be established. A history of APOs is a prompt for more vigorous primordial prevention of CVD risk factors and primary prevention of CVD. Adopting a heart-healthy diet and increasing physical activity among women with APOs, starting in the postpartum setting and continuing across the life span, are important lifestyle interventions to decrease CVD risk. Lactation and breastfeeding may lower a woman’s later cardiometabolic risk. Black and Asian women experience a higher proportion APOs, with more severe clinical presentation and worse outcomes, than White women. More studies on APOs and CVD in non-White women are needed to better understand and address these health disparities. Future studies of aspirin, statins, and metformin may better inform our recommendations for pharmacotherapy in primary CVD prevention among women who have had an APO. Several opportunities exist for health care systems to improve transitions of care for women with APOs and to implement strategies to reduce their long-term CVD risk. One proposed strategy includes incorporation of the concept of a fourth trimester into clinical recommendations and health care policy.
Title:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Publisher:
John Wiley and Sons Inc.
(Hoboken
)
ISSN
(Electronic):
2047-9980
Publication date
(Electronic):
17
October
2022
Publication date Collection: 18
October
2022
Volume: 11
Issue: 20
(
doiID:
10.1002/jah3.v11.20
)
Electronic Location Identifier: e027707
Affiliations
[1]Department of Exercise Science, Arnold School of Public Health
University of South Carolina
Columbia
SC
[2]Department of Epidemiology, School of Public Health
University of Alabama at Birmingham
Birmingham
AL
[3]Division of Research
Kaiser Permanente Northern California
Oakland
CA
[4]Department of Health Systems Science
Kaiser Permanente Bernard J. Tyson School of Medicine
Pasadena
CA
Author notes
[*][*
]Correspondence to: Erica P. Gunderson, PhD, MS, MPH, R.D.Kaiser Permanente Bernard
J. Tyson School of Medicine, Kaiser Permanente Northern California Division of Research,
Cardiovascular and Metabolic Conditions Section, 2000 Broadway, Oakland, CA 94612.
Email:
erica.gunderson@
123456kp.org
This is an open access article under the terms of the
http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original
work is properly cited, the use is non‐commercial and no modifications or adaptations
are made.
History
Date
received
: 02
August
2022
Date
accepted
: 13
September
2022
Page count
Figures: 1,
Tables: 0,
Pages: 5,
Words: 3362
Funding
Funded by: National Heart, Lung and Blood Institute
Award ID: R01 HL145808
Funded by: CARDIA (Coronary Artery Risk Development in Young Adults
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