Clinical Investigation
Coronary Artery Disease
Association of number of live births with left ventricular structure and function. The Multi-Ethnic Study of Atherosclerosis (MESA)

https://doi.org/10.1016/j.ahj.2011.12.011Get rights and content

Background

Pregnancy is associated with marked maternal cardiovascular/hemodynamic changes. A greater number of pregnancies may be associated with long-term subclinical changes in left ventricular (LV) remodeling.

Methods

Among 2,234 white, black, Hispanic, and Chinese women (mean age 62 years) in the MESA, we used linear regression to relate live births and cardiac magnetic resonance imaging LV measures. Covariates included age, ethnicity, height, income, education, birth country, smoking, menopause, and oral contraceptive duration. Models were additionally adjusted for potential mediators: systolic blood pressure, antihypertensive use, total/high-density lipoprotein cholesterol, triglycerides, diabetes, and body mass index. We performed sensitivity analyses excluding 763 women in the lowest socioeconomic group: annual income <$25,000 and lower high school level of education.

Results

With each live birth, LV mass increased 1.26 g; LV end-diastolic volume, 0.74 mL; and LV end-systolic volume, 0.45 mL; LV ejection fraction decreased 0.18% (P trend <0.05). Changes were most notable for the category of women with ≥5 pregnancies. Upon adjustment for potential biologic mediators, live births remained positively associated with LV mass and end-systolic volume. Live births remained significantly associated with LV end-systolic, end-diastolic volumes, and LV mass (P trend ≤0.02) after excluding women in the lowest socioeconomic group.

Conclusions

Number of live births is associated with key LV structural and functional measures in middle to older ages, even after adjustment for sociodemographic factors and cardiovascular disease risk factors. Hemodynamic changes during pregnancy may be associated with cardiac structure/function beyond childbearing years.

Section snippets

Study population

The MESA, begun in July 2000, was designed to investigate the prevalence, correlates, and progression of CVD in individuals without clinically manifest or symptomatic CVD.9 This prospective cohort study enrolled 6,814 participants (including 3,601 women) aged 45 to 84 years from 6 US communities (Baltimore, MD; Chicago, IL; Forsyth County, NC; Los Angeles County, CA; Northern Manhattan, NY; and St Paul, MN). The recruitment of participants has been previously described.9 Cohort participants

Results

The characteristics of the 2,234 women (mean age 62 years) in our study sample are displayed in Table I, stratified by number of live births. The number of live births ranged from 0 to 18. The mean age was greater for women with increasing number of live births. Hispanic and Chinese women had more live births, whereas black and white women had fewer live births. Systolic and diastolic blood pressure and triglycerides were all higher with increasing numbers of live births. Prevalence of current

Summary of findings

Among 2,234 women free of CVD (mean age 62 years), number of live births was positively associated with subsequent LVEDV, LVESV, and LV mass and inversely associated with LVEF. Changes were most notable for women with 5 or more live births. After adjustment for potential biologic mediators, number of live births remained significantly associated with LV mass and LVESV and inversely associated with LVEF at a borderline level of statistical significance. The effects were similar across categories

Conclusions

Number of live births is associated with modest changes in key LV structural and functional measures in middle- to older-aged women, most notably among women reporting 5 or more live births during their lifetime. It is uncertain whether these changes are fully mediated through traditional CVD risk factors or reflect subclinical peripartum LV remodeling that persists postpartum.

Author Contributions

Drs Parikh and Lloyd-Jones had full access to all data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis.

Author Disclosures

None.

Acknowledgements

The authors thank the other investigators, the staff, and the participants of the MESA study for their valuable contributions. A full list of participating MESA investigators and institutions can be found at http://www.mesa-nhlbi.org.

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