TY - JOUR
T1 - Association of Number of Live Births With Electrocardiographic and Cardiac Structural Changes
AU - Harris, Elizabeth
AU - Mauricio, Rina
AU - Ayers, Colby R
AU - Garg, Sonia
AU - Khera, Amit
AU - de Lemos, James A.
AU - Sanghavi, Monika
N1 - Funding Information:
The DHS (Dallas Heart Study) was supported by grants from the Donald W. Reynolds Foundation and the National Center for Advancing Translational Sciences (UL1TR001105).
Publisher Copyright:
© 2022 The Authors.
PY - 2022/11/15
Y1 - 2022/11/15
N2 - BACKGROUND: Pregnancy is a major life event unique to women and leads to significant hemodynamic, hormonal, and metabolic changes. The purpose of this study was to use the DHS (Dallas Heart Study), a multiethnic population-based cohort study of Dallas county adults, to evaluate the association between number of live births and cardiac magnetic resonance imaging and ECG parameters later in life. METHODS AND RESULTS: Women were included if they had data on self-reported live births and ECG or cardiac magnetic resonance imaging measurements. The 3014 women were stratified by number of live births: 0, 1, 2, 3, 4, and ≥5. Higher number of live births was associated with larger left ventricular (LV) end-diastolic volume (β, 1.31±0.41; P<0.01), LV end-systolic volume (β, 0.83±0.24; P<0.01), and LV mass (β, 1.13±0.49; P=0.02) and lower LV ejection fraction (β, −0.004±0.0014; P<0.01). Increasing parity was associated with longer PR intervals (β, 1.07±0.38; P<0.01). Subgroup analysis by race demonstrated that the association between number of live births and magnetic resonance imaging parameters (LV end-diastolic volume, LV end-systolic volume, and LV ejection fraction) only remained significant in Black women (P value for interaction <0.05). CONCLUSIONS: Increasing number of live births was associated with electrocardiographic and cardiac structural changes in a multiethnic population. When stratified by race and ethnicity, magnetic resonance imaging structural changes only remained significant in Black participants. Whether these changes are pathologic and increase the risk of heart failure or arrhythmias in multiparous women warrants further investigation.
AB - BACKGROUND: Pregnancy is a major life event unique to women and leads to significant hemodynamic, hormonal, and metabolic changes. The purpose of this study was to use the DHS (Dallas Heart Study), a multiethnic population-based cohort study of Dallas county adults, to evaluate the association between number of live births and cardiac magnetic resonance imaging and ECG parameters later in life. METHODS AND RESULTS: Women were included if they had data on self-reported live births and ECG or cardiac magnetic resonance imaging measurements. The 3014 women were stratified by number of live births: 0, 1, 2, 3, 4, and ≥5. Higher number of live births was associated with larger left ventricular (LV) end-diastolic volume (β, 1.31±0.41; P<0.01), LV end-systolic volume (β, 0.83±0.24; P<0.01), and LV mass (β, 1.13±0.49; P=0.02) and lower LV ejection fraction (β, −0.004±0.0014; P<0.01). Increasing parity was associated with longer PR intervals (β, 1.07±0.38; P<0.01). Subgroup analysis by race demonstrated that the association between number of live births and magnetic resonance imaging parameters (LV end-diastolic volume, LV end-systolic volume, and LV ejection fraction) only remained significant in Black women (P value for interaction <0.05). CONCLUSIONS: Increasing number of live births was associated with electrocardiographic and cardiac structural changes in a multiethnic population. When stratified by race and ethnicity, magnetic resonance imaging structural changes only remained significant in Black participants. Whether these changes are pathologic and increase the risk of heart failure or arrhythmias in multiparous women warrants further investigation.
KW - ECG
KW - cardiac magnetic resonance imaging
KW - cardiovascular risk factors
KW - parity
KW - women’s health
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U2 - 10.1161/JAHA.122.025805
DO - 10.1161/JAHA.122.025805
M3 - Article
C2 - 36346053
AN - SCOPUS:85141883687
SN - 2047-9980
VL - 11
JO - Journal of the American Heart Association
JF - Journal of the American Heart Association
IS - 22
M1 - e025805
ER -