Early-Life Predictors of Systolic Blood Pressure Trajectories From Infancy to Adolescence: Findings From Project Viva

Author:

Aris Izzuddin M123ORCID,Rifas-Shiman Sheryl L1,Li Ling-Jun145,Belfort Mandy B6,Hivert Marie-France17,Oken Emily18ORCID

Affiliation:

1. Division of Chronic Disease Research Across the Lifecourse, Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, Boston, Massachusetts

2. Department of Obstetrics and Gynecology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore

3. Singapore Institute for Clinical Sciences, Agency for Science, Technology and Research, Singapore

4. Division of Obstetrics and Gynecology, KK Women’s and Children’s Hospital, Singapore

5. Obstetrics and Gynecology Academic Clinical Program, Duke-National University of Singapore Graduate Medical School, Singapore

6. Department of Pediatric Newborn Medicine, Brigham and Women’s Hospital, Boston, Massachusetts

7. Diabetes Unit, Massachusetts General Hospital, Boston, Massachusetts

8. Department of Nutrition, T.H. Chan School of Public Health, Harvard University, Boston, Massachusetts

Abstract

Abstract Childhood blood pressure (BP) is a strong predictor of later risk of cardiovascular disease. However, few studies have assessed dynamic BP trajectories throughout the early-life period. We investigated the relationship between early-life factors and systolic BP (SBP) from infancy to adolescence using linear spline mixed-effects models among 1,370 children from Project Viva, a Boston, Massachusetts-area cohort recruited in 1999–2002. After adjusting for confounders and child height, we observed higher SBP in children exposed to gestational diabetes mellitus (vs. normoglycemia; age 3 years: β = 3.16 mm Hg (95% confidence interval (CI): 0.28, 6.04); age 6 years: β = 1.83 mm Hg (95% CI: 0.06, 3.60)), hypertensive disorders of pregnancy (vs. normal maternal BP; age 6 years: β = 1.39 mm Hg (95% CI: 0.10, 2.67); age 9 years: β = 1.84 mm Hg (95% CI: 0.34, 3.34); age 12 years: β = 1.70 mm Hg (95% CI: 0.48, 2.92)), higher neonatal SBP (per 10-mm Hg increase; age 3 years: β = 1.26 mm Hg (95% CI: 0.42, 2.09); age 6 years: β = 1.00 mm Hg (95% CI: 0.49, 1.51); age 9 years: β = 0.75 mm Hg (95% CI: 0.17, 1.33)), and formula milk in the first 6 months of life (vs. breast milk only; age 12 years: β = 2.10 mm Hg (95% CI: 0.46, 3.74); age 15 years: β = 3.52 mm Hg (95% CI: 1.40, 5.64); age 18 years: β = 4.94 mm Hg (95% CI: 1.88, 7.99)). Our findings provide evidence of programming of offspring SBP trajectories by gestational diabetes, hypertensive disorders of pregnancy, and formula milk intake and of neonatal BP being a potentially useful marker of childhood BP. These factors could be relevant in identifying children who are at risk of developing elevated BP.

Funder

National Institutes of Health

National University of Singapore

Singapore National Medical Council

Publisher

Oxford University Press (OUP)

Subject

Epidemiology

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