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Original Articles

Racial and ethnic differences in the relationship between infant loss after prior live birth and hypertensive disorders in pregnancy

, , , , & ORCID Icon
Pages 9600-9607 | Received 07 Jul 2021, Accepted 01 Mar 2022, Published online: 13 Mar 2022
 

Abstract

Background

Race and ethnicity influence the distribution and severity of hypertensive disorders of pregnancy (HDP) in the U.S. population, although the impact of prior infant loss on this relationship requires further investigation.

Objectives

The aim of this study was to assess the relationship between history of infant loss and the risk of HDP by maternal race and ethnicity.

Methods

For this large cross-sectional study, data were analyzed from the National Center for Health Statistics Vital Statistics Natality Birth Data, 2014–2017. The primary outcome was HDP, and the primary predictor was infant loss after prior live birth. Maternal race/ethnicity was the secondary predictor categorized as Non-Hispanic White (NHW), Non-Hispanic Black (NHB), Hispanic, Asian, or Other. Multiple logistic regression was used to assess the association between history of infant loss and HDP by race and ethnicity.

Results

The 9,439,520 women included in this sample were 51% NHW, 15% NHB, 25% Hispanic, 6% Asian, and 3% Other with a mean age of 29.8 ± 5.3 years. In adjusted analyses, infant loss after prior live birth was significantly associated with an 11% odds of HDP (OR 1.11, 95% CI 1.08, 1.13). Stratified by race, NHB (OR 1.28; 95% CI 1.21, 1.36) women had significantly higher odds of HDP, and Hispanic (OR 0.84, 95% CI 0.79, 0.90) and Asian (OR 0.85, 95% CI 0.75, 0.97) women had significantly lower odds compared to NHW women. Within races, all women with infant loss after prior live birth had significantly higher odds of HDP (p < .001), except Other women (p = .632).

Conclusions

Infant loss after prior live birth was significantly associated with higher odds of HDP among NHB women after adjusting for covariates. Further research is warranted to assess underlying mechanisms associated with higher odds of HDP in NHB women.

Acknowledgments

KW, JSW, AP, and LEE designed the study. AS identified the dataset, and EG and LEE acquired the data. JSW and LEE developed the analyses. EG analyzed the data. KW, JSW, and LEE interpreted the data. All authors critically revised the manuscript for important intellectual content and approved the final manuscript.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

Effort for this study partially supported by the National Institute of Diabetes and Digestive and Kidney Diseases K24Dk093699, R01DK118038, and R01DK120861 (PI: Leonard E. Egede, MD, MS).

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