Sodium intake and the development of hypertensive disorders of pregnancy.


Journal

American journal of obstetrics & gynecology MFM
ISSN: 2589-9333
Titre abrégé: Am J Obstet Gynecol MFM
Pays: United States
ID NLM: 101746609

Informations de publication

Date de publication:
11 2023
Historique:
received: 17 07 2023
revised: 10 09 2023
accepted: 19 09 2023
medline: 6 11 2023
pubmed: 24 9 2023
entrez: 23 9 2023
Statut: ppublish

Résumé

In nonpregnant populations, sodium intake has been associated with the development of chronic hypertension, and sodium restriction has been identified as a strategy to reduce blood pressure. Data regarding the relationship between sodium intake and the development of hypertensive disorders of pregnancy are limited and conflicting. This study aimed to assess the association between daily periconceptional sodium intake and the risk of hypertensive disorders of pregnancy. This was a secondary analysis of the prospective Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-To-Be study. Individuals with nonanomalous, singleton pregnancies who completed food frequency questionnaires with recorded sodium intake in the 3 months before pregnancy were included in the analysis. Individuals whose pregnancies did not progress beyond 20 weeks of gestation were excluded from the analysis. Sodium intake was categorized as low (<2 g per day), medium (2 to <3 g per day), or high (≥3 g per day), based on thresholds used in the nonpregnant population. The primary outcome was the development of a new-onset hypertensive disorder of pregnancy, including gestational hypertension; preeclampsia; hemolysis, elevated liver enzymes, and low platelet count syndrome; superimposed preeclampsia; or eclampsia. Bivariable analyses were performed using Kruskal-Wallis and chi-square tests. Poisson regression was used to estimate adjusted incidence risk ratios with 95% confidence intervals after controlling for potentially confounding factors. Among 7458 individuals included in this analysis, 2336 (31%) reported low sodium intake, 2792 (37%) reported medium sodium intake, and 2330 (31%) reported high sodium intake. Individuals with high sodium intake were more likely to have chronic hypertension, to use tobacco, and to be living with obesity. The risk of developing a hypertensive disorder of pregnancy was similar among groups (medium vs low adjusted incidence risk ratio: 1.10 [95% confidence interval, 0.94-1.28]; high vs low adjusted incidence risk ratio: 1.17 [95% confidence interval, 1.00-1.37]). There was no difference in neonatal outcomes by sodium intake, including preterm birth, small-for-gestational-age neonate, and admission to the neonatal intensive care unit. Sodium intake was not associated with the risk of developing a hypertensive disorder of pregnancy. This lack of association contrasts with that between sodium intake and hypertension in the nonpregnant state and may reflect differences in the pathophysiology underlying pregnancy- vs non-pregnancy-related hypertensive disorders.

Sections du résumé

BACKGROUND
In nonpregnant populations, sodium intake has been associated with the development of chronic hypertension, and sodium restriction has been identified as a strategy to reduce blood pressure. Data regarding the relationship between sodium intake and the development of hypertensive disorders of pregnancy are limited and conflicting.
OBJECTIVE
This study aimed to assess the association between daily periconceptional sodium intake and the risk of hypertensive disorders of pregnancy.
STUDY DESIGN
This was a secondary analysis of the prospective Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-To-Be study. Individuals with nonanomalous, singleton pregnancies who completed food frequency questionnaires with recorded sodium intake in the 3 months before pregnancy were included in the analysis. Individuals whose pregnancies did not progress beyond 20 weeks of gestation were excluded from the analysis. Sodium intake was categorized as low (<2 g per day), medium (2 to <3 g per day), or high (≥3 g per day), based on thresholds used in the nonpregnant population. The primary outcome was the development of a new-onset hypertensive disorder of pregnancy, including gestational hypertension; preeclampsia; hemolysis, elevated liver enzymes, and low platelet count syndrome; superimposed preeclampsia; or eclampsia. Bivariable analyses were performed using Kruskal-Wallis and chi-square tests. Poisson regression was used to estimate adjusted incidence risk ratios with 95% confidence intervals after controlling for potentially confounding factors.
RESULTS
Among 7458 individuals included in this analysis, 2336 (31%) reported low sodium intake, 2792 (37%) reported medium sodium intake, and 2330 (31%) reported high sodium intake. Individuals with high sodium intake were more likely to have chronic hypertension, to use tobacco, and to be living with obesity. The risk of developing a hypertensive disorder of pregnancy was similar among groups (medium vs low adjusted incidence risk ratio: 1.10 [95% confidence interval, 0.94-1.28]; high vs low adjusted incidence risk ratio: 1.17 [95% confidence interval, 1.00-1.37]). There was no difference in neonatal outcomes by sodium intake, including preterm birth, small-for-gestational-age neonate, and admission to the neonatal intensive care unit.
CONCLUSION
Sodium intake was not associated with the risk of developing a hypertensive disorder of pregnancy. This lack of association contrasts with that between sodium intake and hypertension in the nonpregnant state and may reflect differences in the pathophysiology underlying pregnancy- vs non-pregnancy-related hypertensive disorders.

Identifiants

pubmed: 37741626
pii: S2589-9333(23)00308-7
doi: 10.1016/j.ajogmf.2023.101166
pii:
doi:

Substances chimiques

Sodium, Dietary 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

101166

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Auteurs

Tracy Caroline Bank (TC)

Department of Obstetrics and Gynecology, The Ohio State University Wexner Medical Center, Columbus, OH (Drs Bank, Grasch, Grobman, and Frey). Electronic address: tracy.bank@osumc.edu.

Jennifer L Grasch (JL)

Department of Obstetrics and Gynecology, The Ohio State University Wexner Medical Center, Columbus, OH (Drs Bank, Grasch, Grobman, and Frey).

Judith Chung (J)

Department of Obstetrics and Gynecology, University of California, Irvine, Irvine, CA (Dr Chung).

Brian M Mercer (BM)

Department of Obstetrics and Gynecology, The MetroHealth System, Case Western Reserve University, Cleveland, OH (Dr Mercer).

Rebecca B McNeil (RB)

RTI International, Durham, NC (Dr McNeil).

Samuel Parry (S)

Department of Obstetrics and Gynecology, Penn Medicine, Philadelphia, PA (Dr Parry).

George Saade (G)

Department of Obstetrics and Gynecology, Eastern Virginia Medical School, Norfolk, VA (Dr Saade).

Anthony Shanks (A)

Department of Obstetrics and Gynecology, Indiana University, Indianapolis, IN (Dr Shanks).

Robert M Silver (RM)

Department of Obstetrics and Gynecology, University of Utah, Salt Lake City, UT (Dr Silver).

Hyagriv Simhan (H)

Department of Obstetrics and Gynecology, University of Pittsburgh, Pittsburgh, PA (Dr Simhan).

Lynn M Yee (LM)

Department of Obstetrics and Gynecology, Northwestern University Feinberg School of Medicine, Chicago, IL (Dr Yee).

Uma Reddy (U)

Department of Obstetrics and Gynecology, Columbia University, New York, NY (Dr Reddy).

William A Grobman (WA)

Department of Obstetrics and Gynecology, The Ohio State University Wexner Medical Center, Columbus, OH (Drs Bank, Grasch, Grobman, and Frey).

Heather A Frey (HA)

Department of Obstetrics and Gynecology, The Ohio State University Wexner Medical Center, Columbus, OH (Drs Bank, Grasch, Grobman, and Frey).

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