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PeerJ· 2026Q1· Review

Prenatal allostatic load and adverse pregnancy outcomes: a systematic review and meta-analysis

Mengjie Zhao, Hanyue Zheng, Dengyan Qi, Xuening Zhang et al.

Short summary

High prenatal allostatic load (AL) is associated with a 29% increased risk of preterm birth (OR=1.29) and a 131% increased risk of preeclampsia (OR=2.31) in pregnant women.

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Key points

  • High prenatal allostatic load (AL) is associated with increased risk of preterm birth (OR = 1.29, 95% CI [1.04–1.60]).
  • High prenatal AL is associated with increased risk of preeclampsia (OR = 2.31, 95% CI [1.42–3.76]).
  • No statistically significant association was found between high prenatal AL and low birth weight (OR = 1.10, 95% CI [0.95–1.26]).
  • Eight studies involving 8,795 pregnant women were included in the meta-analysis.

AI-generated from the title and abstract; the full text is not read.

Abstract

Background Allostatic load (AL) denotes the cumulative physiological dysregulation resulting from chronic stress exposure. This systematic review and meta-analysis aimed to evaluate the association between prenatal AL and adverse pregnancy outcomes (APOs), and to synthesize current evidence to inform prenatal health strategies and potentially reduce the incidence of APOs. Methodology This study systematically searched PubMed, Web of Science, Embase, PsycINFO, China National Knowledge Infrastructure, Wanfang, VIP China Science and Technology Journal Database, and SinoMed databases for relevant studies examining prenatal AL and APOs published from September 1993 to 22 June 2026. Two researchers independently screened the literature, extracted data, and assessed the risk of bias using the Newcastle-Ottawa scale. Meta-analysis was performed using R software (version 4.4.3). The study protocol is registered in PROSPERO (CRD420251076952). Results Eight original studies involving 8,795 pregnant women were included. High prenatal AL was associated with an increased risk of preterm birth (OR = 1.29, 95% CI [1.04–1.60]) and preeclampsia (OR = 2.31, 95% CI [1.42–3.76]). There was no statistically significant association with low birth weight (OR = 1.10, 95% CI [0.95–1.26]). Furthermore, exploratory subgroup analyses suggested that the gestational period and biomarker composition may influence these associations; however, high methodological heterogeneity limits direct clinical application. Conclusions Elevated prenatal AL is associated with an increased risk of specific APOs, particularly preterm birth and preeclampsia. Future studies should adopt longitudinal designs with repeated AL measurements across pregnancy to clarify temporal dynamics and elucidate underlying biological mechanisms.

The authors' abstract, as published at the source. PeerJ, 2026 · DOI ↗

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Field: Behavioral Neuroscience

Behavioral NeuroscienceNeuroscience