4.7 Article

Proton Pump Inhibitors Use and Risk of Preeclampsia: A Meta-Analysis

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 11, Issue 16, Pages -

Publisher

MDPI
DOI: 10.3390/jcm11164675

Keywords

hypertension; preeclampsia; proton pump inhibitors; PPIs; pregnancy; meta-analysis

Funding

  1. Operational Programme Research, Development and Education-Project, Postdoc2MUNI [CZ.02.2.69/0.0/0.0/18_053/0016952]
  2. INTER-EXCELLENCE grant [LTC20031]

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This study evaluates the association between the use of proton pump inhibitors (PPIs) and the risk of preeclampsia in pregnant women. The findings suggest that the use of PPIs during pregnancy significantly increases the risk of preeclampsia, although the increase is minimal in absolute terms. However, there is no evidence supporting that PPI use decreases the risk of preeclampsia or preterm preeclampsia.
Evidence from preclinical studies suggests a preventive effect of proton pump inhibitors (PPIs) in preeclampsia. Recently, several epidemiological studies have described a conflicting association between the use of PPIs during pregnancy and preeclampsia risk. This study aimed to evaluate the association between PPI use and the risk of preeclampsia. We searched databases, including MEDLINE, Embase, Scopus, Web of Science Core Collection, Emcare, CINAHL, and the relevant grey literature from inception until 13 September 2021. Studies reporting the preeclampsia risk with the use of PPIs were eligible for inclusion. Literature screening, data extraction, and the risk of bias assessment were performed independently by two investigators. Random-effect meta-analysis was performed to generate relative risks (RR) and 95% confidence intervals (CI). The risk of preeclampsia and preterm preeclampsia among women receiving PPIs during pregnancy were the primary outcomes of interest. This meta-analysis comprised three studies involving 4,877,565 pregnant women, of whom 119,017 were PPI users. The included studies were judged to have a low risk of bias. The risk of preeclampsia among pregnant women who received PPIs anytime during pregnancy was significantly increased (RR 1.27 (95% CI: 1.23-1.31)), although the increase was trivial in absolute terms (2 per 1000). The subgroup analysis revealed that the risk was increased in each of the three trimesters. The risk of preterm preeclampsia among pregnant women receiving PPIs anytime during pregnancy was not significantly increased (RR 1.04 (95% CI: 0.70-1.55)). The certainty evaluated by GRADE in these estimates was low. PPI use may be associated with a trivial increase in the risk of preeclampsia in pregnant women. There is no evidence supporting that PPI use decreases the risk of preeclampsia or preterm preeclampsia.

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