Evidence map›Paper›PMID 41346258›Full record

ArticleDiabetes, obesity & metabolism2026

Unintentional periconceptional exposure to glucagon-like peptide-1 receptor agonists and adverse pregnancy outcomes: A nationwide cohort study in Taiwan.

Yi-Chang Chou, Shih-Han Weng, Feng-Shiang Cheng, Chih-Hao Tseng, Hsiao-Yun Hu, Chieh-Hsing Liu

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Article in Diabetes, obesity & metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yi-Chang ChouDepartment of Health Promotion and Health Education, National Taiwan Normal University, Taipei, Taiwan.ORCID 0000-0002-7478-0105
Shih-Han WengDepartment of Education and Research, Taipei City Hospital, Taipei, Taiwan.
Feng-Shiang ChengDepartment of Education and Research, Taipei City Hospital, Taipei, Taiwan.
Chih-Hao TsengDepartment of Education and Research, Taipei City Hospital, Taipei, Taiwan.
Hsiao-Yun HuDepartment of Education and Research, Taipei City Hospital, Taipei, Taiwan.
Chieh-Hsing LiuDepartment of Health Promotion and Health Education, National Taiwan Normal University, Taipei, Taiwan.

Funding

Department of Health, Taipei City Government 11401-62-007
6 · The paper itself

Abstract

aimsTo assess whether periconceptional exposure to glucagon-like peptide-1 receptor agonists (GLP-1 RAs) is associated with adverse outcomes in women with pregestational type 2 diabetes. MATERIALS AND

methodsWe linked Taiwan's Birth Certificate Application and National Health Insurance claims (2013-2022) to assemble a nationwide cohort of singleton births to mothers (18-50 years) with pregestational diabetes. Exposure was any GLP-1 RA dispensed during the 90 days before and after the last menstrual period; insulin without GLP-1 RA was the active comparator. Outcomes were major congenital malformations, stillbirth, preterm birth (<37 weeks) and small for gestational age (SGA, <10th percentile). We used 1:4 propensity-score matching and Poisson generalised estimating equation (GEE); sensitivity analyses required ≥2 prescriptions and restricted exposure to the first trimester.

resultsWe identified 3351 comparison pregnancies (GLP-1 RA 160; insulin 3191); matching yielded 160 versus 606. Risk ratios (GLP-1 RA vs. insulin) were malformations 0.64 (95% confidence interval 0.11-3.83), stillbirth 2.05 (0.82-5.13), preterm birth 1.09 (0.85-1.39) and SGA 0.86 (0.31-2.41). Sensitivity analyses were similar.

conclusionsPericonceptional GLP-1 RA exposure was not associated with increased risks of malformations, stillbirth, preterm birth or SGA versus insulin use. These preliminary data require confirmation in larger agent-specific studies; until then, intentional GLP-1 RA use in planned pregnancy is not advised.

Indexed as

Diabetes Mellitus, Type 2Glucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsPregnancy in DiabeticsPregnancy OutcomeAdolescentAdultCohort StudiesCongenital AbnormalitiesFemaleHumansInfant, NewbornInfant, Small for Gestational AgeInsulinMiddle AgedPregnancyGlucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsInsulinglucagon‐like peptide‐1 receptor agonistspericonceptional exposurepregnancy outcomestype 2 diabetes mellitus

Identifiers

PMID41346258
PMCPMC12803572

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.