Evidence map›Paper›PMID 41284263›Full record

ArticleJAMA2025

Gestational Weight Gain and Pregnancy Outcomes After GLP-1 Receptor Agonist Discontinuation.

Jacqueline Maya, Deepti Pant, Yiran Fu, Kaitlyn James, Carolina Batlle, Sarah Hsu, Diana C Soria-Contreras, Lydia L Shook, Christopher Mow, Marie-France Hivert and 2 more

Registry-linked trialAbstract read
In one paragraph

Article in JAMA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07743567 (Gestational Response, Outcomes, and Weight After GLP-1 Use), which is not on this map. Cited by 36 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT07743567 recruitingnot on this mapstarted 2026, after this paper: background citation

Gestational Response, Outcomes, and Weight After GLP-1 Use

TypeobservationalSponsorUniversity of Kansas Medical CenterRan2026 to 2028Enrolled400ConditionsPregnant Individuals, Obesity & Overweight, Gestational Weight Gain
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Efficacy and safety of cannabinoid-based interventions for behavioral and cognitive symptoms in dementia: systematic review and meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Pooled it
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  4. Hypertension Management in Pregnancy and Postpartum.Journal of the American Society of Nephrology : JASN · 2026
    Review
  5. Hypertensive disorders of pregnancy and women's health throughout the life course: an update review 2025-2026.Hypertension research : official journal of the Japanese Society of Hypertension · 2026
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Jacqueline MayaDiabetes Unit, Department of Medicine, Massachusetts General Hospital, Boston.
Deepti PantMassachusetts General Hospital Biostatistics, Boston.
Yiran FuMassachusetts General Hospital Biostatistics, Boston.
Kaitlyn JamesHarvard Medical School, Boston, Massachusetts.
Carolina BatlleDiabetes Unit, Department of Medicine, Massachusetts General Hospital, Boston.
Sarah HsuDiabetes Unit, Department of Medicine, Massachusetts General Hospital, Boston.
Diana C Soria-ContrerasDiabetes Unit, Department of Medicine, Massachusetts General Hospital, Boston.
Lydia L ShookHarvard Medical School, Boston, Massachusetts.
Christopher MowMass General Brigham Digital Research Data, Boston, Massachusetts.
Marie-France HivertDiabetes Unit, Department of Medicine, Massachusetts General Hospital, Boston.
Tanayott ThaweethaiHarvard Medical School, Boston, Massachusetts.
Camille E PoweDiabetes Unit, Department of Medicine, Massachusetts General Hospital, Boston.

Funding

TRAINING PROGRAM IN ENDOCRINOLOGY AND DIABETEST32DK007028 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Karen K Miller · 1986 to 2026
$18.5M
Mentoring Underrepresented Researchers in Diabetes and Pregnancy InvestigationK26DK138346 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Camille Elise Powe · 2023 to 2026
$529k
NIDDK NIH HHS K26 DK138346NIDDK NIH HHS T32 DK007028
6 · The paper itself

Abstract

Importance: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) are contraindicated in pregnancy. Discontinuation of GLP-1RAs proximal to pregnancy could affect gestational weight gain and pregnancy outcomes. Objective: To compare gestational weight gain and pregnancy outcomes with and without exposure to GLP-1RAs before or during early pregnancy. Design, Setting, and Participants: Retrospective cohort study of 149 790 singleton pregnancies delivered between June 1, 2016, and March 31, 2025, within a single academic health system. Exposure: A GLP-1RA order between 3 years before and 90 days after conception, with propensity score matching of each exposed pregnancy to 3 unexposed pregnancies. Main Outcomes and Measures: The primary outcome was gestational weight gain. Secondary outcomes were excess gestational weight gain, large and small for gestational age birth weight, birth weight percentile for gestational age and sex, birth length, preterm delivery, cesarean delivery, gestational diabetes, and hypertensive disorders of pregnancy. Results: Among 149 790 pregnancies during the study period, 1792 (448 exposed and 1344 unexposed) were matched for the primary analysis. Exposed pregnancies had mean maternal age of 34.0 years (SD, 4.7 years) and prepregnancy body mass index of 36.1 (SD, 6.5; calculated as weight in kilograms divided by height in meters squared); 378 of 448 (84%) had obesity and 104 of 448 (23%) had preexisting diabetes; 136 (30%) were Hispanic, 49 (11%) were non-Hispanic Black, and 223 (50%) were non-Hispanic White; and 43 (10%) had public insurance. The GLP-1RA-exposed pregnancies had greater gestational weight gain (mean, 13.7 kg [SD, 9.2]) than propensity score-matched unexposed pregnancies (mean, 10.5 kg [SD, 8.0]), a difference of 3.3 kg (95% CI, 2.3-4.2; P < .001). The GLP-1RA-exposed group had a higher risk of excess gestational weight gain (65% vs 49%; risk ratio [RR], 1.32; 95% CI, 1.19-1.47), greater mean birth weight percentile (58.4% vs 54.8%; difference, 3.6%; 95% CI, 0.2%-6.9%), and higher risk of preterm delivery (17% vs 13%; RR, 1.34; 95% CI, 1.06-1.69), gestational diabetes (20% vs 15%; RR, 1.30; 95% CI, 1.01-1.68), and hypertensive disorders of pregnancy (46% vs 36%; RR, 1.29; 95% CI, 1.12-1.49). There was no difference in birth length, risk of large or small for gestational age birth weight, or cesarean delivery. Conclusions and Relevance: In a cohort composed primarily of women with obesity, GLP-1RA use with subsequent prepregnancy or early pregnancy discontinuation was associated with more gestational weight gain and a higher risk of preterm delivery, gestational diabetes, and hypertensive disorders of pregnancy.

Indexed as

Gestational Weight GainGlucagon-Like Peptide-1 Receptor AgonistsPregnancy OutcomeAdultBirth WeightCesarean SectionContraindications, DrugDiabetes, GestationalFemaleHumansHypertension, Pregnancy-InducedInfant, NewbornInfant, Small for Gestational AgeObesityPregnancyPremature BirthGlucagon-Like Peptide-1 Receptor Agonists

Identifiers

PMID41284263
PMCPMC12645404

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Registered trials

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.