Evidence mapPaperPMID 41212558Full record

ArticleJAMA network open2025

Early Postpartum Glucose Tolerance Reclassification by Gestational Diabetes Subtype.

Julie A D Van, Joan C Lo, Yeyi Zhu, Alexis S King, Baiyang Sun, Emily Hashimoto-Roth, Hannes Rost, Stacey Alexeeff, Michael B Wheeler, Erica P Gunderson

Abstract read
In one paragraph

Article in JAMA network open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Julie A D VanDepartment of Physiology, University of Toronto, Toronto, Ontario, Canada.
Joan C LoDivision of Research, Kaiser Permanente Northern California, Pleasanton.
Yeyi ZhuDivision of Research, Kaiser Permanente Northern California, Pleasanton.
Alexis S KingDivision of Research, Kaiser Permanente Northern California, Pleasanton.
Baiyang SunDivision of Research, Kaiser Permanente Northern California, Pleasanton.
Emily Hashimoto-RothDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Hannes RostDepartment of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
Stacey AlexeeffDivision of Research, Kaiser Permanente Northern California, Pleasanton.
Michael B WheelerDepartment of Physiology, University of Toronto, Toronto, Ontario, Canada.
Erica P GundersonDivision of Research, Kaiser Permanente Northern California, Pleasanton.

Funding

Metabolite Profiles Preceding Progression to Diabetes Mellitus after Gestational DiabetesR01DK118409 · NIDDK · KAISER FOUNDATION RESEARCH INSTITUTE · PI Erica Pauline Gunderson · 2023 to 2023
$607k
NIDDK NIH HHS R01 DK118409
6 · The paper itself

Abstract

Importance: Gestational diabetes (GD) is a heterogeneous condition that predisposes both mother and offspring to metabolic disorders. GD subtypes defined by antepartum testing results have been associated with adverse perinatal outcomes, but little is known about their relationship to maternal metabolic outcomes soon after pregnancy. Objective: To evaluate early postpartum glucose tolerance reclassification of GD subtypes. Design, Setting, and Participants: This cohort study examined women from the Study of Women, Infant Feeding, and Type 2 Diabetes Mellitus After GD Pregnancy (SWIFT), who were recruited within the Kaiser Permanente Northern California integrated health care system between 2008 and 2011. All women were diagnosed with GD using Carpenter and Coustan criteria with complete glucose measurements at all 4 time points of the diagnostic 3-hour 100-gram oral glucose tolerance test (OGTT). Data analyses were conducted from January to July 2025. Exposure: Three subtypes of GD based on the diagnostic OGTT: (1) postload glucose intolerance (GD-P), as having elevations only at 2 or more postload time points; (2) fasting hyperglycemia (GD-F), as having elevations at fasting and 1 postload time point; and (3) both (GD-M), as having elevations at fasting and 2 or more post-load time points. Main Outcomes and Measures: At 6 to 9 weeks after delivery, glucose tolerance classification was evaluated using 2-hour, 75-g OGTTs. Modified Poisson regression models were used to estimate adjusted prevalence ratios (PRs) of postpartum prediabetes associated with GD subtypes, without and with adjustments for age, race and ethnicity, prepregnancy body mass index, educational level, and gestational weight gain. Results: This study included 1005 women with GD (median [IQR] age, 33.2 [29.8-36.7] years; 368 [36.6%] Asian, 78 [7.8%] Black, 308 [30.6%] Hispanic, 16 [1.6%] multiracial, and 235 [23.4%] White). Prevalence of postpartum prediabetes was 34.5% (347 women), with wide variation across GD subtypes; 23.9% (147 of 616), 41.9% (52 of 124), and 55.8% (148 of 265) for GD-P, GD-F, and GD-M, respectively. Compared with women with GD-P, the adjusted PR for GD-F was 1.74 (95% CI, 1.36-2.24), and for GD-M, it was 2.23 (95% CI, 1.85-2.68) (both P < .001). Pairwise comparisons between GD-F and GD-M were also statistically significant (adjusted PR, 1.28; 95% CI, 1.01-1.61; P = .04). Conclusions and Relevance: In this cohort study, GD subtypes had distinct postpartum prediabetes risks. Early action and intervention to address dysglycemia may be most beneficial for women with fasting or mixed defects.

Indexed as

Diabetes, GestationalGlucose IntolerancePostpartum PeriodAdultBlood GlucoseCaliforniaCohort StudiesDiabetes Mellitus, Type 2FemaleGlucose Tolerance TestHumansPregnancyBlood Glucose

Identifiers

PMID41212558
PMCPMC12603860

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.