Evidence mapPaperPMID 41770725Full record

ArticlePloS one2026

Gestational diabetes-Risk factors and outcomes among American Samoan Women (GROW): A longitudinal cohort study protocol.

Danielle J Carson, Kima Faasalele-Savusa, Miracle Loia, Susie Tasele, Emele Iosefa, Peresia Tupuola, Kelly C Sanchez, Oumaima Kaabi, Rachel K Valencia, Mary G Rossillo and 14 more

Abstract read
In one paragraph

Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors.

Danielle J CarsonDepartment of Epidemiology, Emory University Rollins School of Public Health, Atlanta, Georgia, United States of America.
Kima Faasalele-SavusaObesity, Lifestyle and Genetic Adaptations (OLaGA) Research Center, Nu'uli, American Samoa.
Miracle LoiaObesity, Lifestyle and Genetic Adaptations (OLaGA) Research Center, Nu'uli, American Samoa.
Susie TaseleObesity, Lifestyle and Genetic Adaptations (OLaGA) Research Center, Nu'uli, American Samoa.
Emele IosefaObesity, Lifestyle and Genetic Adaptations (OLaGA) Research Center, Nu'uli, American Samoa.
Peresia TupuolaObesity, Lifestyle and Genetic Adaptations (OLaGA) Research Center, Nu'uli, American Samoa.
Kelly C SanchezDepartment of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, Connecticut, United States of America.ORCID https://orcid.org/0009-0003-2708-8815
Oumaima KaabiDepartment of Epidemiology, Emory University Rollins School of Public Health, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0009-0003-7995-0294
Rachel K ValenciaDepartment of Epidemiology, Emory University Rollins School of Public Health, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0002-9130-7176
Mary G RossilloDivision of Endocrinology, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Neharika MurthyDivision of Endocrinology, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Tolulope AkinadeDepartment of Psychiatry, Yale School of Medicine, New Haven, Connecticut, United States of America.
Lacey W HeinsbergDepartment of Health Promotion and Development, School of Nursing, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Jenna C CarlsonDepartment of Human Genetics, School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.ORCID https://orcid.org/0000-0001-5483-0833
Clare A FlanneryDepartment of Obstetrics, Gynecology, and Reproductive Sciences, Yale School of Medicine, New Haven, Connecticut, United States of America.ORCID https://orcid.org/0000-0002-0219-0907
Stephen T McGarveyDepartment of Epidemiology, Center for Global Public Health, Brown University School of Public Health, Providence, Rhode Island, United States of America.ORCID https://orcid.org/0000-0003-1233-6970
Ashlee N WoodDivision of Endocrinology, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Scott AnesiLyndon B Johnson Tropical Medical Center, Pago Pago, American Samoa.
Va'atausili TofaeonoAmerican Samoa Community Cancer Coalition, Nu'uuli, American Samoa.
Katie DesobryLyndon B Johnson Tropical Medical Center, Pago Pago, American Samoa.
Bethel T Muasau-HowardLyndon B Johnson Tropical Medical Center, Pago Pago, American Samoa.
Angela M BengtsonDepartment of Epidemiology, Emory University Rollins School of Public Health, Atlanta, Georgia, United States of America.
Erin E KershawDivision of Endocrinology, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, United States of America.
Nicola L HawleyDepartment of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, Connecticut, United States of America.ORCID https://orcid.org/0000-0002-2601-3454

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGestational diabetes mellitus (GDM) is linked with adverse health outcomes for both mother and infant and increases the risk of type 2 diabetes mellitus (T2DM) and long-term metabolic dysfunction postpartum. American Samoa experiences among the highest prevalence of GDM globally, with estimates suggesting 26-42% of women develop the condition. To date, no studies have attempted to understand the underlying etiology of GDM in Pacific Islanders or examine population-specific progression from GDM to T2DM. The GROW study will characterize glucose homeostasis, diabetes progression, and the impact of a Pacific-specific variant (rs373863828) in the CREBRF gene, which is known to protect against T2DM, on glucose metabolism during and after pregnancy.

methodsWe will establish a prospective cohort study of 350 pregnant women in American Samoa, enrolled in their first trimester and followed through 18 months postpartum. Participants will be genotyped for CREBRF rs373863828 and undergo frequently-sampled oral glucose tolerance test (fs-OGTTs), glycated hemoglobin (HbA1c), and continuous glucose monitoring (CGM) measurements to identify glycemic patterns across the perinatal period. Participants will complete questionnaires assessing reproductive health history, diet, physical activity, sleep, and psychosocial health. We will examine associations between CREBRF genotype and glucose homeostasis across pregnancy and postpartum and evaluate risk of GDM and subsequent T2DM. We will also explore associations between CREBRF genotype, changes in insulin secretion in pregnancy, and risk of adverse birth outcomes. DISCUSSION: Findings from this study are expected to inform precision medicine approaches to diabetes prevention, refine public health policies and clinical guidelines, and support community-based interventions aimed at reducing GDM and T2DM among Pacific Islander women and more broadly.

Indexed as

Diabetes, GestationalDiabetes Mellitus, Type 2AdultAmerican SamoaBlood GlucoseContinuous Glucose MonitoringFemaleGlucose Tolerance TestGlycated HemoglobinHumansLongitudinal StudiesPregnancyProspective StudiesRisk FactorsBlood GlucoseGlycated Hemoglobin

Identifiers

PMID41770725
PMCPMC12952650

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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 Socratic graph.