Evidence map›Paper›PMID 31958311›Full record

ArticleBMJ open diabetes research & care2020

Genetic factors and risk of type 2 diabetes among women with a history of gestational diabetes: findings from two independent populations.

Mengying Li, Mohammad L Rahman, Jing Wu, Ming Ding, Jorge E Chavarro, Yuan Lin, Sylvia H Ley, Wei Bao, Louise G Grunnet, Stefanie N Hinkle and 15 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open diabetes research & care, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 7% of its field
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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

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  16. Genetic variants ofFrontiers in endocrinology · 2023
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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

25 authors at 12 institutions in 3 countries.

Mengying Li *Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA.ORCID 0000-0002-3713-1683
Mohammad L Rahman *Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA.
Jing WuGlotech, Rockville, Maryland, USA.
Ming DingDepartment of Nutrition, Harvard University T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Jorge E ChavarroDepartment of Nutrition, Harvard University T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Yuan LinEpidemiology Department, Richard M. Fairbanks School of Public Health, Indiana University, Bloomington, Indiana, USA.
Sylvia H LeyDepartment of Nutrition, Harvard University T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Wei BaoDepartment of Epidemiology, College of Public Health, University of Iowa, Iowa City, Iowa, USA.
Louise G GrunnetDepartment of Endocrinology, Rigshospitalet, Copenhagen, Denmark.
Stefanie N HinkleDivision of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA.
Anne Cathrine B ThuesenSteno Diabetes Center Copenhagen, Gentofte, Denmark.
Edwina YeungDivision of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA.
Robert E Gore-LangtonThe Emmes Company, LLC, Rockville, Maryland, USA.
Seth ShermanThe Emmes Company, LLC, Rockville, Maryland, USA.
Line HjortDepartment of Endocrinology, Rigshospitalet, Copenhagen, Denmark.
Freja Bach KampmannDepartment of Endocrinology, Rigshospitalet, Copenhagen, Denmark.
Anne Ahrendt BjerregaardNutrition Group, Statens Serum Institut, Copenhagen, Denmark.
Peter DammDepartments of Obstetrics, Center for Pregnant Women with Diabetes, Rigshospitalet, Copenhagen, Denmark.
Fasil Tekola-AyeleDivision of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA.
Aiyi LiuDivision of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA.
James L MillsDivision of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA.
Allan VaagEarly Clinical Development and Innovative Medicines, AstraZeneca, Mölndal, Sweden.
Sjurdur F OlsenNutrition Group, Statens Serum Institut, Copenhagen, Denmark.
Frank B HuDepartment of Nutrition, Harvard University T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Cuilin ZhangDivision of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland, USA zhangcu@mail.nih.gov.
Eunice Kennedy Shriver National Institute of Child Health and Human Development · USRigshospitalet · DKBrigham and Women's Hospital · USEmmes (United States) · USHarvard University · USStatens Serum Institut · DKUniversity of Copenhagen · DKAstraZeneca (Sweden) · SEGlotech (United States) · USIndiana University Bloomington · USTulane University · USUniversity of Iowa · US

Funding

Risk Factors for Breast Cancer in Younger NursesR01CA050385 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI ELIASSEN, A. HEATHER, WILLETT, WALTER C. · 1989 to 2019
$32.3M
Tulane COBRE in Cardiometabolic Diseases Clinical Research CoreP20GM109036 · NIGMS · TULANE UNIVERSITY OF LOUISIANA · PI JING CHEN · 2016 to 2026
$25.3M
Life Course Cancer Epidemiology Cohort in WomenU01CA176726 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI ELIASSEN, A. HEATHER, WILLETT, WALTER C. · 2018 to 2025
$22.4M
Life Course Cancer Epidemiology Cohort in WomenUM1CA176726 · NCI · HARVARD SCHOOL OF PUBLIC HEALTH · PI WILLETT, WALTER C. · 2013 to 2017
$15.7M
Premonopausal Hormone Levels and Risk of Breast CancerR01CA067262 · NCI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI HANKINSON, SUSAN E · 2002 to 2011
$11.9M
NCI NIH HHS R01 CA050385NCI NIH HHS R01 CA067262NCI NIH HHS U01 CA176726NCI NIH HHS UM1 CA176726NICHD NIH HHS HHSN275201000020CNICHD NIH HHS HHSN275201300026INICHD NIH HHS HHSN275201500003CNIGMS NIH HHS P20 GM109036
6 · The paper itself

Abstract

objectiveWomen with a history of gestational diabetes mellitus (GDM) have an exceptionally high risk for type 2 diabetes (T2D). Yet, little is known about genetic determinants for T2D in this population. We examined the association of a genetic risk score (GRS) with risk of T2D in two independent populations of women with a history of GDM and how this association might be modified by non-genetic determinants for T2D. RESEARCH DESIGN AND

methodsThis cohort study included 2434 white women with a history of GDM from the Nurses' Health Study II (NHSII, n=1884) and the Danish National Birth Cohort (DNBC, n=550). A GRS for T2D was calculated using 59 candidate single nucleotide polymorphisms for T2D identified from genome-wide association studies in European populations. An alternate healthy eating index (AHEI) score was derived to reflect dietary quality after the pregnancy affected by GDM.

resultsWomen on average were followed for 21 years in NHSII and 13 years in DNBC, during which 446 (23.7%) and 155 (28.2%) developed T2D, respectively. The GRS was generally positively associated with T2D risk in both cohorts. In the pooled analysis, the relative risks (RRs) for increasing quartiles of GRS were 1.00, 0.97, 1.25 and 1.19 (p trend=0.02). In both cohorts, the association appeared to be stronger among women with poorer (AHEI <median) than better dietary quality (AHEI ≥median), although the interaction was not significant. For example, in NHSII, the RRs across increasing quartiles of GRS were 1.00, 0.99, 1.51 and 1.29 (p trend=0.06) among women with poorer dietary quality and 1.00, 0.83, 0.81 and 0.94 (p trend=0.79) among women with better dietary quality (p interaction=0.11).

conclusionsAmong white women with a history of GDM, higher GRS for T2D was associated with an increased risk of T2D.

Indexed as

Diabetes, GestationalDiabetes Mellitus, Type 2Cohort StudiesFemaleGenome-Wide Association StudyHumansPolymorphism, Single NucleotidePregnancydietary qualitygenetic risk scoregestational diabetesprospective cohort studiestype 2 diabetes

Identifiers

PMID31958311
PMCPMC7039588
OpenAlexW3005783559

What OpenQuestion holds

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LicenceCC BY-NC
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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.