Evidence map›Paper›PMID 33051273›Full record

ArticleDiabetes2021

Genetic Loci and Physiologic Pathways Involved in Gestational Diabetes Mellitus Implicated Through Clustering.

Camille E Powe, Miriam S Udler, Sarah Hsu, Catherine Allard, Alan Kuang, Alisa K Manning, Patrice Perron, Luigi Bouchard, William L Lowe, Denise Scholtens and 2 more

Open access · greenAbstract read
In one paragraph

Article in Diabetes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.2field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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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

12 authors at 3 institutions in 2 countries.

Camille E PoweDiabetes Unit, Endocrine Division, Massachusetts General Hospital, Boston, MA camille.powe@mgh.harvard.edu.ORCID 0000-0002-7060-7778
Miriam S UdlerDiabetes Unit, Endocrine Division, Massachusetts General Hospital, Boston, MA.ORCID 0000-0003-3824-9162
Sarah HsuDiabetes Unit, Endocrine Division, Massachusetts General Hospital, Boston, MA.
Catherine AllardCentre de Recherche du Centre Hospitalier, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
Alan KuangDivision of Biostatistics, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.
Alisa K ManningBroad Institute, Cambridge, MA.
Patrice PerronDepartment of Medicine, Université de Sherbrooke, Quebec, Canada.
Luigi BouchardCentre de Recherche du Centre Hospitalier, Université de Sherbrooke, Sherbrooke, Quebec, Canada.
William L LoweDepartment of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.ORCID 0000-0001-9467-3422
Denise ScholtensDivision of Biostatistics, Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL.ORCID 0000-0001-9467-3422
Jose C FlorezDiabetes Unit, Endocrine Division, Massachusetts General Hospital, Boston, MA.ORCID 0000-0002-1730-9325
Marie-France HivertDiabetes Unit, Endocrine Division, Massachusetts General Hospital, Boston, MA.ORCID 0000-0001-7752-2585
Broad Institute · USUniversité de Sherbrooke · CANorthwestern University · US

Funding

Hyperglycemia and Adverse Pregnancy Outcome (HAPO)R01HD034243 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI METZGER, BOYD E · 1999 to 2010
$16.2M
HAPO: DATA COORDINATING CENTERR01HD034242 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DYER, ALAN R · 1999 to 2007
$3.0M
Genetics and Genomics of Maternal Glycemia During PregnancyR01DK097534 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2013 to 2017
$2.1M
GWA Mapping: Maternal Metabolism-Birth Weight InteractionsU01HG004415 · NHGRI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2007 to 2009
$1.1M
Elucidating Determinants of Gestational Beta-Cell Adaptation and FailureK23DK113218 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI POWE, CAMILLE ELISE · 2017 to 2021
$1.0M
Clinical Implications of Genetically Defined Diabetes Subtypes and Application to Electronic Health Medical Record SystemsK23DK114551 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI UDLER, MIRIAM SARGON · 2017 to 2021
$1000k
NHGRI NIH HHS U01 HG004415NICHD NIH HHS R01 HD034242NICHD NIH HHS R01 HD034243NIDDK NIH HHS K23 DK113218NIDDK NIH HHS K23 DK114551NIDDK NIH HHS L30 DK106874NIDDK NIH HHS L30 DK114998NIDDK NIH HHS R01 DK097534
6 · The paper itself

Abstract

Hundreds of common genetic variants acting through distinguishable physiologic pathways influence the risk of type 2 diabetes (T2D). It is unknown to what extent the physiology underlying gestational diabetes mellitus (GDM) is distinct from that underlying T2D. In this study of >5,000 pregnant women from three cohorts, we aimed to identify physiologically related groups of maternal variants associated with GDM using two complementary approaches that were based on Bayesian nonnegative matrix factorization (bNMF) clustering. First, we tested five bNMF clusters of maternal T2D-associated variants grouped on the basis of physiology outside of pregnancy for association with GDM. We found that cluster polygenic scores representing genetic determinants of reduced β-cell function and abnormal hepatic lipid metabolism were associated with GDM; these clusters were not associated with infant birth weight. Second, we derived bNMF clusters of maternal variants on the basis of pregnancy physiology and tested these clusters for association with GDM. We identified a cluster that was strongly associated with GDM as well as associated with higher infant birth weight. The effect size for this cluster's association with GDM appeared greater than that for T2D. Our findings imply that the genetic and physiologic pathways that lead to GDM differ, at least in part, from those that lead to T2D.

Indexed as

Genetic LociGenetic Predisposition to DiseaseGenotypePolymorphism, Single NucleotideAdultBirth WeightCluster AnalysisDiabetes, GestationalFemaleHumansLipid MetabolismPregnancy

Identifiers

PMID33051273
PMCPMC7876560
OpenAlexW3091850649

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.