Evidence map›Paper›PMID 23903356›Full record

ArticleDiabetes2013

Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies.

M Geoffrey Hayes, Margrit Urbanek, Marie-France Hivert, Loren L Armstrong, Jean Morrison, Cong Guo, Lynn P Lowe, Douglas A Scheftner, Anna Pluzhnikov, David M Levine and 15 more

Erratum issuedAbstract read
In one paragraph

Article in Diabetes, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 109 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed, 4 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.

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

109 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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  16. HyperCas12a enables multiplexed CRISPRi screens.bioRxiv : the preprint server for biology · 2025
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49 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

25 authors.

M Geoffrey HayesDivision of Endocrinology, Metabolism, and Molecular Medicine, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA. ghayes@northwestern.edu
Margrit Urbanek
Marie-France Hivert
Loren L Armstrong
Jean Morrison
Cong Guo
Lynn P Lowe
Douglas A Scheftner
Anna Pluzhnikov
David M Levine
Caitlin P McHugh
Christine M Ackerman
Luigi Bouchard
Diane Brisson
Brian T Layden
Daniel Mirel
Kimberly F Doheny
Marysa V Leya
Rachel N Lown-Hecht
Alan R Dyer
Boyd E Metzger
Timothy E Reddy
Nancy J Cox
William L Lowe
HAPO Study Cooperative Research Group

Funding

Hyperglycemia and Adverse Pregnancy Outcome (HAPO)R01HD034243 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI METZGER, BOYD E · 1999 to 2010
$16.2M
The function and regulation of the novel pregnancy-specific hexokinase HKDC1R01DK104927 · NIDDK · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LAYDEN, BRIAN THOMAS, REDDY, TIMOTHY E · 2015 to 2024
$7.2M
HAPO: DATA COORDINATING CENTERR01HD034242 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI DYER, ALAN R · 1999 to 2007
$3.0M
Genetics and Evolution of Fetal Human Fat Accretion During DevelopmentR01DK099820 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2013 to 2017
$2.0M
Diabetes Genes: Maternal Glycemia and Birth WeightR01DK067459 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2006 to 2008
$1.4M
GWA Mapping: Maternal Metabolism-Birth Weight InteractionsU01HG004415 · NHGRI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2007 to 2009
$1.1M
Replication of GWAS for Maternal Glycemia, Birthweight and their InteractionR01CA141688 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2009 to 2009
$399k
Role of Short Chain Fatty Acids and their Receptors in Islet FunctionIK2BX001587 · VA · JESSE BROWN VA MEDICAL CENTER · PI LAYDEN, BRIAN THOMAS · 2012 to 2016
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BLRD VA IK2 BX001587NCI NIH HHS CA-141688NCI NIH HHS R01 CA141688NHGRI NIH HHS HG-004415NHGRI NIH HHS U01 HG004415NICHD NIH HHS HD-34242NICHD NIH HHS HD-34243NICHD NIH HHS R01 HD034242NICHD NIH HHS R01 HD034243NIDDK NIH HHS R01 DK067459NIDDK NIH HHS R01 DK099820NIDDK NIH HHS R01 DK104927PHS HHS INMD 110791
6 · The paper itself

Abstract

Maternal metabolism during pregnancy impacts the developing fetus, affecting offspring birth weight and adiposity. This has important implications for metabolic health later in life (e.g., offspring of mothers with pre-existing or gestational diabetes mellitus have an increased risk of metabolic disorders in childhood). To identify genetic loci associated with measures of maternal metabolism obtained during an oral glucose tolerance test at ∼28 weeks' gestation, we performed a genome-wide association study of 4,437 pregnant mothers of European (n = 1,367), Thai (n = 1,178), Afro-Caribbean (n = 1,075), and Hispanic (n = 817) ancestry, along with replication of top signals in three additional European ancestry cohorts. In addition to identifying associations with genes previously implicated with measures of glucose metabolism in nonpregnant populations, we identified two novel genome-wide significant associations: 2-h plasma glucose and HKDC1, and fasting C-peptide and BACE2. These results suggest that the genetic architecture underlying glucose metabolism may differ, in part, in pregnancy.

Indexed as

AdolescentAdultAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesBlood GlucoseC-PeptideFastingFemaleGenome-Wide Association StudyGenotypeGlucose Tolerance TestHumansPregnancyYoung AdultAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesBACE2 protein, humanBlood GlucoseC-Peptide

Identifiers

PMID23903356
PMCPMC3749326

What OpenQuestion holds

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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.