Evidence map›Paper›PMID 22479352›Full record

ArticlePloS one2012

The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy.

Margrit Urbanek, M Geoffrey Hayes, Hoon Lee, Rachel M Freathy, Lynn P Lowe, Christine Ackerman, Nadereh Jafari, Alan R Dyer, Nancy J Cox, David B Dunger and 3 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  15. Genetics, genomics and metabolomics: new insights into maternal metabolism during pregnancy.Diabetic medicine : a journal of the British Diabetic Association · 2014
    Review
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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

13 authors at 5 institutions in 2 countries.

Margrit UrbanekDivision of Endocrinology, Metabolism and Molecular Medicine, Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States of America. m-urbanek@northwestern.edu
M Geoffrey Hayes
Hoon Lee
Rachel M Freathy
Lynn P Lowe
Christine Ackerman
Nadereh Jafari
Alan R Dyer
Nancy J Cox
David B Dunger
Andrew T Hattersley
Boyd E Metzger
William L Lowe
Northwestern University · USPeninsula College of Medicine and Dentistry · GBUniversity of Cambridge · GBUniversity of Chicago · USUniversity of Exeter · GB

Funding

Zosuquidar trihydrochloride for acute myeloid leukemia &refractory anemiaM01RR000080 · NCRR · UNIVERSITY HOSPITALS OF CLEVELAND · PI DEARBORN, DORR GELLATLY · 1985 to 2007
$22.2M
WOMEN'S INTERAGENCY HIV STUDY (WIHS) INTENSIVE PHARMACOKINETICS STUDYM01RR000048 · NCRR · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ARICETA, GEMA · 1985 to 2007
$21.1M
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
The Inflammatory Response Pathway in the Etiology of Polycystic Ovary SyndromeR01HD057450 · NICHD · NORTHWESTERN UNIVERSITY AT CHICAGO · PI URBANEK, MARGRIT · 2009 to 2012
$2.1M
Diabetes Genes: Maternal Glycemia and Birth WeightR01DK067459 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LOWE, WILLIAM L · 2006 to 2008
$1.4M
NCRR NIH HHS M01 RR000048NCRR NIH HHS M01 RR000080NCRR NIH HHS M01-RR00048NCRR NIH HHS M01-RR00080NICHD NIH HHS R01 HD034242NICHD NIH HHS R01 HD034243NICHD NIH HHS R01 HD057450NICHD NIH HHS R01-HD34242NICHD NIH HHS R01-HD34243NIDDK NIH HHS R01 DK067459Wellcome TrustWellcome Trust 085541/Z/08/Z
6 · The paper itself

Abstract

backgroundSince mediators of inflammation are associated with insulin resistance, and the risk of developing diabetes mellitus and gestational diabetes, we hypothesized that genetic variation in members of the inflammatory gene pathway impact glucose levels and related phenotypes in pregnancy. We evaluated this hypothesis by testing for association between genetic variants in 31 inflammatory pathway genes in the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) cohort, a large multiethnic multicenter study designed to address the impact of glycemia less than overt diabetes on pregnancy outcome.

resultsFasting, 1-hour, and 2-hour glucose, fasting and 1-hour C-peptide, and HbA1c levels were measured in blood samples obtained from HAPO participants during an oral glucose tolerance test at 24-32 weeks gestation. We tested for association between 458 SNPs mapping to 31 genes in the inflammatory pathway and metabolic phenotypes in 3836 European ancestry and 1713 Thai pregnant women. The strongest evidence for association was observed with TNF alpha and HbA1c (rs1052248; 0.04% increase per allele C; p-value = 4.4×10(-5)), RETN and fasting plasma glucose (rs1423096; 0.7 mg/dl decrease per allele A; p-value = 1.1×10(-4)), IL8 and 1 hr plasma glucose (rs2886920; 2.6 mg/dl decrease per allele T; p-value = 1.3×10(-4)), ADIPOR2 and fasting C-peptide (rs2041139; 0.55 ug/L decrease per allele A; p-value = 1.4×10(-4)), LEPR and 1-hour C-peptide (rs1171278; 0.62 ug/L decrease per allele T; p-value = 2.4×10(-4)), and IL6 and 1-hour plasma glucose (rs6954897; -2.29 mg/dl decrease per allele G, p-value = 4.3×10(-4)).

conclusionsBased on the genes surveyed in this study the inflammatory pathway is unlikely to have a strong impact on maternal metabolic phenotypes in pregnancy although variation in individual members of the pathway (e.g. RETN, IL8, ADIPOR2, LEPR, IL6, and TNF alpha,) may contribute to metabolic phenotypes in pregnant women.

Indexed as

Polymorphism, Single NucleotideAsian PeopleBlood GlucoseCohort StudiesC-PeptideFastingFemaleGenetic Predisposition to DiseaseGlucose Tolerance TestGlycated HemoglobinHumansHyperglycemiaInflammationInterleukin-6Interleukin-8PregnancyADIPOR2 protein, humanBlood GlucoseC-PeptideGlycated HemoglobinInterleukin-6Interleukin-8Receptors, AdiponectinReceptors, LeptinResistinRETN protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID22479352
PMCPMC3316547
OpenAlexW2148316821

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Registered trials

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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.