Evidence map›Paper›PMID 32710738›Full record

ArticleAmerican journal of hypertension2021

Maternal Hypertension-Related Genotypes and Congenital Heart Defects.

Yunping Lei, Katherine L Ludorf, Xiao Yu, Renata H Benjamin, Xue Gu, Ying Lin, Richard H Finnell, Laura E Mitchell, Fadi I Musfee, Sadia Malik and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of hypertension, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 29% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
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

16 authors at 7 institutions in 1 country.

Yunping LeiDepartment of Molecular and Cellular Biology and Medicine, Baylor College of Medicine, Houston, Texas, USA.
Katherine L LudorfHuman Genetics Center, Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
Xiao YuHuman Genetics Center, Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
Renata H BenjaminHuman Genetics Center, Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
Xue GuCenter for Precision Environmental Health, Baylor College of Medicine, Houston, Texas, USA.
Ying LinCenter for Precision Environmental Health, Baylor College of Medicine, Houston, Texas, USA.
Richard H FinnellCenter for Precision Environmental Health, Baylor College of Medicine, Houston, Texas, USA.
Laura E MitchellHuman Genetics Center, Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
Fadi I MusfeeHuman Genetics Center, Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
Sadia MalikPediatric Cardiology, Department of Pediatrics, UT Southwestern Children's Medical Center, Dallas, Texas, USA.
Mark A CanfieldBirth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas, USA.
Alanna C MorrisonHuman Genetics Center, Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
Charlotte A HobbsRady Children's Institute for Genomic Medicine, San Diego, California, USA.
Alissa R Van ZutphenNew York State Department of Health, Bureau of Environmental and Occupational Epidemiology, Albany, New York, USA.
Sarah FisherNew York State Department of Health, Bureau of Environmental and Occupational Epidemiology, Albany, New York, USA.
A J AgopianHuman Genetics Center, Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
Baylor College of Medicine · USUniversity of Texas Health Science Center at Dallas · USThe University of Texas Health Science Center at Houston · USNew York State Department of Health · USChildren’s Institute · USChildren's Medical Center · USTexas Department of State Health Services · US

Funding

Translational Research Support CoreP30ES030285 · NIEHS · BAYLOR COLLEGE OF MEDICINE · PI Casey W Wright · 2019 to 2026
$14.7M
Project 2: Genetic Mechanisms of Non-syndromic Congenital Cardiac DefectsP01HD070454 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI MORROW, BERNICE E · 2011 to 2020
$14.0M
New York State Component A: BD-STEPS II CoreU01DD001227 · DD · CENTER OF ENVIRONMENTAL HEALTH · PI HOWLEY, MEREDITH M · 2018 to 2022
$4.2M
NCBDD CDC HHS U01 DD001227NICHD NIH HHS P01 HD070454NIEHS NIH HHS P30 ES030285
6 · The paper itself

Abstract

backgroundMaternal hypertension has been associated with congenital heart defect occurrence in several studies. We assessed whether maternal genotypes associated with this condition were also associated with congenital heart defect occurrence.

methodsWe used data from the National Birth Defects Prevention Study to identify non-Hispanic white (NHW) and Hispanic women with (cases) and without (controls) a pregnancy in which a select simple, isolated heart defect was present between 1999 and 2011. We genotyped 29 hypertension-related single nucleotide polymorphisms (SNPs). We conducted logistic regression analyses separately by race/ethnicity to assess the relationship between the presence of any congenital heart defect and each SNP and an overall blood pressure genetic risk score (GRS). All analyses were then repeated to assess 4 separate congenital heart defect subtypes.

resultsFour hypertension-related variants were associated with congenital heart defects among NHW women (N = 1,568 with affected pregnancies). For example, 1 intronic variant in ARHGAP2, rs633185, was associated with conotruncal defects (odds ratio [OR]: 1.3, 95% confidence interval [CI]: 1.1-1.6). Additionally, 2 variants were associated with congenital heart defects among Hispanic women (N = 489 with affected pregnancies). The GRS had a significant association with septal defects (OR: 2.1, 95% CI: 1.2-3.5) among NHW women.

conclusionsWe replicated a previously reported association between rs633185 and conotruncal defects. Although additional hypertension-related SNPs were also associated with congenital heart defects, more work is needed to better understand the relationship between genetic risk for maternal hypertension and congenital heart defects occurrence.

Indexed as

Heart Defects, CongenitalHypertensionPregnancy Complications, CardiovascularAdultCorrelation of DataFemaleGenetic TestingGTPase-Activating ProteinsHumansInfant, NewbornMalePhosphoinositide Phospholipase CPolymorphism, Single NucleotidePregnancyRisk AssessmentUnited StatesARHGAP42 protein, humanGTPase-Activating ProteinsPhosphoinositide Phospholipase Cphospholipase C epsilonblood pressurecongenital heart defectsgenetic risk scorehypertensionmaternal genotype

Identifiers

PMID32710738
PMCPMC7891240
OpenAlexW3044014364

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.