Evidence map›Paper›PMID 39302385›Full record

ArticleJournal of neonatal-perinatal medicine2024

Genetic association study of preterm birth and gestational age in a population-based case-control study in Peru.

D L Juvinao-Quintero, S E Sanchez, T Workalemahu, N Pinto, L Liang, M A Williams, B Gelaye

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Article in Journal of neonatal-perinatal medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

D L Juvinao-QuinteroDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
S E SanchezUniversidad de San Martin de Porres, Facultad de Medicina Humana, Instituto de Investigación, Lima, Peru.
T WorkalemahuDepartment of Obstetrics and Gynecology, University of Utah Health, Salt Lake City, UT, USA.
N PintoAsociación Civil PROESA, Lima, Peru.
L LiangDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
M A WilliamsDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
B GelayeDepartment of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPreterm birth (PTB) affects ∼15 million pregnancies worldwide. Genetic studies have identified several candidate loci for PTB, but results remain inconclusive and limited to European populations. Thus, we conducted a genome-wide association study (GWAS) of PTB and gestational age at delivery (GA) among 2,212 Peruvian women.

methodsPTB cases delivered≥20 weeks' but < 37 weeks' gestation, while controls delivered at term (≥37 weeks but <42 weeks). Multivariable regressions were used to identify genetic markers for PTB and GA (∼6 million SNPs), adjusting for maternal age and the first two genetic principal components. In silico functional analysis was conducted among top signals detected with an arbitrary P < 1.0×10-5 . We sought to replicate genetic markers for PTB and GA identified in Europeans, and we developed a genetic risk score for GA based on European markers.

resultsMean GA was 30 ± 4 weeks in PTB cases (N = 933) and 39 ± 1 in the controls (N = 1,279). No associatiosn were identified at genome-wide level. Nominal PTB variants were enriched for biological pathways associated with polyketide, progesterone, steroid hormones, and glycosyl metabolism. Nominal GA variants were enriched in intronic regions and cancer pathways. Variants in WNT4 associated with GA in Europeans were replicated in our study. A genetic risk score was associated with a 2-day longer GA (P = 0.002) in our sample.

conclusionsThis study identified various signals suggestively associated with PTB and GA in pregnant Peruvian women. None of these variants overlapped with signals previously identified in Europeans.

Indexed as

Genome-Wide Association StudyGestational AgePolymorphism, Single NucleotidePremature BirthAdultCase-Control StudiesFemaleGenetic Predisposition to DiseaseHumansInfant, NewbornPeruPregnancyYoung AdultGenetic risk scoregenome-wide association studygestational age at deliverypregnancypreterm birth

Identifiers

PMID39302385

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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.