Evidence map›Paper›PMID 41467952›Full record

SynthesisMolecular genetics and genomics : MGG2025

A systematic review of genetic association studies on the susceptibility of preterm birth in Asia.

Noor Haliza Mohamed Ibrahim, Shankar Aissvarya, Norshariza Nordin, Habibah Abdul Hamid, Karuppiah Thilakavathy, Amilia Afzan Mohd Jamil, Zurina Zainudin

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Molecular genetics and genomics : MGG, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Noor Haliza Mohamed IbrahimDepartment of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Shankar AissvaryaDepartment of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Norshariza NordinDepartment of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Habibah Abdul HamidDepartment of Obstetrics and Gynaecology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Karuppiah ThilakavathyDepartment of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Amilia Afzan Mohd JamilDepartment of Obstetrics and Gynaecology, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
Zurina ZainudinDepartment of Paediatrics, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, 43400, Serdang, Selangor, Malaysia. zaizurina@upm.edu.my.ORCID http://orcid.org/0000-0002-5660-6058

Funding

Kementerian Pendidikan Malaysia FRGS/1/2020/SKK08/UPM/02/1
6 · The paper itself

Abstract

Preterm birth (PTB) is a leading cause of prenatal and infant mortality and morbidity, yet its molecular mechanisms remain poorly understood. This systematic review aims to enhance understanding of PTB's molecular genetics and to identify potential biomarkers and therapeutic targets by comprehensively analyzing genetic association studies conducted among Asian populations. A systematic search was performed across six online databases, including Google Scholar, Science Direct, Clinical Trials, PubMed, Cochrane, and MyCite, using a combined search strategy of PTB, gene polymorphisms, and Asia (PROSPERO protocol: CRD42023458957). Peer-reviewed articles focusing on the effects of genetic association on labor progression in the Asian population were included. Subsequently, data extraction encompassing study design, demographics, genetic determinants, and effect estimates were collected. Quality assessment was conducted for each study using the Quality of Genetic Association Studies (Q-Genie) tool. Due to heterogeneity among study designs, genetic variants, and reported outcomes, a meta-analysis was not performed; instead, a systematic narrative synthesis was conducted. Out of 2,412 screened articles, 16 met the inclusion criteria and passed the Q-Genie quality assessment. These studies collectively investigated 37 polymorphisms within 25 genes across various Asian ethnic groups. These genes exhibited associations with various aspects of PTB, shedding light on the roles of innate immune responses, inflammation, myometrial quiescence, oxidative stress, and uteroplacental blood flow in PTB pathogenesis. This review highlights the role of genetics role in PTB susceptibility across Asian populations and the need to explore candidate genes and their interactions to uncover the underlying molecular mechanisms.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseasePremature BirthAsiaAsian PeopleFemaleHumansPolymorphism, Single NucleotidePregnancyAsiaBiological pathwaysCandidate gene analysisGene polymorphismPreterm birthSystematic review

Identifiers

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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.