Evidence map›Paper›PMID 41253866›Full record

ArticleScientific reports2025

Effects of rs3802177 G/A polymorphism on SLC30A8 mRNA and hsa-miR-183-5p in Malay women with gestational diabetes mellitus.

Sajad Jamalpour, Phang Kean Chang, Reza Vazifehmand, Hesam Kamyab, Siti Zawiah Omar, Shamsul Mohd Zain

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Article in Scientific reports, 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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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sajad JamalpourDepartment of Medical Microbiology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
Phang Kean ChangDepartment of Pathology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
Reza VazifehmandDepartment of Bioscience, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Kuala Lumpur, Malaysia.
Hesam KamyabCentro de Investigación en Salud Pública y Epidemiología Clínica (CISPEC), Universidad UTE, Quito, 170527, Ecuador. hesam_kamyab@yahoo.com.
Siti Zawiah OmarDepartment of Obstetrics & Gynaecology, University of Malaya, Kuala Lumpur, Malaysia.
Shamsul Mohd ZainDepartment of Pharmacology, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia. shamsul@um.edu.my.

Funding

Fundamental Research Grant Scheme FRGS/1/2023/SKK03/UM/02/2
6 · The paper itself

Abstract

Gestational diabetes mellitus (GDM) is characterized by the initial presentation of impaired glucose tolerance identified during pregnancy. Numerous investigations have explored the associations between single nucleotide polymorphisms (SNPs) and microRNAs in relation to the susceptibility to GDM across diverse populations. This study aimed to investigate the interplay among rs3802177 G/A 3' UTR polymorphism, SLC30A8 mRNA expression, and hsa-miR-183-5p in Malay women with GDM. TargetScanHuman, miRBase, miRRecord, and Sfold bioinformatics tools were applied to predict and select a putative microRNA that has a significant interaction with SLC30A8 mRNA at the 3' UTR region. DNA was extracted and genotyped using the Sequenom Mass ARRAY method. Quantitative PCR was performed to evaluate SLC30A8 mRNA and hsa-miR-183-5p expression levels. Preliminary bioinformatics analysis revealed that hsa-miR-183-5p is a potential target for SLC30A8. Thermodynamic evaluation confirmed a negative association between polymorphisms and SLC30A8 mRNA secondary structure (P = 0.8027). Data analysis showed that the GG genotype in patients with GDM is a risk allele for GDM in the Malay population. Furthermore, the SLC30A8 gene was significantly downregulated (P < 0.05), whereas miR-183-5P was significantly upregulated (P < 0.05) in patients with the GG genotype. In addition, the ROC curve analysis revealed that hsa-miR-183-5p has potential as a biomarker (AUC = 0.7926 ± 0.02045, p = 0.0001) in the first trimester of GDM. In conclusion, this study provides the first evidence of a substantial association in the interplay among the rs3802177 G/A SNP, SLC30A8 mRNA expression, and hsa-miR-183-5p expression levels in the Malay population.

Indexed as

Diabetes, GestationalMicroRNAsPolymorphism, Single NucleotideRNA, MessengerZinc Transporter 83' Untranslated RegionsAdultAllelesFemaleGenetic Predisposition to DiseaseGenotypeHumansMalaysiaPregnancy3' Untranslated RegionsMicroRNAsMIRN183 microRNA, humanRNA, MessengerSLC30A8 protein, humanZinc Transporter 8Gestational diabetes mellitusHsa-miR-183-5pMalaysiaRs3802177 G/ASLC30A8

Identifiers

PMID41253866
PMCPMC12627516

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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.