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Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study.
Bhattacharjee, Esha; Thiruvengadam, Ramachandran; Das, Chitrarpita; Wadhwa, Nitya; Natchu, Uma Chandra Mouli; Kshetrapal, Pallavi; Bhatnagar, Shinjini; Majumder, Partha Pratim; Maitra, Arindam.
Afiliación
  • Bhattacharjee E; National Institute of Biomedical Genomics, PO: NSS, Kalyani, India.
  • Thiruvengadam R; Regional Centre for Biotechnology, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad, India.
  • Ayushi; Translational Health Science and Technology Institute, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad, India.
  • Das C; Pondicherry Institute of Medical Sciences, Ganapathichettikulam, Kalapet, Puducherry, India.
  • Wadhwa N; National Institute of Biomedical Genomics, PO: NSS, Kalyani, India.
  • Kshetrapal P; Translational Health Science and Technology Institute, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad, India.
  • Bhatnagar S; Translational Health Science and Technology Institute, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad, India.
  • Majumder PP; Division of Infectious Diseases, St. John's Research Institute, 100 Feet Road, John Nagar, Koramangala, Bengaluru, India.
  • Maitra A; Translational Health Science and Technology Institute, 3rd Milestone, Faridabad-Gurugram Expressway, Faridabad, India.
Lancet Reg Health Southeast Asia ; 14: 100190, 2023 Jul.
Article en En | MEDLINE | ID: mdl-37492417
Background: Despite having the highest number of preterm births globally, no genomic study on preterm birth was previously published from India or other South-Asian countries. Methods: We conducted a genome-wide association (GWA) study of spontaneous preterm birth (sPTB) on 6211 women from India. We used a novel resampling procedure to identify the associated single nucleotide polymorphisms (SNPs) followed by haplotype association analysis and imputation. Findings: We found that 512 maternal SNPs were associated with sPTB (p < 2.51e-3), of which minor allele at 19 SNPs (after Bonferroni correction) had increased genotype relative risk. Haplotypes containing six of the 19 SNPs (rs13011430, rs8179838, rs2327290, rs4798499, rs7629800, and rs13180906) were associated with sPTB (p < 9.9e-4; Bonferroni adjusted p-value <0.05). After imputation in regions around the 19 SNPs, 15 imputed SNPs were found to be associated with sPTB (Bonferroni adjusted p-value <0.05). One of these imputed SNPs, rs35760881, and three other SNPs (rs17307697, rs4308815, and rs10983507) were also reported to be associated with sPTB in women belonging to European ancestry. Moreover, we found that GG genotype at rs1152954, one of the associated SNPs, enhanced risk of sPTB and reduced telomere length. Interpretation: This is the first study from South Asia on the genome-wide identification of maternal SNPs associated with sPTB. These SNPs are known to alter the expression of genes associated with major pathways in sPTB viz. inflammation, apoptosis, cervical ripening, telomere maintenance, selenocysteine biosynthesis, myometrial contraction, and innate immunity. From a public health perspective, the trans-ethnic association of four SNPs identified in our study may help to stratify women with risk of sPTB in most populations. Funding: Department of Biotechnology (India), Grand Challenges India - All Children Thriving Program and Biotechnology Industry Research Assistance Council (BIRAC).
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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Lancet Reg Health Southeast Asia Año: 2023 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Lancet Reg Health Southeast Asia Año: 2023 Tipo del documento: Article País de afiliación: India