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Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study

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...

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Autores principales: Bhattacharjee, Esha, Thiruvengadam, Ramachandran, Ayushi, Das, Chitrarpita, Wadhwa, Nitya, Natchu, Uma Chandra Mouli, Kshetrapal, Pallavi, Bhatnagar, Shinjini, Majumder, Partha Pratim, Maitra, Arindam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363490/
https://www.ncbi.nlm.nih.gov/pubmed/37492417
http://dx.doi.org/10.1016/j.lansea.2023.100190
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author Bhattacharjee, Esha
Thiruvengadam, Ramachandran
Ayushi
Das, Chitrarpita
Wadhwa, Nitya
Natchu, Uma Chandra Mouli
Kshetrapal, Pallavi
Bhatnagar, Shinjini
Majumder, Partha Pratim
Maitra, Arindam
author_facet Bhattacharjee, Esha
Thiruvengadam, Ramachandran
Ayushi
Das, Chitrarpita
Wadhwa, Nitya
Natchu, Uma Chandra Mouli
Kshetrapal, Pallavi
Bhatnagar, Shinjini
Majumder, Partha Pratim
Maitra, Arindam
author_sort Bhattacharjee, Esha
collection PubMed
description 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: 10.13039/501100001407Department of Biotechnology (India), Grand Challenges India - All Children Thriving Program and 10.13039/501100014825Biotechnology Industry Research Assistance Council (BIRAC).
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spelling pubmed-103634902023-07-25 Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study Bhattacharjee, Esha Thiruvengadam, Ramachandran Ayushi Das, Chitrarpita Wadhwa, Nitya Natchu, Uma Chandra Mouli Kshetrapal, Pallavi Bhatnagar, Shinjini Majumder, Partha Pratim Maitra, Arindam Lancet Reg Health Southeast Asia Articles 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: 10.13039/501100001407Department of Biotechnology (India), Grand Challenges India - All Children Thriving Program and 10.13039/501100014825Biotechnology Industry Research Assistance Council (BIRAC). Elsevier 2023-04-18 /pmc/articles/PMC10363490/ /pubmed/37492417 http://dx.doi.org/10.1016/j.lansea.2023.100190 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Bhattacharjee, Esha
Thiruvengadam, Ramachandran
Ayushi
Das, Chitrarpita
Wadhwa, Nitya
Natchu, Uma Chandra Mouli
Kshetrapal, Pallavi
Bhatnagar, Shinjini
Majumder, Partha Pratim
Maitra, Arindam
Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study
title Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study
title_full Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study
title_fullStr Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study
title_full_unstemmed Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study
title_short Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study
title_sort genetic variants associated with spontaneous preterm birth in women from india: a prospective cohort study
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10363490/
https://www.ncbi.nlm.nih.gov/pubmed/37492417
http://dx.doi.org/10.1016/j.lansea.2023.100190
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