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Genome-wide polygenic risk score for type 2 diabetes in Indian population

Genome-wide polygenic risk scores (PRS) for lifestyle disorders, like Type 2 Diabetes (T2D), are useful in identifying at-risk individuals early on in life, and to guide them towards healthier lifestyles. The current study was aimed at developing PRS for the Indian population using imputed genotype...

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Autores principales: Pemmasani, Sandhya Kiran, Atmakuri, Shravya, Acharya, Anuradha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354074/
https://www.ncbi.nlm.nih.gov/pubmed/37463971
http://dx.doi.org/10.1038/s41598-023-38768-5
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author Pemmasani, Sandhya Kiran
Atmakuri, Shravya
Acharya, Anuradha
author_facet Pemmasani, Sandhya Kiran
Atmakuri, Shravya
Acharya, Anuradha
author_sort Pemmasani, Sandhya Kiran
collection PubMed
description Genome-wide polygenic risk scores (PRS) for lifestyle disorders, like Type 2 Diabetes (T2D), are useful in identifying at-risk individuals early on in life, and to guide them towards healthier lifestyles. The current study was aimed at developing PRS for the Indian population using imputed genotype data from UK Biobank and testing the developed PRS on data from GenomegaDB of Indians living in India. 959 T2D cases and 2,818 controls were selected from Indian participants of UK Biobank to develop the PRS. Summary statistics available for South Asians, from the DIAMANTE consortium, were used to weigh genetic variants. LDpred2 algorithm was used to adjust the effect of linkage disequilibrium among the variants. The association of PRS with T2D, after adjusting for age, sex and top ten genetic principal components, was found to be very significant (AUC = 0.7953, OR = 2.9856 [95% CI: 2.7044–3.2961]). When participants were divided into four PRS quartile groups, the odds of developing T2D increased sequentially with the higher PRS groups. The highest PRS group (top 25%) showed 5.79 fold increased risk compared to the rest of the participants (75%). The PRS derived using the same set of variants was found to be significantly associated with T2D in the test dataset of 445 Indians (AUC = 0.7781, OR = 1.6656 [95%CI = 0.6127–4.5278]). Our study demonstrates a framework to derive Indian-specific PRS for T2D. The accuracy of the derived PRS shows it’s potential to be used as a prognostic metric to stratify individuals, and to recommend personalized preventive strategies.
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spelling pubmed-103540742023-07-20 Genome-wide polygenic risk score for type 2 diabetes in Indian population Pemmasani, Sandhya Kiran Atmakuri, Shravya Acharya, Anuradha Sci Rep Article Genome-wide polygenic risk scores (PRS) for lifestyle disorders, like Type 2 Diabetes (T2D), are useful in identifying at-risk individuals early on in life, and to guide them towards healthier lifestyles. The current study was aimed at developing PRS for the Indian population using imputed genotype data from UK Biobank and testing the developed PRS on data from GenomegaDB of Indians living in India. 959 T2D cases and 2,818 controls were selected from Indian participants of UK Biobank to develop the PRS. Summary statistics available for South Asians, from the DIAMANTE consortium, were used to weigh genetic variants. LDpred2 algorithm was used to adjust the effect of linkage disequilibrium among the variants. The association of PRS with T2D, after adjusting for age, sex and top ten genetic principal components, was found to be very significant (AUC = 0.7953, OR = 2.9856 [95% CI: 2.7044–3.2961]). When participants were divided into four PRS quartile groups, the odds of developing T2D increased sequentially with the higher PRS groups. The highest PRS group (top 25%) showed 5.79 fold increased risk compared to the rest of the participants (75%). The PRS derived using the same set of variants was found to be significantly associated with T2D in the test dataset of 445 Indians (AUC = 0.7781, OR = 1.6656 [95%CI = 0.6127–4.5278]). Our study demonstrates a framework to derive Indian-specific PRS for T2D. The accuracy of the derived PRS shows it’s potential to be used as a prognostic metric to stratify individuals, and to recommend personalized preventive strategies. Nature Publishing Group UK 2023-07-18 /pmc/articles/PMC10354074/ /pubmed/37463971 http://dx.doi.org/10.1038/s41598-023-38768-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pemmasani, Sandhya Kiran
Atmakuri, Shravya
Acharya, Anuradha
Genome-wide polygenic risk score for type 2 diabetes in Indian population
title Genome-wide polygenic risk score for type 2 diabetes in Indian population
title_full Genome-wide polygenic risk score for type 2 diabetes in Indian population
title_fullStr Genome-wide polygenic risk score for type 2 diabetes in Indian population
title_full_unstemmed Genome-wide polygenic risk score for type 2 diabetes in Indian population
title_short Genome-wide polygenic risk score for type 2 diabetes in Indian population
title_sort genome-wide polygenic risk score for type 2 diabetes in indian population
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354074/
https://www.ncbi.nlm.nih.gov/pubmed/37463971
http://dx.doi.org/10.1038/s41598-023-38768-5
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