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Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India
Background: Globally, type 2 diabetes mellitus (T2DM) is one of the fastest-growing noncommunicable multifactorial and polygenic diseases, which leads to many health complications and significant morbidity and mortality. South Asians have a high genetic predisposition to T2DM, with India being home...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9959290/ https://www.ncbi.nlm.nih.gov/pubmed/36834424 http://dx.doi.org/10.3390/ijerph20043729 |
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author | Shitomi-Jones, Lisa Mitsuko Akam, Liz Hunter, David Singh, Puneetpal Mastana, Sarabjit |
author_facet | Shitomi-Jones, Lisa Mitsuko Akam, Liz Hunter, David Singh, Puneetpal Mastana, Sarabjit |
author_sort | Shitomi-Jones, Lisa Mitsuko |
collection | PubMed |
description | Background: Globally, type 2 diabetes mellitus (T2DM) is one of the fastest-growing noncommunicable multifactorial and polygenic diseases, which leads to many health complications and significant morbidity and mortality. South Asians have a high genetic predisposition to T2DM, with India being home to one in six diabetics. This study investigates the association of selected genetic polymorphisms with T2DM risk and develops a polygenic risk score (PRS). Methods: A case–control study recruited fully consented participants from a population of Jat Sikhs in north India. DNA samples were genotyped for a range of polymorphisms and odds ratios were calculated under several genetic association models. Receiver operating characteristic (ROC) curves were produced for combinations of the PRS and clinical parameters. Results: The GSTT1(rs17856199), GSTM1(rs366631), GSTP1(rs1695), KCNQ1(rs2237892), ACE(rs4646994), and TCF7L2(rs12255372; rs7903146; rs7901695) polymorphisms were associated with increased T2DM risk (p ≤ 0.05). No association was observed with IGF2BP2(rs4402960) or PPARG2(rs1801282). The weighted PRS was found to be significantly higher in patients (mean = 15.4, SD = 3.24) than controls (mean = 11.9, SD = 3.06), and t((454)) = −12.2 (p < 0.001). The ROC curve analysis found the weighted PRS in combination with clinical variables to be the most effective predictor of T2DM (area under the curve = 0.844, 95%CI = 0.0.808–0.879). Conclusions: Several polymorphisms were associated with T2DM risk. PRS based on even a limited number of loci improves the prediction of the disease. This may provide a useful method for determining T2DM susceptibility for clinical and public health applications. |
format | Online Article Text |
id | pubmed-9959290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99592902023-02-26 Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India Shitomi-Jones, Lisa Mitsuko Akam, Liz Hunter, David Singh, Puneetpal Mastana, Sarabjit Int J Environ Res Public Health Article Background: Globally, type 2 diabetes mellitus (T2DM) is one of the fastest-growing noncommunicable multifactorial and polygenic diseases, which leads to many health complications and significant morbidity and mortality. South Asians have a high genetic predisposition to T2DM, with India being home to one in six diabetics. This study investigates the association of selected genetic polymorphisms with T2DM risk and develops a polygenic risk score (PRS). Methods: A case–control study recruited fully consented participants from a population of Jat Sikhs in north India. DNA samples were genotyped for a range of polymorphisms and odds ratios were calculated under several genetic association models. Receiver operating characteristic (ROC) curves were produced for combinations of the PRS and clinical parameters. Results: The GSTT1(rs17856199), GSTM1(rs366631), GSTP1(rs1695), KCNQ1(rs2237892), ACE(rs4646994), and TCF7L2(rs12255372; rs7903146; rs7901695) polymorphisms were associated with increased T2DM risk (p ≤ 0.05). No association was observed with IGF2BP2(rs4402960) or PPARG2(rs1801282). The weighted PRS was found to be significantly higher in patients (mean = 15.4, SD = 3.24) than controls (mean = 11.9, SD = 3.06), and t((454)) = −12.2 (p < 0.001). The ROC curve analysis found the weighted PRS in combination with clinical variables to be the most effective predictor of T2DM (area under the curve = 0.844, 95%CI = 0.0.808–0.879). Conclusions: Several polymorphisms were associated with T2DM risk. PRS based on even a limited number of loci improves the prediction of the disease. This may provide a useful method for determining T2DM susceptibility for clinical and public health applications. MDPI 2023-02-20 /pmc/articles/PMC9959290/ /pubmed/36834424 http://dx.doi.org/10.3390/ijerph20043729 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Shitomi-Jones, Lisa Mitsuko Akam, Liz Hunter, David Singh, Puneetpal Mastana, Sarabjit Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India |
title | Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India |
title_full | Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India |
title_fullStr | Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India |
title_full_unstemmed | Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India |
title_short | Genetic Risk Scores for the Determination of Type 2 Diabetes Mellitus (T2DM) in North India |
title_sort | genetic risk scores for the determination of type 2 diabetes mellitus (t2dm) in north india |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9959290/ https://www.ncbi.nlm.nih.gov/pubmed/36834424 http://dx.doi.org/10.3390/ijerph20043729 |
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