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SREBP-2 1784 G/C Genotype is Associated with Non-Alcoholic Fatty Liver Disease in North Indians
Background: Genetics of non-alcoholic fatty liver (NAFLD) in Asian Indians has been inadequately investigated. This study aims to determine the association of the 1784G > C polymorphism in the SREBP-2 gene with NAFLD in Asian Indians in north India. Methods: In this study, (n = 335); 162 obese wi...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
IOS Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826379/ https://www.ncbi.nlm.nih.gov/pubmed/22182810 http://dx.doi.org/10.3233/DMA-2011-0852 |
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author | Bhatt, Surya Prakash Nigam, Priyanka Misra, Anoop Guleria, Randeep Luthra, Kalpana Vaidya, M. Jain, S. K. Pasha, M. A. Qadar |
author_facet | Bhatt, Surya Prakash Nigam, Priyanka Misra, Anoop Guleria, Randeep Luthra, Kalpana Vaidya, M. Jain, S. K. Pasha, M. A. Qadar |
author_sort | Bhatt, Surya Prakash |
collection | PubMed |
description | Background: Genetics of non-alcoholic fatty liver (NAFLD) in Asian Indians has been inadequately investigated. This study aims to determine the association of the 1784G > C polymorphism in the SREBP-2 gene with NAFLD in Asian Indians in north India. Methods: In this study, (n = 335); 162 obese with NAFLD, 91 obese without NAFLD and 82 non-obese without NAFLD subjects were recruited. Abdominal ultrasound, clinical profile, anthropometry, metabolic profile, serum levels of alanine aminotransferase, aspartate aminotransferase, fasting insulin and high sensitivity C-reactive protein (hs-CRP) were analysed. Polymerase chain reaction and restriction fragment length polymorphism were used to identify individual genotypes, and the association of this polymorphism with clinical and biochemical parameters was assessed. Results: The observed frequency of G allele was 0.73 and C allele was 0.27. Frequency of C/C genotype was higher in NAFLD as compared to obese and non-obese subjects (p = 0.003). In NAFLD subjects 57.4% were G/G homozygous, 31.5% G/C heterozygous and 11.1% were C/C homozygous. The SREBP-2 genotype frequencies deviated from the Hardy Weinberg Equilibrium (X(2) = 6.39, p = 0.0114). Mean values of TG (p = 0.002), TC (p = 0.002), ALT (p = 0.04) and AST (p =0.03) levels were significantly higher in NAFLD subjects with G/C genotype as compared to G/G genotypes in obese and non-obese groups. Fasting insulin (p = 0.03), HOMA (p = 0.009) and hs-CRP levels were significantly higher in NAFLD subjects with G/C genotype as compared to obese and non obese subjects with G/G genotypes. Conclusion: In this study, conducted for the first time in Asian Indians, SREBP-2 1784 G > C genotype was associated with NAFLD. |
format | Online Article Text |
id | pubmed-3826379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | IOS Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-38263792013-12-01 SREBP-2 1784 G/C Genotype is Associated with Non-Alcoholic Fatty Liver Disease in North Indians Bhatt, Surya Prakash Nigam, Priyanka Misra, Anoop Guleria, Randeep Luthra, Kalpana Vaidya, M. Jain, S. K. Pasha, M. A. Qadar Dis Markers Other Background: Genetics of non-alcoholic fatty liver (NAFLD) in Asian Indians has been inadequately investigated. This study aims to determine the association of the 1784G > C polymorphism in the SREBP-2 gene with NAFLD in Asian Indians in north India. Methods: In this study, (n = 335); 162 obese with NAFLD, 91 obese without NAFLD and 82 non-obese without NAFLD subjects were recruited. Abdominal ultrasound, clinical profile, anthropometry, metabolic profile, serum levels of alanine aminotransferase, aspartate aminotransferase, fasting insulin and high sensitivity C-reactive protein (hs-CRP) were analysed. Polymerase chain reaction and restriction fragment length polymorphism were used to identify individual genotypes, and the association of this polymorphism with clinical and biochemical parameters was assessed. Results: The observed frequency of G allele was 0.73 and C allele was 0.27. Frequency of C/C genotype was higher in NAFLD as compared to obese and non-obese subjects (p = 0.003). In NAFLD subjects 57.4% were G/G homozygous, 31.5% G/C heterozygous and 11.1% were C/C homozygous. The SREBP-2 genotype frequencies deviated from the Hardy Weinberg Equilibrium (X(2) = 6.39, p = 0.0114). Mean values of TG (p = 0.002), TC (p = 0.002), ALT (p = 0.04) and AST (p =0.03) levels were significantly higher in NAFLD subjects with G/C genotype as compared to G/G genotypes in obese and non-obese groups. Fasting insulin (p = 0.03), HOMA (p = 0.009) and hs-CRP levels were significantly higher in NAFLD subjects with G/C genotype as compared to obese and non obese subjects with G/G genotypes. Conclusion: In this study, conducted for the first time in Asian Indians, SREBP-2 1784 G > C genotype was associated with NAFLD. IOS Press 2011 2011-12-19 /pmc/articles/PMC3826379/ /pubmed/22182810 http://dx.doi.org/10.3233/DMA-2011-0852 Text en Copyright © 2011 Hindawi Publishing Corporation. |
spellingShingle | Other Bhatt, Surya Prakash Nigam, Priyanka Misra, Anoop Guleria, Randeep Luthra, Kalpana Vaidya, M. Jain, S. K. Pasha, M. A. Qadar SREBP-2 1784 G/C Genotype is Associated with Non-Alcoholic Fatty Liver Disease in North Indians |
title | SREBP-2 1784 G/C Genotype is Associated with Non-Alcoholic Fatty Liver Disease in North Indians |
title_full | SREBP-2 1784 G/C Genotype is Associated with Non-Alcoholic Fatty Liver Disease in North Indians |
title_fullStr | SREBP-2 1784 G/C Genotype is Associated with Non-Alcoholic Fatty Liver Disease in North Indians |
title_full_unstemmed | SREBP-2 1784 G/C Genotype is Associated with Non-Alcoholic Fatty Liver Disease in North Indians |
title_short | SREBP-2 1784 G/C Genotype is Associated with Non-Alcoholic Fatty Liver Disease in North Indians |
title_sort | srebp-2 1784 g/c genotype is associated with non-alcoholic fatty liver disease in north indians |
topic | Other |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826379/ https://www.ncbi.nlm.nih.gov/pubmed/22182810 http://dx.doi.org/10.3233/DMA-2011-0852 |
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