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Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population
BACKGROUND: The association between ABCC8 gene C49620T polymorphism and type 2 diabetes (T2D) in populations of diverse ethnic backgrounds has been reported. However, such occurrence in an African population is yet to be established. This case-control study involving 73 T2D and 75 non-diabetic (ND)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5948806/ https://www.ncbi.nlm.nih.gov/pubmed/29751826 http://dx.doi.org/10.1186/s12881-018-0601-1 |
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author | Engwa, Godwill Azeh Nwalo, Friday Nweke Chikezie, Claribel Chidimma Onyia, Christie Oby Ojo, Opeolu Oyejide Mbacham, Wilfred Fon Ubi, Benjamin Ewa |
author_facet | Engwa, Godwill Azeh Nwalo, Friday Nweke Chikezie, Claribel Chidimma Onyia, Christie Oby Ojo, Opeolu Oyejide Mbacham, Wilfred Fon Ubi, Benjamin Ewa |
author_sort | Engwa, Godwill Azeh |
collection | PubMed |
description | BACKGROUND: The association between ABCC8 gene C49620T polymorphism and type 2 diabetes (T2D) in populations of diverse ethnic backgrounds has been reported. However, such occurrence in an African population is yet to be established. This case-control study involving 73 T2D and 75 non-diabetic (ND) patients investigated the occurrence of this polymorphism among T2D patients in Nigeria and assessed its relationship with body lipids of patients. METHODS: Demographic and clinical characteristics of patients were collected and lipid profile indices including total cholesterol (TC), triglyceride (TG), low density lipoprotein (LDL) and high density lipoprotein (HDL) were assayed. Restriction fragment length polymorphism-PCR (RFLP-PCR) was employed to genotype the ABCC8-C49620T polymorphism using PstI restriction enzyme. RESULTS: This study revealed significantly (p < 0.05) higher prevalence of the T allele of the ABCC8 gene in T2D patients (33.1%) compared to ND patients (28.0%). The mutant TT genotype was also higher than the CC and CT genotypes in T2D patients compared to ND patients but did not show any significant risk (p>0.05) of T2D for the unadjusted codominant, dominant and recessive models. Following age adjustment, the mutant genotypes (CT and TT) showed significant (p<0.05) risk of T2D for all the models with the recessive model presenting the greatest risk of T2D (OR: 2.39, 95% CI: 1.16-4.91, p<0.018). The TT genotype significantly (p<0.05) associated with high level of HDL and reduced levels of TC, TG and LDL in non-diabetic patients but was not associated with any of the demographic and clinical characteristics among T2D patients. CONCLUSIONS: ABCC8 C49620T polymorphism showed possible association with T2D marked by predominance of the mutant TT genotype in T2D patients. However, the relationship between TT genotype and lipid abnormalities for possible beneficial effect on people suffering from T2D is unclear. |
format | Online Article Text |
id | pubmed-5948806 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-59488062018-05-18 Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population Engwa, Godwill Azeh Nwalo, Friday Nweke Chikezie, Claribel Chidimma Onyia, Christie Oby Ojo, Opeolu Oyejide Mbacham, Wilfred Fon Ubi, Benjamin Ewa BMC Med Genet Research Article BACKGROUND: The association between ABCC8 gene C49620T polymorphism and type 2 diabetes (T2D) in populations of diverse ethnic backgrounds has been reported. However, such occurrence in an African population is yet to be established. This case-control study involving 73 T2D and 75 non-diabetic (ND) patients investigated the occurrence of this polymorphism among T2D patients in Nigeria and assessed its relationship with body lipids of patients. METHODS: Demographic and clinical characteristics of patients were collected and lipid profile indices including total cholesterol (TC), triglyceride (TG), low density lipoprotein (LDL) and high density lipoprotein (HDL) were assayed. Restriction fragment length polymorphism-PCR (RFLP-PCR) was employed to genotype the ABCC8-C49620T polymorphism using PstI restriction enzyme. RESULTS: This study revealed significantly (p < 0.05) higher prevalence of the T allele of the ABCC8 gene in T2D patients (33.1%) compared to ND patients (28.0%). The mutant TT genotype was also higher than the CC and CT genotypes in T2D patients compared to ND patients but did not show any significant risk (p>0.05) of T2D for the unadjusted codominant, dominant and recessive models. Following age adjustment, the mutant genotypes (CT and TT) showed significant (p<0.05) risk of T2D for all the models with the recessive model presenting the greatest risk of T2D (OR: 2.39, 95% CI: 1.16-4.91, p<0.018). The TT genotype significantly (p<0.05) associated with high level of HDL and reduced levels of TC, TG and LDL in non-diabetic patients but was not associated with any of the demographic and clinical characteristics among T2D patients. CONCLUSIONS: ABCC8 C49620T polymorphism showed possible association with T2D marked by predominance of the mutant TT genotype in T2D patients. However, the relationship between TT genotype and lipid abnormalities for possible beneficial effect on people suffering from T2D is unclear. BioMed Central 2018-05-12 /pmc/articles/PMC5948806/ /pubmed/29751826 http://dx.doi.org/10.1186/s12881-018-0601-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Engwa, Godwill Azeh Nwalo, Friday Nweke Chikezie, Claribel Chidimma Onyia, Christie Oby Ojo, Opeolu Oyejide Mbacham, Wilfred Fon Ubi, Benjamin Ewa Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population |
title | Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population |
title_full | Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population |
title_fullStr | Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population |
title_full_unstemmed | Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population |
title_short | Possible association between ABCC8 C49620T polymorphism and type 2 diabetes in a Nigerian population |
title_sort | possible association between abcc8 c49620t polymorphism and type 2 diabetes in a nigerian population |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5948806/ https://www.ncbi.nlm.nih.gov/pubmed/29751826 http://dx.doi.org/10.1186/s12881-018-0601-1 |
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