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Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study
BACKGROUND: Recently genome-wide association studies identified that NCAN rs2228603 polymorphism was associated with non-alcoholic fatty liver disease (NAFLD) mainly in subjects of European ancestry. While no research have been conducted to demonstrate the relationship between NCAN rs2228603 and NAF...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124242/ https://www.ncbi.nlm.nih.gov/pubmed/27887608 http://dx.doi.org/10.1186/s12944-016-0367-4 |
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author | Wu, Meng-Juan Yuan, Chen Lu, Lin-Lin An, Bai-Quan Xuan, Shi-Ying Xin, Yong-Ning |
author_facet | Wu, Meng-Juan Yuan, Chen Lu, Lin-Lin An, Bai-Quan Xuan, Shi-Ying Xin, Yong-Ning |
author_sort | Wu, Meng-Juan |
collection | PubMed |
description | BACKGROUND: Recently genome-wide association studies identified that NCAN rs2228603 polymorphism was associated with non-alcoholic fatty liver disease (NAFLD) mainly in subjects of European ancestry. While no research have been conducted to demonstrate the relationship between NCAN rs2228603 and NAFLD in Chinese Han adults. The aim of this study was to investigate whether NCAN rs2228603 is associated with NAFLD in Chinese population. METHODS: Gene NCAN rs2228603 was genotyped in 182 patients with NAFLD and 195 healthy controls. The expression of NCAN was tested according to polymerase chain reaction analysis (PCR) and serum lipids were performed by biology techniques. RESULTS: No significant difference was found in genotype and allele frequencies of NCAN rs2228603 between the NAFLD group and the controls (P > 0.05). Subjects with the NCAN rs2228603 CT genotype showed a higher level of alkaline phosphatase (AKP) (P = 0.017) and a higher high-density lipoprotein (HDL) (P < 0.05). CONCLUSIONS: Our study for the first time identified that the gene NCAN rs2228603 is not a risk factor for the incidence of NAFLD in Chinese population. Also we found the dual and opposite role of T variant in protecting liver with a higher level of HDL and conferring risk for liver damage with a higher level of AKP. TRIAL REGISTRATION: Chinese Clinical Trial Register.gov Identifier: ChiCTR-ROC-15006447. |
format | Online Article Text |
id | pubmed-5124242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51242422016-12-08 Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study Wu, Meng-Juan Yuan, Chen Lu, Lin-Lin An, Bai-Quan Xuan, Shi-Ying Xin, Yong-Ning Lipids Health Dis Research BACKGROUND: Recently genome-wide association studies identified that NCAN rs2228603 polymorphism was associated with non-alcoholic fatty liver disease (NAFLD) mainly in subjects of European ancestry. While no research have been conducted to demonstrate the relationship between NCAN rs2228603 and NAFLD in Chinese Han adults. The aim of this study was to investigate whether NCAN rs2228603 is associated with NAFLD in Chinese population. METHODS: Gene NCAN rs2228603 was genotyped in 182 patients with NAFLD and 195 healthy controls. The expression of NCAN was tested according to polymerase chain reaction analysis (PCR) and serum lipids were performed by biology techniques. RESULTS: No significant difference was found in genotype and allele frequencies of NCAN rs2228603 between the NAFLD group and the controls (P > 0.05). Subjects with the NCAN rs2228603 CT genotype showed a higher level of alkaline phosphatase (AKP) (P = 0.017) and a higher high-density lipoprotein (HDL) (P < 0.05). CONCLUSIONS: Our study for the first time identified that the gene NCAN rs2228603 is not a risk factor for the incidence of NAFLD in Chinese population. Also we found the dual and opposite role of T variant in protecting liver with a higher level of HDL and conferring risk for liver damage with a higher level of AKP. TRIAL REGISTRATION: Chinese Clinical Trial Register.gov Identifier: ChiCTR-ROC-15006447. BioMed Central 2016-11-26 /pmc/articles/PMC5124242/ /pubmed/27887608 http://dx.doi.org/10.1186/s12944-016-0367-4 Text en © The Author(s). 2016 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 Wu, Meng-Juan Yuan, Chen Lu, Lin-Lin An, Bai-Quan Xuan, Shi-Ying Xin, Yong-Ning Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study |
title | Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study |
title_full | Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study |
title_fullStr | Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study |
title_full_unstemmed | Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study |
title_short | Role of NCAN rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study |
title_sort | role of ncan rs2228603 polymorphism in the incidence of nonalcoholic fatty liver disease: a case-control study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5124242/ https://www.ncbi.nlm.nih.gov/pubmed/27887608 http://dx.doi.org/10.1186/s12944-016-0367-4 |
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