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Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis
Traditional Chinese medicine (TCM) syndrome is an important basis for TCM diagnosis and treatment. As Child-Pugh classification as well as compensation and decompensation phase in liver cirrhosis, it is also an underlying clinical classification. In this paper, we investigated the correlation betwee...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368439/ https://www.ncbi.nlm.nih.gov/pubmed/22690243 http://dx.doi.org/10.1155/2012/298925 |
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author | Li, Qing-Ya Guo, Zhi-Zhong Liang, Jian Zhang, Wei Xu, Lie-Ming Gao, Yue-Qiu Wang, Xiao-Su Xue, Dong-Ying Su, Shi-Bing |
author_facet | Li, Qing-Ya Guo, Zhi-Zhong Liang, Jian Zhang, Wei Xu, Lie-Ming Gao, Yue-Qiu Wang, Xiao-Su Xue, Dong-Ying Su, Shi-Bing |
author_sort | Li, Qing-Ya |
collection | PubMed |
description | Traditional Chinese medicine (TCM) syndrome is an important basis for TCM diagnosis and treatment. As Child-Pugh classification as well as compensation and decompensation phase in liver cirrhosis, it is also an underlying clinical classification. In this paper, we investigated the correlation between single nucleotide polymorphisms (SNPs) of Interleukin-10 (IL-10) and TCM syndromes in patients with hepatitis B cirrhosis (HBC). Samples were obtained from 343 HBC patients in China. Three SNPs of IL-10 (−592A/C, −819C/T, and −1082A/G) were detected with polymerase chain-reaction-ligase detection reaction (PCR-LDR). The result showed the SNP-819C/T was significantly correlated with Deficiency syndrome (P = 0.031), but none of the 3 loci showed correlation either with Child-Pugh classification and phase in HBC patients. The logistic regression analysis showed that the Excess syndrome was associated with dizzy and spider nevus, and the Deficiency syndrome was associated with dry eyes, aversion to cold, IL-10-819C/T loci, and IL-10-1082A/G loci. The odds ratio (OR) value at IL-10-819C/T was 4.022. The research results suggested that IL-10-819C/T locus (TC plus CC genotype) is probably a risk factor in the occurrence of Deficiency syndrome in HBC patients. |
format | Online Article Text |
id | pubmed-3368439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33684392012-06-11 Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis Li, Qing-Ya Guo, Zhi-Zhong Liang, Jian Zhang, Wei Xu, Lie-Ming Gao, Yue-Qiu Wang, Xiao-Su Xue, Dong-Ying Su, Shi-Bing Evid Based Complement Alternat Med Research Article Traditional Chinese medicine (TCM) syndrome is an important basis for TCM diagnosis and treatment. As Child-Pugh classification as well as compensation and decompensation phase in liver cirrhosis, it is also an underlying clinical classification. In this paper, we investigated the correlation between single nucleotide polymorphisms (SNPs) of Interleukin-10 (IL-10) and TCM syndromes in patients with hepatitis B cirrhosis (HBC). Samples were obtained from 343 HBC patients in China. Three SNPs of IL-10 (−592A/C, −819C/T, and −1082A/G) were detected with polymerase chain-reaction-ligase detection reaction (PCR-LDR). The result showed the SNP-819C/T was significantly correlated with Deficiency syndrome (P = 0.031), but none of the 3 loci showed correlation either with Child-Pugh classification and phase in HBC patients. The logistic regression analysis showed that the Excess syndrome was associated with dizzy and spider nevus, and the Deficiency syndrome was associated with dry eyes, aversion to cold, IL-10-819C/T loci, and IL-10-1082A/G loci. The odds ratio (OR) value at IL-10-819C/T was 4.022. The research results suggested that IL-10-819C/T locus (TC plus CC genotype) is probably a risk factor in the occurrence of Deficiency syndrome in HBC patients. Hindawi Publishing Corporation 2012 2012-05-28 /pmc/articles/PMC3368439/ /pubmed/22690243 http://dx.doi.org/10.1155/2012/298925 Text en Copyright © 2012 Qing-Ya Li et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Li, Qing-Ya Guo, Zhi-Zhong Liang, Jian Zhang, Wei Xu, Lie-Ming Gao, Yue-Qiu Wang, Xiao-Su Xue, Dong-Ying Su, Shi-Bing Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis |
title | Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis |
title_full | Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis |
title_fullStr | Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis |
title_full_unstemmed | Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis |
title_short | Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis |
title_sort | interleukin-10 genotype correlated to deficiency syndrome in hepatitis b cirrhosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368439/ https://www.ncbi.nlm.nih.gov/pubmed/22690243 http://dx.doi.org/10.1155/2012/298925 |
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