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Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis.

Authors :
Qing-Ya Li
Zhi-Zhong Guo
Jian Liang
Wei Zhang
Lie- Ming Xu
Yue-Qiu Gao
Xiao-SuWang
Dong-Ying Xue
Shi-Bing Su
Source :
Evidence-based Complementary & Alternative Medicine (eCAM). 2012, Vol. 2012, p1-6. 6p.
Publication Year :
2012

Abstract

Traditional Chinese medicine (TC M) syndrome is an important basis for TC M 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 TC M 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1741427X
Volume :
2012
Database :
Academic Search Index
Journal :
Evidence-based Complementary & Alternative Medicine (eCAM)
Publication Type :
Academic Journal
Accession number :
86020580
Full Text :
https://doi.org/10.1155/2012/298925