Interleukin-10 Genotype Correlated to Deficiency Syndrome in Hepatitis B Cirrhosis. (28th May 2012)

• Record Type: Journal Article
• Authors: 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
• Other Names: Li Shao Academic Editor.
• Is Part Of: Evidence-based complementary and alternative medicine. Volume 2012(2012)
• Publication Date: 2012-05-28
• Subjects: Alternative medicine -- Periodicals; 615.505
• DOI: 10.1155/2012/298925
• Languages: English
• ISSNs: 1741-427X

Abstract

Abstract : 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.