Polymorphisms in PPARD, PPARG and APM1 associated with four types of Traditional Chinese Medicine constitutions

被引:49
作者
Wu, Yanrui [2 ]
Cun, Yina [2 ]
Dong, Jing [3 ]
Shao, Jingru [2 ]
Luo, Shengjun [2 ]
Nie, Shengjie [2 ]
Yu, Haijing [2 ]
Zheng, Bingrong [2 ]
Wang, Qi [1 ]
Xiao, Chunjie [2 ]
机构
[1] Beijing Univ Chinese Med, Ctr Studies Constitut Res Tradit Chinese Med, Beijing 100029, Peoples R China
[2] Yunnan Univ, Ctr Human Genet, Kunming 650091, Peoples R China
[3] Gen Hosp AF, Beijing 100036, Peoples R China
关键词
Traditional Chinese Medicine; constitution; classification; PPARD; PPARG; APM1; SNP; CARDIOVASCULAR RISK; PLASMA ADIPONECTIN; METABOLIC SYNDROME; GENE; INSULIN; PRO12ALA; OBESITY; WEIGHT; GAMMA; DISEASE;
D O I
10.1016/S1673-8527(09)60055-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Based on the theory of constitution of Traditional Chinese Medicine (TCM), the human population is divided into nine constitutions including one balanced constitution (Normality) and eight unbalanced constitutions (Yang-deficiency, Yin-deficiency, Phlegm-wetness, Qi-deficiency, Wetness-heat, Blood stasis, Depressed constitution, and Inherited special constitution). Different constitutions have specific metabolic features and different susceptibility to certain diseases. However, whether a genetic basis accounts for such constitution classification is yet to be determined. Here we performed a genetic study to assess the association between genetic variations of metabolic genes including PPARD, PPARG and APM1 and the constitutions. A total of 233 individuals of the Han population in China were classified into four groups, Normality, Yang-deficiency, Yin-deficiency and Phlegm-wetness with whom 23 single nucleotide polymorphisms (SNPs) in the three genes were genotyped using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Biased distribution of PPARD rs2267669 and rs2076167, APM1 rs7627128 and rs1063539 in Yang-deficiency, PPARG Pro12Ala in Yin-deficiency and PPARD rs2076167, APM1 rs266729 and rs7627128 in Phlegm-wetness were observed. The frequencies of Haplotype13 (Hap13) of PPARG in Yin-deficiency, Hap25 of APM1 in Yang-deficiency and Hap2 of PPARD and Hap14 of PPARG in Phlegm-wetness, were significantly different from those in Normality, suggesting those might be group-associated haplotypes. These results suggested that single SNP and haplotypes of PPARD, PPARG and APM1 may underlie the genetic basis of the constitutions classified in TCM.
引用
收藏
页码:371 / 379
页数:9
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