Sequence Variants of Peroxisome Proliferator-Activated Receptor-Gamma Gene and the Clinical Courses of Patients with End-Stage Renal Disease

被引:6
作者
Chao, Chia-Ter [1 ,2 ]
Chen, Yen-Ching [3 ]
Chiang, Chih-Kang [1 ,2 ,4 ,5 ]
Huang, Jenq-Wen [4 ]
Hu, Fu-Chang [6 ]
Fang, Cheng-Chung [7 ]
Chang, Chen-Chih [4 ]
Yen, Chung-Jen [4 ,8 ]
机构
[1] Natl Taiwan Univ Hosp, Dept Internal Med, Jinshan Branch, New Taipei 20844, Taiwan
[2] Natl Taiwan Univ, Grad Inst Toxicol, Taipei 10051, Taiwan
[3] Natl Taiwan Univ, Coll Publ Hlth, Inst Epidemiol & Prevent Med, Taipei 10055, Taiwan
[4] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei 10002, Taiwan
[5] Natl Taiwan Univ Hosp, Dept Integrated Diagnost & Therapeut, Taipei 10002, Taiwan
[6] Natl Taiwan Univ, Grad Inst Clin Med, Taipei 10002, Taiwan
[7] Natl Taiwan Univ, Coll Med, Natl Taiwan Univ Hosp, Dept Emergency Med, Taipei 10002, Taiwan
[8] Natl Taiwan Univ, Natl Taiwan Univ Hosp, Dept Geriatr Med & Gerontol, Coll Med, Taipei 10002, Taiwan
关键词
PPAR-GAMMA; PRO12ALA POLYMORPHISM; BODY-MASS; RISK; METAANALYSIS; ASSOCIATION; OBESITY; INFLAMMATION; PROGRESSION; MORTALITY;
D O I
10.1155/2015/763459
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background. PPAR-gamma single nucleotide polymorphisms (SNPs) reportedly play an important role in determining metabolic risk among diverse population. Whether PPAR-gamma SNPs affect the clinical courses in ESRD patients is unknown. Methods. From a multicenter cohort, we identified 698 patients with prevalent ESRD between 2002 and 2003, and other 782 healthy subjects as control. Two PPAR-gamma SNPs, Pro12Ala (rs1801282) and C161T (rs3856806), were genotyped and their association with ESRD was examined. Both groups were prospectively followed until 2007, and the predictability of genotypes for the long-term survival of ESRD patients was analyzed. Results. After multivariable-adjusted regression, GG genotype of Pro12Ala was significantly more likely to associate with ESRD (P < 0.001) among patients with non-diabetes-related ESRD. Cox's proportional hazard regression showed that both Pro12Ala and C161T polymorphisms were significant predictors of mortality in ESRD patients with DM (Pro12Ala: GG versus other genotypes, hazard ratio [HR] <0.01; P < 0.001; for C161T, CC versus TT genotypes, HR 2.86; P < 0.001; CT versus TT genotypes, HR 1.93; P < 0.001). Conclusion. This is the first and largest study to evaluate PPAR-gamma SNPs in ESRD patients. Further mechanistic study is needed to elucidate the role of PPAR-gamma among ESRD patients.
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页码:1 / 7
页数:7
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