Interplay between Superoxide Dismutase, Glutathione Peroxidase, and Peroxisome Proliferator Activated Receptor Gamma Polymorphisms on the Risk of End-Stage Renal Disease among Han Chinese Patients

Author:

Chao Chia-Ter12,Chen Yen-Ching3,Chiang Chih-Kang24,Huang Jenq-Wen5,Fang Cheng-Chung6,Chang Chen-Chih5,Yen Chung-Jen57

Affiliation:

1. Department of Medicine, National Taiwan University Hospital Jinshan Branch, New Taipei City, Taiwan

2. Graduate Institute of Toxicology, College of Medicine, National Taiwan University, No. 1 Jen-Ai Road, Section 1, 10051 Taipei, Taiwan

3. Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, No. 17 Xu-Zhou Road, 10055 Taipei, Taiwan

4. Department of Integrated Diagnostics & Therapeutics, National Taiwan University Hospital, No. 7 Chung-Shan South Road, 10002 Taipei, Taiwan

5. Department of Internal Medicine, National Taiwan University Hospital, No. 7 Chung-Shan South Road, 10002 Taipei, Taiwan

6. Department of Emergency Medicine, National Taiwan University Hospital, No. 7 Chung-Shan South Road, 10002 Taipei, Taiwan

7. Department of Geriatric Medicine and Gerontology, National Taiwan University Hospital, No. 7 Chung-Shan South Road, 10002 Taipei, Taiwan

Abstract

Background. Single nucleotide polymorphisms (SNPs) of antioxidants, including superoxide dismutase 2 (SOD2) and glutathione peroxidase 1 (GPX1), play an important role in the risk for cancer and metabolic disorders. However, little is known regarding the effect of antioxidant SNPs on renal events.Methods. We prospectively enrolled multicenter patients with end-stage renal disease (ESRD) and those without chronic kidney disease (CKD) of Han Chinese origin, with SOD2 (Val16Ala), GPX1 (Pro197Leu), and PPAR-γ(Pro12Ala, C161T) genotyped. Multiple regression analyses were conducted to evaluate the significant risk determinants for ESRD.Results. Compared to ESRD patients, non-CKD subjects were more likely to have T allele at SOD2 Val16Ala (p=0.036) and CC genotype at PPAR-γPro12Ala (p=0.028). Regression analysis showed that TT genotype of SOD2 Val16Ala conferred significantly lower ESRD risk among patients without diabetes (odds ratio 0.699;p=0.018). GPX1 SNP alone did not alter the risk. We detected significant interactions between SNPs including PPAR-γPro12Ala, C161T, and GPX1 regarding the risk of ESRD.Conclusion. This is the first and largest study on the association between adverse renal outcomes and antioxidant SNPs among Han Chinese population. Determination of SOD2 and PPAR-γSNPs status might assist in ESRD risk estimation.

Funder

National Taiwan University Hospital

Publisher

Hindawi Limited

Subject

Cell Biology,Aging,General Medicine,Biochemistry

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