Tohoku J. Exp. Med., 2011, 225(2)

The T-1237C Polymorphism of the Toll-like Receptor-9 Gene Is Associated with Chronic Kidney Disease in a Han Chinese Population

KUO-CHENG LU,1 HSIN-YI YANG,2 YUH-FENG LIN,3,4 SEN-YEONG KAO,5 CHING-HUANG LAI,5 CHI-MING CHU,5 CHIA-CHAO WU4 and SUI-LUNG SU5

1Division of Nephrology, Department of Medicine, Cardinal Tien Hospital, School of Medicine, Fu Jen Catholic University, Taipei, Taiwan, ROC
2Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan, ROC
3Division of Nephrology, Department of Medicine, Shuang Ho Hospital, Graduate Institute of Clinical Medicine, Taipei Medical University, Taipei, Taiwan, ROC
4Division of Nephrology, Department of Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan, ROC
5School of Public Health, National Defense Medical Center, Taipei, Taiwan, ROC

Chronic kidney disease (CKD) is increasingly recognized as a global public health problem. As inflammatory processes and genetic factors are involved in the pathogenesis of CKD, we have investigated the potential genetic contribution of Toll-like receptor (TLR) gene polymorphisms in CKD. In a case-control association study, 149 CKD patients and 429 healthy controls were genotyped by real-time polymerase chain reaction. CKD patients were defined as kidney damage (albuminuria, proteinuria or hematuria) or glomerular filtration rate < 60 ml/min/1.73 m2 for 3 months or more. Single nucleotide polymorphisms (SNPs) at TLR-2 G2408A, TLR-4 A12874G and C13174T, and TLR-9 T-1237C, T-1486C, and G1635A were assessed, and linkage disequilibrium calculations and haplotype association analysis were undertaken. The functions of TLR-9 have been documented to recognize the viral and bacterial CpG DNA sequences, whereas detects microbe-derived peptidoglycan and lipopeptides and TLR-4 binds lipopolysaccharides. SNPs within the TLR genes may influence promoter activity, mRNA conformation and subcellular localization, and/or protein structure and function. Our results show that only the TLR-9 T-1237C and G1635A gene polymorphisms demonstrate an association with CKD (p = 0.002 and p = 0.04, respectively). The TLR-9 TCA haplotype at T-1237C, T-1486C, and G1635A was associated with a lower risk of CKD, whereas the TTA haplotype was associated with a higher risk of CKD. In the Han Chinese population, those who carry the C and A alleles at SNPs T-1237C and G1635A in the TLR-9 gene appear to be more susceptible to the development of CKD.

keywords —— chronic kidney disease; single nucleotide polymorphism; Toll-like receptor 2; Toll-like receptor 4; Toll-like receptor 9

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Tohoku J. Exp. Med., 2011, 225, 109-116

Correspondence: Sui Lung Su, School of Public Health, National Defense Medical Center, No. 161, Sec. 6, Minquan E. Rd., Neihu Dist., Taipei City 114, Taiwan, ROC.

e-mail: a131419@gmail.com