The CNDP1 (CTG)(5) Polymorphism Is Associated with Biopsy-Proven Diabetic Nephropathy, Time on Hemodialysis, and Diabetes Duration

Thomas Albrecht*, Shiqi Zhang, Jana D. Braun, Zuo Li Xia, Angelica Rodriquez, Jiedong Qiu, Verena Peters, Claus P. Schmitt, Jacob van den Born, Stephan J. L. Bakker, Alexander Lammert, Hannes Koeppel, Peter Schnuelle, Bernhard K. Kraemer, Benito A. Yard, Sibylle J. Hauske

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Considering that the homozygous CNDP1 (CTG)(5) genotype affords protection against diabetic nephropathy (DN) in female patients with type 2 diabetes, this study assessed if this association remains gender-specific when applying clinical inclusion criteria (CIC-DN) or biopsy proof (BP-DN). Additionally, it assessed if the prevalence of the protective genotype changes with diabetes duration and time on hemodialysis and if this occurs in association with serum carnosinase (CN-1) activity. Whereas the distribution of the (CTG)(5) homozygous genotype in the no-DN and CIC-DN patients was comparable, a lower frequency was found in the BP-DN patients, particularly in females. We observed a significant trend towards high frequencies of the (CTG)(5) homozygous genotype with increased time on dialysis. This was also observed for diabetes duration but only reached significance when both (CTG)(5) homo- and heterozygous patients were included. CN-1 activity negatively correlated with time on hemodialysis and was lower in (CTG)(5) homozygous patients. The latter remained significant in female subjects after gender stratification. We confirm the association between the CNDP1 genotype and DN to be likely gender-specific. Although our data also suggest that (CTG)(5) homozygous patients may have a survival advantage on dialysis and in diabetes, this hypothesis needs to be confirmed in a prospective cohort study.

Original languageEnglish
Number of pages11
JournalJournal of Diabetes Research
DOIs
Publication statusPublished - 2017

Keywords

  • NONDIABETIC RENAL-DISEASE
  • CARNOSINASE GENE CNDP1
  • AFRICAN-AMERICANS
  • LEUCINE REPEAT
  • KIDNEY-DISEASE
  • RETINOPATHY
  • MELLITUS
  • SUSCEPTIBILITY
  • PROGRESSION
  • RISK

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