Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/36069
Title: Clinical impact of an angiotensin I-converting enzyme insertion/deletion and kinin B2 receptor +9/-9 polymorphisms in the prognosis of renal transplantation
Authors: Amorim, Carlos E. N. [UNIFESP]
Nogueira, Eliana [UNIFESP]
Almeida, Sandro S. [UNIFESP]
Gomes, Pedro P. G. [UNIFESP]
Bacurau, Reury Frank Pereira
Suzete Ozaki, K. [UNIFESP]
Cenedeze, Marcos A. [UNIFESP]
Pacheco-Silva, Alvaro [UNIFESP]
Câmara, Niels Olsen Saraiva [UNIFESP]
Araujo, Ronaldo C. [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Universidade de São Paulo (USP)
Hosp Israelita Albert Einstein
Keywords: angiotensin I-converting enzyme (ACE)
B2 receptor
renal transplantation
Issue Date: 1-Mar-2013
Publisher: Walter de Gruyter & Co
Citation: Biological Chemistry. Berlin: Walter de Gruyter & Co, v. 394, n. 3, p. 369-377, 2013.
Abstract: There is a consensus in the scientific literature that supports the importance of the kallikrein kinin and renin angiotensin systems in renal physiology, but few studies have investigated their importance after renal transplantation. the aim of this study was to investigate the clinical effects of the insertion/deletion polymorphism in the angiotensin I-converting enzyme (ACE) gene and the +9/-9 polymorphism in the kinin B2 receptor (B2R) gene in kidney-transplanted patients (n=215 ACE, n=203 B2R) compared with 443 healthy individuals. Demographic results showed that there is a higher frequency of the D allele (high plasma ACE activity) and +9 allele (lower B2R expression) in transplant patients compared with control individuals. We also observed a higher frequency of these alleles in patients who had an elevated level of plasma creatinine. At day 7 post-transplantation, we found a higher prevalence of individuals with the DD genotype with elevated plasma creatinine level. Furthermore, individuals with the DD genotype had a higher chronic allograft dysfunction and graft loss compared with the II patient genotype, which showed no loss of graft. Taken together, our data suggest that the DD genotype is an indicator of an unfavorable prognosis following renal transplantation and could be related to kinin modulation.
URI: http://repositorio.unifesp.br/handle/11600/36069
ISSN: 1431-6730
Other Identifiers: http://dx.doi.org/10.1515/hsz-2012-0314
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