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Genetic damage in chronic renal failure patients is associated with the glomerular filtration rate index
Author(s) -
Silvia B. Sandoval,
Elitsa Stoyanova,
Elisabeth Coll,
Susana Pastor,
J. Rivera Reyes,
E. Andrés,
José Ballarín,
N. Xamena,
Ricard Marcos
Publication year - 2010
Publication title -
mutagenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.723
H-Index - 91
eISSN - 1464-3804
pISSN - 0267-8357
DOI - 10.1093/mutage/geq047
Subject(s) - renal function , genetic predisposition , medicine , creatinine , population , chronic renal failure , endocrinology , kidney disease , gastroenterology , disease , physiology , environmental health
Chronic renal failure (CRF) patients are considered to present genomic instability and, as a consequence, elevated levels of genetic damage. An open question is whether this damage is related to the stage of the pathology. To determine the background levels of genetic damage, a large population of 258 Caucasian adults (201 CRF patients and 57 controls) was analysed using the micronucleus (MN) assay. The frequency of MN in CRF patients was significantly higher than in controls and correlated with the progression of the disease, according to the glomerular filtration rate. In addition, a significant association was observed between genetic damage and serum creatinine levels. Genetic damage, measured as frequency of MN, increases when renal function decreases. The fact that an increased level of MN is already observed in patients' Stage 2 seems to indicate a genetic predisposition on these patients. Nevertheless, part of the observed damage can be attributed to the uraemic state itself.

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