Results: 7

Screening of family members of chronic kidney disease patients with Fabry disease mutations: a very important and underrated task

J. bras. nefrol; 43 (1), 2021
ABSTRACT Introduction: Fabry disease is a chronic, progressive, and multi-system hereditary condition, related to an Xq22 mutation in X chromosome, which results in deficiency of alpha-galactosidase enzyme, hence reduced capacity of globotriaosylceramide degradation. Objectives: to evaluate the prevale...

Metabolic phenotypes of obese, overweight, and normal weight individuals and risk of chronic kidney disease: a systematic review and meta-analysis

ABSTRACT Objective Chronic kidney disease (CKD) risk is inconsistent in the normal-weight, overweight, and obese individuals due to the heterogeneity of metabolic status. This meta-analysis aimed to examine the combined effects of body mass index (BMI) and metabolic status on CKD risk. Materials and m...

Alelos HLA más comunes y asociados con riesgo o protección en enfermedad renal crónica de etiología no determinada

Gac. méd. Méx; 155 (3), 2019
Resumen Introducción: La enfermedad renal crónica representa parte del gasto en salud en general; una potencial etiología es la relacionada con variaciones, ausencia o presencia de algunos alelos del human leucocyte antigen (HLA). Método: Se realizó el análisis de 1965 reportes de HLA sin etiolog...

Screening potential prognostic biomarkers of long non-coding RNAs for predicting the risk of chronic kidney disease

Braz. j. med. biol. res; 52 (11), 2019
Not much is known about the roles of long non-coding RNAs (lncRNAs) for chronic kidney disease (CKD). In this study, we included CKD patient cohorts and normal controls as a discovery cohort to identify putative lncRNA biomarkers associated with CKD. We first compared the lncRNA expression profiles of CK...

APOL1 risk variants and kidney disease: what we know so far

J. bras. nefrol; 40 (4), 2018
ABSTRACT There are striking differences in chronic kidney disease between Caucasians and African descendants. It was widely accepted that this occurred due to socioeconomic factors, but recent studies show that apolipoprotein L-1 (APOL1) gene variants are strongly associated with focal segmental glomerul...

NOS3 Polymorphisms and Chronic Kidney Disease

J. bras. nefrol; 40 (3), 2018
ABSTRACT Chronic kidney disease (CKD) is a multifactorial pathophysiologic irreversible process that often leads to a terminal state in which the patient requires renal replacement therapy. Most cases of CKD are due to chronic-degenerative diseases and endothelial dysfunction is one of the factors that c...

Nephrin gene expression in chronic kidney disease of dogs with Leishmania (Leishmania) infantum chagasi

Braz. j. infect. dis; 20 (5), 2016