The E 23 K polymorphism of the KCNJ 11 gene is associated with lower insulin release in patients with Autosomal Dominant Polycystic Kidney Disease
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چکیده
[email protected] En los pacientes con IRC, los mecanismos que pueden explicar las elevaciones inespecíficas de TnIc son principalmente el mayor daño cardíaco y la función renal disminuida5. En nuestro estudio, las principales causas de elevación de TnIc en el grupo Otras Patologías Cardíacas (OPC) fueron la insuficiencia cardíaca congestiva, fibrilación auricular y taquicardia, mientras que en el grupo Otras Patologías No Cardíacas (OPNC) fueron hipertensión arterial, accidente cerebrovascular y neumonía, pero consideramos que todas las causas descritas deben tenerse en consideración como posibles factores de confusión cuando se encuentran concentraciones elevadas de TnIc en pacientes con IRC y ausencia de SCA.
منابع مشابه
Exon Sequencing of PKD1 Gene in an Iranian Patient with Autosomal-Dominant Polycystic Kidney Disease
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic kidney disorders with the incidence of 1 in 1,000 births. ADPKD is genetically heterogeneous with two genes identified: PKD1 (16p13.3, 46 exons) and PKD2 (4q21, 15 exons). Eighty five percent of the patients with ADPKD have at least one mutation in the PKD1 gene. Genetic studies have demonstrate...
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Autosomal dominant polycystic kidney disease (ADPKD) is characterized by a significant phenotypic variability in progression of the disease. Vascular endothelial growth factor (VEGF) has been reported to play a major role in renal pathophysiology. The aim of the present case-control study was to evaluate the association of two promoter polymorphisms (-2578C>A and -1154G>A) of VEGF gene and ADPK...
متن کاملThe E23K polymorphism of the KCNJ11gene is associated with lower insulin release in patients with autosomal dominant polycystic kidney disease.
The aim of our study was to investigate an association between E23K KCNJ11 gene polymorphism with anthropometric, biochemical, beta-cell secretion and insulin sensitivity parameters among adult ADPKD patients with normal kidney function and no diagnosis of diabetes. The comparison of genotype-phenotype associations between ADPKD and non-ADPKD subjects could reveal a hypothetical mechanism of ge...
متن کاملHuman Evaluation of the Glu298Asp polymorphism in NOS3 gene and its relationship with onset age of ESRD in Iranian patients suffering from ADPKD
One of the most striking features in autosomal dominant polycystic kidney disease (ADPKD) is the difference at onset age of end-stage renal disease (ESRD). Modifier genes may play a role in this phenotypic variability. The mutated nitric oxide synthase 3 gene (NOS3), have a modifier effect on the severity of ADPKD by impairment of NOS3 activity and decreasing of renal vascular nitric oxide prod...
متن کاملبررسی ارتباط بین پلی‌مورفیسم K23 E پروموتور ژن 11 kcnj و دیابت نوع 2
Background and purpose: The E23K polymorphism of ATP-sensitive potassium channel kcnj11 gene leads to the conversion of glutamate to lysine amino acids and this substitution is associated with increased risk of several diseases such as diabetes. We aimed to examine the association between kcnj11 E23K variation and risk of type 2 diabetes mellitus (T2DM) in a Kurdish population. Materials and m...
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تاریخ انتشار 2015