About: A419C (E111A) polymorphism of the glyoxalase I gene and vascular complications in chronic hemodialysis patients     Goto   Sponge   NotDistinct   Permalink

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  • Advanced glycation end products (AGEs) take part in the pathogenesis of vascular, diabetic, and uremic complications. Their precursors are detoxified by the glyoxalase system. Our aim was to study A419C (E111A) single nucleotide polymorphism (SNP) of the glyoxalase I gene in hemodialysis (HD) patients. A419C SNP, several laboratory parameters including soluble receptor for AGEs (sRAGE), and clinical data were studied in 214 HD patients and 89 controls. Allelic and genotypic frequencies did not differ between HD patients and controls. A419C SNP was significantly linked with serum sRAGE, which sensitively reflects the AGE burden of the organism (3986 +/- 1638 pg/mL in the CC variant versus 3277 +/- 1398 pg/mL in the AC variant and 3297 +/- 1445 pg/mL in the AA variant, P < 0.01). In the CC variant, significantly higher prevalence of cardiovascular disease and peripheral vascular disease was found, while the prevalence of hypertension, diabetes mellitus, and dyslipidemia did not differ between genotyp
  • Advanced glycation end products (AGEs) take part in the pathogenesis of vascular, diabetic, and uremic complications. Their precursors are detoxified by the glyoxalase system. Our aim was to study A419C (E111A) single nucleotide polymorphism (SNP) of the glyoxalase I gene in hemodialysis (HD) patients. A419C SNP, several laboratory parameters including soluble receptor for AGEs (sRAGE), and clinical data were studied in 214 HD patients and 89 controls. Allelic and genotypic frequencies did not differ between HD patients and controls. A419C SNP was significantly linked with serum sRAGE, which sensitively reflects the AGE burden of the organism (3986 +/- 1638 pg/mL in the CC variant versus 3277 +/- 1398 pg/mL in the AC variant and 3297 +/- 1445 pg/mL in the AA variant, P < 0.01). In the CC variant, significantly higher prevalence of cardiovascular disease and peripheral vascular disease was found, while the prevalence of hypertension, diabetes mellitus, and dyslipidemia did not differ between genotyp (en)
Title
  • A419C (E111A) polymorphism of the glyoxalase I gene and vascular complications in chronic hemodialysis patients
  • A419C (E111A) polymorphism of the glyoxalase I gene and vascular complications in chronic hemodialysis patients (en)
skos:prefLabel
  • A419C (E111A) polymorphism of the glyoxalase I gene and vascular complications in chronic hemodialysis patients
  • A419C (E111A) polymorphism of the glyoxalase I gene and vascular complications in chronic hemodialysis patients (en)
skos:notation
  • RIV/60461373:22340/08:00021382!RIV10-MSM-22340___
http://linked.open...avai/riv/aktivita
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  • S, Z(MSM0021620807)
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  • 1126
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  • 357519
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  • RIV/60461373:22340/08:00021382
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  • advanced glycation end products; cardiovascular; glyoxalase; hemodialysis; polymorphisms; sRAGE (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [9BE5141AE7A5]
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  • ANNALS OF THE NEW YORK ACADEMY OF SCIENCES
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  • Jáchymová, Marie
  • Mestek, Oto
  • Zima, Tomáš
  • Kalousova, Marta
  • Germanova, Alexandra
  • Tesák, Vladimír
http://linked.open...ain/vavai/riv/wos
  • 000255833300053
http://linked.open...n/vavai/riv/zamer
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  • 0077-8923
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  • 22340
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