The FTO gene polymorphism is associated with end-stage renal disease: two large independent case-control studies in general population
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023001%3A_____%2F12%3A00056415" target="_blank" >RIV/00023001:_____/12:00056415 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/75010330:_____/12:00009878
Výsledek na webu
<a href="http://ndt.oxfordjournals.org/content/27/3/1030.full" target="_blank" >http://ndt.oxfordjournals.org/content/27/3/1030.full</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1093/ndt/gfr418" target="_blank" >10.1093/ndt/gfr418</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
The FTO gene polymorphism is associated with end-stage renal disease: two large independent case-control studies in general population
Popis výsledku v původním jazyce
Background. Genome-wide association studies identified the FTO (fat mass and obesity gene) gene as an important determinant of body weight. More recently, the FTO gene was reported to be associated with other outcomes, including major risk factors for chronic kidney disease (CKD). We investigated the role of this gene in the risk of end-stage renal disease (ESRD) caused by CM). Methods. We conducted two large population-based case control studies of ESRD. Study 1 compared 984 haemodialysed patients withESRD with 2501 participants in the Czech post-MONICA study; Study 2 compared 1188 patients included in a kidney transplantation programme for ESRD with 6681 participants in the Czech HAPIEE study. The frequencies of the FTO rs17817449 single nucleotidepolymorphism genotype were compared between cases and controls. Results. The FTO rs17817449 genotype was significantly associated with CKD in both studies (P-values 0.00004 and 0.006, respectively). In the pooled data, the odds ratios of
Název v anglickém jazyce
The FTO gene polymorphism is associated with end-stage renal disease: two large independent case-control studies in general population
Popis výsledku anglicky
Background. Genome-wide association studies identified the FTO (fat mass and obesity gene) gene as an important determinant of body weight. More recently, the FTO gene was reported to be associated with other outcomes, including major risk factors for chronic kidney disease (CKD). We investigated the role of this gene in the risk of end-stage renal disease (ESRD) caused by CM). Methods. We conducted two large population-based case control studies of ESRD. Study 1 compared 984 haemodialysed patients withESRD with 2501 participants in the Czech post-MONICA study; Study 2 compared 1188 patients included in a kidney transplantation programme for ESRD with 6681 participants in the Czech HAPIEE study. The frequencies of the FTO rs17817449 single nucleotidepolymorphism genotype were compared between cases and controls. Results. The FTO rs17817449 genotype was significantly associated with CKD in both studies (P-values 0.00004 and 0.006, respectively). In the pooled data, the odds ratios of
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
EB - Genetika a molekulární biologie
OECD FORD obor
—
Návaznosti výsledku
Projekt
<a href="/cs/project/NR7958" target="_blank" >NR7958: Genetická podstata komplikace hemodialyzační léčby - syndromu MIA (Malnutrition-Inflammation-Atherosclerosis)</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2012
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Nephrology Dialysis Transplantation
ISSN
0931-0509
e-ISSN
—
Svazek periodika
27
Číslo periodika v rámci svazku
3
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
6
Strana od-do
1030-1035
Kód UT WoS článku
000301907200028
EID výsledku v databázi Scopus
—