2013
Association of genetic variability in selected regions in visfatin (NAMPT) gene with anthropometric parameters and dietary composition in obese and non-obese Central-European population
ŠŤASTNÝ, Jiří, Julie BIENERTOVÁ VAŠKŮ, Josef TOMANDL, Marie TOMANDLOVÁ, Filip ZLÁMAL et. al.Základní údaje
Originální název
Association of genetic variability in selected regions in visfatin (NAMPT) gene with anthropometric parameters and dietary composition in obese and non-obese Central-European population
Autoři
ŠŤASTNÝ, Jiří (203 Česká republika, domácí), Julie BIENERTOVÁ VAŠKŮ (203 Česká republika, garant, domácí), Josef TOMANDL (203 Česká republika, domácí), Marie TOMANDLOVÁ (203 Česká republika, domácí), Filip ZLÁMAL (203 Česká republika, domácí), Martin FOREJT (203 Česká republika, domácí), Zbyněk ŠPLÍCHAL (203 Česká republika, domácí) a Anna VAŠKŮ (203 Česká republika, domácí)
Vydání
Diabetes & metabolic syndrome, Amsterdam, Elsevier, 2013, 1871-4021
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30105 Physiology
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14110/13:00069379
Organizační jednotka
Lékařská fakulta
UT WoS
000215391200009
Klíčová slova anglicky
Anthropometric parameters; Dietary composition; Extreme obesity; NAMPT; SNP; Visfatin
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 23. 11. 2013 22:06, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Aims Visfatin (NAMPT/PBEF) is a recently identified adipocytokine which harbors strong insulin-mimetic activity and was reported to be associated with obesity. However, nothing is known about whether visfatin is related to specific nutritional behavior which may result in obesity development. This is the first study focusing on genetic variability of the visfatin gene and its association with circulating visfatin, anthropometric parameters and dietary composition. Materials and Methods We analyzed a total of 11 exons and adjacent non-coding regions of the NAMPT gene in 20 extremely obese Czech individuals (mean BMI 52.2 +/- 5.0 SD) using direct sequencing and a frequency of rs2302559 was established in the validation cohort of another 605 individuals with completed 7-day food records and complex anthropometric measurements. Serum levels of visfatin, leptin and leptin-receptor were measured in all sequenced individuals and in part of the validation cohort. Results Three common polymorphisms were identified, two in non-coding regions (rs78411774 A/C, rs71564769 A/C) and one synonymous SNP in exon 7 (rs2302559 A/G). The rs2302559 showed significant correlation with visfatin serum level throughout the entire study cohort (p < 0.001); there was a significant tendency toward higher visfatin levels in G allele carriers with GG homozygotes having the highest visfatin serum levels. Furthermore, a negative correlation was observed between visfatin and leptin serum level (p = 0.01). No association between investigated SNPs and anthropometric parameters or native dietary composition was observed. Conclusion This is the first study to demonstrate that the rs2302559 polymorphism in the PBEF gene is related to circulating levels of visfatin. As the SNP is synonymous, we hypothesize it might be linked to another SNP in the PBEF gene which controls visfatin serum levels.