2003
Association of Two Angiotensinogen Gene Polymorphisms (M235T and G(-6)A) with Chronic Heart Failure
GOLDBERGOVÁ, Monika, Lenka ŠPINAROVÁ, Jindřich ŠPINAR, Jiří TOMAN, Anna VAŠKŮ et. al.Základní údaje
Originální název
Association of Two Angiotensinogen Gene Polymorphisms (M235T and G(-6)A) with Chronic Heart Failure
Autoři
GOLDBERGOVÁ, Monika (203 Česká republika, garant), Lenka ŠPINAROVÁ (203 Česká republika), Jindřich ŠPINAR (203 Česká republika), Jiří TOMAN (203 Česká republika), Anna VAŠKŮ (203 Česká republika) a Jiří VÁCHA (203 Česká republika)
Vydání
International Journal of Cardiology, Ireland, Elsevier, 2003, 0167-5273
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30201 Cardiac and Cardiovascular systems
Stát vydavatele
Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.892
Kód RIV
RIV/00216224:14110/03:00008558
Organizační jednotka
Lékařská fakulta
UT WoS
000183429100018
Klíčová slova anglicky
Chronic heart failure; angiotensinogene gene; polymorphism
Změněno: 22. 6. 2009 10:32, prof. RNDr. Monika Pávková Goldbergová, Ph.D.
Anotace
V originále
The aim of the study was to focus on relationship between the angiotensinogen (AGT) gene polymorphisms, M235T and promoter G(-6)A, and chronic heart failure in the Czech population. 158 patients with chronic heart failure (functional class NYHA II-IV, ejection fraction <40% cardiothoracic index >50%) were compared with control group of 200 subjects of similar age and sex distribution, without any personal history of cardiovascular diseases. The AGT gene polymorphisms were detected by polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP) methods. No significant differences in distributions of AGT genotypes between patients with chronic heart failure (CHF) and controls were found. The differences in distributions of alleles in AGT M235T (Pa=0.02) and genotypes in AGT G(-6)A (Pg=0.017) were found within women groups. Within CHF patients the distribution of AGT G(-6)A genotypes was not consistent with Hardy-Weinberg equilibrium (P=0.0001). We found significant relative risk of CHF for GGMT genotype, OR=2.63 with 95% CI 1.39-4.95, Pcorr=0.01 (in man group OR=1.83, 95% CI 0.92-3.66, Pcorr=0.3; in woman group OR=15.5, 95% CI 1.86-129.42, Pcorr=0.008). We provide evidence of increased risk in subjects with GGMT variant of associated genotype of AGT gene for CHF, especially of fifteen-fold risk of this variant in women.
Návaznosti
MSM 141100002, záměr |
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