2011
Difference in angiotensinogen haplotype frequences between chronic heart failure and advanced atherosclerosis patients - new prognostic factor?
PÁVKOVÁ GOLDBERGOVÁ, Monika; Lenka ŠPINAROVÁ; Jindřich ŠPINAR; Jiří PAŘENICA; Lenka ŠIŠKOVÁ et al.Základní údaje
Originální název
Difference in angiotensinogen haplotype frequences between chronic heart failure and advanced atherosclerosis patients - new prognostic factor?
Autoři
PÁVKOVÁ GOLDBERGOVÁ, Monika; Lenka ŠPINAROVÁ; Jindřich ŠPINAR; Jiří PAŘENICA; Lenka ŠIŠKOVÁ; Ladislav GROCH; Jan MÁCHAL a Anna VAŠKŮ
Vydání
Physiological Research, Praha, Institute of Physiology, Academy of Sci. 2011, 0862-8408
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
Genetika a molekulární biologie
Stát vydavatele
Česká republika
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 1.555
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/11:00064823
Organizační jednotka
Lékařská fakulta
UT WoS
Klíčová slova anglicky
RAAS; heart failure; AGT
Příznaky
Mezinárodní význam
Změněno: 3. 10. 2012 13:57, Mgr. Michal Petr
Anotace
V originále
Numerous association studies have been involved in studying the angiotensinogen (AGT) variants, AGT plasma levels and relations to cardiovascular diseases, such as hypertension, myocardial infarction, coronary heart disease. To investigate a role of AGT G(-6)A and M235T genetic variants for chronic heart failure (CHF) and advanced atherosclerosis (AA), a total of 240 patients with CHF and 200 patients with AA of the Czech origin were evaluated for the study. The study shows the role of polymorphism AGT G(-6)A in genetic background among advanced atherosclerosis patients and chronic heart failure patients (Pg=0.001). This difference was observed also in comparison of AA patients with subgroup of CHF with dilated cardiomyopathy (Pg=0.02; Pa=0.009), and ischemic heart disease (Pg=0.007). The greatest difference between triple-vessel disease and chronic heart failure groups was observed in frequency of GT haplotype (P<0.001) and GGMT associated genotype (P<0.001). Retrospectively, when the subgroups of CHF were compared to AA group (AA vs. IHD with CHF - P < 0.001; and AA vs. DCM - P<0.001) we found the same trend. These results suggest AGT genetic variants as a risk factor for chronic heart failure compared to advanced atherosclerosis disease without heart failure, with a strong difference between IHD patients and chronic heart failure patients with ischemic heart disease, especially in haplotypes and associated genotypes.
Návaznosti
| NR9356, projekt VaV |
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