2001
Polymorphisms in angiotensinogen gene (M235T and G/-6/A) in multifactorial diseases.
VAŠKŮ, Anna, Lydie IZAKOVIČOVÁ HOLLÁ, Vladimír VAŠKŮ, Svatava TSCHÖPLOVÁ, Andrea STEJSKALOVÁ et. al.Základní údaje
Originální název
Polymorphisms in angiotensinogen gene (M235T and G/-6/A) in multifactorial diseases.
Autoři
VAŠKŮ, Anna (203 Česká republika, garant), Lydie IZAKOVIČOVÁ HOLLÁ (203 Česká republika), Vladimír VAŠKŮ (203 Česká republika), Svatava TSCHÖPLOVÁ (203 Česká republika) a Andrea STEJSKALOVÁ (203 Česká republika)
Vydání
Pathophysiology, Amsterdam (Netherlande), Elsevier, 2001, 0928-4680
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Kód RIV
RIV/00216224:14110/01:00005187
Organizační jednotka
Lékařská fakulta
Změněno: 24. 4. 2003 10:13, prof. MUDr. Anna Vašků, CSc.
Anotace
V originále
The aim of the study is to compare results of three association (case-control) studies in three multifactorial disorders (essential hypertension, atopic diseases and psoriasis) with two polymorphisms of angiotensinogen gene (M235T and A(-6)G AGT). The diseases were chosen for their multigenic base and different immunological characteristic (Th1, Th2 and Thps) and angiotensinogen gene for its pleiotropic functional effects in general adaptive reactions. In all (control as well as case) groups, tight linkage disequilibrium between the polymorphisms was found. The strength of linkage (%) differed among the group. The direction of the linkage is identical in all groups (T is combined with A, M is combined with G). In hypertensive-normotensive study, only Hardy-Weinberg disequilibria were found, especially in men. No case-control differences were found for either single alleles or for allelic concurrence of both polymorphisms. In atopy-control study, marginal case-control differences in single allele distribution of both polymorphisms were found, but only in women. In psoriasis-control study, the only significant case-control difference was found when genotypes MTAA and MTGG were present in 2/136 psoriatic patients vs. 20/142 control subjects (OR 0.1, 95% confidence interval 0.02-0.42, P=0.00015). The frequent polymorphisms in pleiotropic genes can form different formulae of genotype distribution in different multigenic diseases according to their contribution to the onset and/or progression of the disease in some evolutionary consequences.
Návaznosti
GA306/93/2192, projekt VaV |
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GA306/96/0099, projekt VaV |
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MSM 141100002, záměr |
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