首页> 美国卫生研究院文献>Disease Markers >TH01 a Tetrameric Short Tandem Repeat Locus in the Tyrosine Hydroxylase Gene: Association with Myocardial Hypertrophy and Death from Myocardial Infarction?
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TH01 a Tetrameric Short Tandem Repeat Locus in the Tyrosine Hydroxylase Gene: Association with Myocardial Hypertrophy and Death from Myocardial Infarction?

机译:TH01酪氨酸羟化酶基因中的四聚体短串联重复序列:与心肌肥大和心肌梗死死亡相关?

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摘要

TH01 is a tetrameric short tandem repeat locus located in intron 01 of the tyrosine hydroxylase gene. The tyrosine hydroxylase catalyzes the hydroxylation of L-tyrosine to L-DOPA and is the rate limiting enzyme in the synthesis of catecholamines like noradrenaline or adrenaline, which are pivotal in the regulation of blood pressure. In a clinical study a strong correlation between alleles *9.3 and *10 and essential hypertension was observed ([2] Hypertension 32: 676–682). To further investigate this association, we typed TH01 in 296 autopsy cases and correlated the genotypes to the heart weight as parameter for myocardial hypertrophy. No significant correlation was observed. Moreover, dividing the studied cases into 2 groups, one including 172 casualties from hypertension-associated diseases (myocardial infarction, left heart failure, aortic aneurysm, spontaneous intracerebral bleeding and cerebral infarction) and one consisting of 124 cases of death unrelated to hypertension, revealed similar allelic frequencies for both groups. Our data thus suggest that TH01 long alleles appear not to lead to a significant increase in the incidence of myocardial hypertrophy or other hypertension associated diseases. This could be explained by a relatively small impact of the TH01 genotype on the blood pressure or by counteraction of another mechanism related to catecholamines and their effect on the human body.
机译:TH01是位于酪氨酸羟化酶基因内含子01上的四聚体短串联重复序列基因座。酪氨酸羟化酶催化L-酪氨酸羟化为L-DOPA,是儿茶酚胺如去甲肾上腺素或肾上腺素的合成中的限速酶,它们在调节血压中起关键作用。在一项临床研究中,观察到等位基因* 9.3和* 10与原发性高血压之间有很强的相关性([2]高血压32:676–682)。为了进一步研究这种关联,我们在296例尸检病例中输入了TH01,并将基因型与心脏重量相关联,作为心肌肥大的参数。没有观察到明显的相关性。此外,将研究病例分为两组,一组包括172例高血压相关疾病(心肌梗塞,左心衰竭,主动脉瘤,自发性脑出血和脑梗塞)造成的伤亡,另一组包括124例与高血压无关的死亡病例两组的等位基因频率相似。因此,我们的数据表明,TH01长等位基因似乎并未导致心肌肥大或其他高血压相关疾病的发生率显着增加。 TH01基因型对血压的影响相对较小,或与儿茶酚胺有关的另一种机制及其对人体的影响,可以解释这一点。

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