原发性高血压年轻患者4个候补基因的多态性

来源 :世界核心医学期刊文摘(儿科学分册) | 被引量 : 0次 | 上传用户:fanny_lizzy
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Aim:To determine whether four potential genetic factors(polymorphisms in genes for alpha-adducin,beta-adducin,the G-protein beta-3 subunit and nitric oxide synthase)are important for the development of essential hypertension(EH)in Slovenian children and young adults with EH.Methods:Both a nuclear families approach and case-control study have been performed.Genotyping of common polymorphisms in these genes using polymerase chain reaction was carried out in 104 nuclear families(an affected child,both parents)and in 200 control patients.Results:Using the transmission disequilibrium test,no statistically significant differences were found between the frequencies of transmitted and non-transmitted alleles in nuclear families for all four investigated polymorphisms.In addition,the distributions of genotypes and alleles for the four polymorphisms did not differ significantly between our children and 200 healthy control patients.The allele frequencies of all polymorphisms were concordant with those observed in some other Caucasian populations.Conclusion:We found no association between the investigated gene variants and EH,so we conclude that they do not confer a significantly increased risk of the development of EH in the Slovenian population of hypertensive children. Aim: To determine whether four potential genetic factors (polymorphisms in genes for alpha-adducin, beta-adducin, the G-protein beta-3 subunit and nitric oxide synthase) are important for the development of essential hypertension (EH) in Slovenian children and young adults with EH. Methods: Both a nuclear families approach and case-control study have been performed. Genotyping of common polymorphisms in these genes using polymerase chain reaction was carried out in 104 nuclear families (an affected child, both parents) and in 200 control patients. Results: Using the transmission disequilibrium test, no significant significant differences found found between the frequencies of transmitted and non-transmitted alleles in nuclear families for all four investigated polymorphisms. In addition, the distributions of genotypes and alleles for the four polymorphisms did not differ significantly between our children and 200 healthy control patients.The allele frequencies of all polymorphisms were concordant with those observed in some other Caucasian populations. Confluence: We found no association between the alleged gene variants and EH, so we conclude that they do not confer a significantly increased risk of the development of EH in the Slovenian population of hypertensive children.
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