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Genetic Determination of the Basic Clinical Components of the Metabolic Syndrome

机译:代谢综合征基本临床组成的遗传测定

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The genetic determination of components of the metabolic syndrome has been studied based on materials including clinical and genealogical data on 510 patients with type 2 diabetes mellitus, 445 individuals with essential hypertension, and 239 abdominal obesity patients and their first-degree relatives. The results of the component analysis revealed the significance of genetic factors in determining the diseases under study and allowed us to conjecture that there exists an interlocus interaction in their genetic control system. Testing Ch. Smith's model revealed the genetic independence of the above conditions and allowed us to determine the coefficient of genetic relatedness of the pathologies under study.
机译:基于包括510例2型糖尿病患者,445例原发性高血压患者和239例腹部肥胖患者及其一级亲属的临床和家谱数据,研究了代谢综合征成分的遗传测定。成分分析的结果揭示了遗传因素在确定所研究疾病中的重要性,并让我们推测其遗传控制系统中存在中间位相互作用。测试通道史密斯的模型揭示了上述条件的遗传独立性,并使我们能够确定所研究病理的遗传相关系数。

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  • 来源
    《Cytology and genetics》 |2010年第1期|P.46-51|共6页
  • 作者单位

    Danilevskii Institute of Endocrine Pathology Problems, Ukraine Academy of Medical Sciences, Kharkov, Ukraine;

    rnRadiation Medicine Center, Ukraine Academy of Medical Sciences, Kiev, Ukraine;

    rnDanilevskii Institute of Endocrine Pathology Problems, Ukraine Academy of Medical Sciences, Kharkov, Ukraine;

    rnMalaya Institute of Therapy, Ukraine Academy of Medical Sciences, Kharkov, Ukraine;

    rnMalaya Institute of Therapy, Ukraine Academy of Medical Sciences, Kharkov, Ukraine;

    rnDanilevskii Institute of Endocrine Pathology Problems, Ukraine Academy of Medical Sciences, Kharkov, Ukraine;

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