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Insertion/deletion polymorphism and serum activity of the angiotensin-converting enzyme in Turkish patients with obstructive sleep apnea syndrome.

机译:土耳其阻塞性睡眠呼吸暂停综合征患者的插入/缺失多态性和血管紧张素转换酶的血清活性。

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摘要

This study determined the allelic frequency and genotypic distribution of an angiotensin-converting enzyme (ACE) polymorphism and serum ACE activity in Turkish patients with obstructive sleep apnea syndrome (OSAS). A colorimetric assay measured serum ACE activity in 73 of 97 subjects. Frequencies for II, ID, and DD genotypes were 19.6, 53.6, and 26.8% in the OSAS group and 15, 38, and 47% in the control group, respectively (P = 0.02). The I allele frequency was higher in the OSAS group than in the healthy control group (P = 0.02). Carrying the I allele (II or ID genotypes) increased OSAS risk 2.41 times in the Turkish population. Mean ACE activity was significantly lower in patients with the II genotype than in the DD genotype (P = 0.011), and ACE activity was significantly lower in patients with severe OSAS than in those with mild OSAS (P = 0.006). Our results suggest that II and ID genotypes of the ACE gene increase the risk of developing OSAS in the Turkish population.
机译:这项研究确定了土耳其阻塞性睡眠呼吸暂停综合症(OSAS)患者的血管紧张素转换酶(ACE)多态性的等位基因频率和基因型分布以及血清ACE活性。比色测定法在97位受试者中的73位测量了血清ACE活性。 II,ID和DD基因型的频率在OSAS组中分别为19.6、53.6和26.8%,在对照组中分别为15、38和47%(P = 0.02)。 OSAS组的I等位基因频率高于健康对照组(P = 0.02)。在土耳其人口中携带I等位基因(II或ID基因型)的OSAS风险增加了2.41倍。 II基因型患者的平均ACE活性显着低于DD基因型(P = 0.011),重度OSAS的患者的ACE活性显着低于轻度OSAS的患者(P = 0.006)。我们的结果表明,ACE基因的II和ID基因型增加了土耳其人群发生OSAS的风险。

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