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ACE Gene Polymorphism and Disease Progression of IgA Nephropathy in Asians in Singapore.

机译:新加坡亚洲人ACE基因多态性与IgA肾病疾病进展。

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The deletion polymorphism of the angiotensin-converting enzyme (ACE) gene has been considered as a risk factor for IgA nephropathy and for its progression to end-stage renal failure. However, results from various studies are conflicting. We had genotyped the ACE gene in 100 patients with IgA nephropathy, 32 of whom were in end-stage renal failure and in 90 normal adult subjects. All DD cases were subjected to confirmation with a second PCR, performed with the insert-specific forward primer. Similar genotype frequencies were obtained for the 90 normal control subjects (II: 47%, ID: 44%, DD: 9%); for the 68 patients not in end-stage renal failure (ESRF) (II: 47%, ID: 46%, DD: 7%) and for the 32 patients with ESRF (II: 53%, ID: 38%, DD: 9%). The genotype frequencies in all 3 series are in Hardy-Weinberg equilibrium. These results suggest that ACE gene polymorphism is not a risk factor for IgA nephropathy and is not a predictor for its progression. Definitive proof of association between ACE gene polymorphism and progression in IgA nephropathy will require a prospective study, controlled for important risk factors, with adequate patient numbers and facility for confirming DD genotypes.
机译:血管紧张素转换酶(ACE)基因的缺失多态性已被认为是IgA肾病及其进展为终末期肾衰竭的危险因素。但是,各种研究的结果相互矛盾。我们对100例IgA肾病患者中的ACE基因进行了基因分型,其中32例处于终末期肾衰竭,并在90例正常成人受试者中进行了基因分型。所有DD病例均接受第二次PCR确认,该第二次PCR使用插入特异性正向引物进行。对于90名正常对照受试者,获得了相似的基因型频率(II:47%,ID:44%,DD:9%);对于没有终末期肾衰竭(ESRF)的68例患者(II:47%,ID:46%,DD:7%)和32例ESRF的患者(II:53%,ID:38%,DD: 9%)。所有3个系列的基因型频率均处于Hardy-Weinberg平衡状态。这些结果表明,ACE基因多态性不是IgA肾病的危险因素,也不是其进展的预测因子。 ACE基因多态性与IgA肾病进展之间相关性的确凿证据将需要进行前瞻性研究,控制重要的危险因素,并有足够的患者人数和设施来证实DD基因型。

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