Chen X, Liu S, Ye Y, Xu Q
Department of Nephrology, General Hospital of Chinese PLA, Military Kidney Center, Beijing, China.
Chin Med J (Engl). 1997 Jul;110(7):526-9.
To investigate the relationship between angiotensin-converting enzyme (ACE) gene insertion/deletion polymorphism and the clinico-pathological manifestations in patients with immunoglobulin nephropathy (IgAN).
A flanking primer pair and an insertion-specific primer pair were used to perform two polymerase chain reactions so as to analyse the insertion/deletion polymorphism of ACE gene.
There was a significantly higher genotype frequency for DD genotype in IgAN patients. The frequencies for DD genotype were also higher in those patients with hypertension and/or heavy proteinuria and/or severe glomerular sclerosis (P < 0.05).
We observed a significant association of the deletion polymorphism of ACE gene with renal insufficiency, hypertension and severe glomerular lesions at biopsy. The deletion allele may play a role, at least to some extent, in the deterioration and progression in IgA nephropathy.
探讨血管紧张素转换酶(ACE)基因插入/缺失多态性与免疫球蛋白肾病(IgAN)患者临床病理表现之间的关系。
使用一对侧翼引物和一对插入特异性引物进行两次聚合酶链反应,以分析ACE基因的插入/缺失多态性。
IgAN患者中DD基因型的基因型频率显著更高。高血压和/或大量蛋白尿和/或严重肾小球硬化的患者中DD基因型频率也更高(P<0.05)。
我们观察到ACE基因的缺失多态性与活检时的肾功能不全、高血压和严重肾小球病变显著相关。缺失等位基因可能至少在一定程度上在IgA肾病的恶化和进展中起作用。