Nephrology Department, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Radiology Department, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Clin Exp Nephrol. 2019 Jun;23(6):792-798. doi: 10.1007/s10157-019-01704-x. Epub 2019 Feb 8.
We aimed to investigate the clinical characteristics of Chinese patients with unilateral renal agenesis.
We enrolled patients with unilateral renal agenesis diagnosed radiologically at the Department of Nephrology from January 2008 to January 2016. Patients with a solitary kidney due to nephrectomy or renal atrophy due to secondary factors were excluded. Clinical data were recorded and analyzed.
In this study, 118 Chinese patients with unilateral renal agenesis were recruited, and the gender ratio (male/female) was 1.11:1. A total of 14 (11.9%) patients had additional abnormalities, 15 (12.7%) had a family history, and 30 (25.4%) presented with renal insufficiency. Kidney length, serum creatinine level and estimated glomerular filtration rate were significantly different between patients with and without family history (P < 0.05, respectively). Gender showed a significant difference between patients with and without other abnormalities. Kidney length and the incidence of proteinuria, hematuria, hypertension, and hyperuricemia were significantly different between patients with and without renal insufficiency. Logistic regression analysis revealed that family history was associated with severe renal failure (OR = 7.11, 95% CI 1.52-33.25).
Renal insufficiency is common in patients with unilateral renal agenesis. Patients with renal insufficiency have shorter kidney lengths and a higher incidence of proteinuria, hypertension, hematuria, and hyperuricemia. Family history is considered a risk factor for severe renal failure.
本研究旨在探讨单侧肾发育不全中国患者的临床特征。
我们纳入了 2008 年 1 月至 2016 年 1 月在肾脏病科经影像学诊断为单侧肾发育不全的患者。排除因肾切除或继发因素导致的孤立肾及肾萎缩患者。记录并分析患者的临床资料。
本研究共纳入 118 例单侧肾发育不全患者,男女比例为 1.11:1。共有 14 例(11.9%)患者存在其他异常,15 例(12.7%)有家族史,30 例(25.4%)存在肾功能不全。有家族史患者的肾脏长度、血肌酐水平和估算肾小球滤过率均显著小于无家族史患者(P 值均<0.05)。性别在有家族史和无家族史患者间存在显著差异。肾脏长度及蛋白尿、血尿、高血压和高尿酸血症的发生率在有和无肾功能不全患者间存在显著差异。Logistic 回归分析显示,家族史与严重肾衰竭相关(OR=7.11,95%CI 1.52-33.25)。
单侧肾发育不全患者中肾功能不全较为常见。肾功能不全患者的肾脏长度较短,蛋白尿、高血压、血尿和高尿酸血症的发生率较高。家族史被认为是严重肾衰竭的危险因素。