Néphrologie pédiatrique, Centre de Référence maladies rénales rares SORARE, CHU Arnaud de Villeneuve, Montpellier, France.
APHP, Génétique moléculaire, Centre de Référence MARHEA, Hôpital Universitaire Necker-Enfants malades, Paris, France.
Pediatr Nephrol. 2020 Jun;35(6):1125-1128. doi: 10.1007/s00467-020-04524-4. Epub 2020 Mar 20.
Bi-allelic loss of function variations in genes encoding proteins of the renin-angiotensin system (AGT, ACE, REN, AGTR1) are associated with autosomal recessive renal tubular dysgenesis, a severe disease characterized by the absence of differentiated proximal tubules leading to fetal anuria and neonatal end-stage renal disease.
CASE-DIAGNOSIS/TREATMENT: We identified bi-allelic loss of function mutations in ACE, the gene encoding angiotensin-converting enzyme, in 3 unrelated cases displaying progressive chronic renal failure, whose DNAs had been sent for suspicion of juvenile hyperuricemic nephropathy, nephronophthisis, and cystic renal disease, respectively. In all cases, patients were affected with anemia whose severity was unexpected regarding the level of renal failure and with important polyuro-polydipsia.
Bi-allelic loss of function mutation of ACE can have atypical and sometimes late presentation with chronic renal failure, anemia (out of proportion with the level of renal failure), and polyuro-polydipsia. These data illustrate the usefulness of next generation sequencing and "agnostic" approaches to elucidate cases with chronic kidney disease of unknown etiology and to broaden the spectrum of phenotypes of monogenic renal diseases. It also raises the question of genetic modifiers involved in the variation of the phenotypes associated with these mutations.
编码肾素-血管紧张素系统(AGT、ACE、REN、AGTR1)蛋白的基因的双等位基因功能丧失变异与常染色体隐性肾小管发育不良有关,这是一种严重的疾病,其特征是缺乏分化的近端肾小管,导致胎儿无尿和新生儿终末期肾病。
病例诊断/治疗:我们在 3 个无关联的病例中发现了编码血管紧张素转换酶的 ACE 基因的双等位基因功能丧失突变,这些病例表现出进行性慢性肾衰竭,其 DNA 分别因怀疑青少年高尿酸血症肾病、肾单位肾病变和囊性肾病而被送检。在所有病例中,患者均伴有贫血,其严重程度与肾衰竭程度不成比例,且伴有明显的多尿多饮。
ACE 的双等位基因功能丧失突变可导致慢性肾衰竭、贫血(与肾衰竭程度不成比例)和多尿多饮等非典型且有时较晚的表现。这些数据说明了下一代测序和“未知”方法在阐明原因不明的慢性肾脏病病例和拓宽单基因肾脏疾病表型谱方面的作用。这也提出了与这些突变相关的表型变化中涉及遗传修饰因子的问题。