Center for Experimental Medicine, The Third Xiangya Hospital, Central South University, Changsha, China.
Department of Clinical Laboratory, the Third Xiangya Hospital, Central South University, Changsha, China.
Curr Mol Med. 2019;19(10):758-765. doi: 10.2174/1566524019666190906144214.
Alport syndrome (AS) is an inherited familial nephropathy, characterized by progressive hematuric nephritis, bilateral sensorineural hypoacusis and ocular abnormalities. X-linked AS (XLAS) is the major AS form and is clinically heterogeneous, and it is associated with defects in the collagen type IV alpha 5 chain gene (COL4A5).
The purpose of this research is to detect the genetic defect responsible for renal disorder in a 3-generation Han-Chinese pedigree.
Detailed family history and clinical data of the family members were collected and recorded. Whole exome sequencing (WES) was applied in the proband to screen potential genetic variants, and then Sanger sequencing was used to verify the variant within the family. Two hundred unrelated ethnically matched normal individuals (male/female: 100/100, age 37.5 ± 5.5 years) without renal disorder were recruited as controls.
Three patients (I:1, II:1 and II:2) presented microscopic hematuria and proteinuria, and the patient I:1 developed uremia and end stage renal disease (ESRD) by age 55 and showed sensorineural hearing loss. Patient II:2 developed mild left ear hearing loss. Cataracts were present in patients I:1 and II:1. A COL4A5 gene missense variant, c.2156G>A (p.G719E), located in the Gly-X-Y repeats of exon 28, was identified to co-segregate with the renal disorder in this family. The variant was absent in 200 ethnically matched controls.
By conducting WES and Sanger sequencing, a COL4A5 missense variant, c.2156G>A (p.G719E), was identified to co-segregate with the renal disorder, and it is possible that this variant is the genetic cause of the disorder in this family. Our study may extend the mutation spectrum of XLAS and may be useful for genetic counseling of this family. Further functional studies associated with genetic deficiency are warranted in the following research.
Alport 综合征(AS)是一种遗传性家族性肾病,其特征为进行性血尿性肾炎、双侧感觉神经性听力损失和眼部异常。X 连锁 AS(XLAS)是主要的 AS 形式,临床上表现多样,与Ⅳ型胶原α 5 链基因(COL4A5)缺陷有关。
本研究旨在检测一个三代汉族家系中导致肾脏疾病的遗传缺陷。
收集并记录家系成员的详细家族史和临床资料。对先证者进行全外显子组测序(WES)以筛选潜在的遗传变异,然后对家系内的变异进行 Sanger 测序验证。招募 200 名无肾脏疾病的、种族匹配的正常对照者(男/女:100/100,年龄 37.5±5.5 岁)。
3 名患者(I:1、II:1 和 II:2)表现为镜下血尿和蛋白尿,患者 I:1 于 55 岁时出现尿毒症和终末期肾病(ESRD),并伴有感觉神经性听力损失。患者 II:2 出现轻度左耳聋。患者 I:1 和 II:1 均有白内障。在该家系中发现 COL4A5 基因错义变异 c.2156G>A(p.G719E),位于外显子 28 的 Gly-X-Y 重复序列中,与肾脏疾病共分离。该变异在 200 名种族匹配的对照者中不存在。
通过进行 WES 和 Sanger 测序,鉴定出 COL4A5 错义变异 c.2156G>A(p.G719E)与肾脏疾病共分离,该变异可能是该家系疾病的遗传原因。本研究可能扩展了 XLAS 的突变谱,有助于该家系的遗传咨询。在后续研究中,需要进行与遗传缺陷相关的功能研究。