Genetic Features of Chinese Patients with Gitelman Syndrome: Sixteen Novel SLC12A3 Mutations Identified in a New Cohort

• Published in: American journal of nephrology Vol. 44; no. 2; p. 113
• Main Authors: Ma, Jun, Ren, Hong, Lin, Li, Zhang, Chunli, Wang, Zhaohui, Xie, Jingyuan, Shen, Ping-Yan, Zhang, Wen, Wang, Weiming, Chen, Xiao-Nong, Chen, Nan
• Format: Journal Article
• Language: English
• Published: Switzerland 01.09.2016
• Subjects: Adolescent; Adult; Alleles; Asian Continental Ancestry Group - genetics; China; Chloride Channels - genetics; Cohort Studies; Exons - genetics; Female; Genetic Testing; Genotype; Gitelman Syndrome - genetics; Humans; Male; Mutation; Phenotype; Sequence Analysis, DNA; Solute Carrier Family 12, Member 3 - genetics; Young Adult
• ISSN: 1421-9670
• DOI: 10.1159/000447366

Gitelman syndrome (GS) is an autosomal recessive renal tubulopathy caused by inactivating mutations in the SLC12A3 gene. Although hundreds of different mutations across the SLC12A3 gene have been reported worldwide, data from mainland China are limited. We investigated the clinical manifestations and genetic features of Chinese patients with GS. Fifty-four unrelated Chinese patients with clinically diagnosed GS were included. Clinical manifestations and biochemical parameters were collected and analyzed. All exons and flanking regions of the SLC12A3 and CLCNKB genes were screened by direct sequencing. Weakness was the most commonly reported symptom in this cohort of patients with GS. In gender-based analyses, higher systolic blood pressure and urine protein excretion were observed in male patients. For genetic screening, 2 pathogenic SLC12A3 mutations were identified in 38 patients (70.4%), 1 mutation in 11 patients (20.4%) and no mutation in 5 patients (9.3%). In total, 42 distinct pathogenic mutations throughout SLC12A3 were identified; 16 were novel, including 9 missense, 1 deletion, 1 insertion, 3 splice site and 2 nonsense mutations. Eleven mutations were recurrently found in different patients. Among them, T60M and D486N were identified in 11 individuals. No CLCNKB mutations were found. Sixteen novel SLC12A3 pathogenic mutations were identified in a cohort of Chinese patients with GS. T60M and D486N were most frequent and appear to be important candidate alleles in Chinese patients with GS.