Department of Internal Medicine, Cheil General Hospital, Kwandong University College of Medicine, Seoul, Korea.
J Korean Med Sci. 2013 Oct;28(10):1489-95. doi: 10.3346/jkms.2013.28.10.1489. Epub 2013 Sep 25.
Isolated hypoparathyroidism (IH) shows heterogeneous phenotypes and can be caused by defects in a variety of genes. The goal of our study was to determine the clinical features and to analyze gene mutations in a large cohort of Korean patients with sporadic or familial IH. We recruited 23 patients. They showed a broad range of onset age and various values of biochemical data. Whole exome sequencing was performed on two affected cases and one unaffected individual in a family. All coding exons and exon-intron borders of GCMB, CASR, and prepro-PTH were sequenced using PCR-amplified DNA. In one family who underwent the whole exome sequencing analysis, approximately 300 single nucleotide changes emerged as candidates for genetic alteration. Among them, we identified a functional mutation in exon 2 of GCMB (C106R) in two affected cases. Besides, heterozygous gain-of-function mutations in the CASR gene were found in other subjects; D410E and P221L. We also found one single nucleotide polymorphism (SNP) in the prepro-PTH gene, five SNPs in the CASR gene, and four SNPs in the GCMB gene. The current study represents a variety of biochemical phenotypes in IH patients with the molecular genetic diagnosis of IH.
孤立性甲状旁腺功能减退症 (IH) 表现出异质性表型,可由多种基因缺陷引起。我们的研究目的是确定大韩民国散发或家族性 IH 患者的临床特征,并分析其基因突变。我们共招募了 23 名患者。他们的发病年龄跨度较大,且各种生化数据值也各不相同。对两例受影响的病例和一例家族中的未受影响个体进行了全外显子组测序。使用 PCR 扩增的 DNA 对 GCMB、CASR 和 prepro-PTH 的所有编码外显子和外显子-内含子边界进行了测序。在进行全外显子组测序分析的一个家族中,大约有 300 个单核苷酸变化被认为是遗传改变的候选者。其中,我们在两个受影响的病例中发现了 GCMB 基因 (C106R) 外显子 2 中的功能突变。此外,还在其他受检者中发现了 CASR 基因的杂合性获得性功能突变,即 D410E 和 P221L。我们还在 prepro-PTH 基因中发现了一个单核苷酸多态性 (SNP),在 CASR 基因中发现了五个 SNPs,在 GCMB 基因中发现了四个 SNPs。本研究代表了 IH 患者的多种生化表型,并对 IH 进行了分子遗传学诊断。