| Endocrine Journal | |
| Establishment of diagnosis by bisulfite-treated methylation-specific PCR method and analysis of clinical characteristics of pseudohypoparathyroidism type 1b | |
| Tomozumi Takatani1  Rieko Takatani1  Mika Ohashi1  Yoichi Kohno1  Masanori Minagawa1  Kaori Kinoshita1  | |
| [1] Department of Pediatrics, Graduate School of Medicine, Chiba University, Chiba 260-8670, Japan | |
| 关键词: Pseudohypoparathyroidism type 1b; GNAS; exon A/B; Differentially methylated region; Methylation-specific polymerase chain reaction; | |
| DOI : 10.1507/endocrj.K10E-364 | |
| 学科分类:内分泌与代谢学 | |
| 来源: Japan Endocrine Society | |
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【 摘 要 】
References(16)Cited-By(9)Pathogenesis of pseudohypoparathyroidism type 1b (PHP-1b) is related to the loss of methylation at the GNAS exon A/B region, which is combined with epigenetic defects at other differentially methylated GNAS regions in most sporadic cases.In this study, we established a method for evaluating the methylation status of a CpG island in exon A/B using a methylation-specific polymerase chain reaction (MSPCR).We designed two primer pairs specific for the methylated and unmethylated alleles and evaluated the methylation status of GNAS exon A/B in samples from PHP-1b patients and normal controls.We examined 20 Japanese patients and 20 normal controls, and one primer set was found to be appropriate for diagnosis.Furthermore, we evaluated the clinical data of patients.Weight and height of patients were not significantly different from the normal population.Short stature (adult height ≤ 2SD) was observed in one patient and short metacarpals in two.Obesity was observed in six patients, and no patient showed ectopic subcutaneous calcification.Seven patients showed subclinical hypothyroidism because of resistance to thyroid stimulating hormone, but no patient had an abnormally low free thyroxine level, and none received oral thyroid hormone replacement.For diagnosis of PHP-1b, only clinical data is not sufficient because a few PHP-1b patients show clinical features similar to PHP-1a, and hence, molecular biology techniques are required for correct diagnosis.We concluded that MSPCR is applicable for rapid molecular diagnosis of PHP-1b.
【 授权许可】
Unknown
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO201911300313250ZK.pdf | 1456KB |
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