Failure of tooth eruption and brachydactyly in pseudohypoparathyroidism are not related to plasma parathyroid hormone-related protein levels

被引:16
作者
Antunes Reis, Mariana Tenorio [1 ]
Matias, Diogo Toledo [2 ]
Justamante de Faria, Maria Estela [2 ]
Martin, Regina Matsunaga [1 ]
机构
[1] Univ Sao Paulo, Hosp Clin, Dept Endocrinol, Osteometab Disorders Unit,Hormone & Mol Genet Lab, Ave Dr Eneas de Carvalho Aguiar 155, BR-05403900 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Hosp Clin, Dent Div, Ave Dr Eneas de Carvalho Aguiar,155,PAMB,6 Andar, BR-05403900 Sao Paulo, SP, Brazil
关键词
Pseudohypoparathyroidism; Failure of tooth eruption; Brachydactyly; Parathyroid hormone related protein (PTHrP); MUTATIONS; CYTOKINE;
D O I
10.1016/j.bone.2016.02.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Pseudohypoparathyroidism (PHP) is a genetic disorder characterized by resistance to the peripheral action of PTH due to maternally inherited heterozygous inactivating mutations in the coding sequence of G(s)alpha or intronic regions of GNAS leading to aberrant splice variants (PHP1A), or methylation defects at GNAS (PHP1B). Brachydactyly is a clinical feature associated with both PHP1A and PHP1B, although it is more frequent in PHP1A patients. Loss-of-function mutations in PTHLH, the gene coding for parathyroid hormone related protein (PTHrP) were previously described in some patients with brachydactyly. Primary failure of tooth eruption (PFE) is related to some syndromes involving skeletal development, but it is also known as a nonsyndromic autosomal dominant condition. Previous studies showed that familial nonsyndromic PFE is caused by heterozygous mutations in the gene encoding the G protein-coupled receptor (PTH1R) for PTH and PTHrP. Thus, we hypothesized that PTHrP resistance could result in failure of tooth eruption (FTE) and/or brachydactyly in PHP. Subjects and methods: Nineteen patients with a molecular diagnosis of PHP underwent dental panoramic radiography (DPR), hand radiography and had their PTHrP levels measured. Patients with alterations at DPR were submitted to clinical dental evaluation. Results: Nine patients had FTE and 7 patients had brachydactyly; 4 patients presented both features and none of them presented high PTHrP levels. Fourteen patients had PTHrP levels within the normal range and only one patient had slightly elevated PTHrP levels. Additionally, three novel GNAS mutations were described. Conclusion: We described the dental abnormalities in a large series of PHP patients that were followed in a single tertiary center. No relationship between plasma PTHrP levels and failure of tooth eruption, dental manifestations of PHP or brachydactyly was found. It is important that doctors pay attention to dental manifestations of the disease in order to refer patients to a proper care with dentists. (C) 2016 Elsevier Inc All rights reserved.
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收藏
页码:138 / 141
页数:4
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