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假性甲状旁腺功能减退症中牙齿萌出失败和短指畸形与血浆甲状旁腺激素相关蛋白水平无关。

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

作者信息

Reis Mariana Tenorio Antunes, Matias Diogo Toledo, Faria Maria Estela Justamante de, Martin Regina Matsunaga

机构信息

Osteometabolic Disorders Unit, Hormone and Molecular Genetics Laboratory (LIM-42), Endocrinology Department, Hospital das Clínicas, University of São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, Prédio dos ambulatórios (PAMB), 8° andar, Bloco 3, CEP: 05403-900, São Paulo, SP, Brazil.

Dentistry Division, Hospital das Clínicas, University of São Paulo, Av. Dr. Enéas de Carvalho Aguiar, 155, PAMB, 6° andar, Bloco 2, CEP: 05403-900, São Paulo, SP, Brazil.

出版信息

Bone. 2016 Apr;85:138-41. doi: 10.1016/j.bone.2016.02.002. Epub 2016 Feb 5.

Abstract

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 Gsα 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.

摘要

背景

假性甲状旁腺功能减退症(PHP)是一种遗传性疾病,其特征是由于Gsα编码序列或GNAS内含子区域的母系遗传杂合失活突变导致异常剪接变体(PHP1A),或GNAS处的甲基化缺陷(PHP1B),从而对外周甲状旁腺激素(PTH)作用产生抵抗。短指畸形是与PHP1A和PHP1B均相关的临床特征,尽管在PHP1A患者中更为常见。甲状旁腺激素相关蛋白(PTHrP)编码基因PTHLH的功能丧失突变先前在一些短指畸形患者中已有描述。原发性牙齿萌出失败(PFE)与一些涉及骨骼发育的综合征有关,但它也被认为是一种非综合征性常染色体显性疾病。先前的研究表明,家族性非综合征性PFE是由编码PTH和PTHrP的G蛋白偶联受体(PTH1R)基因中的杂合突变引起的。因此,我们推测PTHrP抵抗可能导致PHP患者出现牙齿萌出失败(FTE)和/或短指畸形。

研究对象与方法

19例经分子诊断为PHP的患者接受了口腔全景X线摄影(DPR)、手部X线摄影,并检测了他们的PTHrP水平。DPR有异常的患者接受了临床牙科评估。

结果

9例患者出现FTE,7例患者出现短指畸形;4例患者同时出现这两种特征,且他们的PTHrP水平均未升高。14例患者的PTHrP水平在正常范围内,只有1例患者的PTHrP水平略有升高。此外,还描述了3种新的GNAS突变。

结论

我们描述了在一个单一的三级中心随访的一大系列PHP患者的牙齿异常情况。未发现血浆PTHrP水平与牙齿萌出失败、PHP的牙齿表现或短指畸形之间存在关联。医生关注该疾病的牙齿表现以便将患者转介给牙医进行适当治疗很重要。

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