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3
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4
Novel genes and variants associated with congenital pituitary hormone deficiency in the era of next-generation sequencing.与新一代测序技术相关的先天性垂体激素缺乏症的新基因和变异体。
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5
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6
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9
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垂体联合激素缺乏症的病因:GNAO1作为一个新的候选基因。

Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene.

作者信息

Plachy Lukas, Dusatkova Petra, Maratova Klara, Amaratunga Shenali Anne, Zemkova Dana, Neuman Vit, Kolouskova Stanislava, Obermannova Barbora, Snajderova Marta, Sumnik Zdenek, Lebl Jan, Pruhova Stepanka

机构信息

Department of Pediatrics, Second Faculty of Medicine, Charles University and Motol University Hospital, V Úvalu, Prague, Czech Republic.

出版信息

Endocr Connect. 2024 Aug 29;13(10). doi: 10.1530/EC-24-0217. Print 2024 Oct 1.

DOI:10.1530/EC-24-0217
PMID:39078873
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11378134/
Abstract

Because the causes of combined pituitary hormone deficiency (CPHD) are complex, the etiology of congenital CPHD remains unknown in most cases. The aim of the study was to identify the genetic etiology of CPHD in a well-defined single-center cohort. In total, 34 children (12 girls) with congenital CPHD (growth hormone (GH) deficiency and impaired secretion of at least one other pituitary hormone) treated with GH in our center were enrolled in the study. Their median age was 11.2 years, pre-treatment height was -3.2 s.d., and maximal stimulated GH was 1.4 ug/L. Of them, 30 had central adrenal insufficiency, 27 had central hypothyroidism, ten had hypogonadotropic hypogonadism, and three had central diabetes insipidus. Twenty-six children had a midline defect on MRI. Children with clinical suspicion of a specific genetic disorder underwent genetic examination of the gene(s) of interest via Sanger sequencing or array comparative genomic hybridization. Children without a detected causal variant after the first-tier testing or with no suspicion of a specific genetic disorder were subsequently examined using next-generation sequencing growth panel. Variants were evaluated by the American College of Medical Genetics standards. Genetic etiology was confirmed in 7/34 (21%) children. Chromosomal aberrations were found in one child (14q microdeletion involving the OTX2 gene). The remaining 6 children had causative genetic variants in the GLI2, PROP1, POU1F1, TBX3, PMM2, and GNAO1 genes, respectively. We elucidated the cause of CPHD in a fifth of the patients. Moreover, our study supports the PMM2 gene as a candidate gene for CPHD and suggests pathogenic variants in the GNAO1 gene as a potential novel genetic cause of CPHD.

摘要

由于垂体激素联合缺乏症(CPHD)的病因复杂,大多数情况下先天性CPHD的病因仍不清楚。本研究的目的是在一个明确的单中心队列中确定CPHD的遗传病因。本研究共纳入了34名在我们中心接受生长激素(GH)治疗的先天性CPHD儿童(12名女孩)(生长激素缺乏且至少一种其他垂体激素分泌受损)。他们的中位年龄为11.2岁,治疗前身高为-3.2标准差,最大刺激生长激素为1.4μg/L。其中,30例有中枢性肾上腺功能不全,27例有中枢性甲状腺功能减退,10例有低促性腺激素性性腺功能减退,3例有中枢性尿崩症。26名儿童在MRI上有中线缺陷。临床怀疑有特定遗传疾病的儿童通过桑格测序或阵列比较基因组杂交对感兴趣的基因进行基因检测。在一级检测后未检测到因果变异或无特定遗传疾病怀疑的儿童随后使用下一代测序生长面板进行检测。变异按照美国医学遗传学学会标准进行评估。在7/34(21%)的儿童中确定了遗传病因。在1名儿童中发现了染色体畸变(涉及OTX2基因的14q微缺失)。其余6名儿童分别在GLI2、PROP1、POU1F1、TBX3、PMM2和GNAO1基因中存在致病遗传变异。我们阐明了五分之一患者的CPHD病因。此外,我们的研究支持PMM2基因作为CPHD的候选基因,并提示GNAO1基因中的致病变异可能是CPHD的一种新的遗传病因。