NONSYNDROMIC CRANIOSYNOSTOSIS: PHENOTYPE/GENOTYPE STUDY

非综合征性颅缝早闭：表型/基因型研究

• 批准号: 7249417
• 负责人: Simeon A Boyadjiev Boyd
• 金额: $ 41.28万
• 依托单位: UNIVERSITY OF CALIFORNIA AT DAVIS
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-01 至 2011-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7249417
• 关键词: NONSYNDROMIC; CRANIOSYNOSTOSIS; PHENOTYPE; GENOTYPE; STUDY

DESCRIPTION (provided by applicant): Craniosynostosis, the premature fusion of 1 or more cranial sutures is a common malformation occurring in 3 to 5 per 10,000 live births. Most often craniosynostosis occurs as an isolated (i.e. nonsyndromic) anomaly. Nonsyndromic craniosynostosis (NSC) is a heterogeneous condition of multifactorial etiology with evidence of genetic factors. Significant progress has been made in understanding the clinical and molecular aspects of monogenic syndromic craniosynostosis. However, the phenotype characterization of NSC and the variability within diagnostic subgroups is incomplete and the causes of NSC remain unknown. Analysis of the clinical features and the craniofacial anthropometric profiles of a large group of prospectively recruited patients with sagittal and coronal NSC evaluated under a standardized protocol will further characterize these phenotypes. The clinically homogeneous group of patients with isolated nonsyndromic sagittal craniosynostosis will be used to identify causative genes by candidate gene association analysis. We have already enrolled and characterized 100 sagittal and 39 coronal NSC families and our existing recruitment system will ensure at least 250 additional sagittal and coronal NSC families by year 4 of this study. We will use advanced imaging technologies and quantitative morphological tools to characterize and evaluate 3D phenotypic variation within and between the diagnostic categories of sagittal and coronal NSC. The genotyping of the first 47 case-parent trios with isolated sagittal NSC was initiated and the results indicate associations with a region on chromosome 3q and with several of the tested candidate genes. Our efforts will be dedicated to reproducing and validating these associations and to identifying variants within these genes that predispose to NSC. We will also continue SNP-based genotyping and the association analysis of additional candidate genes. In summary, this application proposes a multicenter phenotype and genotype study aimed at determining the clinical, anthropometric, and molecular characteristics of NSC. Our aims are to accrue well-characterized sagittal and coronal patient populations, to identify areas for improved clinical care, and to establish a sample repository available to the scientific community. In addition, we will also identify genes associated with sagittal NSC. The resources that we have amassed and the collaborative and integrated approaches that we will utilize put us in a unique position to accomplish these aims.

描述（由申请方提供）：颅缝早闭，即1条或多条颅缝过早融合，是一种常见畸形，每10，000例活产中发生3 - 5例。最常见的颅缝早闭发生作为一个孤立的（即非综合征）异常。非综合征型颅缝早闭症是一种多因素病因的异质性疾病，有遗传因素的证据。在了解单基因综合征性颅缝早闭的临床和分子方面已经取得了重大进展。然而，NSC的表型特征和诊断亚组内的变异性是不完整的，NSC的原因仍然未知。分析的临床特征和颅面人体测量资料的一个大的前瞻性招募患者的矢状面和冠状面NSC评价下，一个标准化的协议将进一步表征这些表型。临床同质组的患者孤立的非综合征矢状面颅缝早闭将被用来确定致病基因的候选基因关联分析。我们已经招募并鉴定了100个矢状面和39个冠状面NSC家族，我们现有的招募系统将确保到本研究的第4年至少有250个额外的矢状面和冠状面NSC家族。我们将使用先进的成像技术和定量形态学工具来表征和评估矢状面和冠状面NSC诊断类别内和之间的3D表型变化。开始对前47例孤立性矢状面神经干细胞的病例-双亲三联体进行基因分型，结果表明与染色体3q上的一个区域和几个测试的候选基因相关。我们的努力将致力于复制和验证这些关联，并确定这些基因中易患NSC的变异。我们还将继续进行基于SNP的基因分型和其他候选基因的关联分析。总之，本申请提出了一项旨在确定NSC的临床、人体测量学和分子特征的多中心表型和基因型研究。我们的目标是积累特征良好的矢状面和冠状面患者人群，以确定改善临床护理的领域，并建立一个可供科学界使用的样本库。此外，我们还将鉴定与矢状面神经干细胞相关的基因。我们所积累的资源以及我们将利用的协作和综合办法使我们处于实现这些目标的独特地位。