Xiao Jianfeng, Thompson Misty M, Vemula Satya R, LeDoux Mark S
Departments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN, USA.
Departments of Neurology, and Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN, USA.
J Neurol Sci. 2016 Mar 15;362:299-303. doi: 10.1016/j.jns.2016.02.003. Epub 2016 Feb 2.
Isolated blepharospasm (BSP) is a late-onset focal dystonia characterized by involuntary contractions of the orbicularis oculi muscles. Genetic studies of BSP have been limited by the paucity of large multiplex pedigrees. Although sequence variants (SVs) in THAP1 have been reported in rare cases of BSP, the genetic causes of this focal dystonia remain largely unknown. Moreover, in the absence of family history and strong in silico or in vitro evidence of deleteriousness, the pathogenicity of novel SVs in THAP1 and other dystonia-associated genes can be indeterminate.
A large African-American pedigree with BSP was phenotypically characterized and screened for mutations in THAP1, TOR1A and GNAL with Sanger sequencing. Whole-exome sequencing of the proband was used to examine other dystonia-associated genes for potentially pathogenic SVs. In silico and co-segregation analyses were performed for a novel THAP1 SV identified in the proband.
Seven family members exhibited increased blinking and/or stereotyped bilateral and synchronous orbicularis oculi spasms with age of onset ranging from early childhood to late adult life (7 to 54 years). The proband was found to harbor a novel THAP1 SV (c.314T>C, p.L105S). However, the p.L105S SV did not co-segregate with blepharospasm in the pedigree. Moreover, in silico analyses suggest that p.L105S is benign. No pathogenic or likely pathogenic SVs in other dystonia-associated genes were identified with whole-exome sequencing.
Blepharospasm can be familial and may be hereditary in African-Americans. A comprehensive array of in silico tools, and, if possible, co-segregation analysis should be used to classify SVs in dystonia-associated genes.
孤立性眼睑痉挛(BSP)是一种迟发性局灶性肌张力障碍,其特征为眼轮匝肌的不自主收缩。BSP的遗传学研究因大型多位点家系的缺乏而受到限制。尽管在罕见的BSP病例中已报道THAP1存在序列变异(SVs),但这种局灶性肌张力障碍的遗传原因仍 largely未知。此外,在缺乏家族史以及可靠的计算机模拟或体外有害性证据的情况下,THAP1和其他肌张力障碍相关基因中的新型SVs的致病性可能无法确定。
对一个患有BSP的大型非裔美国家系进行表型特征分析,并通过桑格测序筛查THAP1、TOR1A和GNAL中的突变。先证者的全外显子测序用于检查其他肌张力障碍相关基因中潜在的致病性SVs。对先证者中鉴定出的新型THAP1 SV进行计算机模拟和共分离分析。
七名家庭成员表现出随着年龄增长眨眼增加和/或双侧及同步性眼轮匝肌刻板性痉挛,发病年龄从幼儿期到成年晚期(7至54岁)。发现先证者携带一种新型THAP1 SV(c.314T>C,p.L105S)。然而,p.L105S SV在该家系中与眼睑痉挛不共分离。此外,计算机模拟分析表明p.L105S是良性的。全外显子测序未在其他肌张力障碍相关基因中鉴定出致病性或可能致病性的SVs。
眼睑痉挛可能具有家族性,在非裔美国人中可能具有遗传性。应使用一系列全面的计算机模拟工具,并在可能的情况下进行共分离分析,以对肌张力障碍相关基因中的SVs进行分类。