MAPT基因的一种特殊双倍型H1j/H2可能是帕金森病伴痴呆的原因。

Case Reports in Genetics Pub Date : 2020-12-03 eCollection Date: 2020-01-01 DOI:10.1155/2020/8813344
Imane Smaili, Imane Hajjaj, Rachid Razine, Houyam Tibar, Ayyoub Salmi, Naima Bouslam, Ahmed Moussa, Wafa Regragui, Ahmed Bouhouche
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引用次数: 2

摘要

帕金森病(PD)是仅次于阿尔茨海默病的第二常见的神经退行性疾病。5% ~ 10%的患者为单基因型,而散发性PD大多是遗传和环境因素共同作用的结果。微管相关蛋白tau (MAPT)已被认为是包括PD在内的多种神经退行性疾病最重要的危险因素之一。MAPT的特征是在17号染色体上倒置,导致H1和H2两种不同的单倍型。研究描述了MAPT H1j亚单倍型与PD风险的显著关联,而H2单倍型与帕金森病相关,特别是其慢动力学成分。我们在此报告一个孤立的病例,显示了一种动力刚性形式的PD,年龄41岁,左旋多巴反应良好,在7年的疾病进展中逐渐发展为痴呆。该患者未携带LRRK2 G2019S突变、拷贝数变异,也未携带PD相关已知基因的致病性和罕见变异。MAPT亚单倍型基因分型显示患者为H1j/H2双倍型,其母亲为H1j/H1j,其两个健康兄弟为H1j/H1v,其已故父亲为H1v/H2。在80名PD患者中,共有3名患者显示出H1j/H2二倍型,这些患者也没有已知的PD引起突变,在92名健康个体对照中有1名患者显示出H1j/H2二倍型。这三例双倍型患者均具有相似的临床表型。我们的研究结果表明,单倍型H1j和H2是强危险因子等位基因,它们的组合可能是PD伴痴呆早发的原因。
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A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia.

Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer disease. Five to ten percent of patients have monogenic form of the disease, while most of sporadic PD cases are caused by the combination of genetic and environmental factors. Microtubule-associated protein tau (MAPT) has been appointed as one of the most important risk factors for several neurodegenerative diseases including PD. MAPT is characterized by an inversion in chromosome 17 resulting in two distinct haplotypes H1 and H2. Studies described a significant association of MAPT H1j subhaplotype with PD risk, while H2 haplotype was associated with Parkinsonism, particularly to its bradykinetic component. We report here an isolated case displaying an akinetic-rigid form of PD, with age of onset of 41 years and a good response to levodopa, who developed dementia gradually during the seven years of disease progression. The patient does not carry the LRRK2 G2019S mutation, copy number variations, nor pathogenic and rare variants in known genes associated with PD. MAPT subhaplotype genotyping revealed that the patient has the H1j/H2 diplotype, his mother H1j/H1j, his two healthy brothers H1j/H1v and his deceased father was by deduction H1v/H2. The H1j/H2 diplotype was shown in a total of 3 PD patients among 80, who also did not have known PD-causing mutation and in 1 out of 92 healthy individual controls. The three patients with this diplotype all have a similar clinical phenotype. Our results suggest that haplotypes H1j and H2 are strong risk factor alleles, and their combination could be responsible for early onset of PD with dementia.

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