Department of Neurology with Friedrich-Baur Institute, University Hospital of the Ludwig-Maximilians-Universität München, Munich, Germany.
Department of Neuroradiology, University Hospital of the Ludwig-Maximilians-Universität München, Munich, Germany.
J Neurol. 2018 Feb;265(2):388-393. doi: 10.1007/s00415-017-8711-9. Epub 2017 Dec 19.
Cerebrotendinous xanthomatosis (CTX, MIM 213700) is a rare autosomal recessive lipid storage disorder caused by CYP27A1 mutations. Treatment with chenodeoxycholic acid (CDCA) may slow the progression of the disease and reverse some symptoms in a proportion of patients. In a non-consanguineous Caucasian family, two siblings with CTX were evaluated before treatment and prospectively followed-up every 6 months after starting CDCA therapy, using systematic clinical examination, neuropsychological tests, laboratory tests, electroencephalography (EEG) and brain MRI, diffusion tensor imaging (DTI) and tractography. A 30-year-old patient and her 27-year-old brother were referred for progressive spastic paraparesis. Both had epilepsy, learning difficulties, chronic diarrhoea and juvenile-onset cataracts. CTX was diagnosed by increased cholestanol levels and compound heterozygosity for CYP27A1 mutations. Therapy with CDCA led to resolution of chronic diarrhoea, normalisation of serum cholestanol and EEG, and a progressive improvement in gait, cognition and seizure control. Before treatment, conventional brain MRI showed no CTX-related abnormalities for the proband and no cerebellar abnormalities for the brother, while DTI showed reduced fractional anisotropy (FA) and tract-density in the cerebellum and widespread cerebral reductions of FA in both patients, compared to a group of 35 healthy controls. Repeated DTI after starting therapy showed progressive increases of cerebellar tract density and of cerebral FA. In patients with CTX, therapy with CDCA may lead to significant clinical improvement, with normalisation of biochemical and electrophysiological biomarkers. DTI and tractography may detect changes when the conventional MRI is unremarkable and may provide potential neuroimaging biomarkers for monitoring treatment response in CTX, while the conventional MRI remains unchanged.
脑腱黄瘤病(CTX,MIM 213700)是一种罕见的常染色体隐性脂质贮积病,由 CYP27A1 突变引起。使用鹅去氧胆酸(CDCA)治疗可能会减缓疾病的进展,并使一部分患者的一些症状得到逆转。在一个非近亲结婚的白种人家系中,两名 CTX 患者在开始 CDCA 治疗前接受了评估,并在开始 CDCA 治疗后每 6 个月进行一次前瞻性随访,随访内容包括系统的临床检查、神经心理学测试、实验室检查、脑电图(EEG)和脑 MRI、弥散张量成像(DTI)和纤维束追踪。一名 30 岁的女性患者和她 27 岁的哥哥因进行性痉挛性截瘫而就诊。两人均患有癫痫、学习困难、慢性腹泻和青少年期白内障。通过检测胆甾烷醇水平升高和 CYP27A1 基因突变的复合杂合性,诊断为 CTX。CDCA 治疗后,慢性腹泻得到缓解,血清胆甾烷醇恢复正常,脑电图正常,步态、认知和癫痫控制逐渐改善。治疗前,常规脑 MRI 显示先证者无 CTX 相关异常,哥哥无脑干异常,而 DTI 显示与 35 名健康对照组相比,两名患者的小脑纤维束密度和 FA 降低,脑内 FA 普遍降低。开始治疗后重复 DTI 显示小脑纤维束密度和脑内 FA 逐渐增加。CTX 患者接受 CDCA 治疗后可能会有显著的临床改善,生化和电生理生物标志物恢复正常。DTI 和纤维束追踪术可能会在常规 MRI 无异常时发现变化,为监测 CTX 患者的治疗反应提供潜在的神经影像学生物标志物,而常规 MRI 保持不变。