University of Iowa Roy and Lucille Carver College of Medicine, Department of Psychiatry, Iowa City, IA, United States.
Brain Res Bull. 2010 May 31;82(3-4):201-7. doi: 10.1016/j.brainresbull.2010.04.003. Epub 2010 Apr 10.
Previous MRI studies with participants prior to manifest Huntington disease have been conducted in small single-site samples. The current study reports data from a systematic multi-national study during the prodromal period of Huntington disease and examines whether various brain structures make unique predictions about the proximity to manifest disease. MRI scans were acquired from 657 participants enrolled at 1 of 32 PREDICT-HD research sites. Only prodromal Huntington disease participants (those not meeting motor criteria for diagnosis) were included and subgrouped by estimated diagnosis proximity (Near, Mid, and Far) based upon a formula incorporating age and CAG-repeat length. Results show volumes of all three subgroups differed significantly from Controls for total brain tissue, cerebral spinal fluid, white matter, cortical gray matter, thalamus, caudate, and putamen. Total striatal volume demonstrated the largest differences between Controls and all three prodromal subgroups. Cerebral white matter offered additional independent power in the prediction of estimated proximity to diagnosis. In conclusion, this large cross-sectional study shows that changes in brain volume are detectable years to decades prior to estimated motor diagnosis of Huntington disease. This suggests that a clinical trial of a putative neuroprotective agent could begin as much as 15 years prior to estimated motor diagnosis in a cohort of persons at risk for but not meeting clinical motor diagnostic criteria for Huntington disease, and that neuroimaging (striatal and white matter volumes) may be among the best predictors of diagnosis proximity.
先前针对处于亨廷顿病显性期之前的参与者进行的 MRI 研究是在小的单一地点样本中进行的。本研究报告了亨廷顿病前驱期的一项系统多中心研究的数据,并检验了各种大脑结构是否对接近显性疾病做出独特的预测。MRI 扫描从 32 个 PREDICT-HD 研究点中的 1 个招募的 657 名参与者中获取。仅包括处于前驱期的亨廷顿病参与者(不符合运动诊断标准的患者),并根据纳入年龄和 CAG 重复长度的公式,按接近诊断的估计(近、中、远)分组。结果显示,与对照组相比,所有三个亚组的全脑组织、脑脊液、白质、皮质灰质、丘脑、尾状核和壳核的体积均有显著差异。总纹状体体积在对照组和所有三个前驱亚组之间的差异最大。脑白质在预测估计接近诊断方面提供了额外的独立能力。总之,这项大型横断面研究表明,在亨廷顿病显性运动诊断前数年至数十年即可检测到脑容量的变化。这表明,在有亨廷顿病风险但不符合亨廷顿病临床运动诊断标准的人群队列中,在估计的运动诊断前 15 年左右,就可以开始进行潜在神经保护剂的临床试验,而神经影像学(纹状体和白质体积)可能是最接近诊断的最佳预测指标之一。