Department of Epidemiology, University of California Irvine, Irvine, CA, USA; Institute for Interdisciplinary Salivary Bioscience Research, University of California Irvine, Irvine, CA, USA.
Department of Neurosciences, University of California San Diego, San Diego, CA, USA.
Parkinsonism Relat Disord. 2022 Apr;97:25-28. doi: 10.1016/j.parkreldis.2022.02.023. Epub 2022 Mar 4.
The inclusion of premanifest Huntington's Disease (Pre-HD) subjects in clinical trials necessitates selecting those who are near transition to manifest Huntington's disease (Man-HD). We previously determined that plasma neurofilament light (NfL) levels are significantly correlated with predicted years to Man-HD onset, using established formulae. Recently, a new normalized prognostic index (PIN) score for predicting Pre-HD disease progression has been validated. Our objective was to determine whether plasma NfL levels are similarly associated with PIN score and PIN score-derived years to Man-HD onset (PIN-YTO).
112 individuals (46 Pre-HD, 66 Man-HD) underwent blood sample collection and clinical assessment, inclusive of the Symbol Digit Modalities Test and Unified Huntington's Disease Rating Scale Total Motor Score. Plasma NfL levels were measured using a Meso Scale Discovery assay.
Pre-HD and Man-HD cohorts differed by age (p < .0001), and CAG repeat number (p = .004), but not education level or gender. Plasma NfL levels were significantly correlated with PIN scores (r = 0.69, p < .0001) and PIN-YTO (r = -0.69, p < .0001). Plasma NfL levels were similarly correlated with predicted years to onset scores determined using Langbehn and colleague's formula (r = -0.68, p < .0001). All significant correlations endured corrections for age and CAG repeat number. A plasma NfL cut-point of <45.0 pg/ml distinguished Pre-HD participants >10 predicted years from Man-HD onset, compared to those ≤10 predicted years.
We have extensively shown that plasma NfL levels are associated with predicted years to manifest HD onset in Pre-HD participants, and present a plasma NfL cut-point that may help exclude far-from-onset Pre-HD patients from clinical trials.
将处于症状前亨廷顿病(Pre-HD)阶段的受试者纳入临床试验,需要选择那些即将进入亨廷顿病显性期(Man-HD)的患者。我们之前使用既定公式确定了血浆神经丝轻链(NfL)水平与预测的 Man-HD 发病时间之间存在显著相关性。最近,一种新的用于预测 Pre-HD 疾病进展的标准化预后指数(PIN)评分已得到验证。我们的目的是确定血浆 NfL 水平是否与 PIN 评分以及 PIN 评分衍生的 Man-HD 发病时间(PIN-YTO)相关。
112 名个体(46 名 Pre-HD,66 名 Man-HD)接受了血液样本采集和临床评估,包括符号数字模态测试和统一亨廷顿病评定量表运动总评分。使用 Meso Scale Discovery 检测法测量血浆 NfL 水平。
Pre-HD 和 Man-HD 队列在年龄(p<0.0001)和 CAG 重复数(p=0.004)方面存在差异,但在教育程度或性别方面没有差异。血浆 NfL 水平与 PIN 评分(r=0.69,p<0.0001)和 PIN-YTO(r=-0.69,p<0.0001)显著相关。血浆 NfL 水平与 Langbehn 及其同事公式确定的预测发病时间评分(r=-0.68,p<0.0001)也具有相似的相关性。所有显著相关性在年龄和 CAG 重复数校正后仍然存在。血浆 NfL 截断值<45.0pg/ml 可将发病时间预测>10 年的 Pre-HD 参与者与发病时间预测≤10 年的参与者区分开来。
我们已经广泛证明,血浆 NfL 水平与 Pre-HD 参与者的预测 Man-HD 发病时间相关,并提出了一个血浆 NfL 截断值,该值可能有助于将发病时间较远的 Pre-HD 患者排除在临床试验之外。