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Indexing disease progression at study entry with individuals at-risk for Huntington disease.在研究开始时对亨廷顿病高危个体进行疾病进展的指标检测。
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Neural underpinnings of distortions in the experience of time across senses.跨感官体验时间扭曲的神经基础。
Front Integr Neurosci. 2011 Jul 28;5:32. doi: 10.3389/fnint.2011.00032. eCollection 2011.
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The role of physiological arousal in time perception: psychophysiological evidence from an emotion regulation paradigm.生理唤醒在时间感知中的作用:情绪调节范式的心理生理学证据。
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Visuomotor integration deficits precede clinical onset in Huntington's disease.在亨廷顿病中,视动整合缺陷先于临床发病。
Neuropsychologia. 2011 Jan;49(2):264-70. doi: 10.1016/j.neuropsychologia.2010.11.016. Epub 2010 Nov 20.
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Tapping linked to function and structure in premanifest and symptomatic Huntington disease.经颅磁刺激与未出现症状和有症状亨廷顿病的功能和结构相关联。
Neurology. 2010 Dec 14;75(24):2150-60. doi: 10.1212/WNL.0b013e3182020123. Epub 2010 Nov 10.
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Involvement of the anterior cingulate and frontoinsular cortices in rapid processing of salient facial emotional information.前扣带皮层和额极皮层参与显著面部情绪信息的快速处理。
Neuroimage. 2011 Feb 1;54(3):2539-46. doi: 10.1016/j.neuroimage.2010.10.007. Epub 2010 Oct 16.
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Neurocognitive signs in prodromal Huntington disease.前驱期亨廷顿病的神经认知征象。
Neuropsychology. 2011 Jan;25(1):1-14. doi: 10.1037/a0020937.
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Mild cognitive impairment in prediagnosed Huntington disease.亨廷顿病患者的轻度认知障碍。
Neurology. 2010 Aug 10;75(6):500-7. doi: 10.1212/WNL.0b013e3181eccfa2. Epub 2010 Jul 7.
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Self-paced timing detects and tracks change in prodromal Huntington disease.自我调整时间检测和跟踪前驱亨廷顿病的变化。
Neuropsychology. 2010 Jul;24(4):435-42. doi: 10.1037/a0018905.
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Abnormal explicit but normal implicit sequence learning in premanifest and early Huntington's disease.在症状前和早期亨廷顿病中异常外显但正常内隐序列学习。
Mov Disord. 2010 Jul 30;25(10):1343-9. doi: 10.1002/mds.22692.

预测亨廷顿病前驱期诊断时间的认知领域。

Cognitive domains that predict time to diagnosis in prodromal Huntington disease.

机构信息

University of Iowa Carver College of Medicine, Psychiatry Research, Iowa City, IA 52242-1000, USA.

出版信息

J Neurol Neurosurg Psychiatry. 2012 Jun;83(6):612-9. doi: 10.1136/jnnp-2011-301732. Epub 2012 Mar 26.

DOI:10.1136/jnnp-2011-301732
PMID:22451099
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3812822/
Abstract

BACKGROUND

Prodromal Huntington's disease (prHD) is associated with a myriad of cognitive changes but the domains that best predict time to clinical diagnosis have not been studied. This is a notable gap because some domains may be more sensitive to cognitive decline, which would inform clinical trials.

OBJECTIVES

The present study sought to characterise cognitive domains underlying a large test battery and for the first time, evaluate their ability to predict time to diagnosis.

METHODS

Participants included gene negative and gene positive prHD participants who were enrolled in the PREDICT-HD study. The CAG-age product (CAP) score was the measure of an individual's genetic signature. A factor analysis of 18 tests was performed to identify sets of measures or latent factors that elucidated core constructs of tests. Factor scores were then fit to a survival model to evaluate their ability to predict time to diagnosis.

RESULTS

Six factors were identified: (1) speed/inhibition, (2) verbal working memory, (3) motor planning/speed, (4) attention-information integration, (5) sensory-perceptual processing and (6) verbal learning/memory. Factor scores were sensitive to worsening of cognitive functioning in prHD, typically more so than performances on individual tests comprising the factors. Only the motor planning/speed and sensory-perceptual processing factors predicted time to diagnosis, after controlling for CAP scores and motor symptoms. Conclusions The results suggest that motor planning/speed and sensory-perceptual processing are important markers of disease prognosis. The findings also have implications for using composite indices of cognition in preventive Huntington's disease trials where they may be more sensitive than individual tests.

摘要

背景

前驱亨廷顿病(prHD)与许多认知变化有关,但尚未研究哪些领域最能预测临床诊断时间。这是一个显著的差距,因为某些领域可能对认知下降更为敏感,这将为临床试验提供信息。

目的

本研究旨在描述大型测试组合背后的认知领域,并首次评估它们预测诊断时间的能力。

方法

参与者包括基因阴性和基因阳性前驱亨廷顿病参与者,他们参加了 PREDICT-HD 研究。CAG-年龄乘积(CAP)评分是个体遗传特征的衡量标准。对 18 项测试进行因子分析,以确定阐明测试核心结构的测试集或潜在因子。然后将因子得分拟合到生存模型中,以评估其预测诊断时间的能力。

结果

确定了六个因素:(1)速度/抑制,(2)言语工作记忆,(3)运动计划/速度,(4)注意力-信息整合,(5)感觉-知觉加工,(6)言语学习/记忆。因子得分对前驱亨廷顿病认知功能恶化敏感,通常比构成因子的个别测试表现更为敏感。只有运动计划/速度和感觉-知觉加工因子在控制 CAP 评分和运动症状后预测了诊断时间。结论:结果表明,运动计划/速度和感觉-知觉加工是疾病预后的重要标志物。这些发现还对使用预防亨廷顿病试验中的认知综合指数具有影响,因为它们可能比个别测试更为敏感。