Alcalay Roy N, Mejia-Santana Helen, Mirelman Anat, Saunders-Pullman Rachel, Raymond Deborah, Palmese Christina, Caccappolo Elise, Ozelius Laurie, Orr-Urtreger Avi, Clark Lorraine, Giladi Nir, Bressman Susan, Marder Karen
Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY, USA; Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Columbia University, New York, NY, USA.
Department of Neurology, College of Physicians and Surgeons, Columbia University, New York, NY, USA.
Parkinsonism Relat Disord. 2015 Feb;21(2):106-10. doi: 10.1016/j.parkreldis.2014.09.033. Epub 2014 Nov 20.
Ashkenazi Jewish (AJ) LRRK2 carriers are more likely to manifest the postural instability gait difficulty (PIGD) motor phenotype than non-carriers but perform similarly to non-carriers on cognitive screening tests.
To compare the cognitive profiles of AJ with Parkinson's disease (PD) with and without LRRK2 G2019S mutations using a comprehensive neuropsychological battery.
We administered a neuropsychological battery to PD participants in the Michael J. Fox Foundation AJ consortium. Participants (n = 236) from Beth Israel Medical Center, NY, Columbia University Medical Center, NY and Tel Aviv Medical Center, Israel included 116 LRRK2 G2019S carriers and 120 non-carriers. Glucocerbrosidase mutation carriers were excluded. We compared performance on each neuropsychological test between carriers and non-carriers. Participants in New York (n = 112) were evaluated with the entire battery. Tel Aviv participants (n = 124) were evaluated on attention, executive function and psychomotor speed tasks. The association between G2019S mutation status (predictor) and each neuropsychological test (outcome) was assessed using linear regression models adjusted for PIGD motor phenotype, site, sex, age, disease duration, education, Unified Parkinson's Disease Rating Scale (UPDRS) Part III, levodopa equivalent dose, and Geriatric Depression Score (GDS).
Carriers had longer disease duration (p < 0.001) and were more likely to manifest the PIGD phenotype (p = 0.024). In adjusted regression models, carriers performed better than non-carriers in Stroop Word Reading (p < 0.001), Stroop Interference (p = 0.011) and Category Fluency (p = 0.026).
In AJ-PD, G2019S mutation status is associated with better attention (Stroop Word Reading), executive function (Stroop Interference) and language (Category Fluency) after adjustment for PIGD motor phenotype.
与非携带者相比,阿什肯纳兹犹太(AJ)LRRK2基因携带者更有可能表现出姿势不稳步态障碍(PIGD)运动表型,但在认知筛查测试中的表现与非携带者相似。
使用一套全面的神经心理学测试,比较携带和不携带LRRK2 G2019S突变的AJ帕金森病(PD)患者的认知概况。
我们对迈克尔·J·福克斯基金会AJ联盟中的PD参与者进行了一套神经心理学测试。来自纽约贝斯以色列医疗中心、纽约哥伦比亚大学医学中心和以色列特拉维夫医疗中心的参与者(n = 236)包括116名LRRK2 G2019S基因携带者和120名非携带者。排除了葡萄糖脑苷脂酶突变携带者。我们比较了携带者和非携带者在每项神经心理学测试中的表现。纽约的参与者(n = 112)接受了整套测试。特拉维夫的参与者(n = 124)接受了注意力、执行功能和精神运动速度任务的评估。使用针对PIGD运动表型、地点、性别、年龄、病程、教育程度、统一帕金森病评定量表(UPDRS)第三部分、左旋多巴等效剂量和老年抑郁量表(GDS)进行调整的线性回归模型,评估G2019S突变状态(预测因素)与每项神经心理学测试(结果)之间的关联。
携带者的病程更长(p < 0.001),且更有可能表现出PIGD表型(p = 0.024)。在调整后的回归模型中,携带者在Stroop单词阅读(p < 0.001)、Stroop干扰(p = 0.011)和类别流畅性(p = 0.026)方面的表现优于非携带者。
在AJ-PD中,在对PIGD运动表型进行调整后,G2019S突变状态与更好的注意力(Stroop单词阅读)、执行功能(Stroop干扰)和语言能力(类别流畅性)相关。