Department of Neurology Boston University School of Medicine Boston MA USA.
Brain Behav. 2016 Oct 19;7(1):e00590. doi: 10.1002/brb3.590. eCollection 2017 Jan.
Parkinson's disease (PD) usually emerges with a unilateral side-of-onset (left-onset: LOPD; right-onset: ROPD; Marinus & van Hilten, 2015) due to an asymmetrical degeneration of striatal dopaminergic neurons (Donnemiller et al., , 135, 2012, 3348). This has led to a body of research exploring the cognitive, neuropsychological, and clinical differences between LOPD and ROPD (e.g., Verreyt et al., , 21, 2011, 405).
Thirty ROPD and 14 LOPD cases were drawn from a Boston clinic specializing in PD. Various cognitive and neuropsychological measures were used in an attempt to discover if there were indeed any differences between LOPD and ROPD in this cohort.
For LOPD, duration of illness was found to be significantly greater than that of ROPD. However, further testing was able to confirm that despite this difference, it was not the cause of the other significant differences found. Furthermore, this increased duration was consistent with a previous study (Munhoz et al., , 19, 2013, 77). Performance on the Digit Span Backward (DSB) was found to be significantly poorer in LOPD than ROPD, suggesting compromised executive function in LOPD. Additionally, LOPD had significantly greater anxiety on the DASS Anxiety scales than ROPD. However, unlike Foster et al (, 23, 2010, 4), this increased anxiety could not account for the poorer performance on the DSB for LOPD. Finally, ROPD had significantly greater magical ideation than LOPD, which can be explained by the theory put forth by Brugger and Graves (, 247, 1997, 55).
Clear and significant differences between LOPD and ROPD were found within our cohort. LOPD showed greater impairment of working memory, greater anxiety, and greater duration of illness-all independent of one another; whereas, those with ROPD had greater magical ideation, also independent of any other variables.
帕金森病(PD)通常以单侧起病(左侧起病:LOPD;右侧起病:ROPD;Marinus 和 van Hilten,2015)为特征,这是由于纹状体多巴胺能神经元的不对称变性(Donnemiller 等人,2012 年,第 135 页,3348)。这导致了大量研究探索 LOPD 和 ROPD 之间的认知、神经心理学和临床差异(例如,Verreyt 等人,2011 年,第 21 页,405)。
从专门研究 PD 的波士顿诊所中抽取了 30 例 ROPD 和 14 例 LOPD 病例。使用各种认知和神经心理学测量方法试图发现该队列中 LOPD 和 ROPD 是否确实存在差异。
对于 LOPD,发病时间明显长于 ROPD。然而,进一步的测试能够证实,尽管存在这种差异,但它不是发现的其他显著差异的原因。此外,这种持续时间的增加与之前的一项研究一致(Munhoz 等人,2013 年,第 19 页,77)。LOPD 的数字广度后向(DSB)测试表现明显差于 ROPD,表明 LOPD 的执行功能受损。此外,LOPD 在 DASS 焦虑量表上的焦虑明显高于 ROPD。然而,与 Foster 等人(2010 年,第 23 页,4)不同的是,这种增加的焦虑并不能解释 LOPD 在 DSB 测试中的较差表现。最后,ROPD 的魔幻思维明显多于 LOPD,可以用 Brugger 和 Graves 的理论来解释(1997 年,第 247 页,55)。
在我们的队列中发现了 LOPD 和 ROPD 之间明显而显著的差异。LOPD 表现出更大的工作记忆损伤、更大的焦虑和更长的发病时间——所有这些都是独立的;而那些 ROPD 的患者则有更大的魔幻思维,这也与任何其他变量无关。