Claassen Daniel O, McDonell Katherine E, Donahue Manus, Rawal Shiv, Wylie Scott A, Neimat Joseph S, Kang Hakmook, Hedera Peter, Zald David, Landman Bennett, Dawant Benoit, Rane Swati
Department of Neurology Vanderbilt University Nashville TN USA.
Vanderbilt University Institute of Imaging Science Nashville TN USA.
Brain Behav. 2016 Oct 6;6(12):e00573. doi: 10.1002/brb3.573. eCollection 2016 Dec.
Clinically, Parkinson's disease (PD) presents with asymmetric motor symptoms. The left nigrostriatal system appears more susceptible to early degeneration than the right, and a left-lateralized pattern of early neuropathological changes is also described in several neurodegenerative conditions, including Alzheimer's disease, frontotemporal dementia, and Huntington's disease. In this study, we evaluated hemispheric differences in estimated rates of atrophy in a large, well-characterized cohort of PD patients.
Our cohort included 205 PD patients who underwent clinical assessments and T1-weighted brain MRI's. Patients were classified into Early (= 109) and Late stage (= 96) based on disease duration, defined as greater than or less than 10 years of motor symptoms. Cortical thickness was determined using FreeSurfer, and a bootstrapped linear regression model was used to estimate differences in rates of atrophy between Early and Late patients.
Our results show that patients classified as Early stage exhibit a greater estimated rate of cortical atrophy in left frontal regions, especially the left insula and olfactory sulcus. This pattern was replicated in left-handed patients, and was not influenced by the degree of motor symptom asymmetry (i.e., left-sided predominant motor symptoms). Patients classified as Late stage exhibited greater atrophy in the bilateral occipital, and right hemisphere-predominant cortical areas.
We show that cortical degeneration in PD differs between cerebral hemispheres, and findings suggest a pattern of early left, and late right hemisphere with posterior cortical atrophy. Further investigation is warranted to elucidate the underlying mechanisms of this asymmetry and pathologic implications.
临床上,帕金森病(PD)表现为不对称运动症状。左侧黑质纹状体系统似乎比右侧更容易早期退化,并且在包括阿尔茨海默病、额颞叶痴呆和亨廷顿病在内的几种神经退行性疾病中也描述了早期神经病理变化的左侧化模式。在本研究中,我们评估了一大群特征明确的PD患者中估计萎缩率的半球差异。
我们的队列包括205例接受临床评估和T1加权脑MRI检查的PD患者。根据疾病持续时间将患者分为早期(=109例)和晚期(=96例),疾病持续时间定义为运动症状大于或小于10年。使用FreeSurfer确定皮质厚度,并使用自抽样线性回归模型估计早期和晚期患者之间萎缩率的差异。
我们的结果表明,分类为早期的患者在左侧额叶区域,尤其是左侧岛叶和嗅沟,表现出更高的估计皮质萎缩率。这种模式在左撇子患者中也有体现,并且不受运动症状不对称程度(即左侧为主的运动症状)的影响。分类为晚期的患者在双侧枕叶和以右侧半球为主的皮质区域表现出更大的萎缩。
我们表明,PD中的皮质退化在大脑半球之间存在差异,研究结果提示了一种早期左侧和晚期右侧半球伴后部皮质萎缩的模式。有必要进一步研究以阐明这种不对称的潜在机制和病理意义。