Emerging Concepts of Motor Reserve in Parkinson's Disease

被引:39
作者
Chung, Seok Jong [1 ,2 ]
Lee, Jae Jung [3 ]
Lee, Phil Hyu [1 ,4 ]
Sohn, Young H. [1 ]
机构
[1] Yonsei Univ, Dept Neurol, Coll Med, 50 Yonsei Ro, Seoul 03722, South Korea
[2] Yonsei Univ Hlth Syst, Yongin Severance Hosp, Dept Neurol, Yongin, South Korea
[3] Inje Univ, Ilsan Paik Hosp, Dept Neurol, Coll Med, Goyang, South Korea
[4] Yonsei Univ, Severance Biomed Sci Inst, Coll Med, Seoul, South Korea
关键词
Dopamine transporter; Motor reserve; Parkinson's disease; Positron-emission tomography; SLEEP BEHAVIOR DISORDER; WHITE-MATTER HYPERINTENSITIES; STRIATAL DOPAMINE DEPLETION; BODY-MASS INDEX; COGNITIVE RESERVE; OLFACTORY DYSFUNCTION; GENDER-DIFFERENCES; NONMOTOR SYMPTOMS; BASAL GANGLIA; 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE-INDUCED NEUROTOXICITY;
D O I
10.14802/jmd.20029
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The concept of cognitive reserve (CR) in Alzheimer's disease (AD) explains the differences between individuals in their susceptibility to AD-related pathologies. An enhanced CR may lead to less cognitive deficits despite severe pathological lesions. Parkinson's disease (PI)) is also a common neurodegenerative disease and is mainly characterized by motor dysfunction related to striatal dopaminergic depletion. The degree of motor deficits in PD is closely correlated to the degree of dopamine depletion; however, significant individual variations still exist. Therefore, we hypothesized that the presence of motor reserve (MR) in PD explains the individual differences in motor deficits despite similar levels of striatal dopamine depletion. Since 2015, we have performed a series of studies investigating MR in de novo patients with PD using the data of initial clinical presentation and dopamine transporter PET scan. In this review, we summarized the results of these published studies. In particular, some premorbid experiences (i.e., physical activity and education) and modifiable factors (i.e., body mass index and white matter hyperintensity on brain image studies) could modulate an individual's capacity to tolerate PD pathology, which can be maintained throughout disease progression.
引用
收藏
页码:171 / 184
页数:14
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