Patterns of Sulcal depth and cortical thickness in Parkinson’s disease

Author(s):  
Erlei Wang ◽  
Yujing Jia ◽  
Yang Ya ◽  
Jin Xu ◽  
Chengjie Mao ◽  
...  
2020 ◽  
Vol 42 (1) ◽  
pp. 139-153
Author(s):  
Carla Silva‐Batista ◽  
Anjanibhargavi Ragothaman ◽  
Martina Mancini ◽  
Patricia Carlson‐Kuhta ◽  
Graham Harker ◽  
...  

2017 ◽  
Vol 90 ◽  
pp. 40-45 ◽  
Author(s):  
Marcos Hortes N. Chagas ◽  
Vitor Tumas ◽  
Márcio A. Pena-Pereira ◽  
João Paulo Machado-de-Sousa ◽  
Antonio Carlos dos Santos ◽  
...  

2011 ◽  
Vol 33 (11) ◽  
pp. 2521-2534 ◽  
Author(s):  
Joana Braga Pereira ◽  
Naroa Ibarretxe-Bilbao ◽  
Maria-Jose Marti ◽  
Yaroslau Compta ◽  
Carme Junqué ◽  
...  

Aging ◽  
2021 ◽  
Author(s):  
LiQin Sheng ◽  
PanWen Zhao ◽  
HaiRong Ma ◽  
Joaquim Radua ◽  
ZhongQuan Yi ◽  
...  

2021 ◽  
Vol 13 ◽  
Author(s):  
Lin Zhang ◽  
Qin Shen ◽  
Haiyan Liao ◽  
Junli Li ◽  
Tianyu Wang ◽  
...  

There is increasing evidence to show that motor symptom lateralization in Parkinson’s disease (PD) is linked to non-motor features, progression, and prognosis of the disease. However, few studies have reported the difference in cortical complexity between patients with left-onset of PD (LPD) and right-onset of PD (RPD). This study aimed to investigate the differences in the cortical complexity between early-stage LPD and RPD. High-resolution T1-weighted magnetic resonance images of the brain were acquired in 24 patients with LPD, 34 patients with RPD, and 37 age- and sex-matched healthy controls (HCs). Cortical complexity including gyrification index, fractal dimension (FD), and sulcal depth was analyzed using surface-based morphometry via CAT12/SPM12. Familywise error (FWE) peak-level correction at p < 0.05 was performed for significance testing. In patients with RPD, we found decreased mean FD and mean sulcal depth in the banks of the left superior temporal sulcus (STS) compared with LPD and HCs. The mean FD in the left superior temporal gyrus (STG) was decreased in RPD compared with HCs. However, in patients with LPD, we did not identify significantly abnormal cortical complex change compared with HCs. Moreover, we observed that the mean FD in STG was negatively correlated with the 17-item Hamilton Depression Scale (HAMD) among the three groups. Our findings support the specific influence of asymmetrical motor symptoms in cortical complexity in early-stage PD and reveal that the banks of left STS and left STG might play a crucial role in RPD.


2016 ◽  
Vol 24 ◽  
pp. 119-125 ◽  
Author(s):  
Alessandro Tessitore ◽  
Gabriella Santangelo ◽  
Rosa De Micco ◽  
Carmine Vitale ◽  
Alfonso Giordano ◽  
...  

2017 ◽  
Vol 43 (8) ◽  
pp. 863-869
Author(s):  
I. V. Litvinenko ◽  
E. V. Boyko ◽  
A. N. Kulikov ◽  
P. S. Dynin ◽  
A. G. Trufanov ◽  
...  

2015 ◽  
Vol 30 (5) ◽  
pp. 688-695 ◽  
Author(s):  
Roberta Biundo ◽  
Luca Weis ◽  
Silvia Facchini ◽  
Patrizia Formento-Dojot ◽  
Annamaria Vallelunga ◽  
...  

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Sang-Won Yoo ◽  
Joong-Seok Kim ◽  
Ji-Yeon Yoo ◽  
Eunkyeong Yun ◽  
Uicheul Yoon ◽  
...  

AbstractOrthostatic hypotension (OH) is relatively common in the early stage of Parkinson’s disease (PD). It is divided into delayed OH and classical OH. Classical OH in PD has been investigated widely, however, the clinical implications of delayed OH in PD have seldom been studied. The purpose of this study is to characterize delayed OH in PD. A total of 285 patients with early drug-naïve PD were enrolled and divided into three groups according to orthostatic change: no-OH, delayed OH, and classical OH. The disease severity in terms of motor, non-motor, and cognitive functions was assessed. The cortical thickness of 82 patients was analyzed with brain magnetic resonance imaging. The differences among groups and linear tendency in the order of no-OH, delayed OH, and classical OH were investigated. Seventy-seven patients were re-evaluated. Initial and follow-up evaluations were explored to discern any temporal effects of orthostasis on disease severity. Sixty-four (22.5%) patients were defined as having delayed OH and 117 (41.1%) had classical OH. Between-group comparisons revealed that classical OH had the worst outcomes in motor, non-motor, cognitive, and cortical thickness, compared to the other groups. No-OH and delayed OH did not differ significantly. Linear trends across the pre-ordered OH subtypes found that clinical parameters worsened along with the orthostatic challenge. Clinical scales deteriorated and the linear gradient was maintained during the follow-up period. This study suggests that delayed OH is a mild form of classical OH in PD. PD with delayed OH has milder disease severity and progression.


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