2022
DOI: 10.1007/s10072-022-06563-1
|View full text |Cite
|
Sign up to set email alerts
|

The impact of cerebral small vessel disease burden and its imaging markers on gait, postural control, and cognition in Parkinson’s disease

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
4
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 6 publications
(4 citation statements)
references
References 59 publications
0
4
0
Order By: Relevance
“…In line with the previous study, our study also found that patients with CSVD had an impaired stride length. Similar to stride speed, researchers found decreased cadence in CSVD patients [15,[18][19][20]. Interestingly, a cross-sectional study with large samples showed that patients with CSVD had step length, step speed, swing time and stance time impaired and age was associated with step length, step speed, swing time and stance time [21].…”
Section: Discussionmentioning
confidence: 99%
“…In line with the previous study, our study also found that patients with CSVD had an impaired stride length. Similar to stride speed, researchers found decreased cadence in CSVD patients [15,[18][19][20]. Interestingly, a cross-sectional study with large samples showed that patients with CSVD had step length, step speed, swing time and stance time impaired and age was associated with step length, step speed, swing time and stance time [21].…”
Section: Discussionmentioning
confidence: 99%
“…The presence and size of WMH increase with age even in apparently healthy individuals and can be larger in those with medical and neuropsychiatric disorders, for example, HIV infection and alcohol use disorder (AUD) [1,2], Alzheimer's disease [3], Parkinson's disease [4]; mild stroke [5][6][7][8], small cerebrovascular disease [9,10], depression [11].…”
Section: Introductionmentioning
confidence: 99%
“…A visually distinctive, neuroradiological marker of brain degradation is white matter hyperintense (WMH) signal occurring at the borders of the lateral ventricles and in deep white matter of cortical, cerebellar, and subcortical tissue. The presence and size of WMH increase with age even in apparently healthy individuals and can be larger in those with medical and neuropsychiatric disorders, for example, HIV infection and alcohol use disorder (AUD) [1,2], Alzheimer's disease [3], Parkinson's disease [4]; mild stroke [5–8], small cerebrovascular disease [9,10], depression [11]. Initial reports were skeptical about the functional ramifications of the ‘unidentified bright objects’, also known as UBOs [12], now called WMH, but dozens of reports have since noted variables that are common correlates of WMH number and size, implicating WMH as underlying functional declines in normal aging [13–19], age-related frailty [20], and numerous neuropsychiatric disorders.…”
Section: Introductionmentioning
confidence: 99%
“…Furthermore, the association between WMHs and cognitive performance, motor function and core clinical features in LBD has also provided mixed results. Greater WMH burden is associated with worse cognitive performance, executive functioning, language and information processing [15, 16], and CMBs are positively correlated with the severity of motor and emotional impairments [17]. Few studies have investigated the association of WMHs with clinical features of DLB.…”
Section: Introductionmentioning
confidence: 99%