Severity: Warning
Message: file_get_contents(https://...@gmail.com&api_key=61f08fa0b96a73de8c900d749fcb997acc09&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests
Filename: helpers/my_audit_helper.php
Line Number: 176
Backtrace:
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url
File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML
File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global
File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword
File: /var/www/html/index.php
Line: 316
Function: require_once
Purpose: The endocannabinoid system plays a regulatory role in a number of physiological functions, including motor control but also mood, emotion, and cognition. A number of preclinical studies in Parkinson's disease (PD) models demonstrated that modulating the type 1 cannabinoid receptor (CBR) may improve motor symptoms and components of cognitive processing. However, the relation between CBR, cognitive decline and behavioral symptoms has not been investigated in PD patients so far. The aim of this study was to examine whether CBR availability is associated with measures of cognitive and behavioral function in PD patients.
Methods: Thirty-eight PD patients and ten age- and gender-matched controls underwent a [F]MK-9470 PET scan to assess CBR availability, as well as volumetric MR imaging. Neuropsychological symptoms were evaluated using an extensive cognitive and behavioral battery covering the five cognitive domains, depression, anxiety, apathy, and psychiatric complications, and were correlated to CBR availability using vowel-wise regression analysis (P < 0.05, corrected for familywise error).
Results: PD patients with poorer performance in episodic memory, executive functioning, speed and mental flexibility (range P 0.003-0.03) showed lower CBR availability in predominantly the midcingulate cortex and middle to superior frontal gyrus (T > 4.0). Also, PD patients with more severe visuospatial dysfunction showed decreased CBR availability in the precuneus, midcingulate, supplementary motor cortex, inferior orbitofrontal gyrus and thalamus (T = 5.5). These correlations were not related to cortical gray matter atrophy. No relationship was found between CBR availability and mood or behavioral symptom scores.
Conclusions: Decreased CBR availability in the prefrontal and midcingulate cortex in PD patients is strongly correlated with disturbances in executive functioning, episodic memory, and visuospatial functioning. Further investigation of regional CB1R expression in groups of PD patients with mild cognitive impairment or dementia is warranted in order to further investigate the role of CB1R expression in different levels of cognitive impairment in PD.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1007/s00259-019-04445-x | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!