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Tytuł pozycji:

Assessment of cytokines, microRNA and patient related outcome measures in conversion disorder/functional neurological disorder (CD/FND): The CANDO clinical feasibility study

Tytuł:
Assessment of cytokines, microRNA and patient related outcome measures in conversion disorder/functional neurological disorder (CD/FND): The CANDO clinical feasibility study
Autorzy:
Christina van der Feltz-Cornelis
Sally Brabyn
Jonathan Ratcliff
Danielle Varley
Victoria Allgar
Simon Gilbody
Chris Clarke
Dimitris Lagos
Temat:
Conversion disorder/functional neurological disorder
Functional movement disorder
Cytokines
Systemic low-grade inflammation
microRNA
Neurocognitive symptoms
Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Źródło:
Brain, Behavior, & Immunity - Health, Vol 13, Iss , Pp 100228- (2021)
Wydawca:
Elsevier, 2021.
Rok publikacji:
2021
Kolekcja:
LCC:Neurosciences. Biological psychiatry. Neuropsychiatry
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
English
ISSN:
2666-3546
Relacje:
http://www.sciencedirect.com/science/article/pii/S2666354621000314; https://doaj.org/toc/2666-3546
DOI:
10.1016/j.bbih.2021.100228
Dostęp URL:
https://doaj.org/article/e4f13d2415cf44ccbd997aa47ce06e06  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.4f13d2415cf44ccbd997aa47ce06e06
Czasopismo naukowe
Background: Conversion disorder/functional neurological disorder (CD/FND) occurs often in neurological settings and can lead to long-term distress, disability and demand on health care services. Systemic low-grade inflammation might play a role, however, the pathogenic mechanism is still unknown. Aim: 1) To explore the feasibility to establish and assess a cohort of CD/FND with motor symptoms, involving persons with lived experience (PPI). 2) To generate proof of concept regarding a possible role for cytokines, microRNA, cortisol levels and neurocognitive symptoms in patients with motor CD/FND. Method: Feasibility study. Results: The study showed active involvement of patients despite high clinical illness burden and disability, neurocognitive symptoms, childhood adverse experiences (ACE) and current life events. The study provided valuable knowledge regarding the feasibility of conducting a study in these patients that will inform future study phases. In the sample there were elevated levels of IL6, IL12, IL17A, IFNg, TNFa and VEGF-a, suggesting systemic low-grade inflammation. Also, microRNAs involved in inflammation and vascular inflammation were correlated with TNFa and VEGFa respectively, suggesting proof of concept for an epigenetic mechanism. Owing to the COVID-19 outbreak, the patient sample was limited to 15 patients. Conclusion: It is a novelty that this study is conducted in the clinical setting. This innovative, translational study explores stress-related SLI in CD/FND patients and the feasibility of a larger project aiming to develop new treatments for this vulnerable population. Given the positive findings, there is scope to conduct further research into the mechanism of disease in CD/FND.

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