Predictors of clinically significant anhedonia in refractory epilepsy.

Anhedonia Antiseizure medication Depression Epilepsy

Journal

Journal of the neurological sciences
ISSN: 1878-5883
Titre abrégé: J Neurol Sci
Pays: Netherlands
ID NLM: 0375403

Informations de publication

Date de publication:
02 Dec 2023
Historique:
received: 28 08 2023
revised: 08 11 2023
accepted: 28 11 2023
medline: 8 12 2023
pubmed: 8 12 2023
entrez: 7 12 2023
Statut: aheadofprint

Résumé

Anhedonia, the inability to feel pleasure or motivation for reward, is a core feature of depression in epilepsy, but can occur independent from depression. It is reported in over a third of people with epilepsy and has a significant impact on quality of life. This study determined whether specific features of medication refractory epilepsy are predictive of anhedonia. We assessed 267 patients with medication refractory epilepsy for anhedonia, primarily using the clinically validated Snaith-Hamilton Pleasure Scale (SHAPS) scale. Patients with clinically significant anhedonia were compared with those without for key demographics, epilepsy characteristics and medication using a logistic regression analysis. We found that seizure frequency (p < 0.01) but not duration of epilepsy was significantly associated with anhedonia. We also found that benzodiazepine use was significantly associated (p = 0.01) with anhedonia, and levetiracetam/brivaracetam and sodium valproate were significantly negatively associated with anhedonia (0.01 and 0.03 respectively). High seizure burden in medication refractory epilepsy is significantly associated with anhedonia. Specific antiseizure medications are also associated with the development of anhedonia, but it is unclear whether their use is causative or influenced by the presence of anhedonia.

Sections du résumé

BACKGROUND BACKGROUND
Anhedonia, the inability to feel pleasure or motivation for reward, is a core feature of depression in epilepsy, but can occur independent from depression. It is reported in over a third of people with epilepsy and has a significant impact on quality of life.
OBJECTIVES OBJECTIVE
This study determined whether specific features of medication refractory epilepsy are predictive of anhedonia.
DESIGN METHODS
We assessed 267 patients with medication refractory epilepsy for anhedonia, primarily using the clinically validated Snaith-Hamilton Pleasure Scale (SHAPS) scale.
METHODS METHODS
Patients with clinically significant anhedonia were compared with those without for key demographics, epilepsy characteristics and medication using a logistic regression analysis.
RESULTS RESULTS
We found that seizure frequency (p < 0.01) but not duration of epilepsy was significantly associated with anhedonia. We also found that benzodiazepine use was significantly associated (p = 0.01) with anhedonia, and levetiracetam/brivaracetam and sodium valproate were significantly negatively associated with anhedonia (0.01 and 0.03 respectively).
CONCLUSION CONCLUSIONS
High seizure burden in medication refractory epilepsy is significantly associated with anhedonia. Specific antiseizure medications are also associated with the development of anhedonia, but it is unclear whether their use is causative or influenced by the presence of anhedonia.

Identifiants

pubmed: 38061273
pii: S0022-510X(23)02288-8
doi: 10.1016/j.jns.2023.122826
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

122826

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest none.

Auteurs

Surapi Wijayendran (S)

National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.

Rofael Jabr (R)

National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.

Lucy Roberts-West (L)

National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.

Dorothea Bindman (D)

National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.

Matthew C Walker (MC)

National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, WC1N 3BG, UK.

Sallie Baxendale (S)

National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK.

Umesh Vivekananda (U)

National Hospital for Neurology and Neurosurgery, Queen Square, London WC1N 3BG, UK; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, WC1N 3BG, UK. Electronic address: u.vivekananda@ucl.ac.uk.

Classifications MeSH