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Deep brain stimulation for the treatment of severe intractable anorexia nervosa.

Authors :
Sobstyl M
Stapińska-Syniec A
Sokół-Szawłowska M
Kupryjaniuk A
Source :
British journal of neurosurgery [Br J Neurosurg] 2019 Dec; Vol. 33 (6), pp. 601-607. Date of Electronic Publication: 2019 Sep 25.
Publication Year :
2019

Abstract

Anorexia nervosa (AN) is a challenging multifactorial disorder with the highest mortality rate among all psychiatric disorders. Due to the low rate of long-term treatment success, new treatment options are needed. Here, we review Deep Brain Stimulation (DBS) as a treatment of Severe Intractable AN. The mechanisms of AN have shown significant involvement of the central nervous system especially the same brain regions which are involved with obsessive-compulsive disorder (OCD) and major depressive disorder (MDD). AN and OCD display many similarities in psychiatric practice such as compulsive behaviours and anxiety levels, which are related to networks in the brain, that can be altered using DBS. Our literature search revealed 8 studies totalling 28 individuals with AN and comorbid OCD or MDD. The most common stereotactic targets included the sub-callosal cingulate cortex (Brodmann area 25)/medial forebrain bundle (MFB) for AN and comorbid MDD and nucleus accumbens (NAc)/ventral striatum for AN and comorbid OCD. In most cases bilateral DBS of various structures of the reward system achieved good results in BMI, and core AN symptoms and psychiatric comorbidities showed sustained improvement. DBS is a promising treatment modality for AN and comorbid OCD or MDD. These results highlight promise and hope for patients with AN. However, further studies with larger patient populations are needed to shed light on the long-term outcomes of DBS and its effects in AN treatment.

Details

Language :
English
ISSN :
1360-046X
Volume :
33
Issue :
6
Database :
MEDLINE
Journal :
British journal of neurosurgery
Publication Type :
Academic Journal
Accession number :
31550921
Full Text :
https://doi.org/10.1080/02688697.2019.1667484