English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Association between depression subtypes and response to repeated‐dose intravenous ketamine

MPS-Authors
/persons/resource/persons222389

Li,  M
Max Planck Institute for Biological Cybernetics, Max Planck Society;
Department High-Field Magnetic Resonance, Max Planck Institute for Biological Cybernetics, Max Planck Society;

External Resource
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Wang, C., Zhou, Y., Zheng, W., Liu, W., Zhan, Y., Li, H., et al. (in press). Association between depression subtypes and response to repeated‐dose intravenous ketamine. Acta Psychiatrica Scandinavica, Epub ahead. doi:10.1111/acps.13096.


Cite as: https://hdl.handle.net/21.11116/0000-0004-9B48-D
Abstract
Objective

About half or more of treatment‐resistant depressed patients do not respond to ketamine, and few clinical predictors to gauge the most likely antidepressant response have been proposed. We explored whether depression subtypes are associated with response to ketamine.
Methods

Ninety‐seven participants with depression were administered six repeated‐dose intravenous ketamine and assessed for depression (Montgomery‐Åsberg Depression Rating Scale, MADRS), anxiety (Hamilton Anxiety Rating Scale, HAMA), and suicidal ideation (Beck Scale for Suicidal Ideation, SSI) at baseline, 24 hours after each infusion, and 2 weeks after the whole treatment. Participants were classified by melancholic/anxious subtype. Individuals who met criteria for neither or both subtypes were classified separately, resulting in four mutually exclusive groups.
Results

Patients with melancholic or melancholic‐anxious features were less likely to respond (e.g. day 13, melancholic‐anxious vs. anxious, OR 0.138, 95% CI 0.032–0.584, p = 0.007) or remit (e.g. day 26, melancholic vs. no subtype, OR 0.182, 95% CI 0.035–0.960, p = 0.045) and took longer to achieve response/remission than those with anxious or no subtype features. Faster HAMA score reductions were observed in patients with anxious or melancholic‐anxious features, and faster SSI score reductions were observed among those with melancholic‐anxious features.
Conclusions

Our study shows promising results for ketamine as a novel antidepressant preferentially for the treatment of non‐melancholic or anxious depression.