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New drug candidates for depression - a nationwide population-based study
L V Kessing1, H C Rytgaard2, T A Gerds2
1Copenhagen Affective Disorder reaserch Center (CADIC), Psychiatric Center Copenhagen, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Continued use of low-dose aspirin, statins, allopurinol, and angiotensin agents may decrease depression rates. However, non-aspirin NSAIDs and high-dose aspirin were linked to increased depression risk.
Area of Science:
- Pharmacology
- Psychiatry
- Epidemiology
Background:
- Depression is a significant public health concern.
- Medications targeting inflammation and stress response pathways are being explored for depression treatment.
Purpose of the Study:
- To examine the association between continued use of specific medications and the incidence of depression.
- To identify potential drug repurposing opportunities for depression treatment.
Main Methods:
- Utilized Danish nationwide population-based registers from 1995-2015.
- Included over 1.5 million subjects exposed to non-aspirin NSAIDs, low-dose aspirin, high-dose aspirin, statins, allopurinol, or angiotensin agents.
- Assessed depression using psychiatric diagnoses and antidepressant use.
Main Results:
- Continued use of low-dose aspirin, statins, allopurinol, and angiotensin agents was associated with a reduced rate of incident depression.
- Continued use of non-aspirin NSAIDs and high-dose aspirin was linked to an increased rate of incident depression.
Conclusions:
- Findings suggest that agents modulating inflammation and stress response may have a role in depression.
- Population-based registers are valuable for identifying drugs with repurposing potential for depression.
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