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Volume 58, Issue 12, Pages 955-962 (15 December 2005)


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Platelet Adenylyl Cyclase Activity: A Biological Marker for Major Depression and Recent Drug Use

WHO/ISBRA Study on State and Trait Markers of Alcohol Use and Dependence InvestigatorsLisa M. HinesCorresponding Author Informationemail address, Boris Tabakoff

Received 14 January 2005; received in revised form 29 March 2005; accepted 27 May 2005. published online 11 August 2005.

Background

Adenylyl cyclase (AC) is an enzyme that can regulate the physiologic effects of numerous drugs and hormones through the production of cyclic adenosine-3′,5′-monophosphate (cAMP). Some studies suggest that certain measures of AC activity are lower among depressed subjects. We examined the relationship between various measures of AC activity and major depression, taking into account potential confounders, such as drug use and gender.

Methods

We assessed the relationship between platelet levels of AC activity and lifetime diagnosis of major depression among 1481 participants (226 subjects with a history of major depression and 1255 control subjects) in an international, cross-sectional study initiated by the World Health Organization and the International Society on Biomedical Research on Alcoholism.

Results

After accounting for recent drug use, subjects with a history of major depression had markedly lower mean levels for all measures of platelet AC activity compared with control subjects. The adjusted odds ratios for major depression comparing the bottom to the top quartile of AC activity were 2.69 for basal (95% confidence interval [CI] 1.30–5.56), 3.72 for cesium fluoride-stimulated (95% CI 1.54–8.98), 6.20 for forskolin-stimulated (95% CI 2.04–18.80), and 2.20 for Gpp(NH)p-stimulated (95% CI 1.03–4.70).

Conclusions

Subjects with major depression have lower platelet AC activity levels, and this relationship is dramatically attenuated by various types of drug use.

Department of Pharmacology, University of Colorado Health Sciences Center, Denver, Colorado.

Corresponding Author InformationAddress reprint requests to Lisa M. Hines, Sc.D., University of Colorado Health Sciences Center at Fitzsimons, School of Medicine, Department of Pharmacology, Mail Stop F-8303, P.O. Box 6511, Aurora, CO 80045-0511.

PII: S0006-3223(05)00690-6

doi:10.1016/j.biopsych.2005.05.040


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