Depressive symptomatology in young adults with a history of MDMA use: a longitudinal analysis
Rüssel S. Falck, Jichuan Wang, Robert G. Carlson
Journal of Psychopharmacology August 22, 2007 DOI: 10.1177/0269881107078293 via OpenAlex
Summary
AI-generated from the abstractAmong 402 young adult MDMA users followed for two years, depressive symptoms measured by the Beck Depression Inventory (BDI-II) declined from an average score of 9.8 at baseline to 7.7 at 24 months, decreasing by 0.36 points every six months. People with higher initial scores showed greater declines. Men and white participants had lower scores than women and non-whites; those with some university education had lower scores than those without. Current benzodiazepine or opioid users and people who had used MDMA more than 50 times had higher scores. The low and declining average scores suggest that for most people, MDMA use does not lead to long-term depressive symptoms.
Study at a glance
| Characteristics | Longitudinal study Peer reviewed |
|---|---|
| Sample size | 402 |
| Population | Young adult MDMA/ecstasy users from the community |
| Duration | 2-year follow-up with assessments every six months |
| Topics | Anxiety MDMA |
| Keywords | Depression economics Longitudinal study Beck depression inventory |
| Citations | 45 |
| Key finding | Depressive symptoms declined over two years among young adult MDMA users, suggesting that MDMA use does not result in long-term depressive symptomatology for most people. |
Abstract
Research suggests that methylenedioxymethamphetamine (MDMA)/`ecstasy' can cause serotonin depletion as well as serotonergic neurodegradation that may result in depression. This longitudinal study used the Beck Depression Inventory (BDI-II) to assess depressive symptomatology every six months over a two-year period among a community sample of young adult MDMA/`ecstasy' users ( n = 402). Multilevel growth modeling was used to analyze changes in BDI scores. Between baseline and 24 months, the mean BDI score declined from 9.8 to 7.7. Scores varied significantly across individuals at baseline and declined at a rate of 0.36 points every six months. Persons with higher baseline scores were more likely to have their scores decrease over time. Several factors were significantly associated with score levels, independent of time: gender — men's scores were lower than women's; ethnicity — whites' scores were lower than those of non-whites; education — persons with at least some university education had scores that were lower than those without any college experience; benzodiazepines — current users' scores were higher than non-users'; opioids — current users' scores were higher than non-users'; and cumulative ecstasy use — people who had used MDMA more than 50 times had scores that were higher than persons who had used the drug less often. The results reported here show low levels of depressive symptoms among a sample that, after 24 months, consisted of both current and former MDMA users. The low and declining mean scores suggest that for most people MDMA/`ecstasy' use does not result in long-term depressive symptomatology.