Evidence map›Paper›PMID 16133393›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2006

Reversibility of ecstasy-induced reduction in serotonin transporter availability in polydrug ecstasy users.

Ralph Buchert, Rainer Thomasius, Kay Petersen, Florian Wilke, Jost Obrocki, Bruno Nebeling, Lutz Wartberg, Pavlina Zapletalova, Malte Clausen

Abstract read
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In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 63 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Brain serotonin function in MDMA (ecstasy) users: evidence for persisting neurotoxicity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2013
    Review
  5. Article
  6. Methodological weaknesses in non-randomized studies of ecstasy (MDMA) use: a cautionary note to readers and reviewers.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2012
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Effects of cocaine and MDMA self-administration on serotonin transporter availability in monkeys.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2008
    Article
  13. Review
  14. Article
  15. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Ralph BuchertDepartment of Nuclear Medicine, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246 Hamburg, Germany. buchert@uke.uni-hamburg.de
Rainer Thomasius
Kay Petersen
Florian Wilke
Jost Obrocki
Bruno Nebeling
Lutz Wartberg
Pavlina Zapletalova
Malte Clausen
University Medical Center Hamburg-Eppendorf · DEUniversität Hamburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAnimal data suggest that the synthetic drug ecstasy may damage brain serotonin neurons. Previously we reported protracted reductions in the availability of the serotonin transporter (SERT), an index of integrity of the axon terminals of brain serotonergic neurons, in SERT-rich brain regions in current human ecstasy users. Comparison of current ecstasy users and former ecstasy users yielded some evidence that this reduction might be reversible. However, participant selection effects could not be ruled out. Therefore, follow-up examinations were performed in these subjects to test the following a priori hypothesis in a prospective longitudinal design that eliminates participant selection effects to a large extent: availability of the SERT increases towards normal levels when ecstasy use is stopped, and remains unchanged or is further decreased if use is continued.

methodsTwo follow-up positron emission tomography measurements using the SERT ligand [11C](+)McN5652 were completed by 15 current and nine former ecstasy users. All subjects used illicit drugs other than ecstasy, too. The time interval between repeated measurements was about 1 year. The time course of the availability of the SERT was analysed in the following SERT-rich regions: mesencephalon, putamen, caudate and thalamus.

resultsCurrent ecstasy users showed a consistent increase in the availability of the SERT in the mesencephalon during the study (Friedman test: p = 0.010), which most likely was caused by a decrease in the intensity of ecstasy consumption (Spearman correlation coefficient -0.725, p = 0.002). Former ecstasy users showed a consistent increase in SERT availability in the thalamus (Friedman test: p = 0.006).

conclusionEcstasy-induced protracted alterations in the availability of the SERT might be reversible.

Indexed as

AdolescentAdultBrainFemaleFollow-Up StudiesHumansIsoquinolinesMaleNeuronsN-Methyl-3,4-methylenedioxyamphetaminePositron-Emission TomographySerotonin AntagonistsSerotonin Plasma Membrane Transport ProteinsSubstance-Related DisordersIsoquinolinesMcN 5652N-Methyl-3,4-methylenedioxyamphetamineSerotonin AntagonistsSerotonin Plasma Membrane Transport Proteins

Identifiers

PMID16133393
OpenAlexW2058524677

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.