Evidence map›Paper›PMID 25427171›Full record

Trial reportJournal of clinical psychopharmacology2015

Zonisamide, topiramate, and levetiracetam: efficacy and neuropsychological effects in alcohol use disorders.

Clifford M Knapp, Domenic A Ciraulo, Ofra Sarid-Segal, Mark A Richardson, Eric Devine, Chris C Streeter, Marlene Oscar-Berman, Caitlin Surprise, Laurie Colaneri, Meghan Putnam and 2 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical psychopharmacology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 3 pooled it
2.5field-weighted citation impact, top 12% 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

25 citing papers in PubMed, 3 syntheses or guidelines pooled it, 70 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. The Effect of Zonisamide and Ethanol on Various Types of Memory in Rats.International journal of environmental research and public health · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Pharmacogenetics of alcohol addiction: current perspectives.The application of clinical genetics · 2019
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Clifford M KnappFrom the Departments of *Psychiatry, †Psychology and Brain Sciences, and ‡Neurology, Boston University School of Medicine; §Department of Psychiatry, Harvard Medical School; and ∥Department of Anatomy and Neurobiology, Boston University School of Medicine, Boston, MA.
Domenic A Ciraulo
Ofra Sarid-Segal
Mark A Richardson
Eric Devine
Chris C Streeter
Marlene Oscar-Berman
Caitlin Surprise
Laurie Colaneri
Meghan Putnam
Megan Waters
Courtney Richambault
Doctors Hospital · USBoston University · USHarvard University · US

Funding

Interdisciplinary Study of Two Novel Anticonvulsants in AlcoholismR01AA015923 · NIAAA · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI FARCHIONE, TODD J. · 2009 to 2020
$6.4M
NIAAA NIH HHS R01 AA 015923NIAAA NIH HHS R01 AA015923
6 · The paper itself

Abstract

The anticonvulsant topiramate not only decreases ethanol consumption in alcohol dependence (AD) but also may produce several adverse events including cognitive impairment. Zonisamide is a structurally related anticonvulsant that is a promising agent for the treatment of AD and may have greater tolerability than topiramate. This study evaluated the effects of zonisamide (400 mg/d) on alcohol consumption and its neurotoxic effects in subjects with AD. A double-blind placebo-controlled clinical trial was conducted using 2 comparator anticonvulsant drugs, topiramate (300 mg/d) and levetiracetam (2000 mg/d), which does not impair cognition. Study medications were administered for 14 weeks, including a 2-week taper period. Medication adherence was facilitated using Brief Behavioral Compliance Enhancement Treatment. The neurotoxicity of the study drugs was assessed using neuropsychological tests and the AB-Neurotoxicity Scale. Compared with placebo, both zonisamide and topiramate produced significant reductions in the drinks consumed per day, percent days drinking, and percent days heavy drinking. Only the percent days heavy drinking was significantly decreased in the levetiracetam group. The topiramate cell was the only group that had a significant increase on the mental slowing subscale of the Neurotoxicity Scale compared with placebo at study weeks 11 and 12. Topiramate and zonisamide both produced modest reductions in verbal fluency and working memory. These findings indicate that zonisamide may have efficacy in the treatment of AD, with effect sizes similar to topiramate. Both of these drugs produced similar patterns of cognitive impairment, although only the topiramate group reported significant increases in mental slowing.

Indexed as

Neuropsychological TestsAdultAgedAlcohol DrinkingAlcohol-Related DisordersAnticonvulsantsCognition DisordersDouble-Blind MethodFemaleFructoseHumansIsoxazolesLevetiracetamMaleMiddle AgedPiracetamAnticonvulsantsFructoseIsoxazolesLevetiracetamPiracetamTopiramateZonisamide

Identifiers

PMID25427171
PMCPMC4276485
OpenAlexW1987065152

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.