Evidence map›Paper›PMID 23948785›Full record

Trial reportJournal of clinical psychopharmacology2013

A placebo-controlled trial of acetyl-L-carnitine and α-lipoic acid in the treatment of bipolar depression.

Brian P Brennan, John Eric Jensen, James I Hudson, Caitlin E Coit, Ashley Beaulieu, Harrison G Pope, Perry F Renshaw, Bruce M Cohen

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical psychopharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 4 pooled it
1.9field-weighted citation impact, top 14% 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

24 citing papers in PubMed, 4 syntheses or guidelines pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. A Systematic Review of Nutraceuticals for the Treatment of Bipolar Disorder.Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2021
    Pooled it
  3. Pooled it
  4. Guideline
  5. Trial
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Carnitine and Depression.Frontiers in nutrition · 2022
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Targeting Mitochondrial Dysfunction for Bipolar Disorder.Current topics in behavioral neurosciences · 2021
    Review
  17. Review
  18. Article
  19. Review
  20. Review
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

8 authors at 4 institutions in 1 country.

Brian P BrennanBiological Psychiatry Laboratory, McLean Hospital, Belmont, MA 02478, USA. bbrennan@partners.org
John Eric Jensen
James I Hudson
Caitlin E Coit
Ashley Beaulieu
Harrison G Pope
Perry F Renshaw
Bruce M Cohen
Harvard University · USMcLean Hospital · USImaging Center · USUniversity of Utah · US

Funding

PROTON MRSI STUDIES OF BIPOLAR DISORDERR01MH058681 · NIMH · UNIVERSITY OF UTAH · PI RENSHAW, PERRY FRANKLIN · 1999 to 2009
$3.0M
DRUG ABUSE RESEARCH TRAINING PROGRAMT32DA007252 · NIDA · MC LEAN HOSPITAL (BELMONT, MA) · PI MELLO, NANCY K. · 1991 to 2011
$3.0M
Mentoring in Drug Abuse NeuroimagingK05DA031247 · NIDA · UNIVERSITY OF UTAH · PI RENSHAW, PERRY FRANKLIN · 2011 to 2015
$661k
NIDA NIH HHS K05 DA031247NIDA NIH HHS T32 DA007252NIDA NIH HHS T32-DA07252NIMH NIH HHS R01 MH058681
6 · The paper itself

Abstract

backgroundBipolar disorder may be associated with mitochondrial dysfunction. Therefore, agents that enhance mitochondrial functioning may be efficacious in bipolar disorder. We performed a randomized placebo-controlled trial of the mitochondrial enhancers acetyl-L-carnitine (ALCAR) and α-lipoic acid (ALA) in patients with bipolar depression, and assessed markers of cerebral energy metabolism using phosphorus magnetic resonance spectroscopy.

methodsWe administered ALCAR (1000-3000 mg daily) plus ALA (600-1800 mg daily) or placebo for 12 weeks to 40 patients with bipolar depression and obtained imaging data at baseline, week 1, and week 12 of treatment in 20 patients using phosphorus 3-dimensional chemical-shift imaging at 4 T. Statistical analysis used random effects mixed models.

resultsWe found no significant difference between ALCAR/ALA and placebo on change from baseline in the Montgomery-Asberg Depression Rating Scale in both the longitudinal (mean difference [95% confidence interval], -1.4 [-6.2 to 3.4], P = 0.58) and last-observation-carried-forward (-3.2 [-7.2 to 0.9], P = 0.12) analyses. ALCAR/ALA treatment significantly reduced phosphocreatine levels in the parieto-occipital cortex at week 12 (P = 0.002). Reduction in whole brain total nucleoside triphosphate levels from baseline to week 1 was associated with reduction in Montgomery-Asberg Depression Rating Scale scores (P = 0.02) in patients treated with ALCAR/ALA. However, this was likely a chance finding attributable to multiple statistical comparisons.

conclusionsTreatment with ALCAR and ALA at the dose and duration used in this study does not have antidepressant effects in depressed bipolar patients and does not significantly enhance mitochondrial functioning in this patient group.

Indexed as

AcetylcarnitineAdultAntidepressive AgentsBipolar DisorderBrainChi-Square DistributionDrug Therapy, CombinationEnergy MetabolismFemaleHumansLinear ModelsMagnetic Resonance SpectroscopyMaleMiddle AgedMitochondriaPhosphocreatineAcetylcarnitineAntidepressive AgentsPhosphocreatineThioctic Acid

Identifiers

PMID23948785
PMCPMC4699308
OpenAlexW2320624499

What OpenQuestion holds

Textmetadata
LicenceTDM
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.