Evidence map›Paper›PMID 28031712›Full record

ArticleNeuropsychiatric disease and treatment2017

Minocycline and celecoxib as adjunctive treatments for bipolar depression: a study protocol for a multicenter factorial design randomized controlled trial.

Muhammad I Husain, Imran B Chaudhry, Munir M Hamirani, Fareed A Minhas, Ajmal Kazmi, John Hodsoll, Peter M Haddad, John Fw Deakin, Nusrat Husain, Allan H Young

Open access · goldAbstract read
In one paragraph

Article in Neuropsychiatric disease and treatment, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Anti-Inflammatory Therapy as a Promising Target in Neuropsychiatric Disorders.Advances in experimental medicine and biology · 2023
    Review
  4. New Pharmacological Interventions in Bipolar Disorder.Current topics in behavioral neurosciences · 2021
    Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Altered neuro-inflammatory gene expression in hippocampus in major depressive disorder.Progress in neuro-psychopharmacology & biological psychiatry · 2018
    Article
  10. Inflammatory Mediators in Mood Disorders: Therapeutic Opportunities.Annual review of pharmacology and toxicology · 2018
    Review
  11. Article
  12. 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

10 authors at 7 institutions in 4 countries.

Muhammad I HusainCamden and Islington NHS Foundation Trust, St Pancras Hospital, London, UK.
Imran B ChaudhryPakistan Institute of Learning and Living.
Munir M HamiraniDepartment of Psychiatry, Abbasi Shaheed Hospital, Karachi.
Fareed A MinhasInstitute of Psychiatry, Rawalpindi Medical College, Rawalpindi.
Ajmal KazmiDepartment of Psychiatry, Karwan-e-Hayat Hospital, Karachi, Pakistan.
John HodsollDepartment of Psychological Medicine, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London.
Peter M HaddadDivision of Psychology and Mental Health, University of Manchester, Manchester.
John Fw DeakinDivision of Psychology and Mental Health, University of Manchester, Manchester.
Nusrat HusainDivision of Psychology and Mental Health, University of Manchester, Manchester.
Allan H YoungCentre for Affective Disorders, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
University of Manchester · GBKing's College London · GBAbbasi Shaheed Hospital · PKCivil Hospital Karachi · PKPakistan Institute of Learning and Living · PKRawalpindi Medical University · PKSt Pancras Hospital · GB

Funding

Medical Research Council MC_PC_11003
6 · The paper itself

Abstract

backgroundEvidence suggests that the use of anti-inflammatory agents may improve depressive symptoms in patients with bipolar affective disorder. However, there are few well-designed clinical trials demonstrating the efficacy of these newer treatment strategies. PATIENTS AND

methodsThis is a multicenter, 3-month, randomized, placebo-controlled, double-blind, factorial design trial of minocycline and/or celecoxib added to TAU for the treatment of depressive symptoms in patients experiencing a DSM-5 bipolar I or II disorder and a current major depressive episode. A total of 240 participants will undergo screening and randomization followed by four assessment visits. The primary outcome measure will be mean change from baseline to week 12 on the Hamilton Depression Scale scores. Clinical assessments using the Clinical Global Impression scale, Patient Health Questionnaire-9, and the Generalized Anxiety Disorder 7-item scale will be carried out at every visit as secondary outcomes. Side-effect checklists will be used to monitor the adverse events at each visit. Complete blood count and plasma C-reactive protein will be measured at baseline and at the end of the treatment. Minocycline will be started at 100 mg once daily and increased to 200 mg at 2 weeks. Celecoxib will be started at 200 mg once daily and increased to 400 mg at 2 weeks. DISCUSSION: Anti-inflammatory agents have been shown to be potentially efficacious in the treatment of depressive symptoms. The aim of this study is to determine whether the addition of minocycline and/or celecoxib to TAU improves depressive symptoms in patients with bipolar affective disorder.

Indexed as

anti-inflammatorybipolar disordercelecoxibdepressioninflammationminocycline

Identifiers

PMID28031712
PMCPMC5182039
OpenAlexW2564816824

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.