Evidence map›Paper›PMID 28696415›Full record

ArticleThe pharmacogenomics journal2018

Genome-wide association studies of placebo and duloxetine response in major depressive disorder.

M Maciukiewicz, V S Marshe, A K Tiwari, T M Fonseka, N Freeman, J L Kennedy, S Rotzinger, J A Foster, S H Kennedy, D J Müller

Abstract read
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Precision Medicine in Antidepressants Treatment.Handbook of experimental pharmacology · 2023
    Review
  8. Article
  9. Article
  10. Article
  11. Drug-Placebo Additivity in Randomized Clinical Trials.Clinical pharmacology and therapeutics · 2019
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. 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

10 authors at 5 institutions in 1 country.

M MaciukiewiczPharmacogenetic Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
V S MarshePharmacogenetic Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
A K TiwariPharmacogenetic Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
T M FonsekaPharmacogenetic Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
N FreemanPharmacogenetic Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
J L KennedyPharmacogenetic Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
S RotzingerDepartment of Psychiatry, University of Toronto, Toronto, ON, Canada.
J A FosterDepartment of Psychiatry and Behavioral Neurosciences, McMaster University, Hamilton, ON, Canada.
S H KennedyDepartment of Psychiatry, University of Toronto, Toronto, ON, Canada.
D J MüllerPharmacogenetic Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON, Canada.
Centre for Addiction and Mental Health · CAUniversity Health Network · CAMcMaster University · CASt. Michael's Hospital · CAUniversity of Toronto · CA

Funding

CIHR
6 · The paper itself

Abstract

We investigated variants associated with treatment response in depressed patients treated with either the antidepressant duloxetine or placebo using a genome-wide approach. Our sample (N=391) included individuals aged 18-75 years, diagnosed with major depressive disorder and treated with either duloxetine or placebo for up to 8 weeks. We conducted genome-wide associations for treatment response as operationalized by percentage change in Montgomery-Åsberg Depression Rating Scale score from baseline, as well as mixed models analyses across five time points. In the placebo-treated subsample (N=205), we observed a genome-wide association with rs76767803 (β=0.69, P=1.25 × 10

Indexed as

Genome-Wide Association StudyAdolescentAdultAgedAntidepressive AgentsCD56 AntigenDNA-Binding ProteinsDouble-Blind MethodDuloxetine HydrochlorideFemaleGenotypeHumansMajor Depressive DisorderMaleMiddle AgedNerve Tissue ProteinsAntidepressive AgentsCD56 AntigenDNA-Binding ProteinsDuloxetine HydrochlorideKMT2E protein, humanNCAM1 protein, humanNerve Tissue ProteinsPlacebosSTAC protein, humanTranscription FactorsZNF385D protein, human

Identifiers

PMID28696415
OpenAlexW2734841827

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.