Evidence map›Paper›PMID 19676097›Full record

Trial reportAmerican journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics2010

FKBP5 polymorphisms and antidepressant response in geriatric depression.

Jane E Sarginson, Laura C Lazzeroni, Heather S Ryan, Alan F Schatzberg, Greer M Murphy

Open access · greenAbstract readRandomized Controlled Trial
In one paragraph

Trial report in American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 3 pooled it
1.6field-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

16 citing papers in PubMed, 3 syntheses or guidelines pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Mirtazapine versus other antidepressive agents for depression.The Cochrane database of systematic reviews · 2011
    Pooled it
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. From pharmacogenetics to pharmacogenomics: the way toward the personalization of antidepressant treatment.Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2014
    Review
  14. Review
  15. Article
  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

5 authors at 1 institution in 1 country.

Jane E SarginsonDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California.
Laura C LazzeroniDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California.
Heather S RyanDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California.
Alan F SchatzbergDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California.
Greer M MurphyDepartment of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California.
Stanford University · US

Funding

Pharmacogenetics of the Antidepressant Response in Geriatric Major DepressionR01MH073914 · NIMH · STANFORD UNIVERSITY · PI MURPHY, GREER M · 2006 to 2010
$1.8M
NIMH NIH HHS R01 MH073914
6 · The paper itself

Abstract

Genetic variation at the FKBP5 locus has been reported to affect clinical outcomes in patients treated with antidepressant medications in several studies. However, other reports have not confirmed this association. FKBP5 may regulate the sensitivity of the hypothalamic-pituitary-adrenal axis. We tested two FKBP5 single nucleotide polymorphisms (rs1360780 and rs3800373) in a sample of 246 geriatric patients treated for 8 weeks in a double-blind randomized comparison trial of paroxetine and mirtazapine. These two polymorphisms had previously been reported to predict efficacy in depressed patients treated with selective serotonin reuptake inhibitors such as paroxetine, and those treated with mirtazapine, an agent with both serotonergic and noradrenergic actions. However, we found no significant associations between these FKBP5 genetic variants and clinical outcomes. Neither mean Hamilton Depression Rating Scale scores nor time to remission or response were predicted by FKBP5 genetic variation. These results suggest that FKBP5 is unlikely to play a major role in determining antidepressant treatment outcomes in geriatric patients.

Indexed as

Polymorphism, GeneticAgedAntidepressive AgentsDepressionDouble-Blind MethodFemaleGenetic VariationGeriatricsHumansMaleMianserinMirtazapineParoxetineSequence Analysis, DNATacrolimus Binding Protein 5Tacrolimus Binding ProteinsAntidepressive AgentsMianserinMirtazapineParoxetineTacrolimus Binding Protein 5Tacrolimus Binding Proteins

Identifiers

PMID19676097
PMCPMC2897151
OpenAlexW2156586486

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.