Evidence map›Paper›PMID 25980509›Full record

ReviewCurrent psychiatry reports2015

Pharmacogenetics of major depressive disorder: top genes and pathways toward clinical applications.

Chiara Fabbri, Alessandro Serretti

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Current psychiatry reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02625155 (Standard of Care Versus Urine Testing With Selective PHarmacogenomics for Effective Drug and Dosing REgimens), which is not on this map. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 pooled it
3.7field-weighted citation impact, top 6% 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.

NCT02625155 phase4unknown statusnot on this map

Standard of Care Versus Urine Testing With Selective PHarmacogenomics for Effective Drug and Dosing REgimens: SPHERE

TypeinterventionalSponsorInSource DiagnosticsRan2015Enrolled14,000ConditionsTarget Drug-related Adverse EventsArmsUrine diagnostic testing as SOC, drug regimen changes per SOC, Urine diagnostic testing with selective PGx testing, drug regimen changes based on PGx test results
3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 3 syntheses or guidelines pooled it, 85 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
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  8. Precision medicine in mental health: applications, challenges, and recommendations.European psychiatry : the journal of the Association of European Psychiatrists · 2026
    Review
  9. Article
  10. Review
  11. Review
  12. E3 Ubiquitin LigaseInternational journal of molecular sciences · 2024
    Article
  13. Article
  14. Precision medicine in mood disorders.PCN reports : psychiatry and clinical neurosciences · 2022
    Review
  15. Review
  16. Article
  17. Review
  18. The genetics of bipolar disorder.Molecular psychiatry · 2020
    Review
  19. Review
  20. 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

2 authors at 1 institution in 1 country.

Chiara FabbriDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Viale Carlo Pepoli 5, 40123, Bologna, Italy, chiara.fabbri@yahoo.it.
Alessandro Serretti
University of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pharmacogenetics of antidepressants has been not only a challenging but also frustrating research field since its birth in the 1990s. Indeed, great expectations followed the first evidence of familiar aggregation of antidepressant response. Despite the progress from candidate gene studies to genome-wide association studies (GWAS), results fell out the expectations and they were often inconsistent. Anyway, the cumulative evidence supports the involvement of some genes and molecular pathways in antidepressant efficacy. The best single genes are SLC6A4, HTR2A, BDNF, GNB3, FKBP5, ABCB1, and cytochrome P450 genes (CYP2D6 and CYP2C19). Molecular pathways involved in inflammation and neuroplasticity show the greatest support. The first studies evaluating benefits of genotype-guided antidepressant treatments provided encouraging results and confirmed the relevance of SLC6A4, HTR2A, ABCB1, and cytochrome P450 genes. Further progress in genotyping and data analysis would allow to move forward and complete the understanding of antidepressant pharmacogenetics and its translation into clinical applications.

Indexed as

Signal TransductionAntidepressive AgentsATP Binding Cassette Transporter, Subfamily BCytochrome P-450 Enzyme SystemGenome-Wide Association StudyGenotypeHumansMajor Depressive DisorderNeuronal PlasticityPharmacogeneticsReceptors, Serotonin, 5-HT2Serotonin Plasma Membrane Transport ProteinsABCB1 protein, humanAntidepressive AgentsATP Binding Cassette Transporter, Subfamily BCytochrome P-450 Enzyme SystemReceptors, Serotonin, 5-HT2Serotonin Plasma Membrane Transport ProteinsSLC6A4 protein, human

Identifiers

PMID25980509
OpenAlexW2096927391

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.