Evidence map›Paper›PMID 42056077›Full record

Observational studyThe pharmacogenomics journal2026

CYPRI: a clinical decision-making tool to select psychiatric patients for pharmacogenetic testing.

Ivana Tašková, Nicole Šafářová, Martina Hahn

Abstract readObservational Study
In one paragraph

Observational study in The pharmacogenomics journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

3 authors.

Ivana TaškováDepartment of Clinical Pharmacy, Psychiatric Hospital Bohnice, Prague, Czech Republic.ORCID 0000-0001-8866-3834
Nicole ŠafářováDepartment of Clinical Pharmacy, Psychiatric Hospital Bohnice, Prague, Czech Republic.
Martina HahnDepartment of Psychiatry, Psychosomatics and Psychotherapy, University Medicine Frankfurt, Goethe University, Frankfurt am Main, Germany. m.hahn@med.uni-frankfurt.de.ORCID 0000-0001-8355-8584

Funding

Non-US Government Research Support type
6 · The paper itself

Abstract

Pharmacogenetic (PGx) testing of cytochrome P450 (CYP) enzymes CYP2D6 and CYP2C19 is increasingly utilised to personalise psychopharmacological treatment, but clear criteria for patient selection are lacking. We developed and conducted a pilot evaluation of a clinical decision-making tool, the CYPRI (CYP Pharmacogenetic Risk Index), which uses routinely available clinical and pharmacological data to estimate the likelihood of a clinically relevant and actionable PGx testing result. A pilot observational study involving 34 patients was conducted at Psychiatric Hospital Bohnice in Prague, Czech Republic. A significant correlation was observed between the CYPRI score and the IMPACT score (ordinal logistic regression: t = 3.279, p = 0.0011; Kendall's τ = 0.46, p = 0.0011). Discriminative ability was high, with an area under the curve (AUC) of 0.83 (95% CI: 0.69-0.97), based on ROC analysis performed using two outcome categories (0-2 vs. ≥ 2 points of IMPACT score). The optimal cut-off was 4. The CYPRI score offers a straightforward method to prioritise patients for PGx testing, potentially enhancing cost-effectiveness and clinical outcomes in psychiatric care.

Indexed as

Clinical Decision-MakingCytochrome P-450 CYP2C19Cytochrome P-450 CYP2D6Mental DisordersPatient SelectionPharmacogenomic TestingAdultFemaleHumansMaleMiddle AgedPharmacogeneticsPilot ProjectsCYP2C19 protein, humanCytochrome P-450 CYP2C19Cytochrome P-450 CYP2D6

Identifiers

PMID42056077
PMCPMC13128436

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Registered trials

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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.