Evidence map›Paper›PMID 42516561›Full record

ArticleFrontiers in pharmacology2026

Association of decreased CYP2C9 function,

Chutima Seree-Aphinan, Antida Sangiemchoey, Suwanna Setthawatcharawanich, Sutthiporn Pattharachayakul, Areerat Hnoonual, Warit Ruanglertboon, Porntip Intapiboon, Anukoon Kaewborisutsakul, Titaporn Thamcharoenvipas, Pornruedee Rachatawiriyakul and 4 more

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Chutima Seree-AphinanDepartment of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai/Songkhla, Thailand.
Antida SangiemchoeyDivision of Pharmacy, Songklangarind Hospital, Faculty of Medicine, Prince of Songkla University, Hat Yai/Songkhla, Thailand.
Suwanna SetthawatcharawanichDepartment of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai/Songkhla, Thailand.
Sutthiporn PattharachayakulDepartment of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai/Songkhla, Thailand.
Areerat HnoonualDepartment of Pathology, Faculty of Medicine, Prince of Songkla University, Hat Yai/Songkhla, Thailand.
Warit RuanglertboonDepartment of Pharmacology, Faculty of Science, Prince of Songkla University, Hat Yai/Songkhla, Thailand.
Porntip IntapiboonDepartment of Internal Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai/Songkhla, Thailand.
Anukoon KaewborisutsakulNeurological Surgery Unit, Department of Surgery, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, Thailand.
Titaporn ThamcharoenvipasDepartment of Pediatrics, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
Pornruedee RachatawiriyakulDepartment of Pediatrics, Faculty of Medicine, Prince of Songkla University, Songkhla, Thailand.
Tabtim ChongsuvivatwongDivision of Neurology, Department of Medicine, Hat Yai Medical Education Center, Hat Yai, Songkhla, Thailand.
Sirianong SittipongSongkhla Hospital, Songkhla, Thailand.
Chonlaphat SukasemDepartment of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Kanoot JaruthamsophonDepartment of Pathology, Faculty of Medicine, Prince of Songkla University, Hat Yai/Songkhla, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Phenytoin is an anticonvulsant used to treat epilepsy and prevent perioperative seizures. However, genetic prediction of phenytoin-induced cutaneous adverse reactions (PHT-cADRs) and the co-contributing role of non-genetic factors remain unclear. We aimed to evaluate genetic and non-genetic factors associated with PHT-cADRs in a Southern Thai population. Methods: A case-control study was conducted involving 104 patients (26 with PHT-cADRs confirmed by a dermatologist or allergist and 78 phenytoin-tolerant controls). Patient history (demographics, comorbidities, and co-medications) and laboratory parameters (complete blood count and clinical chemistry indicators) during phenytoin initiation were reviewed. Genetic markers including Results: A significant difference in sex was observed among the patients (73.1% female patients in the PHT-cADR group vs. 44.9% in the control group; P = 0.014). Baseline clinical indications differed marginally between the groups; the case group had more neurosurgical patients and fewer patients with epilepsy than the control group. Other non-genetic factors were not significantly associated with PHT-cADRs. For laboratory data, the case group showed significantly lower mean hemoglobin (11.73 g/dL vs. 13.48 g/dL, P = 0.0005) and hematocrit levels (35.94% vs. 40.29%, P = 0.0019) and a higher mean white blood cell count (10.19 × 10 Conclusion:

Indexed as

drug allergydrug eruptionspharmacogeneticspharmacological biomarkersprecision medicine

Identifiers

PMID42516561
PMCPMC13402506

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.