Evidence map›Paper›PMID 35535391›Full record

ArticleJournal of clinical laboratory analysis2022

CYP2S1 rs338599 polymorphism confers reduced risk to anti-tuberculosis drug-induced liver injury and may be a novel marker for its risk prediction.

Liyuan Wang, Hui Wang, Ying Qi

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

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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 at 1 institution in 1 country.

Liyuan WangDepartment of Tuberculosis, Affiliated Hospital of Hebei University, Baoding, China.
Hui WangDepartment of Tuberculosis, Affiliated Hospital of Hebei University, Baoding, China.
Ying QiDepartment of Tuberculosis, Affiliated Hospital of Hebei University, Baoding, China.ORCID https://orcid.org/0000-0003-4987-0982
Affiliated Hospital of Hebei University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn the present study, we would like to explore whether Cytochrome P450 2S1 (CYP2S1) rs338599 polymorphism confers risk to anti-tuberculosis drug-induced liver injury (ADLI) and provide evidence of being used as novel marker for ADLI risk prediction. PATIENTS AND

methodsA total of 162 pulmonary tuberculosis patients admitted to Affiliated Hospital of Hebei University from August 2018 to March 2021 were selected. Patients who developed into ADLI were assigned as ADLI group (n = 50), and those who did not developed into ADLI were assigned as non-ADLI group (n = 112). The CYP2S1 rs338599 polymorphism was detected by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method using binary logistic regression analyses through adjusting for age and sex.

resultsNo difference was detected in age, sex, smoking status, profession, education level, marital status, alcohol consumption, or using liver-protecting drugs (p > 0.05). Compared with non-ADLI group, GG genotype and G allele were significantly higher in ADLI group (p < 0.05).

conclusionOur results indicated that CYP2S1 rs338599 polymorphism conferred reduced risk to ADLI. The tuberculosis patients who had GG genotype or G allele were not susceptible to ADLI. CYP2S1 rs338599 polymorphism may be a novel marker for ADLI risk prediction.

Indexed as

Chemical and Drug Induced Liver InjuryTuberculosisBiomarkersCytochrome P-450 Enzyme SystemHumansPolymorphism, GeneticPolymorphism, Restriction Fragment LengthBiomarkersCYP2S1 protein, humanCytochrome P-450 Enzyme Systemanti-tuberculosis drug-induced liver injuryCYP2S1gene polymorphismnovel markerrisk prediction

Identifiers

PMID35535391
PMCPMC9169199
OpenAlexW4229444052

What OpenQuestion holds

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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.