Evidence map›Paper›PMID 30487649›Full record

Observational studyActa pharmacologica Sinica2019

Influences of an NR1I2 polymorphism on heterogeneous antiplatelet reactivity responses to clopidogrel and clinical outcomes in acute ischemic stroke patients.

Yi-Bei Chen, Zi-Yi Zhou, Guo-Min Li, Can-Xing Xiao, Wei-Bang Yu, Shi-Long Zhong, Ye-Feng Cai, Jing Jin, Min Huang

Open access · bronzeAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Acta pharmacologica Sinica, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.2field-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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. The role ofExpert review of clinical pharmacology · 2022
    Pooled it
  2. Recent research progress on the mechanisms of clopidogrel resistance.European journal of clinical pharmacology · 2026
    Review
  3. Article
  4. Mechanisms and Therapeutic Advances of PXR in Metabolic Diseases and Cancer.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Article
  7. Aspects of xenobiotics and their receptors in stroke.Neuroprotection (Chichester, England) · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. 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

9 authors at 3 institutions in 1 country.

Yi-Bei ChenInstitute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Zi-Yi ZhouGuangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.
Guo-Min LiGuangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China.
Can-Xing XiaoInstitute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Wei-Bang YuInstitute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Shi-Long ZhongMedical Research Center of Guangdong General Hospital, Guangzhou, 510080, China. zhongsl@hotmail.com.
Ye-Feng CaiGuangdong Provincial Hospital of Chinese Medicine, Guangzhou, 510120, China. caiyefeng@126.com.
Jing JinInstitute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China. jinjing@mail.sysu.edu.cn.
Min HuangInstitute of Clinical Pharmacology, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Sun Yat-sen University · CNGuangdong Provincial Hospital of Traditional Chinese Medicine · CNGuangdong General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pregnane X receptor (PXR) is a member of nuclear receptor subfamily 1 (NR1I2) that is a transcriptional regulator of several metabolic enzymes involved in clopidogrel metabolism. In this study we identified and evaluated the contributions of single nucleotide polymorphisms (SNPs) in NR1I2 and cytochrome P450 (CYP) 2C19 alleles to clopidogrel resistance (CR) and long-term clinical outcomes in acute ischemic stroke (IS) patients. A total of 634 patients with acute IS were recruited, who received antiplatelet medication (clopidogrel or aspirin) every day and completed a 1-year follow-up. The selected SNPs were genotyped, and platelet function was measured. Modified Rankin Scale (mRS) scores and main adverse cardiovascular and cerebrovascular events (MACCE) were noted to assess the prognosis. We showed that SNPs NR1I2 rs13059232 and CYP2C19 alleles (2*/3*) were related to CR. SNP NR1I2 (rs13059232) was identified as an independent risk factor for the long-term clinical outcomes in the clopidogrel cohorts (P < 0.001), but similar results were not observed in a matched aspirin cohort (P > 0.05). Our results suggest that NR1I2 variant (rs13059232) could serve as biomarker for clopidogrel therapy and individualized antiplatelet medications in the treatment of acute IS patients.

Indexed as

Polymorphism, Single NucleotideAcute DiseaseAgedAged, 80 and overAspirinBrain InfarctionClopidogrelCohort StudiesCytochrome P-450 CYP2C19FemaleHumansMaleMiddle AgedPlatelet AggregationPlatelet Aggregation InhibitorsPregnane X ReceptorAspirinClopidogrelCYP2C19 protein, humanCytochrome P-450 CYP2C19NR1I2 protein, humanPlatelet Aggregation InhibitorsPregnane X Receptoracute ischemic strokeanti-platelet medicationaspirinclopidogrelindividualized medicationNR1I2

Identifiers

PMID30487649
PMCPMC6786370
OpenAlexW2902200738

What OpenQuestion holds

Textmetadata
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.