Evidence map›Paper›PMID 38939036›Full record

ArticleJACC. Advances2023

Genetic Backgrounds Associated With Stent Thrombosis: A Pilot Study From a Percutaneous Coronary Intervention Registry.

Satoshi Shoji, Mitsuaki Sawano, Taku Inohara, Takahiro Hiraide, Ikuko Ueda, Masahiro Suzuki, Shigetaka Noma, Keiichi Fukuda, Shun Kohsaka

Abstract read
In one paragraph

Article in JACC. Advances, 2023. 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

9 authors.

Satoshi ShojiDepartment of Cardiology, Keio University School of Medicine, Tokyo, Japan.
Mitsuaki SawanoDepartment of Cardiology, Keio University School of Medicine, Tokyo, Japan; Section of Cardiovascular Medicine, Department of Internal Medicine, Center for Outcomes Research and Evaluation, Yale New Haven Hospital, New Haven, Connecticut, USA.
Taku InoharaDepartment of Cardiology, Keio University School of Medicine, Tokyo, Japan.
Takahiro HiraideDepartment of Cardiology, Keio University School of Medicine, Tokyo, Japan.
Ikuko UedaDepartment of Cardiology, Keio University School of Medicine, Tokyo, Japan.
Masahiro SuzukiDepartment of Cardiology, National Hospital Organization Saitama Hospital, Saitama, Japan.
Shigetaka NomaDepartment of Cardiology, Saiseikai Utsunomiya Hospital, Tochigi, Japan.
Keiichi FukudaDepartment of Cardiology, Keio University School of Medicine, Tokyo, Japan.
Shun KohsakaDepartment of Cardiology, Keio University School of Medicine, Tokyo, Japan. Electronic address: sk@keio.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Stent thrombosis (ST) is a rare, yet devastating, complication following percutaneous coronary intervention (PCI), with poorly understood pathophysiologic characteristics and genetic backgrounds. Objectives: The authors performed a genome-wide association study to identify the common genetic loci associated with early stent thrombosis (EST) and late/very late ST (LST/VLST) in a contemporary Japanese multicenter PCI registry. Methods: Among 8,642 PCI patients included in the registry, 42 who experienced stent thrombosis [EST (n = 15) and LST/VLST (n = 27)] were included (mean age, 67.6 ± 10.8 years; and 88.1% men). We conducted a genome-wide association study using the BioBank Japan patient population as the control (control #1: acute coronary syndrome [n = 29,542] and control #2: effort angina [n = 8,900]) to identify significant single nucleotide polymorphisms (SNPs) and evaluate the performance of polygenic risk scores (PRSs) for predicting these conditions. Results: We compared patients with EST with controls #1 and #2 and identified SNPs (rs565401593 and rs561634568) in Conclusions: We identified different genetic predispositions between EST and LST/VLST and demonstrated that the incorporation of PRS may aid in risk prediction of this highly fatal event.

Indexed as

early stent thrombosisgenome-wide association studylate stent thrombosispercutaneous coronary interventionpolygenic risk scoresingle nucleotide polymorphism

Identifiers

PMID38939036
PMCPMC11198226

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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.