Evidence map›Paper›PMID 26256966›Full record

ArticleYonsei medical journal2015

eNOS3 Genetic Polymorphism Is Related to Post-Ablation Early Recurrence of Atrial Fibrillation.

Jaemin Shim, Jae Hyung Park, Ji-Young Lee, Jae Sun Uhm, Boyoung Joung, Moon-Hyoung Lee, Patrick T Ellinor, Hui-Nam Pak

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Yonsei medical journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Functional Role and Mechanism of microRNA-28b in Atrial Myocyte in a Persistent Atrial Fibrillation Rat Model.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Jaemin ShimDepartment of Cardiology, Korea University Anam Hospital, Seoul, Korea.
Jae Hyung ParkDepartment of Cardiology, Yonsei University Health System, Seoul, Korea.
Ji-Young LeeDepartment of Cardiology, Yonsei University Health System, Seoul, Korea.
Jae Sun UhmDepartment of Cardiology, Yonsei University Health System, Seoul, Korea.
Boyoung JoungDepartment of Cardiology, Yonsei University Health System, Seoul, Korea.
Moon-Hyoung LeeDepartment of Cardiology, Yonsei University Health System, Seoul, Korea.
Patrick T EllinorCardiac Arrhythmia Service & Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA.
Hui-Nam PakCardiovascular Genome Center, Yonsei University Health System, Seoul, Korea.
Yonsei University Health System · KRKorea University Medical Center · KRMassachusetts General Hospital · US

Funding

IDENTIFICATION OF COMMON GENETIC VARIANTS FOR ATRIAL FIBRILLATION AND PR INTERVALR01HL092577 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2009 to 2025
$20.6M
NHLBI NIH HHS R01 HL092577
6 · The paper itself

Abstract

purposePrevious studies have demonstrated an association between eNOS polymorphisms and atrial fibrillation (AF). We sought to determine whether eNOS polymorphisms are associated with AF recurrence after a radiofrequency catheter ablation (RFCA). MATERIALS AND

methodsA total of 500 consecutive patients (56±11 years, 77% male) with paroxysmal (68%) or persistent (32%) AF who underwent RFCA and 500 age, gender-matched controls were genotyped for the eNOS3 single nucleotide polymorphism (rs1799983). AF recurrence was monitored according to 2012 ACC/AHA/ESC guidelines.

resultsThe frequencies of the rs1799983 variant alleles (T) in the case and control group were not significantly different (OR 1.05, 95% CI 0.75-1.46, p=0.798). AF patients with rs1799983 variants were more likely to have coronary artery disease or stroke than those without genetic variant at this gene (31.0% vs. 17.3%, p=0.004). During mean 17 months follow-up, early recurrence of AF (ERAF; within 3 months) and clinical recurrence (CR) of AF were 31.8% and 24.8%, respectively. The rs1799983 variant was associated with higher risk of ERAF (OR 1.71, 95% CI 1.06-2.79, p=0.028), but not with CR. ERAF occurred earlier (11±16 days) in variant group than those without variant allele (20±25 days, p=0.016). A multiple logistic regression analysis showed that presence of the rs1799983 variant (OR 1.75, 95% CI 1.07-2.86, p=0.026) and persistent AF were independent predictors for ERAF after AF ablation.

conclusionThe rs1799983 variant of the eNOS3 gene was associated with ERAF, but not with CR, after RFCA. eNOS3 gene variants may have a potential role for stratification of post-ablation management.

Indexed as

Catheter AblationAgedAllelesAtrial FibrillationCase-Control StudiesCoronary Artery DiseaseFemaleFollow-Up StudiesGenotypeHumansLogistic ModelsMaleMiddle AgedNitric Oxide Synthase Type IIIPolymorphism, Single NucleotideRecurrenceNitric Oxide Synthase Type IIINOS3 protein, humanAtrial fibrillationcatheter ablationeNOS generecurrence

Identifiers

PMID26256966
PMCPMC4541653
OpenAlexW1951243362

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.