Evidence map›Paper›PMID 31895922›Full record

ArticlePloS one2020

Fragmented QRS complex in patients with systemic lupus erythematosus at the time of diagnosis and its relationship with disease activity.

Masahiro Hosonuma, Nobuyuki Yajima, Ryo Takahashi, Ryo Yanai, Taka-Aki Matsuyama, Eiji Toyosaki, Jumpei Saito, Kengo Kusano, Hiroshi Morita

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. 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
0.9field-weighted citation impact, top 27% 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, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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 4 institutions in 1 country.

Masahiro HosonumaDivision of Rheumatology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.ORCID 0000-0002-5861-7543
Nobuyuki YajimaDivision of Rheumatology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Ryo TakahashiDivision of Rheumatology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Ryo YanaiDivision of Rheumatology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Taka-Aki MatsuyamaDepartment of Legal Medicine, Showa University, School of Medicine, Tokyo, Japan.
Eiji ToyosakiDivision of Cardiology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Jumpei SaitoDivision of Cardiology, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Kengo KusanoDivision of Arrhythmia and Electrophysiology, Department of Cardiovascular Medicine, National Cerebral and Cardiovascular Center, Osaka, Japan.
Hiroshi MoritaDepartment of Cardiovascular Therapeutics, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.
Showa University · JPNational Cerebral and Cardiovascular Center · JPOkayama University · JPShowa University Northern Yokohama Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCardiovascular disease is an important contributor to the mortality rate of patients with systemic lupus erythematosus (SLE), which is related to SLE disease activity. Fragmented QRS (fQRS) complexes, defined by additional spikes in the QRS complex, are useful for identifying myocardial scars on electrocardiography and can be an independent predictor of cardiac events. We aimed to assess the relationship between disease activity in patients with SLE and fQRS at the time of diagnosis.

methodsForty-four patients with SLE were included. Patients with cardiac diseases, other rheumatic diseases, and prior treatment at the time of electrocardiography measurement were excluded. The appearance of fQRS represented exposure. The primary outcome was SLE Disease Activity Index 2000 (SLEDAI-2K). Multiple regression analysis was conducted to assess the association between fQRS and SLEDAI-2K adjusted for age, sex, and time from the estimated onset date to the date of diagnosis.

resultsAmong patients with SLE at diagnosis, 26 (59.1%) had fQRS. The median SLEDAI-2K was 18 (interquartile range [IQR], 12-22) and 9 (IQR, 8-15) in the fQRS(+) and fQRS(-) groups, respectively. SLEDAI-2K was significantly higher in the fQRS(+) group than in the fQRS(-) group (regression coefficient, 2.69; 95% confidence interval, 0.76-4.61; p = 0.008).

conclusionOur results suggested that fQRS(+) patients with SLE had high disease activity. fQRS could likely detect subclinical myocardial involvement in patients with SLE and predict long-term occurrence of cardiac events.

Indexed as

AdolescentAdultChildDiagnostic Techniques, CardiovascularElectrocardiographyFemaleHeart DiseasesHumansLupus Erythematosus, SystemicMaleMiddle AgedMultivariate AnalysisPredictive Value of TestsRetrospective StudiesSeverity of Illness IndexYoung Adult

Identifiers

PMID31895922
PMCPMC6939939
OpenAlexW2997378949

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.