Evidence map›Paper›PMID 33533258›Full record

Observational studyJournal of the American Heart Association2021

Risk of QTc Interval Prolongation Associated With Circulating Anti-Ro/SSA Antibodies Among US Veterans: An Observational Cohort Study.

Pietro Enea Lazzerini, Gabriele Cevenini, Yongxia Sarah Qu, Frank Fabris, Nabil El-Sherif, Maurizio Acampa, Alessandra Cartocci, Franco Laghi-Pasini, Pier Leopoldo Capecchi, Mohamed Boutjdir and 1 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Journal of the American Heart Association, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 27 citations in OpenAlex.

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  3. Arrhythmias in Autoimmune Diseases: Immune-Mediated Mechanisms and Management.Journal of cardiovascular development and disease · 2026
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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

11 authors at 3 institutions in 2 countries.

Pietro Enea LazzeriniDepartment of Medical Sciences Surgery and Neurosciences University of Siena Italy.
Gabriele CeveniniDepartment of Medical Biotechnologies University of Siena Italy.
Yongxia Sarah QuVA New York Harbor Healthcare SystemSUNY Downstate Medical Center New York NY.
Frank FabrisVA New York Harbor Healthcare SystemSUNY Downstate Medical Center New York NY.
Nabil El-SherifVA New York Harbor Healthcare SystemSUNY Downstate Medical Center New York NY.
Maurizio AcampaStroke Unit University Hospital of Siena Italy.
Alessandra CartocciDepartment of Medical Biotechnologies University of Siena Italy.
Franco Laghi-PasiniDepartment of Medical Sciences Surgery and Neurosciences University of Siena Italy.
Pier Leopoldo CapecchiDepartment of Medical Sciences Surgery and Neurosciences University of Siena Italy.
Mohamed BoutjdirVA New York Harbor Healthcare SystemSUNY Downstate Medical Center New York NY.
Deana LazaroVA New York Harbor Healthcare SystemSUNY Downstate Medical Center New York NY.
University of Siena · ITSUNY Downstate Health Sciences University · USNewYork–Presbyterian Brooklyn Methodist Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Anti-Sjögren's syndrome-related antigen A-antibodies (anti-Ro/SSA-antibodies) are responsible for a novel form of acquired long-QT syndrome, owing to autoimmune-mediated inhibition of cardiac human ether-a-go-go-related gene-potassium channels. However, current evidence derives only from basic mechanistic studies and relatively small sample-size clinical investigations. Hence, the aim of our study is to estimate the risk of QTc prolongation associated with the presence of anti-Ro/SSA-antibodies in a large population of unselected subjects. Methods and Results This is a retrospective observational cohort study using the Veterans Affairs Informatics and Computing Infrastructure. Participants were veterans who were tested for anti-Ro/SSA status and had an ECG. Descriptive statistics and univariate and multivariate logistic regression analyses were performed to identify risk factors for heart rate-corrected QT interval (QTc) prolongation. The study population consisted of 7339 subjects (61.4±12.2 years), 612 of whom were anti-Ro/SSA-positive (8.3%). Subjects who were anti-Ro/SSA-positive showed an increased prevalence of QTc prolongation, in the presence of other concomitant risk factors (crude odds ratios [OR], 1.67 [1.26-2.21] for QTc >470/480 ms; 2.32 [1.54-3.49] for QTc >490 ms; 2.77 [1.66-4.60] for QTc >500 ms), independent of a connective tissue disease history. Adjustments for age, sex, electrolytes, cardiovascular risk factors/diseases, and medications gradually attenuated QTc prolongation estimates, particularly when QT-prolonging drugs were added to the model. Nevertheless, stepwise-fully adjusted OR for the higher cutoffs remained significantly increased in anti-Ro/SSA-positive subjects, particularly for QTc >500 ms (2.27 [1.34-3.87]). Conclusions Anti-Ro/SSA-antibody positivity was independently associated with an increased risk of marked QTc prolongation in a large cohort of US veterans. Our data suggest that within the general population individuals who are anti-Ro/SSA-positive may represent a subgroup of patients particularly predisposed to ventricular arrhythmias/sudden cardiac death.

Indexed as

ElectrocardiographyVeteransAntibodies, AntinuclearBiomarkersCross-Sectional StudiesFemaleFollow-Up StudiesHeart RateHumansIncidenceLong QT SyndromeMaleMiddle AgedRetrospective StudiesRisk FactorsUnited StatesAntibodies, AntinuclearBiomarkersSS-A antibodiesanti‐Ro/SSAconnective tissue diseasesgeneral populationQTc prolongationsudden death risk

Identifiers

PMID33533258
PMCPMC7955337
OpenAlexW3127449994

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.