POS1490 ANTI-RO/SSA-ANTIBODIES AND ELECTROCARDIOGRAPHIC ABNORMALITIES IN PATIENTS WITH SYSTEMIC LUPUS ERYHEMATOSUS (SLE): DATA OF A MULTIDISCIPLINARY STUDY IN A MONOCENTRIC COHORT

BackgroundCardiovascular involvement is common in patients with SLE and heart rhythm disorders are frequent in addition to the manifestations included in the classification criteria ACR/EULAR 2019. Previous studies provided evidence that anti-Ro/SSA-positivity is an independent risk factor for marke...

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Published inAnnals of the rheumatic diseases Vol. 82; no. Suppl 1; pp. 1101 - 1102
Main Authors Fredi, M., Bertocchi, S., Pedretti, E., Rovelli, R., Drera, A., Ravasio, F., Riccardi, M., Serafini, L., Cavazzana, I., Vizzardi, E., Franceschini, F.
Format Journal Article
LanguageEnglish
Published Kidlington BMJ Publishing Group Ltd and European League Against Rheumatism 01.06.2023
Elsevier Limited
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ISSN0003-4967
1468-2060
DOI10.1136/annrheumdis-2023-eular.1309

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Summary:BackgroundCardiovascular involvement is common in patients with SLE and heart rhythm disorders are frequent in addition to the manifestations included in the classification criteria ACR/EULAR 2019. Previous studies provided evidence that anti-Ro/SSA-positivity is an independent risk factor for marked QTc prolongation; suggesting that subjects who are anti-Ro/SSA-positive may represent a subgroup with an increased predisposition to ventricular arrhythmias, particularly when other QT-prolonging risk factors are concomitantly present [1].ObjectivesThe aim of this study is to estimate the prevalence of QTc-prolongation in a monocentric cohort and to evaluate possible correlation with the presence of anti-Ro/SSA-antibodies and other QT-prolonging risk factors.MethodsAn electrocardiographic study (ECG) was proposed to patients affected by SLE consecutively attending our Lupus Clinic from November 2021 to March 2022. All subjects were tested for anti-Ro/SSA-antibodies. Exclusion criteria included: severe valvulopathies, hypertrophic or dilated cardiomyopathy, previous implantation of pacemaker or implantable cardioverter-defibrillator.QTc measurement was calculated using the Bazett’s formula and QTc-prolongation was defined according to American College of Cardiology (ACC)/American Heart Association (AHA) recommendations (QTc>470 ms for males, QTc>480 ms for females) [2]. Data on 24-hour ECG holter were available in 26 patients.ResultsOne hundred and forty-one patients with SLE, consecutively attending our clinic, accepted to undergo an ECG, 128 (91%) females, 13 (9%) males; 124 (88%) Caucasians (median age 53.2 [IQR 42.3-58.7], median disease duration 20.0 years [12.0-28.2]).Median QTc was 415ms [IQR 394-436]; only 4/141 (2.8%), all Caucasian and female, had a prolonged QTc (Table 1).Table 1Features of patients with prolonged QTcageAnti-Ro/SSAQTcCardiological historyHCQ therapy156Positive492 msnoneyes257Negative488 msHT, Dno360Positive480 msHTyes463Positive508 msDnoHT: hypertension, D: dyslipidaemiaSixty-eight (48%) patients were positive for anti-Ro/SSA-antibodies. No significant differences were observed between anti-Ro/SSA-positive vs. negative patients in term of QTc intervals (416.0 [395-437] ms vs 413.0 [392-432] ms; p=0.545) using Mann-Withney Test.Other electrocardiographic alterations were found: 4 first-degree atrioventricular blocks, 25 bundle branch blocks (BBB), 31 repolarization anomalies, 1 Wolff-Parkinson-White.Patients were grouped according to hydroxychloroquine (HCQ) therapy and antibody profile into 4 groups: HCQ+/Ro/SSA+(56, 39.7%), HCQ+/Ro/SSA-(58, 41.1%), HCQ-/Ro/SSA+ (12, 8.5%) and HCQ-/Ro/SSA- (15,106%); no statistical differences (p=0.178) were observed in QTc length comparing the 4 groups using ANOVA test.Twenty-six (18.4%) underwent a 24-hour ECG holter evaluation. None of these patients had a QTc prolongation, and no major elettrocardiographic anomalies were found. These patients were divided in 4 groups (as previously done for all patients). No statistical differences were found comparing the QTc of groups of patients (p=0.783).ConclusionThese preliminary data show a lower prevalence of QTc prolongation compared to previous studies, with no differences between anti-Ro/SSA-positive and anti-Ro/SSA-negative patients. Otherwise, considering previous studies which observed a role of anti-Ro/SSA antibodies as an independent risk factor for QTc prolongation, further analysis will be performed in order to identify standardized markers for cardiovascular risk stratification. The evaluation of 24-hour ECG Holter in a larger number of patients and the characterization of anti-Ro/SSA (anti-Ro/SSA-52kD and anti-Ro/SSA-60kD) are ongoing.References[1]Lazzerini et al, Journal of the American Heart Association, 2021[2]Drew BJ et Al. Circulation, 2010Acknowledgements:NIL.Disclosure of InterestsNone Declared.
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ISSN:0003-4967
1468-2060
DOI:10.1136/annrheumdis-2023-eular.1309