A retrospective study of electrocardiographic alterations in primary Sjögren's syndrome: role of anti-SSA positivity and disease duration.

IF 2.9 3区 医学 Q2 RHEUMATOLOGY
Clinical Rheumatology Pub Date : 2025-06-01 Epub Date: 2025-05-10 DOI:10.1007/s10067-025-07477-x
Sibel Ösken, Altuğ Ösken, Fuat Polat, Duygu Şahin, Nihan Neval Uzun, Nesrin Şen, Mehmet Engin Tezcan
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引用次数: 0

Abstract

Background: Primary Sjögren's Syndrome (pSS) is a chronic autoimmune disorder affecting exocrine glands and potentially leading to cardiovascular complications. The impact of anti-SSA antibody seropositivity on cardiac function, particularly ECG parameters, is not well understood.

Aims: This study aims to explore the association between anti-SSA antibody seropositivity and various ECG parameters, including the QT interval, corrected QT interval (QTc), QT dispersion, and T peak to T end (TP-TE) interval, in patients with pSS.

Methods: A retrospective observational study was conducted involving 57 pSS patients. Participants were divided into seropositive (n = 32) and seronegative (n = 25) groups based on anti-SSA antibody status. ECG parameters were assessed, including QT interval, QTc interval, QT dispersion, and TP-TE interval. Statistical comparisons were made using independent t-tests, Mann-Whitney U tests, or chi-square tests, with a significance threshold of p < 0.05.

Results: The seropositive group showed significantly prolonged QT interval (403.1 ± 28.7 ms) compared to the seronegative group (381.8 ± 28.2 ms, p < 0.01). Similarly, the QTc interval was longer in seropositive patients (430.1 ± 28.6 ms) compared to seronegative patients (412.6 ± 31.8 ms, p = 0.03). QT dispersion was greater in the seropositive group (43.5 ± 3.6 ms) compared to the seronegative group (40.8 ± 4.6 ms, p = 0.02). The TP-TE interval was also significantly prolonged in seropositive patients (67.9 ± 7.5 ms) compared to seronegative patients (63.4 ± 4.8 ms, p < 0.01). The TP-TE/QTc ratio did not differ significantly between the two groups.

Conclusions: Anti-SSA seropositivity in pSS patients is associated with significant alterations in ECG parameters indicative of impaired ventricular repolarization. These findings suggest that seropositive pSS patients may have an increased risk of cardiovascular complications, emphasizing the importance of ECG monitoring in this patient population. Key Points •Anti-Ro/SSA seropositivity in pSS patients is linked to prolonged QT and QTc intervals, indicating impaired ventricular repolarization. •Seropositive pSS patients show increased QT dispersion, which may reflect a higher risk for arrhythmias. •The TP-TE interval is significantly prolonged in seropositive pSS patients, suggesting a higher risk for ventricular arrhythmias. •ECG monitoring is crucial in seropositive pSS patients to detect early cardiac abnormalities and guide treatment.

原发性Sjögren综合征心电图改变的回顾性研究:抗ssa阳性和病程的作用
背景:原发性Sjögren综合征(pSS)是一种影响外分泌腺并可能导致心血管并发症的慢性自身免疫性疾病。抗ssa抗体血清阳性对心功能,特别是心电图参数的影响尚不清楚。目的:本研究旨在探讨抗ssa抗体血清阳性与pSS患者QT间期、校正QT间期(QTc)、QT离散度、T峰至T端(TP-TE)间期等心电图参数的关系。方法:对57例pSS患者进行回顾性观察研究。根据抗ssa抗体水平将参与者分为血清阳性组(n = 32)和血清阴性组(n = 25)。评估心电图参数,包括QT间期、QTc间期、QT离散度、TP-TE间期。采用独立t检验、Mann-Whitney U检验或卡方检验进行统计学比较,显著性阈值为p。结果:血清阳性组QT间期(403.1±28.7 ms)明显延长,血清阴性组QT间期(381.8±28.2 ms)显著延长,p。结论:pSS患者抗ssa血清阳性与心电参数显著改变相关,提示心室复极受损。这些发现提示血清pSS阳性患者可能有心血管并发症的风险增加,强调了ECG监测在这类患者群体中的重要性。•pSS患者的抗ro /SSA血清阳性与QT和QTc间期延长有关,表明心室复极受损。•血清pSS阳性患者QT离散度增加,这可能反映心律失常的风险较高。•血清pSS阳性患者TP-TE间期明显延长,提示室性心律失常的风险较高。•心电图监测对于血清阳性pSS患者早期发现心脏异常并指导治疗至关重要。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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