Pons Isaac, Louro Joana, Sitges Marta, Vidal Bàrbara, Cervera Ricard, Espinosa Gerard
Department of Autoimmune Diseases, Reference Centre (UEC/CSUR) for Systemic Autoimmune Diseases of the Catalan and Spanish Health Systems, Hospital Clínic, Universitat de Barcelona, 08036 Barcelona, Spain.
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 08036 Barcelona, Spain.
J Clin Med. 2023 Apr 20;12(8):2996. doi: 10.3390/jcm12082996.
Valve involvement is the most common cardiac manifestation in antiphospholipid syndrome (APS). The objective of the study was to describe the prevalence, clinical and laboratory features, and evolution of APS patients with heart valve involvement.
A retrospective longitudinal and observational study of all APS patients followed by a single centre with at least one transthoracic echocardiographic study.
144 APS patients, 72 (50%) of them with valvular involvement. Forty-eight (67%) had primary APS, and 22 (30%) were associated with systemic lupus erythematosus (SLE). Mitral valve thickening was the most frequent valve involvement present in 52 (72%) patients, followed by mitral regurgitation in 49 (68%), and tricuspid regurgitation in 29 (40%) patients. Female sex (83% vs. 64%; = 0.013), arterial hypertension (47% vs. 29%; = 0.025), arterial thrombosis at APS diagnosis (53% vs. 33%; = 0.028), stroke (38% vs. 21%; = 0.043), livedo reticularis (15% vs. 3%; = 0.017), and lupus anticoagulant (83% vs. 65%; = 0.021) were more prevalent in those with valvular involvement. Venous thrombosis was less frequent (32% vs. 50%; = 0.042). The valve involvement group suffered from higher mortality (12% vs. 1%; = 0.017). Most of these differences were maintained when we compared patients with moderate-to-severe valve involvement ( = 36) and those with no or mild involvement ( = 108).
Heart valve disease is a frequent manifestation in our cohort of APS patients and is associated with demographic, clinical and laboratory features, and increased mortality. More studies are needed, but our results suggest that there may be a subgroup of APS patients with moderate-to-severe valve involvement with its own characteristics that differs from the rest of the patients with mild valve involvement or without valve involvement.
瓣膜受累是抗磷脂综合征(APS)最常见的心脏表现。本研究的目的是描述心脏瓣膜受累的APS患者的患病率、临床和实验室特征以及病情演变。
对一家单一中心随访的所有APS患者进行回顾性纵向观察研究,这些患者至少接受过一次经胸超声心动图检查。
144例APS患者中,72例(50%)有瓣膜受累。48例(67%)为原发性APS,22例(30%)与系统性红斑狼疮(SLE)相关。二尖瓣增厚是最常见的瓣膜受累表现,见于52例(72%)患者,其次是二尖瓣反流49例(68%),三尖瓣反流29例(40%)。瓣膜受累患者中女性(83%对64%;P = 0.013)、动脉高血压(47%对29%;P = 0.025)、APS诊断时的动脉血栓形成(53%对33%;P = 0.028)、中风(38%对21%;P = 0.043)、网状青斑(15%对3%;P = 0.017)和狼疮抗凝物(83%对65%;P = 0.021)更为常见。静脉血栓形成较少见(32%对50%;P = 0.042)。瓣膜受累组死亡率更高(12%对1%;P = 0.017)。当我们比较中度至重度瓣膜受累患者(n = 36)和无或轻度受累患者(n = 108)时,这些差异大多仍然存在。
心脏瓣膜病在我们的APS患者队列中是一种常见表现,与人口统计学、临床和实验室特征以及死亡率增加相关。需要更多的研究,但我们的结果表明,可能存在一个中度至重度瓣膜受累的APS患者亚组,其具有与轻度瓣膜受累或无瓣膜受累的其他患者不同的自身特征。