Section of Dermatology, Department of Health Sciences (DISSAL), 9302University of Genoa, Genoa, Italy.
Dermatology Unit, 9246Ospedale Policlinico San MartinoIRCCS, Genoa, Italy.
Int J Immunopathol Pharmacol. 2021 Jan-Dec;35:20587384211042115. doi: 10.1177/20587384211042115.
Hypercoagulability is a risk factor of thromboembolic events in COVID-19. Anti-phospholipid (aPL) antibodies have been hypothesized to be involved. Typical COVID-19 dermatological manifestations of livedo reticularis and digital ischemia may resemble cutaneous manifestations of anti-phospholipid syndrome (APS).
To investigate the association between aPL antibodies and thromboembolic events, COVID-19 severity, mortality, and cutaneous manifestations in patients with COVID-19.
aPL antibodies [anti-beta2-glycoprotein-1 (B2GP1) and anti-cardiolipin (aCL) antibodies] were titered in frozen serum samples from hospitalized COVID-19 patients and the patients' clinical records were retrospectively analyzed.
173 patients were enrolled. aPL antibodies were detected in 34.7% of patients, anti-B2GP1 antibodies in 30.1%, and aCL antibodies in 10.4%. Double positivity was observed in 5.2% of patients. Thromboembolic events occurred in 9.8% of patients, including 11 pulmonary embolisms, 1 case of celiac tripod thrombosis, and six arterial ischemic events affecting the cerebral, celiac, splenic, or femoral-popliteal arteries or the aorta. aPL antibodies were found in 52.9% of patients with vascular events, but thromboembolic events were not correlated to aPL antibodies (adjusted OR = 1.69, = 0.502). Ten patients (5.8%) had cutaneous signs of vasculopathy: nine livedo reticularis and one acrocyanosis. No significant association was observed between the presence of cutaneous vasculopathy and aPL antibodies ( = 0.692).
Anti-phospholipid antibodies cannot be considered responsible for hypercoagulability and thrombotic events in COVID-19 patients. In COVID-19 patients, livedo reticularis and acrocyanosis do not appear to be cutaneous manifestations of APS.
高凝状态是 COVID-19 血栓栓塞事件的危险因素。抗磷脂(aPL)抗体被认为与此相关。COVID-19 特有的网状青斑和指(趾)缺血等皮肤表现可能类似于抗磷脂综合征(APS)的皮肤表现。
探讨 COVID-19 患者抗磷脂抗体与血栓栓塞事件、COVID-19 严重程度、死亡率及皮肤表现的相关性。
对住院 COVID-19 患者的冷冻血清样本进行 aPL 抗体(抗β2-糖蛋白 1(B2GP1)抗体和抗心磷脂(aCL)抗体)滴度检测,并对患者的临床记录进行回顾性分析。
共纳入 173 例患者。34.7%的患者检测到 aPL 抗体,其中抗 B2GP1 抗体阳性率为 30.1%,aCL 抗体阳性率为 10.4%。5.2%的患者同时存在两种抗体阳性。9.8%的患者发生血栓栓塞事件,包括 11 例肺栓塞、1 例腹腔干三脚架血栓形成和 6 例累及脑、腹腔干、脾或股-腘动脉或主动脉的动脉缺血性事件。血管事件患者中 52.9%检测到 aPL 抗体,但血栓栓塞事件与 aPL 抗体无关(调整后 OR = 1.69, = 0.502)。10 例(5.8%)患者出现血管病变皮肤表现:9 例网状青斑和 1 例肢端发绀。皮肤血管病变的存在与 aPL 抗体之间无显著相关性( = 0.692)。
在 COVID-19 患者中,抗磷脂抗体不能被认为是导致高凝状态和血栓形成事件的原因。在 COVID-19 患者中,网状青斑和肢端发绀似乎不是 APS 的皮肤表现。