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[斯内登综合征患者的抗磷脂酰乙醇胺抗体]

[Anti-phosphatidylethanolamine antibodies in patients with Sneddon's syndrome].

作者信息

Kalashnikova L A, Aleksandrova E N, Novikov A A, Dobrynina L A, Nasonov E L, Sergeeva E V, Berkovskiĭ A L

出版信息

Klin Med (Mosk). 2005;83(5):46-9.

Abstract

Anti-phosphatidylethanolamine antibodies (aPE) belong to the group of anti-phospholipid antibodies (aPL) and are directed against neutral phospholipid, connected with co-factor protein, while cardiolipin antibodies (aKL) are directed against negative phospholipid. The paper presents a study of prevalence and clinical significance of IgG aPE in 28 patients (22 women and 6 men, mean age 47.6 +/- 11.6 years) with Sneddon's syndrome (SS), which consists in cerebrovascular disturbances and extensive livedo reticularis. IgG aPE were detected by immune-enzyme assay. The upper normal limit, calculated as mean + 3SD after studying 19 healthy donors, was 0.303 optic density units. aPE were found in 15 (54%), aKL and/or lupus anticoagulant (LA)--in 6 (21%) patients with SS. aPE were found in 10 (46%) out of 22 aKL- and LA-negative patients. Among the aPE-positive patients there was a higher incidence of cortic dementia (53% vs. 8%, p = 0.02), the widening of cortical sulci, detected by means of computed tomography and magnetic resonance imaging (73% vs. 31%, p = 0.05), and mild renal syndrome (73% vs. 16%, p = 0.03). Besides, they displayed a higher rate of headaches (87% vs. 62%), chorea (33% vs. 8%), epilepsy (27% vs. 8%), non-carrying of pregnancy (91% vs. 50%), peripheral venous thrombosis (27% vs. 15%), coronary heart disease (47% vs. 31%), cardiac valvular thickening, detected by means of EchoCG (93% vs. 69%), arterial hypertension (87% vs. 54%), thrombocytopenia (20% vs. 0), anemia (40% vs. 15%); however, the difference was not significant. The results show that aPE detection, performed in addition to detection of classic immunological antiphospholipid syndrome markers (aKL and LA), increases the portion of aPE-positive patients with SS by 33%. aPE are often (in 46% of cases) found in aKL- and LA-negative patients with SS. aPE is likely to be the most significant factor of thrombosis in small arteries of the brain cortex and kidneys, which could explain their association with dementia and renal syndrome.

摘要

抗磷脂酰乙醇胺抗体(aPE)属于抗磷脂抗体(aPL)组,针对与辅因子蛋白相连的中性磷脂,而抗心磷脂抗体(aKL)则针对负电荷磷脂。本文介绍了对28例(22名女性和6名男性,平均年龄47.6±11.6岁)患有斯内登综合征(SS)患者的IgG aPE患病率及临床意义的研究,该综合征表现为脑血管紊乱和广泛的网状青斑。通过免疫酶测定法检测IgG aPE。在研究了19名健康供体后,计算得出的正常上限为平均+3标准差,即0.303光密度单位。在15例(54%)SS患者中发现了aPE,6例(21%)患者发现了aKL和/或狼疮抗凝物(LA)。在22例aKL和LA阴性的患者中,10例(46%)发现了aPE。在aPE阳性患者中,皮质性痴呆的发生率较高(53%对8%,p = 0.02),通过计算机断层扫描和磁共振成像检测到的皮质沟增宽(73%对31%,p = 0.05),以及轻度肾综合征(73%对16%,p = 0.03)。此外,他们还表现出较高的头痛发生率(87%对62%)、舞蹈症(33%对8%)、癫痫(27%对8%)、妊娠失败(91%对50%)、外周静脉血栓形成(27%对15%)、冠心病(47%对31%)、通过超声心动图检测到的心脏瓣膜增厚(93%对69%)、动脉高血压(87%对54%)、血小板减少症(20%对0)、贫血(40%对15%);然而,差异不显著。结果表明,除了检测经典的免疫性抗磷脂综合征标志物(aKL和LA)外,进行aPE检测可使SS患者中aPE阳性患者的比例增加33%。在aKL和LA阴性的SS患者中,aPE经常(46%的病例)被发现。aPE可能是大脑皮质和肾脏小动脉血栓形成的最重要因素,这可以解释它们与痴呆和肾综合征的关联。

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