血浆源性c1抑制剂浓缩物成功长期预防遗传性妊娠相关血管性水肿1例报告

D. V. Demina, A. O. Makeeva, L. M. Kudelya, E. V. Novikova, V. Kozlov
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引用次数: 0

摘要

遗传性血管性水肿(HAE)是一种罕见的常染色体显性遗传病,由C1酯酶抑制剂(C1- inh)数量(I型)或功能(II型)缺乏引起。它可能是由多达20%的患者的新突变引起的。HAE的患病率尚不确定,但估计约为每5万人中有1例,在种族群体中没有已知的差异。C1-INH蛋白是一种丝氨酸蛋白酶抑制剂,通过作用于补体激活、凝血和纤溶的初始阶段,在控制血管通透性方面起重要作用。缺乏功能性C1-INH蛋白允许缓激肽的释放,缓激肽是血管通透性的关键介质。症状通常从童年开始,在青春期恶化,并持续一生,具有不可预测的临床病程。HAE患者患有反复发作的急性水肿,可影响身体任何部位,引起潜在的危及生命的疾病(喉水肿)。临床研究结果表明,轻微的创伤、压力和医疗干预可能是肿胀发作的频繁诱因,但许多发作没有明显的原因。妊娠相关的激素变化可能会加重、改善或完全没有影响C1-INH血管性水肿发作的过程,但更高比例的孕妇经历了C1-INH- hae发作率的增加。妊娠期HAE患者的治疗选择有限。C1-INH浓缩物由于其安全性和有效性,被推荐作为HAE孕妇按需治疗、短期和长期预防的一线治疗。其他治疗方法,例如,用新鲜冷冻血浆、雄激素、icatibant、抗纤溶药物治疗,可能表现出不同的疗效,或引起不良的副作用。下面的病例说明了C1酯酶抑制剂(C1- inh)浓缩物成功治疗孕妇HAE。该患者一生中患有非常轻微的HAE,并没有接受任何治疗。在怀孕期间,她经历了发作频率的显著增加,并决定开始使用血浆来源的双重病毒灭活C1-INH浓缩物作为替代治疗,作为整个怀孕期间,剖宫产分娩之前,期间和之后的长期预防治疗。
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Successful long-term prophylaxis of hereditary pregnancy-associated angioedema with plasma-derived C1-inhibitor concentrate: a case report
Hereditary angioedema (HAE) is a rare autosomal dominant disease caused by quantitative (type I) or functional (type II) deficiency in C1 esterase inhibitor (C1-INH). It may be caused by new mutations in up to 20% of patients. Prevalence of HAE is uncertain but is estimated to be approximately 1 case per 50,000 persons, without known differences among ethnic groups. C1-INH protein is a serine protease inhibitor that is important in controlling vascular permeability by acting on the initial phase of the complement activation, blood clotting, and fibrinolysis. Deficiency in functional C1-INH protein permits release of bradykinin, a key mediator of vascular permeability. Symptoms typically begin since childhood, worsening at puberty, and persist throughout the life, with unpredictable clinical course. The patients with HAE suffer from recurrent, acute attacks of edema that can affect any body sites, causing potentially life-threatening disorders (laryngeal edema). Results of clinical studies show that minor traumas, stress and medical interventions may be frequent precipitants of swelling episodes, but many attacks occur without an apparent cause. Pregnancy-associated hormonal changes may affect the course of C1-INH angioedema attacks by worsening, improving, or having no impact at all, but a higher percentage of pregnant women experienced an increase in C1-INH-HAE attack rates. Therapeutic options for patients with HAE are limited during pregnancy. C1-INH concentrate is recommended as the first-line therapy for pregnant women with HAE for on-demand treatment, shortterm and long-term prophylaxis, due to its safety and efficiency. Other therapies, e.g., treatment with fresh frozen plasma, androgens, icatibant, antifibrinolytics, may show variable efficacy, or cause undesirable side effects. The case below illustrates the successful treatment of HAE in a pregnant woman with C1 esterase inhibitor (C1-INH) concentrate. This patient had a very mild course of HAE during her lifetime and didn’t get any treatment. During pregnancy, she experienced a significant increase in the frequency of attacks, and the decision was made to start replacement therapy with a plasma-derived, double virus-inactivated C1-INH concentrate as a long-term prophylaxis throughout the full term of her pregnancy, before, during and after the cesarean section delivery.
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