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瑞士C1抑制剂缺乏所致遗传性血管性水肿:队列研究中的临床特征与治疗方式

Hereditary angioedema due to C1 - inhibitor deficiency in Switzerland: clinical characteristics and therapeutic modalities within a cohort study.

作者信息

Steiner Urs C, Weber-Chrysochoou Christina, Helbling Arthur, Scherer Kathrin, Grendelmeier Peter Schmid, Wuillemin Walter A

机构信息

Division of Clinical Immunology, University Hospital Zurich, Zurich, Switzerland.

Allergy Unit, Department of Dermatology, University Hospital Zurich, Zurich, Switzerland.

出版信息

Orphanet J Rare Dis. 2016 Apr 21;11:43. doi: 10.1186/s13023-016-0423-1.

Abstract

BACKGROUND

Registration of trigger factors, prodromal symptoms, swelling localization, therapeutic behavior and gender-specific differences of the largest cohort of patients with hereditary angioedema due to C1-Inhibitor deficiency (C1-INH-HAE) in Switzerland.

METHODS

Questionnaire survey within a cohort study: Consenting eligible patients with diagnosed HAE according to clinical history, physical examination and laboratory results, including plasma values for C1-INH and C4 were selected. To each participant we sent a questionnaire assessing patients' birthday, sex, date of first symptoms and diagnosis, trigger factors, prodromal symptoms, frequency and localization of angioedema, medication use and co-morbidities. Clinical information was collected in each center and then transmitted to the cohort database. Frequencies and distributions were summarized. Associations between gender and trigger factors or prodromal symptoms or localization of angioedema were assessed in multivariate analyses correcting for patients' age.

RESULTS

Of 135 patients, data from 104 patients (77%) were available for analysis. Fifty- four percent were female, mean age at diagnosis was 19.5 years (SD 14.1), Mean age when completing the questionnaire was 44.0 (SD 19.8). More women than men were symptomatic (44/57 vs. 36/47; p = 0.005). This association remained when correcting for age at diagnosis (16.10. 95%CI (5.17 to 26.70); p = 0.004). Swelling episodes ranged between 1 and 136 episodes/year. Swelling was more common among female than among male (-13.15 (95% CI; -23.10 to -3.22), p = 0.010). Age at diagnosis was inversely associated with the total number of attacks 0.50 (-0.88 to -.011); p = 0.012). One third of patients were on danazol prophylaxis.

CONCLUSION

We found large differences of HAE in male and female both in terms of symptom number and swelling episodes. Women are more affected by intensity and frequency of angioedema episodes than men. Danazol treatment remains widely used as effective prophylaxis despite its side effects. New therapies which selectively influence the hormonal estrogen balance could open new therapeutic options mainly for women and maybe also for men.

摘要

背景

对瑞士最大规模的C1抑制剂缺乏所致遗传性血管性水肿(C1-INH-HAE)患者队列的触发因素、前驱症状、肿胀部位、治疗行为及性别差异进行登记。

方法

在一项队列研究中进行问卷调查:根据临床病史、体格检查及实验室检查结果(包括C1-INH和C4的血浆值),选取确诊为HAE且同意参与的合格患者。我们向每位参与者发送了一份问卷,评估患者的生日、性别、首次出现症状和确诊的日期、触发因素、前驱症状以及血管性水肿的发作频率和部位、用药情况及合并症。各中心收集临床信息,然后传输至队列数据库。汇总频率和分布情况。在对患者年龄进行校正的多变量分析中,评估性别与触发因素、前驱症状或血管性水肿部位之间的关联。

结果

135例患者中,104例(77%)的数据可供分析。54%为女性,确诊时的平均年龄为19.5岁(标准差14.1),完成问卷时的平均年龄为44.0岁(标准差19.8)。有症状的女性多于男性(44/57对36/47;p = 0.005)。在校正确诊年龄后,这种关联仍然存在(16.10,95%置信区间(5.17至26.70);p = 0.004)。肿胀发作次数为每年1至136次。女性肿胀比男性更常见(-13.15(95%置信区间;-23.10至-3.22),p = 0.010)。确诊年龄与发作总数呈负相关0.50(-0.88至-0.011);p = 0.012)。三分之一的患者接受达那唑预防治疗。

结论

我们发现HAE在男性和女性中的症状数量和肿胀发作次数存在很大差异。女性比男性更容易受到血管性水肿发作强度和频率的影响。尽管达那唑有副作用,但它作为有效的预防药物仍被广泛使用。选择性影响激素雌激素平衡的新疗法可能为女性甚至男性开辟新的治疗选择。

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