Stray-Pedersen A, Abrahamsen T G, Frøland S S
The Centre for Rare Disorders, Department of Medicine, Rikshospitalet, University of Oslo, Norway.
J Clin Immunol. 2000 Nov;20(6):477-85. doi: 10.1023/a:1026416017763.
This study represents the first national epidemiological survey of primary immunodeficiency diseases in Norway. Uniform questionnaires were sent out in April 1998 to all hospital departments considered relevant. As of February 1999, a total of 372 patients have been registered, of whom 69 patients are deceased. With a population of 4.45 million people, the total prevalence of primary immunodeficiency diseases in Norway February 1, 1999 is 6.82 per 100000 inhabitants. Distribution between the main immunodeficiency diagnoses is (a) antibody deficiencies 50.8%, (b) combined deficiencies included other immunodeficiency syndromes 12.4%, (c) complement deficiencies 21.0%, (d) phagocytic disorders 6.7%, (e) and immunodeficiency associated with other congenital diseases 9. 1%. Compared to previous reports from other European countries, there is a smaller proportion of antibody deficiencies due to few IgA deficiencies registered and a large proportion of complement deficiencies due to many patients with hereditary angioedema.
本研究是挪威首次针对原发性免疫缺陷疾病开展的全国性流行病学调查。1998年4月,向所有相关医院科室发放了统一问卷。截至1999年2月,共登记了372例患者,其中69例已死亡。挪威人口为445万,1999年2月1日原发性免疫缺陷疾病的总患病率为每10万居民6.82例。主要免疫缺陷诊断的分布情况如下:(a)抗体缺陷占50.8%,(b)联合缺陷(包括其他免疫缺陷综合征)占12.4%,(c)补体缺陷占21.0%,(d)吞噬细胞疾病占6.7%,(e)与其他先天性疾病相关的免疫缺陷占9.1%。与其他欧洲国家之前的报告相比,由于登记的IgA缺陷较少,抗体缺陷的比例较小;由于遗传性血管性水肿患者较多,补体缺陷的比例较大。