Suppr超能文献

家族性疱疹样皮炎的发病率。

Incidence of familial dermatitis herpetiformis.

作者信息

Reunala T

机构信息

Department of Dermatology, University of Helsinki, Finland.

出版信息

Br J Dermatol. 1996 Mar;134(3):394-8.

PMID:8731659
Abstract

Dermatitis herpetiformis (DH) and coeliac disease (CD) are gluten-sensitive diseases which have a common immunogenetic background, with the histocompatibility locus antigen (HLA) alleles DQ A10501 and B10201 in the short arm of chromosome 6. CD is well known to cluster in families whereas DH has not been generally regarded as a familial disease. To study the familial incidence of DH, a prospective study was started in 1969 at the Department of Dermatology of Helsinki University Hospital and in 1976 at the Department of Dermatology of Tampere University Hospital. A total of 1018 patients with DH were diagnosed and questioned for positive family histories. Of the 999 unrelated DH patients, 105 (10.5%) had one or several affected first-degree relatives. The disease in the relatives was either DH (4.4%) or CD (6.1%). Analysis of the 105 families showed that 13.6% of parents, 18.7% of siblings and 14.0% of children were affected, a segregation pattern which fits well to a dominant mode of Mendelian inheritance. Gender may also be important because the first-degree relatives affected with DH were more often females and those affected with CD twice as often females as males. In contrast, there were more males among the 105 propositi with DH and also among the 894 DH patients with no affected relatives. The present study clearly shows that DH is a familial disease in which the first-degree relatives can be affected both with DH and CD, presumably because of a common genetic background. The environmental factors which could cause the rather high penetrance of DH and CD in the first-degree relatives of DH patients remain unknown.

摘要

疱疹样皮炎(DH)和乳糜泻(CD)是麸质敏感疾病,它们具有共同的免疫遗传背景,与6号染色体短臂上的组织相容性位点抗原(HLA)等位基因DQ A10501和B10201有关。众所周知,CD在家族中具有聚集性,而DH一般不被视为家族性疾病。为了研究DH的家族发病率,1969年在赫尔辛基大学医院皮肤科以及1976年在坦佩雷大学医院皮肤科开展了一项前瞻性研究。共诊断出1018例DH患者,并询问其家族病史。在999例无亲缘关系的DH患者中,105例(10.5%)有一个或多个患病的一级亲属。亲属所患疾病为DH(4.4%)或CD(6.1%)。对这105个家庭的分析表明,13.6%的父母、18.7%的兄弟姐妹和14.0%的子女患病,这种分离模式非常符合孟德尔显性遗传模式。性别可能也很重要,因为患DH的一级亲属中女性更为常见,而患CD的一级亲属中女性是男性的两倍。相比之下,在105例患DH的先证者以及894例无患病亲属的DH患者中,男性更多。本研究清楚地表明,DH是一种家族性疾病,其一级亲属可能同时患DH和CD,推测是由于共同的遗传背景。导致DH患者一级亲属中DH和CD具有较高外显率的环境因素尚不清楚。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验