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分析影响日本先天性血友病患者抑制剂形成发生率的因素。

An analysis of factors affecting the incidence of inhibitor formation in patients with congenital haemophilia in Japan.

机构信息

Department of Paediatrics, University of Occupational and Environmental Health, Kitakyushu, Fukuoka, Japan.

出版信息

Haemophilia. 2011 Sep;17(5):771-6. doi: 10.1111/j.1365-2516.2011.02599.x. Epub 2011 Jun 20.

Abstract

Studies conducted in European and North American countries have demonstrated that various factors including races affect the frequency of inhibitor formation in haemophilia patients. The present study was undertaken to analyse factors affecting the incidence of inhibitor formation in Japanese haemophilia A and B patients. Analytical data were retrospectively collected from haemophilia A and B patients born after 1988, the year when monoclonal antibody-purified factor VIII products were first marketed in Japan. Various data were collected from 184 patients (153 cases of haemophilia A; 31 cases of haemophilia B). The sample size of haemophilia B cases was too small to reveal any significant differences between the inhibitor formation group and the inhibitor-free group in any of background variables. For patients with haemophilia A, on the other hand, univariate analysis identified the severity of haemophilia and a positive family history of inhibitor development as risk factors for the formation of inhibitors. In analyses of the clotting factor products used, the incidence of inhibitor formation did not differ significantly between the group treated with plasma-derived products (29.7%) and the group treated with recombinant products (25.0%). When background variables were compared, age was higher in the group treated with plasma-derived products but none of the other background variables differed between the two groups. These results suggest that in Japanese haemophilia patients, the type of clotting factor preparations used for therapy has not influenced the incidence of inhibitor formation.

摘要

在欧洲和北美国家进行的研究表明,包括种族在内的各种因素都会影响血友病患者抑制剂形成的频率。本研究旨在分析影响日本血友病 A 和 B 患者抑制剂形成的因素。分析数据是从 1988 年后出生的血友病 A 和 B 患者中回顾性收集的,这一年日本首次推出了单克隆抗体纯化的凝血因子 VIII 产品。从 184 名患者(153 例血友病 A;31 例血友病 B)中收集了各种数据。血友病 B 病例的样本量太小,无法在任何背景变量中揭示抑制剂形成组与无抑制剂组之间的任何显著差异。另一方面,对于血友病 A 患者,单因素分析确定了血友病的严重程度和抑制剂发展的阳性家族史是抑制剂形成的危险因素。在对使用的凝血因子产品进行分析时,用血浆衍生产品治疗的组(29.7%)和用重组产品治疗的组(25.0%)之间抑制剂形成的发生率没有显著差异。在比较背景变量时,用血浆衍生产品治疗的组的年龄较高,但两组之间没有其他背景变量存在差异。这些结果表明,在日本血友病患者中,用于治疗的凝血因子制剂类型并未影响抑制剂形成的发生率。

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