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德国原发性免疫缺陷登记处(2012-2017 年)。

The German National Registry of Primary Immunodeficiencies (2012-2017).

机构信息

Institute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

RESIST - Cluster of Excellence 2155 to Hanover Medical School, Satellite Center Freiburg, Freiburg, Germany.

出版信息

Front Immunol. 2019 Jul 19;10:1272. doi: 10.3389/fimmu.2019.01272. eCollection 2019.

Abstract

The German PID-NET registry was founded in 2009, serving as the first national registry of patients with primary immunodeficiencies (PID) in Germany. It is part of the European Society for Immunodeficiencies (ESID) registry. The primary purpose of the registry is to gather data on the epidemiology, diagnostic delay, diagnosis, and treatment of PIDs. Clinical and laboratory data was collected from 2,453 patients from 36 German PID centres in an online registry. Data was analysed with the software Stata® and Excel. The minimum prevalence of PID in Germany is 2.72 per 100,000 inhabitants. Among patients aged 1-25, there was a clear predominance of males. The median age of living patients ranged between 7 and 40 years, depending on the respective PID. Predominantly antibody disorders were the most prevalent group with 57% of all 2,453 PID patients (including 728 CVID patients). A gene defect was identified in 36% of patients. Familial cases were observed in 21% of patients. The age of onset for presenting symptoms ranged from birth to late adulthood (range 0-88 years). Presenting symptoms comprised infections (74%) and immune dysregulation (22%). Ninety-three patients were diagnosed without prior clinical symptoms. Regarding the general and clinical diagnostic delay, no PID had undergone a slight decrease within the last decade. However, both, SCID and hyper IgE- syndrome showed a substantial improvement in shortening the time between onset of symptoms and genetic diagnosis. Regarding treatment, 49% of all patients received immunoglobulin G (IgG) substitution (70%-subcutaneous; 29%-intravenous; 1%-unknown). Three-hundred patients underwent at least one hematopoietic stem cell transplantation (HSCT). Five patients had gene therapy. The German PID-NET registry is a precious tool for physicians, researchers, the pharmaceutical industry, politicians, and ultimately the patients, for whom the outcomes will eventually lead to a more timely diagnosis and better treatment.

摘要

德国 PID-NET 注册中心成立于 2009 年,是德国首个原发性免疫缺陷病(PID)国家注册中心。它是欧洲免疫缺陷学会(ESID)注册中心的一部分。该注册中心的主要目的是收集 PID 的流行病学、诊断延迟、诊断和治疗数据。临床和实验室数据是从德国 36 个 PID 中心的 2453 名患者的在线注册中收集的。使用 Stata®和 Excel 软件对数据进行了分析。德国 PID 的最低患病率为每 10 万人 2.72 人。在 1-25 岁的患者中,男性明显居多。存活患者的中位年龄在 7 至 40 岁之间,具体取决于各自的 PID。主要抗体疾病是最常见的疾病组,占所有 2453 名 PID 患者的 57%(包括 728 名 CVID 患者)。36%的患者发现有基因缺陷。21%的患者为家族病例。出现症状的发病年龄从出生到成年晚期(0-88 岁)不等。首发症状包括感染(74%)和免疫失调(22%)。93 名患者在没有先前临床症状的情况下被诊断出患有 PID。关于一般和临床诊断延迟,过去十年中没有 PID 出现轻微减少。然而,SCID 和高 IgE 综合征在缩短症状出现和基因诊断之间的时间方面都有了实质性的改善。在治疗方面,所有患者中有 49%接受了免疫球蛋白 G(IgG)替代治疗(70%-皮下;29%-静脉内;1%-未知)。300 名患者接受了至少一次造血干细胞移植(HSCT)。5 名患者接受了基因治疗。德国 PID-NET 注册中心是医生、研究人员、制药行业、政治家和最终患者的宝贵工具,这些患者的最终结果将导致更及时的诊断和更好的治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e05/6659583/f75b35073c46/fimmu-10-01272-g0001.jpg

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