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

Authors :
El-Helou SM
Biegner AK
Bode S
Ehl SR
Heeg M
Maccari ME
Ritterbusch H
Speckmann C
Rusch S
Scheible R
Warnatz K
Atschekzei F
Beider R
Ernst D
Gerschmann S
Jablonka A
Mielke G
Schmidt RE
Schürmann G
Sogkas G
Baumann UH
Klemann C
Viemann D
von Bernuth H
Krüger R
Hanitsch LG
Scheibenbogen CM
Wittke K
Albert MH
Eichinger A
Hauck F
Klein C
Rack-Hoch A
Sollinger FM
Avila A
Borte M
Borte S
Fasshauer M
Hauenherm A
Kellner N
Müller AH
Ülzen A
Bader P
Bakhtiar S
Lee JY
Heß U
Schubert R
Wölke S
Zielen S
Ghosh S
Laws HJ
Neubert J
Oommen PT
Hönig M
Schulz A
Steinmann S
Schwarz K
Dückers G
Lamers B
Langemeyer V
Niehues T
Shai S
Graf D
Müglich C
Schmalzing MT
Schwaneck EC
Tony HP
Dirks J
Haase G
Liese JG
Morbach H
Foell D
Hellige A
Wittkowski H
Masjosthusmann K
Mohr M
Geberzahn L
Hedrich CM
Müller C
Rösen-Wolff A
Roesler J
Zimmermann A
Behrends U
Rieber N
Schauer U
Handgretinger R
Holzer U
Henes J
Kanz L
Boesecke C
Rockstroh JK
Schwarze-Zander C
Wasmuth JC
Dilloo D
Hülsmann B
Schönberger S
Schreiber S
Zeuner R
Ankermann T
von Bismarck P
Huppertz HI
Kaiser-Labusch P
Greil J
Jakoby D
Kulozik AE
Metzler M
Naumann-Bartsch N
Sobik B
Graf N
Heine S
Kobbe R
Lehmberg K
Müller I
Herrmann F
Horneff G
Klein A
Peitz J
Schmidt N
Bielack S
Groß-Wieltsch U
Classen CF
Klasen J
Deutz P
Kamitz D
Lassay L
Tenbrock K
Wagner N
Bernbeck B
Brummel B
Lara-Villacanas E
Münstermann E
Schneider DT
Tietsch N
Westkemper M
Weiß M
Kramm C
Kühnle I
Kullmann S
Girschick H
Specker C
Vinnemeier-Laubenthal E
Haenicke H
Schulz C
Schweigerer L
Müller TG
Stiefel M
Belohradsky BH
Soetedjo V
Kindle G
Grimbacher B
Source :
Frontiers in immunology [Front Immunol] 2019 Jul 19; Vol. 10, pp. 1272. Date of Electronic Publication: 2019 Jul 19 (Print Publication: 2019).
Publication Year :
2019

Abstract

Introduction: 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. Methods: 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. Results: 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. Conclusion: 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.

Details

Language :
English
ISSN :
1664-3224
Volume :
10
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
31379802
Full Text :
https://doi.org/10.3389/fimmu.2019.01272