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

Sabine M El-Helou1,2, Anika-Kerstin Biegner1, Sebastian Bode1,3

  • 1Institute for Immunodeficiency, Center for Chronic Immunodeficiency (CCI), Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Insights

The German PID-NET registry provides crucial data on primary immunodeficiencies (PID), revealing insights into prevalence, diagnosis, and treatment. This national registry aids in improving patient outcomes through timely diagnosis and enhanced care strategies.

Area of Science:

  • Immunology
  • Genetics
  • Epidemiology

Background:

  • The German PID-NET registry, established in 2009, is Germany's first national registry for primary immunodeficiencies (PID).
  • It functions as part of the European Society for Immunodeficiencies (ESID) registry.
  • The registry aims to collect comprehensive data on PID epidemiology, diagnosis, and treatment.

Purpose of the Study:

  • To analyze epidemiological data, diagnostic delays, and treatment modalities for primary immunodeficiencies in Germany.
  • To provide insights into the prevalence and characteristics of various PID types.
  • To evaluate the effectiveness of diagnostic and therapeutic strategies for PID patients.

Main Methods:

  • Clinical and laboratory data were collected from 2,453 patients across 36 German PID centers.
  • Data was managed through an online registry and analyzed using Stata® and Excel.
  • Prevalence, demographic, clinical presentation, genetic, and treatment data were systematically gathered and assessed.

Main Results:

  • The minimum prevalence of PID in Germany is 2.72 per 100,000 inhabitants.
  • Predominantly antibody disorders were the most common PID group (57%), with infections being the most frequent presenting symptom (74%).
  • Diagnostic delay showed minimal decrease overall, but significant improvements were noted for Severe Combined Immunodeficiency (SCID) and Hyper IgE syndrome, with 49% of patients receiving immunoglobulin G (IgG) substitution and 300 undergoing hematopoietic stem cell transplantation (HSCT).

Conclusions:

  • The German PID-NET registry is an invaluable resource for clinicians, researchers, and policymakers.
  • The registry's data supports efforts to achieve more timely diagnoses and optimize treatment for PID patients.
  • Continued data collection and analysis are essential for advancing the understanding and management of primary immunodeficiencies.

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