Back to Search
Start Over
The German National Registry of Primary Immunodeficiencies (2012–2017)
- Source :
- Frontiers in Immunology, Vol 10 (2019), FRONTIERS IN IMMUNOLOGY, Frontiers in Immunology, Frontiers in immunology 10, 1272 (2019). doi:10.3389/fimmu.2019.01272
- Publication Year :
- 2019
- Publisher :
- Frontiers Media S.A., 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. peerReviewed
- Subjects :
- Male
0301 basic medicine
Pediatrics
Delayed Diagnosis
medicine.medical_treatment
CVID
European Society for Immunodeficiencies (ESID)
German PID-NET registry
IgG substitution therapy
PID prevalence
primary immunodeficiency (PID)
registry for primary immunodeficiency
Prevalence
Hematopoietic stem cell transplantation
medicine.disease_cause
German
0302 clinical medicine
Germany
Epidemiology
Immunology and Allergy
Registries
Child
Original Research
Aged, 80 and over
Hematopoietic Stem Cell Transplantation
Middle Aged
ddc
3. Good health
Child, Preschool
language
Female
Adult
lcsh:Immunologic diseases. Allergy
medicine.medical_specialty
Adolescent
Immunology
Immunoglobulins
Young Adult
03 medical and health sciences
medicine
Humans
ddc:610
Aged
business.industry
Immunologic Deficiency Syndromes
Infant, Newborn
Infant
Genetic Therapy
Immune dysregulation
language.human_language
030104 developmental biology
National registry
Age of onset
business
Genetic diagnosis
lcsh:RC581-607
030215 immunology
Subjects
Details
- Language :
- English
- ISSN :
- 16643224
- Volume :
- 10
- Database :
- OpenAIRE
- Journal :
- Frontiers in Immunology
- Accession number :
- edsair.doi.dedup.....548173fd8c7c0b6b3554a9823dcf9999