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Article detail · 2024 · article

Allergic reactions to enzyme replacement therapy in children with lysosomal storage diseases and their management

YÖKSİS OpenAlex
Year2024
Citations4OpenAlex
Percentile%74.7
FWCI0.921.00 = world average
Scopus (SJR)Q2
WoS (JCR)Q3

Data source split

  • YÖKSİSYÖKSİS article record
  • YÖKSİS venueJournal of Pediatric Endocrinology and Metabolism
  • Catalog match (ISSN)Journal of Pediatric Endocrinology and Metabolism
  • OpenAlexOpenAlex enrichment (abstract, citations, topics)
  • Semantic Scholarcitation count (not merged with OpenAlex)

Abstract

OpenAlex English

OBJECTIVES: Human recombinant enzyme replacement therapy, given to compensate for genetic enzyme deficiency in lysosomal storage diseases, delays the progression of the disease and improves the quality of life. However, enzyme replacement therapy may cause hypersensitivity reactions. Within the scope of this research, we aimed to elucidate the frequency and clinical features of hypersensitivity reactions against enzyme replacement therapy in children with lysosomal storage diseases and clarify the management of these reactions. METHODS: Medical records of pediatric patients with lysosomal storage disease and receiving enzyme replacement therapy were retrospectively reviewed, and patients who experienced allergic reactions were included in the study. The demographic characteristics of the patients, their diagnosis, the responsible enzyme, the time at which the reaction started and at what dose, the signs and symptoms associated with the reaction, diagnostic tests, the management of the reaction, and the protocol applied for the maintenance of enzyme replacement therapy after the reaction were recorded. RESULTS: Hypersensitivity reactions developed in 18 of 71 patients (25.3 %) who received enzyme replacement therapy. The most common cutaneous findings were observed. Anaphylaxis developed in 6 of 18 patients. Patients who experienced recurrent hypersensitivity reactions with premedication or a slower infusion rate, those with positive skin test results, and patients who developed anaphylaxis were given enzyme replacement therapy with desensitization. CONCLUSIONS: HSR may develop during enzyme replacement therapy, which are vital in lysosomal storage diseases, and discontinuation of enzyme replacement therapy is a significant loss for patients with metabolic disorders. These reactions can be treated with premedication and long-term infusions, but some patients may require desensitization protocols for continued treatment.

Topics

Citations

OpenAlex cited_by_count. Not a WoS or Scopus citation count; those sources have no separate column here.

4citationsOpenAlex · cited_by_count (cache / database)

3 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).

  1. 2026 Phenotypes of Elosulfase Alfa-Induced Immediate Hypersensitivity Reactions and Long-Term Outcomes of Desensitization in Mucopolysaccharidosis IVACitations 0 · OpenAlex
  2. 2026 Phenotypes of Elosulfase Alfa-Induced Immediate Hypersensitivity Reactions and Long-term Outcomes of Desensitization in Mucopolysaccharidosis IVACitations 0 · OpenAlex
  3. 2026 Phenotypes of Elosulfase Alfa-Induced Immediate Hypersensitivity Reactions and Long-Term Outcomes of Desensitization in Mucopolysaccharidosis IVACitations 0 · OpenAlex

Authors

9
  1. ELİF ARIK 1
  2. ÖZLEM KESKİN 2
  3. SERPİL ALBAYRAK 3
  4. MEHMET KESKİN 4
  5. MAHMUT CESUR 5
  6. MURAT KARAOĞLAN GAZİANTEP ÜNİVERSİTESİ 6
  7. GAYE İNAL 7
  8. AHMET YILDIRIM 8
  9. ERCAN KÜÇÜKOSMANOĞLU 9