Journals / Astım Allerji İmmünoloji / 2020 / Cilt: 18 - Sayı: 1

To What Extent do Transient Hypogammaglobulinemia of the Infancy and Allergic Diseases Coexist?

Pages
23–29
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In patients who are admitted with allergic disease symptoms, underlying hypogammaglobulinemia should also be investigated.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Objective: To investigate the clinical features and follow-up results of the patients with transient hypogammaglobulinemia of infancy (THI) and to understand to what extent the condition coexists with allergic diseases.
📊
Key Findings & Data:Materials and Methods: Between January 2010 and February 2019, 172 patients who had been referred to Ankara University Faculty of Medicine’s Pediatric Immunology and Allergy Outpatient Department for findings of atopic disease or for frequent infections with a suspicion of PID, who were diagnosed with THI, and followed-up for at least one year were included in this study.
💡
Conclusion & Impact:In patients who are admitted with allergic disease symptoms, underlying hypogammaglobulinemia should also be investigated.
🔬Design:Research Article
📍Scope:2010 Verileri
⚙️Variables:Domain Parameters

Özet

Objective: To investigate the clinical features and follow-up results of the patients with transient hypogammaglobulinemia of infancy (THI) and to understand to what extent the condition coexists with allergic diseases. Materials and Methods: Between January 2010 and February 2019, 172 patients who had been referred to Ankara University Faculty of Medicine’s Pediatric Immunology and Allergy Outpatient Department for findings of atopic disease or for frequent infections with a suspicion of PID, who were diagnosed with THI, and followed-up for at least one year were included in this study. Their clinical and immunological features and follow-up results were evaluated retrospectively. Results: Of the 172 patients, 59% were boys. Median time of symptom onset was 14 months (1-46 months), median time of admission was 20 months (6-30 months), and consanguineous marriages were seen in 20% of the families. The most common referral complaints were respiratory tract infections and non-wheezing allergic diseases with rates of 71.5% and 27%, respectively. Cellular immune system analyses were normal. During a median follow-up time of 36 months, 42% of the patients recovered, 25% (n=43) still had THI, 25% (n=43) had unclassified hypogammaglobulinemia (UCG), 4% (n=7) had partial IgA deficiency, and 4% (n=7) had partial IgM deficiency. Allergic diseases were seen in 46% of the patients. An asthma diagnosis was made in 35.4% of the patients, allergic rhinitis in 5% and atopic dermatitis in 12.7%. The skin prick test was positive in 15% of them. Conclusion: THI mostly improves spontaneously in time. However, hypogammaglobulinemia can last until later years in life in a group of patients. Allergic diseases increase with the presence of THI. In patients who are admitted with allergic disease symptoms, underlying hypogammaglobulinemia should also be investigated.

🔖

Cite This Article

HASKALOĞLU, Ş. (2020). To What Extent do Transient Hypogammaglobulinemia of the Infancy and Allergic Diseases Coexist?. Astım Allerji İmmünoloji, Cilt: 18 - Sayı: 1, 23–29. https://ajindex.com/articles/141887

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (13)

  1. Gitlinn D, Janeway CA. Agammaglobulinemia, congenital, acquired and transient forms. Prog Hematol 1956;1:318-29
  2. Picard C, Al-Herz W, Bousfiha A, Casanova JL, Chatila T, Conley ME, et al. Primary immunodeficiency diseases: An update on the classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015. J Clin Immunol 2015; 35:696-726
  3. Schatorje EJ, Gathmann B, vanHout RW, de Vries E, PedPADconsortium. The PedPAD study: Boys predominate in the hypogammaglobulinaemia registry of the ESID online database. Clin Exp Immunol 2014;176:387‐93
  4. Ameratunga R, Ahn Y, Steele R, Woon ST. Transient hypogammaglobulinaemia of infancy: Many patients recover in adolescence and adulthood. Clin Exp Immunol 2019;198:224-32
  5. Kutukculer N, Gulez N. The outcome of patients with unclassified hypogammaglobulinemia in early childhood. Pediatr Allergy Immunol 2009:20:693-8
  6. Dorsey MJ, Orange JS. Impaired specific antibody response and increased B-cell population in transient hypogammaglobulinemia of infancy. Ann Allergy Asthma Immunol 2006;(97):590-5
  7. Walker AM, Kemp AS, Hill DJ, Shelton MJ. Features of transient hypogammaglobulinaemia in infants screened for immunological abnormalities. Arch Dis Child 1994;70:183-6
  8. Keles S, Artac H, Kara R, Gokturk B, Ozen A, Reisli I. Transient hypogammaglobulinemia and unclassified hypogammaglobulinemia: ‘Similarities and differences”. Pediatr Allergy Immunol 2010:21:843-51
  9. Dadkhah M, Aghamohammadi A, Movahedi M, Gharagozlou M. Atopic manifestations: Dermatitis, allergic rhinitis and asthma in patients with hypogammaglobulinemia. Iran J Pediatr 2015;25(5):e2786
  10. Tezcan I, Berkel AI, Ersoy F, Sanal O. Sağlıklı Türk çocukları ve erişkinlerde turbidimetrik yöntemle bakılan serum immünoglobülin düzeyleri. Çocuk Sağlığı ve Hastalıkları Dergisi 1996;39:649-56
  11. Kendirli T, Ikincioğullari A, Doğu F, Babacan E. Peripheral blood lymphocyte subsets in children with frequent upper respiratory tract infections. Turk J Pediatr 2008;50(1):63-6
  12. Hanifin JM, Cooper KD, Ho VC, Kang S, Krafchik BR, Margolis DJ, et al. Guidelines of care for atopic dermatitis developed in accordance with the American Academy of Dermatology (AAD)/ American Academy of Dermatology Association “Administrative Regulations for Evidence-Based Clinical Practice Guidelines”. J Am Acad Dermatol 2004; 50:391-404
  13. GINA Report, Global Strategy for Asthma Management and Prevention. Erişim tarihi