Kazan (Volga region) Federal University, KFU
KAZAN
FEDERAL UNIVERSITY
 
PERIOSTIN AS A BIOMARKER OF ALLERGIC INFLAMMATION IN ATOPIC BRONCHIAL ASTHMA AND ALLERGIC RHINITIS (A PILOT STUDY)
Form of presentationArticles in Russian journals and collections
Year of publication2020
Языканглийский
  • Kubysheva Nailya Iskhakovna, author
  • Eliseeva Tatyana , author
  • Frolov Pavel , author
  • Krasilnikova Svetlana , author
  • Ovsyannikov Dmitry , author
  • Terentyeva Anna , author
  • Tush Elena , author
  • Bibliographic description in the original language Krasilnikova, S. V., Tush, E. V., Frolov, P. A., Ovsyannikov, D. Y., Terentyeva, A. B., Kubysheva, N. I., & Eliseeva, T. I. (2020). Periostin as a Biomarker of Allergic Inflammation in Atopic Bronchial Asthma and Allergic Rhinitis (a Pilot Study). Sovremennye tekhnologii v medicine, 12(5 (eng)).
    Annotation The involvement of periostin in Th2-dependent allergic inflammation has been documented. However, the significance of periostin as a biomarker of local allergic inflammation in the nasal mucosa (NM) of patients with atopic bronchial asthma (BA) and allergic rhinitis (AR) is yet to be determined. The aim of the study was to determine the presence of periostin and evaluate its role as a non-invasive marker of allergic inflammation in the nasal secretions of children with atopic BA and AR. Materials and Methods. In 43 patients aged 4–17 years with atopic BA and AR, the NM was examined using nasal video-endoscopy and (if indicated) computed tomography; the amount of periostin in the nasal secretion was determined by the enzyme immunoassay. Results. Exacerbation ofAR was accompanied by a statistically significant increase in the level of periostin in the nasal secretion: up to 0.84 [0.06; 48.79] ng/mg, whereas in remission, that was 0.13 [0.00; 0.36] ng/mg; p=0.04. This value increased progressively as the severity of AR increased from 0.16 [0.00; 0.36] ng/mg in the mild course to 0.20 [0.00; 9.03] ng/mg in AR of moderate severity, and to 10.70 [0.56; 769.20] ng/mg in most severe cases; p=0.048. Hypertrophy or polyposis of the nasal and/or paranasal mucosa was detected in 34.9% (15/43) of the examined patients. The concentration of periostin in the nasal secretion was lower in children without NM hypertrophy: 0.18 [0.001; 4.30] ng/mg vs 0.78 [0.13; 162.10] ng/mg in patients with NM hypertrophy; the differences were close to statistically significant: p=0.051. The level of nasal periostin depended on the clinical form of hypertrophy in the sinonasal mucosa, reaching 0.17 [0.00; 0.32] ng/mg in children with polyposis hyperplasia of NM and 21.6 [10.70; 1516.80] ng/mg — with hypertrophy of the NM in the medial surface of the concha; p=0.02. Conclusion. Exacerbation and increased severity of AR in patients with atopic BA are accompanied by an increased level of periostin in the nasal secretion. This allows us to consider the level of nasal periostin as a biomarker of local allergic inflammation in the NM of patients with atopic BA combined with AR. Hypertrophic changes in the sinonasal mucosa are generally accompanied by an increased level of nasal periostin; specifically, this level significantly depends on the clinical form of mucous membrane hypertrophy and requires additional studies.
    Keywords periostin, bronchial asthma, allergic rhinitis, chronic rhinosinusitis with polyps
    The name of the journal SOVREMENNYE TEHNOLOGII V MEDICINE
    URL http://www.stm-journal.ru/ru/numbers/2020/5/1666
    Please use this ID to quote from or refer to the card https://repository.kpfu.ru/eng/?p_id=244281&p_lang=2
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