INFLUENCE OF THE AGE OF THE DIAGNOSIS AND THE BEGINNING OF SPECIFIC THERAPY ON MAIN CLINICAL AND LABORATORY MANIFESTATIONS OF A DISEASE IN PATIENTS WITH CYSTIC FIBROSIS

Background: To establish features of a clinical course of a disease at patients depending on age of firstly determine diagnosis of cystic fibrosis. Patients and methods: We examined 130 patients with cystic fibrosis aged under 25 years old. Depending on the age of diagnosis 3 groups of patients were...

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Main Authors: S. A. Krasovskii, N. Yu. Kashirskaya, M. V. Usacheva, E. L. Amelina, A. V. Chernyak, Zh.K. Naumenko
Format: Article
Language:English
Published: "Paediatrician" Publishers LLC 2014-03-01
Series:Вопросы современной педиатрии
Subjects:
Online Access:https://vsp.spr-journal.ru/jour/article/view/205
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author S. A. Krasovskii
N. Yu. Kashirskaya
M. V. Usacheva
E. L. Amelina
A. V. Chernyak
Zh.K. Naumenko
author_facet S. A. Krasovskii
N. Yu. Kashirskaya
M. V. Usacheva
E. L. Amelina
A. V. Chernyak
Zh.K. Naumenko
author_sort S. A. Krasovskii
collection DOAJ
description Background: To establish features of a clinical course of a disease at patients depending on age of firstly determine diagnosis of cystic fibrosis. Patients and methods: We examined 130 patients with cystic fibrosis aged under 25 years old. Depending on the age of diagnosis 3 groups of patients were formed: diagnosed at the age of 0–7, 8–18 and 18–25 years old. Results: There were no differences in the main anthropometric, functional, microbiological characteristics and frequency of complications at the age of 25 years between the patients of all three groups. However significant differences in «severity» of genotypes are defined: in group with the diagnosis established at preschool age, «severe» genotypes dominated, in group with the diagnosis established in 7–18 and 18–25 years, — «mild» genotypes. Importance of treatment with dornase alfa in all patients with cystic fibrosis regarding age of establishment of the diagnosis was shown. Conclusion: Early diagnostics determines appropriate beginning of the treatment, which can improve the further prognosis of the disease course. However late diagnostics in patients with «mild» genotype does not have significant influence on the clinical course at the age of 25 years old, which proves protective effects of «mild» mutations.
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spelling doaj.art-b34b275b0d2c4dc6aed3a9e34d11d79f2025-03-02T11:34:07Zeng"Paediatrician" Publishers LLCВопросы современной педиатрии1682-55271682-55352014-03-01132364310.15690/vsp.v13i2.971205INFLUENCE OF THE AGE OF THE DIAGNOSIS AND THE BEGINNING OF SPECIFIC THERAPY ON MAIN CLINICAL AND LABORATORY MANIFESTATIONS OF A DISEASE IN PATIENTS WITH CYSTIC FIBROSISS. A. Krasovskii0N. Yu. Kashirskaya1M. V. Usacheva2E. L. Amelina3A. V. Chernyak4Zh.K. Naumenko5Scientific Research Institute of Pulmonology, MoscowResearch Centre of Medical Genetics, MoscowScientific Research Institute of Pulmonology, MoscowScientific Research Institute of Pulmonology, MoscowScientific Research Institute of Pulmonology, MoscowScientific Research Institute of Pulmonology, MoscowBackground: To establish features of a clinical course of a disease at patients depending on age of firstly determine diagnosis of cystic fibrosis. Patients and methods: We examined 130 patients with cystic fibrosis aged under 25 years old. Depending on the age of diagnosis 3 groups of patients were formed: diagnosed at the age of 0–7, 8–18 and 18–25 years old. Results: There were no differences in the main anthropometric, functional, microbiological characteristics and frequency of complications at the age of 25 years between the patients of all three groups. However significant differences in «severity» of genotypes are defined: in group with the diagnosis established at preschool age, «severe» genotypes dominated, in group with the diagnosis established in 7–18 and 18–25 years, — «mild» genotypes. Importance of treatment with dornase alfa in all patients with cystic fibrosis regarding age of establishment of the diagnosis was shown. Conclusion: Early diagnostics determines appropriate beginning of the treatment, which can improve the further prognosis of the disease course. However late diagnostics in patients with «mild» genotype does not have significant influence on the clinical course at the age of 25 years old, which proves protective effects of «mild» mutations.https://vsp.spr-journal.ru/jour/article/view/205cystic fibrosisdiagnosticsage«severity» of genotypedornase alfa
spellingShingle S. A. Krasovskii
N. Yu. Kashirskaya
M. V. Usacheva
E. L. Amelina
A. V. Chernyak
Zh.K. Naumenko
INFLUENCE OF THE AGE OF THE DIAGNOSIS AND THE BEGINNING OF SPECIFIC THERAPY ON MAIN CLINICAL AND LABORATORY MANIFESTATIONS OF A DISEASE IN PATIENTS WITH CYSTIC FIBROSIS
Вопросы современной педиатрии
cystic fibrosis
diagnostics
age
«severity» of genotype
dornase alfa
title INFLUENCE OF THE AGE OF THE DIAGNOSIS AND THE BEGINNING OF SPECIFIC THERAPY ON MAIN CLINICAL AND LABORATORY MANIFESTATIONS OF A DISEASE IN PATIENTS WITH CYSTIC FIBROSIS
title_full INFLUENCE OF THE AGE OF THE DIAGNOSIS AND THE BEGINNING OF SPECIFIC THERAPY ON MAIN CLINICAL AND LABORATORY MANIFESTATIONS OF A DISEASE IN PATIENTS WITH CYSTIC FIBROSIS
title_fullStr INFLUENCE OF THE AGE OF THE DIAGNOSIS AND THE BEGINNING OF SPECIFIC THERAPY ON MAIN CLINICAL AND LABORATORY MANIFESTATIONS OF A DISEASE IN PATIENTS WITH CYSTIC FIBROSIS
title_full_unstemmed INFLUENCE OF THE AGE OF THE DIAGNOSIS AND THE BEGINNING OF SPECIFIC THERAPY ON MAIN CLINICAL AND LABORATORY MANIFESTATIONS OF A DISEASE IN PATIENTS WITH CYSTIC FIBROSIS
title_short INFLUENCE OF THE AGE OF THE DIAGNOSIS AND THE BEGINNING OF SPECIFIC THERAPY ON MAIN CLINICAL AND LABORATORY MANIFESTATIONS OF A DISEASE IN PATIENTS WITH CYSTIC FIBROSIS
title_sort influence of the age of the diagnosis and the beginning of specific therapy on main clinical and laboratory manifestations of a disease in patients with cystic fibrosis
topic cystic fibrosis
diagnostics
age
«severity» of genotype
dornase alfa
url https://vsp.spr-journal.ru/jour/article/view/205
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