The influence of various factors on the forced expiratory volume in 1 second in children and adults with cystic fibrosis not taking CFTR-modulators
https://doi.org/10.18093/0869-0189-2026-36-1-43-51
Abstract
One of the most important predictors of the prognosis of cystic fibrosis (CF) is the pulmonary function test – forced expiratory volume in 1 second (FEV1). It is important for physicians to understand the factors associated with changes in FEV1 in patients not receiving CFTR modulators.
The aim of this study was to identify factors influencing changes in FEV1 in patients with CF not receiving CFTR modulators.
Methods. Retrospective analysis was conducted using medical records of patients (n = 225) under 18 years who received inpatient treatment in the pediatric department of the Russian Children’s Clinical Hospital, the Branch of the Russian National Research Medical University named after N.I.Pirogov, as well as patients over 18 years (n = 181) who were followed by specialists of the Pulmonology Scientific Research Institute under Federal Medical and Biological Agency of Russian Federation.
Results. Nutritional status and the nature of pathogenic microflora of the lower respiratory tract have a key impact on the FEV1 indicator in childhood. In the group of adult patients, the leading role belongs to complications such as CF-associated diabetes mellitus and the presence of pneumothorax.
Conclusion. Regular monitoring of external respiratory function is an integral part of patient management in CF. This study demonstrates the relationship between FEV1 and a number of factors in patients not receiving pathogenetic therapy.
About the Authors
O. G. КositskaiaRussian Federation
Oksana G. Кositskaia, Assistant Professor, Academician V.A.Tabolin Department of Hospital Paediatrics, Institute of Motherhood and Childhood
ul. Ostrovityanova 1, Moscow, 117997
tel.: (495) 936-93-74
Author ID: 881007
Competing Interests:
The authors declare no conflicts of interest.
S. A. Krasovskiy
Russian Federation
Stanislav А. Krasovskiy, Candidate of Medicine, Senior Researcher, Acting Head of the Cystic Fibrosis Laboratory; Leading Researcher, Scientific and Clinical Department
Orekhovyy bul’var 28, Moscow, 115682
ul. Moskvorechye 1, Moscow, 115522
tel.: (495) 111-03-03
Author ID: 688178
Competing Interests:
The authors declare no conflicts of interest.
P. V. Shumilov
Russian Federation
Petr V. Shumilov, Doctor of Medicine, Professor, Head of the Academician V.A.Tabolin Department of Hospital Paediatrics, Institute of Motherhood and Childhood
ul. Ostrovityanova 1, Moscow, 117997
tel.: (495) 936-93-74
Competing Interests:
The authors declare no conflicts of interest.
S. Yu. Semykin
Russian Federation
Sergey Yu. Semykin, Сandidate of Medicine, Head of the Pediatric Department
Leninskiy prospect 117, build. 1, Moscow, 119571
tel.: (495) 965-45-20
Competing Interests:
The authors declare no conflicts of interest.
O. V. Ryazanovа
Russian Federation
Olga V. Ryazanovа, Сandidate of Medicine, Associate Professor, Academician V.A.Tabolin Department of Hospital Paediatrics, Institute of Motherhood and Childhood
ul. Ostrovityanova 1, Moscow, 117997
tel.: (495) 936-93-74
Competing Interests:
The authors declare no conflicts of interest.
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Review
For citations:
Кositskaia O.G., Krasovskiy S.A., Shumilov P.V., Semykin S.Yu., Ryazanovа O.V. The influence of various factors on the forced expiratory volume in 1 second in children and adults with cystic fibrosis not taking CFTR-modulators. PULMONOLOGIYA. 2026;36(1):43-51. (In Russ.) https://doi.org/10.18093/0869-0189-2026-36-1-43-51
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