The Influence of Body Mass Index on Monocytes and Eosinophil Levels and Their Relationship With Spirometric Parameters in Children and Adolescents With Bronchial Asthma
Regina N. Khramova, Tatyana I. Eliseeva, Dmitry Y. Ovsyannikov, Elena V. Tush, Maxim A. Karpenko, Anastasia A. Shamrikova, Nailya I. Kubysheva, Vilya A. Bulgakova, Olga V. Khaletskaya, Natalia A. Geppe, Ildar Z. Batyrshin

TL;DR
This study explores how body mass index affects monocyte and eosinophil levels in children with asthma and how these relate to lung function.
Contribution
The study is the first to characterize the effect of BMI on monocyte levels in children with asthma and their relationship with spirometric parameters.
Findings
Overweight/obese children with asthma had significantly higher monocyte levels compared to normal weight children.
Eosinophil levels were lower in overweight/obese children compared to normal weight children.
Monocyte and eosinophil levels correlated negatively with spirometric parameters in overweight/obese and normal weight groups, respectively.
Abstract
Objectives: Excess adipose tissue induces low-intensity inflammation, which is an important pathogenetic factor adversely affecting the course of bronchial asthma (BA) in overweight/obese patients. The key effector cells of this inflammation are monocytes and macrophages. However, there are currently no studies characterising the effect of body mass index (BMI) on peripheral blood monocyte levels in children and adolescents with BA and their relationship with spirometric parameters reflecting bronchial patency. The aim of this study was to investigate the effect of BMI on peripheral blood monocyte and eosinophil levels and their relationship with spirometric parameters in children and adolescents with asthma. Methods: A single-centre, observational cross-sectional study was conducted. A total of 212 patients with asthma aged 7–17 years were studied. Anthropometric and spirometric…
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Taxonomy
TopicsAsthma and respiratory diseases · Chronic Obstructive Pulmonary Disease (COPD) Research · IL-33, ST2, and ILC Pathways
