The Levels of Serum Biomarkers in Stable Asthma Patients with Comorbidities

• Published in: Iranian journal of allergy, asthma, and immunology Vol. 18; no. 1; pp. 27 - 37
• Main Authors: Ceylan, Emel, Bulut, Sertan, Yilmaz, Mustafa, Örün, Hüseyin, Karadağ, Fisun, Ömürlü, İmran Kurt, Kirdar, Sevin, Karul, Aslıhan
• Format: Journal Article
• Language: English
• Published: Iran Tehran University of Medical Sciences 01.02.2019
• Subjects: Adiponectin; Allergic rhinitis; Asthma; Biomarkers; Body mass index; C-reactive protein; Comorbidities; Cytokines; Diabetes mellitus; Disease control; Gastritis; Gastroesophageal reflux; Gender; Inflammation; Interleukin 13; Interleukin 6; Interleukin 8; Leukocytes (eosinophilic); Osteopontin; Patients; Serum interleukin 6; Serum interleukin 8; Sinusitis; Biomarkers; Serum interleukin 6; Comorbidities; Serum interleukin 8; Asthma
• ISSN: 1735-1502; 1735-5249
• DOI: 10.18502/ijaai.v18i1.628

The effects of comorbidities on systemic inflammation markers in stable asthmatics and the consequences of such effects have not been well evaluated. We aimed to evaluate the effect of comorbidities on clinical manifestations and systemic inflammation in asthmatic patients under control. The study group consisted of asthmatic patients who applied to our pulmonology outpatient clinic and volunteered to participate. 120 clinically stable asthma patients (71 females and 49 males) and 35 healthy controls (19 females and 16 males) with similar age, gender, and body mass index distributions were admitted to the study. The levels of osteopontin, interleukin 6 (IL-6), interleukin 8 (IL-8), interleukin 13 (IL-13), eosinophilic cationic protein, adiponectin, and high-sensitivity C-reactive protein of the individuals were evaluated using commercial ELISA kits by taking venous blood samples. Of 120 asthmatic subjects, 47 (39, 2%) had comorbidities and allergic rhinitis (15%) coexisted most frequently. Other comorbidities associated with asthma were gastroesophageal reflux, sinusitis, hypertension, diabetes, gastritis, and peptic ulcus respectively. There was no physician-diagnosed comorbidity in the control group. The levels of IL-6 and IL-8 were found higher in asthma group with comorbidities when compared to those with no comorbidities (p were 0.032 and 0.046, respectively). Comorbidities interfere with the diagnosis and treatment of asthma, besides affecting the disease control. Our findings suggest the possibility of the impact of comorbidities on systemic inflammation markers, especially IL-6 and IL-8. To evaluate the impact of comorbidities on asthma control and systemic markers, further studies are needed.