The MEGA Project: A Study of the Mechanisms Involved in the Genesis and Disease Course of Asthma. Asthma Cohort Creation and Long-Term Follow-Up.
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Muñoz Xavier, Álvarez-Puebla María José, Arismendi Ebymar, Arochena Lourdes, Ausín María Del Pilar, Barranco Pilar, Bobolea Irina, Cañas Jose Antonio, Cardaba Blanca, Crespo Astrid, Del Pozo Victora, Domínguez-Ortega Javier, Fernandez-Nieto María Del Mar, Giner Jordi, González-Barcala Francisco Javier, Luna Juan Alberto, Mullol Joaquim, Ojanguren Iñigo, Olaguibel José María, Picado César, Plaza Vicente, Quirce Santiago, Ramos David, Rial Manuel, Romero-Mesones Christian, Salgado Francisco Javier, San-José María Esther, Sánchez-Diez Silvia, Sastre Beatriz, Sastre Joaquin, Soto Lorena, Torrejón Montserrat, Urnadoz Marisa, Valdes Luis, Valero Antonio, Cruz María Jesús
Аннотация
The general aim of this study is to create a cohort of asthma patients with varying grades of severity in order to gain greater insight into the mechanisms underlying the genesis and course of this disease. The specific objectives focus on various studies, including imaging, lung function, inflammation, and bronchial hyperresponsiveness, to determine the relevant events that characterize the asthma population, the long-term parameters that can determine changes in the severity of patients, and the treatments that influence disease progression. The study will also seek to identify the causes of exacerbations and how this affects the course of the disease. Patients will be contacted via the outpatient clinics of the 8 participating institutions under the auspices of the Spanish Respiratory Diseases Networking System (CIBER). In the inclusion visit, a standardized clinical history will be obtained, a clinical examination, including blood pressure, body mass index, complete respiratory function tests, and FENO will be performed, and the Asthma Control Test (ACT), Morisky-Green test, Asthma Quality of Life Questionnaire (Mini AQLQ), the Sino-Nasal Outcome Test 22 (SNOT-22), and the Hospital Anxiety and Depression scale (HADS) will be administered. A specific electronic database has been designed for data collection. Exhaled breath condensate, urine and blood samples will also be collected. Non-specific bronchial hyperresponsiveness testing with methacholine will be performed and an induced sputum sample will be collected at the beginning of the study and every 24 months. A skin prick test for airborne allergens and a chest CT will be performed at the beginning of the study and repeated every 5 years.