Influence of Genetics on the Response to Omalizumab in Patients with Severe Uncontrolled Asthma with an Allergic Phenotype

被引:3
|
作者
Rojo-Tolosa, Susana [1 ,2 ,3 ]
Sanchez-Martinez, Jose Antonio [1 ]
Pineda-Lancheros, Laura Elena [2 ,3 ]
Galvez-Navas, Jose Maria [2 ,3 ,4 ]
Gonzalez-Gutierrez, Maria Victoria [1 ]
Jimenez-Galvez, Gonzalo [1 ]
Perez-Ramirez, Cristina [3 ]
Morales-Garcia, Concepcion [1 ]
Jimenez-Morales, Alberto [2 ]
机构
[1] Univ Hosp Virgen De Las Nieves, Resp Med Dept, Granada 18014, Spain
[2] Univ Hosp Virgen De Las Nieves, Pharm Serv, Pharmacogenet Unit, Granada 18014, Spain
[3] Univ Granada, Inst Nutr & Food Technol Jose Mataix, Ctr Biomed Res, Dept Biochem & Mol Biol 2, Avda Conocimiento s-n, Granada 18016, Spain
[4] Andalusian Sch Publ Hlth, Canc Registry Granada, Carretera Observ 4, Granada 18011, Spain
关键词
severe uncontrolled asthma; omalizumab; effectiveness; polymorphisms; EPSILON-RI-BETA; RECEPTOR-LIKE; IMMUNOGLOBULIN-E; CHILDHOOD ASTHMA; LUNG-FUNCTION; ASSOCIATION; IGE; POLYMORPHISMS; THERAPY; VARIANTS;
D O I
10.3390/ijms24087029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Omalizumab is a monoclonal antibody indicated for the treatment of severe uncontrolled asthma with an allergic phenotype. Its effectiveness could be influenced by clinical variables and single nucleotide polymorphisms (SNPs) in one or more of the genes involved in the mechanism of action and process of response to omalizumab, and these could be used as predictive biomarkers of response. We conducted an observational retrospective cohort study that included patients with severe uncontrolled allergic asthma treated with omalizumab in a tertiary hospital. Satisfactory response after 12 months of treatment was defined as (1) Reduction >= 50% of exacerbations or no exacerbations, (2) Improvement of lung function >= 10% FEV1, and (3) Reduction >= 50% of OCS courses or no OCS. Polymorphisms in the FCER1A (rs2251746, rs2427837), FCER1B (rs1441586, rs573790, rs1054485, rs569108), C3 (rs2230199), FCGR2A (rs1801274), FCGR2B (rs3219018, rs1050501), FCGR3A (rs10127939, rs396991), IL1RL1 (rs1420101, rs17026974, rs1921622), and GATA2 (rs4857855) genes were analyzed by real-time polymerase chain reaction (PCR) using TaqMan probes. A total of 110 patients under treatment with omalizumab were recruited. After 12 months of treatment, the variables associated with a reduction in exacerbations were the absence of polyposis (odds ratio [OR] = 4.22; 95% confidence interval [CI] = 0.95-19.63), IL1RL1 rs17026974-AG (OR = 19.07; 95% CI = 1.27-547), and IL1RL1 rs17026974-GG (OR = 16.76; 95% CI = 1.22-438.76). Reduction in oral corticosteroids (OCS) was associated with age of starting omalizumab treatment (OR = 0.95; 95% CI = 0.91-0.99) and blood eosinophil levels > 300 cells/mu L (OR = 2.93; 95% CI = 1.01-9.29). Improved lung function showed a relationship to the absence of chronic obstructive pulmonary disease (COPD) (OR = 12.16; 95% CI = 2.45-79.49), FCGR2B rs3219018-C (OR = 8.6; 95% CI = 1.12-117.15), GATA2 rs4857855-T (OR = 15.98; 95% CI = 1.52-519.57) and FCGR2A rs1801274-G (OR = 13.75; 95% CI = 2.14-142.68; AG vs. AA and OR = 7.46; 95% CI = 0.94-89.12; GG vs. AA). Meeting one response criterion was related to FCER1A rs2251746-TT (OR = 24; 95% CI = 0.77-804.57), meeting two to age of asthma diagnosis (OR = 0.93; 95% CI = 0.88-0.99), and meeting all three to body mass index (BMI) < 25 (OR = 14.23; 95% CI = 3.31-100.77) and C3 rs2230199-C (OR = 3; 95% CI = 1.01-9.92). The results of this study show the possible influence of the polymorphisms studied on the response to omalizumab and the clinical benefit that could be obtained by defining predictive biomarkers of treatment response.
引用
收藏
页数:16
相关论文
共 50 条
  • [31] Cost-effectiveness of omalizumab in real world uncontrolled allergic asthma patients
    Arrobas, A.
    Barbosa, M. P.
    Rabiais, S.
    Vandewalle, B.
    Felix, J.
    PULMONOLOGY, 2021, 27 (02): : 124 - 133
  • [32] Use of Omalizumab in patients with uncontrolled persistent allergic asthma: first experience in Kuwait
    Al-Ahmad, M.
    Arifhodzic, N.
    Al Ahmed, N.
    al Enizi, A.
    Fakim, N.
    ALLERGY, 2010, 65 : 553 - 553
  • [33] Response to Omalizumab in Black and White Patients with Allergic Asthma
    Szefler, Stanley J.
    Jerschow, Elina
    Yoo, Bongin
    Janampally, Pranathi
    Pazwash, Hooman
    Holweg, Cecile T. J.
    Hudes, Golda
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2021, 9 (11): : 4021 - 4028
  • [34] Adherence and effectiveness of omalizumab treatment in severe allergic asthma patients
    Ozseker, Z. F.
    Bulut, I
    Erdenen, F.
    Erdogdu, D.
    Asli, G.
    Ersoy, R.
    Kutlu, A.
    Ozturk, S.
    ALLERGY, 2013, 68 : 363 - 364
  • [35] Omalizumab decreases IgE production in patients with severe allergic asthma
    Huebner, Marisa
    Korn, Stephanie
    Jung, Matthias
    Buhl, Roland
    EUROPEAN RESPIRATORY JOURNAL, 2012, 40
  • [36] Improvement in quality of life with omalizumab in patients with severe allergic asthma
    Chipps, Bradley
    Buhl, Roland
    Beeh, Kai-Michael
    Fox, Howard
    Thomas, Karen
    Reisner, Colin
    CURRENT MEDICAL RESEARCH AND OPINION, 2006, 22 (11) : 2201 - 2208
  • [37] Omalizumab Improves Quality of Life in Adults and Adolescents (≥ 12 Years) With Uncontrolled Severe Allergic Asthma
    Siergiejko, Z.
    Swiebocka, E.
    Peckitt, C.
    Maykut, R.
    Peachey, G.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2010, 181
  • [38] Omalizumab shows two different response patterns in severe allergic asthma
    Proenca, M.
    Marcelino, J.
    Farinha, S.
    Silva, R.
    Tomaz, E.
    ALLERGY, 2021, 76 : 178 - 179
  • [39] OMALIZUMAB TREATMENT RESPONSE IN A SEVERE ALLERGIC ASTHMA POPULATION WITH OVERLAPPING COPD
    Maltby, Steven
    Gibson, Peter G.
    Powell, Heather
    Mcdonald, Vanessa M.
    RESPIROLOGY, 2017, 22 : 83 - 83
  • [40] Omalizumab Treatment Response in a Population With Severe Allergic Asthma and Overlapping COPD
    Maltby, Steven
    Gibson, Peter G.
    Powell, Heather
    McDonald, Vanessa M.
    CHEST, 2017, 151 (01) : 78 - 89