Influence of Genetics on the Response to Omalizumab in Patients with Severe Uncontrolled Asthma with an Allergic Phenotype
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Rojo Tolosa, Susana; Pineda Lancheros, Laura Elena; Gálvez Navas, José María; Pérez Ramírez, CristinaEditorial
MDPI
Materia
Severe uncontrolled asthma Omalizumab Effectiveness Polymorphism
Date
2023-04-10Referencia bibliográfica
Rojo-Tolosa, S.; Sánchez- Martínez, J.A.; Pineda-Lancheros, L.E.; Gálvez-Navas, J.M.; González- Gutiérrez, M.V.; Jiménez-Gálvez, G.; Pérez-Ramírez, C.;Morales-García, C.; Jiménez-Morales, A. Influence of Genetics on the Response to Omalizumab in Patients with Severe Uncontrolled Asthma with an Allergic Phenotype. Int. J. Mol. Sci. 2023, 24, 7029. https://doi.org/10.3390/ijms24087029
Sponsorship
Instituto de Salud Carlos III (PT13/0010/0039); Biobank of the Hospital Universitario Virgen de las Nieves.Abstract
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/ 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.