Quality of life in adult patients using dialyzable leukocyte extract for allergic rhinitis

Author:

Homberg Toni Angela1,Lara Ivan1,Andaluz Consuelo1,Cervantes-Trujano Edgar1,Hernández-Martínez Pedro Martín1,Pérez-Tapia Sonia Mayra234,Jiménez-Martínez María Carmen56

Affiliation:

1. Unidad de Servicios Externos e Investigación Clínica (USEIC), Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de Mexico, Mexico

2. Unidad de Desarrollo e Investigación en Bioterapéuticos (UDIBI), Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de Mexico, Mexico

3. Departamento de Inmunología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de Mexico, Mexico

4. Laboratorio Nacional para Servicios Especializados de Investigación, Desarrollo e Innovación (I+D+i) para Farmacoquímicos y Biotecnológicos, LANSEIDI-FarBiotec-CONACyT, Ciudad de Mexico, Mexico

5. Departamento de Bioquímica, Facultad de Medicina, Universidad Nacional Autónoma de México, Ciudad de Mexico, Mexico

6. Departamento de Inmunología, Unidad de Investigación, Instituto de Oftalmología Fundación “Conde de Valenciana”, Ciudad DE Mexico, Mexico.

Abstract

Allergic rhinitis (AR) has considerable impact on the general health of individuals. Therefore, treatment trials should include an evaluation of quality of life. We aimed to determine changes in the quality of life of moderate/severe AR patients treated with standard treatment in addition to dialyzable leukocyte extract (DLE), a peptide-based immunomodulator. In a prospective, non-controlled trial, DLE was added to the standard treatment regimen for patients with moderate/severe AR. DLE was administered orally at 2 mg per day for 5 days, followed by 4 mg per week for 5 weeks, and then 2 mg per week for 5 weeks. The primary endpoints were overall improved Standardized Rhinoconjunctivitis Quality of Life Questionnaire (RQLQ) scores, domain scores, and individual item scores of 0.5 points or higher. Statistical significance was defined as P < .05. Thirty patients (50% female) aged 14 to 60 years old (33.4 ± 11.9) were enrolled in this study. The mean overall basal quality of life score was 3.41 ± 1.22. After 11 weeks, the mean RQLQ score was 1.74 ± 1.09 (P < .0001; 95% confidence interval [CI], 1.05-2.33), and all the domain scores improved (daily activities P < .001, 95% CI 0.91–2.15, sleep P < .001, 95% CI 0.9–2.26, non-hay fever symptoms P = .001, 95% CI 0.51–1.82, practical problems P < .001, 95% CI 1.55–2.85, nasal symptoms P < .001, 95% CI 1.36–2.67, ocular symptoms P < .001, 95% CI 1.05–2.17, emotional P < .001, 95% CI 1.23–2.55). Each of the 28 individual item scores on the RQLQ showed clinical (minimal important difference [MID] ≥ 0.5) and statistical (P < .05) improvements. DLE might be a beneficial adjuvant treatment for AR. Our results provide preliminary data for future research. Clinical trials registration ID: NCT02506998

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

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