Do Probiotics have a role in the Treatment of Allergic Rhinitis? A Comprehensive Systematic Review and Metaanalysis

Author:

Güvenç Işil Adadan1,Muluk Nuray Bayar2,Mutlu Fezan Şahin3,Eşki Erkan4,Altıntoprak Niyazi5,Oktemer Tugba6,Cingi Cemal7

Affiliation:

1. Department of Otorhinolaryngology, Çigli Regional Education Hospital, Izmir, Turkey

2. Department of Otorhinolaryngology, Kirikkale University, Medical Faculty, Kirikkale, Turkey

3. Department of Biostatistics, Medical Faculty, Eskisehir Osmangazi University, Eskisehir, Turkey

4. Department of Otorhinolaryngology, Zubeyde Hanım Research and Training Center, Medical Faculty, Baskent University, Izmir, Turkey

5. Ear, Nose and Throat (ENT) Department, Tuzla State Hospital, Istanbul, Turkey

6. ENT Department, Private Polath Can Hospital, Ankara, Turkey

7. Department of Otorhinolaryngology, Medical Faculty, Eskisehir Osmangazi University, Eskisehir, Turkey

Abstract

Objective To investigate clinical evidence for the efficacy of probiotics in the treatment of allergic rhinitis (AR). Methods A systematic search was conducted to review the results of all randomized, double-blind, placebo-controlled trials by following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Statement. Primary outcome measurements were total nasal and ocular symptom scores (SS) and quality of life (QoL) questionnaires. Secondary outcome measurements were individual nasal SS and immunologic parameters. Results Twenty-two randomized, double-blind, placebo-controlled studies were included. Seventeen trials showed significant benefit of probiotics clinically, whereas eight trials showed significant improvement in immunologic parameters compared with placebo. All five studies with Lactobacillus paracasei (LP) strains demonstrated clinically significant improvements compared with placebo. Probiotics showed significant reduction in nasal and ocular SS (standardized mean difference [SMD], -1.23, p < 0.001; and SMD, -1.84, p < 0.001; respectively), total, nasal, and ocular QoL scores compared with placebo (SMD, -1.84, p < 0.001; SMD, -2.30, p = 0.006; and SMD, -3.11, p = 0.005; respectively). Although heterogeneity was high, in subgroup analysis, SMD for total nasal and ocular symptoms with patients with seasonal AR and for nasal QoL scores for studies with LP-33 strain were significant and homogenous. Scores of nasal blockage, rhinorrhea, and nasal itching were significantly lower in the probiotic group compared with placebo. The meta-analysis studies SS the Japanese guidelines revealed a significant, homogenous SMD score of -0.34 for individual nasal SS, above the minimal important clinical difference value of 0.3. The T-helper 1 to T-helper 2 ratio was significantly lower in the probiotic group compared with placebo (SMD, -0.78; p = 0.045). Conclusion Despite high variability among the studies, synthesis of available data provided significant evidence of beneficial clinical and immunologic effects of probiotics in the treatment of AR, especially with seasonal AR and LP-33 strains. With the rising pool of studies, the most promising strains in specific allergies can be revealed and adjuvant therapy with probiotics can be recommended for the treatment of AR.

Publisher

SAGE Publications

Subject

General Medicine,Otorhinolaryngology,Immunology and Allergy

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