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鼻内皮质类固醇对变应性鼻炎患者睡眠障碍的疗效:一项系统评价和荟萃分析。

Effectiveness of Intranasal Corticosteroids for Sleep Disturbances in Patients with Allergic Rhinitis: A Systematic Review and Meta-Analysis.

作者信息

Tabata Kenshiro, Sumi Yukiyoshi, Sasaki Hatoko, Kojimahara Noriko

机构信息

Department of Biochemistry and Cellular Biology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.

Department of Psychiatry, Shiga University of Medical Science, Otsu, Japan.

出版信息

Int Arch Allergy Immunol. 2025;186(4):330-344. doi: 10.1159/000541389. Epub 2024 Oct 29.

DOI:10.1159/000541389
PMID:39471798
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11939832/
Abstract

INTRODUCTION

Allergic rhinitis (AR) is a chronic condition caused by an immunoglobulin E-mediated response to environmental allergens, which affects 10-40% of the global population. AR symptoms, such as nasal congestion and rhinorrhea, significantly reduce quality of life and are associated with sleep disturbances, further exacerbating the condition's burden. Despite the known impact of AR on sleep, the effects of intranasal corticosteroids on sleep quality have not been comprehensively reviewed. Therefore, this systematic review and meta-analysis aimed to investigate the efficacy of intranasal corticosteroids in improving sleep quality among patients with AR.

METHODS

This systematic review and meta-analysis followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. The study protocol was registered with PROSPERO (CRD42023460698). A comprehensive search was conducted on PubMed, Cochrane Central Register of Controlled Trials, and Ichushi-Web. Randomized controlled trials (RCTs) comparing intranasal corticosteroids with placebos in patients with AR were included. Data extraction and risk of bias assessment were independently performed by two authors. The primary outcome was the improvement in sleep quality measured by standardized questionnaires. Meta-analyses were performed using a random-effects model. The risk of bias was assessed using the RoB2 tool.

RESULTS

Eighteen RCTs involving 6,019 participants were included. The meta-analysis of 12 comparisons from eight studies for the Rhinoconjunctivitis Quality of Life Questionnaire sleep domain showed significant improvement in sleep quality with a standardized mean difference (SMD) of 0.292 (95% confidence interval [CI]: 0.235-0.350, p < 0.0001, I2 = 0.0%). The Nocturnal Rhinoconjunctivitis Quality of Life Questionnaire also showed improvement with an SMD of 0.284 (95% CI: 0.164-0.404, p < 0.0001) based on two comparisons from one study. However, the Epworth Sleepiness Scale did not show significant results (SMD: 0.027, 95% CI: -0.429 to 0.483, p = 0.907) based on two comparisons from two studies. Sensitivity analysis, excluding two studies with high risk of bias according to RoB2, confirmed the robustness of these results. Subgroup analyses for patients with seasonal or perennial AR showed significant improvements in both groups.

CONCLUSION

This study demonstrates that intranasal corticosteroids significantly improve sleep quality in patients with AR. These findings support the use of intranasal corticosteroids as a first-line treatment for AR, not only for managing daytime symptoms but also for enhancing sleep quality. Future research should focus on sleep quality changes as a primary outcome and incorporate both subjective and objective measures to better understand the relationship between sleep and AR symptoms.

INTRODUCTION

Allergic rhinitis (AR) is a chronic condition caused by an immunoglobulin E-mediated response to environmental allergens, which affects 10-40% of the global population. AR symptoms, such as nasal congestion and rhinorrhea, significantly reduce quality of life and are associated with sleep disturbances, further exacerbating the condition's burden. Despite the known impact of AR on sleep, the effects of intranasal corticosteroids on sleep quality have not been comprehensively reviewed. Therefore, this systematic review and meta-analysis aimed to investigate the efficacy of intranasal corticosteroids in improving sleep quality among patients with AR.

METHODS

This systematic review and meta-analysis followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. The study protocol was registered with PROSPERO (CRD42023460698). A comprehensive search was conducted on PubMed, Cochrane Central Register of Controlled Trials, and Ichushi-Web. Randomized controlled trials (RCTs) comparing intranasal corticosteroids with placebos in patients with AR were included. Data extraction and risk of bias assessment were independently performed by two authors. The primary outcome was the improvement in sleep quality measured by standardized questionnaires. Meta-analyses were performed using a random-effects model. The risk of bias was assessed using the RoB2 tool.

RESULTS

Eighteen RCTs involving 6,019 participants were included. The meta-analysis of 12 comparisons from eight studies for the Rhinoconjunctivitis Quality of Life Questionnaire sleep domain showed significant improvement in sleep quality with a standardized mean difference (SMD) of 0.292 (95% confidence interval [CI]: 0.235-0.350, p < 0.0001, I2 = 0.0%). The Nocturnal Rhinoconjunctivitis Quality of Life Questionnaire also showed improvement with an SMD of 0.284 (95% CI: 0.164-0.404, p < 0.0001) based on two comparisons from one study. However, the Epworth Sleepiness Scale did not show significant results (SMD: 0.027, 95% CI: -0.429 to 0.483, p = 0.907) based on two comparisons from two studies. Sensitivity analysis, excluding two studies with high risk of bias according to RoB2, confirmed the robustness of these results. Subgroup analyses for patients with seasonal or perennial AR showed significant improvements in both groups.

CONCLUSION

This study demonstrates that intranasal corticosteroids significantly improve sleep quality in patients with AR. These findings support the use of intranasal corticosteroids as a first-line treatment for AR, not only for managing daytime symptoms but also for enhancing sleep quality. Future research should focus on sleep quality changes as a primary outcome and incorporate both subjective and objective measures to better understand the relationship between sleep and AR symptoms.

摘要

引言

变应性鼻炎(AR)是一种由免疫球蛋白E介导的针对环境过敏原的反应所引起的慢性疾病,全球10%-40%的人口受其影响。AR症状,如鼻塞和流涕,会显著降低生活质量,并与睡眠障碍相关,进一步加重了该病的负担。尽管已知AR对睡眠有影响,但鼻用糖皮质激素对睡眠质量的影响尚未得到全面综述。因此,本系统评价和荟萃分析旨在研究鼻用糖皮质激素改善AR患者睡眠质量的疗效。

方法

本系统评价和荟萃分析遵循系统评价和荟萃分析的首选报告项目指南。研究方案已在国际前瞻性系统评价注册库(PROSPERO,注册号:CRD42023460698)注册。在PubMed、Cochrane对照试验中心注册库和日本医学中央杂志网络版上进行了全面检索。纳入了比较鼻用糖皮质激素与安慰剂治疗AR患者的随机对照试验(RCT)。由两位作者独立进行数据提取和偏倚风险评估。主要结局是通过标准化问卷测量的睡眠质量改善情况。使用随机效应模型进行荟萃分析。使用RoB2工具评估偏倚风险。

结果

纳入了18项RCT,涉及6019名参与者。对八项研究中关于鼻结膜炎生活质量问卷睡眠领域的12项比较进行的荟萃分析显示,睡眠质量有显著改善,标准化平均差(SMD)为0.292(95%置信区间[CI]:0.235-0.350,p<0.0001,I2=0.0%)。基于一项研究的两项比较,夜间鼻结膜炎生活质量问卷也显示有改善,SMD为0.284(95%CI:0.164-0.404,p<0.0001)。然而,基于两项研究的两项比较,爱泼沃斯思睡量表未显示出显著结果(SMD:0.027,95%CI:-0.429至0.483,p=0.907)。敏感性分析排除了根据RoB2判断有高偏倚风险的两项研究,证实了这些结果的稳健性。对季节性或常年性AR患者的亚组分析显示两组均有显著改善。

结论

本研究表明,鼻用糖皮质激素可显著改善AR患者的睡眠质量。这些发现支持将鼻用糖皮质激素作为AR的一线治疗药物,不仅用于控制白天症状,还可提高睡眠质量。未来的研究应将睡眠质量变化作为主要结局,并纳入主观和客观测量方法,以更好地理解睡眠与AR症状之间的关系。

引言

变应性鼻炎(AR)是一种由免疫球蛋白E介导的针对环境过敏原的反应所引起的慢性疾病,全球10%-40%的人口受其影响。AR症状,如鼻塞和流涕,会显著降低生活质量,并与睡眠障碍相关,进一步加重了该病的负担。尽管已知AR对睡眠有影响,但鼻用糖皮质激素对睡眠质量的影响尚未得到全面综述。因此,本系统评价和荟萃分析旨在研究鼻用糖皮质激素改善AR患者睡眠质量的疗效。

方法

本系统评价和荟萃分析遵循系统评价和荟萃分析的首选报告项目指南。研究方案已在国际前瞻性系统评价注册库(PROSPERO,注册号:CRD42023460698)注册。在PubMed、Cochrane对照试验中心注册库和日本医学中央杂志网络版上进行了全面检索。纳入了比较鼻用糖皮质激素与安慰剂治疗AR患者的随机对照试验(RCT)。由两位作者独立进行数据提取和偏倚风险评估。主要结局是通过标准化问卷测量的睡眠质量改善情况。使用随机效应模型进行荟萃分析。使用RoB2工具评估偏倚风险。

结果

纳入了18项RCT,涉及6019名参与者。对八项研究中关于鼻结膜炎生活质量问卷睡眠领域的12项比较进行的荟萃分析显示,睡眠质量有显著改善,标准化平均差(SMD)为0.292(95%置信区间[CI]:0.235-0.350,p<0.0001,I2=0.0%)。基于一项研究的两项比较,夜间鼻结膜炎生活质量问卷也显示有改善,SMD为0.284(95%CI:0.164-0.404,p<0.0001)。然而,基于两项研究的两项比较,爱泼沃斯思睡量表未显示出显著结果(SMD:0.027,95%CI:-0.429至0.483,p=0.907)。敏感性分析排除了根据RoB2判断有高偏倚风险的两项研究,证实了这些结果的稳健性。对季节性或常年性AR患者的亚组分析显示两组均有显著改善。

结论

本研究表明,鼻用糖皮质激素可显著改善AR患者的睡眠质量。这些发现支持将鼻用糖皮质激素作为AR的一线治疗药物,不仅用于控制白天症状,还可提高睡眠质量。未来的研究应将睡眠质量变化作为主要结局,并纳入主观和客观测量方法,以更好地理解睡眠与AR症状之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc6e/11939832/b12e4e44c7c6/iaa-2025-0186-0004-541389_F07.jpg
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