The prevalence of spontaneous pneumothorax in patients with BHD syndrome: a systematic review and meta-analysis.

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Yanan Zhang, Yuling Wang, Jinxia Wang, Ping Li, Ruonan Lv, Juan Chen
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引用次数: 0

Abstract

Background: Birt-Hogg-Dubé (BHD) syndrome is associated with an increased risk of pneumothorax. This study aimed to determine the prevalence of spontaneous pneumothorax among individuals diagnosed with BHD syndrome.

Method: A comprehensive literature search was conducted across PubMed, EMBASE, Cochrane Controlled Register of Trials (CENTRAL), and Web of Science databases up to March 10, 2024. Studies reporting on the prevalence of spontaneous pneumothorax in BHD syndrome patients were included. Eligibility assessment, data extraction, and quality assessment were performed independently by two reviewers. Random-effects or fixed-effect models were conducted to calculate pooled incidence rates, and subgroup analyses were performed to explore sources of heterogeneity. The publication bias was assessed by funnel plot and Egger's test.

Results: Eighteen studies, conducted between 2009 and 2023, were included in the systematic review. The meta-analysis revealed a pooled incidence rate of spontaneous pneumothorax in BHD syndrome patients at 0.61 (95% CI 0.46; 0.76). Subgroup analyses based on region, study design, and diagnostic methods further elucidated variations in incidence rates among different patient groups. Specifically, the Asian subgroup demonstrated a higher pooled incidence rate of 0.71 (95% CI 0.60; 0.81), while the Caucasian subgroup showed a lower pooled incidence rate of 0.43 (95% CI 0.26; 0.60). The subgroup analysis by study design revealed a pooled incidence rate of 0.60 (95% CI 0.45; 0.76) for retrospective studies and 0.70 (95% CI 0.42; 0.98) for the sole prospective study. Additionally, the subgroup analysis by diagnostic methods showed pooled incidence rates of 0.64 (95% CI 0.48; 0.81) for studies using FLCN mutation testing and 0.51 (95% CI 0.33; 0.70) for those using clinical criteria and imaging findings. Potential publication bias was identified by Egger's test (P < 0.05).

Conclusion: The study indicated a pooled prevalence rate of 61% for pneumothorax in BHD syndrome patients, with subgroup analyses revealing higher rates among Asian individuals and in prospective studies. Further researches, particularly large-sample prospective studies, are needed to address publication bias and improve the reliability of prevalence estimates.

Prospero: CRD42024567520.

BHD综合征患者自发性气胸的患病率:系统回顾和荟萃分析。
背景:birt - hogg - dub (BHD)综合征与气胸风险增加有关。本研究旨在确定诊断为BHD综合征的个体中自发性气胸的患病率。方法:综合检索PubMed、EMBASE、Cochrane Controlled Register of Trials (CENTRAL)和Web of Science数据库,检索时间截止到2024年3月10日。纳入了有关BHD综合征患者自发性气胸患病率的研究报告。资格评估、数据提取和质量评估由两名审稿人独立完成。采用随机效应或固定效应模型计算合并发病率,并进行亚组分析以探索异质性来源。采用漏斗图和Egger检验评估发表偏倚。结果:2009年至2023年间进行的18项研究被纳入系统评价。荟萃分析显示,BHD综合征患者自发性气胸的总发病率为0.61 (95% CI 0.46;0.76)。基于地区、研究设计和诊断方法的亚组分析进一步阐明了不同患者组之间发病率的差异。具体来说,亚洲亚组的合并发病率更高,为0.71 (95% CI 0.60;0.81),而高加索亚组的合并发病率较低,为0.43 (95% CI 0.26;0.60)。研究设计的亚组分析显示合并发病率为0.60 (95% CI 0.45;0.76)为回顾性研究,0.70 (95% CI 0.42;0.98)作为唯一的前瞻性研究。此外,诊断方法的亚组分析显示合并发病率为0.64 (95% CI 0.48;使用FLCN突变检测的研究为0.81),0.51 (95% CI 0.33;0.70),适用于临床标准和影像学表现。结论:该研究表明BHD综合征患者气胸的总患病率为61%,亚组分析显示亚洲个体和前瞻性研究中气胸的发生率更高。需要进一步的研究,特别是大样本前瞻性研究来解决发表偏倚和提高患病率估计的可靠性。普洛斯彼罗:CRD42024567520。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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