华东地区 100 例 Birt-Hogg-Dubé 综合征患者的临床和遗传特征。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Daiju Hu, Rui Wang, Jinli Liu, Xianmeng Chen, Xianliang Jiang, Jun Xiao, Jay H Ryu, Xiaowen Hu
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引用次数: 0

摘要

背景:尽管中国有越来越多的伯-霍格-杜贝综合征(BHD)患者,但其临床和遗传特征尚未明确。此外,2023 年提出了针对中国人群的修订诊断标准,我们旨在探索这些标准在罕见肺病中心临床实践中的实用性:我们回顾性分析了 2017 年 1 月至 2023 年 6 月期间在中国科学技术大学附属第一医院连续接诊的 100 例根据中国 BHD 修订标准诊断的 BHD 患者的数据:100名患者(包括63名女性)来自华东地区(主要是安徽省)65个无血缘关系的家庭。常见表现为肺囊肿(99%)、气胸(60%)和皮肤病变(77%)。肾癌和肾血管脂肪瘤各占 5 例。37%的患者没有 BHD 家族史。共检测到25个FLCN种系突变,包括6个新型突变。除了FLCN的热点突变c.1285delC/dupC(17%)外,最常见的突变是c.1015 C > T(16%)、c.1579_1580insA(14%)和外显子1-3缺失(11%)。与热点突变c.1285dupC相比,外显子1-3缺失突变和c.1177-5_1177-3de1CTC导致气胸的风险更高(分别为91% [95% CI: 0.31, 46.82, p = 0.015] 和67% [95% CI: 0.35, 71.9, p = 0.302] vs. 30%)。诊断平均延迟时间为初始症状出现后 7.6 年。中国的诊断标准大多与典型的肺部表现一致,并有遗传学支持证据:结论:在华东地区,BHD 患者最常见的症状是肺囊肿伴有气胸和皮肤病变。结论:在华东地区,BHD 患者最常见的症状是肺囊肿伴有气胸和皮肤病变,但肾癌和意外的肾血管肌脂肪瘤的发病率较低。基因型谱与全球其他地区的报告不同,气胸的基因型相关性值得进一步研究。修订后的中国鼻咽癌诊断标准似乎更适合诊断中国患者的鼻咽癌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and genetic characteristics of 100 consecutive patients with Birt-Hogg-Dubé syndrome in Eastern Chinese region.

Background: Although an increasing number of patients with Birt-Hogg-Dubé syndrome (BHD) are being recognized in China, clinical and genetic characteristics are not well-defined. In addition, revised diagnostic criteria for the Chinese population was proposed in 2023, we aimed to explore their utility in clinical practice at a rare lung disease center.

Methods: We retrospectively analyzed the data of 100 consecutive patients with BHD diagnosed according to the revised Chinese BHD criteria, encountered at the First Affiliated Hospital of University of Science and Technology of China from Jan 2017 to June 2023.

Results: There were 100 patients (including 63 females) from 65 unrelated families in Eastern China, mostly Anhui Province. The common manifestations were pulmonary cysts (99%), pneumothorax (60%), and skin lesions (77%). Renal cancer and renal angiomyolipoma were detected in 5 patients each. 37% of patients had no family history of BHD. In total, 25 FLCN germline mutations were detected, including 6 novel mutations. In addition to hotspot mutation c.1285delC/dupC (17%), the most common mutations were c.1015 C > T (16%), c.1579_1580insA (14%), and exons 1-3 deletion (11%) in FLCN. Higher risk of pneumothorax was associated with exons 1-3 deletion mutation and c.1177-5_1177-3de1CTC compared to the hotspot mutation c.1285dupC (91% [95% CI: 0.31, 46.82, p = 0.015] and 67% [95% CI: 0.35, 71.9, p = 0.302] vs. 30%, respectively). The average delay in diagnosis was 7.6 years after initial symptoms. Chinese diagnostic criteria were mostly consistent with typical pulmonary presentations with supportive genetic evidence.

Conclusion: In the Eastern Chinese region, patients with BHD present most commonly with pulmonary cysts associated with pneumothorax and skin lesions. However, low incidence of renal cancer along with unexpected renal angiomyolipoma was observed. Genotypic spectrum differed from that reported from other global regions, and genotype association of pneumothorax warrants further research. The revised Chinese criteria for BHD seem more appropriate in diagnosing BHD in Chinese patients.

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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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