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

Clinical and genetic characteristics of 100 consecutive patients with Birt-Hogg-Dubé syndrome in Eastern Chinese region.

机构信息

Department of Pulmonary and Critical Care Medicine, Hefei, China.

Department of Dermatology, Hefei, China.

出版信息

Orphanet J Rare Dis. 2024 Sep 19;19(1):348. doi: 10.1186/s13023-024-03360-1.

Abstract

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.

摘要

背景

尽管越来越多的 Birt-Hogg-Dubé 综合征(BHD)患者在中国被识别,但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,我们旨在探讨其在罕见肺病中心的临床应用。

方法

我们回顾性分析了 2017 年 1 月至 2023 年 6 月期间在科技大学第一附属医院根据修订的中国 BHD 标准诊断的 100 例 BHD 连续患者的数据。

结果

来自华东地区(主要是安徽省)65 个无关家庭的 100 名患者(包括 63 名女性),常见表现为肺囊肿(99%)、气胸(60%)和皮肤病变(77%)。各有 5 例患者患有肾癌和肾血管平滑肌脂肪瘤。37%的患者无 BHD 家族史。共检测到 25 个 FLCN 种系突变,包括 6 个新突变。除热点突变 c.1285delC/dupC(17%)外,最常见的突变为 c.1015C>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 与气胸风险更高相关(91%[95%CI:0.31,46.82,p=0.015]和 67%[95%CI:0.35,71.9,p=0.302]与 30%,分别)。首次出现症状后,平均诊断延迟 7.6 年。中国的诊断标准与具有支持性遗传证据的典型肺部表现大多一致。

结论

在中国东部地区,BHD 患者最常见的表现为与气胸和皮肤病变相关的肺囊肿。然而,观察到肾癌发病率较低,以及意外的肾血管平滑肌脂肪瘤。基因型谱与其他全球地区报道的不同,气胸的基因型相关性值得进一步研究。修订后的中国 BHD 标准似乎更适合在中国患者中诊断 BHD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f09/11414263/3c3dddfd545f/13023_2024_3360_Fig1_HTML.jpg

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