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香港中文人群中由 FLNC 相关肌原纤维肌病的创始变体 c.8129G>A 引起的临床和病理特征。

Clinical and pathological characterization of FLNC-related myofibrillar myopathy caused by founder variant c.8129G>A in Hong Kong Chinese.

机构信息

Department of Pathology, Princess Margaret Hospital, Hong Kong.

Pathology Department, St. Paul's Hospital, Hong Kong.

出版信息

Clin Genet. 2020 May;97(5):747-757. doi: 10.1111/cge.13715. Epub 2020 Feb 23.

DOI:10.1111/cge.13715
PMID:32022900
Abstract

FLNC-related myofibrillar myopathy could manifest as autosomal dominant late-onset slowly progressive proximal muscle weakness; involvements of cardiac and/or respiratory functions are common. We describe 34 patients in nine families of FLNC-related myofibrillar myopathy in Hong Kong ethnic Chinese diagnosed over the last 12 years, in whom the same pathogenic variant c.8129G>A (p.Trp2710*) was detected. Twenty-six patients were symptomatic when diagnosed; four patients died of pneumonia and/or respiratory failure. Abnormal amorphous material or granulofilamentous masses were detected in half of the cases, with mitochondrial abnormalities noted in two-thirds. We also show by haplotype analysis the founder effect associated with this Hong Kong variant, which might have occurred 42 to 71 generations ago or around Tang and Song dynasties, and underlain a higher incidence of myofibrillar myopathy among Hong Kong Chinese. The late-onset nature and slowly progressive course of the highly penetrant condition could have significant impact on the family members, and an early diagnosis could benefit the whole family. Considering another neighboring founder variant in FLNC in German patients, we advocate development of specific therapies such as chaperone-based or antisense oligonucleotide strategies for this particular type of myopathy.

摘要

FLNC 相关肌纤维病可表现为常染色体显性遗传的迟发性进行性近端肌无力;常伴有心脏和/或呼吸功能受累。我们描述了过去 12 年中在香港汉族人群中诊断出的 9 个家族的 34 例 FLNC 相关肌纤维病患者,这些患者均携带相同的致病性变异 c.8129G>A(p.Trp2710*)。26 名患者在诊断时出现症状;4 名患者因肺炎和/或呼吸衰竭死亡。一半的病例中检测到异常无定形物质或颗粒状团块,三分之二的病例中存在线粒体异常。通过单体型分析,我们还显示了与该香港变异相关的起源效应,该变异可能发生在 42 到 71 代或唐宋时期,导致香港汉族人群中肌纤维病的发病率更高。这种高外显率疾病的迟发性和缓慢进行性可能对家庭成员产生重大影响,早期诊断可能对整个家庭都有益。考虑到德国患者中 FLNC 的另一个邻近的起源变异,我们提倡针对这种特定类型的肌病开发基于伴侣蛋白或反义寡核苷酸的特定治疗方法。

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1
Clinical and pathological characterization of FLNC-related myofibrillar myopathy caused by founder variant c.8129G>A in Hong Kong Chinese.香港中文人群中由 FLNC 相关肌原纤维肌病的创始变体 c.8129G>A 引起的临床和病理特征。
Clin Genet. 2020 May;97(5):747-757. doi: 10.1111/cge.13715. Epub 2020 Feb 23.
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First clinical and myopathological description of a myofibrillar myopathy with congenital onset and homozygous mutation in FLNC.首例先天性肌纤维病的临床和肌病理表现及肌联蛋白 FLNC 纯合突变
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FLNC myofibrillar myopathy results from impaired autophagy and protein insufficiency.腓骨肌萎缩症相关肌原纤维肌病由自噬受损和蛋白质不足引起。
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引用本文的文献

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Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems.新型原肌球蛋白 Filamin C 肌病的变异导致不同的病理机制和蛋白质质量控制系统的改变。
Cells. 2023 May 5;12(9):1321. doi: 10.3390/cells12091321.
2
FLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic Data.与肌联蛋白相关的肌原纤维肌病:新的临床、功能和蛋白质组学数据。
Neurol Genet. 2021 May 18;7(3):e590. doi: 10.1212/NXG.0000000000000590. eCollection 2021 Jun.
3
Expanding the Clinico-Genetic Spectrum of Myofibrillar Myopathy: Experience From a Chinese Neuromuscular Center.
扩大肌原纤维肌病的临床-遗传谱:来自中国神经肌肉中心的经验
Front Neurol. 2020 Sep 15;11:1014. doi: 10.3389/fneur.2020.01014. eCollection 2020.
4
Homozygous expression of the myofibrillar myopathy-associated p.W2710X filamin C variant reveals major pathomechanisms of sarcomeric lesion formation.致同态表达的肌原纤维肌病相关 p.W2710X 细丝蛋白 C 变体揭示了肌节损伤形成的主要病理机制。
Acta Neuropathol Commun. 2020 Sep 4;8(1):154. doi: 10.1186/s40478-020-01001-9.