Clinical and biochemical characterization of asymptomatic carriers and symptomatic patients with hereditary transthyretin amyloidosis caused by TTR V30L mutation

IF 2.7 4区 医学 Q2 CLINICAL NEUROLOGY Neurological Sciences Pub Date : 2024-09-14 DOI:10.1007/s10072-024-07765-5
Hao Jiao, Mengdie Wang, Kang Du, Jialu Sun, Xujun Chu, Junsu Yang, He Lv, Wei Zhang, Zhaoxia Wang, Yun Yuan, Yu Liu, Lingchao Meng
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Abstract

Background

Hereditary transthyretin amyloidosis (ATTR) is an autosomal dominant disease characterized by amyloid fibril deposition. The TTR c.148G > T mutation (V30L) in ATTR is rarely reported, and its biochemical properties are unknown.

Methods

Seven patients and two asymptomatic carriers from two unrelated families diagnosed with V30L variant of ATTR were included. Data on clinical manifestations, laboratory examination, electrophysiology, ophthalmological corneal confocal microscopy (CCM), pathology and molecular biological experiments was collected and analyzed.

Results

Most patients initially experienced paresthesia, with varying degrees of peripheral neuropathy, autonomic dysfunction, and cardiac involvement. Nerve conduction studies showed extensive motor and sensory nerve involvement in upper and lower limbs. CCM revealed reduced corneal nerve density and fiber length. Sural nerve biopsies indicated loss of myelinated nerve fibers, with neurogenic patterns in gastrocnemius muscle biopsies. Asymptomatic carriers had nearly normal electrophysiology but mild reductions in corneal nerve fiber density and length. Sural nerve biopsies in carriers showed mild reductions in small myelinated nerve fibers. V30L mutation impaired thermodynamic and kinetic stability of the mutant protein. Plasma TTR tetramer concentration was lower in ATTR V30L patients compared to healthy donors. Small molecule stabilizers failed to exhibit satisfactory inhibition on fibril formation of V30L mutation in vitro.

Conclusion

This study highlights the multisystem involvement in ATTR V30L patients, including neuropathy and cardiac issues. Both patients and carriers showed abnormalities in nerve conduction, corneal microscopy, and pathology. The V30L mutation impaired protein stability and reduced plasma TTR tetramer levels. Small molecule stabilizers were ineffective, indicating a need for alternative treatments.

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由 TTR V30L 基因突变引起的遗传性转甲状腺素淀粉样变性无症状携带者和有症状患者的临床和生化特征分析
背景遗传性转甲状腺素淀粉样变性(ATTR)是一种以淀粉样纤维沉积为特征的常染色体显性遗传病。方法纳入了7名患者和2名无症状携带者,他们来自两个无血缘关系的家庭,被诊断为ATTR V30L变异型。收集并分析了临床表现、实验室检查、电生理学、眼科角膜共聚焦显微镜(CCM)、病理学和分子生物学实验等方面的数据。神经传导研究显示,上肢和下肢的运动和感觉神经广泛受累。CCM显示角膜神经密度和纤维长度降低。硬膜神经活检显示髓鞘神经纤维缺失,腓肠肌活检显示神经源性模式。无症状携带者的电生理学几乎正常,但角膜神经纤维密度和长度轻度减少。携带者的耳神经活检结果显示,有髓小神经纤维轻度减少。V30L突变损害了突变蛋白的热力学和动力学稳定性。与健康供体相比,ATTR V30L 患者的血浆 TTR 四聚体浓度较低。小分子稳定剂未能在体外对 V30L 突变的纤维形成表现出令人满意的抑制作用。患者和携带者均表现出神经传导、角膜显微镜检查和病理学方面的异常。V30L 突变损害了蛋白质的稳定性,降低了血浆中 TTR 四聚体的水平。小分子稳定剂效果不佳,表明需要替代治疗。
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来源期刊
Neurological Sciences
Neurological Sciences 医学-临床神经学
CiteScore
6.10
自引率
3.00%
发文量
743
审稿时长
4 months
期刊介绍: Neurological Sciences is intended to provide a medium for the communication of results and ideas in the field of neuroscience. The journal welcomes contributions in both the basic and clinical aspects of the neurosciences. The official language of the journal is English. Reports are published in the form of original articles, short communications, editorials, reviews and letters to the editor. Original articles present the results of experimental or clinical studies in the neurosciences, while short communications are succinct reports permitting the rapid publication of novel results. Original contributions may be submitted for the special sections History of Neurology, Health Care and Neurological Digressions - a forum for cultural topics related to the neurosciences. The journal also publishes correspondence book reviews, meeting reports and announcements.
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