Unit of Neurology and Neuromuscular Diseases, Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
J Peripher Nerv Syst. 2020 Sep;25(3):273-278. doi: 10.1111/jns.12385. Epub 2020 May 29.
V122I is one of more than 130 mutations in transthyretin gene associated with hereditary TTR (ATTRv) amyloidosis. Main clinical expression is an infiltrative pseudohypertrophic cardiomyopathy with mild or no neurological symptoms. It is particularly common among African-Americans (prevalence: 3%-4%). We report 12 subjects from seven unrelated Caucasian families hailing from Sicily and carrying the V122I mutation. One patient was homozygous for V122I and in another family two subjects also carried the E89Q variant in compound heterozygosity. All the subjects underwent neurologic/neurophysiologic evaluation and cardiologic baseline tests; in five of them, cardiac magnetic resonance and/or (99 m) Tc-DPD scintigraphy were performed. Three of 12 subjects were asymptomatic carriers. Of the remaining nine subjects, in four of nine patients, the nerve conduction studies revealed a polyneuropathy; in one of them, this represents the only sign of disease after 5 years of follow-up. In eight of nine subjects, we found a hypertrophic restrictive cardiomyopathy and cardiac failure, associated with a carpal tunnel syndrome. Although in non-Afro-American individuals V122I prevalence is low, subjects carrying this mutation have been identified in the United Kingdom, Italy, and France. Our report describes a large cohort of V122I Caucasian patients from a non-endemic area, confirming the possible underestimation of this mutation in the non-African population. Moreover, it highlights the heterogeneity in the genotype-phenotype correlation of ATTRv mutations, suggesting that the presence of a polyneuropathy has to be identified as soon as possible, since available treatments are, in Europe, so far authorized only for ATTRv amyloid peripheral neuropathy.
V122I 是与遗传性 TTR(ATTRv)淀粉样变性相关的超过 130 种转甲状腺素蛋白基因突变之一。主要临床表现为浸润性假性肥大性心肌病,伴有轻度或无神经症状。它在非裔美国人中尤为常见(患病率:3%-4%)。我们报告了来自西西里岛的七个无关的白人家庭的 12 名携带 V122I 突变的患者。一名患者为 V122I 纯合子,另一个家族中有两名患者也为复合杂合子携带 E89Q 变异。所有患者均接受了神经/神经生理评估和心脏基线测试;其中 5 人进行了心脏磁共振和/或(99m)Tc-DPD 闪烁扫描。12 名患者中有 3 名无症状携带者。在其余 9 名患者中,有 4 名患者的神经传导研究显示多发性神经病;其中 1 名患者在 5 年随访后出现这种疾病的唯一迹象。在 9 名患者中的 8 名中,我们发现了肥厚性限制性心肌病和心力衰竭,伴有腕管综合征。尽管在非非裔美国人中 V122I 的患病率较低,但在英国、意大利和法国也发现了携带这种突变的患者。我们的报告描述了来自非流行地区的大量 V122I 白人患者,证实了在非非洲人群中对这种突变的可能低估。此外,它强调了 ATTRv 突变的基因型-表型相关性的异质性,表明应尽快发现多发性神经病的存在,因为在欧洲,目前仅授权使用可用于治疗 ATTRv 淀粉样周围神经病的治疗方法。