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与异染性脑白质营养不良认知功能衰退及运动功能长期保留相关的芳基硫酸酯酶A变体

ARSA Variants Associated With Cognitive Decline and Long-Term Preservation of Motor Function in Metachromatic Leukodystrophy.

作者信息

Beerepoot Shanice, Schoenmakers Daphne H, Fumagalli Francesca, Groeschel Samuel, Schöls Ludger, Schiffmann Raphael, Wong Sheila, Boespflug-Tanguy Odile, Sevin Caroline, Nadjar Yann, Bley Annette, Mochel Fanny, Horn Morten A, Baldoli Cristina, Locatelli Sara, Hengel Holger, Laugwitz Lucia, Hollak Carla E M, Gieselmann Volkmar, van der Knaap Marjo S, Wolf Nicole I

机构信息

Amsterdam Leukodystrophy Center, Department of Child Neurology, Emma Children's Hospital, Amsterdam UMC, Location Vrije Universiteit, Amsterdam, the Netherlands.

Amsterdam Neuroscience, Cellular & Molecular Mechanisms, Vrije Universiteit, Amsterdam, the Netherlands.

出版信息

J Inherit Metab Dis. 2025 Sep;48(5):e70072. doi: 10.1002/jimd.70072.

Abstract

Patients with metachromatic leukodystrophy (MLD) show variable motor and cognitive decline. The ARSA variants c.256C>T, p.(Arg86Trp), c.257G>A, p.(Arg86Gln) and c.542T>G, p.(Ile181Ser) are associated with predominantly cognitive decline. This multinational study analyzed MLD onset type, presenting signs/symptoms, cognitive function, gross motor function, central motor tract involvement, MRI severity score, peripheral neuropathy, and survival of 47 patients (three homozygous for c.256C>T and five, twelve and 27 compound heterozygous for c.256C>T, c.257G>A, or c.542T>G and another ARSA variant, respectively). Eleven underwent hematopoietic stem cell transplantation (HSCT). Onset was late-juvenile (46.8%) or adult (44.7%) with predominantly cognitive decline (n = 40/41 symptomatic patients). At diagnosis, untreated patients typically retained independent walking (100%), sparing of central motor tracts (87.5%), and absence of demyelinating neuropathy (95.5%), which persisted in follow-up for most (76.5%, 71.4%, and 64.7%, respectively). Early-juvenile onset and rapid motor decline occurred only in patients compound heterozygous for c.256C>T and a severe second variant (n = 4), showing central motor tract involvement at diagnosis. One untreated and one treated patient died of disease progression, and another from HSCT complications. All other treated patients retained independent walking, and four of five tested normal cognitive function. Median MRI severity score remained lower in treated (13) than untreated patients (25). The phenotype of c.256C>T carriers depends on the severity of the second ARSA variant. Patients harboring c.257G>A or c.542T>G show late-juvenile or adult onset with cognitive decline and preserved motor function, usually associated with sparing of central motor tracts. In these patients, cognitive function and MRI severity score should be preferred treatment outcomes.

摘要

异染性脑白质营养不良(MLD)患者表现出不同程度的运动和认知功能衰退。ARSA基因变体c.256C>T、p.(Arg86Trp),c.257G>A、p.(Arg86Gln)以及c.542T>G、p.(Ile181Ser)主要与认知功能衰退相关。这项跨国研究分析了47例患者的MLD发病类型、出现的体征/症状、认知功能、粗大运动功能、中枢运动神经束受累情况、MRI严重程度评分、周围神经病变以及生存情况(其中3例为c.256C>T纯合子,另外5例、12例和27例分别为c.256C>T与c.257G>A或c.542T>G以及另一个ARSA基因变体的复合杂合子)。11例患者接受了造血干细胞移植(HSCT)。发病类型为青少年晚期(46.8%)或成人期(44.7%),主要表现为认知功能衰退(41例有症状患者中有40例)。在诊断时,未经治疗的患者通常仍能独立行走(100%),中枢运动神经束未受累(87.5%),且无脱髓鞘性神经病变(95.5%),在随访中大多数患者这些情况仍持续存在(分别为76.5%、71.4%和64.7%)。青少年早期发病和快速运动功能衰退仅发生在c.256C>T与严重的第二个变体的复合杂合子患者中(n = 4),这些患者在诊断时显示中枢运动神经束受累。1例未经治疗和1例接受治疗的患者死于疾病进展,另1例死于HSCT并发症。所有其他接受治疗的患者仍能独立行走,5例接受测试的患者中有4例认知功能正常。接受治疗患者的MRI严重程度评分中位数(13)低于未经治疗的患者(25)。c.256C>T携带者的表型取决于第二个ARSA基因变体的严重程度。携带c.257G>A或c.542T>G的患者表现为青少年晚期或成人期发病,伴有认知功能衰退但运动功能保留,通常与中枢运动神经束未受累有关。对于这些患者,认知功能和MRI严重程度评分应作为首选的治疗效果指标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f277/12317651/c8722911fad8/JIMD-48-0-g004.jpg

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