皮肤磷酸化突触核蛋白:纯自律神经衰竭的早期诊断生物标志物。

IF 8.7 1区 医学 Q1 CLINICAL NEUROLOGY
Shiwen Koay, Vincenzo Provitera, Giuseppe Caporaso, Ekawat Vichayanrat, Fernanda Valerio, Annamaria Stancanelli, Ilaria Borreca, Michael P Lunn, Maria Nolano, Valeria Iodice
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引用次数: 0

摘要

背景:单纯自主神经衰竭(PAF)表现为进行性自主神经衰竭,无其他神经学特征。不典型的表现可能导致诊断的不确定性。我们研究了皮肤磷酸化α -突触核蛋白(p-syn)是否可以区分PAF、多系统萎缩(MSA)和非突触核蛋白病相关的自主神经衰竭,并研究了其与心血管自主神经衰竭的定量标志物的关系。方法:所有个体均接受自主神经症状综合评分-31自主神经问卷调查、心血管自主神经测试和双侧小腿远端皮肤活检。我们注意到p-syn是否存在于供给自主神经附件的神经中,包括汗腺、血管、立毛肌、皮下纤维、真皮纤维和神经束(每个样本的最大自主神经亚分为3分,总p-syn分为6分,两侧计算平均值)。结果:共36例,其中PAF 11例,MSA 13例,非突触核蛋白病相关性自主神经衰竭12例。在22/22 (100%)PAF活检,19/26 (73%)MSA活检和0/22(0%)非突触核病活检中存在P-syn。PAF的平均总p-syn评分明显高于MSA(中位数为4.5 vs 1, p3区分PAF和MSA的特异性为100%,敏感性为82%)。自主神经p-syn亚评分与倾斜时直立不耐受比(ρ=0.63, p=0.0004)、Valsalva运动后血压恢复时间(r=0.44, p=0.03)和患者报告的直立不耐受(ρ=0.57, p=0.006)相关。结论:皮肤p-syn在PAF中丰富,主要是外周α -突触核蛋白病。它是一个很有前途的生物标志物,可以帮助区分PAF、MSA和非突触核蛋白病相关的自主神经衰竭,以帮助早期诊断和招募未来的临床试验。P-syn沉积在自主神经上可能损害对总外周阻力的控制,从而引起症状性直立性低血压。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cutaneous phosphorylated-synuclein: an early diagnostic biomarker for pure autonomic failure.

Background: Pure autonomic failure (PAF) presents with progressive autonomic failure without other neurological features. Atypical presentations may lead to diagnostic uncertainty. We studied whether cutaneous phosphorylated-alpha-synuclein (p-syn) could distinguish between PAF, multiple system atrophy (MSA) and non-synucleinopathy-related autonomic failure, and examined its relationship with quantitative markers of cardiovascular autonomic failure.

Methods: All individuals underwent Composite Autonomic Symptom Score-31 autonomic questionnaires, cardiovascular autonomic testing and bilateral distal leg skin biopsies. We noted whether p-syn was present in nerves supplying autonomic adnexa, including sweat glands, blood vessels, arrector pili muscles, and subepidermal fibres, dermal fibres and nerve fascicles (maximum autonomic subscore 3, total p-syn score 6 for each sample, average calculated for both sides).

Results: 36 individuals were studied: 11 PAF, 13 MSA and 12 non-synucleinopathy-related autonomic failure. P-syn was present in 22/22 (100%) PAF biopsies, 19/26 (73%) MSA biopsies and 0/22 (0%) non-synucleinopathy biopsies. Mean total p-syn score was significantly higher in PAF compared with MSA (median 4.5 vs 1, p<0.001). Total p-syn score >3 distinguished PAF from MSA with 100% specificity and 82% sensitivity. Autonomic p-syn subscores correlated with orthostatic intolerance ratio on tilt (ρ=0.63, p=0.0004), blood pressure recovery time following Valsalva manoeuvre (r=0.44, p=0.03) and patient-reported orthostatic intolerance (ρ=0.57, p=0.006).

Conclusion: Cutaneous p-syn was abundant in PAF, a predominantly peripheral alpha-synucleinopathy. It is a promising biomarker to help distinguish between PAF, MSA and non-synucleinopathy-related autonomic failure to aid early diagnosis and recruitment to future clinical trials. P-syn deposition on autonomic nerves may impair control of total peripheral resistance giving rise to symptomatic orthostatic hypotension.

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来源期刊
CiteScore
15.70
自引率
1.80%
发文量
888
审稿时长
6 months
期刊介绍: The Journal of Neurology, Neurosurgery & Psychiatry (JNNP) aspires to publish groundbreaking and cutting-edge research worldwide. Covering the entire spectrum of neurological sciences, the journal focuses on common disorders like stroke, multiple sclerosis, Parkinson’s disease, epilepsy, peripheral neuropathy, subarachnoid haemorrhage, and neuropsychiatry, while also addressing complex challenges such as ALS. With early online publication, regular podcasts, and an extensive archive collection boasting the longest half-life in clinical neuroscience journals, JNNP aims to be a trailblazer in the field.
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