唾液中的α-突触核蛋白是22q11.2缺失综合征帕金森病的候选生物标记物

M. Fanella, Emanuele Cerulli Irelli, T. Accinni, F. Di Fabio, Carolina Putotto, Federica Pulvirenti, Francesco E Bellomi, C. Di Bonaventura, Giorgio Vivacqua
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摘要

背景22q11.2缺失综合征(22q11.2DS)与早发帕金森病的风险增加有关。方法这项横断面研究纳入了 10 名伴有帕金森病的 22q11.2DS 患者(Park+)、10 名不伴有帕金森病的 22q11.2DS 患者(Park-)以及 10 名年龄和性别相当的健康受试者(HS)。结果Park(+)患者唾液总α-突触核蛋白浓度明显低于Park(-)患者和HS(P = 0.007)。此外,唾液中的α-突触核蛋白在区分帕金森(+)和帕金森(-)患者方面显示出良好的准确性(曲线下面积 = 0.86),并与运动严重程度和认知障碍相关。
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Salivary α-Synuclein as a Candidate Biomarker of Parkinsonism in 22q11.2 Deletion Syndrome.
BACKGROUND 22q11.2 deletion syndrome (22q11.2DS) has been linked to an increased risk of early-onset Parkinson's disease. However, the pathophysiological mechanisms underlying parkinsonism remain poorly understood. OBJECTIVE The objective is to investigate salivary total α-synuclein levels in 22q11.2DS patients with and without parkinsonian motor signs. METHODS This cross-sectional study included 10 patients with 22q11.2DS with parkinsonism (Park+), ten 22q11.2DS patients without parkinsonism (Park-), and 10 age and sex-comparable healthy subjects (HS). Salivary and serum α-synuclein levels were measured using enzyme-linked immunosorbent assay. RESULTS Salivary total α-synuclein concentration was significantly lower in Park (+) patients than in Park (-) patients and HS (P = 0.007). In addition, salivary α-synuclein showed good accuracy in discriminating Park (+) from Park (-) patients (area under the curve = 0.86) and correlated with motor severity and cognitive impairment. CONCLUSION This exploratory study suggests that the parkinsonian phenotype of 22q11.2DS is associated with a reduced concentration of monomeric α-synuclein in biological fluids.
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Parkinson's Disease Associated with G2019S LRRK2 Mutations without Lewy Body Pathology. Salivary α-Synuclein as a Candidate Biomarker of Parkinsonism in 22q11.2 Deletion Syndrome. Early Screening for the Parkinson Variant of Multiple System Atrophy: A 6-Item Score. Dystonic Tremor: Time to Change. Atypical Mowat-Wilson Syndrome: Dystonia, Choreoathetosis and Cognitive Features.
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