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评估唾液血红素加氧酶-1 作为早期帕金森病的潜在生物标志物。

Evaluation of salivary heme oxygenase-1 as a potential biomarker of early Parkinson's disease.

机构信息

Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.

Department of Dentistry, Jewish General Hospital, Montreal, QC, Canada.

出版信息

Mov Disord. 2018 Apr;33(4):583-591. doi: 10.1002/mds.27328. Epub 2018 Feb 28.

DOI:10.1002/mds.27328
PMID:29488275
Abstract

BACKGROUND AND HYPOTHESIS

To date, there are no chemical analytes, including biochemical indices of oxidative stress, metabolites of α-synuclein protein, and differential protein expression patterns on proteomic profiling, for use in clinics as a diagnostic biomarker of idiopathic PD.

OBJECTIVES

Heme oxygenase-1 has been implicated in the pathogenesis of PD. The objective of this study is to ascertain whether salivary heme oxygenase-1 may serve as a biomarker for early idiopathic PD.

METHODS

Fifty-eight PD patients and 59 non-neurological disease controls were recruited. Levels of heme oxygenase-1 expression were assayed using enzyme-linked immunosorbent assay and western blot analysis of whole, unstimulated saliva. Analyses were adjusted by sex, l-dopa exposure, and relevant comorbidities.

RESULTS

We documented: (1) the presence of 32-kDa heme oxygenase-1 protein in human saliva; (2) significantly higher mean heme oxygenase-1 protein concentrations in saliva of PD patients relative to control values; (3) no variability in salivary heme oxygenase-1 levels with sex, age, l-dopa equivalence, or comorbidities; and (4) significantly higher mean salivary heme oxygenase-1 concentrations in patients with H & Y stage 1 PD (early) than control subjects and stage 2 and stage 3 PD patients. The area under the receiver operating characteristic curve that separated controls from PD H & Y stage 1 was 76% (95% confidence interval: 63-90).

CONCLUSIONS

Salivary heme oxygenase-1 concentrations may provide a useful, noninvasive, and relatively inexpensive biomarker of early idiopathic PD. © 2018 International Parkinson and Movement Disorder Society.

摘要

背景与假说

迄今为止,还没有任何化学分析物(包括氧化应激的生化指标、α-突触核蛋白的代谢物和蛋白质组学分析中的差异蛋白表达模式)可用于临床作为特发性 PD 的诊断生物标志物。

目的

血红素加氧酶-1 已被牵涉到 PD 的发病机制中。本研究的目的是确定唾液血红素加氧酶-1 是否可作为早期特发性 PD 的生物标志物。

方法

招募了 58 名 PD 患者和 59 名非神经疾病对照者。使用酶联免疫吸附试验和全唾液非刺激物的 Western blot 分析检测血红素加氧酶-1 的表达水平。通过性别、l-多巴暴露和相关合并症进行分析调整。

结果

我们记录到:(1)人唾液中存在 32-kDa 血红素加氧酶-1 蛋白;(2)与对照值相比,PD 患者的唾液血红素加氧酶-1 蛋白浓度明显更高;(3)唾液血红素加氧酶-1 水平不受性别、年龄、l-多巴等效物或合并症的影响;(4)H & Y 分期 1(早期)的 PD 患者的平均唾液血红素加氧酶-1 浓度明显高于对照者和 H & Y 分期 2 和 3 的 PD 患者。将对照者与 PD H & Y 分期 1 区分开的接收者操作特征曲线下面积为 76%(95%置信区间:63-90)。

结论

唾液血红素加氧酶-1 浓度可能为早期特发性 PD 提供一个有用的、非侵入性的和相对廉价的生物标志物。 © 2018 国际帕金森和运动障碍学会。

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