Carlomagno Cristiano, Bertazioli Dario, Gualerzi Alice, Picciolini Silvia, Andrico Michele, Rodà Francesca, Meloni Mario, Banfi Paolo Innocente, Verde Federico, Ticozzi Nicola, Silani Vincenzo, Messina Enza, Bedoni Marzia
IRCCS Fondazione Don Carlo Gnocchi ONLUS, Milan, Italy.
Università degli Studi di Milano-Bicocca, Milan, Italy.
Front Neurosci. 2021 Oct 26;15:704963. doi: 10.3389/fnins.2021.704963. eCollection 2021.
Despite the wide range of proposed biomarkers for Parkinson's disease (PD), there are no specific molecules or signals able to early and uniquely identify the pathology onset, progression and stratification. Saliva is a complex biofluid, containing a wide range of biological molecules shared with blood and cerebrospinal fluid. By means of an optimized Raman spectroscopy procedure, the salivary Raman signature of PD can be characterized and used to create a classification model. Raman analysis was applied to collect the global signal from the saliva of 23 PD patients and related pathological and healthy controls. The acquired spectra were computed using machine and deep learning approaches. The Raman database was used to create a classification model able to discriminate each spectrum to the correct belonging group, with accuracy, specificity, and sensitivity of more than 97% for the single spectra attribution. Similarly, each patient was correctly assigned with discriminatory power of more than 90%. Moreover, the extracted data were significantly correlated with clinical data used nowadays for the PD diagnosis and monitoring. The preliminary data reported highlight the potentialities of the proposed methodology that, once validated in larger cohorts and with multi-centered studies, could represent an innovative minimally invasive and accurate procedure to determine the PD onset, progression and to monitor therapies and rehabilitation efficacy.
尽管针对帕金森病(PD)提出了各种各样的生物标志物,但尚无能够早期且唯一地识别该疾病发病、进展和分层的特定分子或信号。唾液是一种复杂的生物流体,含有与血液和脑脊液共有的多种生物分子。通过优化的拉曼光谱程序,可以对PD的唾液拉曼特征进行表征,并用于创建分类模型。应用拉曼分析从23名PD患者以及相关病理对照和健康对照的唾液中收集全局信号。使用机器学习和深度学习方法对获取的光谱进行计算。利用拉曼数据库创建了一个分类模型,该模型能够将每个光谱正确地判别到所属组,单光谱归属的准确率、特异性和灵敏度均超过97%。同样,每位患者的判别能力超过90%时也能被正确分类。此外,提取的数据与目前用于PD诊断和监测的临床数据显著相关。所报告的初步数据突出了所提出方法的潜力,一旦在更大的队列中并通过多中心研究得到验证,该方法可能代表一种创新的微创且准确的程序,用于确定PD的发病、进展以及监测治疗和康复效果。