Serum Biomarkers of Olfactory Identification Deficits in Patients with Parkinson’s Disease

Fu-Jia Li, Yangdanyu Li, Xu Liu, J. Zu, Wei Zhang, Qi-Hua Xiao, Xue-Bin Niu, Li Du, Chen-Chen Cui, Ru-Yu Zhang, Xiao-Qing He, Gui-Yun Cui, Chuan-Ying Xu
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Abstract

To investigate whether glial fibrillary acidic protein (GFAP), neurofilament light chain (NFL), and 12 cytokines can serve as serum biomarkers of olfactory identification dysfunction in patients with Parkinson’s disease (PD). GFAP and NFL levels were measured in 75 patients with PD and 36 healthy controls (HCs). The levels of 12 cytokines were assayed in 41 patients with PD. The 16-item Sniffin’ Sticks test and the Mini-Mental State Examination (MMSE) were used to assess olfactory identification ability and cognitive function, respectively. Linear regression models were applied to control for confounding effects. Receiver operating characteristic curves were used to examine the diagnostic accuracy of serum NFL, GFAP, and interleukin-6 (IL-6) levels. The cut-off value for the SS-16 test in diagnosing dysosmia was equal to 9.5 points. Serum GFAP levels were higher in patients with PD with olfactory identification dysfunction than in those without. GFAP, NFL, and IL-6 levels were correlated with SS-16 scores. Moreover, combining these three biomarkers yielded the best-fitting model for distinguishing patients with PD with or without dysosmia. We found a prominent indirect effect of GFAP on MMSE scores through its contribution to SS-16 scores. GFAP, NFL, and IL-6 can serve as serum biomarkers for olfactory identification dysfunctions in PD. We inferred that astrogliosis might promote the occurrence of dysosmia by releasing proinflammatory factors and causing neuronal damage and may indirectly impair cognition through its effect on olfactory function.
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帕金森病患者嗅觉识别障碍的血清生物标记物
目的:研究神经胶质纤维酸性蛋白(GFAP)、神经丝蛋白轻链(NFL)和 12 种细胞因子是否可作为帕金森病(PD)患者嗅觉识别功能障碍的血清生物标记物。对 75 名帕金森病患者和 36 名健康对照者(HCs)的 GFAP 和 NFL 水平进行了测定。对 41 名帕金森病患者的 12 种细胞因子水平进行了检测。16项嗅棒测试和迷你精神状态检查(MMSE)分别用于评估嗅觉识别能力和认知功能。采用线性回归模型控制混杂效应。受试者操作特征曲线用于检测血清 NFL、GFAP 和白细胞介素-6(IL-6)水平的诊断准确性。SS-16测试诊断发育不良的临界值为9.5分。有嗅觉识别功能障碍的帕金森病患者血清GFAP水平高于无嗅觉识别功能障碍的患者。GFAP、NFL和IL-6水平与SS-16评分相关。此外,将这三种生物标志物结合在一起可得出最佳拟合模型,用于区分伴有或不伴有嗅觉障碍的帕金森病患者。我们发现,GFAP通过对SS-16评分的贡献,对MMSE评分产生了显著的间接影响。GFAP、NFL和IL-6可作为PD患者嗅觉识别功能障碍的血清生物标志物。我们推断星形胶质细胞增多症可能会通过释放促炎因子和造成神经元损伤来促进嗅觉障碍的发生,并可能通过影响嗅觉功能间接损害认知能力。
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Neurofilament and Brain Atrophy and Their Association with Cognition in Multiple Sclerosis: A 10-Year Follow-Up Study Serum Biomarkers of Olfactory Identification Deficits in Patients with Parkinson’s Disease Erratum to “Changes in Retinal Thickness and Brain Volume during 6.8-Year Escalating Therapy for Multiple Sclerosis”
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