Sun Wenhua, Zheng Jinhua, Ma Jianjun, Wang Zhidong, Shi Xiaoxue, Li Mingjian, Huang Shen, Hu Shiyu, Zhao Zhenxiang, Li Dongsheng
Department of Neurology, People's Hospital of Zhengzhou University, Zhengzhou, China.
Department of Neurology, Henan Provincial People's Hospital, Zhengzhou, China.
Front Aging Neurosci. 2021 Feb 12;13:621508. doi: 10.3389/fnagi.2021.621508. eCollection 2021.
: Heme oxygenase-1 (HO-1) is a 32 kDa stress-response protein implicated in the pathogenesis of Parkinson's disease (PD). Biliverdin is derived from heme through a reaction mediated by HO-1 and protects cells from oxidative stress. However, iron and carbon monoxide produced by the catabolism of HO-1 exert detrimental effects on patients with PD. The purpose of this study was to determine whether plasma HO-1 levels represent a biomarker of PD and to further explore the underlying mechanism of increased HO-1 levels by applying voxel-based morphometry (VBM).: We measured plasma HO-1 levels using an enzyme-linked immunosorbent assay (ELISA) in 156 subjects, including 81 patients with early- and advanced-stage PD and 75 subjects without PD. The analyses were adjusted to control for confounders such as age, sex, and medication. We analyzed T1-weighted magnetic resonance imaging (MRI) data from 74 patients with PD using VBM to elucidate the association between altered brain volumes and HO-1 levels. Then, we compared performance on MMSE sub-items between PD patients with low and high levels of HO-1 using Mann-Whitney tests.: Plasma HO-1 levels were significantly elevated in PD patients, predominantly those with early-stage PD, compared with controls ( < 0.05). The optimal cutoff value for patients with early PD was 2.245 ng/ml HO-1 [area under the curve (AUC) = 0.654]. Plasma HO-1 levels were unaffected by sex, age, and medications ( > 0.05). The right hippocampal volume was decreased in the subset of PD patients with high HO-1 levels ( < 0.05). A weak correlation was observed between right hippocampal volume and plasma HO-1 levels ( = -0.273, = 0.018). There was no difference in total MMSE scores between the low- and high-HO-1 groups ( > 0.05), but the high-HO-1 group had higher language scores than the low-HO-1 group ( < 0.05).: Plasma HO-1 levels may be a promising biomarker of early PD. Moreover, a high plasma concentration of the HO-1 protein is associated with a reduction in right hippocampal volume.
血红素加氧酶-1(HO-1)是一种32 kDa的应激反应蛋白,与帕金森病(PD)的发病机制有关。胆绿素通过HO-1介导的反应从血红素衍生而来,可保护细胞免受氧化应激。然而,HO-1分解代谢产生的铁和一氧化碳对PD患者产生有害影响。本研究的目的是确定血浆HO-1水平是否代表PD的生物标志物,并通过应用基于体素的形态测量法(VBM)进一步探索HO-1水平升高的潜在机制。
我们使用酶联免疫吸附测定(ELISA)测量了156名受试者的血浆HO-1水平,其中包括81例早期和晚期PD患者以及75名非PD受试者。分析进行了调整,以控制年龄、性别和药物等混杂因素。我们使用VBM分析了74例PD患者的T1加权磁共振成像(MRI)数据,以阐明脑容量改变与HO-1水平之间的关联。然后,我们使用曼-惠特尼检验比较了HO-1水平低和高的PD患者在简易精神状态检查表(MMSE)子项目上的表现。
与对照组相比,PD患者的血浆HO-1水平显著升高,主要是早期PD患者(<0.05)。早期PD患者的最佳截断值为2.245 ng/ml HO-1[曲线下面积(AUC)=0.654]。血浆HO-1水平不受性别、年龄和药物的影响(>0.05)。HO-1水平高的PD患者亚组右侧海马体积减小(<0.05)。右侧海马体积与血浆HO-1水平之间观察到弱相关性(=-0.273,=0.018)。HO-1水平低和高的组之间总MMSE评分没有差异(>0.05),但HO-1水平高的组语言评分高于HO-1水平低的组(<0.05)。
血浆HO-1水平可能是早期PD的一个有前景的生物标志物。此外,HO-1蛋白的高血浆浓度与右侧海马体积减小有关。