Liu Chuan Ze, Guo Da Shuai, Ma Jian Jun, Dong Lin Rui, Chang Qing Qing, Yang Hong Qi, Liang Ke Ke, Li Xiao Huan, Yang Da Wei, Fan Yong Yan, Gu Qi, Chen Si Yuan, Li Dong Sheng
Department of Neurology, Henan University People's Hospital, Zhengzhou, China.
Department of Neurology, Henan Provincial People's Hospital, Zhengzhou, China.
Front Aging Neurosci. 2022 Aug 22;14:889257. doi: 10.3389/fnagi.2022.889257. eCollection 2022.
Matrix metalloproteinases (MMPs) are essential for tissue formation, neuronal network remodeling, and blood-brain barrier integrity. MMPs have been widely studied in acute brain diseases. However, the relationship with Parkinson's disease (PD) remains unclear. The purpose of this study was to evaluate the serum MMP3 and MMP9 levels of PD patients and analyze their correlation with non-motor symptoms.
In this cross-sectional study, we recruited 73 patients with idiopathic PD and 64 healthy volunteers. Serum MMP3 and MMP9 levels were measured by enzyme-linked immunosorbent assay (ELISA). Patients with PD were assessed for non-motor symptoms using the Non-motor Symptoms Scale (NMSS) and Parkinson's disease sleep scale (PDSS) and Mini Mental State Examination (MMSE).
Serum MMP3 levels were significantly decreased in PD patients, predominantly those with early-stage PD, compared with controls [12.56 (9.30, 17.44) vs. 15.37 (11.33, 24.41) ng/ml; = 0.004], and the serum MMP9 levels of PD patients were significantly higher than those of healthy controls [522 (419, 729) vs. 329 (229, 473) ng/ml; < 0.001]. MMP3 levels were positively correlated with the NMSS total score ( = 0.271, = 0.020) and the single-item scores for item six, assessing the gastrointestinal tract ( = 0.333, = 0.004), and there was an inverse correlation between serum MMP3 levels and PDSS score ( = -0.246, = 0.036); meanwhile, MMP9 levels were positively correlated with the NMSS total score ( = 0.234, = 0.047), and higher serum MMP9 levels were detected in the cognitive dysfunction subgroup than in the cognitively intact subgroup [658 (504, 877) vs. 502 (397, 608) ng/ml, = 0.008].
The serum MMP3 level of PD patients (especially early-stage patients) was significantly lower than that of the healthy control group, and the MMP9 level was significantly higher than that of the healthy control group. MMP3 and MMP9 levels correlate with sleep disturbance and cognitive function in PD patients, respectively.
基质金属蛋白酶(MMPs)对于组织形成、神经网络重塑和血脑屏障完整性至关重要。MMPs在急性脑疾病中已得到广泛研究。然而,其与帕金森病(PD)的关系仍不明确。本研究旨在评估PD患者的血清MMP3和MMP9水平,并分析它们与非运动症状的相关性。
在这项横断面研究中,我们招募了73例特发性PD患者和64名健康志愿者。采用酶联免疫吸附测定(ELISA)法检测血清MMP3和MMP9水平。使用非运动症状量表(NMSS)、帕金森病睡眠量表(PDSS)和简易精神状态检查表(MMSE)对PD患者的非运动症状进行评估。
与对照组相比,PD患者(主要是早期PD患者)的血清MMP3水平显著降低[12.56(9.30,17.44)对15.37(11.33,24.41)ng/ml;P = 0.004],且PD患者的血清MMP9水平显著高于健康对照组[522(419,729)对329(229,473)ng/ml;P < 0.001]。MMP3水平与NMSS总分呈正相关(r = 0.271,P = 0.020),与评估胃肠道的第6项单项评分呈正相关(r = 0.333,P = 0.004),血清MMP3水平与PDSS评分呈负相关(r = -0.246,P = 0.036);同时,MMP9水平与NMSS总分呈正相关(r = 0.234,P = 0.047),认知功能障碍亚组的血清MMP9水平高于认知功能正常亚组[658(504,877)对502(397,608)ng/ml,P = 0.008]。
PD患者(尤其是早期患者)的血清MMP3水平显著低于健康对照组,MMP9水平显著高于健康对照组。MMP3和MMP9水平分别与PD患者的睡眠障碍和认知功能相关。