文章摘要
帕金森病患者血清Sirt1-6水平与认知功能障碍的关系
Relationship between serum Sirt1-6 levels and cognitive dysfunction in patients with Parkinson's disease
投稿时间:2025-04-28  
DOI:10.3969/j.issn.1000-0399.2026.07.009
中文关键词: 帕金森病  认知功能障碍  血清沉默信息调节因子1-6  关系研究
英文关键词: Parkinson's disease  Cognitive dysfunction  Sirt1-6  Relationship study
基金项目:河北省医学科学研究课题计划资助(编号:20232121)
作者单位E-mail
连雅君 056000 河北邯郸 邯郸明仁医院脑病三科  
彭营影 061001 河北沧州 沧州市中心医院眩晕一科  
朱明肃 061001 河北沧州 沧州市中心医院眩晕一科  
杨潮萍 061001 河北沧州 沧州市中心医院眩晕一科  
朱兰 061001 河北沧州 沧州市中心医院眩晕一科 17717736624@163.com 
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中文摘要:
      目的 探讨帕金森病(PD)患者血清沉默信息调节因子(Sirts)1-6水平与认知功能障碍的关系。方法 回顾性选取2021年4月至2023年5月于邯郸明仁医院收治的121例PD患者为研究组。根据蒙特利尔认知评估量表(MoCA)评分将其分为痴呆组(MoCA评分≤17分,n=37)、轻度认知功能障碍组(即PD-MCI组,MoCA评分为18~25分,n=45)和认知功能正常组(即PD组,MoCA评分≥26分,n=39)。另同期选择121例体检健康者作为对照组。比较各组研究对象血清中Sirt1-6表达水平;采用Spearman相关性分析血清Sirt1、Sirt2、Sirt3水平与认知功能障碍的相关性;采用有序多分类logistic回归分析筛选PD患者认知功能障碍的影响因素;采用受试者工作特征(ROC)曲线及曲线下面积(AUC)分析血清Sirt1、Sirt2、Sirt3水平预测PD患者发生认知功能障碍的诊断效能。结果 研究组患者血清Sirt2水平高于对照组(P<0.05),血清Sirt1和Sirt3水平低于对照组(P<0.05)。PD组、PD-MCI组和痴呆组3组患者Sirt4、Sirt5以及Sirt6的表达水平比较,差异无统计学意义(P>0.05);痴呆组患者血清Sirt2水平高于PD-MCI组和PD组,血清Sirt1和Sirt3水平低于PD-MCI组和PD组(P<0.05),且PD-MCI组和PD组间差异有统计学意义(P<0.05)。Spearman相关性分析结果显示,血清Sirt2与MoCA评分呈负相关(P<0.05),血清Sirt1、Sirt3与MoCA评分呈正相关(P<0.05)。有序多分类logistic回归分析显示,Sirt2、病程、UPDRSⅢ评分是PD患者发生认知功能障碍的危险因素(P<0.05),血清Sirt1、Sirt3均是其保护因素(P<0.05)。ROC曲线结果显示,血清Sirt1、Sirt2以及Sirt3水平联合预测的AUC高于Sirt1(0.837)、Sirt2(0.748)以及Sirt3(0.802)单独使用时的AUC。结论 PD患者血清Sirt2水平的升高以及Sirt1和Sirt3水平的降低与认知功能障碍密切相关,且这3种标志物的联合检测在预测PD患者发生认知功能障碍方面表现出最佳的预测效能。
英文摘要:
      Objective To investigate the relationship between serum levels of silent information regulator(Sirtuin) 1-6 and cognitive impairment in Parkinson's disease(PD) patients. Methods A retrospective cohort study was conducted on 121 patients with Parkinson's disease(PD) admitted to Handan Mingren Hospital between April 2021 and May 2023. Based on MoCA scores, the patients were categorized into three groups: dementia group(MoCA score≤17, n=37), mild cognitive impairment group(PD-MCI group)(MoCA score 18-25, n=45), and normal cognitive function group(PD group)(MoCA score≥26, n=39). Additionally, 121 healthy individuals undergoing routine physical examinations were selected as the control group during the same period. Serum expression levels of Sirt1-6 were compared among the study groups. Spearman correlation analysis was used to assess the relationship between serum Sirt1, Sirt2, and Sirt3 levels and cognitive impairment. Ordered multinomial logistic regression was used to identify factors influencing cognitive impairment in patients with Parkinson's disease. Receiver operating characteristic(ROC) curves and area under the curve(AUC) values were analyzed to evaluate the diagnostic efficacy of serum Sirt1, Sirt2, and Sirt3 levels in predicting cognitive impairment in PD patients. Results Serum Sirt2 levels in the study group were higher than those in the control group(P<0.05), while serum Sirt1 and Sirt3 levels were lower than those in the control group(P<0.05). Comparisons of Sirt4, Sirt5, and Sirt6 expression levels among the PD group, PD-MCI group, and dementia group showed no statistically significant differences(P>0.05). Patients in the dementia group exhibited higher serum Sirt2 levels than those in the PD-MCI and PD groups, while their serum Sirt1 and Sirt3 levels were lower than those in the PD-MCI and PD groups(P<0.05). Additionally, statistically significant differences were observed between the PD-MCI and PD groups(P<0.05). Spearman correlation analysis revealed a negative correlation between serum Sirt2 and MoCA scores(P<0.05), while serum Sirt1 and Sirt3 showed positive correlations with MoCA scores(P<0.05). Ordered multivariate logistic regression analysis revealed that Sirt2, disease duration, and the UPDRS Ⅲ score were risk factors for cognitive impairment in patients with Parkinson's disease(P<0.05), while serum Sirt1 and Sirt3 were protective factors(P<0.05). ROC curve results indicated that the combined AUC for predicting PD using serum Sirt1, Sirt2, and Sirt3 levels was higher than the AUC when using Sirt1 alone(0.837), Sirt2 alone(0.748), or Sirt3 alone(0.802). Conclusion Elevated serum Sirt2 levels as well as decreased Sirt1 and Sirt3 levels in PD patients are strongly associated with cognitive dysfunction, and the combined testing of these three markers shows the best predictive efficacy in predicting the occurrence of cognitive dysfunction in PD patients.
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