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帕金森病合并便秘患者的血清微小 RNA 29c 表达较高,突出的神经精神障碍,可能发生 RBD 转化,生活质量较差。

Parkinson's disease patients combined with constipation tend to have higher serum expression of microRNA 29c, prominent neuropsychiatric disorders, possible RBD conversion, and a substandard quality of life.

机构信息

Department of Neurology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai, 200120, China.

出版信息

Neurol Sci. 2023 Sep;44(9):3141-3150. doi: 10.1007/s10072-023-06793-x. Epub 2023 Apr 17.

Abstract

INTRODUCTION

The symptom of constipation has been confirmed as an early diagnose criteria for Parkinson's disease (PD). Furthermore, evidences suggest that pathogenesis of PD initiates in gut, rather than brain. If so, identifying biomarkers for constipation in PD might have potentials to assist early diagnosis and initial treatment.

METHOD

We first identified that microRNA 29c (miR-29c) was dysregulated both in PD and constipation patients through bioinformatics analysis. Then, serological analysis of the expression of miR-29c in 67 PD patients with constipation (PD-C), 51 PD patients without constipation (PD-NC), and 50 healthy controls (HC) was carried out by qPCR. Demographic and clinical features were also compared. Patients in PD-C group were further classified into two groups: those with prodromal stage constipation (PD-C-Pro) (n = 36) and those with clinical stage constipation (PD-C-Clinic) (n = 31), to explore their different characteristics.

RESULTS

The levels of miR-29c in PD-C group were higher than that in PD-NC group, both higher than HC group. PD-C-Pro group's miR-29c levels were statistically higher compared with PD-C-Clinic group's. What is more, PD-C group had higher scores of MDS-UPDRS-I, NMSS, NMSS3, NMSS4, NMSS6, NMSS9, SCOPA-AUT, HAMD, HAMA, RBDSQ, CSS, and PACQOL compared with PD-NC party. Relative to the PD-C-Clinic, patients in PD-C-Pro group had higher MDS-UPDRS-I, NMSS, NMSS3, HAMD, and HAMA scores, and were more likely to have RBD.

CONCLUSION

Our results indicated that miR-29c seems to be an underlying cause for developing constipation in patients with PD and PD-C identifies a group of patients with more severe non-motor impairment, prominent neuropsychiatric disorders, and possible RBD conversion as well as a substandard quality of life. We further confirmed that there is a close relationship between symptoms representing the same pathological origin, especially constipation and RBD.

摘要

简介

便秘症状已被确认为帕金森病(PD)的早期诊断标准。此外,有证据表明 PD 的发病机制始于肠道,而不是大脑。如果是这样,那么识别 PD 患者便秘的生物标志物可能有助于早期诊断和初始治疗。

方法

我们首先通过生物信息学分析发现 microRNA 29c(miR-29c)在 PD 和便秘患者中均失调。然后,通过 qPCR 对 67 例 PD 伴便秘(PD-C)患者、51 例 PD 无便秘(PD-NC)患者和 50 例健康对照(HC)的血清 miR-29c 表达进行了血清学分析。还比较了人口统计学和临床特征。PD-C 组患者进一步分为两个亚组:前驱期便秘(PD-C-Pro)(n=36)和临床期便秘(PD-C-Clinic)(n=31),以探讨它们的不同特征。

结果

PD-C 组的 miR-29c 水平高于 PD-NC 组,均高于 HC 组。PD-C-Pro 组的 miR-29c 水平明显高于 PD-C-Clinic 组。此外,PD-C 组的 MDS-UPDRS-I、NMSS、NMSS3、NMSS4、NMSS6、NMSS9、SCOPA-AUT、HAMD、HAMA、RBDSQ、CSS 和 PACQOL 评分均高于 PD-NC 组。与 PD-C-Clinic 相比,PD-C-Pro 组患者的 MDS-UPDRS-I、NMSS、NMSS3、HAMD 和 HAMA 评分更高,发生 RBD 的可能性更大。

结论

我们的结果表明,miR-29c 似乎是 PD 患者便秘的潜在原因,PD-C 可识别出一组具有更严重非运动障碍、突出神经精神障碍和可能 RBD 转化以及生活质量较差的患者。我们进一步证实,代表相同病理起源的症状之间存在密切关系,特别是便秘和 RBD。

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