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Mitochondrial Creatine Kinase is Decreased in the Serum of Idiopathic Parkinson’s Disease Patients

机译:特发性帕金森病患者血清中的线粒体肌酸激酶减少

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Mitochondrial creatine kinase (MtCK) is vital in the process of mitochondrial energy metabolism, and mitochondrial dysfunction has been implicated in the pathogenesis of Parkinson’s disease (PD). Therefore, we speculated that MtCK activity could be altered in the serum of PD patients. However, no studies to date have investigated this specific topic, so we sought to investigate the serum MtCK activities among a cohort of PD patients. 50 patients with PD and 30 age-matched controls were recruited for this study. Serum ubiquitous MtCK (uMtCK) and sarcomeric MtCK (sMtCK) activities were assayed using an immunoinhibition method. Correlations between serum uMtCK/sMtCK activities and clinical features/parameters were explored in the PD group. Our study revealed a significant decrease in the uMtCK activity in the PD group when compared with the control group. No significant difference was found in the serum sMtCK activity between the PD and control groups. There was a significant correlation between serum uMtCK activities and the disease progression rate, duration, and age at onset in PD patients. While no significant relationship was found between the serum uMtCK activities and the Hoehn & Yahr stage or main non-motor symptoms scale. There was a significant decrease in the uMtCK activity in the serum of PD patients, which was associated with the rate of disease progression, duration, and age at onset of disease. Therefore, uMtCK activity in serum offers a useful clue for identification of PD biomarkers.
机译:线粒体肌酸激酶(MtCK)在线粒体能量代谢过程中至关重要,而线粒体功能障碍与帕金森氏病(PD)的发病机理有关。因此,我们推测PD患者血清中的MtCK活性可能改变。但是,迄今为止,尚无研究调查此特定主题,因此我们试图研究一组PD患者的血清MtCK活性。该研究招募了50名PD患者和30名年龄匹配的对照者。使用免疫抑制方法测定血清普遍存在的MtCK(uMtCK)和肌节MtCK(sMtCK)的活性。 PD组探讨了血清uMtCK / sMtCK活性与临床特征/参数之间的相关性。我们的研究显示,与对照组相比,PD组的uMtCK活性显着降低。 PD和对照组之间的血清sMtCK活性没有发现显着差异。 PD患者的血清uMtCK活性与疾病进展率,病程和发病年龄之间存在显着相关性。虽然血清uMtCK活性与Hoehn&Yahr分期或主要非运动症状量表之间无显着相关性。 PD患者血清中的uMtCK活性显着降低,这与疾病进展的速度,持续时间和发病年龄相关。因此,血清中的uMtCK活性为PD生物标志物的鉴定提供了有用的线索。

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