血清检测或成阿尔茨海默病检测新方法

2011-12-20 EurekAlert中文 EurekAlert中文

12月14日,芬兰国家技术研究中心发表新闻公报说,由该中心和芬兰东部大学共同完成的研究发现,一种指示组织缺氧和磷酸戊糖途径的分子信号,是阿尔茨海默氏症的前兆。 所谓磷酸戊糖途径,是葡萄糖氧化分解的一种方式。由于阿尔茨海默氏症(早老性痴呆症)目前无法治愈,因此尽早检测和及早治疗非常重要。芬兰研究人员最近发现,可以通过检测血清在症状出现前数月甚至数年就查出这种疾病。 公报说,研究人员分别采集阿

12月14日,芬兰国家技术研究中心发表新闻公报说,由该中心和芬兰东部大学共同完成的研究发现,一种指示组织缺氧和磷酸戊糖途径的分子信号,是阿尔茨海默氏症的前兆。

所谓磷酸戊糖途径,是葡萄糖氧化分解的一种方式。由于阿尔茨海默氏症(早老性痴呆症)目前无法治愈,因此尽早检测和及早治疗非常重要。芬兰研究人员最近发现,可以通过检测血清在症状出现前数月甚至数年就查出这种疾病。

公报说,研究人员分别采集阿尔茨海默氏症患者、轻度认知障碍患者及健康对照组的血清样本,并对他们进行跟踪观察。27个月内,143名轻度认知障碍患者中的52人患上阿尔茨海默氏症。这52人的血清样本中均可检测到一种指示组织缺氧和磷酸戊糖途径的分子信号。通过对代谢途径的数据分析,研究人员发现磷酸戊糖途径与阿尔茨海默氏症的病变有关,组织缺氧和氧化应激是早期病变的反映。

芬兰国家技术研究中心指出,医生评估患者的神经认知功能时可以配合这种血清检测方法,来辨别需要接受综合治疗的高危患者。

阿尔茨海默氏症是一种脑部病变,发病原因尚不明确。临床症状表现为认知、记忆和语言功能障碍等。目前还没有有效的治愈疗法,现有药物只能缓解症状和减缓病程的进展。(生物谷Bioon.com)

Biochemical signature predicts progression to Alzheimer's disease

EurekAlert 14-Dec-2011

A study led by Research Professor Matej Orešič from VTT Technical Research Centre of Finland suggests that Alzheimer's disease is preceded by a molecular signature indicative of hypoxia and up-regulated pentose phosphate pathway. This indicator can be analysed as a simple biochemical assay from a serum sample months or even years before the first symptoms of the disease occur. In a healthcare setting, the application of such an assay could therefore complement the neurocognitive assessment by the medical doctor and could be applied to identify the at-risk patients in need of further comprehensive follow-up. Alzheimer's disease (AD) is a growing challenge to the health care systems and economies of developed countries with millions of patients suffering from this disease and increasing numbers of new cases diagnosed annually with the increasing ageing of populations. The progression of Alzheimer's disease (AD) is gradual, with the subclinical stage of illness believed to span several decades. The pre-dementia stage, also termed mild cognitive impairment (MCI), is characterised by subtle symptoms that may affect complex daily activities. MCI is considered as a transition phase between normal aging and AD. MCI confers an increased risk of developing AD, although the state is heterogeneous with several possible outcomes, including even improvement back to normal cognition.

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