Comparative proteomic profiling of cerebrospinal fluid between living and post mortem ALS and control subjects.

Comparative proteomic profiling of cerebrospinal fluid between living and post mortem ALS and control subjects.
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活体和死后 ALS 与对照受试者之间脑脊液的比较蛋白质组学分析。

DOI:
10.1080/17482960701549681
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发表时间:
2007
期刊:
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases
影响因子:
--
通讯作者:
Bowser,Robert
Bowser,Robert
中科院分区:
--
文献类型:
--
作者:
Ranganathan,Srikanth;Nicholl,GeorginaCB;Henry,Sarah;Lutka,Fran;Sathanoori,Ramasri;Lacomis,David;Bowser,Robert

文献摘要

相似文献

Neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS), lack definitive diagnostic tests or biomarkers of disease progression. Most studies that investigate protein abnormalities in ALS have used biofluids such as blood or cerebrospinal fluid (CSF), while some have used post mortem tissue or CSF samples. Since ALS disease progression and post mortem effects probably induce significant alterations to protein modifications or proteolysis, we directly examined the CSF proteome from ALS subjects at various lengths of time from symptom onset and at autopsy by mass spectrometry based proteomics. CSF was also obtained from both healthy age‐matched control subjects and at autopsy from healthy and Alzheimer's disease (AD) controls. We identified significant differences in the CSF proteome between living and post mortem ALS subjects, as well as living and post mortem control subjects. We also noted differences in the CSF proteome of ALS subjects that have exhibited symptoms for varying lengths of time and between ALS and AD subjects at end‐stage of disease. This is the first study describing differences in the CSF proteome from post mortem and living ALS subjects using a mass spectrometric approach. These differences highlight the importance of utilizing CSF from living ALS subjects near the time of symptom onset for the identification of early protein biomarkers, although some protein alterations that occur early in the disease process are maintained throughout the course of disease and in post mortem samples.