| Literature DB >> 29226874 |
Han-Hsing Tsou1, Wen-Chin Hsu2, Jong-Ling Fuh3,4,5, Shih-Pin Chen3,4,5,6, Tsung-Yun Liu1,7, Hsiang-Tsui Wang2.
Abstract
Alzheimer's disease (AD) is a detrimental neurodegenerative disease, and early diagnosis appears to be the key to successful treatment. Acrolein, a byproduct of lipid peroxidation, has been shown to contribute to the pathological process of AD. This study recruited 118 elderly subjects consisting of 58 non-demented control subjects and 62 AD patients. We analyzed the acrolein-related metabolites in the plasma, cerebrospinal fluid (CSF), and urine of all subjects. We found that the levels of acrolein-conjugated protein (Acr-PC) in the plasma (p = 0.00012) and CSF (p = 0.00161) of AD patients were significantly higher than those of control subjects, whereas the levels of a urinary acrolein metabolite, 3-hydroxypropyl mercapturic acid (3-HPMA), were markedly decreased (p = 0.00882) in AD patients. These data suggest that deregulated acrolein metabolism may be correlated with neuronal damage in AD patients, which might provide further insights into the disease progression and early diagnosis of AD.Entities:
Keywords: 3-HPMA; Acrolein; Alzheimer’s disease; acrolein-conjugated protein (Acr-PC)
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Year: 2018 PMID: 29226874 DOI: 10.3233/JAD-170736
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472