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• W2904136079 startingPage "242" @default.
• W2904136079 abstract "Alzheimer’s disease (AD) is the most common age-related, progressive neurodegenerative disease. It is characterized by memory loss and cognitive decline and responsible for most cases of dementia in the elderly. Late-onset or sporadic AD accounts for > 95% of cases, with age at onset > 65 years. Currently there are no drugs or other therapeutic agents available to prevent or delay the progression of AD. The cellular and molecular changes occurring in the brains of individuals with AD include accumulation of β-amyloid peptide and hyperphosphorylated tau protein, decrease of acetylcholine neurotransmitter, inflammation, and oxidative stress. Aggregation of β-amyloid peptide in extracellular plaques and the hyperphosphorylated tau protein in intracellular neurofibrillary tangles are characteristic of AD. A major challenge is identifying molecular biomarkers of the early-stage AD in patients as most studies have been performed with blood or brain tissue samples (postmortem) at late-stage AD. Subjects with mild cognitive impairment almost always have the neuropathologic features of AD with about 50% of mild cognitive impairment patients progressing to AD. They could provide important information about AD pathomechanism and potentially also highlight minimally or noninvasive, easy-to-access biomarkers. MicroRNAs are dysregulated in AD, and may facilitate the early detection of the disease and potentially the continual monitoring of disease progression and allow therapeutic interventions to be evaluated. Four recent reviews have been published of microRNAs in AD, each of which identified areas of weakness or limitations in the reported studies. Importantly, studies in the last three years have shown considerable progress in overcoming some of these limitations and identifying specific microRNAs as biomarkers for AD and mild cognitive impairment. Further large-scale human studies are warranted with less disparity in the study populations, and using an appropriate method to validate the findings." @default.
• W2904136079 created "2018-12-22" @default.
• W2904136079 creator A5025212321 @default.
• W2904136079 creator A5045986795 @default.
• W2904136079 date "2019-01-01" @default.
• W2904136079 modified "2023-10-16" @default.
• W2904136079 title "MicroRNAs as diagnostic and therapeutic tools for Alzheimer’s disease: advances and limitations" @default.
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• W2904136079 doi "https://doi.org/10.4103/1673-5374.244784" @default.
• W2904136079 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6301178" @default.
• W2904136079 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30531004" @default.
• W2904136079 hasPublicationYear "2019" @default.
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