Key result
Long noncoding RNAs are dysregulated in neurodegenerative diseases and represent promising therapeutic targets for diabetic Alzheimer's disease by modulating neurogenesis and insulin resistance.
Why the study?
Diabetic Alzheimer's disease has emerged as an important issue due to metabolic risk factors like brain insulin resistance, motivating a review to understand the role of lncRNAs across both conditions.
This review summarizes the role of long noncoding RNAs in the pathogenesis of diabetic Alzheimer's disease, highlighting their potential as therapeutic targets.
LncRNA modulation should not yet alter diabetic Alzheimer's management; leaves open their therapeutic potential pending interventional studies.
Long noncoding RNAs (lncRNAs) are involved in diverse physiological and pathological processes by modulating gene expression. They have been found to be dysregulated in the brain and cerebrospinal fluid of patients with neurodegenerative diseases, and are considered promising therapeutic targets for treatment. Among the various neurodegenerative diseases, diabetic Alzheimer's disease (AD) has been recently emerging as an important issue due to several unexpected reports suggesting that metabolic issues in the brain, such as insulin resistance and glucose dysregulation, could be important risk factors for AD. To facilitate understanding of the role of lncRNAs in this field, here we review recent studies on lncRNAs in AD and diabetes, and summarize them with different categories associated with the pathogenesis of the diseases including neurogenesis, synaptic dysfunction, amyloid beta accumulation, neuroinflammation, insulin resistance, and glucose dysregulation. It is essential to understand the role of lncRNAs in the pathogenesis of diabetic AD from various perspectives for therapeutic utilization of lncRNAs in the near future.
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Kim et al. (2018) conducted a review in Diabetic Alzheimer's disease. Long noncoding RNAs (lncRNAs) was evaluated. Long noncoding RNAs are dysregulated in neurodegenerative diseases and represent promising therapeutic targets for diabetic Alzheimer's disease by modulating neurogenesis and insulin resistance.
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