Serum microRNA‐501‐3p is a potential diagnostic tool for detecting mild cognitive impairment: Ehime genome study
Abstract
Tight junction disruption and dysfunction are involved in the progression of blood–brain barrier (BBB) breakdown. Recent investigations have revealed BBB disruption in patients with vascular cognitive decline. Our previous studies showed that miR‐501‐3p negatively regulates cerebral endothelial tight junction protein‐1, resulting in the disruption of the BBB, and playing an important role in the development of vascular cognitive impairment. BBB breakdown in white matter lesions is often seen in the patients with vascular mild cognitive impairment (MCI). We therefore hypothesize that most early‐phase MCI patients may demonstrate elevated expression of miR‐501‐3p and sought to investigate whether serum exosome miR‐501‐3p levels could be a clinical indicator for detecting mild cognitive impairment. One hundred and seventy‐eight subjects (aged 73 [68–75] years, 53% male) were recruited for this study. The Japanese version of the Montreal Cognitive Assessment (MoCA‐J) was used for detecting MCI. Serum exosome miR‐501‐3p expression levels were measured by qPCR methods. Patients were divided into two groups depending on whether their miR‐501‐3p ∆Ct values were above (“High”; n = 74) or below (“Low”; n = 104) cutoff levels determined by ROC curve. MCI was detected significantly more often in the miR‐501‐3p‐High group (vs. ‐Low group, 63.5% vs. 47.1%, respectively; p < 0.05). Multivariate logistic regression analysis showed a significant association between MCI status and High miR‐501‐3p (odds ratio 2.662; p < 0.01), improved vs. known risk factors. In non‐diabetic patients, High miR‐501‐3p was positively associated with MCI status (odds ratio 3.633; p < 0.01) and also positively associated with MCI status in those with atherosclerosis (odds ratio 3.219; p < 0.01). The present study demonstrates that elevated expression of blood exosomal miR‐501‐3p can indicate the presence of MCI in human patients. Early detection of vascular injuries may allow a reduction in progressive dementia through the management of vascular risk factors.image
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TNF-induced miR-501-3p directly targets claudin-5 and ZO-1, causing BBB leakage and cognitive deficits in mouse models.
“TNF-induced miR-501-3p directly targets claudin-5 and ZO-1, causing BBB leakage and cognitive deficits in mouse models, while serum and exosomal miR-501-3p are elevated in individuals with mild cognitive impairment (MCI) and early AD (Toyama et al., 2023).”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Toyama et al., 2023
Serum and exosomal miR-501-3p are elevated in individuals with MCI and early AD.
“TNF-induced miR-501-3p directly targets claudin-5 and ZO-1, causing BBB leakage and cognitive deficits in mouse models, while serum and exosomal miR-501-3p are elevated in individuals with mild cognitive impairment (MCI) and early AD (Toyama et al., 2023).”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Toyama et al., 2023
Cites
Gorelick, P. B., Scuteri, A., Black, S. E., DeCarli, C., Greenberg, S. M., Iadecola, C., Launer, L. J., Laurent, S., Lopez, O. L., Nyenhuis, D., et al. (2011) · Stroke · doi:10.1161/str.0b013e3182299496 · Cited by 3,811 · see citing works
Donanemab in Early Alzheimer’s Disease
Mintun, M. A., Lo, A. C., Duggan Evans, C., Wessels, A. M., Ardayfio, P. A., Andersen, S. W., Shcherbinin, S., Sparks, J., Sims, J. R., Brys, M., et al. (2021) · New England Journal of Medicine · doi:10.1056/nejmoa2100708 · Cited by 1,728 · cited 1× · see citing works
“As described previously (Morioka et al., 2010), CAVI was measured using an automatic vascular screening system (VaSera VS 1500E, Fukuda Denshi).”
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Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease
Donepudi, K., Eadha, S., Rodarte, D., Sharma, B., & Kumar, S. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103211
- Authors
- Toyama, K., Spin, J. M., Tsao, P. S., Maruyama, K., Osawa, H., Mogi, M., & Takata, Y.
- Affiliations
- Department of Pharmacology Ehime University Graduate School of Medicine Ehime Japan
- VA Palo Alto Health Care System Palo Alto California USA
- Department of Bioscience, Graduate School of Agriculture Ehime University Ehime Japan
- Precision Medicine Translational Research Unit Ehime University Ehime Japan
- ORCID
- Toyama, Kensuke
- Venue
- Journal of Neurochemistry
- Publisher
- Wiley
- Published
- 2023-07-13
- Volume
- 166
- Issue
- 6
- Pages
- 960-971
- ISSN
- 0022-3042
- 1471-4159
- Cited by
- 11
- References
- 2
- Language
- en
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