Please use this identifier to cite or link to this item: https://doi.org/10.18632/aging.101924
Title: Identification of inflammatory and vascular markers associated with mild cognitive impairment
Authors: Shen, Xue-Ning
Lu, Yanxia 
Tan, Crystal Tze Ying
Liu, Ling-Yun
Yu, Jin-Tai
Feng, Lei 
Larbi, Anis 
Keywords: Science & Technology
Life Sciences & Biomedicine
Cell Biology
Geriatrics & Gerontology
mild cognitive impairment
TNF-alpha
C-peptide
VEGF-A
PAI-1
sTNFR-1
sIL-2R alpha
PLASMINOGEN-ACTIVATOR INHIBITOR-1
NECROSIS-FACTOR-ALPHA
ALZHEIMERS-DISEASE
MOUSE MODEL
TNF-ALPHA
NEUROINFLAMMATION
EXPRESSION
MEMORY
RISK
MOCA
Issue Date: 30-Apr-2019
Publisher: IMPACT JOURNALS LLC
Citation: Shen, Xue-Ning, Lu, Yanxia, Tan, Crystal Tze Ying, Liu, Ling-Yun, Yu, Jin-Tai, Feng, Lei, Larbi, Anis (2019-04-30). Identification of inflammatory and vascular markers associated with mild cognitive impairment. AGING-US 11 (8) : 2403-2419. ScholarBank@NUS Repository. https://doi.org/10.18632/aging.101924
Abstract: Biochemical processes have been associated with the pathogenesis of mild cognitive impairment (MCI) and dementia, including chronic inflammation, dysregulation of membrane lipids and disruption of neurotransmitter pathways. However, research investigating biomarkers of these processes in MCI remained sparse and inconsistent. To collect fresh evidence, we evaluated the performance of several potential markers in a cohort of 57 MCI patients and 57 cognitively healthy controls. MCI patients showed obviously increased levels of plasma TNF-α (p = 0.045) and C-peptide (p = 0.004) as well as decreased levels of VEGF-A (p = 0.042) and PAI-1 (p = 0.019), compared with controls. In addition, our study detected significant correlations of plasma sTNFR-1 (MCI + Control: B = -6.529, p = 0.020; MCI: B = -9.865, p = 0.011) and sIL-2Rα (MCI + Control: B = -7.010, p = 0.007; MCI: B = -11.834, p = 0.003) levels with MoCA scores in the whole cohort and the MCI group. These findings corroborate the inflammatory and vascular hypothesis for dementia. Future studies are warranted to determine their potential as early biomarkers for cognitive deficits and explore the related mechanisms.
Source Title: AGING-US
URI: https://scholarbank.nus.edu.sg/handle/10635/235238
ISSN: 1945-4589
DOI: 10.18632/aging.101924
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