血小板总PLA2活性、血清氧化水平和血浆铜/锌比:监测MCI和阿尔茨海默病进展的潜在作用的恶性循环

IF 2.2 4区 医学 Q3 GERIATRICS & GERONTOLOGY Rejuvenation research Pub Date : 2022-02-01 DOI:10.1089/rej.2021.0020
Marta Balietti, Tiziana Casoli, Robertina Giacconi, Cinzia Giuli
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引用次数: 1

摘要

阿尔茨海默病(AD)无法治愈,主要是因为诊断晚。早期诊断生物标志物至关重要。磷脂酶A2 (PLA2)是一种在大脑中具有多种功能的水解酶,然而它们的失调会导致神经退行性变。我们评估了健康老年受试者(HE, n = 102)、轻度认知障碍患者(MCI, n = 90)和AD患者(n = 91)的血小板总PLA2活性(ptotPLA2)。血小板被认为是“循环神经元”,ptotPLA2似乎反映了大脑活动。三个队列的ptotPLA2相似,但在MCI中,ptotPLA2越高,整体认知状态(Mini Mental State Examination score [MMSE])越差,在AD中,ptotPLA2越低,病理分期(Clinical Dementia Rating [CDR])越严重。相应的,MMSE≥26的MCI与HE重叠,MMSE的MCI中totPLA2升高,CDR 2的AD中ptotPLA2降低。在MCI中,ptotPLA2与血液氧化和炎症呈正相关,而在AD中则相反。最后,判别指数(DI)——计算ptotPLA2、氧化水平和Cu/Zn比值(炎症参数)的乘积——区分在接下来的24个月内进展为痴呆的MCI患者和病理发展较差的AD患者。综上所述,ptotPLA2在MCI和AD进展过程中的变化与MCI和AD的氧化/炎症状态相反,当纳入DI时,可能有助于识别预后更严重的MCI转化为痴呆和AD患者。ptotPLA2可能具有诊断/预后价值,是一个潜在的治疗靶点。
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Platelet Total PLA2 Activity, Serum Oxidative Level, and Plasma Cu/Zn Ratio: A Vicious Cycle with a Potential Role to Monitor MCI and Alzheimer's Disease Progression.

Alzheimer's disease (AD) has no cure, mainly because of late diagnosis. Early diagnostic biomarkers are crucial. Phospholipases A2 (PLA2) are hydrolases with several functions in the brain, nevertheless their deregulation contributes to neurodegeneration. We evaluated platelet total PLA2 activity (ptotPLA2) in healthy elderly subjects (HE, n = 102), patients suffering from mild cognitive impairment (MCI, n = 90) and AD (n = 91). Platelets are considered "circulating neurons" and ptotPLA2 appears to mirror the cerebral activity. ptotPLA2 of the three cohorts was similar, but in MCI the higher ptotPLA2 the worse the global cognitive status (Mini Mental State Examination score [MMSE]) and in AD the lower ptotPLA2 the more severe the pathology stage (Clinical Dementia Rating [CDR]). Accordingly, MCI with MMSE ≥26 overlapped HE, in MCI with MMSE <26 and in AD with CDR 1 ptotPLA2 increased, in AD with CDR 2 ptotPLA2 decreased. In MCI ptotPLA2 positively correlated with blood oxidation and inflammation, in AD it was the opposite. Finally, Discrimination Index (DI)-calculated multiplying ptotPLA2, oxidative level and Cu/Zn ratio (an inflammation parameter)-differentiated MCI patients who progressed to dementia in the following 24 months and AD patients with the worse pathology development. Summarizing, ptotPLA2 changes during MCI and AD progression, is linked, in opposite way, to oxidative/inflammatory status in MCI and AD and might help, when included in DI, to identify MCI converters to dementia and AD patients with the more severe prognosis. ptotPLA2 may have a diagnostic/prognostic value and be a potential therapeutic target.

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来源期刊
Rejuvenation research
Rejuvenation research 医学-老年医学
CiteScore
4.50
自引率
0.00%
发文量
41
审稿时长
3 months
期刊介绍: Rejuvenation Research publishes cutting-edge, peer-reviewed research on rejuvenation therapies in the laboratory and the clinic. The Journal focuses on key explorations and advances that may ultimately contribute to slowing or reversing the aging process, and covers topics such as cardiovascular aging, DNA damage and repair, cloning, and cell immortalization and senescence. Rejuvenation Research coverage includes: Cell immortalization and senescence Pluripotent stem cells DNA damage/repair Gene targeting, gene therapy, and genomics Growth factors and nutrient supply/sensing Immunosenescence Comparative biology of aging Tissue engineering Late-life pathologies (cardiovascular, neurodegenerative and others) Public policy and social context.
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