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Identification of inflammatory and vascular markers associated with mild cognitive impairment

机译:识别与轻度认知障碍有关的炎症和血管标志物

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摘要

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.
机译:生化过程已与轻度认知障碍(MCI)和痴呆症的发病机制相关,包括慢性炎症,膜脂调节异常和神经递质途径破坏。但是,研究MCI中这些过程的生物标记物的研究仍然很少且不一致。为了收集新的证据,我们评估了57名MCI患者和57名认知健康对照人群中几种潜在标志物的表现。与之相比,MCI患者的血浆TNF-α(p = 0.045)和C肽(p = 0.004)明显升高,而VEGF-A(p = 0.042)和PAI-1(p = 0.019)降低。与控件。此外,我们的研究还发现血浆sTNFR-1(MCI +对照:B = -6.529,p = 0.020; MCI:B = -9.865,p = 0.011)与sIL-2Rα(MCI +对照:B =-)存在显着相关性。 7.010,p = 0.007; MCI:B = -11.834,p = 0.003)水平,整个队列和MCI组均具有MoCA评分。这些发现证实了痴呆的炎症和血管假说。有必要进行进一步的研究以确定它们作为认知缺陷早期生物标志物的潜力,并探索相关的机制。

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