阿尔茨海默氏症患者血清 Sirtuin-1、HMGB1-TLR4、NF-KB 和 IL-6 水平:神经炎症通路与痴呆症严重程度的关系

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY Current Alzheimer research Pub Date : 2022-01-01 DOI:10.2174/1567205020666221226140721
Nazrin Gulmammadli, Dildar Konukoğlu, Eda Merve Kurtuluş, Didem Tezen, Muhammed Ibrahim Erbay, Melda Bozluolçay
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引用次数: 0

摘要

阿尔茨海默病(AD)影响着全球老龄人口,是一种进行性神经退行性疾病,需要标记物或工具来准确、简便地诊断和监测这一过程:本研究对根据 NINCS-ADRA 标准确诊的 AD 患者的血清 Sirtuin-1(SIRT-1)、高迁移率组框 1(HMGB1)、Toll-Like Receptor-4 (TLR4)、核因子卡巴 B(NF-kB)、白细胞介素-6(IL-6)、淀粉样蛋白 βeta-42 (Aβ-42)和 p-tau181 水平进行了研究。我们研究了导致神经元逐渐丧失的炎症途径,并强调了它们与全身循环中痴呆严重程度的可能关系:根据标准小型智力测验结果、核磁共振成像和/或氟化葡萄糖正电子发射断层扫描结果或根据 CT 结果将 60 岁以上的患者分组为:对照组 n:20;AD 组 n:32;血管性痴呆(VD)组 n:17;AD + VD 组 n=21。对全血计数、葡萄糖、维生素 B12、叶酸、酶、尿素、肌酐、电解质、胆红素和甲状腺功能检测进行了评估。使用 ELISA 分析血清 SIRT1、HMGB1、TLR4、NF-kB、IL-6、Aβ-42 和 p-tau181 水平:结果:血清中 Aβ-42、SIRT1、HMGB1 和 IL-6 的水平显著升高(p˂0.001,p 结论:我们的研究结果表明,血清中 Aβ-42、SIRT1、HMGB1 和 IL-6 的水平显著升高:我们的研究结果表明,AD 和 VD 中 Aβ42、SIRT 1、HMGB1 和 TLR4 通路的水平发生了改变。SIRT 1的活性在痴呆症发展的炎症途径中起着重要作用,尤其是在AD中。
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Serum Sirtuin-1, HMGB1-TLR4, NF-KB and IL-6 Levels in Alzheimer's: The Relation Between Neuroinflammatory Pathway and Severity of Dementia.

Alzheimer's disease (AD), which affects the world's aging population, is a progressive neurodegenerative disease requiring markers or tools to accurately and easily diagnose and monitor the process.

Objective: In this study, serum Sirtuin-1(SIRT-1), High Mobility Group Box 1 (HMGB1), Toll-Like Receptor-4 (TLR4), Nuclear Factor Kappa B (NF-kB), Interleukin-6 (IL-6), Amyloid βeta-42 (Aβ- 42), and p-tau181 levels in patients diagnosed with AD according to NINCS-ADRA criteria were studied. We investigated the inflammatory pathways that lead to progressive neuronal loss and highlight their possible relationship with dementia severity in the systemic circulation.

Methods: Patients over 60 years of age were grouped according to their Standard Mini Mental Test results, MRI, and/or Fludeoxyglucose positron emission tomography or according to their CT findings as Control n:20; AD n:32; Vascular Dementia (VD) n:17; AD + VD; n = 21. Complete blood count, Glucose, Vitamin B12, Folic Acid, Enzymes, Urea, Creatinine, Electrolytes, Bilirubin, and Thyroid Function tests were evaluated. ELISA was used for the analysis of serum SIRT1, HMGB1, TLR4, NF-kB, IL-6, Aβ-42, and p-tau181 levels.

Results: Levels of serum Aβ-42, SIRT1, HMGB1, and IL-6 were significantly higher (p< 0.001, p< 0.01, p< 0.001, and p< 0.001, respectively), and TLR4 levels were significantly lower (p< 0.001) in the dementia group than in the control group. No significant difference was observed between dementia and control groups for serum NF-kB and p-tau181 levels.

Conclusion: Our results show that the levels of the Aβ42, SIRT 1, HMGB1, and TLR4 pathways are altered in AD and VD. SIRT 1 activity plays an important role in the inflammatory pathway of dementia development, particularly in AD.

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来源期刊
Current Alzheimer research
Current Alzheimer research 医学-神经科学
CiteScore
4.00
自引率
4.80%
发文量
64
审稿时长
4-8 weeks
期刊介绍: Current Alzheimer Research publishes peer-reviewed frontier review, research, drug clinical trial studies and letter articles on all areas of Alzheimer’s disease. This multidisciplinary journal will help in understanding the neurobiology, genetics, pathogenesis, and treatment strategies of Alzheimer’s disease. The journal publishes objective reviews written by experts and leaders actively engaged in research using cellular, molecular, and animal models. The journal also covers original articles on recent research in fast emerging areas of molecular diagnostics, brain imaging, drug development and discovery, and clinical aspects of Alzheimer’s disease. Manuscripts are encouraged that relate to the synergistic mechanism of Alzheimer''s disease with other dementia and neurodegenerative disorders. Book reviews, meeting reports and letters-to-the-editor are also published. The journal is essential reading for researchers, educators and physicians with interest in age-related dementia and Alzheimer’s disease. Current Alzheimer Research provides a comprehensive ''bird''s-eye view'' of the current state of Alzheimer''s research for neuroscientists, clinicians, health science planners, granting, caregivers and families of this devastating disease.
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