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本文引用的文献

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2
Ranking the risk factors for Alzheimer's disease; findings from the UK Biobank study.阿尔茨海默病风险因素的排名;来自英国生物银行研究的结果。
Aging Brain. 2023 Jun 17;3:100081. doi: 10.1016/j.nbas.2023.100081. eCollection 2023.
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With Teeth, Broken, or Fixed: The Challenges of Linking Periodontitis, Neuroepidemiology, and Biomarkers of Disease.有牙、缺牙或镶牙:牙周炎、神经流行病学和疾病生物标志物关联的挑战。
J Alzheimers Dis. 2023;93(3):991-994. doi: 10.3233/JAD-230346.
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Poor Oral Health and Risk of Incident Dementia: A Prospective Cohort Study of 425,183 Participants.口腔健康状况不佳与痴呆症发病风险的前瞻性队列研究:一项纳入 425183 名参与者的研究。
J Alzheimers Dis. 2023;93(3):977-990. doi: 10.3233/JAD-221176.
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血浆蛋白质组生物标志物对口腔健康问题与痴呆症发病相关性的中介和调节作用:英国生物银行研究。

Mediating and moderating effects of plasma proteomic biomarkers on the association between poor oral health problems and incident dementia: The UK Biobank study.

机构信息

US Department of Veterans Affairs, VA National Center On Homelessness Among Veterans, Washington, DC, 20420, USA.

Department of Management, Policy, and Community Health, School of Public Health, University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.

出版信息

Geroscience. 2024 Oct;46(5):5343-5363. doi: 10.1007/s11357-024-01202-3. Epub 2024 May 29.

DOI:10.1007/s11357-024-01202-3
PMID:38809392
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11336161/
Abstract

The plasma proteome can mediate poor oral health problems (POHP)'s link to incident dementia. We screened 37,269 UK Biobank participants 50-74 years old (2006-2010) for prevalent POHP, further tested against 1463 plasma proteins and incident dementia over up to 15 years of follow-up. Total effect (TE) of POHP-dementia through plasma proteomic markers was decomposed into pure indirect effect (PIE), interaction referent (INTREF), controlled direct effect (CDE), or mediated interaction (INTMED). POHP increased the risk of all-cause dementia by 17% (P < 0.05). Growth differentiation factor 15 (GDF15) exhibited the strongest mediating effects (PIE > 0, P < 0.001), explaining 28% the total effect of POHP on dementia, as a pure indirect effect. A first principal component encompassing top 4 mediators (GDF15, IL19, MMP12, and ACVRL1), explained 11% of the POHP-dementia effect as a pure indirect effect. Pathway analysis including all mediators (k = 173 plasma proteins) revealed the involvement of the immune system, signal transduction, metabolism, disease, and gene expression, while STRING analysis indicated that top mediators within the first principal component were also represented in the two largest proteomic clusters. The dominant biological GO pathway for the GDF15 cluster was GO:0007169 labeled as "transmembrane receptor protein tyrosine kinase signaling pathway." Dementia is linked to POHP mediated by GDF15 among several proteomic markers.

摘要

血浆蛋白质组可以介导口腔健康不良问题 (POHP) 与痴呆症发病之间的联系。我们筛选了 37269 名年龄在 50-74 岁的英国生物库参与者 (2006-2010 年),以确定现患 POHP,并对 1463 种血浆蛋白和长达 15 年的随访期间的痴呆症发病进行了进一步检测。通过血浆蛋白质组学标志物,将 POHP-痴呆症的总效应 (TE) 分解为纯间接效应 (PIE)、交互参照 (INTREF)、受控直接效应 (CDE) 或介导交互 (INTMED)。POHP 使全因痴呆症的风险增加了 17% (P<0.05)。生长分化因子 15 (GDF15) 表现出最强的中介作用 (PIE>0,P<0.001),占 POHP 对痴呆症总效应的 28%,作为纯间接效应。包含前 4 个中介物 (GDF15、IL19、MMP12 和 ACVRL1) 的第一主成分解释了 POHP 对痴呆症的 11% 效应,作为纯间接效应。包括所有中介物 (k=173 种血浆蛋白) 的途径分析表明,免疫系统、信号转导、代谢、疾病和基因表达都参与其中,而 STRING 分析表明,第一主成分中的前几个中介物也代表了两个最大蛋白质组簇中的一部分。GDF15 簇的主要生物学 GO 途径是 GO:0007169,标记为 "跨膜受体蛋白酪氨酸激酶信号通路"。GDF15 等多种蛋白质标志物介导的痴呆症与 POHP 有关。