• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Association of subjective memory complaints with serum biomarkers of neurodegeneration and cognition: A population-based study.主观记忆主诉与神经退行性变及认知的血清生物标志物的关联:一项基于人群的研究。
J Am Geriatr Soc. 2025 Mar;73(3):859-866. doi: 10.1111/jgs.19300. Epub 2024 Dec 3.
2
APOE4, Blood Neurodegenerative Biomarkers, and Cognitive Decline in Community-Dwelling Older Adults.载脂蛋白E4、血液神经退行性生物标志物与社区居住老年人的认知衰退
JAMA Netw Open. 2025 May 1;8(5):e258903. doi: 10.1001/jamanetworkopen.2025.8903.
3
Alzheimer's and neurodegenerative disease biomarkers in blood predict brain atrophy and cognitive decline.血液中的阿尔茨海默病和神经退行性疾病生物标志物可预测脑萎缩和认知能力下降。
Alzheimers Res Ther. 2024 Apr 30;16(1):94. doi: 10.1186/s13195-024-01459-y.
4
Perceived Stress, Blood Biomarkers, and Cognitive Functioning in Older Adults.老年人的感知压力、血液生物标志物与认知功能。
Psychosom Med. 2024;86(6):507-511. doi: 10.1097/PSY.0000000000001317. Epub 2024 Apr 16.
5
Association of Plasma Amyloid, P-Tau, GFAP, and NfL With CSF, Clinical, and Cognitive Features in Patients With Dementia With Lewy Bodies.血浆淀粉样蛋白、P-tau、GFAP 和 NfL 与路易体痴呆患者脑脊液、临床和认知特征的关联。
Neurology. 2024 Jun 25;102(12):e209418. doi: 10.1212/WNL.0000000000209418. Epub 2024 Jun 3.
6
Plasma neurofilament light, glial fibrillary acid protein, and phosphorylated tau 181 as biomarkers for neuropsychiatric symptoms and related clinical disease progression.血浆神经丝轻链、胶质纤维酸性蛋白和磷酸化 tau181 作为神经精神症状和相关临床疾病进展的生物标志物。
Alzheimers Res Ther. 2024 Jul 25;16(1):165. doi: 10.1186/s13195-024-01526-4.
7
Association of Subjective Memory Complaints With White Matter Hyperintensities and Cognitive Decline Among Older Adults in Chicago, Illinois.伊利诺伊州芝加哥市老年人主观记忆主诉与脑白质高信号和认知能力下降的相关性研究。
JAMA Netw Open. 2022 Apr 1;5(4):e227512. doi: 10.1001/jamanetworkopen.2022.7512.
8
Pathologic and cognitive correlates of plasma biomarkers in neurodegenerative disease.神经退行性疾病中血浆生物标志物的病理和认知相关性。
Alzheimers Dement. 2024 Jun;20(6):3889-3905. doi: 10.1002/alz.13777. Epub 2024 Apr 21.
9
Predicting Longitudinal Cognitive Decline and Alzheimer's Conversion in Mild Cognitive Impairment Patients Based on Plasma Biomarkers.基于血浆生物标志物预测轻度认知障碍患者的纵向认知下降和阿尔茨海默病转化。
Cells. 2024 Jun 22;13(13):1085. doi: 10.3390/cells13131085.
10
Comparison of plasma and neuroimaging biomarkers to predict cognitive decline in non-demented memory clinic patients.比较血浆和神经影像学生物标志物以预测非痴呆记忆门诊患者的认知下降。
Alzheimers Res Ther. 2024 May 16;16(1):110. doi: 10.1186/s13195-024-01478-9.

本文引用的文献

1
Subjective cognitive complaints and blood biomarkers of neurodegenerative diseases: a longitudinal cohort study.主观认知主诉与神经退行性疾病的血液生物标志物:一项纵向队列研究。
Alzheimers Res Ther. 2023 Nov 11;15(1):198. doi: 10.1186/s13195-023-01341-3.
2
Blood Biomarkers in Neurodegenerative Diseases: Implications for the Clinical Neurologist.神经退行性疾病中的血液生物标志物:对临床神经科医生的影响。
Neurology. 2023 Jul 25;101(4):172-180. doi: 10.1212/WNL.0000000000207193. Epub 2023 Mar 6.
3
Tau levels are higher in objective subtle cognitive decline but not subjective memory complaint.客观认知衰退但无主观记忆主诉者的 Tau 水平更高。
Alzheimers Res Ther. 2022 Aug 22;14(1):114. doi: 10.1186/s13195-022-01060-1.
4
Association of Subjective Memory Complaints With White Matter Hyperintensities and Cognitive Decline Among Older Adults in Chicago, Illinois.伊利诺伊州芝加哥市老年人主观记忆主诉与脑白质高信号和认知能力下降的相关性研究。
JAMA Netw Open. 2022 Apr 1;5(4):e227512. doi: 10.1001/jamanetworkopen.2022.7512.
5
Association of Neurofilament Light With the Development and Severity of Parkinson Disease.神经丝轻链与帕金森病的发生发展及严重程度的关系。
Neurology. 2022 May 31;98(22):e2185-e2193. doi: 10.1212/WNL.0000000000200338. Epub 2022 Apr 13.
6
Early-stage Alzheimer disease: getting trial-ready.早期阿尔茨海默病:做好试验准备。
Nat Rev Neurol. 2022 Jul;18(7):389-399. doi: 10.1038/s41582-022-00645-6. Epub 2022 Apr 4.
7
Examination of Neurofilament Light Chain Serum Concentrations, Physical Activity, and Cognitive Decline in Older Adults.神经丝轻链血清浓度、身体活动与老年人认知能力下降的检查。
JAMA Netw Open. 2022 Mar 1;5(3):e223596. doi: 10.1001/jamanetworkopen.2022.3596.
8
Association of plasma glial fibrillary acidic protein (GFAP) with neuroimaging of Alzheimer's disease and vascular pathology.血浆胶质纤维酸性蛋白(GFAP)与阿尔茨海默病神经影像学及血管病理学的关联
Alzheimers Dement (Amst). 2022 Feb 28;14(1):e12291. doi: 10.1002/dad2.12291. eCollection 2022.
9
Blood GFAP as an emerging biomarker in brain and spinal cord disorders.血液 GFAP 作为脑和脊髓疾病的新兴生物标志物。
Nat Rev Neurol. 2022 Mar;18(3):158-172. doi: 10.1038/s41582-021-00616-3. Epub 2022 Feb 3.
10
Association of CSF, Plasma, and Imaging Markers of Neurodegeneration With Clinical Progression in People With Subjective Cognitive Decline.脑脊液、血浆和神经退行性病变影像学标志物与主观认知下降患者临床进展的相关性。
Neurology. 2022 Mar 29;98(13):e1315-e1326. doi: 10.1212/WNL.0000000000200035. Epub 2022 Feb 2.

主观记忆主诉与神经退行性变及认知的血清生物标志物的关联:一项基于人群的研究。

Association of subjective memory complaints with serum biomarkers of neurodegeneration and cognition: A population-based study.

作者信息

Dhana Anisa, DeCarli Charles S, Dhana Klodian, Desai Pankaja, Krueger Kristin, Evans Denis A, Rajan Kumar B

机构信息

Rush Institute for Healthy Aging, Rush University Medical Center, Chicago, Illinois, USA.

Department of Internal Medicine, Rush University Medical Center, Chicago, Illinois, USA.

出版信息

J Am Geriatr Soc. 2025 Mar;73(3):859-866. doi: 10.1111/jgs.19300. Epub 2024 Dec 3.

DOI:10.1111/jgs.19300
PMID:39625703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11908938/
Abstract

BACKGROUND

Subjective memory complaints (SMCs) refer to memory concerns reported by an individual, regardless of objective test impairment. We conducted a study to evaluate the association of SMCs with serum biomarkers of neurodegeneration, including neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP), and total tau (t-tau). In addition, we evaluated the association of SMCs with the rate of cognitive decline.

METHODS

This study included 1096 individuals participating in the Chicago Health and Aging Project, with data on SMCs, neurodegenerative biomarkers (NfL, GFAP, and t-tau), and global cognitive scores. The SMC score ranges from 0 to 8 and higher scores reflect more memory complaints. Linear regression models were developed to investigate the association of SMCs with serum biomarkers, adjusted by age, sex, race, education, and APOE e4. Linear mixed-effects models were used to examine the independent association of SMCs with cognitive decline in a multivariable model that was additionally adjusted by biomarkers of neurodegeneration.

RESULTS

Of the 1096 individuals, 665 (60.7%) were female, 643 (58.7%) were African Americans, and the mean (SD) age at the baseline was 78.0 (5.8) years. Compared to individuals with fewer memory complaints (i.e., people in the first tertile of SMCs), those reporting more memory complaints (i.e., people in the third tertile of SMCs) had a 12.0% increase in serum concentrations of NfL and an 9.4% increase in GFAP. In addition, individuals reporting more memory complaints (i.e., those in the 3rd versus the 1st tertile of SMCs) had a faster rate of cognitive decline by 0.029 ( -0.029, 95% CI -0.046 to -0.013) standardized units per year.

CONCLUSIONS

Individuals who reported more memory complaints had higher levels of biomarkers of neurodegeneration and a faster rate of cognitive decline, suggesting that SMCs may be valuable for identifying people at high risk of cognitive impairment.

摘要

背景

主观记忆抱怨(SMCs)是指个体报告的记忆方面的担忧,无论客观测试是否存在损害。我们开展了一项研究,以评估SMCs与神经退行性变血清生物标志物之间的关联,这些生物标志物包括神经丝轻链(NfL)、胶质纤维酸性蛋白(GFAP)和总tau蛋白(t-tau)。此外,我们还评估了SMCs与认知衰退率之间的关联。

方法

本研究纳入了1096名参与芝加哥健康与老龄化项目的个体,他们有关于SMCs、神经退行性生物标志物(NfL、GFAP和t-tau)以及整体认知得分的数据。SMCs评分范围为0至8分,分数越高反映记忆抱怨越多。建立线性回归模型来研究SMCs与血清生物标志物之间的关联,并根据年龄、性别、种族、教育程度和载脂蛋白E4(APOE e4)进行调整。线性混合效应模型用于在一个多变量模型中检验SMCs与认知衰退的独立关联,该模型还根据神经退行性变生物标志物进行了调整。

结果

在这1096名个体中,665名(60.7%)为女性,643名(58.7%)为非裔美国人,基线时的平均(标准差)年龄为78.0(5.8)岁。与记忆抱怨较少的个体(即SMCs处于第一三分位数的人群)相比,报告记忆抱怨较多的个体(即SMCs处于第三三分位数的人群)血清NfL浓度升高了12.0%,GFAP升高了9.4%。此外,报告记忆抱怨较多的个体(即SMCs处于第三三分位数与第一三分位数相比)认知衰退速度更快,每年快0.029(-0.029,95%置信区间-0.046至-0.013)个标准化单位。

结论

报告记忆抱怨较多的个体神经退行性变生物标志物水平较高,认知衰退速度更快,这表明SMCs可能对识别认知障碍高危人群有价值。