Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Blood Studies for Cardiovascular System I: Cardiac Biomarkers01:20

Blood Studies for Cardiovascular System I: Cardiac Biomarkers

749
Cardiac biomarkers are enzymes, proteins, and hormones released into the blood when cardiac cells are injured. They are powerful tools for triaging.
The essential diagnostic tools for detecting myocardial necrosis and monitoring individuals suspected of having acute coronary syndrome (ACS) include:
Troponins
Troponins, particularly cardiac troponins I and T, are the most precise and sensitive markers of myocardial injury. They are detectable within 4-6 hours of myocardial injury and remain...
749
Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers01:19

Blood Studies for Cardiovascular System II: CRP, Hcy, and Cardiac Natriuretic Peptide Markers

516
Cardiac biomarkers are critical in diagnosing, prognosing, and managing cardiovascular diseases. Routine measurement of specific biomarkers such as B-type natriuretic peptide (BNP), C-reactive protein (CRP), and homocysteine (Hcy) is common practice in clinical settings to evaluate heart function and predict cardiovascular events.
These markers indicate stress or strain on the heart muscle:
Natriuretic Peptides (BNP)
Cardiac myocytes produce these hormones in response to ventricular stretching...
516

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

A combination of ketones and NAD<sup>+</sup> precursor preserves white matter integrity in mild cognitive impairment.

Alzheimer's & dementia (New York, N. Y.)·2026
Same author

Investigating Physical Exercise and Cognitive Training Effects on Cognition and Brain Health in Men and Women with Heart Failure: The ReCARDIO Trial.

CJC open·2026
Same author

EXPRESS: Kinetic modeling of the Tropomyosin Receptor Kinases radioligand [<sup>18</sup>F]TRACK in human brain with high-resolution positron emission tomography.

Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism·2026
Same author

Plasma p-tau markers, vascular factors, and cognitive decline in the CIMA-Q cohort.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same author

Tau extent outperforms tau load as a predictor of neurodegeneration in Alzheimer's disease.

Molecular neurodegeneration·2026
Same author

Tau-PET and CSF MTBR-tau243 comparisons validate increased tau aggregation in females.

European journal of nuclear medicine and molecular imaging·2026
Same journal

Inflammation profiles in Alzheimer's disease relate to cognition and neurodegeneration.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same journal

Cardiovascular-kidney-metabolic syndrome stage modifies the efficacy of intensive blood pressure control on cognitive outcomes: A post hoc analysis of SPRINT MIND.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same journal

Evidence of APOE4-related brain vulnerabilities in verbal memory systems in midlife women.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same journal

Changes in DNA methylation-based aging predicts brain damage and dementia and reflects life-course cardiovascular risk.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same journal

Elimination of tau tangles and soluble aggregates with the small molecule ACI-16664 prevents neurodegeneration in vivo.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
Same journal

Altered brain glucose metabolism and connectivity in young adults with obstructive sleep apnea.

Alzheimer's & dementia : the journal of the Alzheimer's Association·2026
查看所有相关文章
  1. 首页
  2. 生物标志物 生物标志物
  1. 首页
  2. 生物标志物 生物标志物

相关实验视频

Dried Blood Spot Collection of Health Biomarkers to Maximize Participation in Population Studies
07:20

Dried Blood Spot Collection of Health Biomarkers to Maximize Participation in Population Studies

Published on: January 28, 2014

37.1K

生物标志物 生物标志物

Ting Qiu1,2,3,4, Zhen-Qi Liu5,6, Jonathan Gallego Rudolf5,7,8

  • 1Integrated Program in Neurosciences, McGill University, Montréal, QC, Canada.

Alzheimer's & dementia : the journal of the Alzheimer's Association
|December 25, 2025

在PubMed 上查看摘要

概括
此摘要是机器生成的。

阿尔茨海默病 (AD) 的脑部变化,包括皮质厚度和扩散性,在症状出现前几年就开始. 这些结构变化遵循非线性模式,以应对粉样β (Aβ) 病理.

更多相关视频

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances
07:35

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances

Published on: October 11, 2018

7.9K
Ecotoxicological Methodologies to Evaluate Biomarkers at Different Scales in Neotropical Anurans
08:14

Ecotoxicological Methodologies to Evaluate Biomarkers at Different Scales in Neotropical Anurans

Published on: April 28, 2023

702

相关实验视频

Dried Blood Spot Collection of Health Biomarkers to Maximize Participation in Population Studies
07:20

Dried Blood Spot Collection of Health Biomarkers to Maximize Participation in Population Studies

Published on: January 28, 2014

37.1K
Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances
07:35

Selecting Multiple Biomarker Subsets with Similarly Effective Binary Classification Performances

Published on: October 11, 2018

7.9K
Ecotoxicological Methodologies to Evaluate Biomarkers at Different Scales in Neotropical Anurans
08:14

Ecotoxicological Methodologies to Evaluate Biomarkers at Different Scales in Neotropical Anurans

Published on: April 28, 2023

702

科学领域:

  • 神经成像是一种神经成像.
  • 阿尔茨海默氏症疾病研究研究
  • 大脑结构分析 分析大脑结构

背景情况:

  • 阿尔茨海默病 (AD) 涉及粉样β (Aβ) 和病理,通常与灰质损失有关.
  • 临床前的AD可能会显示皮质厚度 (CT) 增加,与后期的减少形成鲜明对比.
  • 纵向数据对于了解AD进展中的早期结构变化至关重要.

研究的目的:

  • 为了研究Aβ和tau病理和大脑结构 (CT,平均扩散率,海马体积) 在10年内之间的关联.
  • 为了确定与Aβ阳性相对的结构性大脑变化的纵向轨迹.
  • 探索阿尔茨海默病的临床前和临床前阶段的变化.

主要方法:

  • 部分最小方形分析 (PLS) 用于识别Aβ阴性和Aβ阳性组中的病理结构关联.
  • 评估了AD病理和结构性措施之间的截面和纵向关联.
  • 从Aβ阳性开始的时间被估计跟踪随时间的结构变化.

主要成果:

  • 较高的Aβ沉积与Aβ阴性个体的MDT降低和CT增加相关.
  • 具有Aβ阳性的个体表现出相反的关联 (增加MDT,减少CT).
  • MDT遵循U形模式,CT则遵循Aβ病理的反向U形模式,出现在Aβ阳性之前的几年.

结论:

  • 作为对Aβ病理的反应,大脑的结构变化在临床症状出现前几十年就开始了.
  • 这些变化呈现出高度非线性轨迹,可能涉及神经炎症或大脑胀.
  • 了解这些早期的非线性变化是临床前AD干预的关键.