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Updated: Sep 18, 2025

Evaluation of the Cognitive Performance of Hypertensive Patients with Silent Cerebrovascular Lesions
Published on: April 23, 2021
Subclinical Myocardial Injury and Global Cognitive Performance: MESA (Multi-Ethnic Study of Atherosclerosis)
Shubham Tomar1, Karita C F Lidani1, Aline A I Moraes2
1Division of Cardiovascular Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Insights
Elevated or rising high-sensitivity cardiac troponin T (hs-cTnT) levels are linked to increased odds of future cognitive decline in individuals with cardiovascular disease (CVD). This highlights a potential biomarker for monitoring brain health in at-risk populations.
Area of Science:
- Cardiology
- Neurology
- Biomarker Research
Background:
- Cognitive impairment is a frequent complication among patients diagnosed with cardiovascular disease (CVD).
- Understanding the underlying mechanisms linking CVD to cognitive decline is crucial for patient management.
- Myocardial injury biomarkers may offer insights into this relationship.
Purpose of the Study:
- To investigate the association between myocardial injury, quantified by high-sensitivity cardiac troponin T (hs-cTnT), and cognitive function.
- To determine if hs-cTnT levels predict global cognitive performance and its longitudinal decline over time.
Main Methods:
- Longitudinal study of 4,445 participants, assessing hs-cTnT at baseline and exam 5.
- Cognitive function evaluated using the Cognitive Abilities Screening Instrument (CASI) at exams 5 and 6.
- Subclinical myocardial injury defined as hs-cTnT between limits of detection and 19 ng/L; clinical injury >19 ng/L. Cognitive decline defined as a >5 point CASI decrease.
Main Results:
- Higher baseline and exam 5 hs-cTnT levels, and increases between these time points, were associated with lower cognitive scores.
- These associations lost significance after adjusting for CVD risk factors.
- However, higher or increasing hs-cTnT levels were significantly associated with a greater odds of cognitive decline over 6 years in fully adjusted models.
Conclusions:
- In a community-based cohort, elevated or increasing hs-cTnT levels are linked to an increased risk of future cognitive decline.
- hs-cTnT may serve as a valuable biomarker for predicting cognitive trajectory in individuals with or at risk for CVD.
Background:
Cognitive impairment is common in cardiovascular disease (CVD) patients.
Objectives:
The purpose of this study was to evaluate the relationship of myocardial injury, measured by high-sensitivity cardiac troponin T (hs-cTnT), with global cognitive performance and its decline over time.
Methods:
Hs-cTnT assessed at baseline (2000-2002) and exam 5 (2010-2012) in 4,445 participants. Cognitive function evaluated using the Cognitive Abilities Screening Instrument (CASI) at exams 5 and 6 (2016-2018). Subclinical myocardial injury defined as hs-cTnT above limits of detection but below 19 ng/L, while clinical myocardial injury >19 ng/L. Cognitive decline was a >5 point decrease in CASI scores from exam 5 to 6. Regression analysis assessed the association of hs-cTnT levels with CASI scores and their decline.
Results:
Mean age at baseline was 60 years with 53% females. At baseline and exam 5, 63% and 87% had subclinical myocardial injury, respectively. Higher Log10(hs-cTnT) at baseline (β = -1.45 [95% CI: -2.5 to -0.41]), exam 5 (β = -1.63 [95% CI: -2.7 to -0.59]), and greater baseline to exam 5 increase (β = -1.42 [95% CI: -2.8 to -0.06]) were associated with lower CASI scores at exam 5, after adjusting for demographics, education, language, and apolipoprotein E status. These estimate lost significance after CVD risk factor adjustment. Higher Log10(hs-cTnT) at baseline (OR: 2.02 [95% CI: 1.29-3.12]), exam 5 (OR: 2.52 [95% CI: 1.56-4.05]), or greater baseline to exam 5 increase (OR: 2.22 [95% CI: 1.18-4.15]) were associated with higher odds of cognitive decline in fully adjusted models.
Conclusions:
In community-based cohort, higher or increasing hs-cTnT was associated with greater odds of future cognitive decline over 6 years of follow-up.
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