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Related Concept Videos

Regulation of Stroke Volume01:27

Regulation of Stroke Volume

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The regulation of stroke volume, which is the amount of blood the heart pumps out during each heartbeat, is critical for maintaining a healthy circulatory system. Stroke volume is influenced by three main factors: preload, contractility, and afterload.
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Ischemic heart disease occurs when the heart's blood supply dwindles, causing an ominous lack of oxygen and nutrients. This deficiency, stemming from reduced or obstructed blood flow, spells danger, leading to heart muscle damage and dysfunction.
Atherosclerosis, the primary malefactor, orchestrates this dangerous condition. It manifests as the accumulation of fatty deposits, akin to insidious plaques, within arterial walls. As time elapses, these plaques metamorphose, hardening and...
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Cardiac output (CO) is an integral aspect of human physiology, reflecting the heart's efficiency and responsiveness to the body's needs. It represents the volume of blood that the left or right ventricle ejects into the aorta or pulmonary trunk each minute. The CO is calculated by multiplying the heart rate (HR)—the number of heartbeats per minute—by the stroke volume (SV)—the amount of blood pumped out with each heartbeat.
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Cardiac Output II: Effect of Stroke Volume on Cardiac Output01:22

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Cardiac output (CO), the amount of blood the heart pumps per minute, is a parameter in cardiovascular physiology determined by stroke volume and heart rate. Stroke volume, the amount of blood pushed from one of the ventricles per heartbeat, is influenced by preload, afterload, and contractility.
Preload
Preload refers to the initial elongation of the cardiac myocytes before contraction and is related to the volume of blood filling the heart at the end of diastole, or end-diastolic volume. The...
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Amyloid fibrils are aggregates of misfolded proteins.  Under most circumstances, misfolded proteins are either refolded by chaperone proteins or degraded by the proteasome. However, in the case of a mutation or a disease, these proteins can accumulate to form large clusters and often further assemble to form elongated fibers, called fibrils. 
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Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
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Related Experiment Video

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Modeling Stroke in Mice: Focal Cortical Lesions by Photothrombosis
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Ischemic stroke lesion segmentation using stacked sparse autoencoder.

G B Praveen1, Anita Agrawal1, Ponraj Sundaram2

  • 1Department of Electrical and Electronics Engineering, BITS PILANI - K.K Birla Goa Campus, Goa, India.

Computers in Biology and Medicine
|June 9, 2018
PubMed
Summary

This study introduces an unsupervised feature learning method using stacked sparse autoencoders (SSAE) for accurate ischemic stroke lesion segmentation in brain MRI scans. The approach significantly outperforms existing methods in precision, Dice coefficient, and recall.

Keywords:
Ischemic stroke lesion segmentationMagnetic resonance imagingSVMStacked sparse autoencodersUnsupervised feature learning

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Area of Science:

  • Medical Imaging
  • Artificial Intelligence
  • Neurology

Background:

  • Accurate segmentation of ischemic stroke lesions in multi-spectral MRI is crucial for patient care.
  • Current methods often rely on complex, hand-crafted features that struggle to differentiate lesions from normal tissue.

Purpose of the Study:

  • To develop an unsupervised feature learning approach for automatic and accurate segmentation of ischemic stroke lesions.
  • To overcome the limitations of hand-crafted features in stroke lesion segmentation.

Main Methods:

  • Proposed a stacked sparse autoencoder (SSAE) framework for unsupervised feature learning.
  • Integrated SSAE with a support vector machine (SVM) classifier for lesion segmentation.
  • Validated the approach on the Ischemic Stroke Lesion Segmentation (ISLES) 2015 dataset.

Main Results:

  • Achieved high performance metrics: mean precision of 0.968, mean Dice coefficient (DC) of 0.943, mean recall of 0.924, and mean accuracy of 0.904.
  • Demonstrated significant improvements over state-of-the-art methods, with precision, DC, and recall increases of 25.71%, 36.67%, and 16.96%, respectively.
  • Unsupervised features learned via SSAE outperformed hand-crafted features.

Conclusions:

  • The proposed unsupervised SSAE framework enables accurate automatic segmentation of ischemic stroke lesions from brain MRI.
  • This method offers a robust alternative to traditional feature engineering, with potential for efficient training on large datasets.