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Related Concept Videos

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Aging is a complex biological phenomenon influenced by various processes that affect cellular and systemic functions. Several prominent theories attempt to explain its mechanisms, highlighting cellular limitations, oxidative damage, and hormonal changes as central factors in aging.
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Cognitive development continues throughout adulthood, undergoing significant shifts across early, middle, and late stages. Individual transition occurs from adolescent idealism to pragmatic and adaptable thinking in early adulthood. During this period, individuals learn to integrate personal beliefs with the recognition that other perspectives are equally valid. Exposure to the complexities of modern society, diverse experiences, and higher education contribute to this adaptive thought process,...
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Alzheimer's Disease (AD) is a continually advancing neurodegenerative disorder, distinguished by escalating memory loss, cognitive dysfunction, and dementia. The disease unfolds in three stages: preclinical, mild cognitive impairment (MCI), and dementia. Its onset is insidious, and the progression gradual, with the cause not well explained by other disorders.
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Related Experiment Video

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The Multiple Sclerosis Performance Test MSPT: An iPad-Based Disability Assessment Tool
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"Brain age" predicts disability accumulation in multiple sclerosis.

Matthew R Brier1, Zhuocheng Li1, Maria Ly2,3

  • 1Department of Neurology, Washington University in St. Louis, St Louis, Missouri, USA.

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|April 29, 2023
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Summary
This summary is machine-generated.

Brain age analysis reveals that a younger-appearing brain in multiple sclerosis (MS) patients correlates with less disability. Advanced brain age predicts future disability accumulation in MS.

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Area of Science:

  • Neuroimaging and computational neuroscience
  • Clinical neurology and neuroimmunology

Background:

  • Neurodegenerative diseases like multiple sclerosis (MS) often show signs of premature aging on medical imaging.
  • While MS lesion biomarkers are established, reliable measures for neurodegeneration are still developing.
  • Machine learning-based 'brain age' analysis quantifies apparent aging from structural MRI, offering a potential neurodegeneration metric.

Purpose of the Study:

  • To evaluate the utility of brain age analysis as a biomarker for neurodegeneration in MS.
  • To determine the explanatory and predictive power of brain age for disability in a large MS cohort.
  • To assess how brain age relates to MS disease course, lesion burden, and treatment efficacy.

Main Methods:

  • Utilized a large, real-world longitudinal dataset of over 13,000 imaging sessions from more than 6,000 MS patients.
  • Compared the performance of three distinct brain age algorithms.
  • Employed linear mixed-effects models to analyze associations with MS, disease course, disability, lesion burden, and disease-modifying therapy (DMT) efficacy.

Main Results:

  • All three brain age algorithms indicated that MS is associated with advanced predicted brain age cross-sectionally and accelerated brain aging longitudinally.
  • Patient disability was the strongest correlate of advanced brain age, more so than MS disease course (relapsing vs. progressive).
  • Advanced brain age at the study's start predicted greater disability accumulation over time, while a younger brain age correlated with decreased disability.

Conclusions:

  • Brain age analysis is a feasible and clinically significant biomarker for MS pathology.
  • Advanced brain age in MS patients strongly correlates with and predicts increasing disability.
  • This neuroimaging biomarker holds promise for monitoring disease progression and predicting outcomes in multiple sclerosis.