4.4 Article

Imaging subtle leaks in the blood-brain barrier in the aging human brain: potential pitfalls, challenges, and possible solutions

期刊

GEROSCIENCE
卷 44, 期 3, 页码 1339-1351

出版社

SPRINGER
DOI: 10.1007/s11357-022-00571-x

关键词

Blood-brain barrier permeability; Aging population; Cognitive impairment; Alzheimer's disease; Dementia; Small vessel disease; Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI)

资金

  1. National Institutes of Health [P01AG052350, P41EB015922, P30AG066530, R01AG023084, R01NS090904, R01NS034467, R01AG039452, 1R01NS100459, 5P01AG052350, P30AG06653, R01AG064228, R01AG060049, P30AG066519]
  2. Foundation Leducq Transatlantic Network of Excellence for the Study of Perivascular Spaces in Small Vessel Disease [16 CVD 05]
  3. UK Dementia Research Institute (MRC)
  4. UK Dementia Research Institute (Alzheimer's Society)
  5. UK Dementia Research Institute (ARUK)
  6. UKRI Medical Research Council [MR/V032488/1]
  7. Alzheimer's Association [AARG-17-532905]

向作者/读者索取更多资源

Recent studies have found subtle blood-brain barrier leaks in the human brain during normal aging, age-related cognitive dysfunction, genetic risk for Alzheimer's disease, mild cognitive impairment, early Alzheimer's disease, cerebral small vessel disease, and other neurodegenerative disorders using dynamic contrast-enhanced magnetic resonance imaging. The quantified leaks are typically much lower than those in brain tumors, stroke, and multiple sclerosis relapses. The challenges lie in improving the detectability, reliability, and reproducibility of the technique, as well as standardizing and harmonizing data between different scanners.
Recent studies using dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) with gadolinium-based contrast agents (GBCA) have demonstrated subtle blood-brain barrier (BBB) leaks in the human brain during normal aging, in individuals with age-related cognitive dysfunction, genetic risk for Alzheimer's disease (AD), mild cognitive impairment, early AD, cerebral small vessel disease (SVD), and other neurodegenerative disorders. In these neurological conditions, the BBB leaks, quantified by the unidirectional BBB GBCA tracer's constant K-trans maps, are typically orders of magnitude lower than in brain tumors, after stroke and/or during relapsing episodes of multiple sclerosis. This puts extra challenges for the DCE-MRI technique by pushing calculations towards its lower limits of detectability. In addition, presently, there are no standardized multivendor protocols or evidence of repeatability and reproducibility. Nevertheless, subtle BBB leaks may critically contribute to the pathophysiology of cognitive impairment and dementia associated with AD or SVD, and therefore, efforts to improve sensitivity of detection, reliability, and reproducibility are warranted. A larger number of participants scanned by different MR scanners at different clinical sites are sometimes required to detect differences in BBB integrity between control and at-risk groups, which impose additional challenges. Here, we focus on these new challenges and propose some approaches to normalize and harmonize DCE data between different scanners. In brief, we recommend specific regions to be used for the tracer's vascular input function and DCE data processing and how to find and correct negative K-trans values that are physiologically impossible. We hope this information will prove helpful to new investigators wishing to study subtle BBB damage in neurovascular and neurodegenerative conditions and in the aging human brain.

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