4.5 Article

Decreased CSF clearance and increased brain amyloid in Alzheimer's disease

期刊

FLUIDS AND BARRIERS OF THE CNS
卷 19, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12987-022-00318-y

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资金

  1. NIH/NIA [AG057848, RF1AG057570, R56 AG058913, AG022374, AG013616, AG012101, T32AG052909-01A1, NIH-HLB HL111724]
  2. Health and Labor Sciences research grants from the Ministry of Health, Labor, and Welfare of Japan [23390297, 26117003]
  3. Japan Advanced Molecular Imaging Program (J-AMP) of the Ministry of Education, Culture, Sports, Science and Technology
  4. GE Healthcare
  5. Sumitomo Electric Industries, Ltd.
  6. Grants-in-Aid for Scientific Research [26117003, 23390297] Funding Source: KAKEN

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This study found reduced CSF clearance in Alzheimer's disease, which is associated with brain amyloid-beta deposition and cognitive decline.
Background In sporadic Alzheimer's disease (AD), brain amyloid-beta (A beta) deposition is believed to be a consequence of impaired A beta clearance, but this relationship is not well established in living humans. CSF clearance, a major feature of brain glymphatic clearance (BGC), has been shown to be abnormal in AD murine models. MRI phase contrast and intrathecally delivered contrast studies have reported reduced CSF flow in AD. Using PET and tau tracer F-18-THK5117, we previously reported that the ventricular CSF clearance of the PET tracer was reduced in AD and associated with elevated brain A beta levels. Methods In the present study, we use two PET tracers, F-18-THK5351 and C-11-PiB to estimate CSF clearance calculated from early dynamic PET frames in 9 normal controls and 15 AD participants. Results we observed that the ventricular CSF clearance measures were correlated (r = 0.66, p < 0.01), with reductions in AD of 18 and 27%, respectively. We also replicated a significant relationship between ventricular CSF clearance (F-18-THK5351) and brain A beta load (r = - 0.64, n = 24, p < 0.01). With a larger sample size, we extended our observations to show that reduced CSF clearance is associated with reductions in cortical thickness and cognitive performance. Conclusions Overall, the findings support the hypothesis that failed CSF clearance is a feature of AD that is related to A beta deposition and to the pathology of AD. Longitudinal studies are needed to determine whether failed CSF clearance is a predictor of progressive amyloidosis or its consequence.

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