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Non-Invasive MRI of Blood–Cerebrospinal Fluid Barrier Function

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  • P. G. Evans

    (University College London)

  • M. Sokolska

    (University College London Hospitals NHS Foundation Trust)

  • A. Alves

    (University College London Cancer Institute)

  • I. F. Harrison

    (University College London)

  • Y. Ohene

    (University College London)

  • P. Nahavandi

    (University College London)

  • O. Ismail

    (University College London)

  • E. Miranda

    (University College London Cancer Institute)

  • M. F. Lythgoe

    (University College London)

  • D. L. Thomas

    (UCL Queen Square Institute of Neurology
    UCL Queen Square Institute of Neurology)

  • J. A. Wells

    (University College London)

Abstract

The blood–cerebrospinal fluid barrier (BCSFB) is a highly dynamic transport interface that serves brain homeostasis. To date, however, understanding of its role in brain development and pathology has been hindered by the absence of a non-invasive technique for functional assessment. Here we describe a method for non-invasive measurement of BSCFB function by using tracer-free MRI to quantify rates of water delivery from arterial blood to ventricular cerebrospinal fluid. Using this method, we record a 36% decrease in BCSFB function in aged mice, compared to a 13% decrease in parenchymal blood flow, itself a leading candidate biomarker of early neurodegenerative processes. We then apply the method to explore the relationship between BCSFB function and ventricular morphology. Finally, we provide proof of application to the human brain. Our findings position the BCSFB as a promising new diagnostic and therapeutic target, the function of which can now be safely quantified using non-invasive MRI.

Suggested Citation

  • P. G. Evans & M. Sokolska & A. Alves & I. F. Harrison & Y. Ohene & P. Nahavandi & O. Ismail & E. Miranda & M. F. Lythgoe & D. L. Thomas & J. A. Wells, 2020. "Non-Invasive MRI of Blood–Cerebrospinal Fluid Barrier Function," Nature Communications, Nature, vol. 11(1), pages 1-11, December.
    • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-16002-4
    DOI: 10.1038/s41467-020-16002-4
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