Evidence map›Paper›PMID 31810839›Full record

ArticleNeuron2020

Vasomotion as a Driving Force for Paravascular Clearance in the Awake Mouse Brain.

Susanne J van Veluw, Steven S Hou, Maria Calvo-Rodriguez, Michal Arbel-Ornath, Austin C Snyder, Matthew P Frosch, Steven M Greenberg, Brian J Bacskai

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 325 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
325citing papers in PubMed, 1 pooled it
26.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

325 citing papers in PubMed, 1 synthesis or guideline pooled it, 489 citations in OpenAlex.

  1. Pooled it
  2. Trial
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  4. Trial
  5. Article
  6. Article
  7. Article
  8. Ultrafast venous and sagittal sinus constrictions in the brain driven by abdominal pressure.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  17. Infra-slow (<0.1 Hz) Modulation of Human Brain Pulsations in Awake and Sleep States.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  18. Article
  19. Article
  20. Review

265 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Susanne J van VeluwJ. Philip Kistler Stroke Research Center, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA; MassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital and Harvard Medical School, Charlestown Navy Yard, MA 02129, USA. Electronic address: svanveluw@mgh.harvard.edu.
Steven S HouMassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital and Harvard Medical School, Charlestown Navy Yard, MA 02129, USA.
Maria Calvo-RodriguezMassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital and Harvard Medical School, Charlestown Navy Yard, MA 02129, USA.
Michal Arbel-OrnathMassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital and Harvard Medical School, Charlestown Navy Yard, MA 02129, USA.
Austin C SnyderMassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital and Harvard Medical School, Charlestown Navy Yard, MA 02129, USA.
Matthew P FroschMassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital and Harvard Medical School, Charlestown Navy Yard, MA 02129, USA; Neuropathology Service, C.S. Kubik Laboratory for Neuropathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
Steven M GreenbergJ. Philip Kistler Stroke Research Center, Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
Brian J BacskaiMassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital and Harvard Medical School, Charlestown Navy Yard, MA 02129, USA.
Harvard University · USMassachusetts General Hospital · USMaineGeneral Medical Center · US

Funding

CEREBRAL AMYLOID ANGIOPATHY AND MECHANISMS OF BRAIN AMYLOID ACCUMULATIONR01NS096730 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI BACSKAI, BRIAN J, GREENBERG, STEVEN M · 2016 to 2020
$5.7M
Multiphoton microscopy for in vivo neural imaging.R01EB000768 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI BACSKAI, BRIAN J · 2002 to 2015
$5.0M
The role of astrocytes in Alzheimer's disease pathogenesisR01AG054598 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI Brian J Bacskai · 2017 to 2026
$4.4M
Mechanisms of Vasomotion-mediated Perivascular Clearance in Cerebral Amyloid AngiopathyR01NS128790 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI Steven M Greenberg · 2022 to 2026
$2.9M
Cerebral microvascular lesions and vascular and neuronal networksRF1NS110054 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI BACSKAI, BRIAN J · 2018 to 2020
$2.7M
Multiphoton microscopy for in vivo neural imagingR56AG060974 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI BACSKAI, BRIAN J · 2019 to 2019
$598k
A replacement multiphoton microscope for in vivo imaging in rodent models of neurS10RR025645 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI BACSKAI, BRIAN J · 2009 to 2009
$492k
Unraveling the mechanisms of microhemorrhages in cerebral amyloid angiopathy; from ex vivo MRI in humans to in vivo optics in miceK99AG059893 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI VAN VELUW, SUSANNE JANNEKE · 2018 to 2019
$273k
NCRR NIH HHS S10 RR025645NIA NIH HHS K99 AG059893NIA NIH HHS R01 AG054598NIA NIH HHS R56 AG060974NIBIB NIH HHS R01 EB000768NINDS NIH HHS R01 NS096730NINDS NIH HHS R01 NS128790NINDS NIH HHS RF1 NS110054
6 · The paper itself

Abstract

Paravascular drainage of solutes, including β-amyloid (Aβ), appears to be an important process in brain health and diseases such as Alzheimer's disease (AD) and cerebral amyloid angiopathy (CAA). However, the major driving force for clearance remains largely unknown. Here we used in vivo two-photon microscopy in awake head-fixed mice to assess the role of spontaneous vasomotion in paravascular clearance. Vasomotion correlated with paravascular clearance of fluorescent dextran from the interstitial fluid. Increasing the amplitude of vasomotion by means of visually evoked vascular responses resulted in increased clearance rates in the visual cortex of awake mice. Evoked vascular reactivity was impaired in mice with CAA, which corresponded to slower clearance rates. Our findings suggest that low-frequency arteriolar oscillations drive drainage of solutes. Targeting naturally occurring vasomotion in patients with CAA or AD may be a promising early therapeutic option for prevention of Aβ accumulation in the brain.

Indexed as

Amyloid beta-PeptidesAnimalsBrainCapillariesExtracellular FluidFemaleMaleMiceMice, Inbred C57BLMice, TransgenicMuscle, Smooth, VascularPhotic StimulationVasomotor SystemVisual CortexWakefulnessAmyloid beta-PeptidesAlzheimer’s diseasecerebral amyloid angiopathyfunctional hyperemiaglymphaticsintra-mural peri-arterial drainageperivascular spacevascular smooth muscle cellsvasomotion

Identifiers

PMID31810839
PMCPMC7028316
OpenAlexW2993316870

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.