Evidence map›Paper›PMID 35237142›Full record

ArticleFrontiers in aging neuroscience2021

Gradual Not Sudden Change: Multiple Sites of Functional Transition Across the Microvascular Bed.

Kira Shaw, Katie Boyd, Silvia Anderle, Matthew Hammond-Haley, Davina Amin, Orla Bonnar, Catherine N Hall

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Neurophotonics · 2025
    Article
  3. Article
  4. Article
  5. APOE4 expression confers a mild, persistent reduction in neurovascular function in the visual cortex and hippocampus of awake mice.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2023
    Article
  6. Review
  7. Review
  8. Article
  9. Neurophotonics · 2022
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Kira ShawSussex Neuroscience, School of Psychology, University of Sussex, Falmer, United Kingdom.
Katie BoydSussex Neuroscience, School of Psychology, University of Sussex, Falmer, United Kingdom.
Silvia AnderleSussex Neuroscience, School of Psychology, University of Sussex, Falmer, United Kingdom.
Matthew Hammond-HaleyBrighton and Sussex Medical School, Brighton, United Kingdom.
Davina AminDepartment of Neuroscience, Physiology and Pharmacology, University College London, London, United Kingdom.
Orla BonnarMassGeneral Institute for Neurodegenerative Disease, Massachusetts General Hospital and Harvard Medical School, Charlestown Navy Yard, MA, United States.
Catherine N HallSussex Neuroscience, School of Psychology, University of Sussex, Falmer, United Kingdom.

Funding

Medical Research Council MC_PC_15071Medical Research Council MR/S026495/1Medical Research Council MR/V036750/1
6 · The paper itself

Abstract

In understanding the role of the neurovascular unit as both a biomarker and target for disease interventions, it is vital to appreciate how the function of different components of this unit change along the vascular tree. The cells of the neurovascular unit together perform an array of vital functions, protecting the brain from circulating toxins and infection, while providing nutrients and clearing away waste products. To do so, the brain's microvasculature dilates to direct energy substrates to active neurons, regulates access to circulating immune cells, and promotes angiogenesis in response to decreased blood supply, as well as pulsating to help clear waste products and maintain the oxygen supply. Different parts of the cerebrovascular tree contribute differently to various aspects of these functions, and previously, it has been assumed that there are discrete types of vessel along the vascular network that mediate different functions. Another option, however, is that the multiple transitions in function that occur across the vascular network do so at many locations, such that vascular function changes gradually, rather than in sharp steps between clearly distinct vessel types. Here, by reference to new data as well as by reviewing historical and recent literature, we argue that this latter scenario is likely the case and that vascular function gradually changes across the network without clear transition points between arteriole, precapillary arteriole and capillary. This is because classically localized functions are in fact performed by wide swathes of the vasculature, and different functional markers start and stop being expressed at different points along the vascular tree. Furthermore, vascular branch points show alterations in their mural cell morphology that suggest functional specializations irrespective of their position within the network. Together this work emphasizes the need for studies to consider where transitions of different functions occur, and the importance of defining these locations, in order to better understand the vascular network and how to target it to treat disease.

Indexed as

arteriolebraincapillaryendothelial cellmural cellneurovascularpericyte

Identifiers

PMID35237142
PMCPMC8885127

What OpenQuestion holds

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Registered trials

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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.