Evidence map›Paper›PMID 35592552›Full record

ArticleFrontiers in bioengineering and biotechnology2022

Angiographic Pulse Wave Coherence in the Human Brain.

Matthew J Koch, Phan Q Duy, Benjamin L Grannan, Aman B Patel, Scott B Raymond, Pankaj K Agarwalla, Kristopher T Kahle, William E Butler

Open access · goldAbstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

8 authors at 6 institutions in 1 country.

Matthew J KochDepartment of Neurosurgery, University of Florida, Gainesville, FL, United States.
Phan Q DuyMedical Scientist Training Program, Yale University School of Medicine, New Haven, CT, United States.
Benjamin L GrannanDepartment of Neurosurgery, University of Washington Medicine, Seattle, WA, United States.
Aman B PatelDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA, United States.
Scott B RaymondDepartment of Radiology, University of Vermont, Burlington, VT, United States.
Pankaj K AgarwallaDepartment of Neurosurgery, Rutgers New Jersey Medical School, Newark, NJ, United States.
Kristopher T KahleDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA, United States.
William E ButlerDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA, United States.
Massachusetts General Hospital · USRutgers, The State University of New Jersey · USUniversity of Florida · USUniversity of Vermont · USUniversity of Washington · USYale University · US

Funding

Role of TRIM71 in neural stem cell biology and congenital hydrocephalusF30HD106694 · NICHD · YALE UNIVERSITY · PI PHAN, DUY · 2021 to 2022
$56k
NICHD NIH HHS F30 HD106694
6 · The paper itself

Abstract

A stroke volume of arterial blood that arrives to the brain housed in the rigid cranium must be matched over the cardiac cycle by an equivalent volume of ejected venous blood. We hypothesize that the brain maintains this equilibrium by organizing coherent arterial and venous pulse waves. To test this hypothesis, we applied wavelet computational methods to diagnostic cerebral angiograms in four human patients, permitting the capture and analysis of cardiac frequency phenomena from fluoroscopic images acquired at faster than cardiac rate. We found that the cardiac frequency reciprocal phase of a small region of interest (ROI) in a named artery predicts venous anatomy pixel-wise and that the predicted pixels reconstitute venous bolus passage timing. Likewise, a small ROI in a named vein predicts arterial anatomy and arterial bolus passage timing. The predicted arterial and venous pixel groups maintain phase complementarity across the bolus travel. We thus establish a novel computational method to analyze vascular pulse waves from minimally invasive cerebral angiograms and provide the first direct evidence of arteriovenous coupling in the intact human brain. This phenomenon of arteriovenous coupling may be a physiologic mechanism for how the brain precisely maintains mechanical equilibrium against volume displacement and kinetic energy transfer resulting from cyclical deformations with each heartbeat. The study also paves the way to study deranged arteriovenous coupling as an underappreciated pathophysiologic disturbance in a myriad of neurological pathologies linked by mechanical disequilibrium.

Indexed as

angiographybiomechanicscerebral circulationhydrocephaluspulse waves

Identifiers

PMID35592552
PMCPMC9110661
OpenAlexW4225381900

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.