Evidence map›Paper›PMID 29312121›Full record

ArticleFrontiers in neurology2017

Predictive Model of Spread of Progressive Supranuclear Palsy Using Directional Network Diffusion.

Sneha Pandya, Chris Mezias, Ashish Raj

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Stepwise Functional Brain Architecture Correlates with Atrophy in Progressive Supranuclear Palsy.Movement disorders : official journal of the Movement Disorder Society · 2024
    Article
  8. Connectome-based biophysics models of Alzheimer's disease diagnosis and prognosis.Translational research : the journal of laboratory and clinical medicine · 2023
    Review
  9. Review
  10. Article
  11. Prefrontal connectomics: from anatomy to human imaging.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
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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

3 authors at 1 institution in 1 country.

Sneha PandyaDepartment of Radiology, Weill Cornell Medicine, New York, NY, United States.
Chris MeziasDepartment of Neuroscience, Weill Cornell Medicine, New York, NY, United States.
Ashish RajDepartment of Radiology, Weill Cornell Medicine, New York, NY, United States.
Weill Cornell Medicine · US

Funding

Predictive model of spread of Parkinson's pathology using network diffusionR01NS092802 · NINDS · WEILL MEDICAL COLL OF CORNELL UNIV · PI GUPTA, AJAY, RAJ, ASHISH · 2016 to 2020
$2.8M
Multimodal modeling framework for fusing structural and functional connectome dataR01EB022717 · NIBIB · WEILL MEDICAL COLL OF CORNELL UNIV · PI NAGARAJAN, SRIKANTAN S., RAJ, ASHISH · 2016 to 2018
$1.6M
NIBIB NIH HHS R01 EB022717NINDS NIH HHS R01 NS092802
6 · The paper itself

Abstract

Several neurodegenerative disorders including Alzheimer's disease (AD), frontotemporal dementia (FTD), Parkinson's disease (PD), amyotrophic lateral sclerosis, and Huntington's disease report aggregation and transmission of pathogenic proteins between cells. The topography of these diseases in the human brain also, therefore, displays a well-characterized and stereotyped regional pattern, and a stereotyped progression over time. This is most commonly true for AD and other dementias characterized by hallmark misfolded tau or alpha-synuclein pathology. Both tau and synuclein appear to propagate within brain circuits using a shared mechanism. The most canonical synucleopathy is PD; however, much less studied is a rare disorder called progressive supranuclear palsy (PSP). The hallmark pathology and atrophy in PSP are, therefore, also highly stereotyped: initially appearing in the striatum, followed by its neighbors and connected cortical areas. In this study, we explore two mechanistic aspects hitherto unknown about the canonical network diffusion model (NDM) of spread: (a) whether the NDM can apply to other common degenerative pathologies, specifically PSP, and (b) whether the directionality of spread is important in explaining empirical data. Our results on PSP reveal two important findings: first, that PSP is amenable to the connectome-based ND modeling in the same way as previously applied to AD and FTD and, second, that the NDM fit with empirical data are significantly enhanced by using the directional rather than the non-directional form of the human connectome. Specifically, we show that both the anterograde model of transmission (some to axonal terminal) and retrograde mode explain PSP topography more accurately than non-directional transmission. Collectively, these data show that the intrinsic architecture of the structural network mediates disease spread in PSP, most likely

Indexed as

4Rdirectionalitynetwork diffusionprogressive supranuclear palspytauopathies

Identifiers

PMID29312121
PMCPMC5742613
OpenAlexW2779111914

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.