Evidence map›Paper›PMID 29609518›Full record

ArticleJournal of neurotrauma2018

Vascular Abnormalities within Normal Appearing Tissue in Chronic Traumatic Brain Injury.

Margalit Haber, Franck Amyot, Kimbra Kenney, Tawny Meredith-Duliba, Carol Moore, Erika Silverman, Jamie Podell, Yi-Yu Chou, Dzung L Pham, John Butman and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of neurotrauma, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Persistent dysmorphology and dysfunction of the brain microvasculature following repeated trauma.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Potential Neuroprotective Role of Neurotrophin in Traumatic Brain Injury.CNS & neurological disorders drug targets · 2024
    Review
  9. Review
  10. Article
  11. Imaging biomarkers of vascular and axonal injury are spatially distinct in chronic traumatic brain injury.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  12. Impaired capillary-to-arteriolar electrical signaling after traumatic brain injury.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  13. Impairment of cerebrovascular reactivity in response to hypercapnic challenge in a mouse model of repetitive mild traumatic brain injury.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  14. Repetitive mTBI is associated with age-related reductions in cerebral blood flow but not cortical thickness.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
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

13 authors at 4 institutions in 1 country.

Margalit Haber1 Department of Neurology, University of Pennsylvania Perelman School of Medicine , Philadelphia, Pennsylvania.
Franck Amyot6 National Intrepid Center of Excellence, Walter Reed National Military Medical Center, Bethesda, Maryland.
Kimbra Kenney2 Department of Neurology, Uniformed Services University of the Health Sciences , Bethesda, Maryland.
Tawny Meredith-Duliba1 Department of Neurology, University of Pennsylvania Perelman School of Medicine , Philadelphia, Pennsylvania.
Carol Moore2 Department of Neurology, Uniformed Services University of the Health Sciences , Bethesda, Maryland.
Erika Silverman1 Department of Neurology, University of Pennsylvania Perelman School of Medicine , Philadelphia, Pennsylvania.
Jamie Podell1 Department of Neurology, University of Pennsylvania Perelman School of Medicine , Philadelphia, Pennsylvania.
Yi-Yu Chou3 Center for Neuroscience and Regenerative Medicine , Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland.
Dzung L Pham3 Center for Neuroscience and Regenerative Medicine , Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, Maryland.
John Butman4 National Institutes of Health , Clinical Center, Radiology and Imaging Sciences, Bethesda, Maryland.
Hanzhang Lu5 Department of Radiology, Johns Hopkins University Baltimore , Maryland.
Ramon Diaz-Arrastia1 Department of Neurology, University of Pennsylvania Perelman School of Medicine , Philadelphia, Pennsylvania.
Danielle Sandsmark1 Department of Neurology, University of Pennsylvania Perelman School of Medicine , Philadelphia, Pennsylvania.
University of Pennsylvania · USUniformed Services University of the Health Sciences · USNational Institutes of Health Clinical Center · USWalter Reed National Military Medical Center · US

Funding

Natural History of Traumatic Microvascular InjuryK23NS104239 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI SANDSMARK, DANIELLE KAYE · 2017 to 2021
$929k
NINDS NIH HHS K23 NS104239
6 · The paper itself

Abstract

Magnetic resonance imaging (MRI) is a powerful tool for visualizing traumatic brain injury(TBI)-related lesions. Trauma-induced encephalomalacia is frequently identified by its hyperintense appearance on fluid-attenuated inversion recovery (FLAIR) sequences. In addition to parenchymal lesions, TBI commonly results in cerebral microvascular injury, but its anatomical relationship to parenchymal encephalomalacia is not well characterized. The current study utilized a multi-modal MRI protocol to assess microstructural tissue integrity (by mean diffusivity [MD] and fractional aniosotropy [FA]) and altered vascular function (by cerebral blood flow [CBF] and cerebral vascular reactivity [CVR]) within regions of visible encephalomalacia and normal appearing tissue in 27 chronic TBI (minimum 6 months post-injury) subjects. Fifteen subjects had visible encephalomalacias whereas 12 did not have evident lesions on MRI. Imaging from 14 age-matched healthy volunteers were used as controls. CBF was assessed by arterial spin labeling (ASL) and CVR by measuring the change in blood-oxygen-level-dependent (BOLD) MRI during a hypercapnia challenge. There was a significant reduction in FA, CBF, and CVR with a complementary increase in MD within regions of FLAIR-visible encephalomalacia (p < 0.05 for all comparisons). In normal-appearing brain regions, only CVR was significantly reduced relative to controls (p < 0.05). These findings indicate that vascular dysfunction represents a TBI endophenotype that is distinct from structural injury detected using conventional MRI, may be present even in the absence of visible structural injury, and persists long after trauma. CVR may serve as a useful diagnostic and pharmacodynamic imaging biomarker of traumatic microvascular injury.

Indexed as

Cerebrovascular CirculationAdultBrain Injuries, TraumaticBrain Injury, ChronicFemaleHumansMagnetic Resonance ImagingMaleNeuroimagingcerebral blood flowcerebral vascular reactivitydiffusion tensor imagingFLAIRtraumatic brain injury

Identifiers

PMID29609518
PMCPMC6157375
OpenAlexW2796396777

What OpenQuestion holds

Textmetadata
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.