Evidence map›Paper›PMID 36670596›Full record

ArticleChildren (Basel, Switzerland)2022

Evidence of Chronic Complement Activation in Asymptomatic Pediatric Brain Injury Patients: A Pilot Study.

Scott A Holmes, Joud Mar'i, Jordan Lemme, Anne Margarette Maallo, Alyssa Lebel, Laura Simons, Michael J O'Brien, David Zurakowski, Rami Burnstein, David Borsook

Open access · goldAbstract read
In one paragraph

Article in Children (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

10 authors at 4 institutions in 1 country.

Scott A HolmesDepartment of Anesthesia, Critical Care and Pain Medicine, Pediatric Pain Pathway Lab 1, Boston, MA 02215, USA.
Joud Mar'iDepartment of Anesthesia, Critical Care and Pain Medicine, Pediatric Pain Pathway Lab 1, Boston, MA 02215, USA.
Jordan LemmeDepartment of Anesthesia, Critical Care and Pain Medicine, Pediatric Pain Pathway Lab 1, Boston, MA 02215, USA.ORCID 0000-0002-1367-5555
Anne Margarette MaalloDepartment of Anesthesia, Critical Care and Pain Medicine, Pediatric Pain Pathway Lab 1, Boston, MA 02215, USA.ORCID 0000-0002-5456-208X
Alyssa LebelDepartment of Anesthesia, Critical Care and Pain Medicine, Boston Children's Hospital, Boston, MA 02215, USA.
Laura SimonsDepartment of Anesthesia, Stanford University, Stanford, CA 94305, USA.ORCID 0000-0002-3395-9483
Michael J O'BrienSports Medicine Division, Boston Children's Hospital, Boston, MA 02215, USA.ORCID 0000-0003-1334-6513
David ZurakowskiDepartment of Anesthesia, Critical Care and Pain Medicine, Boston Children's Hospital, Boston, MA 02215, USA.ORCID 0000-0003-3610-6942
Rami BurnsteinDepartment of Anesthesia, Beth Israel Deaconness Medical Center, Boston, MA 02215, USA.
David BorsookDepartment of Radiology, Massachuetts General Hospital, Boston, MA 02114, USA.
Boston Children's Hospital · USBeth Israel Deaconess Medical Center · USMassachusetts General Hospital · USStanford University · US

Funding

Post-Traumatic Headache (PTH) in Children: Alterations of Brain Function, Blood Flow and Inflammatory ProcessesR01NS095655 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI HOLMES, SCOTT · 2015 to 2019
$2.7M
NINDS NIH HHS 5R01NS095655-05
6 · The paper itself

Abstract

Physical insult from a mild Traumatic Brain Injury (mTBI) leads to changes in blood flow in the brain and measurable changes in white matter, suggesting a physiological basis for chronic symptom presentation. Post-traumatic headache (PTH) is frequently reported by persons after an mTBI that may persist beyond the acute period (>3 months). It remains unclear whether ongoing inflammation may contribute to the clinical trajectory of PTH. We recruited a cohort of pediatric subjects with PTH who had an acute or a persistent clinical trajectory, each around the 3-month post-injury time point, as well as a group of age and sex-matched healthy controls. We collected salivary markers of mRNA expression as well as brain imaging and psychological testing. The persistent PTH group showed the highest levels of psychological burden and pain symptom reporting. Our data suggest that the acute and persistent PTH cohort had elevated levels of complement factors relative to healthy controls. The greatest change in mRNA expression was found in the acute-PTH cohort wherein the complement cascade and markers of vascular health showed a prominent role for C1Q in PTH pathophysiology. These findings (1) underscore a prolonged engagement of what is normally a healthy response and (2) show that a persistent PTH symptom trajectory may parallel a poorly regulated inflammatory response.

Indexed as

brain injuryinflammationpediatrics

Identifiers

PMID36670596
PMCPMC9856304
OpenAlexW4313414102

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.