Evidence map›Paper›PMID 34683918›Full record

ReviewPharmaceutics2021

Traumatic Brain Injury: An Age-Dependent View of Post-Traumatic Neuroinflammation and Its Treatment.

Clément Delage, Toufik Taib, Célia Mamma, Dominique Lerouet, Valérie C Besson

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Clément DelageUniversité de Paris, Inserm UMR-S 1144-Optimisation Thérapeutique en Neuropsychopharmacologie, Faculté de Pharmacie de Paris, 4 Avenue de l'Observatoire, 75006 Paris, France.ORCID 0000-0003-0710-1659
Toufik TaibUniversité Paris Descartes, EA4475-Pharmacologie de la Circulation Cérébrale, Faculté de Pharmacie de Paris, 4 Avenue de l'Observatoire, 75006 Paris, France.
Célia MammaUniversité Paris Descartes, EA4475-Pharmacologie de la Circulation Cérébrale, Faculté de Pharmacie de Paris, 4 Avenue de l'Observatoire, 75006 Paris, France.
Dominique LerouetUniversité de Paris, Inserm UMR-S 1144-Optimisation Thérapeutique en Neuropsychopharmacologie, Faculté de Pharmacie de Paris, 4 Avenue de l'Observatoire, 75006 Paris, France.ORCID 0000-0002-5656-8768
Valérie C BessonUniversité de Paris, Inserm UMR-S 1144-Optimisation Thérapeutique en Neuropsychopharmacologie, Faculté de Pharmacie de Paris, 4 Avenue de l'Observatoire, 75006 Paris, France.ORCID 0000-0002-1491-2380
Inserm · FRUniversité Paris Cité · FR

Funding

Union des Blessés de la Face et de la Tête 10-2020
6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a leading cause of death and disability all over the world. TBI leads to (1) an inflammatory response, (2) white matter injuries and (3) neurodegenerative pathologies in the long term. In humans, TBI occurs most often in children and adolescents or in the elderly, and it is well known that immune responses and the neuroregenerative capacities of the brain, among other factors, vary over a lifetime. Thus, age-at-injury can influence the consequences of TBI. Furthermore, age-at-injury also influences the pharmacological effects of drugs. However, the post-TBI inflammatory, neuronal and functional consequences have been mostly studied in experimental young adult animal models. The specificity and the mechanisms underlying the consequences of TBI and pharmacological responses are poorly understood in extreme ages. In this review, we detail the variations of these age-dependent inflammatory responses and consequences after TBI, from an experimental point of view. We investigate the evolution of microglial, astrocyte and other immune cells responses, and the consequences in terms of neuronal death and functional deficits in neonates, juvenile, adolescent and aged male animals, following a single TBI. We also describe the pharmacological responses to anti-inflammatory or neuroprotective agents, highlighting the need for an age-specific approach to the development of therapies of TBI.

Indexed as

adolescentagedjuvenileneonatesneuroinflammationneuroprotectionpreclinicaltraumatic brain injury

Identifiers

PMID34683918
PMCPMC8537402
OpenAlexW3202285645

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.