Evidence map›Paper›PMID 37900152›Full record

ReviewFrontiers in aging2023

Immunosenescence and multiple sclerosis: inflammaging for prognosis and therapeutic consideration.

Smathorn Thakolwiboon, Elizabeth A Mills, Jennifer Yang, Jonathan Doty, Martin I Belkin, Thomas Cho, Charles Schultz, Yang Mao-Draayer

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in aging, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
9.7field-weighted citation impact, top 1% 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

30 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
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  11. Impact of Age on Switching or Stopping Disease Modifying Therapies in Multiple Sclerosis.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2025
    Review
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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

8 authors at 2 institutions in 1 country.

Smathorn ThakolwiboonDepartment of Neurology, University of Michigan, Ann Arbor, MI, United States.
Elizabeth A MillsDepartment of Neurology, University of Michigan, Ann Arbor, MI, United States.
Jennifer YangDepartment of Neurology, University of Michigan, Ann Arbor, MI, United States.
Jonathan DotyMichigan Institute for Neurological Disorders, Farmington Hills, MI, United States.
Martin I BelkinMichigan Institute for Neurological Disorders, Farmington Hills, MI, United States.
Thomas ChoDepartment of Neurology, University of Michigan, Ann Arbor, MI, United States.
Charles SchultzDepartment of Neurology, University of Michigan, Ann Arbor, MI, United States.
Yang Mao-DraayerDepartment of Neurology, University of Michigan, Ann Arbor, MI, United States.
University of Michigan–Ann Arbor · USMichigan Institute for Neurological Disorders · US

Funding

University of Michigan Clinical Autoimmunity Center of ExcellenceUM1AI144298 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FOX, DAVID ALAN, KHANNA, DINESH · 2019 to 2023
$546k
University of Michigan Autoimmunity Center of Excellence, Clinical Research ProgrUM1AI110557 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FOX, DAVID ALAN · 2014 to 2018
$543k
NIAID NIH HHS UM1 AI110557NIAID NIH HHS UM1 AI144298
6 · The paper itself

Abstract

Aging is associated with a progressive decline of innate and adaptive immune responses, called immunosenescence. This phenomenon links to different multiple sclerosis (MS) disease courses among different age groups. While clinical relapse and active demyelination are mainly related to the altered adaptive immunity, including invasion of T- and B-lymphocytes, impairment of innate immune cell (e.g., microglia, astrocyte) function is the main contributor to disability progression and neurodegeneration. Most patients with MS manifest the relapsing-remitting phenotype at a younger age, while progressive phenotypes are mainly seen in older patients. Current disease-modifying therapies (DMTs) primarily targeting adaptive immunity are less efficacious in older patients, suggesting that immunosenescence plays a role in treatment response. This review summarizes the recent immune mechanistic studies regarding immunosenescence in patients with MS and discusses the clinical implications of these findings.

Indexed as

immunosenescenceinflammagingmultiple sclerosisneurodegenerationneuroinflammation

Identifiers

PMID37900152
PMCPMC10603254
OpenAlexW4387607347

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.