Evidence map›Paper›PMID 36361845›Full record

ReviewInternational journal of molecular sciences2022

Targeting Immune Senescence in Atherosclerosis.

Danusha Michelle Vellasamy, Sin-Jye Lee, Khang Wen Goh, Bey-Hing Goh, Yin-Quan Tang, Long Chiau Ming, Wei Hsum Yap

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

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  5. Translational Geroscience Strategies for Delaying Multimorbidity.ACS pharmacology & translational science · 2026
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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

7 authors at 4 institutions in 3 countries.

Danusha Michelle VellasamySchool of Biosciences, Faculty of Medical and Health Sciences, Taylor's University, Subang Jaya 47500, Malaysia.
Sin-Jye LeeSchool of Biosciences, Faculty of Medical and Health Sciences, Taylor's University, Subang Jaya 47500, Malaysia.
Khang Wen GohFaculty of Data Science and Information Technology, INTI International University, Nilai 71800, Malaysia.ORCID 0000-0001-6686-7019
Bey-Hing GohBiofunctional Molecule Exploratory (BMEX) Research Group, School of Pharmacy, Monash University Malaysia, Bandar Sunway 47500, Malaysia.ORCID 0000-0003-1006-3649
Yin-Quan TangSchool of Biosciences, Faculty of Medical and Health Sciences, Taylor's University, Subang Jaya 47500, Malaysia.ORCID 0000-0001-7327-2830
Long Chiau MingPAP Rashidah Sa'adatul Bolkiah Institute of Health Sciences, Universiti Brunei Darussalam, Gadong BE1410, Brunei.ORCID 0000-0002-6971-1383
Wei Hsum YapSchool of Biosciences, Faculty of Medical and Health Sciences, Taylor's University, Subang Jaya 47500, Malaysia.ORCID 0000-0001-8116-6018
Taylor's University · MYINTI International University · MYMonash University Malaysia · MYUniversiti Brunei Darussalam · BN

Funding

Ministry of Higher Education (MOHE) Malaysia through Fundamental Research Grant Scheme FRGS/1/2019/SKK08/TAYLOR/02/2 and FRGS/1/2020/SKK0/TAYLOR/02/2
6 · The paper itself

Abstract

Atherosclerosis is one of the main underlying causes of cardiovascular diseases (CVD). It is associated with chronic inflammation and intimal thickening as well as the involvement of multiple cell types including immune cells. The engagement of innate or adaptive immune response has either athero-protective or atherogenic properties in exacerbating or alleviating atherosclerosis. In atherosclerosis, the mechanism of action of immune cells, particularly monocytes, macrophages, dendritic cells, and B- and T-lymphocytes have been discussed. Immuno-senescence is associated with aging, viral infections, genetic predispositions, and hyperlipidemia, which contribute to atherosclerosis. Immune senescent cells secrete SASP that delays or accelerates atherosclerosis plaque growth and associated pathologies such as aneurysms and coronary artery disease. Senescent cells undergo cell cycle arrest, morphological changes, and phenotypic changes in terms of their abundances and secretome profile including cytokines, chemokines, matrix metalloproteases (MMPs) and Toll-like receptors (TLRs) expressions. The senescence markers are used in therapeutics and currently, senolytics represent one of the emerging treatments where specific targets and clearance of senescent cells are being considered as therapy targets for the prevention or treatment of atherosclerosis.

Indexed as

AtherosclerosisCellular SenescenceAgingCytokinesHumansInflammationCytokinesatherosclerosisimmune cellsenescence

Identifiers

PMID36361845
PMCPMC9658319
OpenAlexW4307423296

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.