Evidence map›Paper›PMID 34342127›Full record

ArticleAging cell2021

Aging influences the cardiac macrophage phenotype and function during steady state and during inflammation.

Noushin Saljoughian Esfahani, Qian Wu, Naresh Kumar, Latha Prabha Ganesan, William P Lafuse, Murugesan V S Rajaram

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
5.2field-weighted citation impact, top 3% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 45 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Immunometabolism in the Aging Heart.Journal of the American Heart Association · 2025
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Hallmarks of cardiovascular ageing.Nature reviews. Cardiology · 2023
    Review
  18. Review
  19. Kielin/chordin-like protein deficiency causes cardiac aging in male mice.Journal of molecular medicine (Berlin, Germany) · 2023
    Article
  20. 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

6 authors at 1 institution in 1 country.

Noushin Saljoughian EsfahaniDepartment of Microbial Infection and Immunity/ College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Qian WuDepartment of Microbial Infection and Immunity/ College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Naresh KumarDepartment of Microbial Infection and Immunity/ College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Latha Prabha GanesanDepartment of Internal Medicine, College of Medicine, The Ohio State University, Wexner Medical Center, Columbus, OH, USA.
William P LafuseDepartment of Microbial Infection and Immunity/ College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, USA.
Murugesan V S RajaramDepartment of Microbial Infection and Immunity/ College of Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, USA.ORCID 0000-0002-1515-1122
The Ohio State University Wexner Medical Center · US

Funding

Molecular mechanism of cardiac inflammation and dysfunction in Pseudomonas aeruginosa infectionR01AI146252 · NIAID · OHIO STATE UNIVERSITY · PI RAJARAM, MURUGESAN · 2019 to 2023
$2.2M
Role of Aging on cardiac macrophage dysfunction and heart failure during infectionR21AG073720 · NIA · OHIO STATE UNIVERSITY · PI RAJARAM, MURUGESAN · 2022 to 2023
$433k
Mechanisms of Cardioprotection by the Innate Immune System During Influenza Virus InfectionsR21AI146690 · NIAID · OHIO STATE UNIVERSITY · PI RAJARAM, MURUGESAN, YOUNT, JACOB · 2019 to 2020
$415k
NIAID NIH HHS R01 AI146252NIAID NIH HHS R21 AI146690NIA NIH HHS R21 AG073720
6 · The paper itself

Abstract

Aging-mediated immune dysregulation affects the normal cardiac immune cell phenotypes and functions, resulting in cardiac distress. During cardiac inflammation, immune activation is critical for mounting the regenerative responses to maintain normal heart function. We investigated the impact of aging on myeloid cell phenotype and function during cardiac inflammation induced by a sub-lethal dose of LPS. Our data show that hearts of old mice contain more myeloid cells than the hearts of young mice. However, while the number of monocytic-derived suppressor cells did not differ between young and old mice, monocytic-derived suppressor cells from old mice were less able to suppress T-cell proliferation. Since cardiac resident macrophages (CRMs) are important for immune surveillance, clearance of dead cells, and tissue repair, we focused our studies on CRMs phenotype and function during steady state and LPS treatment. In the steady state, we observed significantly more MHC-II

Indexed as

AgingAnimalsHeartHumansInflammationMacrophagesMicePhenotypeagingcardiac macrophagesinfection and inflammation

Identifiers

PMID34342127
PMCPMC8373275
OpenAlexW3192690180

What Socratic 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 Socratic graph.