Evidence map›Paper›PMID 35563294›Full record

ArticleInternational journal of molecular sciences2022

The Anti-Atherosclerosis Effect of Anakinra, a Recombinant Human Interleukin-1 Receptor Antagonist, in Apolipoprotein E Knockout Mice.

Eu Jeong Ku, Bo-Rahm Kim, Jee-In Lee, Yun Kyung Lee, Tae Jung Oh, Hak C Jang, Sung Hee Choi

Open access · goldAbstract read
In one paragraph

Article 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 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Review
  3. Targeted drug delivery systems for atherosclerosis.Journal of nanobiotechnology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Endothelial mechanobiology in atherosclerosis.Cardiovascular research · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. 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

7 authors at 3 institutions in 1 country.

Eu Jeong KuDepartment of Internal Medicine, Chungbuk National University Hospital, Cheongju 28644, Korea.ORCID 0000-0001-5533-4989
Bo-Rahm KimDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam 13620, Korea.
Jee-In LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam 13620, Korea.
Yun Kyung LeeDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam 13620, Korea.ORCID 0000-0002-6476-0135
Tae Jung OhDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam 13620, Korea.ORCID 0000-0002-5078-6123
Hak C JangDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam 13620, Korea.ORCID 0000-0002-4188-6536
Sung Hee ChoiDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seongnam 13620, Korea.
Seoul National University · KRSeoul National University Bundang Hospital · KRChungbuk National University · KR

Funding

National Research Foundation of Korea NRF-2018R1A5A2024425
6 · The paper itself

Abstract

Interleukin (IL)-1β plays an important role in atherosclerosis pathogenesis. We aimed to investigate the effect of anakinra, a recombinant human IL-1 receptor antagonist, on the progression of atherosclerosis in apolipoprotein E knockout (ApoE−/−) mice. ApoE−/− mice (8-week male) were treated with saline (control), anakinra 10, 25, and 50 mg/kg, respectively (n = 10 in each group). Mice were fed a standard chow (4 weeks) followed by an atherogenic diet (35kcal% fat, 1.25% cholesterol, 12 weeks). Atheromatous plaques in ApoE−/− mice and the expression of inflammatory genes and signaling pathways in human umbilical vein endothelial cells (HUVECs), rat aortic smooth muscle cells (RAOSMCs), and 3T3-L1 adipocytes were assessed. Anakinra reduced the plaque size of the aortic arch (30.6% and 25.2% at the 25 mg/kg and 50 mg/kg doses, both p < 0.05) and serum triglyceride in ApoE−/− mice and suppressed inflammatory genes (IL-1β and IL-6) expressions in HUVECs and RAOSMCs (all p < 0.05). In RAOSMCs, anakinra reduced metalloproteinase-9 expression in a dose-dependent manner and inhibited cell migration. Anakinra-treated mice exhibited trends of lower CD68+ macrophage infiltration in visceral fat and monocyte chemoattractant protein-1 expression was reduced in 3T3-L1 adipocytes. Anakinra could be a useful component for complementary treatment with a standard regimen to reduce the residual cardiovascular risk.

Indexed as

AtherosclerosisInterleukin 1 Receptor Antagonist ProteinPlaque, AtheroscleroticAnimalsApolipoproteins EHumansHuman Umbilical Vein Endothelial CellsMaleMiceMice, Inbred C57BLMice, KnockoutRatsReceptors, Interleukin-1Apolipoproteins EInterleukin 1 Receptor Antagonist ProteinReceptors, Interleukin-1anakinraanti-inflammationatherosclerosisIL-1 receptor blockersmooth muscle cell migration

Identifiers

PMID35563294
PMCPMC9104865
OpenAlexW4225480849

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.