Evidence map›Paper›PMID 38214259›Full record

ArticleJournal of the American Heart Association2024

Novel UV-B Phototherapy With a Light-Emitting Diode Device Prevents Atherosclerosis by Augmenting Regulatory T-Cell Responses in Mice.

Toru Tanaka, Naoto Sasaki, Aga Krisnanda, Masakazu Shinohara, Hilman Zulkifli Amin, Sayo Horibe, Ken Ito, Motoaki Iwaya, Atsushi Fukunaga, Ken-Ichi Hirata and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

Toru TanakaLaboratory of Medical Pharmaceutics Kobe Pharmaceutical University Kobe Japan.ORCID 0000-0002-1054-9211
Naoto SasakiLaboratory of Medical Pharmaceutics Kobe Pharmaceutical University Kobe Japan.ORCID 0000-0002-7760-6129
Aga KrisnandaLaboratory of Medical Pharmaceutics Kobe Pharmaceutical University Kobe Japan.ORCID 0009-0005-6417-2738
Masakazu ShinoharaDivision of Molecular Epidemiology Kobe University Graduate School of Medicine Kobe Japan.ORCID 0000-0001-8724-0071
Hilman Zulkifli AminLaboratory of Medical Pharmaceutics Kobe Pharmaceutical University Kobe Japan.ORCID 0000-0003-0659-9678
Sayo HoribeLaboratory of Medical Pharmaceutics Kobe Pharmaceutical University Kobe Japan.ORCID 0000-0002-4111-2426
Ken ItoLaboratory of Medical Pharmaceutics Kobe Pharmaceutical University Kobe Japan.ORCID 0009-0007-8678-1862
Motoaki IwayaDepartment of Materials Science and Engineering Meijo University Nagoya Japan.ORCID 0000-0002-4889-706X
Atsushi FukunagaDepartment of Dermatology, Division of Medicine for Function and Morphology of Sensory Organs, Faculty of Medicine Osaka Medical and Pharmaceutical University, Takatsuki Osaka Japan.ORCID 0000-0003-2026-8154
Ken-Ichi HirataDivision of Cardiovascular Medicine, Department of Internal Medicine Kobe University Graduate School of Medicine Kobe Japan.
Yoshiyuki RikitakeLaboratory of Medical Pharmaceutics Kobe Pharmaceutical University Kobe Japan.ORCID 0000-0001-7207-4656
Kobe Pharmaceutical University · JPKobe University · JPMeijo University · JPOsaka University of Pharmaceutical Sciences · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUltraviolet B (UV-B) irradiation is an effective treatment for human cutaneous disorders and was shown to reduce experimental atherosclerosis by attenuating immunoinflammatory responses. The aim of this study was to clarify the effect of specific wavelengths of UV-B on atherosclerosis and the underlying mechanisms focusing on immunoinflammatory responses. METHODS AND

resultsBased on light-emitting diode technology, we developed novel devices that can emit 282 nm UV-B, which we do not receive from natural sunlight, 301 nm UV-B, and clinically available 312 nm UV-B. We irradiated 6-week-old male atherosclerosis-prone

conclusionsWe demonstrated that 282 nm UV-B irradiation effectively reduces aortic inflammation and the development of atherosclerosis by systemically augmenting regulatory T-cell responses and modulating the balance between proresolving and proinflammatory lipid mediators in the skin. Our findings indicate that a novel 282 nm UV-B phototherapy could be an attractive approach to treat atherosclerosis.

Indexed as

AtherosclerosisPlaque, AtheroscleroticUltraviolet TherapyAnimalsApolipoproteins EHumansInflammationLipidsMaleMiceMice, Inbred C57BLMice, KnockoutT-Lymphocytes, RegulatoryApolipoproteins ELipidsatherosclerosisimmunologyinflammationultraviolet B

Identifiers

PMID38214259
PMCPMC10926836
OpenAlexW4390793172

What OpenQuestion holds

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LicenceCC BY-NC
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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.