Evidence map›Paper›PMID 25119884›Full record

ArticlePloS one2014

Persistent release of IL-1s from skin is associated with systemic cardio-vascular disease, emaciation and systemic amyloidosis: the potential of anti-IL-1 therapy for systemic inflammatory diseases.

Keiichi Yamanaka, Takehisa Nakanishi, Hiromitsu Saito, Junko Maruyama, Kenichi Isoda, Ayumu Yokochi, Kyoko Imanaka-Yoshida, Kenshiro Tsuda, Masato Kakeda, Ryuji Okamoto and 9 more

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

32 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. ABCB5Cytotherapy · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Skin-Derived ABCB5International journal of molecular sciences · 2022
    Review
  14. Article
  15. Article
  16. Special Issue: "Skin Disease and Comorbidities".Journal of clinical medicine · 2021
    Article
  17. Article
  18. Skin and metabolic syndrome: A review of the possible associations.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2021
    Review
  19. Article
  20. Article
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

19 authors.

Keiichi YamanakaDepartment of Dermatology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Takehisa NakanishiDepartment of Dermatology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Hiromitsu SaitoDepartment of Animal Genomics, Functional Genomics Institute, Mie University Life Science Research Center, Tsu, Mie, Japan.
Junko MaruyamaDepartment of Clinical Engineering, Suzuka University of Medical Science, Suzuka, Mie, Japan.
Kenichi IsodaDepartment of Dermatology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Ayumu YokochiAnesthesiology and Critical Care Medicine, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Kyoko Imanaka-YoshidaPathology and Matrix Biology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan; Mie University Research Center for Matrix Biology, Tsu, Mie, Japan.
Kenshiro TsudaDepartment of Dermatology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Masato KakedaDepartment of Dermatology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Ryuji OkamotoCardiology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Satoshi FujitaCardiology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Yoichiro IwakuraDivision of Experimental Animal Immunology, Tokyo University of Science, Noda, Chiba, Japan.
Noboru SuzukiDepartment of Animal Genomics, Functional Genomics Institute, Mie University Life Science Research Center, Tsu, Mie, Japan.
Masaaki ItoCardiology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Kazuo MaruyamaAnesthesiology and Critical Care Medicine, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Esteban C GabazzaImmunology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Toshimichi YoshidaPathology and Matrix Biology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan; Mie University Research Center for Matrix Biology, Tsu, Mie, Japan.
Motomu ShimaokaMolecular Pathology and Cell Adhesion Biology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.
Hitoshi MizutaniDepartment of Dermatology, Mie University, Graduate School of Medicine, Tsu, Mie, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The skin is an immune organ that contains innate and acquired immune systems and thus is able to respond to exogenous stimuli producing large amount of proinflammatory cytokines including IL-1 and IL-1 family members. The role of the epidermal IL-1 is not limited to initiation of local inflammatory responses, but also to induction of systemic inflammation. However, association of persistent release of IL-1 family members from severe skin inflammatory diseases such as psoriasis, epidermolysis bullosa, atopic dermatitis, blistering diseases and desmoglein-1 deficiency syndrome with diseases in systemic organs have not been so far assessed. Here, we showed the occurrence of severe systemic cardiovascular diseases and metabolic abnormalities including aberrant vascular wall remodeling with aortic stenosis, cardiomegaly, impaired limb and tail circulation, fatty tissue loss and systemic amyloid deposition in multiple organs with liver and kidney dysfunction in mouse models with severe dermatitis caused by persistent release of IL-1s from the skin. These morbid conditions were ameliorated by simultaneous administration of anti-IL-1α and IL-1β antibodies. These findings may explain the morbid association of arteriosclerosis, heart involvement, amyloidosis and cachexia in severe systemic skin diseases and systemic autoinflammatory diseases, and support the value of anti-IL-1 therapy for systemic inflammatory diseases.

Indexed as

AmyloidosisAnimalsAntibodies, NeutralizingCardiovascular DiseasesCholesterolCytokinesEmaciationEnzyme-Linked Immunosorbent AssayInterleukin-1MiceMice, TransgenicSkinSystemic Inflammatory Response SyndromeTomography, X-Ray ComputedAntibodies, NeutralizingCholesterolCytokinesInterleukin-1

Identifiers

PMID25119884
PMCPMC4131904

What OpenQuestion holds

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Registered trials

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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.