Evidence map›Paper›PMID 28566901›Full record

ArticleAnnals of dermatology2017

Periostin in Mature Stage Localized Scleroderma.

Min-Woo Kim, Jung Tae Park, Jung Ho Kim, Seong-Joon Koh, Hyun-Sun Yoon, Soyun Cho, Hyun-Sun Park

Open access · hybridAbstract read
In one paragraph

Article in Annals of dermatology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Emerging Roles of Matricellular Proteins in Systemic Sclerosis.International journal of molecular sciences · 2020
    Review
  4. NRF2 Activation Inhibits Both TGF-Oxidative medicine and cellular longevity · 2018
    Article
  5. Periostin in the pathogenesis of skin diseases.Cellular and molecular life sciences : CMLS · 2017
    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 1 institution in 1 country.

Min-Woo KimDepartment of Dermatology, SMG-SNU Boramae Medical Center, Seoul, Korea.
Jung Tae ParkDepartment of Dermatology, SMG-SNU Boramae Medical Center, Seoul, Korea.
Jung Ho KimDepartment of Pathology, SMG-SNU Boramae Medical Center, Seoul, Korea.
Seong-Joon KohDepartment of Internal Medicine, SMG-SNU Boramae Medical Center, Seoul, Korea.
Hyun-Sun YoonDepartment of Dermatology, SMG-SNU Boramae Medical Center, Seoul, Korea.
Soyun ChoDepartment of Dermatology, SMG-SNU Boramae Medical Center, Seoul, Korea.
Hyun-Sun ParkDepartment of Dermatology, SMG-SNU Boramae Medical Center, Seoul, Korea.
SNUH SMG-SNU Boramae Medical Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeriostin is a novel matricellular protein expressed in many tissues, including bone, periodontal ligament, and skin. Although its expression is prominent in various fibrotic conditions, studies of periostin in localized scleroderma are rare.

objectiveTo investigate the expression of periostin and other molecules in localized scleroderma.

methodsA retrospective study of 14 patients with confirmed mature stage localized scleroderma was undertaken. Fourteen age-matched and biopsy site-matched subjects with normal skin were included as controls. Collagen fiber deposition, periostin, procollagen, transforming growth factor-β, and matrix metalloproteinase (MMP)-1 expression were assessed and compared between the two groups. Co-localization of α-smooth muscle actin and periostin was evaluated using confocal microscopy.

resultsPeriostin was predominantly expressed along the dermo-epidermal junction in the controls. Conversely, patients with localized scleroderma demonstrated increased collagen fiber deposition and periostin expression that was more widely distributed along the entire dermis. MMP-1 staining showed increased expression in the epidermis and dermis of patients compared to scanty expression in the controls. A semi-quantitative evaluation showed a higher proportion of excessive collagen bundle deposition (57.1% vs. 7.1%,

conclusionCompared to the controls, patients with localized scleroderma had enhanced periostin expression corresponding to increased collagen fiber deposition and unexpected overexpression of MMP-1. The results of this human

Indexed as

CollagenLocalized sclerodermaPathogenesisPeriostinSclerosis

Identifiers

PMID28566901
PMCPMC5438931
OpenAlexW2615040789

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.