Evidence map›Paper›PMID 31804582›Full record

ArticleScientific reports2019

Expression of apoptotic and proliferation factors in gastric mucosa of patients with systemic sclerosis correlates with form of the disease.

Katarina Boric, Snjezana Mardesic, Dusanka Martinovic Kaliterna, Mislav Radic, Ivana Tadin Hadjina, Katarina Vukojevic, Ivona Kosovic, Ivana Solic, Sandra Zekic Tomas, Mirna Saraga-Babic

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

10 authors at 1 institution in 1 country.

Katarina BoricDepartment of Internal Medicine, University Hospital Center Split, Split, Croatia.
Snjezana MardesicDepartment of Anatomy, Histology and Embryology, University of Split, School of Medicine, Split, Croatia.
Dusanka Martinovic KaliternaDepartment of Internal Medicine, University Hospital Center Split, Split, Croatia.
Mislav RadicDepartment of Internal Medicine, University Hospital Center Split, Split, Croatia.
Ivana Tadin HadjinaDepartment of Internal Medicine, University Hospital Center Split, Split, Croatia.
Katarina VukojevicDepartment of Anatomy, Histology and Embryology, University of Split, School of Medicine, Split, Croatia.ORCID http://orcid.org/0000-0003-2182-2890
Ivona KosovicDepartment of Anatomy, Histology and Embryology, University of Split, School of Medicine, Split, Croatia.
Ivana SolicDepartment of Anatomy, Histology and Embryology, University of Split, School of Medicine, Split, Croatia.
Sandra Zekic TomasDepartment of Pathology, University Hospital Center Split, Split, Croatia.
Mirna Saraga-BabicDepartment of Anatomy, Histology and Embryology, University of Split, School of Medicine, Split, Croatia. mirna.saraga-babic@mefst.hr.
University of Split · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite high prevalence of patients with gastric disease in systemic sclerosis (SSc), its pathogenesis is still poorly understood. We immunohistochemically analysed biopsies of gastric mucosa (GM) in 5 controls and 15 patients with different forms of SSc: limited cutaneous (lc), diffuse cutaneous moderate (sys1) and severe (sys2). The number of positive cells was analysed by a Kruskall-Wallis test, P < 0.05 was considered statistically significant. Percentage of proliferating (Ki-67 positive) cells was highest in sys1 (3% in superficial and 4,6% in deeper parts of GM), which dropped to 1% in sys2. Percentage of α-smooth muscle actin (α-SMA) positive cells was 5% in controls, 9% in superficial GM, while in deeper GM rose from 7% to 19% in sys1 and sys2, thus indicating increased myofibroblast population. Caspase-3 positive apoptotic cells characterized 1,5-2% of controls, 8% of superficial and 6% of deeper GM cells in sys1. In sys2, apoptosis affected 50% of surface epithelial and gland cells and 30% of deeper glands, and correlated with increased fibrosis and decreased syndecan-1 expression. Our data demonstrate that sys1 is the most "active" proliferating form of SSc. Sys2 characterize collagen deposition, surface epithelium defects, extensive apoptosis and low proliferation, GM atrophy and loss of function.

Indexed as

ActinsAdultAgedApoptosisAtrophyBiopsyCase-Control StudiesCaspase 3Cell ProliferationCollagenFemaleGastric MucosaHumansKi-67 AntigenMaleMiddle AgedACTA2 protein, humanActinsCASP3 protein, humanCaspase 3CollagenKi-67 AntigenMKI67 protein, humanSDC1 protein, humanSyndecan-1

Identifiers

PMID31804582
PMCPMC6895086
OpenAlexW2993146541

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.