Evidence map›Paper›PMID 37762589›Full record

ReviewInternational journal of molecular sciences2023

The Pathogenesis of Systemic Sclerosis: The Origin of Fibrosis and Interlink with Vasculopathy and Autoimmunity.

Junsuk Ko, Maria Noviani, Vasuki Ranjani Chellamuthu, Salvatore Albani, Andrea Hsiu Ling Low

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
14.3field-weighted citation impact, top 1% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 56 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Junsuk KoDuke-National University of Singapore Medical School, Singapore 169857, Singapore.
Maria NovianiDuke-National University of Singapore Medical School, Singapore 169857, Singapore.
Vasuki Ranjani ChellamuthuTranslational Immunology Institute, SingHealth Duke-National University of Singapore Academic Medical Centre, Singapore 169856, Singapore.
Salvatore AlbaniDuke-National University of Singapore Medical School, Singapore 169857, Singapore.
Andrea Hsiu Ling LowDuke-National University of Singapore Medical School, Singapore 169857, Singapore.ORCID 0000-0002-5244-686X
National University of Singapore · SG

Funding

National Medical Research Council MN is supported by the National Medical Research Council (NMRC) Clinician Scientist Seed Funding (MOH-001324-00). SA holds grant support from NMRC (NMRC/OFLCG/002/2018, CIRG19may0052), MOH-STaR19nov-0002, A*STAR PEC21-H22P0M0003, Duke-NUS and SingHealth ASingHealth Academy of Medicine JK is supported by the SingHealth Medical Student Talent Development Awards (SMSTDA, Project and Travel Awards).
6 · The paper itself

Abstract

Systemic sclerosis (SSc) is an autoimmune disease associated with increased mortality and poor morbidity, impairing the quality of life in patients. Whilst we know that SSc affects multiple organs via vasculopathy, inflammation, and fibrosis, its exact pathophysiology remains elusive. Microvascular injury and vasculopathy are the initial pathological features of the disease. Clinically, the vasculopathy in SSc is manifested as Raynaud's phenomenon (reversible vasospasm in reaction to the cold or emotional stress) and digital ulcers due to ischemic injury. There are several reports that medications for vasculopathy, such as bosentan and soluble guanylate cyclase (sGC) modulators, improve not only vasculopathy but also dermal fibrosis, suggesting that vasculopathy is important in SSc. Although vasculopathy is an important initial step of the pathogenesis for SSc, it is still unclear how vasculopathy is related to inflammation and fibrosis. In this review, we focused on the clinical evidence for vasculopathy, the major cellular players for the pathogenesis, including pericytes, adipocytes, endothelial cells (ECs), and myofibroblasts, and their signaling pathway to elucidate the relationship among vasculopathy, inflammation, and fibrosis in SSc.

Indexed as

AutoimmunityScleroderma, SystemicVascular DiseasesAnimalsEndothelial CellsFibrosisHumansSignal TransductionautoimmunityfibrosisinflammationpathogenesisRaynaudsclerodermasystemic sclerosisvasculopathy

Identifiers

PMID37762589
PMCPMC10532389
OpenAlexW4386895064

What Socratic 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 Socratic graph.