TY - JOUR
T1 - What have we learned on pre, very early, and early systemic sclerosis microcirculatory pathophysiology? A scoping review
AU - Caetano, Joana
AU - Rodrigues, Luís Monteiro
AU - Alves, José Delgado
N1 - Copyright © 2024 Elsevier B.V. All rights reserved.
PY - 2024/5/1
Y1 - 2024/5/1
N2 - Objective: Microvascular dysfunction is an early event in the pathogenesis of systemic sclerosis (SSc). The objective of this scoping review is to update the current information and the level of knowledge about the mechanisms of microvascular dysfunction in pre-SSc, very early diagnosis of SSc (VEDOSS) and early SSc. Methods: A PubMed® database search allowed us to include original data from full-length articles in English in which the main topic was microvascular dysfunction in pre-SSC, VEDOSS or early SSc. Data was extracted using a customized form. Results: In the present review 437 articles were identified, and 42 studies included, reporting data from a total of 1069 patients with pre-SSc, VEDOSS or early-SSc. Distinct mechanisms of microvascular injury were identified comprising, angiogenesis and vasculogenesis, cell surface proteins and adhesion, molecules expression, cytokines profile, inflammatory and oxidation pathways, and skin perfusion determinants. Most of the studies were conducted in early SSc, with a reduced number in pre-disease stages, in which the prompt recognition of specific mechanisms and biomarkers may allow targeted treatment to prevent disease progression. Conclusions: Although different molecular expression patterns and signaling pathways related to microvascular dysfunction in pre-SSc, VEDOSS, and early SSc were identified, additional prospective longitudinal studies and combined work with functional evaluation of peripheral skin perfusion are needed.
AB - Objective: Microvascular dysfunction is an early event in the pathogenesis of systemic sclerosis (SSc). The objective of this scoping review is to update the current information and the level of knowledge about the mechanisms of microvascular dysfunction in pre-SSc, very early diagnosis of SSc (VEDOSS) and early SSc. Methods: A PubMed® database search allowed us to include original data from full-length articles in English in which the main topic was microvascular dysfunction in pre-SSC, VEDOSS or early SSc. Data was extracted using a customized form. Results: In the present review 437 articles were identified, and 42 studies included, reporting data from a total of 1069 patients with pre-SSc, VEDOSS or early-SSc. Distinct mechanisms of microvascular injury were identified comprising, angiogenesis and vasculogenesis, cell surface proteins and adhesion, molecules expression, cytokines profile, inflammatory and oxidation pathways, and skin perfusion determinants. Most of the studies were conducted in early SSc, with a reduced number in pre-disease stages, in which the prompt recognition of specific mechanisms and biomarkers may allow targeted treatment to prevent disease progression. Conclusions: Although different molecular expression patterns and signaling pathways related to microvascular dysfunction in pre-SSc, VEDOSS, and early SSc were identified, additional prospective longitudinal studies and combined work with functional evaluation of peripheral skin perfusion are needed.
KW - Biomarkers
KW - Disease Progression
KW - Early Diagnosis
KW - Humans
KW - Microcirculation
KW - Neovascularization, Pathologic
KW - Scleroderma, Systemic/physiopathology
KW - Skin/blood supply
UR - http://www.scopus.com/inward/record.url?scp=85190267528&partnerID=8YFLogxK
U2 - 10.1016/j.autrev.2024.103540
DO - 10.1016/j.autrev.2024.103540
M3 - Article
C2 - 38604463
AN - SCOPUS:85190267528
SN - 1568-9972
VL - 23
SP - 103540
JO - Autoimmunity Reviews
JF - Autoimmunity Reviews
IS - 5
M1 - 103540
ER -