Cargando…

An Integrated Approach to Unravel Hidradenitis Suppurativa Etiopathogenesis

Hidradenitis suppurativa/acne inversa (HS) is a chronic inflammatory disease involving hair follicles that presents with painful nodules, abscesses, fistulae, and hypertrophic scars, typically occurring in apocrine gland bearing skin. Establishing a diagnosis of HS may take up to 7 years after disea...

Descripción completa

Detalles Bibliográficos
Autores principales: Tricarico, Paola M., Boniotto, Michele, Genovese, Giovanni, Zouboulis, Christos C., Marzano, Angelo V., Crovella, Sergio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494959/
https://www.ncbi.nlm.nih.gov/pubmed/31105704
http://dx.doi.org/10.3389/fimmu.2019.00892
_version_ 1783415310738522112
author Tricarico, Paola M.
Boniotto, Michele
Genovese, Giovanni
Zouboulis, Christos C.
Marzano, Angelo V.
Crovella, Sergio
author_facet Tricarico, Paola M.
Boniotto, Michele
Genovese, Giovanni
Zouboulis, Christos C.
Marzano, Angelo V.
Crovella, Sergio
author_sort Tricarico, Paola M.
collection PubMed
description Hidradenitis suppurativa/acne inversa (HS) is a chronic inflammatory disease involving hair follicles that presents with painful nodules, abscesses, fistulae, and hypertrophic scars, typically occurring in apocrine gland bearing skin. Establishing a diagnosis of HS may take up to 7 years after disease onset. HS severely impairs the quality of life of patients and its high frequency causes significant costs for health care system. HS patients have an increased risk of developing associated diseases, such as inflammatory bowel diseases and spondyloarthropathies, thereby suggesting a common pathophysiological mechanism. Familial cases, which are around 35% of HS patients, have allowed the identification of susceptibility genes. HS is perceived as a complex disease where environmental factors trigger chronic inflammation in the skin of genetically predisposed individuals. Despite the efforts made to understand HS etiopathogenesis, the exact mechanisms at the basis of the disease need to be still unraveled. In this review, we considered all OMICs studies performed on HS and observed that OMICs contribution in the context of HS appeared as not clear enough and/or rich of useful clinical information. Indeed, most studies focused only on one aspect—genome, transcriptome, or proteome—of the disease, enrolling small numbers of patients. This is quite limiting for the genetic studies, from different geographical areas and looking at a few aspects of HS pathogenesis without any integration of the findings obtained or a comparison among different studies. A strong need for an integrated approach using OMICs tools is required to discover novel actors involved in HS etiopathogenesis. Moreover, we suggest the constitution of consortia to enroll a higher number of patients to be analyzed following common and consensus OMICs strategies. Comparison and integration with the findings present in the OMICs repositories are mandatory. In a theoretic pipeline, the Skin-OMICs profile obtained from each HS patient should be compared and integrated with repositories and literature data by using appropriate InterOMICs approach. The final goal is not only to improve the knowledge of HS etiopathogenesis but also to provide novel tools to the clinicians with the eventual aim of offering a tailored treatment for HS patients.
format Online
Article
Text
id pubmed-6494959
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-64949592019-05-17 An Integrated Approach to Unravel Hidradenitis Suppurativa Etiopathogenesis Tricarico, Paola M. Boniotto, Michele Genovese, Giovanni Zouboulis, Christos C. Marzano, Angelo V. Crovella, Sergio Front Immunol Immunology Hidradenitis suppurativa/acne inversa (HS) is a chronic inflammatory disease involving hair follicles that presents with painful nodules, abscesses, fistulae, and hypertrophic scars, typically occurring in apocrine gland bearing skin. Establishing a diagnosis of HS may take up to 7 years after disease onset. HS severely impairs the quality of life of patients and its high frequency causes significant costs for health care system. HS patients have an increased risk of developing associated diseases, such as inflammatory bowel diseases and spondyloarthropathies, thereby suggesting a common pathophysiological mechanism. Familial cases, which are around 35% of HS patients, have allowed the identification of susceptibility genes. HS is perceived as a complex disease where environmental factors trigger chronic inflammation in the skin of genetically predisposed individuals. Despite the efforts made to understand HS etiopathogenesis, the exact mechanisms at the basis of the disease need to be still unraveled. In this review, we considered all OMICs studies performed on HS and observed that OMICs contribution in the context of HS appeared as not clear enough and/or rich of useful clinical information. Indeed, most studies focused only on one aspect—genome, transcriptome, or proteome—of the disease, enrolling small numbers of patients. This is quite limiting for the genetic studies, from different geographical areas and looking at a few aspects of HS pathogenesis without any integration of the findings obtained or a comparison among different studies. A strong need for an integrated approach using OMICs tools is required to discover novel actors involved in HS etiopathogenesis. Moreover, we suggest the constitution of consortia to enroll a higher number of patients to be analyzed following common and consensus OMICs strategies. Comparison and integration with the findings present in the OMICs repositories are mandatory. In a theoretic pipeline, the Skin-OMICs profile obtained from each HS patient should be compared and integrated with repositories and literature data by using appropriate InterOMICs approach. The final goal is not only to improve the knowledge of HS etiopathogenesis but also to provide novel tools to the clinicians with the eventual aim of offering a tailored treatment for HS patients. Frontiers Media S.A. 2019-04-25 /pmc/articles/PMC6494959/ /pubmed/31105704 http://dx.doi.org/10.3389/fimmu.2019.00892 Text en Copyright © 2019 Tricarico, Boniotto, Genovese, Zouboulis, Marzano and Crovella. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Tricarico, Paola M.
Boniotto, Michele
Genovese, Giovanni
Zouboulis, Christos C.
Marzano, Angelo V.
Crovella, Sergio
An Integrated Approach to Unravel Hidradenitis Suppurativa Etiopathogenesis
title An Integrated Approach to Unravel Hidradenitis Suppurativa Etiopathogenesis
title_full An Integrated Approach to Unravel Hidradenitis Suppurativa Etiopathogenesis
title_fullStr An Integrated Approach to Unravel Hidradenitis Suppurativa Etiopathogenesis
title_full_unstemmed An Integrated Approach to Unravel Hidradenitis Suppurativa Etiopathogenesis
title_short An Integrated Approach to Unravel Hidradenitis Suppurativa Etiopathogenesis
title_sort integrated approach to unravel hidradenitis suppurativa etiopathogenesis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6494959/
https://www.ncbi.nlm.nih.gov/pubmed/31105704
http://dx.doi.org/10.3389/fimmu.2019.00892
work_keys_str_mv AT tricaricopaolam anintegratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT boniottomichele anintegratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT genovesegiovanni anintegratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT zouboulischristosc anintegratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT marzanoangelov anintegratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT crovellasergio anintegratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT tricaricopaolam integratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT boniottomichele integratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT genovesegiovanni integratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT zouboulischristosc integratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT marzanoangelov integratedapproachtounravelhidradenitissuppurativaetiopathogenesis
AT crovellasergio integratedapproachtounravelhidradenitissuppurativaetiopathogenesis