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...
Autores principales: | , , , , , |
---|---|
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 |