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1.
Sci Rep ; 12(1): 8415, 2022 05 19.
Artículo en Inglés | MEDLINE | ID: mdl-35589750

RESUMEN

Hidradenitis suppurativa (HS) is a recurrent inflammatory skin disease with a complex etiopathogenesis whose treatment poses a challenge in the clinical practice. Here, we present a novel integrated pipeline produced by the European consortium BATMAN (Biomolecular Analysis for Tailored Medicine in Acne iNversa) aimed at investigating the molecular pathways involved in HS by developing new diagnosis algorithms and building cellular models to pave the way for personalized treatments. The objectives of our european Consortium are the following: (1) identify genetic variants and alterations in biological pathways associated with HS susceptibility, severity and response to treatment; (2) design in vitro two-dimensional epithelial cell and tri-dimensional skin models to unravel the HS molecular mechanisms; and (3) produce holistic health records HHR to complement medical observations by developing a smartphone application to monitor patients remotely. Dermatologists, geneticists, immunologists, molecular cell biologists, and computer science experts constitute the BATMAN consortium. Using a highly integrated approach, the BATMAN international team will identify novel biomarkers for HS diagnosis and generate new biological and technological tools to be used by the clinical community to assess HS severity, choose the most suitable therapy and follow the outcome.


Asunto(s)
Dermatitis , Hidradenitis Supurativa , Biomarcadores , Dermatitis/complicaciones , Hidradenitis Supurativa/diagnóstico , Hidradenitis Supurativa/genética , Hidradenitis Supurativa/terapia , Salud Holística , Humanos , Piel
2.
J Dermatol Sci ; 99(1): 17-22, 2020 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-32518053

RESUMEN

BACKGROUND: Diagnosis of pyoderma gangrenosum, acne and hidradenitis suppurativa (PASH) and pyogenic arthritis, pyoderma gangrenosum, acne, and hidradenitis suppurativa (PAPASH) patients, in spite of recently identified genetic variations, is just clinical, since most patients do not share the same mutations, and the mutations themselves are not informative of the biological pathways commonly disrupted in these patients. OBJECTIVE: To reveal genetic changes more closely related to PASH and PAPASH etiopathogenesis, identifying novel common pathways involved in these diseases. METHODS: Cohort study on PASH (n = 4) and PAPASH (n = 1) patients conducted using whole exome sequencing (WES) approach and a novel bioinformatic pipeline aimed at discovering potentially candidate genes selected from density mutations and involved in pathways relevant to the disease. RESULTS: WES results showed that patients presented 90 genes carrying mutations with deleterious and/or damage impact: 12 genes were in common among the 5 patients and bared 237 ns ExonVar (54 and 183 in homozygosis and heterozygosis, respectively). In the pathway enrichment analysis, only 10 genes were included, allowing us to retrieve 4 pathways shared by all patients: (1) Vitamin D metabolism, (2) keratinization, (3) formation of the cornified envelope and (4) steroid metabolism. Interestingly, all patients had vitamin D levels lower than normal, with a mean value of 10 ng/mL. CONCLUSION: Our findings, through a novel strategy for analysing the genetic background of syndromic HS patients, suggested that vitamin D metabolism dysfunctions seem to be crucial in PASH and PAPASH pathogenesis. Based on low vitamin D serum levels, its supplementation is envisaged.


Asunto(s)
Acné Vulgar/diagnóstico , Artritis Infecciosa/diagnóstico , Secuenciación del Exoma , Hidradenitis Supurativa/diagnóstico , Piodermia Gangrenosa/diagnóstico , Piel/patología , Vitamina D/metabolismo , Acné Vulgar/genética , Acné Vulgar/metabolismo , Acné Vulgar/patología , Adolescente , Adulto , Artritis Infecciosa/genética , Artritis Infecciosa/metabolismo , Artritis Infecciosa/patología , Biología Computacional , Femenino , Estudios de Seguimiento , Hidradenitis Supurativa/genética , Hidradenitis Supurativa/metabolismo , Hidradenitis Supurativa/patología , Humanos , Queratinocitos/patología , Masculino , Piodermia Gangrenosa/genética , Piodermia Gangrenosa/metabolismo , Piodermia Gangrenosa/patología , Piel/citología , Síndrome , Adulto Joven
4.
Molecules ; 19(12): 21127-53, 2014 Dec 16.
Artículo en Inglés | MEDLINE | ID: mdl-25521115

RESUMEN

Curcumin belongs to the family of natural compounds collectively called curcuminoids and it possesses remarkable beneficial anti-oxidant, anti-inflammatory, anti-cancer, and neuroprotective properties. Moreover it is commonly assumed that curcumin has also been suggested as a remedy for digestive diseases such as inflammatory bowel diseases (IBD), a chronic immune disorder affecting the gastrointestinal tract and that can be divided in two major subgroups: Crohn's disease (CD) and Ulcerative Colitis (UC), depending mainly on the intestine tract affected by the inflammatory events. The chronic and intermittent nature of IBD imposes, where applicable, long-term treatments conducted in most of the cases combining different types of drugs. In more severe cases and where there has been no good response to the drugs, a surgery therapy is carried out. Currently, IBD-pharmacological treatments are generally not curative and often present serious side effects; for this reason, being known the relationship between nutrition and IBD, it is worthy of interesting the study and the development of new dietary strategy. The curcumin principal mechanism is the suppression of IBD inflammatory compounds (NF-κB) modulating immune response. This review summarizes literature data of curcumin as anti-inflammatory and anti-oxidant in IBD, trying to understand the different effects in CD e UC.


Asunto(s)
Antiinflamatorios no Esteroideos/uso terapéutico , Curcumina/uso terapéutico , Enfermedades Inflamatorias del Intestino/tratamiento farmacológico , Animales , Antiinflamatorios no Esteroideos/farmacología , Química Farmacéutica , Ensayos Clínicos como Asunto , Curcumina/análogos & derivados , Curcumina/farmacología , Humanos , Enfermedades Inflamatorias del Intestino/diagnóstico , Enfermedades Inflamatorias del Intestino/etiología , Terapia Molecular Dirigida , Nanotecnología , Resultado del Tratamiento
5.
Biomed Res Int ; 2013: 715465, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-24073415

RESUMEN

Mevalonate Kinase Deficiency (MKD) is a rare autosomal recessive inborn disorder of cholesterol biosynthesis caused by mutations in the mevalonate kinase (MK) gene, leading to MK enzyme decreased activity. The consequent shortage of mevalonate-derived isoprenoid compounds results in an inflammatory phenotype, caused by the activation of the NALP3 inflammasome that determines an increased caspase-1 activation and IL-1 ß release. In MKD, febrile temperature can further decrease the residual MK activity, leading to mevalonate pathway modulation and to possible disease worsening. We previously demonstrated that the administration of exogenous isoprenoids such as geraniol or the modulation of the enzymatic pathway with drugs, such as Tipifarnib, partially rescues the inflammatory phenotype associated with the defective mevalonic pathway. However, it has not been investigated yet how temperature can affect the success of these treatments. Thus, we investigated the effect of temperature on primary human monocytes from MKD patients. Furthermore the ability of geraniol and Tipifarnib to reduce the abnormal inflammatory response, already described at physiological temperature in MKD, was studied in a febrile condition. We evidenced the role of temperature in the modulation of the inflammatory events and suggested strongly considering this variable in future researches aimed at finding a treatment for MKD.


Asunto(s)
Deficiencia de Mevalonato Quinasa/tratamiento farmacológico , Quinolonas/uso terapéutico , Temperatura , Terpenos/uso terapéutico , Monoterpenos Acíclicos , Antiinflamatorios/farmacología , Apoptosis/efectos de los fármacos , Vías Biosintéticas/efectos de los fármacos , Proteínas Portadoras/metabolismo , Niño , Citocinas/sangre , Femenino , Humanos , Inflamasomas/metabolismo , Interleucina-1beta/metabolismo , Lipopolisacáridos/farmacología , Masculino , Deficiencia de Mevalonato Quinasa/sangre , Ácido Mevalónico/metabolismo , Proteína con Dominio Pirina 3 de la Familia NLR , Quinolonas/farmacología , Terpenos/farmacología
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