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Dive into the research topics where Giulia Ganzetti is active.

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Featured researches published by Giulia Ganzetti.


Dermatologic Surgery | 2010

Effect of Allium Cepa-Allantoin-Pentaglycan Gel on Skin Hypertrophic Scars: Clinical and Video-Capillaroscopic Results of an Open-Label, Controlled, Nonrandomized Clinical Trial

Anna Campanati; Andrea Savelli; Lucia Sandroni; Barbara Marconi; Angela Giuliano; Katia Giuliodori; Giulia Ganzetti; Annamaria Offidani

BACKGROUND Hypertrophic scar formation is a process in which prolonged angiogenesis sustained by vascular endothelial growth factor cutaneous expression plays an important role. OBJECTIVE This in vivo study was conducted to evaluate the clinical effect of a topical gel containing onion extract, allantoin, and pentaglycan on hypertrophic scars and keloids. MATERIALS AND METHODS Thirty people with hypertrophic scars or keloids were examined. Fifteen patients received a topical application of a gel containing allium cepa, allantoin, and pentaglycan twice a day for 24 weeks, the remaining 15 patients received no topical treatments. A clinical evaluation and an intravital videocapillaroscopy were performed on every patient at baseline (T0) and 24 weeks (T24) after the treatment. RESULTS Only the patients who received the topical treatment showed a significant reduction in neoangiogenetic features, demonstrated through an improvement of erythema and all videocapillaroscopic markers of neoangiogenesis. These changes induced by therapy led to a general improvement of the lesions. CONCLUSION Topical applications of a gel containing allium cepa, pentaglycan, and allantoin twice a day for 24 weeks seems to be useful in reducing neoangiogenesis in hypertrophic scars and keloids, resulting in clinical improvement of skin lesions. The authors have indicated no significant interest with commercial supporters.


American Journal of Clinical Dermatology | 2010

A Patient with Psoriasis and Vitiligo Treated with Etanercept

Anna Campanati; Katia Giuliodori; Giulia Ganzetti; Giulia Liberati; Anna Maria Offidani

Psoriasis is a chronic, immune-mediated, inflammatory dermatosis whose aetiopathogenesis remains unclear, although tumour necrosis factor alpha (TNFα) appears to play a crucial role. The biological potential of TNFα inhibitors, such as etanercept, which reduce the inflammatory cascade, has radically changed the therapeutic management of patients with psoriasis and other immunomediated inflammatory diseases, associated with TNFα. The pathogenesis of the selective destruction of melanocytes in vitiligo is not fully understood, although there is growing evidence that several T helper type 1 cytokines, particularly TNFα, may be involved in the depigmentation process.A patient is described who presented with both psoriasis and vitiligo, and was treated with etanercept. After 24 weeks of therapy, the patient’s psoriasis had improved markedly and the patient noted a mild improvement of vitiligo, with a reduction in macules and repigmentation in the scapular region.


British Journal of Dermatology | 2007

CTACK /CCL27 expression in psoriatic skin and its modification after administration of etanercept

Anna Campanati; G. Goteri; Oriana Simonetti; Giulia Ganzetti; Katia Giuliodori; D. Stramazzotti; D. Morichetti; Maria Luisa Bernardini; B. Mannello; G. Fabris; Annamaria Offidani

Background  Tumour necrosis factor‐α upregulates the expression of a cutaneous T cell‐attracting chemokine (CTACK/CCL27), that promotes migration of cutaneous lymphocyte‐associated antigen‐positive lymphocytes into the skin. The role of CTACK/CCL27 in pathogenesis of psoriasis has recently been documented but no data are available at the present time on its modification in psoriatic cutaneous tissue after administration of etanercept.


Archives of Dermatological Research | 2014

Characterization and profiling of immunomodulatory genes in resident mesenchymal stem cells reflect the Th1-Th17/Th2 imbalance of psoriasis.

Anna Campanati; Monia Orciani; Veronica Consales; Raffaella Lazzarini; Giulia Ganzetti; G. Di Benedetto; R. Di Primio; Annamaria Offidani

The expression of genes encoding for Th1, Th2 and Th17 cytokines has been extensively evaluated in differentiated skin cells of psoriatic patients. The microenvironment exerts a control on the phenotype of resident mesenchymal stem cells (MSCs) into the skin of psoriasis patients. Aim of the study was to extensively evaluate the relative expression of 43 genes encoding for Th1, Th2 and Th17 cytokines in MSCs isolated from skin of psoriasis patients. MSCs resident into psoriatic skin were isolated, characterized and profiled by PCR array for the relative expression of genes encoding for cytokines involved in Th1, Th2 and Th17 pathways. MSCs isolated from the skin of healthy subjects were used as control. The MSCs isolated from skin of psoriasis patients showed a greater relative expression of the most part of the analyzed genes encoding for Th1 and Th17 cytokines: INF-γ, CCR5, CXCL9, CXCL10, IL6, IL8, TNF-α, IL23A, CCL2, CCL20, CXCL2, CXCL5, IL17C, IL17F, IL17RA, IL21, TLR2 than healthy subjects. On the contrary, the relative expression of genes encoding for Th2 cytokines: CCL1, CCL22, CXCL12, IL2, IL3, IL4, IL13B, IL 22, IL 27, TGF-β1, was similar between the MSCs isolated from psoriasis and healthy subjects. In conclusion, the MSCs isolated from psoriasis show an imbalance between the Th1-Th17 and Th2 pathways, which reflects the well-known abnormal balance observed in differentiated skin cells. This evidence could strengthen the hypothesis of an early involvement of resident MSCs in the pathogenesis of psoriasis.


Journal of Crohns & Colitis | 2012

Alopecia Areata: A possible extraintestinal manifestation of Crohn's disease

Giulia Ganzetti; Anna Campanati; Annamaria Offidani

Alopecia Areata (AA) is a chronic inflammatory hair disease resulting in a non-scarring hair loss.1 The CD4+ and CD8+ T lymphocytes peri- and intra-follicular infiltration emphasizes that an abnormal immune response may be involved in AA pathogenesis.1 Although many molecular pathways are implicated, Th1 cytokine profile seems to play a crucial role: a greater expression of IFN- γ , IL-1, TNF- α have been extensively showed in serum and tissue of AA patients than in healthy controls.1 Inflammatory bowel diseases (IBD) are idiopathic and inflammatory diseases of the intestinal tract including two major …


Burns | 2013

Topical ozonated oil versus hyaluronic gel for the treatment of partial- to full-thickness second-degree burns: A prospective, comparative, single-blind, non-randomised, controlled clinical trial.

Anna Campanati; S. De Blasio; Angela Giuliano; Giulia Ganzetti; Katia Giuliodori; T. Pecora; Veronica Consales; Ilaria Minnetti; Annamaria Offidani

INTRODUCTION AND AIM Several studies have demonstrated that ozonated oil is effective on cutaneous wound healing. This in vivo study has been conducted to evaluate the clinical effect of the topical application of ozonated oil for 12 weeks on second-degree skin burns. METHOD A total of 30 patients suffering from second-degree skin burns in the phase of re-epithelisation were included in this study. Every skin burn was subdivided in two symmetrical parts. One part was treated with occlusive application of ozonated oil; the contralateral part of the lesion was treated with topical application of hyaluronic acid gel, once a day for 12 weeks. A clinical evaluation and an intra-vital video-capillaroscopy were performed on every patient at baseline, 6 and 12 weeks after. RESULTS All treated lesions improved regardless of the treatment used. Ozonated oil was as effective as hyaluronic acid in improving erythema, tension, itching and burning sensation reported by patients, and it does not exert a specific anti-angiogenic effect compared to hyaluronic acid. However it seems more effective than hyaluronic acid in reducing post-lesional hyperpigmentation. CONCLUSION Ozonated oil, topically applied for 12 weeks, seems to be as effective as hyaluronic acid in reducing symptoms related to skin burns, but it could be more effective in preventing the post-lesional hyperpigmentation.


Medical Mycology | 2009

In vitro susceptibility of dermatophytes to conventional and alternative antifungal agents

Francesco Barchiesi; Carmela Silvestri; Daniela Arzeni; Giulia Ganzetti; Sefora Castelletti; Oriana Simonetti; Oscar Cirioni; Wojciech Kamysz; Elzbieta Kamysz; Elisabetta Spreghini; Alessandra Abruzzetti; Alessandra Riva; Anna Maria Offidani; Andrea Giacometti; Giorgio Scalise

The minimum inhibitory concentrations (MICs), the minimal fungicidal concentrations (MFCs), the fungal biomass (FB) and hyphal viability employing the dye 3-4,5 dimethyl- 2-thiazolyl- 2,5- diphenyl- 2H tetrazolium bromide (MTT) were used to compare the in vitro effects of fluconazole (FLU) with those of the N-terminal palmitoyl-lipidated peptide, Pal-Lys-Lys-NH(2) (PAL), and a tea tree oil component, gamma-Terpinene (TER), against several clinical isolates of Microsporum canis and Trichophyton rubrum. In general, FLU and PAL MICs were significantly lower than those observed with TER, while no differences in the three drugs were found in the MFCs. However, they were from two to 16-times higher than their respective MICs. FB of M. canis treated with either FLU or PAL, but not with TER, was significantly reduced over untreated controls. Only PAL and TER, in a medium-dependent fashion, but not FLU, reduced the FB of T. rubrum. Finally, PAL was found to be significantly more active than FLU at reducing the hyphal viability against both genera of dermatophytes. This study shows that PAL exerts an in vitro activity against dermatophytes at least similar to that observed with FLU and suggests that this compound might be a promising candidate in the treatment of infections due to dermatophytes.


International Journal of Dermatology | 2015

Serum levels of adipocytokines in psoriasis patients receiving tumor necrosis factor-α inhibitors: results of a retrospective analysis

Anna Campanati; Giulia Ganzetti; Katia Giuliodori; Maurizio Marra; Annarita Bonfigli; Roberto Testa; Annamaria Offidani

Adipocytokines are bioactive molecules that are deeply involved in the occurrence of atherosclerosis, obesity, and autoimmune inflammatory diseases.


World Journal of Hepatology | 2015

Non-alcoholic fatty liver disease and psoriasis: So far, so near.

Giulia Ganzetti; Anna Campanati; Annamaria Offidani

Psoriasis is a chronic inflammatory immune-mediated skin diseases which is frequently associated to comorbidities. Non-alcoholic fatty liver disease (NAFLD) is defined as an excessive accumulation of triglycerides in hepatocytes and includes a wide spectrum of liver conditions ranging from relatively benign steatosis to non-alcoholic steatohepatitis with fatty infiltration and lobular inflammation and to cirrhosis and end-stage liver disease. Actually, psoriasis is considered a systemic diseases associated to comorbidities, as metabolic syndrome and NAFLD is seen the hepatic manifestation of the metabolic syndrome. The possible link between psoriasis, obesity and metabolic syndrome, which are known risk factors for NAFLD has been recently documented focusing in the crucial role of the adipose tissue in the development of the inflammatory background sharing by the above entities. According to recent data, patients with psoriasis show a greater prevalence of NAFLD and metabolic syndrome than the general population. Moreover, patients with NAFLD and psoriasis are at higher risk of severe liver fibrosis than those with NAFLD and without psoriasis. The link between these pathological conditions appears to be a chronic low-grade inflammatory status. The aim of this review is to focus on the multiple aspects linking NAFLD and psoriasis, only apparently far diseases.


European Journal of Clinical Microbiology & Infectious Diseases | 2012

In vitro activity and in vivo efficacy of tigecycline alone and in combination with daptomycin and rifampin against Gram-positive cocci isolated from surgical wound infection

Carmela Silvestri; Oscar Cirioni; Daniela Arzeni; Roberto Ghiselli; Oriana Simonetti; Fiorenza Orlando; Giulia Ganzetti; Silvia Staffolani; Lucia Brescini; Mauro Provinciali; Annamaria Offidani; Mario Guerrieri; Andrea Giacometti

The aim of this work was to determine the in vitro activity of tigecycline and its bactericidal effect for a large number of Gram-positive cocci, as well as to investigate its in vitro interaction with six clinically used antibiotics. In vivo, a wound model was established through the panniculus carnosus of BALB/c mice, and then inoculated with 5 × 107 colony-forming units (CFU) of Staphylococcus aureus or Enterococcus faecalis. For each bacterial strain, the study included an infected or non-infected group that did not receive any treatment, three groups singly treated with tigecycline, rifampin, and daptomycin, and two groups that received tigecycline treatment plus rifampin or daptomycin. In the in vitro studies, tigecycline, daptomycin, and teicoplanin were active against all of the 48 Gram-positive isolates. The combination of tigecycline with rifampicin and daptomycin was synergistic against S. aureus and Enterococcus spp. In the in vivo studies, all groups treated with single drugs showed statistically significant results compared to the control group. The two groups treated with a combination of drugs showed the highest antimicrobial efficacy. In conclusion, our results suggested a strong activity of tigecycline alone and in combination with other antimicrobial agents against multi-resistant Gram-positive organisms isolated from wound infections.

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Dive into the Giulia Ganzetti's collaboration.

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Anna Campanati

Marche Polytechnic University

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Annamaria Offidani

Marche Polytechnic University

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Katia Giuliodori

Marche Polytechnic University

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Oriana Simonetti

Marche Polytechnic University

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Anna Maria Offidani

Marche Polytechnic University

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Elisa Molinelli

Marche Polytechnic University

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Veronica Consales

Marche Polytechnic University

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Barbara Marconi

Marche Polytechnic University

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Corrado Rubini

Marche Polytechnic University

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Ivana Cataldi

Marche Polytechnic University

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