36 research outputs found

    New Directions in Understanding Atopic March Starting from Atopic Dermatitis

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    Recent evidence showed that the postulated linear progression of the atopic march, from atopic dermatitis to food and respiratory allergies, does not capture the heterogeneity of allergic phenotypes, which are influenced by complex interactions between environmental, genetic, and psychosocial factors. Indeed, multiple atopic trajectories are possible in addition to the classic atopic march. Nevertheless, atopic dermatitis is often the first manifestation of an atopic march. Improved understanding of atopic dermatitis pathogenesis is warranted as this could represent a turning point in the prevention of atopic march. In this review, we outline the recent findings on the pathogenetic mechanisms leading to atopic dermatitis that could be targeted by intervention strategies for the prevention of atopic march

    Glycated ACE2 reduces anti-remodeling effects of renin-angiotensin system inhibition in human diabetic hearts

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    High glycated-hemoglobin (HbA1c) levels correlated with an elevated risk of adverse cardiovascular outcomes despite renin-angiotensin system (RAS) inhibition in type-2 diabetic (T2DM) patients with reduced ejection fraction. Using the routine biopsies of non-T2DM heart transplanted (HTX) in T2DM recipients, we evaluated whether the diabetic milieu modulates glycosylated ACE2 (GlycACE2) levels in cardiomyocytes, known to be affected by non-enzymatic glycosylation, and the relationship with glycemic control

    Consensus Conference on Clinical Management of pediatric Atopic Dermatitis

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    Abstracts from the Food Allergy and Anaphylaxis Meeting 2016

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    New Directions in Understanding Atopic March Starting from Atopic Dermatitis

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    Recent evidence showed that the postulated linear progression of the atopic march, from atopic dermatitis to food and respiratory allergies, does not capture the heterogeneity of allergic phenotypes, which are influenced by complex interactions between environmental, genetic, and psychosocial factors. Indeed, multiple atopic trajectories are possible in addition to the classic atopic march. Nevertheless, atopic dermatitis is often the first manifestation of an atopic march. Improved understanding of atopic dermatitis pathogenesis is warranted as this could represent a turning point in the prevention of atopic march. In this review, we outline the recent findings on the pathogenetic mechanisms leading to atopic dermatitis that could be targeted by intervention strategies for the prevention of atopic march

    Stafilococco aureo e dermatite atopica

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    La dermatite atopica riconosce tra i fattori eziopatogenetici una complessa interazione tra difetti genetici/immunologici e fattori ambientali; tra questi lo Stafilococco aureo gioca un ruolo predominante. In condizioni normali, la barriera cutanea con le sue propriet\ue0 antimicrobiche impedisce l\u2019invasione e la colonizzazione della cute da parte di microrganismi patogeni. Con l\u2018avvento della metagenomica, la possibilit\ue0 di studiare il microbiota cutaneo ha offerto nuove affascinanti acquisizioni; \ue8 emerso in particolare il concetto di disbiosi, ovvero di alterazione della composizione relativa dei microrganismi in alcune condizioni patologiche. Lo Stafilococco aureo rappresenta infatti il batterio pi\uf9 comunemente riscontrato sulla cute affetta da dermatite atopica, dal momento che oltre il 90% dei pazienti risultano colonizzati a livello cutaneo vs il 5-30% dei soggetti sani. Con i suoi numerosi meccanismi di virulenza, \ue8 in grado di interagire con i meccanismi dell\u2019immunit\ue0 innata e acquisita dell\u2019ospite, sostenendo e contribuendo a perpetuare le riacutizzazioni della DA e determinando una maggior severit\ue0 del quadro clinico

    Fetal lung lesions diagnosis: the crucial role of ultrasonography

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    Fetal lung lesions may cause significant effects of mass and may evolve into a non-immune hydrops and lead to the death of the fetus or the child. Treatment options for these severely affected infants are constantly evolving. The widespread use of ultrasound in prenatal diagnosis, in tertiary center like ours, allows us to identify the fetus, including lung lesions more ‘small. Prenatal diagnosis and possible therapeutic intervention in the immediate prenatal or postnatal period has significantly changed the quality of life and the survival of fetuses and infants, especially those who were completely asymptomatic at birth. Object of our interest is the pulmonary sequestration and congenital pulmonary malformation is the second in order of frequency, with an incidence between 0.15% and 6.4% of cases

    Bifidobacterium mixture (B longum BB536, B infantis M-63, B breve M-16V) treatment in children with seasonal allergic rhinitis and intermittent asthma

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    Background: Allergic rhinitis (AR) and allergic asthma are caused by an IgE-mediated inflammatory reaction. Probiotics may exert anti-inflammatory and immune-modulatory activity. Thus, this study aimed at investigating whether a Bifidobacteria mixture could be able to relieve nasal symptoms, and affect quality of life (QoL) in children with AR and intermittent asthma due to Parietaria allergy. Materials and methods: The present study was conducted as placebo-controlled, double-blinded, and randomized. Globally, 40 children (18 males; mean age 9 ± 2.2 years) were enrolled. They were treated with probiotics or placebo: 1 sachet/day for 4 weeks. AR symptoms, and QoL were assessed at baseline and after treatment. Use of rescue medications, such as cetirizine syrup and salbutamol spray, was also permitted and recorded. Results: Children treated with probiotic mixture achieved a significant improvement of symptoms (p < 0.005), and QoL ((p < 0.001). Placebo group had worsening of symptoms (p < 0.005) and QoL (p < 0.001). The use of rescue medications was overlapping in the two groups. The intergroup analysis showed that probiotic mixture was significantly superior than placebo for all parameters. Conclusions: The current study demonstrated that a Bifidobacteria mixture was able of significantly improving AR symptoms and QoL in children with pollen-induced AR and intermittent asthma. Clinical trial registration: ClinicalTrials.gov ID NCT02807064
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