Probiotic Lactobacillus Rhamnosus GG for Pediatric Atopic Dermatitis
- Conditions
- Atopic Dermatitis
- Interventions
- Other: placeboDietary Supplement: Lactobacillus rhamnosus GG
- Registration Number
- NCT03863418
- Lead Sponsor
- Federico II University
- Brief Summary
Atopic dermatitis (AD) is a multifactorial, chronic inflammatory skin disorder that results in areas of dry, itchy skin. AD affects up to 20% of children in Western societies and represents a prevalent, burdensome, and psychologically important pediatric concern.
It often appears in infancy and may persist into adolescence and adulthood. This complex disease is typified by defective skin barrier function with activation of abnormal immunological and inflammatory pathways upon exposure to ubiquitous environmental allergens.
It often appears in infancy and may persist into adolescence and adulthood. This complex disease is typified by defective skin barrier function with activation of abnormal immunological and inflammatory pathways upon exposure to ubiquitous environmental allergens.
This complex disease is typified by defective skin barrier function with activation of abnormal immunological and inflammatory pathways upon exposure to ubiquitous environmental allergens. This phenomenon may be primarily related to mutations in important barrier proteins, in the same fashion as filaggrin in the atopic skin, or may be secondary, reflecting the intestinal mucosal damage caused by local hypersensitivity reactions to food antigens or to microbial components as in inflammatory bowel disease. Conventional therapy for AD consists of elimination of exacerbating factors, moisturizers to maintain skin hydration, antihistamines to alleviate pruritus, topically applied corticosteroids, or topical calcineurin inhibitors to control inflammation. Severe forms of atopic dermatitis may need systemic corticosteroids, oral cyclosporine, and/or phototherapy.
Probiotics have been suggested as a novel treatment approach for atopic dermatitis. Specific probiotics have been shown to normalize intestinal permeability, to counteract intestinal immune dysfunction and to normalize gut dysbiosis. Hence, their clinical benefit may reside in the control of gut inflammation induced by various intraluminal antigens and enhancement of adaptive and especially innate immune responses.
Indeed, above and beyond balancing the gut microecology and promoting host immune defences, specific probiotics might further aid in controlling the microbial colonization of the skin, thereby reducing proneness to secondary infections which typically cause sustained symptoms. However, there are conflicting evidence on the utility of selected probiotic strains for atopic dermatitis, and major problems are due to dose and viability of strain used, duration of treatment, study population.
The aim of this randomized, double-blind, placebo-controlled study is to evaluate the efficacy of the most studied probiotic in the pediatric allergy field - Lactobacillus rhamnosus GG (LGG) - in children affected by atopic dermatitis.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 100
- Children aged 6-36 months
- diagnosis of Atopic Dermatitis according to SCORAD index
Exclusion Criteria
- Age < 6 months
- age > 36 months,
- skin infections,
- ichthyosis,
- food allergies,
- other allergic diseases,
- chronic systemic diseases,
- congenital cardiac defects,
- active tuberculosis,
- autoimmune diseases,
- immunodeficiency,
- chronic inflammatory bowel diseases,
- celiac disease,
- cystic fibrosis,
- metabolic diseases,
- malignancy,
- chronic pulmonary diseases,
- malformations of the gastrointestinal and/or respiratory tract,
- administration of prebiotics/ probiotics/symbiotic/systemic immunomodulators during the 4 weeks before enrolment,
- treatments with topical immunomodulators (Tacrolimus or Pimecrolimus) over the three months prior to enrolment;
- use of corticosteroids or calcineurin antagonists or phototherapy in the previous 4 weeks,
- use of systemic antibiotics or anti-mycotic drugs during 4 weeks before study entry;
- investigator's uncertainty about the willingness or ability of the subject to comply with the protocol requirements;
- participation in any other studies involving investigational or marketed products concomitantly or within two weeks prior to entry into the study;
- hypersensitivity to components contained in study product.
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description placebo placebo maltodextrin Lactobacillus rhamnosus GG Lactobacillus rhamnosus GG Lactobacillus rhamnosus GG (10 billion Colony Forming Units/CAPSULE)
- Primary Outcome Measures
Name Time Method Reduction of SCORing Atopic Dermatitis (SCORAD) after 12-week treatment The efficacy of LGG supplementation on clinical course of children in terms of reduction of SCORAD index (score minimum 0 - maximum 60)
- Secondary Outcome Measures
Name Time Method Composition of gut microbiota metabolomic feature after 12-week treatment Determination of short chain fatty acids
Composition of gut microbiota after 12-week treatment gut microbiota metagenomic in term of total genomic DNA
evaluation acquired immunity after 12-week treatment evaluation acquired immunity by determining fecal Immunoglobulin A levels
evaluation of quality of life after 12-week treatment evaluation of Infant Dermatitis Quality of Life Questionnaire (IDQOL) (score minimum 0 - maximum 30)
Trial Locations
- Locations (1)
University of Naples Federico II
🇮🇹Naples, Italy