A5066553445- Diet and metabolism studies
- Pancreatitis Pathology and Treatment
- Obesity, Physical Activity, Diet
- Gut microbiota and health
- Nutritional Studies and Diet
- Nutrition, Genetics, and Disease
- Pituitary Gland Disorders and Treatments
- Infant Health and Development
- Phytase and its Applications
- Thyroid Disorders and Treatments
- Neonatal Respiratory Health Research
- Pediatric health and respiratory diseases
- Gastrointestinal motility and disorders
- Adipokines, Inflammation, and Metabolic Diseases
- Genetics and Neurodevelopmental Disorders
- Adrenal Hormones and Disorders
- Growth Hormone and Insulin-like Growth Factors
- Food composition and properties
- Genetic Syndromes and Imprinting
- Probiotics and Fermented Foods
- Neonatal Health and Biochemistry
- Nutrition and Health in Aging
- Health and Lifestyle Studies
- Renal and related cancers
- Pediatric Urology and Nephrology Studies
Università degli Studi del Piemonte Orientale “Amedeo Avogadro”
2018-2025
Ospedale Regina Margherita
2023
Department of Medical Sciences
2019
The purposes of this study were to evaluate the differences in Mediterranean diet and its components among primary secondary school children adolescents living northern Italy, associations with weight status. Adherence was assessed by KIDMED (Mediterranean Diet Quality Index) questionnaire on 669 subjects (6⁻16 years) attending five schools Novara. adherence poor 16.7%, average 63.7%, high 19.6% students. Poor more frequent than (20.7% vs. 13.7%,
Variations in gut microbiota might impact metabolism leading to body weight excess. We assessed the of a probiotic supplementation pediatric obesity on weight, metabolic alterations, selected microbial groups, and functionality.Cross-over, double-blind, randomized control trial (BIFI-OBESE trial; NCT03261466). 101 youths (6-18 years, Tanner stage ≥2) with insulin-resistance diet were 2 × 109 CFU/AFU/day Bifidobacterium breve BR03 (DSM 16604) B. B632 24706) (51) or placebo (50) for 8 weeks...
Abstract Aim To assess the efficacy of combined administration myo‐inositol and zinc, a mineral involved in insulin pathway, paediatric obesity with resistance on HOMA‐IR, glucose‐insulin metabolism, lipid profile. Materials Methods Double‐blind, randomized, placebo‐controlled study conducted North Italy. Fifty‐six patients (10–18 years, Tanner stage ≥3) were randomized to (2000 mg), zinc gluconate (5 galactooligosaccharides (GOS) from plant‐based origin (1000 mg) (TRT) or placebo (PLC)...
Infantile functional gastrointestinal disorders are common in the first months of life. Their pathogenesis remains unknown although evidences suggest multiple independent causes, including gut microbiota modifications. Feeding type, influencing composition intestinal microbiota, could play a significant role pathogenesis. Previous studies supported probiotic supplementation success against colics, however mainly Lactobacillus spp. were tested. The aim this study was to evaluate effectiveness...
Data on metabolic impairments in Cushing's syndrome and GH deficiency all suggest that the relationship between cortisol GH/IGF-I axis obesity may have a role related diseases. However, studies focusing only one of these hormones are often controversial paediatrics. We aimed to explore simultaneous IGF-I with alterations paediatric obesity.Retrospective cross-sectional study tertiary care center. recruited 876 (441 males 435 females) overweight obese children adolescents. A complete clinical...
Abstract Disclosure: V. Antoniotti: None. Mancioppi: A. Solito: C. Partenope: Petri: I. Rabbone: L. Scotti: F. Prodam: Background: In the last decades, pediatric obesity and cardiovascular-associated risks have been relevant challenges. The first treatment against is a lifestyle change, nevertheless, no intervention seems to be effective in evolution of condition, especially long term. Thus, interest non-pharmaceutical as well pharmaceutical compounds growing. Inositol recently studied...
Background: Subclinical hypothyroidism (SH) management in neonatal age opens important questions. We aimed to describe the evolution over time of subclinical diagnosed first three months life a population full-term neonates. Methods: A single-center longitudinal retrospective cohort study tertiary care center was conducted. recruited 32 subjects with SH within life. collected clinical, biochemical, and ultrasound data for every subject at examination six until four years age. Results: total...
Abstract Background and Aims Renal cystic disease (RCD) includes a spectrum of disorders with heterogenous clinical presentation. Among RCD are autosomal dominant polycystic kidney (ADPKD), recessive (ARPKD), ciliopathies, HNF1B-nephropathy, congenital anomalies the kidneys urinary tract (CAKUT). Diagnosis is based on criteria, yet, given extreme genetic heterogeneity phenotypic overlap among different conditions, confirmation by testing paramount for correct management recurrence risk...
Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | 1479-6848 (online)
Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | 1479-6848 (online)
Searchable abstracts of presentations at key conferences in endocrinology ISSN 1470-3947 (print) | 1479-6848 (online)