Funded under the National Recovery and Resilience Plan (NRRP), Mission 4 Component 2 Investment 1.3, Theme 10.
Highlights
Profiling of vulnerable targets (in connection with SPOKE 5) through: a) analyses of existing data in children affected by obesity and ageing population at risk of malnutrition and non-communicable diseases (NCDs) b) screening of socioeconomic factors, lifestyle and dietary habits, environmental factors, food knowledge, nutritional status, body composition, functional status and disability, quality of life, genetic, metagenetic, phenotypic profiles, exposure to endocrine disruptors chemicals (EDCs), immune system functions in children and aging population with malnutrition c) human-derived biological samples analysis (including samples for the gut microbiome structure analysis and function).
Identification of sustainable tailored multidimensional approach including nutritional strategies aimed at reducing malnutrition in target specific populations by exploiting the interactions between environment, food, genotype and phenotype: a) analysis of the positive and negative interactions between lifestyle, socioeconomic status, clinical condition, psychological distress, medical treatment and diet for the implementation of sustainable dietary patterns; b) malnutrition biomarker validation; c) draft of sustainable nutritional protocols (in connection with Spoke 1 and 4).
Systematic evaluation of existing data on nutritional status and critical issues for target specific groups with malnutrition (M8)
Identification and mapping of specific target groups with malnutrition (M24)
Report on lifestyle, socioeconomic status, clinical condition, psychological distress, medical treatment, diet, cultural and environmental determinants of malnutrition in target specific populations (M24)
Evaluation and harmonisation of existing nutritional protocol, dietary guidelines for specific target groups with malnutrition (M10)
New sustainable nutrition protocols for specific target groups with malnutrition (M20)
Inflammatory bowel disease (IBD) is an immune-mediate, multifactorial, chronic, and disabling disorder which includes Crohn’s disease (CD), that may affect any part of the gastrointestinal tract, and ulcerative colitis (UC), that affects the colon. IBD is a common disease with an estimated incidence of UC at 24.3/100000 and CD at 12.7/100000 person years in Europe. Among factors that may affect the response to treatments, the nutritional status, along with malnutrition, may play a major role. Little is known regarding its pathogenesis and a reliable tool for predicting response to treatments, in relation to the nutritional status and disease phenotype, is not available. In fact, while some patients may experience long periods of remission, others may experience an aggressive course. The nutritional status in these patients, at different ages (i.e., transitional age, adulthood, elderly) may have a different impact in determining the outcomes.
At least 150 consecutive active IBD patients will be enrolled at the Fondazione IRCCS Policlinico San Matteo (IBD outpatient clinic), stratifying them into three age categories, namely the transitional age (i.e., 12 to 18 years), adults (18-65 years), and elderly (>65 years). Patients will be included in the study only if these criteria are fulfilled: a) written informed consent; b) >12 years of age; c) confirmed diagnosis of IBD according to international guidelines. Patients will be excluded from the study in case of: a) Inability to conform to the protocol; b) Any subject not able to express/understand the informed consent; c) inconclusive diagnosis of IBD. Disease activity will be assessed with serum and faecal biomarkers, clinical indexes, endoscopy (ileo-colonoscopy with biopsies), and bowel abdominal ultrasound. Morphogram Pro, bioimpedentiometry, Mass-Q gastropack I permeability test, and microbiota sequencing will be assessed at the time of disease flare and 3 months after stable remission, along with clinical indexes and bowel abdominal ultrasound. The time needed to achieve remission will be assessed.
It is expected that a poor nutritional status at baseline is associated with longer time to reaching remission. It is expected that some sociodemographic and clinical factors (e.g., greater disease activity as assessed with endoscopy and bowel abdominal ultrasound) are associated to both a poor nutritional status and a poor disease outcome.