Slowly progressive autoimmune diabetes: a clinical model for novel pathways of ß-cell protection

Anno
2020
Proponente Raffaella Buzzetti - Professore Ordinario
Sottosettore ERC del proponente del progetto
LS4_3
Componenti gruppo di ricerca
Componente Categoria
Giuseppe Pugliese Componenti strutturati del gruppo di ricerca / Structured participants in the research project
Maria Gisella Cavallo Componenti strutturati del gruppo di ricerca / Structured participants in the research project
Susanna Morano Componenti strutturati del gruppo di ricerca / Structured participants in the research project
Ernesto Maddaloni Dottorando/Assegnista/Specializzando componente non strutturato del gruppo di ricerca / PhD/Assegnista/Specializzando member non structured of the research group
Vincenzo Trischitta Componenti strutturati del gruppo di ricerca / Structured participants in the research project
Componente Qualifica Struttura Categoria
Carmen Mignogna Specializzando Medicina Sperimentale Altro personale aggregato Sapienza o esterni, titolari di borse di studio di ricerca / Other aggregate personnel Sapienza or other institution, holders of research scholarships
Abstract

Rationale. A consistent group of subjects with autoimmune diabetes (AD) is affected by a slowly progressive form of the disease, known as Latent Autoimmune Diabetes in Adults (LADA). This suggests that progression towards absolute insulin deficiency is not ineluctable. We hypothesize that LADA may offer a novel model to search for endogenous disease modifiers. These may be discovered by looking at differences between LADA and type 1 diabetes (T1D) in humoral features, proteomics, and in the clinical history of disease development.
Aim. To identify novel endogenous pathways of protection from disease progression in AD by carrying out a humoral, proteomic and phenotypic characterization of T1D and LADA.
Methods. In this cross-sectional study we will enroll two groups of subjects affected by AD representing the two extreme phenotypes of the disease: 100 subjects affected by T1D with no detectable C-peptide and 100 subjects affected by LADA with preserved ß-cell function after 5 years from the diagnosis. Novel candidate autoantibodies possibly related to lower autoimmune load (IA-2JM(601-630)) and quantitative proteomic profiles will be measured. Quantitative proteomic profiles will be compared between 50 T1D and 50 LADA matched for gender, kidney function and metabolic control by propensity score matching. Clinical history of the three years before diabetes development, including infectious diseases, allergies, surgery, pharmacotherapy, will be collected. Differences between the three groups will be evaluated and association with clinical features will be tested.
Novelty. We will investigate mechanisms of natural protection from AD by taking advantage from a population with the unique features of slow diabetes progression, free from insulin dependence, despite the presence of autoimmunity. This proposal is novel in that the heterogeneity of AD is proposed for the first time as an opportunity for understanding AD, with potential applications to precision medicine.

ERC
LS4_3, LS4_5
Keywords:
DIABETE, MALATTIE AUTOIMMUNI, PROTEOMICA

© Università degli Studi di Roma "La Sapienza" - Piazzale Aldo Moro 5, 00185 Roma