From Metabolic Syndrome to Type 2 Diabetes in Youth

Author:

Iafusco Dario1,Franceschi Roberto2ORCID,Maguolo Alice3ORCID,Guercio Nuzio Salvatore4,Crinò Antonino5,Delvecchio Maurizio6ORCID,Iughetti Lorenzo7ORCID,Maffeis Claudio3ORCID,Calcaterra Valeria89ORCID,Manco Melania10ORCID

Affiliation:

1. Department of Woman, Child and General and Specialistic Surgery, Regional Center of Pediatric Diabetes, University of Campania “L. Vanvitelli”, 80131 Naples, Italy

2. Pediatric Department, S. Chiara Hospital of Trento, APSS, 38122 Trento, Italy

3. Section of Pediatric Diabetes and Metabolism, Department of Surgery, Dentistry, Pediatrics, and Gynecology, University of Verona, 37129 Verona, Italy

4. Pediatric Unit, Department of Women’s and Children’s Health, S. Maria della Speranza Hospital of Battipaglia, 84091 Salerno, Italy

5. Center for Rare Diseases and Congenital Defects—Fondazione Policlinico Universitario “Agostino Gemelli” IRCCS, 00168 Rome, Italy

6. Metabolic Disorders and Diabetes Unit, “Giovanni XXIII” Children’s Hospital, A.O.U. Policlinico di Bari, 70124 Bari, Italy

7. Department of Medical and Surgical Sciences for Mothers, Children and Adults, Post Graduate School of Pediatrics, University of Modena and Reggio Emilia, 41121 Modena, Italy

8. Department of Internal Medicine, University of Pavia, 27100 Pavia, Italy

9. Pediatric Department, “V. Buzzi” Children’s Hospital, 20154 Milan, Italy

10. Preventive and Predictive Medicine Unit, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy

Abstract

In the frame of metabolic syndrome, type 2 diabetes emerges along a continuum of the risk from the clustering of all its components, namely visceral obesity, high blood pressure and lipids, and impaired glucose homeostasis. Insulin resistance is the hallmark common to all the components and, in theory, is a reversible condition. Nevertheless, the load that this condition can exert on the β-cell function at the pubertal transition is such as to determine its rapid and irreversible deterioration leading to plain diabetes. The aim of this review is to highlight, in the context of metabolic syndrome, age-specific risk factors that lead to type 2 diabetes onset in youth; resume age specific screening and diagnostic criteria; and anticipate potential for treatment. Visceral obesity and altered lipid metabolism are robust grounds for the development of the disease. Genetic differences in susceptibility to hampered β-cell function in the setting of obesity and insulin resistance largely explain why some adolescents with obesity do develop diabetes at a young age and some others do not. Lifestyle intervention with a healthy diet and physical activity remains the pillar of the type 2 diabetes treatment in youth. As to the pharmacological management, metformin and insulin have failed to rescue β-cell function and to ensure long-lasting glycemic control in youth. A new era might start with the approval for use in pediatric age of drugs largely prescribed in adults, such as dipeptidyl peptidase-4 and sodium-dependent glucose transport inhibitors, and of new weight-lowering drugs in the pipeline such as single and multiple agonists of the glucagon-like peptide 1 receptor. The latter drugs can have tremendous impact on the natural history of the disease. By treating diabetes, they will reduce the burden of all the metabolic abnormalities belonging to the syndrome while causing a tremendous weight loss hitherto never seen before.

Funder

Italian Ministry of Health

Publisher

MDPI AG

Subject

Pediatrics, Perinatology and Child Health

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