TY - JOUR
T1 - Efficacy of myo-inositol and zinc on insulin resistance in a paediatric population with obesity
AU - Antoniotti, Valentina
AU - Partenope, Cristina
AU - Solito, Arianna
AU - Mancioppi, Valentina
AU - Baima, Jessica
AU - Medina, Federico
AU - Dimarakis, Sotirios
AU - Agostini, Alida
AU - Sista, Maria T.
AU - Monzani, Alice
AU - Scotti, Lorenza
AU - Rabbone, Ivana
AU - Prodam, Flavia
AU - Bellone, Simonetta
N1 - Publisher Copyright:
© 2025 John Wiley & Sons Ltd.
PY - 2025/4
Y1 - 2025/4
N2 - Aim: To assess the efficacy of the combined administration of myo-inositol and zinc, a mineral involved in the insulin pathway, in paediatric obesity with insulin resistance on HOMA-IR, glucose-insulin metabolism, and lipid profile. Materials and Methods: Double-blind, randomized, placebo-controlled study conducted in North Italy. Fifty-six patients (10–18 years, Tanner stage ≥3) with obesity and insulin resistance were randomized to myo-inositol (2000 mg), zinc gluconate (5 mg), and galactooligosaccharides (GOS) from plant-based origin (1000 mg) (TRT) or placebo (PLC) containing only GOS from plant-based origin (1000 mg). All patients received an isocaloric diet following the Mediterranean diet style. Data were collected at baseline (V0) and after 3 months (V1). The primary outcome was the insulin resistance index (HOMA-IR). Results: Fifty out of 56 recruited subjects completed the study. TRT improved HDL cholesterol level compared to PLC (p = 0.05) but not insulin resistance. A stratified post hoc analysis was performed by sex, BMI, and subgroups of adherence to the Mediterranean diet. Subjects were divided for obesity grade, fasting insulin (p = 0.0137) and HOMA-IR (p = 0.0273) were lower in TRT than in PLC patients, with a greater effect on severe obesity. No adverse events were detected. Conclusion: Three months of supplementation with myo-inositol and zinc were beneficial on lipid profile and in managing obesity complications at least in subjects with severe phenotype. Thus, myo-inositol and zinc could be used as non-pharmacological agents. This work suggests a long-term study with a larger sample size to enrich the findings.
AB - Aim: To assess the efficacy of the combined administration of myo-inositol and zinc, a mineral involved in the insulin pathway, in paediatric obesity with insulin resistance on HOMA-IR, glucose-insulin metabolism, and lipid profile. Materials and Methods: Double-blind, randomized, placebo-controlled study conducted in North Italy. Fifty-six patients (10–18 years, Tanner stage ≥3) with obesity and insulin resistance were randomized to myo-inositol (2000 mg), zinc gluconate (5 mg), and galactooligosaccharides (GOS) from plant-based origin (1000 mg) (TRT) or placebo (PLC) containing only GOS from plant-based origin (1000 mg). All patients received an isocaloric diet following the Mediterranean diet style. Data were collected at baseline (V0) and after 3 months (V1). The primary outcome was the insulin resistance index (HOMA-IR). Results: Fifty out of 56 recruited subjects completed the study. TRT improved HDL cholesterol level compared to PLC (p = 0.05) but not insulin resistance. A stratified post hoc analysis was performed by sex, BMI, and subgroups of adherence to the Mediterranean diet. Subjects were divided for obesity grade, fasting insulin (p = 0.0137) and HOMA-IR (p = 0.0273) were lower in TRT than in PLC patients, with a greater effect on severe obesity. No adverse events were detected. Conclusion: Three months of supplementation with myo-inositol and zinc were beneficial on lipid profile and in managing obesity complications at least in subjects with severe phenotype. Thus, myo-inositol and zinc could be used as non-pharmacological agents. This work suggests a long-term study with a larger sample size to enrich the findings.
KW - insulin resistance
KW - lipid
KW - nutrition
KW - obesity
KW - paediatric
UR - http://www.scopus.com/inward/record.url?scp=85214673676&partnerID=8YFLogxK
U2 - 10.1111/dom.16185
DO - 10.1111/dom.16185
M3 - Article
SN - 1462-8902
VL - 27
SP - 1932
EP - 1939
JO - Diabetes, Obesity and Metabolism
JF - Diabetes, Obesity and Metabolism
IS - 4
ER -