Abstract
Objectives
A connection between thyroid hormones (THs) and diverse metabolic pathways has been reported. We evaluated thyroid function and tissue sensitivity to THs in children and adolescents with T1D in comparison to euthyroid controls. Additionally, we investigate whether a relationship exists between sensitivity indices and metabolic parameters.
Methods
A retrospective analysis was conducted on 80 pediatric patients diagnosed with T1D. Clinical parameters, TSH, FT3, FT4, and the presence of MS were documented. Additionally, indices of peripheral sensitivity (FT3/FT4 ratio) and central sensitivity (TSH index, TSHI; TSH T4 resistance index, TT4RI; TSH T3 resistance index, TT3RI) were assessed. Thirty healthy subjects were considered as controls.
Results
The overall prevalence of MS was 7.27 %, with MS identified in 8 out of 80 (10 %) T1D subjects; none of the controls manifested MS (p<0.01). No significant differences were observed in indexes of tissue sensitivity to THs between subjects with or without MS (all p>0.05). Correlations between THs and indexes of THs tissue sensitivity and metabolic parameters in controls and T1D patients were noted.
Conclusions
This study affirms a heightened prevalence of MS in children with T1D compared to controls and underscores the potential role of THs in maintaining metabolic equilibrium.
Acknowledgments
The authors thank Dr. N. Bladen for English revision. Valeria Calcaterra and Chiara Mameli contributed equally to this work.
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Research ethics: This study was authorized by the local Review Board (Milano Area 1, Protocol number n. 2021/ST/207) and adhered to the principles of the 1975 Declaration of Helsinki, as revised in 2008.
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Informed consent: All participants, or their legal guardians, provided written consent after being informed about the nature of the study.
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Author contributions: VC, CM, GZ conceptualized and designed the study, reviewed and revised the manuscript, and approved the final manuscript as submitted; AD performed statistical analysis, drafted the initial manuscript, and approved the final manuscript as submitted. MM, LS, FN, FCR, AP, AB drafted the initial manuscript, and approved the final manuscript as submitted.
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Competing interests: The authors report no conflict of interest. The authors have no relevant financial or non-financial interests to disclose.
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Research funding: None declared.
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Data availability: All data are reported in the paper.
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© 2024 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Review
- The effect of GnRH analog treatment on BMI in children treated for precocious puberty: a systematic review and meta-analysis
- Original Articles
- Association of hepatokines with markers of endothelial dysfunction and vascular reactivity in obese adolescents
- Evaluation of cardiac electrophysiological features in patients with premature adrenarche
- Growth hormone treatment in children with short stature: impact of the diagnosis on parents
- Ovarian reserve and fertility parameters in post-pubertal females with congenital adrenal hyperplasia: a case-control study
- Early change of retinal nerve fiber layer in children with type 1 diabetes mellitus in northern China
- Investigating the connection among thyroid function, sensitivity to thyroid hormones, and metabolic syndrome in euthyroid children and adolescents affected by type 1 diabetes
- Surgical treatment of secondary hyperparathyroidism in children with chronic kidney disease. Experience in 19 patients
- Short Communication
- Decline in case rates of youth onset type 2 diabetes in year three of the COVID-19 pandemic
- Letters to the Editor
- The effect of phenylketonuria on family quality of life
- Struggle for the future health of adolescent patients with phenylketonuria and parents with a sick child due to the economic crisis
- Case Reports
- A new onset drug induced diabetes mellitus presenting with diabetic ketoacidosis in a child undergoing treatment for B cell acute lymphoblastic leukemia. A case report and review of literature
- Late diagnosis of the X-linked MCT8 deficiency (Allan–Herndon–Dudley syndrome) in a teenage girl with primary ovarian insufficiency
- An infant developing hypercalcemia and hypophosphatemia due to the use of exclusively almond milk
- New data supporting that early diagnosis and treatment are possible and necessary in intracellular cobalamin depletion: the case of transcobalamin II deficiency
Articles in the same Issue
- Frontmatter
- Review
- The effect of GnRH analog treatment on BMI in children treated for precocious puberty: a systematic review and meta-analysis
- Original Articles
- Association of hepatokines with markers of endothelial dysfunction and vascular reactivity in obese adolescents
- Evaluation of cardiac electrophysiological features in patients with premature adrenarche
- Growth hormone treatment in children with short stature: impact of the diagnosis on parents
- Ovarian reserve and fertility parameters in post-pubertal females with congenital adrenal hyperplasia: a case-control study
- Early change of retinal nerve fiber layer in children with type 1 diabetes mellitus in northern China
- Investigating the connection among thyroid function, sensitivity to thyroid hormones, and metabolic syndrome in euthyroid children and adolescents affected by type 1 diabetes
- Surgical treatment of secondary hyperparathyroidism in children with chronic kidney disease. Experience in 19 patients
- Short Communication
- Decline in case rates of youth onset type 2 diabetes in year three of the COVID-19 pandemic
- Letters to the Editor
- The effect of phenylketonuria on family quality of life
- Struggle for the future health of adolescent patients with phenylketonuria and parents with a sick child due to the economic crisis
- Case Reports
- A new onset drug induced diabetes mellitus presenting with diabetic ketoacidosis in a child undergoing treatment for B cell acute lymphoblastic leukemia. A case report and review of literature
- Late diagnosis of the X-linked MCT8 deficiency (Allan–Herndon–Dudley syndrome) in a teenage girl with primary ovarian insufficiency
- An infant developing hypercalcemia and hypophosphatemia due to the use of exclusively almond milk
- New data supporting that early diagnosis and treatment are possible and necessary in intracellular cobalamin depletion: the case of transcobalamin II deficiency