Serum Levels of Soluble Receptor for Advanced Glycation End Products Are Reduced in Euthyroid Children with Newly Diagnosed Hashimoto's Thyroiditis: A Pilot Study.

Advanced glycation end products Autoimmunity Hashimoto’s thyroiditis Oxidative stress Receptor for advanced glycation end products

Journal

Hormone research in paediatrics
ISSN: 1663-2826
Titre abrégé: Horm Res Paediatr
Pays: Switzerland
ID NLM: 101525157

Informations de publication

Date de publication:
2021
Historique:
received: 07 03 2021
accepted: 20 05 2021
pubmed: 9 7 2021
medline: 27 1 2022
entrez: 8 7 2021
Statut: ppublish

Résumé

No data are available on advanced glycation end products (AGEs) and their soluble receptor (sRAGE) in pediatric patients with Hashimoto's thyroiditis (HT). The present study was aimed to simultaneously evaluate serum levels of sRAGE, AGEs, and advanced oxidation protein products (AOPPs) and investigate the relationships between these oxidative stress markers and clinical and biochemical parameters of thyroid function in euthyroid children with HT. This is a case-control study carried out in a single university hospital center. We enrolled 19 newly diagnosed euthyroid HT pediatric patients (3 M, 16 F; median age 12.44 years, range 6.54-15.81 years) and 16 age-, sex-, and BMI-matched healthy controls (5 M, 11 F; median age 12.83 years, range 5.68-15.07 years). None was on levothyroxine treatment. The exclusion criteria were autoimmune, inflammatory, and infection comorbidities. Patients did not differ significantly from controls with regard to lipid or for anthropometric parameters. sRAGE levels were significantly lower in HT patients (median 414.30 pg/mL, range 307.30-850.30 pg/mL) than in controls (561.30, 273.20-1121.60 pg/mL; p = 0.034). No differences emerged between patients and controls with regard to serum AGEs (124.25 AU/g prot, 71.98-186.72 vs. 133.90, 94.06-200.78 AU/g prot, p = 0.707) and AOPPs (1.13 nmol/mL, 0.62-1.83 vs. 1.17, 0.76-1.42 nmol/mL, p = 0.545). sRAGE levels were decreased in euthyroid children/adolescents at the onset of HT, suggesting that autoimmunity per se seems to play an important role in such a reduction of sRAGE, irrespective of any functional alteration. Children and adolescents suffering from HT may exhibit increased susceptibility to oxidative damage, even when in euthyroid status.

Identifiants

pubmed: 34237741
pii: 000517341
doi: 10.1159/000517341
doi:

Substances chimiques

AGER protein, human 0
Receptor for Advanced Glycation End Products 0

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

144-150

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Tommaso Aversa (T)

Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy.

Rosaria Maddalena Ruggeri (RM)

Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
Endocrine Unit at University Hospital AOU Policlinico "G. Martino", Messina, Italy.

Domenico Corica (D)

Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy.

Maria Teresa Cristani (MT)

Department of Chemical, Biological, Pharmaceutical and Environmental Sciences, University of Messina, Messina, Italy.

Giorgia Pepe (G)

Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy.

Teresa Manuela Vicchio (TM)

Endocrine Unit at University Hospital AOU Policlinico "G. Martino", Messina, Italy.

Angela Alibrandi (A)

Department of Economics, Unit of Statistical and Mathematical Sciences, University of Messina, Messina, Italy.

Francesco Trimarchi (F)

Accademia Peloritana dei Pericolanti, University of Messina, Messina, Italy.

Salvatore Cannavò (S)

Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy.
Endocrine Unit at University Hospital AOU Policlinico "G. Martino", Messina, Italy.

Giovanni Battista Pajno (GB)

Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy.

Malgorzata Gabriela Wasniewska (MG)

Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy.

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