Comparative analyses of surrogates of metabolic syndrome in children and adolescents with metabolically healthy obesity vs. metabolically unhealthy obesity according to Damanhoury’s criteria
Abstract
Objectives
Metabolically healthy obesity (MHO) has been reported with varying frequencies in children. The reasons of metabolically healthy phenotype in some obese subjects are unclear. Our aim was to identify the frequency of MHO in obese subjects, to assess the potential associations of demographic characteristics, serum uric acid, alanine transaminase (ALT), pediatric nonalcoholic fatty liver disease fibsosis score probability (PNFS p) with MHO status and to evaluate the differences between MHO and metabolically unhealthy obesity (MUO) with regard to metabolic syndrome surrogates.
Methods
251 consecutive obese subjects (125 females) aged 7–18 years were included. Subjects were classified as having MHO according to Damanhoury’s criteria. Several metabolic variables were measured, PNFS p was calculated by using the formula: z=1.1+(0.34*sqrt(ALT))+ (0.002*ALP)–(1.1*log(platelets)–(0.02*GGT).
Results
Median age of the subjects was 12.5 yr (range: 7.0–17.0 yr). The frequency of MHO was 41 %. Subjects with MHO were significantly younger, had lower waist circumference (WC) and waist height ratio (WHtR) and lower HOMA-IR than those without MHO(p<0.05 for all). Frequencies of hyperuricemia, hypertransaminasemia, hepatosteatosis and PNFS p values≥8 were similar betwen the groups. When putatively influential factors associated with MHO status were assessed with logistic regression analysis, only WC(β=1.03) and HOMA-IR(β=1.166) emerged as significant factors(Nagelkerke R2=0.142). None of the investigated demographic factors were associated with MHO status.
Conclusions
We found a remarkably high frequency of MHO status. Nevertheless, the absence of decreased frequencies of hyperuricemia, hypertransaminasemia and PNFS in subjects with MHO may suggest the need to reconsider the validity of the criteria defining MHO.
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Research funding: None declared.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Informed consent: Informed consent was obtained from all individuals included in this study.
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Ethical approval: The study protocol was approved by the local Ethics Committee (number: 3109).
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- Comparative analyses of surrogates of metabolic syndrome in children and adolescents with metabolically healthy obesity vs. metabolically unhealthy obesity according to Damanhoury’s criteria
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Articles in the same Issue
- Frontmatter
- Original Articles
- Comparison of internet usage and internet addiction scores in healthy children and children with type 1 diabetes mellitus
- Prevalence of nonalcoholic fatty liver disease increased with type 2 diabetes mellitus in overweight/obese youth with polycystic ovary syndrome
- Comparison of regular with NPH insulin vs. premix insulin in children and adolescents with type 1 diabetes in a resources-limited setting: a retrospective data analysis
- Comparative analyses of surrogates of metabolic syndrome in children and adolescents with metabolically healthy obesity vs. metabolically unhealthy obesity according to Damanhoury’s criteria
- Response to vitamin D replacement therapy in obese children and adolescents with vitamin D deficiency: a randomized controlled trial
- Clinical profile of Laron dwarfism – experience from a tertiary care institute in Chennai
- 10.1515/jpem-2022-0462
- Identifying elevated plasma free triiodothyronine levels: age-adapted reference intervals for pediatrics
- Benefits and risks evaluation of recombinant human growth hormone replacement therapy in children with GHD after craniopharyngioma surgery
- Copeptin levels in hospitalized infants and children with suspected vasopressin-dependent disorders: a case series
- Case Reports
- Activating calcium-sensing receptor gene variants in China: a case report of hypocalcaemia and literature review
- Hypoparathyroidism and medium-chain Acyl-CoA dehydrogenase deficiency, an unusual association
- An 11-year-old girl with Autoimmune Polyglandular Syndrome (APS) type 2: a case report and review of literature
- An exceptionally rare case of Cushing’s syndrome caused by ectopic ACTH syndrome due to olfactory neuroblastoma in childhood