Abstract
Objective: To examine the relationships of 25-hydroxyvitamin D (25-OHD) levels with the measures of insulin resistance and cardiovascular risk, and identify the clinical factors associated with low 25-OHD in young obese children.
Design and methods: Data from 83 children ages 2–6 years seen for obesity care (clinic latitude 42°N) were analyzed. Insulin resistance [homeostasis model assessment of insulin resistance (HOMA-IR)] and cardiovascular risks were examined in relationship to 25-OHD levels using correlation statistics. χ2 and logistic regression models were applied to identify the factors associated with vitamin D deficiency (25-OHD levels <20 ng/mL) and insufficiency (<30 ng/mL).
Results: Children’s mean age was mean 4.9 years and they were predominantly Hispanic. Mean body mass index (BMI) Z-score was 3.2 and mean HOMA-IR was 2.8. Mean 25-OHD was 30.9 ng/mL (6% <20 ng/mL and 46% 20–29 ng/mL). There were no significant correlations between 25-OHD and BMI (Spearman’s ρ=–0.096, p=0.389), BMI Z-score (Spearman’s ρ=0.104, p=0.350), HOMA-IR (Spearman’s ρ=–0.144, p=0.269), total cholesterol (Spearman’s ρ=–0.028, p=0.833), or triglycerides (Spearman’s ρ=–0.026, p=0.846). Vitamin D deficiency was significantly associated with older age, lower milk intake, and testing in winter months. 25-OHD level <30 ng/mL was associated with older age, African-American and Hispanic race/ethnicity, and testing in winter months. All factors retained significance in a multivariate logistic regression model, with African-American (odds ratio=14.4) and Hispanic (odds ratio=7.2) race/ethnicity being the strongest predictors of 25-OHD levels <30 ng/mL.
Conclusions: In these children, 25-OHD was not associated with insulin resistance or cardiovascular risks. Considering age, race/ethnicity, diet, and season may help identify young obese children needing vitamin D management.
©2013 by Walter de Gruyter Berlin Boston
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Articles in the same Issue
- Masthead
 - Masthead
 - Review Article
 - Clinical and diagnostic characteristics of hyperprolactinemia in childhood and adolescence
 - Images in Pediatric Endocrinology
 - Early occurrence of cerebral white matter abnormality detected in a neonate with salt-wasting congenital adrenal hyperplasia
 - Original Articles
 - Pentoxifylline treatment for protecting diabetic retinopaty in children with type 1 diabetes
 - Absence of diabetes mellitus type 2 in obese children and adolescents in the north of Spain
 - Ceramide mediates inhibition of the Akt/eNOS pathway by high levels of glucose in human vascular endothelial cells
 - Short- and middle-term continuous use of cinacalcet in children on peritoneal dialysis
 - Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 (DUOX2) gene
 - Arginine-guanidinoacetate-creatine pathway in preterm newborns: creatine biosynthesis in newborns
 - The effect of different nutritional states on puberty onset and the expression of hypothalamic Kiss1/kisspepetin
 - Celiac disease and dermatitis herpetiformis in Brazilian twins: a long-term follow-up and screening of their relatives
 - Glucocorticoid receptor expression in whole blood with preterm infants
 - Trends in hospitalizations among children with type 1 diabetes in Spain, 2001–2009
 - Effects of a combined intervention for treating severely obese prepubertal children
 - Vitamin D levels, insulin resistance, and cardiovascular risks in very young obese children
 - Prevalence of metabolic syndrome in children and adolescents — the recent trends in South Korea
 - Elevated visfatin levels in obese children are related to proinflammatory factors
 - Patient reports
 - A clinically euthyroid child with a large goiter due to a thyroglobulin gene defect: clinical features and genetic studies
 - Immune thrombocytopenic purpura in a child with thyroid hormone resistance – a rare presentation
 - Attempted suicide with levothyroxine in an adolescent girl
 - Differentiated thyroid carcinoma in a girl with resistance to thyroid hormone management with triiodothyroacetic acid
 - Brothers with germline PTEN mutations and persistent hypoglycemia, macrocephaly, developmental delay, short stature, and coagulopathy
 - DEND syndrome due to V59A mutation in KCNJ11 gene: unresponsive to sulfonylureas
 - Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation
 - Mild form of 3-methylglutaconic aciduria type IV and mutation in the TMEM70 genes
 - Conn syndrome and Crohn disease in a pediatric case: an interesting parallel
 - Adolescent ischemic stroke associated with anabolic steroid and cannabis abuse
 - Anorexia nervosa in a patient with congenital adrenal hyperplasia
 - Severe hypothalamopituitary dysfunction accompanied by influenza-associated encephalopathy: report of two pediatric cases
 - Octreotide-induced hepatitis in a child with persistent hyperinsulinemia hypoglycemia of infancy
 - Hepatitis in an infant treated with octreotide for congenital hyperinsulinism
 - Letters to the Editor
 - Delayed cord clamping in full-term neonates: is it time for outlining exclusion criteria?
 - And what about cord blood cardiac troponin I (cTnI) levels as an inclusion criterion for therapeutic hypothermia after perinatal asphyxia?
 - Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD
 - Association of the interferon-γ (IFN-γ) gene polymorphism with endometriosis: is epidermal growth factor (EGF) the key-mediator?