Frequency of the E23K polymorphism of the KCNJ11 gene in children born small for gestational age and its influence on auxological and metabolic parameters in the prepubertal period
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Renata Stawerska
Abstract
Background: The E23K variant of the KCNJ11 gene is possibly responsible for changes in insulin secretion during the fetal life. We tried to assess the influence of the E23K variant on birth weight and metabolic profile in prepubertal children born small for gestational age (SGA).
Subjects: One hundred and twenty-three SGA and 132 born appropriate for gestational age (AGA) children were genotyped for the E23K variant. Lipids, glucose, and insulin concentrations during oral glucose tolerance test were assessed in 112 SGA prepubertal children.
Results: There were no significant differences between the frequency of the E23K variant in SGA and AGA children. In SGA children with E23K, the mean birth weight was significantly higher than in the E23E group. Body mass index, glucose, insulin, and lipids were not different between the E23K, E23E, and K23K groups.
Conclusions: The higher birth weight in SGA children with the E23K variant may be related to higher insulin concentrations in the fetal period. The E23K variant did not affect metabolic disorders in prepubertal SGA children.
This study was supported by funds from the Ministry of Scientific Research and Information Technology of Poland, project no. 2751/P01/2007/32.
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©2013 by Walter de Gruyter Berlin Boston
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- Meetings
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Articles in the same Issue
- Masthead
- Masthead
- Editorial
- Success has many fathers, failure is orphan
- Review Article
- Normosmic idiopathic hypogonadotropic hypogonadism: update on the genetic background and future challenges
- Original Articles
- Temporary brittle bone disease: association with intracranial bleeding
- Asymmetric dimethylarginine (ADMA) and L-arginine levels in children with glycogen storage disease type I
- Application of liquid chromatography-tandem mass spectrometry in the diagnosis and follow-up of maple syrup urine disease in a Chinese population
- The role of uncoupling protein 2 and 3 genes polymorphism and energy expenditure in obese Indonesian children
- Thyroid dysfunctions of prematurity and their impacts on neurodevelopmental outcome1)
- Frequency of the E23K polymorphism of the KCNJ11 gene in children born small for gestational age and its influence on auxological and metabolic parameters in the prepubertal period
- Reference intervals for serum thyroid hormones in preterm hospitalized infants1)
- The clinical and biochemical presentation of vitamin D deficiency and insufficiency in children and adolescents
- A risk score for identifying overweight adolescents with dysglycemia in primary care settings1)
- Thyroid function and morphology in overweight and obese children and adolescents in a Chinese population
- Propionic acidaemia: demographic characteristics and complicationsa
- Negative correlation between serum IL-6 level and cardiorespiratory fitness in 10- to 11-year-old boys with increased BMI
- Penile length and genital anomalies in Egyptian male newborns: epidemiology and influence of endocrine disruptors
- Efficacy of vitamin D loading doses on serum 25-hydroxy vitamin D levels in school going adolescents: an open label non-randomized prospective trial
- Characteristics of infants admitted with hypoglycemia to a neonatal unit
- Increasing thyroid-stimulating hormone is associated with impaired glucose metabolism in euthyroid obese children and adolescents
- The role of FTO genotype on eating behavior in obese Sardinian children and adolescents
- Prevalence of multiple forms of autoimmunity in Egyptian patients with Turner syndrome: relation to karyotype
- A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigree
- Patient Reports
- Pseudohypoparathyroidism type Ia: a novel GNAS mutation in a Brazilian boy presenting with an early primary hypothyroidism
- Diabetic ketoacidosis with cerebral hemorrhage and alpha coma in an adolescent female
- A novel mutation in thyrotropin (thyroid-stimulating hormone) gene in congenital hypothyroidism
- Citric acid as the last therapeutic approach in an acute life-threatening metabolic decompensation of propionic acidaemia
- A case of autosomal dominant osteopetrosis type II with a novel TCIRG1 gene mutation
- The interpretation of color – an endocrine cause of skin discoloration mimicking cyanosis
- Novel heterozygous thyrotropin receptor mutation presenting with neonatal hyperthyrotropinaemia, mild thyroid hypoplasia and absent uptake on radioisotope scan
- Turner Syndrome and apparent absent uterus: a case report and review of the literature
- 10.1515/jpem-2012-0133
- Vaginal bleeding in a 4-month-old preterm girl: extreme minipuberty mimicking central precocious puberty
- A rare case of isolated Cushing syndrome in a 3-month-old boy
- Letters to the Editors
- Gynecomastia in puberty is usually asymptomatic and regresses spontaneously
- Is endometriosis ultimately the end result of the interplay between interferon-γ (IFN-γ) and the HOXA10 gene network?
- Does treatment with L-selenomethionine reduce thyroid volume in euthyroid children with autoimmune thyroiditis?
- Meetings
- Meetings Calendar