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1.
Annals of Pediatric Endocrinology & Metabolism ; : 176-182, 2017.
Article in English | WPRIM | ID: wpr-99769

ABSTRACT

PURPOSE: Precocious puberty has significantly increased recently. While obesity is associated with puberty timing, the relationship between obesity and central precocious puberty (CPP) remains controversial. The purpose of this study was to determine whether insulin resistance is associated with bone age (BA) advancement in girls with CPP. METHODS: We retrospectively analyzed the records of 804 girls referred for puberty evaluation. Anthropometric measurements, BA, sex hormone, sex hormone binding globulin (SHBG), and insulin levels, lipid profiles, and gonadotropin releasing hormone stimulation tests were assessed. Insulin resistance parameters were calculated using the homeostasis model assessment-insulin resistance (HOMA-IR) and quantitative insulin sensitivity check index (QUICKI) models. RESULTS: BA, BA advancement, free estradiol index, insulin, and HOMA-IR increased significantly in girls with high body mass index (BMI) compared with that of girls with low BMI in cases of CPP. HOMA-IR was positively correlated with BA advancement and BMI but negatively correlated with SHBG. QUICKI was negatively correlated with BA advancement and BMI and positively correlated with SHBG. When HOMA-IR increased by 1, the odds for BA advancement increased 120% after adjusting for age and BMI (P=0.033). CONCLUSION: Insulin resistance could be associated with BA advancement in girls with CPP.


Subject(s)
Adolescent , Female , Humans , Body Mass Index , Estradiol , Gonadotropin-Releasing Hormone , Homeostasis , Insulin Resistance , Insulin , Luteinizing Hormone , Obesity , Puberty , Puberty, Precocious , Retrospective Studies , Sex Hormone-Binding Globulin
2.
Annals of Pediatric Endocrinology & Metabolism ; : 125-128, 2017.
Article in English | WPRIM | ID: wpr-45448

ABSTRACT

Heterotaxy syndrome (HS) is a congenital disorder resulting from an abnormal arrangement of visceral organs across the normal left-right axis in the embryonic period. HS is usually associated with multiple anomalies, including defects of the major cardiovascular system and the extracardiovascular system such as intestinal malrotation, abnormal lung lobulation, bronchus anomalies, and pancreatic dysplasia. Although pancreatic dysplasia is occasionally accompanied with HS, the occurrence of diabetes mellitus (DM) due to pancreatic dysplasia in HS is rarely reported. We here report a case involving 13-year-old girl with DM caused by agenesis of the dorsal pancreas and HS diagnosed on the basis of the presence of a double-outlet right ventricle with bilateral pulmonary stenosis and intestinal malrotation with duodenal cyst. Timely diagnosis and treatment with insulin improved glycemic control.


Subject(s)
Adolescent , Female , Humans , Bronchi , Cardiovascular System , Congenital, Hereditary, and Neonatal Diseases and Abnormalities , Diabetes Mellitus , Diagnosis , Double Outlet Right Ventricle , Heterotaxy Syndrome , Insulin , Lung , Pancreas , Pulmonary Valve Stenosis
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