Thyroid function and volume in epileptic children using carbamazepine, oxcarbazepine and valproate

BACKGROUND: The aim of the present study was to investigate the effects of carbamazepine (CBZ), oxcarbazepine (OXC), and valproic acid (VPA) on thyroid function and volume in epileptic children. METHODS: Fifty-three epileptic children (age, 3-17 years) treated with OXC (n = 10), CBZ (n = 12), or VPA (n = 31) at least for 1 year were evaluated in terms of thyroid hormones, thyroid-stimulating hormone (TSH) levels, response to thyrotropin-releasing hormone (TRH) stimulation test, and thyroid volumes. RESULTS: The patients in the OXC and CBZ groups had similar total thyroxin (TT4) and free T4 (fT4) median levels that were significantly lower than those of the VPA group (P < 0.016). Total tri-iodothyrosin median levels were lower in the CBZ group compared to the VPA group (P < 0.016). Basal TSH levels and thyroid volumes were similar in all groups (P > 0.016). One child from the OXC group (10%), one from the CBZ group (%8.3), and six from the VPA group (19.3%) had hypothyroidic status according to the TRH stimulation test. No statistically significant correlations were found between thyroid gland volume and thyroid function variables and between anti-epileptic drug receiving time and thyroid function or thyroid volume, respectively, in any of the groups (P > 0.05). CONCLUSIONS: Thyroid function should be evaluated periodically in children using CBZ, OXC or VPA. The children taking VPA seems to be at greater risk compared to children onr CBZ or OXC therapy. Except for the basal TSH values in the VPA group, the parameters predictive for the subclinical hypothyroid status remain to be evaluated in further studies.     

Role of hemoglobin A1c, duration and puberty on bone mineral density in diabetic children

BACKGROUND: The aim of the present was to determine bone mineral density (BMD) in type 1 diabetic children and the roles of hemoglobin A(1c), disease duration and pubertal stage on BMD changes. METHODS: Fifty-eight patients were investigated: 16 had been newly diagnosed (Diabetes(New)) and 42 were already on follow up (Diabetes(Follow up)). BMD of the lumbar vertebrae, HbA1c(HbA1c(last)), Ca, P, Mg were measured. Mean HbA1c of the previous year (HbA1c(1year)), the whole duration of diabetes (HbA1c(whole)), and diabetic impact index (HbA1c(whole) x diabetes duration) were calculated in the Diabetes(Follow up) group. RESULTS: Mean BMD-Z score (-0.61 +/- 0.99 g/cm(2)) of the whole group was significantly lower than zero. Osteopenia was present in 14 (24.1%), and osteoporosis in three (5.2%). HbA1c(whole) was the most important determinant effecting BMD-Z (r = -0.35, P < 0.05) with the cut-off for osteopenia and osteoporosis being 9.8% and 12.1%, respectively. The cut-off of diabetes duration for osteopenia was 3.6 years and it was more predictive for osteopenia compared to HbA1c(whole). In the Diabetes(New) group, the BMD-Z score of the early pubertal group was significantly lower than those in other pubertal groups. CONCLUSION: BMD is affected in diabetic children, and HbA1c(whole) and diabetes duration are the most important determinants. Pubertal stage is another determinant of BMD, especially in newly diagnosed patients.