Abstract
Objective: To determine the oxidative stress and trace element levels in vivo in patients with nutritional rachitism associated with vitamin D deficiency.
Materials and method: A total of 30 patients, 18 males and 12 females, were included in the study. Age, sex, medical history, vital, and physical examination findings of each patient documented at presentation were recorded. Serum calcium, phosphorus, alkaline phosphatase, parathormone, and 25-OH vitamin D levels, as well as oxidant and antioxidant system parameters and trace element levels were studied. After being diagnosed with rachitism, the patients were administered a single dose of 300,000 IU vitamin D by intramuscular injection. The same analyses were repeated post-treatment. Thirty children with normal anthropometric measurements were included as the control group. The analyses described above were performed only once for the control group.
Results: Serum calcium, phosphorus, alkaline phosphatase, parathormone, and 25-OH vitamin D levels were different between the controls and children in the patient group (p<0.001). Analysis of trace element levels demonstrated markedly lower pretreatment zinc levels for the patient group compared to the controls, with a statistically significant difference (p=0.001). Comparison of pretreatment oxidant and antioxidant system markers between the patient and control groups demonstrated higher values for vitamin C, β-carotene, reduced glutathione, and superoxide dismutase in the control group, whereas MDA was higher in the patient group.
Conclusion: The present study demonstrated increased oxidative stress, reduced antioxidant defence system in patients with nutritional rachitism, with reduced oxidative stress and a pronounced improvement in the antioxidant system with vitamin D treatment.
©2012 by Walter de Gruyter Berlin Boston
Articles in the same Issue
- Masthead
- Masthead
- Review article
- The pros and cons of sex steroid priming in growth hormone stimulation testing
- Images in pediatric endocrinology
- Tuber sinerium hamartoma causing precocious puberty in a child
- Original articles
- Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche
- Disorders of sex development among Sudanese children: 5-year experience of a pediatric endocrinology clinic
- Anti-Müllerian hormone levels in serum 1 year after unilateral orchiopexy
- Clinical and genetic analysis of three Chinese patients with steroid 5α-reductase type 2 deficiency
- Apparent mineralocorticoid excess syndrome: report of one family with three affected children
- A decrease in fasting FGF19 levels is associated with the development of non-alcoholic fatty liver disease in obese adolescents
- Acanthosis nigricans predicts the clustering of metabolic syndrome components in Hispanic elementary school-aged children
- Nutritional and metabolic findings in patients with Prader-Willi syndrome diagnosed in early infancy
- Increased endothelial microparticles in obese and overweight children
- The treatment effect of diazoxide on 44 patients with congenital hyperinsulinism
- Hyperprolactinemia in children: clinical features and long-term results
- Oxidant/antioxidant system markers and trace element levels in children with nutritional rickets
- Single-nucleotide polymorphism of the osteoprotegerin gene and its association with bone mineral density in Chinese postmenopausal women
- A case of complete androgen insensitivity syndrome with a novel androgen receptor mutation
- Patient reports
- Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation
- An unusual cause of delayed puberty: Berardinelli-Seip syndrome
- Primary hypogonadism in a case with XLAG syndrome
- Precocious puberty produced by an osteolipoma of the tuber cinereum
- A case of Mayer-Rokitansky-Küster-Hauser syndrome presenting as Graves disease
- Priapism in teenage boys following depot testosterone
- Spontaneous resolution of pituitary apoplexy in a giant boy under 10 years old
- Congenital craniopharyngioma: a case report and literature review
- Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency
- Chylomicron retention disease: report of two cases from a Greek Island
- Cerebellar metastatic papillary thyroid carcinoma in a pediatric patient with complex congenital heart disease
- Hepatic subcapsular steatosis: a rare complication of high dose insulin therapy
- Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemia
- Unusual presentations of a girl with Down syndrome: Van Wyk-Grumbach syndrome
- Short communications
- Cortisol response to the Trier Social Stress Test among Chinese adolescents
- Inhaled fluticasone propionate does not influence salivary cortisol when measured with tandem mass spectrometry
Articles in the same Issue
- Masthead
- Masthead
- Review article
- The pros and cons of sex steroid priming in growth hormone stimulation testing
- Images in pediatric endocrinology
- Tuber sinerium hamartoma causing precocious puberty in a child
- Original articles
- Clinical features suggestive of non-classical 21-hydroxylase deficiency in children presenting with precocious pubarche
- Disorders of sex development among Sudanese children: 5-year experience of a pediatric endocrinology clinic
- Anti-Müllerian hormone levels in serum 1 year after unilateral orchiopexy
- Clinical and genetic analysis of three Chinese patients with steroid 5α-reductase type 2 deficiency
- Apparent mineralocorticoid excess syndrome: report of one family with three affected children
- A decrease in fasting FGF19 levels is associated with the development of non-alcoholic fatty liver disease in obese adolescents
- Acanthosis nigricans predicts the clustering of metabolic syndrome components in Hispanic elementary school-aged children
- Nutritional and metabolic findings in patients with Prader-Willi syndrome diagnosed in early infancy
- Increased endothelial microparticles in obese and overweight children
- The treatment effect of diazoxide on 44 patients with congenital hyperinsulinism
- Hyperprolactinemia in children: clinical features and long-term results
- Oxidant/antioxidant system markers and trace element levels in children with nutritional rickets
- Single-nucleotide polymorphism of the osteoprotegerin gene and its association with bone mineral density in Chinese postmenopausal women
- A case of complete androgen insensitivity syndrome with a novel androgen receptor mutation
- Patient reports
- Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation
- An unusual cause of delayed puberty: Berardinelli-Seip syndrome
- Primary hypogonadism in a case with XLAG syndrome
- Precocious puberty produced by an osteolipoma of the tuber cinereum
- A case of Mayer-Rokitansky-Küster-Hauser syndrome presenting as Graves disease
- Priapism in teenage boys following depot testosterone
- Spontaneous resolution of pituitary apoplexy in a giant boy under 10 years old
- Congenital craniopharyngioma: a case report and literature review
- Growth and hormonal profile from birth to adolescence of a girl with aromatase deficiency
- Chylomicron retention disease: report of two cases from a Greek Island
- Cerebellar metastatic papillary thyroid carcinoma in a pediatric patient with complex congenital heart disease
- Hepatic subcapsular steatosis: a rare complication of high dose insulin therapy
- Infantile malignant osteopetrosis: a rare cause of neonatal hypocalcemia
- Unusual presentations of a girl with Down syndrome: Van Wyk-Grumbach syndrome
- Short communications
- Cortisol response to the Trier Social Stress Test among Chinese adolescents
- Inhaled fluticasone propionate does not influence salivary cortisol when measured with tandem mass spectrometry