Startseite Vitamin D status and insulin requirements in children and adolescent with type 1 diabetes
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

Vitamin D status and insulin requirements in children and adolescent with type 1 diabetes

  • Ozgul Tunc , Semra Cetinkaya EMAIL logo , Murat Kızılgün und Zehra Aycan
Veröffentlicht/Copyright: 1. November 2011
Journal of Pediatric Endocrinology and Metabolism
Aus der Zeitschrift Band 24 Heft 11-12

Abstract

Background: Vitamin D and its active form are potent immuno­modulators and are known to play an important role in the glucose/insulin metabolism. Studies on type 2 diabetes mellitus (T2DM) have shown that vitamin D increases insulin efficacy; however, there are no studies that define a similar relationship in type 1 diabetes mellitus (T1DM). The aim of this study was to investigate the relation between serum vitamin D levels and the insulin requirement used in children with T1DM.

Subjects and methods: A total of 100 patients with T1DM aged 4.7–19.9 years were included in the study. Serum calcium, phosphorus, alkaline phosphatase, parathyroid hormone, 25-hydroxyvitamin D (25OHD), and 1,25-dihydroxyvitamin D were measured. A serum 25OHD level of <10 ng/mL was accepted as vitamin D deficiency, whereas <20 ng/mL was accepted as vitamin D insufficiency.

Results: We found vitamin D deficiency in 28% and vitamin D insufficiency in 43% of our patients, whereas 29% had normal serum 25OHD levels. The insulin requirement of patients with a serum 25OHD level below 10 ng/mL were significantly higher than those of patients with a serum 25OHD level above 10 ng/mL (p=0.012). This result did not change in those with diabetes duration of over 1 year. There was weak correlation between the daily insulin requirements and serum vitamin D levels (r=–0.212, p=0.032).

Conclusion: We found a significantly higher insulin requirement in T1DM children with decreased serum 25OHD levels and decreased insulin sensitivity. We recommend checking the level of serum 25OHD in children with diabetes and starting treatment if it is deficient/inadequate.


Corresponding author: Semra Cetinkaya, MD, Kozluevler, 3251 Cadde, 2/28, Yasamkent, Ankara TR-06810, Turkey Phone: +90 505 3884403, Fax: +90 312 3170353

Received: 2011-3-10
Accepted: 2011-9-3
Published Online: 2011-11-01
Published in Print: 2011-12-01

©2011 by Walter de Gruyter Berlin Boston

Artikel in diesem Heft

  1. Editorial
  2. Intracranial cysts: large-scale information is needed
  3. Reviews
  4. The endocrine spectrum of intracranial cysts in childhood and review of the literature
  5. Radioiodine treatment in pediatric Graves disease and thyroid carcinoma
  6. Images in Pediatric Endocrinology
  7. Perineal ectopic testis: a rare cause of empty scrotum
  8. Original Articles
  9. Normal thyroid function in young adults who were born very preterm
  10. Does clinical management impact height potential in children with severe acquired hypothyroidism?
  11. Neurodevelopment of preterm infants born at 28 to 36 weeks of gestational age: the role of hypothyroxinemia and long-term outcome at 4 years
  12. Central hypothyroidism following chemotherapy for acute lymphoblastic leukemia
  13. The prevalence of non-alcoholic fatty liver disease and metabolic syndrome in obese children
  14. Retinol binding protein 4 is associated with adiposity-related co-morbidity risk factors in children
  15. Circulating adipocyte fatty acid-binding protein, juvenile obesity, and metabolic syndrome
  16. Obesity and associated cardiovascular risk factors among schoolchildren in Greece: a cross-sectional study and review of the literature
  17. Peptides from adipose tissue in monitoring energy balance in infants
  18. Effectiveness of pentoxifylline on the cross-sectional area of intima media thickness and functions of the common carotid artery in adolescents with type 1 diabetes
  19. Common adipokine features of neonates and centenarians
  20. Congenital adrenal hyperplasia: as viewed by parents of affected children in India – a pilot study
  21. Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V281l mutation in patients with premature pubarche
  22. Contribution of bone turnover markers to bone mass in pubertal boys and girls
  23. Modifiable factors associated with low bone mineral content in underprivileged premenarchal Indian girls
  24. Effect of GnRH analogue on height potential in patients with severe growth hormone insensitivity syndrome treated with IGF-I
  25. Measurement of amino-terminal propeptide of C-type natriuretic peptide in patients with idiopathic short stature or isolated growth hormone deficiency
  26. Growth hormone treatment, final height, insulin-like growth factors, ghrelin, and adiponectin in four siblings with Seckel syndrome
  27. Health promotion intervention in Arab-Israeli kindergarten children
  28. Validation of automatic bone age rating in children with precocious and early puberty
  29. Interrelationship of carpal angle and bone age in children of different generations: a retrospective study
  30. Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell
  31. Use of nocturnal melatonin concentration and urinary 6-sulfatoxymelatonin excretion to evaluate melatonin status in children with severe sepsis
  32. Primary ovarian dysfunction after hematopoietic stem cell transplantation during childhood: busulfan-based conditioning is a major concern
  33. Vitamin D status and insulin requirements in children and adolescent with type 1 diabetes
  34. Patient Reports
  35. Homozygosity for two missense mutations in the leptin receptor gene (P316T;W646C) in a Turkmenian girl with severe early-onset obesity
  36. A 3-year-old girl with Graves’ disease with hypoglycemia following transient adrenal hyporesponsiveness
  37. Papillary carcinoma masquerading as clinically toxic adenoma in very young children
  38. Hyperandrogenism in a set of triplets with modification of clinical course by hyperthyroidism
  39. A case of Langerhans cell histiocytosis with thyroid involvement
  40. Congenital rhabdomyosarcoma, central precocious puberty, hemihypertrophy and hypophosphatemic rickets associated with epidermal nevus syndrome
  41. Precocious puberty and empty sella syndrome in a girl cured of acute lymphoblastic leukemia
  42. Sex of rearing seems to exert a powerful influence on gender identity in the absence of strong hormonal influence: report of two siblings with PAIS assigned different sex of rearing
  43. Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant
  44. Persistent hypoglycemia caused by umbilical arterial catheterization
  45. Congestive heart failure as an initial manifestation of reninoma
  46. Multiple pterygium syndrome: mimicking the findings of Turner syndrome
  47. A neonate with contiguous deletion syndrome in XP21
  48. Kocher-Debré-Sémélaigne syndrome with pericardial effusion
  49. Meetings
  50. Meetings Calendar
Heruntergeladen am 5.9.2025 von https://www.degruyterbrill.com/document/doi/10.1515/JPEM.2011.213/html?lang=de
Button zum nach oben scrollen