The utility of neonatal dried blood spots for the assessment of neonatal vitamin D status.

Evidence suggests that low concentrations of 25-hydroxyvitamin D(3) (25OHD3) during gestation may be associated with a range of adverse health outcomes in later life. Retrospective estimation of perinatal vitamin D status using questionnaires is extremely unreliable and stored serum samples are rarely available. We aimed to validate the use of dried blood spots (DBS) to estimate perinatal vitamin D status and to determine whether inter-group differences in cord serum 25OHD3 are reflected in DBS. We examined 25OHD3 in 4-year-old frozen cord sera and matched DBS from neonates born at a hospital in Melbourne, Australia (n = 100). We examined the correlation between these values and also investigated whether the expected seasonal (winter/spring vs. summer/autumn) difference in serum 25OHD3 was reflected in DBS values. 25OHD3 was assayed in triplicate using tandem mass spectroscopy in both a 3 microL sample of cord serum and in matched 3 mm punches from archived DBS. 25OHD3 concentrations in neonatal cord serum and DBS were highly correlated (r = 0.85, P < 0.0001). As expected, serum 25OHD3 concentrations were higher in neonates born in summer/autumn (December to March) vs. winter/spring (April to November) (median 46.6 vs. 23.7 nmol/L, P < 0.0001). A comparable difference was seen in DBS values (17.8 vs. 10.5 nmol/L, P = 0.0001). Archived DBS samples provided a valid measure of perinatal vitamin D status and identified inter-seasonal differences in perinatal 25OHD3 concentrations. They could be used for case-control studies investigating the association between perinatal vitamin D status and later health outcomes.

[1]  P. Mortensen,et al.  A sensitive LC/MS/MS assay of 25OH vitamin D3 and 25OH vitamin D2 in dried blood spots. , 2009, Clinica chimica acta; international journal of clinical chemistry.

[2]  M. Holick,et al.  Prolapsed intervertebral disc , 2008, British medical journal.

[3]  T. Higashi,et al.  Liquid chromatography–tandem mass spectrometric method for the determination of salivary 25-hydroxyvitamin D3: a noninvasive tool for the assessment of vitamin D status , 2008, Analytical and bioanalytical chemistry.

[4]  C. Wagner,et al.  Neonatal vitamin D status at birth at latitude 32°72′: evidence of deficiency , 2007, Journal of Perinatology.

[5]  A. Olshan Meeting Report: The Use of Newborn Blood Spots in Environmental Research: Opportunities and Challenges , 2007, Environmental health perspectives.

[6]  M. Holick Vitamin D deficiency. , 2007, The New England journal of medicine.

[7]  T. Dwyer,et al.  The High Prevalence of Vitamin D Insufficiency across Australian Populations Is Only Partly Explained by Season and Latitude , 2007, Environmental health perspectives.

[8]  L. Bodnar,et al.  High prevalence of vitamin D insufficiency in black and white pregnant women residing in the northern United States and their neonates. , 2007, The Journal of nutrition.

[9]  M. Holick,et al.  Vitamin D Deficiency in a Healthy Group of Mothers and Newborn Infants , 2007, Clinical pediatrics.

[10]  G. Heinze,et al.  Influence of hematocrit and localisation of punch in dried blood spots on levels of amino acids and acylcarnitines measured by tandem mass spectrometry. , 2006, Clinica chimica acta; international journal of clinical chemistry.

[11]  C. Wagner,et al.  Vitamin D deficiency during pregnancy: an ongoing epidemic. , 2006, The American journal of clinical nutrition.

[12]  A. Papadopoulou,et al.  Low Vitamin D Status in Mother-Newborn Pairs in Greece , 2006, Calcified Tissue International.

[13]  C. Wagner,et al.  Nutritional vitamin D status during pregnancy: reasons for concern , 2006, Canadian Medical Association Journal.

[14]  Wielders Jp,et al.  Ernstige vitamine D-deficiëntie bij ruim de helft van de niet-westerse allochtone zwangeren en hun pasgeborenen , 2006 .

[15]  C. Cooper,et al.  Maternal vitamin D status during pregnancy and childhood bone mass at age 9 years: a longitudinal study , 2006, The Lancet.

[16]  P. Rothwell,et al.  Timing of birth and risk of multiple sclerosis: population based study , 2004, BMJ : British Medical Journal.

[17]  R. Yolken,et al.  Low maternal vitamin D as a risk factor for schizophrenia: a pilot study using banked sera , 2003, Schizophrenia Research.

[18]  N. Ozbek,et al.  Significant differences between capillary and venous complete blood counts in the neonatal period. , 2003, Clinical and laboratory haematology.

[19]  Eric Sampson,et al.  DNA Banking for Epidemiologic Studies: A Review of Current Practices , 2002, Epidemiology.

[20]  Elina Hyppönen,et al.  Intake of vitamin D and risk of type 1 diabetes: a birth-cohort study , 2001, The Lancet.

[21]  J. McGrath,et al.  Does 'imprinting' with low prenatal vitamin D contribute to the risk of various adult disorders? , 2001, Medical hypotheses.

[22]  J. Haddad,et al.  Assessment of the free fraction of 25-hydroxyvitamin D in serum and its regulation by albumin and the vitamin D-binding protein. , 1986, The Journal of clinical endocrinology and metabolism.

[23]  F. Glorieux,et al.  Vitamin D supplementation during pregnancy: effect on neonatal calcium homeostasis. , 1986, The Journal of pediatrics.

[24]  C. Lamberg‐Allardt,et al.  25-Hydroxyvitamin D concentrations in maternal and cord blood at delivery and in maternal blood during lactation in Finland. , 1984, Human nutrition. Clinical nutrition.

[25]  F. Glorieux,et al.  Vitamin D metabolism in preterm infants: serum calcitriol values during the first five days of life. , 1981, The Journal of pediatrics.

[26]  H. DeLuca,et al.  Vitamin D homeostasis in the perinatal period: 1,25-dihydroxyvitamin D in maternal, cord, and neonatal blood. , 1980, The New England journal of medicine.