Relationship Between the Levels of Holotranscobalamin and Vitamin B in Children.

Indian J Hematol Blood Transfus

Department of Pediatric Hematology, Ankara Children's Hematology Oncology Hospital, Kurtdereli Sokak, Irfan Bastug Cad. No: 10, 06110 Diskapi, Ankara, Turkey.

Published: December 2017

AI Article Synopsis

  • * A total of 155 children were divided into two groups: those with low vitamin B levels (≤200 pg/mL) and those with normal levels (>200 pg/mL), with average holoTC levels significantly different between the groups.
  • * The research identified an optimum cutoff value for vitamin B at 165 pg/mL, showing a positive correlation with holoTC, but suggested further studies with additional markers like MMA and tHcy are necessary to validate these findings.

Article Abstract

The purpose of this study was to evaluate the relationship between the plasma holoTC and serum vitamin B in children and to identify a cutoff cobalamin values according to holoTC. One hundred and fifty-five children were enrolled into the study. All children were evaluated for hemoglobin, vitamin B, folate, ferritin and holoTC levels. Children were grouped as with low vitamin B level (≤200 pg/mL, group I) and normal vitamin B (>200 pg/mL, group II). Serum vitamin B, and holoTC levels were performed in each patient in the study. In 101 patients with low vitamin B (group I) the mean holoTC was 21.74 ± 1.14 pmol/L. In 54 children with normal vitamin B (group II) mean holoTC was 44.0 ± 2.7 pmol/L ( < 0.01). A ROC curve analysis was performed to delineate the optimum cut-off point for vitamin B level and it was found to be 165 pg/mL with a sensitivity of 70% and specificity of 74%; the area under curve was 0.783 ( < 0.01). Our study displayed a positive correlation between vitamin B and holoTC, and defined an optimum cutoff value for vitamin B as 165 pg/mL. Further studies using the markers both MMA, tHcy and holoTC to confirm the findings are needed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5640542PMC
http://dx.doi.org/10.1007/s12288-017-0789-9DOI Listing

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