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Metabolomic analysis reveals extended metabolic consequences of marginal vitamin B-6 deficiency in healthy human subjects.

Publication ,  Journal Article
Gregory, JF; Park, Y; Lamers, Y; Bandyopadhyay, N; Chi, Y-Y; Lee, K; Kim, S; da Silva, V; Hove, N; Ranka, S; Kahveci, T; Muller, KE ...
Published in: PLoS One
2013

Marginal deficiency of vitamin B-6 is common among segments of the population worldwide. Because pyridoxal 5'-phosphate (PLP) serves as a coenzyme in the metabolism of amino acids, carbohydrates, organic acids, and neurotransmitters, as well as in aspects of one-carbon metabolism, vitamin B-6 deficiency could have many effects. Healthy men and women (age: 20-40 y; n = 23) were fed a 2-day controlled, nutritionally adequate diet followed by a 28-day low-vitamin B-6 diet (<0.5 mg/d) to induce marginal deficiency, as reflected by a decline of plasma PLP from 52.6±14.1 (mean ± SD) to 21.5±4.6 nmol/L (P<0.0001) and increased cystathionine from 131±65 to 199±56 nmol/L (P<0.001). Fasting plasma samples obtained before and after vitamin B6 restriction were analyzed by (1)H-NMR with and without filtration and by targeted quantitative analysis by mass spectrometry (MS). Multilevel partial least squares-discriminant analysis and S-plots of NMR spectra showed that NMR is effective in classifying samples according to vitamin B-6 status and identified discriminating features. NMR spectral features of selected metabolites indicated that vitamin B-6 restriction significantly increased the ratios of glutamine/glutamate and 2-oxoglutarate/glutamate (P<0.001) and tended to increase concentrations of acetate, pyruvate, and trimethylamine-N-oxide (adjusted P<0.05). Tandem MS showed significantly greater plasma proline after vitamin B-6 restriction (adjusted P<0.05), but there were no effects on the profile of 14 other amino acids and 45 acylcarnitines. These findings demonstrate that marginal vitamin B-6 deficiency has widespread metabolic perturbations and illustrate the utility of metabolomics in evaluating complex effects of altered vitamin B-6 intake.

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Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2013

Volume

8

Issue

6

Start / End Page

e63544

Location

United States

Related Subject Headings

  • Young Adult
  • Vitamin B 6 Deficiency
  • Vitamin B 6
  • Pyridoxal Phosphate
  • Proline
  • Metabolomics
  • Male
  • Ketoglutaric Acids
  • Humans
  • Glutamine
 

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Gregory, J. F., Park, Y., Lamers, Y., Bandyopadhyay, N., Chi, Y.-Y., Lee, K., … Jones, D. P. (2013). Metabolomic analysis reveals extended metabolic consequences of marginal vitamin B-6 deficiency in healthy human subjects. PLoS One, 8(6), e63544. https://doi.org/10.1371/journal.pone.0063544
Gregory, Jesse F., Youngja Park, Yvonne Lamers, Nirmalya Bandyopadhyay, Yueh-Yun Chi, Kichen Lee, Steven Kim, et al. “Metabolomic analysis reveals extended metabolic consequences of marginal vitamin B-6 deficiency in healthy human subjects.PLoS One 8, no. 6 (2013): e63544. https://doi.org/10.1371/journal.pone.0063544.
Gregory JF, Park Y, Lamers Y, Bandyopadhyay N, Chi Y-Y, Lee K, et al. Metabolomic analysis reveals extended metabolic consequences of marginal vitamin B-6 deficiency in healthy human subjects. PLoS One. 2013;8(6):e63544.
Gregory, Jesse F., et al. “Metabolomic analysis reveals extended metabolic consequences of marginal vitamin B-6 deficiency in healthy human subjects.PLoS One, vol. 8, no. 6, 2013, p. e63544. Pubmed, doi:10.1371/journal.pone.0063544.
Gregory JF, Park Y, Lamers Y, Bandyopadhyay N, Chi Y-Y, Lee K, Kim S, da Silva V, Hove N, Ranka S, Kahveci T, Muller KE, Stevens RD, Newgard CB, Stacpoole PW, Jones DP. Metabolomic analysis reveals extended metabolic consequences of marginal vitamin B-6 deficiency in healthy human subjects. PLoS One. 2013;8(6):e63544.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2013

Volume

8

Issue

6

Start / End Page

e63544

Location

United States

Related Subject Headings

  • Young Adult
  • Vitamin B 6 Deficiency
  • Vitamin B 6
  • Pyridoxal Phosphate
  • Proline
  • Metabolomics
  • Male
  • Ketoglutaric Acids
  • Humans
  • Glutamine