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Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease.

Publication ,  Journal Article
Doss, JF; Jonassaint, JC; Garrett, ME; Ashley-Koch, AE; Telen, MJ; Chi, J-T
Published in: PLoS One
2016

Sickle cell disease (SCD) is the most common inherited hemoglobinopathy worldwide. Our previous results indicate that the reduced oxidative stress capacity of sickle erythrocytes may be caused by decreased expression of NRF2 (Nuclear factor (erythroid-derived 2)-like 2), an oxidative stress regulator. We found that activation of NRF2 with sulforaphane (SFN) in erythroid progenitors significantly increased the expression of NRF2 targets HMOX1, NQO1, and HBG1 (subunit of fetal hemoglobin) in a dose-dependent manner. Therefore, we hypothesized that NRF2 activation with SFN may offer therapeutic benefits for SCD patients by restoring oxidative capacity and increasing fetal hemoglobin concentration. To test this hypothesis, we performed a Phase 1, open-label, dose-escalation study of SFN, contained in a broccoli sprout homogenate (BSH) that naturally contains SFN, in adults with SCD. The primary and secondary study endpoints were safety and physiological response to NRF2 activation, respectively. We found that BSH was well tolerated, and the few adverse events that occurred during the trial were not likely related to BSH consumption. We observed an increase in the mean relative whole blood mRNA levels for the NRF2 target HMOX1 (p = 0.02) on the last day of BSH treatment, compared to pre-treatment. We also observed a trend toward increased mean relative mRNA levels of the NRF2 target HBG1 (p = 0.10) from baseline to end of treatment, but without significant changes in HbF protein. We conclude that BSH, in the provided doses, is safe in stable SCD patients and may induce changes in gene expression levels. We therefore propose investigation of more potent NRF2 inducers, which may elicit more robust physiological changes and offer clinical benefits to SCD patients. Trial registration: ClinicalTrials.gov NCT01715480.

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Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2016

Volume

11

Issue

4

Start / End Page

e0152895

Location

United States

Related Subject Headings

  • Sulfoxides
  • RNA, Messenger
  • Oxidative Stress
  • NF-E2-Related Factor 2
  • Middle Aged
  • Male
  • Isothiocyanates
  • Humans
  • Heme Oxygenase-1
  • General Science & Technology
 

Citation

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Doss, J. F., Jonassaint, J. C., Garrett, M. E., Ashley-Koch, A. E., Telen, M. J., & Chi, J.-T. (2016). Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease. PLoS One, 11(4), e0152895. https://doi.org/10.1371/journal.pone.0152895
Doss, Jennifer F., Jude C. Jonassaint, Melanie E. Garrett, Allison E. Ashley-Koch, Marilyn J. Telen, and Jen-Tsan Chi. “Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease.PLoS One 11, no. 4 (2016): e0152895. https://doi.org/10.1371/journal.pone.0152895.
Doss JF, Jonassaint JC, Garrett ME, Ashley-Koch AE, Telen MJ, Chi J-T. Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease. PLoS One. 2016;11(4):e0152895.
Doss, Jennifer F., et al. “Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease.PLoS One, vol. 11, no. 4, 2016, p. e0152895. Pubmed, doi:10.1371/journal.pone.0152895.
Doss JF, Jonassaint JC, Garrett ME, Ashley-Koch AE, Telen MJ, Chi J-T. Phase 1 Study of a Sulforaphane-Containing Broccoli Sprout Homogenate for Sickle Cell Disease. PLoS One. 2016;11(4):e0152895.

Published In

PLoS One

DOI

EISSN

1932-6203

Publication Date

2016

Volume

11

Issue

4

Start / End Page

e0152895

Location

United States

Related Subject Headings

  • Sulfoxides
  • RNA, Messenger
  • Oxidative Stress
  • NF-E2-Related Factor 2
  • Middle Aged
  • Male
  • Isothiocyanates
  • Humans
  • Heme Oxygenase-1
  • General Science & Technology