Effect of Broccoli Sprouts Homogenate on SS RBC



Status:Completed
Conditions:Other Indications
Therapuetic Areas:Other
Healthy:No
Age Range:18 - Any
Updated:7/11/2015
Start Date:March 2012
End Date:September 2015
Contact:Sonja G Hunter, AAS
Email:sonja.hunter@duke.edu
Phone:919-668-6035

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Physiological Effect of Sulforaphane Obtained From Broccoli Sprouts Homogenates (BSH) on the HbF and Anti-oxidative Capacity of Human Sickle Red Blood Cells (SS RBC)

The overall purpose of this study is to obtain a better understanding of the biological
response of red blood cells to sulforaphane contained in fresh broccoli sprouts that have
been put through a blending process. This study will use commercially available fresh
broccoli sprouts certified by Brassica Protection Products LLC (BroccoSprouts®). This
product can also be purchased at some local grocery stores in the produce section. It is
believed that NRF2, a transcription factor encoded by the NFE2L2 gene, plays a role in the
regulation of defense against oxidative stress. The detrimental accelerated breakdown of
sickle cell disease (SCD) red blood cells (SS RBC) is partially due to reduced
anti-oxidative capacity. Previous analysis of SS RBC microRNAs revealed that a reduced level
of NRF2, the master regulator of anti-oxidative stress capacity, contributes to reduced
resistance to oxidative stress and increased hemolysis; NRF2 also induces fetal hemoglobin
(HbF), which is known to prevent SS RBC sickling.

First, erythroid progenitors from normal and SCD subjects will be tested ex-vivo to find out
how sulforaphane, a natural NRF2 activator, affects the oxidative stress capacity, HbF
expression, and microRNA expression of red cells.

Second, a pilot clinical trial will be conducted to determine the safety and physiological
effects of 3 weeks of daily consumption of broccoli sprout homogenate in a cohort of Hb
SS/SB0 thalassemia adult SCD patients. During this study, subjects RBCs will be assayed for
changes in anti-oxidative stress capacity and microRNA composition in mature SCD red blood
cells.


Inclusion Criteria:

- Diagnosis of Hemoglobin (Hb) SS or Hb Sβ0 thalassemia by electrophoresis

- Age ≥18 years

- Hematocrit (Hct) ≥ 20% and Hb > 6.0 g/dL

- Capacity to understand and sign informed consent and can adhere to the daily regimen
of BSH

Exclusion Criteria:

- RBC transfusion or change in hydroxyurea dose during the 3 months prior to study
entry

- Ongoing pregnancy

- Diabetes

- Renal insufficiency (BUN >21 mg/dL and/or Creatinine >1.4 mg/dL)

- History of allergy to sulfonamides
We found this trial at
1
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2301 Erwin Rd
Durham, North Carolina 27710
919-684-8111
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