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Study of Beet Juice for Patients With Sickle Cell Anemia

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status and phase

Withdrawn
Phase 2

Conditions

Sickle Cell Anemia

Treatments

Drug: beet juice (Unbeetable)

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02162225
Wake-58091
R37HL058091 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The investigators hypothesize that increasing plasma nitrite using dietary nitrate will improve platelet function and red cell deformability and decrease MCHC in patients with sickle cell disease. The investigators will test this hypothesis through administration of daily intake of beetroot juice (Unbeetable - Performance Drink) to patients with sickle cell disease for 28 days. The investigators will evaluate the safety of daily beet root juice intake in patients with sickle cell disease. In addition, the investigators will measure MCHC, red cell deformability, and platelet function (activation and aggregation) in response to daily intake of beet root juice in this patient population.

Full description

Sickle cell disease is caused by dysfunction of a mutant form of hemoglobin which polymerizes under hypoxic conditions, sickling the red blood cell. Sickling makes the cells rigid which contributes to vascular occlusion and much morbidity and mortality. Cycles of sickling and unsickling leads to calcium (Ca) influx which activates the gardos channel which pumps out potassium from the cells. Loss of potassium leads to dehydration, poor deformability, and increased mean corpuscular hemoglobin concentration (MCHC) in red blood cells. Increased MCHC leads to increased polymerization. Thus, a significant therapeutic goal for sickle cell disease has been to decrease MCHC by blocking the Ca-influx induced dehydration.

Rifkind and coworkers have shown that the NO+ donor sodium nitrosoprusside (SNP) can block Ca-induced loss of deformability when normal red blood cells are exposed to Ca and a Ca ionophore. The investigators have preliminary data showing that both NO activity donors SNP and nitrite can partially relieve loss of deformability due to cycles of sickling and unsickling in red cells from patients with sickle cell disease.

Low nitric oxide (NO) bioavailabilty secondary to red cell hemolysis has been proposed to contribute to pathology in sickle cell disease. Low NO could lead to poor protection against Ca-induced potassium loss described above. Another consequence of low NO is likely to be increased platelet activation; sickle cell disease is pro-thrombotic disease. NO reduces platelet aggregation and activation. It has been shown that an acute dietary nitrate intervention can reduce platelet aggregation in healthy volunteers. Nitrate is converted to nitrite which is converted to NO in the body.6 Improved platelet function is likely due to increasing NO bioavailability through the nitrate intervention.

In this pilot study, the safety of Beet Juice intake in patients with sickle cell disease will be evaluated using a self-administered health survey. Physiological effects of the Beet Juice will also be examined and the investigators hypothesize that increasing plasma nitrite using dietary nitrate will improve platelet function and red cell deformability and decrease MCHC in patients with sickle cell disease. The investigators will test this hypothesis through administration of daily intake of Beet Juice to patients with sickle cell disease for 28 days. The investigators will measure MCHC, red cell deformability, and platelet function (activation and aggregation) in response to the intervention.

Sex

All

Ages

19 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • diagnosis of sickle cell anemia (Hb S/S or Hb S/beta thal0)
  • no acute illness at the time of obtaining the study
  • willingness to adhere to the study preparatory procedures including drinking the beet juice product daily
  • willingness to give consent in order to participate

Exclusion criteria

  • less than 19 years in age or older than 65
  • smoke or chew tobacco
  • currently take medications that affect stomach pH
  • atrophic gastritis
  • hypo-or hyperthyroidism
  • Type I or II diabetes
  • history of gout, kidney stones or hypotension
  • pregnant
  • aversion to the study-related testing procedures
  • allergy, sensitivity or aversion to the study beetroot juice beverage
  • suffered an acute sickle cell episode (involving hospitalization or a visit to the emergency room) within the past six months

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Beet Juice
Experimental group
Description:
Volunteers will drink a single 8 ounce bottle of beet juice (Unbeetable) per day for 28 days. On days 1,14, and 28, the juice will be drunk just prior to having blood drawn. Blood will also be drawn 1.5 hours after drinking the juice on days 1,14, and 28.
Treatment:
Drug: beet juice (Unbeetable)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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