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Omega-3 fatty acids are a potential therapy for patients with sickle cell disease

Nature Reviews Disease Primersvolume 4, Article number: 15 (2018) | Download Citation

We have read with interest the excellent review on sickle cell disease (SCD) recently published in Nature Reviews Disease Primers (Sickle cell disease. Nat. Rev. Dis. Primers 4, 18010 (2018))1. The Primer succinctly highlights the recent advances in the molecular pathology of SCD, medical management options and future challenges. However, the article did not underscore the crucial role of abnormality in the membrane lipids of blood cells in the pathogenesis of the disease, as well as the therapeutic potential of long-chain omega-3 fatty acids demonstrated in pilot and randomized studies2,3,4,5,6.

The authors stated, “HbS polymerization directly or indirectly alters the typical lipid bilayer and proteins of the erythrocyte membrane”; however, they did not mention that the plasma membrane of red blood cells, white blood cells and platelets of patients with SCD has an abnormal fatty acid composition, characterized by decreased levels of docosahexaenoic acid (DHA, 22:6ω3) and eicosapentaenoic acid (EPA, 20:5ω3), and a concomitant increase in arachidonic acid (AA, 20:4ω6)5. These findings suggest that membrane lipid perturbation and its manifestations, including the exposure of phosphatidyl serine on the exterior of red blood cell membranes and the propensity of red blood cells, white blood cells and platelets to adhere and aggregate, is fundamental to SCD pathology.

Tomer et al.2 reported a lower frequency of pain episodes in patients with SCD who were treated with omega-3 fatty acids than in patients treated with placebo (olive oil). Subsequently, Daak et al.5 conducted a large (n = 140) single-centre randomized, double-blind, placebo-controlled trial with omega-3 fatty acids in patients with homozygous sickle cell anaemia (HbSS). The annualized vaso-occlusive crisis (VOC) rate and the rate and length of hospitalizations for VOC were significantly lower in the omega-3 group than in patients who received placebo capsules. We have recently concluded a phase II multi-centre randomized, double-blind, placebo-controlled, parallel-group, dose-finding trial (SCOT) in the United States. Consistent with previous findings, our data reveals a >53% reduction in clinical VOCs in patients with SCD treated with DHA. A detailed protocol of the SCOT trial is provided on the ClinicalTrials.gov website.

These clinical studies provide evidence that omega-3 fatty acids are effective and safe treatment options for patients with SCD. The specific mechanisms through which these fatty acids ameliorate VOCs are yet to be elucidated. Nevertheless, omega-3 fatty acids and their active metabolites have well-substantiated pleiotropic biological actions — anti-inflammatory, inflammation resolving, anti-adhesion, anti-aggregation, vasodilatory and antioxidant7,8,9,10. In addition, there is evidence that abnormality of membrane fatty acids, rheological abnormalities of red blood cells, inflammation and haemolysis in patients with SCD are ameliorated by treatment with omega-3 fatty acids10,11,12,13.

After hydroxycarbamide received approval >20 years ago, only one drug, l-glutamine, has been recently approved for SCD, whereas most drug development programmes have failed to live up to their earlier promise. This is to be expected because of the complex nature of SCD pathophysiology. Hence, a multimodal therapy or a single drug with multiple mechanisms of action may be necessary to achieve clinical effectiveness14,15. The multipronged biological and pleiotropic effects of omega-3 fatty acids could make them a new therapeutic option for patients with SCD.

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SCOT trial: https://clinicaltrials.gov/ct2/show/NCT02973360

References

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    Daak, A. A. et al. Docosahexaenoic and eicosapentaenoic acid supplementation does not exacerbate oxidative stress or intravascular haemolysis in homozygous sickle cell patients. Prostaglandins Leukot Essent. Fatty Acids 89, 305–311 (2013).

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Affiliations

  1. Center of Molecular Biology and Biotechnology (CMBB), Florida Atlantic University, Jupiter, FL, USA

    • Ahmed Daak
    •  & Adrian Rabinowicz
  2. Sancilio Pharmaceuticals Company, Riviera Beach, FL, USA

    • Ahmed Daak
    •  & Adrian Rabinowicz
  3. Lipidomics and Nutrition Research Centre, London Metropolitan University, London, UK

    • Kebreab Ghebremeskel

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Competing interests

A.D. and A.R. are employees of Sancilio Pharmaceuticals Inc (SCI). K.G. declares no competing interests.

Corresponding author

Correspondence to Ahmed Daak.

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https://doi.org/10.1038/s41572-018-0012-9

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