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Randomized Controlled Trial
. 2013 Aug 29;8(8):e73387.
doi: 10.1371/journal.pone.0073387. eCollection 2013.

The effect of lutein supplementation on blood plasma levels of complement factor D, C5a and C3d

Affiliations
Randomized Controlled Trial

The effect of lutein supplementation on blood plasma levels of complement factor D, C5a and C3d

Yuan Tian et al. PLoS One. .

Abstract

Lutein is selectively taken up by the primate retina and plays an important role as a filter for harmful blue light and as an antioxidant. Recent studies have shown that lutein has systemic anti-inflammatory properties. Dietary lutein has been associated with reduced circulating levels of inflammatory biomarkers such as CRP and sICAM. Whether lutein also affects activation of the complement system has not yet been addressed and was the purpose of the study described here. Seventy-two subjects with signs of early macular degeneration were randomly assigned to receive either a 10 mg lutein supplement or a placebo during one year. EDTA blood samples were collected at 0, 4, 8 and 12 months. Complement factor D (CFD), a rate limiting component of the alternative pathway of complement activation and the complement activation products C5a and C3d were determined in the plasma samples by ELISA. A significant 0.11 µg/ml monthly decrease in plasma CFD concentration was observed in the lutein group (p<0.001), resulting in a 51% decrease from 2.3 µg/ml at baseline to 1.0 µg/ml at 12 months. The C5a concentration showed a significant 0.063ng/ml monthly decrease in the lutein group (p<0.001) resulting in a 36% decrease from 2.2ng/ml at baseline to 1.6ng/ml at 12 months. The C3d concentration showed a significant 0.19µg/ml monthly decrease in the lutein group (p=0.004) that gave rise to a 9% decrease from 15.4µg/ml at baseline to 14.4µg/ml at 12 months. In the placebo group we found a significant 0.04 µg/ml monthly decrease in plasma CFD concentration, whereas no changes were observed for C5a and C3d. Lutein supplementation markedly decreases circulating levels of the complement factors CFD, C5a and C3d levels, which might allow a simple method to control this inflammatory pathway of the innate immune system.

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Conflict of interest statement

Competing Interests: This study was sponsored by the Landelijke Stichting voor Blinden en Slechtzienden, the Stichting Nederlands Oogheelkundig Onderzoek, the Macula Degeneratie Fonds and Cognis GmbH. Cognis was a company who made and marketed lutein. They funded the study and prepared the lutein and placebo supplements. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The commercial funder does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.

Figures

Figure 1
Figure 1. Mean relative plasma concentration of complement factor D (CFD) (left), C5a concentration (middle) and C3d (right) in time for the lutein (solid line) and placebo group (dotted line).
Values at baseline were taken as the reference, i.e. 1.0.
Figure 2
Figure 2. Change in serum concentration from baseline to 12 months for C5a (left) and C3d (right) as a function of the change in CFD concentration from baseline to 12 months (r=0.37, p=0.004 and r=0.18, p=0.16 respectively).

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