Abstract

Ferrous sulphate (FS) is a cost effective, readily available iron supplement for iron deficiency (ID). The pro-oxidant effect of oral ferrous iron is known to induce inflammation, causing gastric side-effects and resulting in poor compliance. Curcumin is a potent antioxidant and has also been shown to exhibit iron chelation in-vitro, although it is not established whether these effects are retained in-vivo. The aim of this study was therefore to assess the influence of a formulated bioavailable form of curcumin (HydroCurcTM; 500 mg) on acute iron absorption and status in a double blind, placebo-controlled randomized trial recruiting 155 healthy participants (79 males; 26.42 years ± 0.55 and 76 females; 25.82 years ± 0.54). Participants were randomly allocated to five different treatment groups: iron and curcumin placebo (FS0_Plac), low dose (18 mg) iron and curcumin placebo (FS18_Plac), low dose iron and curcumin (FS18_Curc), high dose (65 mg) iron and curcumin placebo (FS65_Plac), and high dose iron and curcumin (FS65_Curc). Participants were provided with the supplements according to their relevant treatment groups at baseline (0 min), and blood collection was carried out at 0 min and at 180 min following supplementation. In the treatment groups, significant difference was observed in mean serum iron between baseline (0 min) and at end-point (180 min) (F (1, 144) = 331.9, p < 0.0001) with statistically significant intra-group increases after 180 min (p < 0.0001) in the FS18_Plac (8.79 µmol/L), FS18_Curc (11.41 µmol/L), FS65_Plac (19.09 µmol/L), and FS65_Curc (16.39 µmol/L) groups. A significant difference was also observed between the two time points in serum TIBC levels and in whole blood haemoglobin (HGB) in the treatment groups, with a significant increase (1.55%/2.04 g/L) in HGB levels from baseline to end-point observed in the FS65_Curc group (p < 0.05). All groups receiving iron demonstrated an increase in transferrin saturation (TS%) in a dose-related manner, demonstrating that increases in serum iron are translated into increases in physiological iron transportation. This study demonstrates, for the first time, that regardless of ferrous dose, formulated curcumin in the form of HydroCurc™ does not negatively influence acute iron absorption in healthy humans.

Highlights

  • IntroductionIron is an essential mineral nutrient that plays a key role in most biological processes necessary to sustain life [1,2]

  • Participant 105 was excluded from further analysis (Figure S1) due to BMI of 49.65 kg/m2, the only BMI that fell in class 3 obese category (≥40 kg/m2 ) [55,56] and the only value detected as 3*IQR or an extreme outlier in SPSS

  • This study utilised curcumin supplement in the form of HydroCurcTM, a formulation consisting of 85% total curcuminoids entrapped in a proprietary delivery system (LipiSperse®) that has been shown to enhance bioavailability in humans [47]

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Summary

Introduction

Iron is an essential mineral nutrient that plays a key role in most biological processes necessary to sustain life [1,2]. ID has been attributed to more than 60% of all anaemia cases worldwide and is associated with reduced life expectancy, altered immune response, developmental delays, and adverse pregnancy outcomes [3,6]. As iron is fundamental for growth and metabolism, ID even without anaemia can lead to impaired cognitive and physical development in children, compromise physical and cognitive performance in adults [3,7,8,9], and has been linked with fatigue [10], impaired quality of life [11], and reduced mood [3,9]

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