Safety, Tolerability, and Pharmacokinetics of β-Cryptoxanthin Supplementation in Healthy Women: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial

Author:

Tan Karen M. L.12ORCID,Chee Jolene1,Lim Kezlyn L. M.1,Ng Maisie13,Gong Min1,Xu Jia1,Tin Felicia1,Natarajan Padmapriya45,Lee Bee Lan5,Ong Choon Nam5,Tint Mya Thway16,Kee Michelle Z. L.1,Müller-Riemenschneider Falk57,Gluckman Peter D.18,Meaney Michael J.19,Kumar Mukkesh13,Karnani Neerja1310,Eriksson Johan G.1461112,Nandanan Bindu13,Wyss Adrian13,Cameron-Smith David114ORCID

Affiliation:

1. Singapore Institute for Clinical Sciences, Agency for Science Technology and Research Singapore, Singapore 117609, Singapore

2. Department of Laboratory Medicine, National University Hospital, Singapore 119074, Singapore

3. Bioinformatics Institute, Agency for Science Technology and Research Singapore, Singapore 138671, Singapore

4. Department of Obstetrics and Gynaecology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore

5. Saw Swee Hock School of Public Health, National University of Singapore, Singapore 117549, Singapore

6. Human Potential Translational Research Program, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore

7. Digital Health Centre, Berlin Institute of Health, Charité—Universitätsmedizin Berlin, 10179 Berlin, Germany

8. Liggins Institute, University of Auckland, Auckland 1023, New Zealand

9. Douglas Mental Health University Institute, McGill University, Montreal, QC H4H 1R3, Canada

10. Department of Biochemistry, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore

11. Department of General Practice and Primary Health Care, University of Helsinki, 00100 Helsinki, Finland

12. Folkhälsan Research Center, 00250 Helsinki, Finland

13. DSM Nutritional Products Ltd., 4001 Basel, Switzerland

14. School of Environmental and Life Sciences, University of Newcastle, Callaghan, NSW 2308, Australia

Abstract

Background: β-cryptoxanthin is a dietary carotenoid for which there have been few studies on the safety and pharmacokinetics following daily oral supplementation. Methods: 90 healthy Asian women between 21 and 35 years were randomized into three groups: 3 and 6 mg/day oral β-cryptoxanthin, and placebo. At 2, 4, and 8 weeks of supplementation, plasma carotenoid levels were measured. The effects of β-cryptoxanthin on blood retinoid-dependent gene expression, mood, physical activity and sleep, metabolic parameters, and fecal microbial composition were investigated. Results: β-cryptoxanthin supplementation for 8 weeks (3 and 6 mg/day) was found to be safe and well tolerated. Plasma β-cryptoxanthin concentration was significantly higher in the 6 mg/day group (9.0 ± 4.1 µmol/L) compared to 3 mg/day group (6.0 ± 2.6 µmol/L) (p < 0.03), and placebo (0.4 ± 0.1 µmol/L) (p < 0.001) after 8 weeks. Plasma all-trans retinol, α-cryptoxanthin, α-carotene, β-carotene, lycopene, lutein, and zeaxanthin levels were not significantly changed. No effects were found on blood retinol-dependent gene expression, mood, physical activity and sleep, metabolic parameters, and fecal microbial composition. Conclusions: Oral β-cryptoxanthin supplementation over 8 weeks lead to high plasma concentrations of β-cryptoxanthin, with no impact on other carotenoids, and was well tolerated in healthy women.

Funder

DSM Nutritional Products Ltd.

Publisher

MDPI AG

Subject

Food Science,Nutrition and Dietetics

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