Beta-cryptoxanthin Supplement: Absorption and Function (BETA+)

Beta-Cryptoxanthin (BCX) Supplementation and Circulating Carotenoid Concentrations in Women: A Randomized, Controlled, Double-blinded and 8 Week Parallel Trial

Beta-cryptoxanthin (BCX) is a naturally occurring member of the carotenoid family, found in a wide range of fruits and vegetables. The unique biological functions of BCX have not been well-established, although BCX, like other members of the carotenoids have antioxidant functions. BCX, may also serve as a precursor of Vitamin A. Vitamin A has a wide range of functions including maintain immunity, vision, growth and development. Whilst not specific for BCX, epidemiological studies indicate that dietary intake of carotenoids may be of benefit in maintaining cognitive health and reducing stress via its antioxidant, anti-inflammatory and immunomodulatory properties. This pilot study aims to establish the relationship between supplemental dose and circulating concentrations of BCX and related carotenoids in circulation. Results obtained from this study will provide greater insight of bioavailability and carotenoid metabolism, necessary for larger supplementation in selected target populations.

Study Overview

• Status: Completed
• Conditions: Beta-cryptoxanthin Supplementation
• Intervention / Treatment: Dietary supplement: Beta-cryptoxanthin (BCX)

Detailed Description

In previous Singapore maternal and child health cohort study, Growing up towards healthy outcomes (GUSTO), it established potentially significant health function to be significantly correlated with BCX. At childbirth, mothers' blood concentrations of carotenoids, including α-, β-carotene and BCX were simultaneously measured by ultra-performance liquid chromatography. Unique to the carotenoids, there was a correlation between higher maternal plasma concentrations of BCX with lower rates of depression and reduced anxiety scores during pregnancy for the mother. Furthermore, the concentrations of BCX were uniquely correlated with child neurocognitive function by age 2 years.

Current studies have only been food-based efficacy trials with an increase of dietary BCX intake through BCX-rich foods in humans. There have been no direct assessments of risk associated with BCX exposure, and current evidence in the literature does not identify any consistent, substantial risks for any level of BCX supplementation. Overall, the utility of BCX as a pro-vitamin A is clear, but evidence towards benefits beyond this role is inconsistent.

Hence, this is a pilot study that will aim to examine bioavailability of a novel BCX preparation supplemented at 2 doses (3mg and 6mg daily) versus placebo, consumed once daily in a randomised, doubled-blinded parallel trial, in healthy female subjects of reproductive age.

• Study Type: Interventional
• Enrollment (Actual): 90
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Singapore
  • Singapore, Singapore
    • Singapore Institute for Clinical Sciences

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 21 years to 35 years (ADULT)
• Accepts Healthy Volunteers: Yes
• Genders Eligible for Study: Female

Description

Inclusion Criteria:

1. Women aged 21 - 35 years old, residing in Singapore
2. Body mass index (BMI) between 18.5 to 27.5 kg/m2
3. Subject should not be pregnant or breastfeeding during study period
4. Subject should not be planning to conceive within 3 months from enrolment
5. Subject must voluntarily consent to participate in this study and provide their written informed consent prior to start of study
6. Subject is always willing to comply with study regulations and instructions

Exclusion Criteria:

1. Any current diagnosis or history of cardiovascular, hepatic, renal, metabolic (e.g. diabetes), immunological, gastrointestinal diseases, psychiatric disorders or chronic diseases
2. Participation in another simultaneous clinical study
3. Ongoing adherence to weight reduction diet and/or programs
4. Use of medication and supplementation with other carotenoids reasonable expected to impact on primary outcome (e.g. drug treatment for hyperlipidemia)
5. A history of drug abuse
6. Current smoker or excessive alcohol intake (>4 standard drinks per day)
7. Subject has a known allergy or sensitivity to BCX or any ingredients of the study products provided

Study Plan

How is the study designed?

Design Details

• Primary Purpose: BASIC_SCIENCE
• Allocation: RANDOMIZED
• Interventional Model: PARALLEL
• Masking: TRIPLE

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
EXPERIMENTAL: 3mg BCX supplement; One 3mg BCX capsule + one placebo capsule to be taken once per day for 8 weeks	Dietary supplement: Beta-cryptoxanthin (BCX); Subjects will be randomised into one of the three study treatment arms.
EXPERIMENTAL: 6mg BCX supplement; Two 3mg BCX capsules to be taken once per day for 8 weeks	Dietary supplement: Beta-cryptoxanthin (BCX); Subjects will be randomised into one of the three study treatment arms.
PLACEBO_COMPARATOR: 0mg BCX supplementation; Two placebo capsules to be taken once per day for 8 weeks	Dietary supplement: Beta-cryptoxanthin (BCX); Subjects will be randomised into one of the three study treatment arms.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in plasma concentration of BCX over 8 weeks	Fasting plasma carotenoids concentrations	Baseline, Week 2, Week 4, Week 8

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Height measurement	Height in centimeters (cm)	Baseline
Change in weight	Weight in kilograms (kg)	Baseline, Week 8
Change in Body Mass Index (BMI)	BMI in kg/m^2 (from converted height in centimeters to meters)	Baseline, Week 8
Change in waist circumference	Waist circumference in centimeters (cm)	Baseline, Week 8
Change in body composition - Total body fat	Body fat analysis in percentage (%)	Baseline, Week 8
Changes in General Health Questionnaire (GHQ-12) scores	- GHQ-12 scores for measure of physiological distress	Baseline, Week 8
Change in Pittsburgh Sleep Quality Index (PSQI) scores	- PSQI scores for measures of sleep quality and patterns	Baseline, Week 8
Change in State-Trait Anxiety Inventory (STAI) scores	- STAI scores for measures of anxiety	Baseline, Week 8
Change in Perceived Stress Scale (PSS) scores	- PSS scores for measures of stress perceptions	Baseline, Week 8
Change in Quality of Life Enjoyment and Satisfaction Questionnaire (QLES) scores	- QLES scores for measures of the degree of life satisfaction	Baseline, Week 8
Change in Satisfaction with Life Scale (SLS) scores	- SLS scores for measures of subjective well-being	Baseline, Week 8
Change in Depression Anxiety Stress Scales (DASS) scores	- DASS scores for measures of the negative emotional states of depression, anxiety and stress	Baseline, Week 2, Week 4, Week 8
Change in gut microbiota composition	- Assessed by 16S rRNA gene sequencing of stool sample	Baseline, Week 8
Change in sleep/wake time	- Assessed with 7 consecutive days of total sleep time and wake after sleep onset measured using a wrist worn accelerometer	Baseline, Week 8
Change in physical activity	- Assessed with 7 consecutive days of raw acceleration, steps taken and activity counts measured using a wrist worn accelerometer	Baseline, Week 8

Collaborators and Investigators

• Sponsor: Singapore Institute for Clinical Sciences
• Collaborators: DSM Nutritional Products, Inc.
• Investigators: Principal Investigator: Karen Tan Mei Ling, PhD, Singapore Institute for Clinical Sciences

Study record dates

Study Major Dates

• Study Start (ACTUAL): September 7, 2021
• Primary Completion (ACTUAL): March 31, 2022
• Study Completion (ACTUAL): March 31, 2022

Study Registration Dates

• First Submitted: August 23, 2021
• First Submitted That Met QC Criteria: September 7, 2021
• First Posted (ACTUAL): September 16, 2021

Study Record Updates

• Last Update Posted (ACTUAL): April 13, 2022
• Last Update Submitted That Met QC Criteria: April 5, 2022
• Last Verified: April 1, 2022

More Information

Terms related to this study

• Keywords: Supplementation; Bioavailability; Carotenoids; Beta-cryptoxanthin
• Additional Relevant MeSH Terms: Physiological Effects of Drugs; Micronutrients; Vitamins; Provitamins; Beta-Cryptoxanthin
• Other Study ID Numbers: 2021/00455

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No