Macroalgae Consumption - a Pilot Study

Sponsor
University of Bergen (Other)
Overall Status
Completed
CT.gov ID
NCT05940727
Collaborator
Institute of Marine Research (Other)
49
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2
12
4.1

Study Details

Study Description

Brief Summary

In this study, the aim is to investigate the food safety of macroalgae. There will be an analysis of macroalgae products for the concentration of cadmium, inorganic arsenic, and iodine in macroalgae, as well as measure the status of these elements in consumers. An investigation of the thyroid function of macroalgae consumers and the use of metabolomics to explore which biological changes occur when consuming seaweed and kelp and when the consumer excludes macroalgae from their diet will be performed.

Condition or Disease Intervention/Treatment Phase
  • Other: Habitual macroalgae consumption
  • Other: No macroalgae consumption
N/A

Detailed Description

A group of consumers of macroalgae will be recruited to investigate their macroalgae intake and iodine, cadmium, and inorganic arsenic status and thyroid function. Iodine, cadmium, and inorganic arsenic have been selected since these elements have been described as relatively high in a previously published report from Norway. The goal is to recruit consumers of brown algae - especially kelp, and certain types of red algae, as these were the species with the highest content of iodine, cadmium, and arsenic, described in a previous publication. The participants will be asked to abstain from macroalgae for 6 weeks and again examine iodine status, cadmium and arsenic exposure, and thyroid function after the cessation period. A withdrawal period of 6 weeks has been chosen on the basis that it is calculated 6-8 weeks after Levaxin treatment for hypothyroidism before a new equilibrium can be expected and the effect of treatment on TSH can be assessed.

This study will provide new insight into the status of iodine, cadmium, and inorganic arsenic that macroalgae consumers have in urine and thyroid function after regular macroalgae consumption and after cessation of macroalgae intake. In addition, the study will provide descriptive data on macroalgae consumption, how it is eaten, how often, and how much. This can provide critical knowledge to the national and European authorities for food safety and public health advisers to evaluate the food safety of macroalgae.

Study Design

Study Type:
Interventional
Actual Enrollment :
49 participants
Allocation:
Non-Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Macroalgae Consumption - a Pilot Study
Actual Study Start Date :
Jan 1, 2022
Actual Primary Completion Date :
Dec 15, 2022
Actual Study Completion Date :
Jan 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Usual macroalgae consumption

Crossover design with habitual macroalgae consumption at baseline

Other: Habitual macroalgae consumption
The participant have a habitual macroalgae consumption at baseline.

Other: No macroalgae consumption
The participants exclude any macroalgae products from their diet

Experimental: Cessation of macroalgae consumption

Cessation of macroalgae consumption as an experimental intervention.

Other: Habitual macroalgae consumption
The participant have a habitual macroalgae consumption at baseline.

Other: No macroalgae consumption
The participants exclude any macroalgae products from their diet

Outcome Measures

Primary Outcome Measures

  1. Consumption of macroalgae products [Through study completion, on average 6 weeks]

    Assess the dietary consumption of macroalgae in consumers in the Bergen and Oslo area by 24hr recall and food frequency questionnaire

  2. Levels of iodine, cadmium and inorganic arsenic in macroalgae products [Through study completion, on average 6 weeks]

    Analyse the levels of iodine, cadmium and inorganic arsenic in macroalgae products used by the participants

Secondary Outcome Measures

  1. Levels of iodine [6 weeks]

    Analyse the levels of iodine in urine after intervention/usual macroalgae consumption

  2. Levels of cadmium in urine [6 weeks]

    Analyse the levels of cadmium urine after intervention/usual macroalgae consumption

  3. Levels of inorganic arsenic in urine [6 weeks]

    Analyse the levels of inorganic arsenic in urine after intervention/usual macroalgae consumption

  4. Levels of creatinine in urine [6 weeks]

    Analyse the of creatinine in urine after intervention/usual macroalgae consumption

  5. Thyroid function measure by thyroid-stimulating hormon [6 weeks]

    Measurement of thyroid-stimulating hormon (TSH) in serum after intervention/usual macroalgae consumption

  6. Thyroid function measure by ree-triiodinetyronin [6 weeks]

    Measurement of free-triiodinetyronin (fT3) in serum after intervention/usual macroalgae consumption

  7. Thyroid function measure by free thyroxine [6 weeks]

    Measurement of free thyroxine (fT4) in serum after intervention/usual macroalgae consumption

  8. Thyroid function measure by Thyroid peroxidase antibody [6 weeks]

    Measurement of Thyroid peroxidase antibody (TPOAb) in serum after intervention/usual macroalgae consumption

  9. Thyroid function measured by thyroglobulin [6 weeks]

    Measurement of thyroglobulin (Tg) in serum after intervention/usual macroalgae consumption

  10. Thyroid function [6 weeks]

    Measurement of thyroid-stimulating hormon (TSH), free-triiodinetyronin (fT3), free thyroxine (fT4), Thyroid peroxidase antibody (TPOAb), thyroglobulin (Tg) in serum after intervention/usual macroalgae consumption

  11. Metabolic changes [6 weeks]

    Measurement of metabolic changes by non-targeted metabolomics after intervention/usual macroalage consumption

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • adults

  • weekly consumer of macroalgae

Exclusion Criteria:
  • pregnant

  • known disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Bergen Bergen Norway 5021

Sponsors and Collaborators

  • University of Bergen
  • Institute of Marine Research

Investigators

  • Principal Investigator: Inger Aakre, PhD, Institute of Marine Research

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Bergen
ClinicalTrials.gov Identifier:
NCT05940727
Other Study ID Numbers:
  • 332865
First Posted:
Jul 11, 2023
Last Update Posted:
Jul 11, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Bergen

Study Results

No Results Posted as of Jul 11, 2023