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Fibromyalgia Treatment With Enzyme DAO

Primary Purpose

Fibromyalgia

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
fibroDAO®
Placebo
Sponsored by
Centros de Investigación de Nutrición y Salud
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Fibromyalgia focused on measuring Fibromyalgia, Diamine Oxidase, Supplementation, Genetics, Treatment

Eligibility Criteria

30 Years - 59 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Female
  • Age between 30 and 59 years (included)
  • Diagnosis of fibromyalgia
  • Must sign an informed consent
  • Able to follow-up at 2 and 6 months

Exclusion Criteria:

  • Pregnant or possibly pregnant
  • Patients with change of pharmacological treatment in the last 3 months
  • Patients with DAO enzyme treatment
  • Patients diagnosed with other severe diseases (i.e. cancer, cardiovascular disease, autoimmune disease or metabolic disease)
  • Patients with multiple chemical sensitivity

Sites / Locations

  • Hospital Ruber Internacional

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Enzyme DAO administration

Placebo administration

Arm Description

DAO enzyme supplementation for 6 months

Placebo supplementation for 6 months

Outcomes

Primary Outcome Measures

Patient status, progress and outcomes
Change from baseline in fibromyalgia status on the Fibromyalgia Impact Questionnaire (FIQ). The FIQ has10 items. Each item has a maximum possible score of 10. The maximum possible score is 100. A higher score indicates a greater impact of the syndrome.
Sleep quality
Change from baseline in sleep quality on the Pittsburgh Sleep Quality Index (PSQI). The PSQI contains 19 questions scored from 0 (no difficulty) to 3 (severe difficulty). The overall score is from 0 to 21. Higher scores indicate poorer sleep quality.
Pain experience
Change from baseline in pain on the Pain Catastrophizing Scale (PCS). The PCS contains 13 items that are rated on 5-point Likert scales, from 0 (not at all) to 4 (all the time). The minimum total score is 0 and the maximum is 52. A higher score indicates a higher level of catastrophizing.
Extent and severity of eczema
Change from baseline in eczema on the SCORing Atopic Dermatitis (SCORAD). The extension can be scored from 0 to 100, intensity from 0 to 18, and subjective symptoms from 0 to 20. The final score is achieved using the formula A / 5 + 7B / 2 + C.
Impact of headache
Change from baseline in headache on the Headache Impact Test-6 (HIT-6). HIT-6 has six questions, each with five response categories: never = 6, rarely = 8, sometimes = 10, very often = 11, and always = 13. The total score is obtained by adding the responses to the six items. Scores ≥ 60 indicate severe life impact, 56-59 substantial life impact, 50-55 some life impact, and ≤ 49 minimal or no life impact.

Secondary Outcome Measures

Prevalence of DAO deficiency
Genetic analysis of DAO deficiency
Analgesic intake
Changes in analgesics intake. An ad-hoc questionnaire is used, where patients are asked to indicate the analgesics they take.

Full Information

First Posted
May 9, 2022
Last Updated
March 22, 2023
Sponsor
Centros de Investigación de Nutrición y Salud
Collaborators
AB Biotek
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1. Study Identification

Unique Protocol Identification Number
NCT05389761
Brief Title
Fibromyalgia Treatment With Enzyme DAO
Official Title
Evaluation of the Efficacy of Fibromyalgia Treatment With Enzyme DAO (Diamine-oxidase)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
February 22, 2022 (Actual)
Primary Completion Date
May 5, 2022 (Actual)
Study Completion Date
November 18, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centros de Investigación de Nutrición y Salud
Collaborators
AB Biotek

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Fibromyalgia is a complex and common chronic pain disorder that affects 12 million Europeans. Fibromyalgia causes persistent widespread pain in muscles, tendons, ligaments, and joints, as well as widespread tenderness to touch and the presence of extreme fatigue and weakness. Histamine is a molecule derived from an essential amino acid, histidine. It is stored in mast cells and basophils and is excreted through the intestine, being degraded as it passes through the intestinal mucosa by the enzyme Diamine Oxidase (DAO), which is found in this area. If there is any alteration in its metabolism and normal concentrations of histamine in the blood (50-70 mg/l) are not maintained, the free circulation of this amine in high concentrations triggers undesired effects, such as migraine, fibromyalgia, asthenia and atopy. DAO deficiency is an alteration in the metabolism of dietary histamine that occurs when there is little activity of the DAO enzyme. The low activity of the enzyme causes that a concentration considered normal of histamine from food cannot be metabolized and a transepithelial penetration of exogenous histamine occurs. In this way, histamine passes into the bloodstream, increasing its plasma concentration and once located freely in the blood, it is distributed throughout different parts of the body, producing adverse effects. One of the factors that causes DAO deficiency is genetics. The genetic sequence of DAO is found in a fragment located on chromosome 7 (7q34-q36) of the human genome. There are 85 single nucleotide variants (SNPs) located and identified in the human DAO gene (AOC1). Seven of these SNPs produce amino acid substitution, being candidates to cause alterations in the metabolic capacity of the enzyme. Since histamine accumulation can trigger fibromyalgia, and the enzyme DAO has been shown to degrade histamine, oral supplementation with DAO food supplements, prepared from pig kidney, is suggested as a treatment for fibromyalgia. The objective of this study is to analyze whether DAO enzyme supplementation reduces the characteristic symptoms of fibromyalgia. In addition, the prevalence of DAO deficiency in women with fibromyalgia will be identified by genetic analysis of DAO deficiency from a saliva sample. It will also be evaluated if patients require a lower intake of analgesics after supplementation with the enzyme DAO.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
Fibromyalgia, Diamine Oxidase, Supplementation, Genetics, Treatment

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Enzyme DAO administration
Arm Type
Experimental
Arm Description
DAO enzyme supplementation for 6 months
Arm Title
Placebo administration
Arm Type
Placebo Comparator
Arm Description
Placebo supplementation for 6 months
Intervention Type
Dietary Supplement
Intervention Name(s)
fibroDAO®
Intervention Description
One DAO enzyme capsule is taken with water 20 minutes before each meal, 3 times a day. DAO enzyme capsules contains 0.3 mg DAO enzyme divided into 2 white/beige tablets (each gastro-resistant tablet contains 0.15 mg DAO enzyme) and 80 mg magnesium divided into 2 lilac tablets (each immediate-release tablet contains 40 mg of Mg).
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
One placebo capsule is taken with water 20 minutes before each meal, 3 times a day. Placebo capsules consist of microcrystalline cellulose and gelatin capsules with the same shape, size and colour as the DAO enzyme.
Primary Outcome Measure Information:
Title
Patient status, progress and outcomes
Description
Change from baseline in fibromyalgia status on the Fibromyalgia Impact Questionnaire (FIQ). The FIQ has10 items. Each item has a maximum possible score of 10. The maximum possible score is 100. A higher score indicates a greater impact of the syndrome.
Time Frame
Baseline, 2 months and 6 months
Title
Sleep quality
Description
Change from baseline in sleep quality on the Pittsburgh Sleep Quality Index (PSQI). The PSQI contains 19 questions scored from 0 (no difficulty) to 3 (severe difficulty). The overall score is from 0 to 21. Higher scores indicate poorer sleep quality.
Time Frame
Baseline, 2 months and 6 months
Title
Pain experience
Description
Change from baseline in pain on the Pain Catastrophizing Scale (PCS). The PCS contains 13 items that are rated on 5-point Likert scales, from 0 (not at all) to 4 (all the time). The minimum total score is 0 and the maximum is 52. A higher score indicates a higher level of catastrophizing.
Time Frame
Baseline, 2 months and 6 months
Title
Extent and severity of eczema
Description
Change from baseline in eczema on the SCORing Atopic Dermatitis (SCORAD). The extension can be scored from 0 to 100, intensity from 0 to 18, and subjective symptoms from 0 to 20. The final score is achieved using the formula A / 5 + 7B / 2 + C.
Time Frame
Baseline, 2 months and 6 months
Title
Impact of headache
Description
Change from baseline in headache on the Headache Impact Test-6 (HIT-6). HIT-6 has six questions, each with five response categories: never = 6, rarely = 8, sometimes = 10, very often = 11, and always = 13. The total score is obtained by adding the responses to the six items. Scores ≥ 60 indicate severe life impact, 56-59 substantial life impact, 50-55 some life impact, and ≤ 49 minimal or no life impact.
Time Frame
Baseline, 2 months and 6 months
Secondary Outcome Measure Information:
Title
Prevalence of DAO deficiency
Description
Genetic analysis of DAO deficiency
Time Frame
Baseline
Title
Analgesic intake
Description
Changes in analgesics intake. An ad-hoc questionnaire is used, where patients are asked to indicate the analgesics they take.
Time Frame
Baseline, 2 months and 6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
59 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female Age between 30 and 59 years (included) Diagnosis of fibromyalgia Must sign an informed consent Able to follow-up at 2 and 6 months Exclusion Criteria: Pregnant or possibly pregnant Patients with change of pharmacological treatment in the last 3 months Patients with DAO enzyme treatment Patients diagnosed with other severe diseases (i.e. cancer, cardiovascular disease, autoimmune disease or metabolic disease) Patients with multiple chemical sensitivity
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ismael San Mauro Martin, PhD
Organizational Affiliation
Centros de Investigación de Nutrición y Salud
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Ruber Internacional
City
Madrid
ZIP/Postal Code
28036
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No

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Fibromyalgia Treatment With Enzyme DAO

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