Metabolic Biomarkers in Hashimoto's Thyroiditis and Psoriasis

Not Applicable

Active, not recruiting

• Conditions: Hashimoto Disease; Psoriasis
• Interventions: Combination Product: Nutraceutical Combination Plan

• Registration Number: NCT04693936
• Lead Sponsor: University of Crete

Brief Summary

Hashimoto's disease (HT) and psoriasis (PsO) have a significant impact on patient's quality of everyday life, and early diagnosis is critical for the symptoms management and prognosis. There is evidence that HT and PsO share common metabolic pathways that relate to their pathogenesis, and are affected by dietary and lifestyle factors. Previous studies have identified potential metabolic biomarkers, although the small number of studies hamper their validation. Of note, most studies are not longitudinal thus do not capture the metabolic fluctuations in response to disease progression or dietary changes. Thus, the purpose of this study is to identify metabolic biomarkers of HT and PsO and study the role of epigenetic factors (diet and lifestyle) on the involved metabolic pathways . In addition, a comparative analysis of the disease-related quality of life (QoL) will be performed in relation to dietary changes to unravel possible links between the QoL and the associated metabolic pathways in HT and PsO.

Detailed Description

Patients with Hashimoto's thyroiditis (HT), patients with psoriasis (PsO), and healthy individuals aged 18-60 will be recruited and assessed according to inclusion/exclusion criteria. Eligible participants will be randomized to two groups. The intervention group will receive a combinational nutraceuticals plan for 6 months as part of a Mediterranean diet and the control group will follow usual diet. Data will be collected at baseline and at the end of the study including levels of organic and fatty acids, lifestyle and anthropometric measurements, adherence to Mediterranean diet through the Mediterranean Diet Score (MDS) and disease-specific quality of life through the Thyroid Patient Report Outcome (THYPRO) and the Dermatology Life Quality Index (DLQI) questionnaires for the HT and the PsO group respectively.

Study Timeline

• Study First Submitted: 2020-12-23
• Study First Submitted QC: 2020-12-30
• Study First Posted: 2021-01-05
• Study Start: 2021-02-02
• Status Verified: 2024-06
• Last Update Submitted: 2024-06-26
• Last Update Posted: 2024-06-28
• Primary Completion: 2024-09
• Study Completion: 2024-12

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 200

Inclusion Criteria

Not provided

Exclusion Criteria

• malignant or congenital goiter
• thyroidectomy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Nutraceuticals	Nutraceutical Combination Plan	Participants will receive a combination of nutraceuticals and will be instructed to follow a Mediterranean diet

Primary Outcome Measures

Name	Time	Method
Differential levels of urinary organic acids in patients with Hashimoto's thyroiditis and psoriasis compared to healthy individuals as assessed by GC-MS	Baseline	Levels of organic acids will be quantified in the urine of patients with Hashimoto's diseases and psoriasis and the healthy group at baseline. Concentrations will be calculated in relation to creatinine (mmol/mol Crea) using Gas Chromatography-Mass Spectrometry (GC-MS).; Comparisons will be made at organic acids concentrations between the HT, the PSO and the healthy group to determine disease-related differences
Differential levels of peripheral blood fatty acids in patients with Hashimoto's thyroiditis and psoriasis compared to healthy individuals as assessed by GC-MS	Baseline	Levels of total fatty acids will be quantified (μmol/l) in the peripheral blood of patients with Hashimoto's diseases and psoriasis and the healthy group at baseline using Gas Chromatography-Mass Spectrometry (GC-MS); Comparisons will be made at fatty acids concentrations between the HT, the PSO and the healthy group to determine disease-related differences
Change from baseline psoriasis-related quality of life at 6-months of intervention with nutraceuticals as assessed by the DLQI questionnaire	6 months	The Dermatology Life Quality Index (DLQI) will be completed by the HT group and the PSO group (both arms) at baseline and 6 months post intervention.; DLQI score (0-30) after the intervention will be compared with baseline.
Change from baseline peripheral blood fatty acids levels after the 6-month intervention with nutraceuticals as assessed by GC-MS	6 months	Levels of total fatty acids will be quantified (μmol/l) in the peripheral blood of patients with Hashimoto's diseases and psoriasis and the healthy group after 6 months of intervention.; Comparisons will be made at fatty acids concentrations between baseline levels and post 6 months of treatment in the HT, the PSO and the healthy group to determine intervention-related differences
Change from baseline Mediterranean diet adherence at 6 months of intervention with nutraceuticals as assessed by the MDS questionnaire	6 months	The Mediterranean Diet Score (MDS) questionnaire will be collected for all participants (both arms) at baseline and 6 months post the intervention.; MDS (0-17) after the intervention will be compared with baseline.
Change from baseline urinary organic acids levels after 6-month intervention with nutraceuticals as assessed by GC-MS	6 months	Levels of organic acids will be quantified in the urine of patients with Hashimoto's diseases and psoriasis and the healthy group after 6 months of intervention. Concentrations will be calculated in relation to creatinine (mmol/mol Crea).; Comparisons will be made at organic acids concentrations between baseline levels and post 6 months treatment in the HT, the PSO and the healthy group to determine intervention-related differences
Change from baseline thyroid disease-related quality of life at 6-months of intervention with nutraceuticals as assessed by the THYPRO questionnaire	6 months	The Thyroid Patient Response Outcome (THYPRO) questionnaire will be completed by the HT group at baseline and 6 months post intervention (both arms).; THYPRO score (0-100) after the intervention will be compared with baseline.

Secondary Outcome Measures

Name	Time	Method
Change from baseline Body Mass Index at 6 months of intervention with nutraceuticals	6 months	BMI will be estimated at baseline and 6 months post the intervention for the three groups (both arms).; For the estimation of BMI (kg/m\^2) weight and height will be combined
Change from baseline alcohol consumption at 6 months of intervention with nutraceuticals	6 months	Alcohol consumption (number of glasses per week) will be assessed at baseline and 6 months post the intervention for all participants (both arms).
Change from baseline waist circumference at 6 months of intervention with nutraceuticals	6 months	Waist circumference (cm) will be measured at baseline and 6 months post the intervention for the three groups (both arms).
Change from baseline physical activity at 6 months of intervention with nutraceuticals	6 months	Physical activity frequency (times per week) will be assessed at baseline and 6 months post the intervention for all participants (both arms).
Change from baseline smoking at 6 months of intervention with nutraceuticals	6 months	Smoking (cigars per day) will be assessed at baseline and 6 months post the intervention for all participants(both arms).

Trial Locations

Locations (1)

Metabolomic Medicine, Private Health Clinics; 🇬🇷 Athens, Greece