Metabolic Biomarkers in Hashimoto's Thyroiditis and Psoriasis

Psoriasis Clinical Trial

Official title:

Study of Metabolic Pathways for the Identification of Biomarkers in Hashimoto's Thyroiditis and Psoriasis

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04693936
• Other study ID #: 147/26.06.2020
• Status: Recruiting
• Phase: N/A
• Start date: February 2, 2021
• Est. completion date: January 2024

Study information

• Verified date: April 2023
• Source: University of Crete
• Contact: Evangelia Sarandi, MSc, PhDc
• Phone: +306945546993
• Email: esarandi6[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: January 2024
• Est. primary completion date: September 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 60 Years

Eligibility

Hashimoto's Thyroiditis:

• Clinical findings
• Presence of thyroid autoantibodies (anti-TPO) in laboratory tests
• Gray-scale Ultrasound findings.

Psoriasis:

• Presence of psoriatic lesions
• Psoriasis Area and Severity Index score (PASI). Healthy group: Non-obese (BMI<30)
• non-athletes
• non-pregnant or lactating women
• not been diagnosed with a chronic or acute disease
• not receiving antidepressants, drugs and supplements
• normal Thyroid Stimulating Hormone (TSH) levels or high TSH and absence of other clinical findings of thyroid malfunction.

Exclusion Criteria:

• malignant or congenital goiter
• thyroidectomy

Related Conditions & MeSH terms

• Hashimoto Disease
• Psoriasis
• Thyroiditis

Intervention

Combination Product:
• Nutraceutical Combination Plan
Multivitamin (My Total Health) 1 tablet per day Vitamin C (My Immuno) 1 scoop per day Calcium-Magnesium combination (My Calmag) 1 scoop per day Omega 3-6-9 My Omega Krill. 1 capsule per day Glutamine (L-Glutamin &Chios Mastiha) 1 tablet per day Probiotics 40 billion 1 capsule per day Nutraceuticals will be received daily along with the patient's customary psoriasis/Hashimoto's disease treatment.

Locations

Country	Name	City	State
Greece	Metabolomic Medicine, Private Health Clinics	Athens

Sponsors (1)

Lead Sponsor	Collaborator
University of Crete

Country where clinical trial is conducted

Greece, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Differential levels of urinary organic acids in patients with Hashimoto's thyroiditis and psoriasis compared to healthy individuals as assessed by GC-MS	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	Baseline
Primary	Differential levels of peripheral blood fatty acids in patients with Hashimoto's thyroiditis and psoriasis compared to healthy individuals as assessed by GC-MS	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	Baseline
Primary	Change from baseline urinary organic acids levels after 6-month intervention with nutraceuticals as assessed by GC-MS	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	6 months
Primary	Change from baseline peripheral blood fatty acids levels after the 6-month intervention with nutraceuticals as assessed by GC-MS	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	6 months
Primary	Change from baseline thyroid disease-related quality of life at 6-months of intervention with nutraceuticals as assessed by the THYPRO questionnaire	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.	6 months
Primary	Change from baseline psoriasis-related quality of life at 6-months of intervention with nutraceuticals as assessed by the DLQI questionnaire	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.	6 months
Primary	Change from baseline Mediterranean diet adherence at 6 months of intervention with nutraceuticals as assessed by the MDS questionnaire	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.	6 months
Secondary	Change from baseline Body Mass Index at 6 months of intervention with nutraceuticals	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	6 months
Secondary	Change from baseline waist circumference at 6 months of intervention with nutraceuticals	Waist circumference (cm) will be measured at baseline and 6 months post the intervention for the three groups (both arms).	6 months
Secondary	Change from baseline alcohol consumption at 6 months of intervention with nutraceuticals	Alcohol consumption (number of glasses per week) will be assessed at baseline and 6 months post the intervention for all participants (both arms).	6 months
Secondary	Change from baseline physical activity at 6 months of intervention with nutraceuticals	Physical activity frequency (times per week) will be assessed at baseline and 6 months post the intervention for all participants (both arms).	6 months
Secondary	Change from baseline smoking at 6 months of intervention with nutraceuticals	Smoking (cigars per day) will be assessed at baseline and 6 months post the intervention for all participants(both arms).	6 months