First Department of Medicine, Medical School, University of Pécs
Pécs, Baranya, 7624, Hungary
Location status: Recruiting
NCT Number: NCT05530070
This investigation examines the most important cardiovascular risk factors (e.g., metabolic parameters, body composition) and their changes in coeliac disease. The series of studies allow to assess body composition and cardiovascular risk-related metabolic parameters of newly diagnosed and treated coeliac patients in their complexity and to test if they change during therapy. The interventional part of the investigation aims to answer the question if a dietary intervention mitigates the unfavorable effects of unbalanced diet.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Pécs, Baranya, 7624, Hungary
Location status: Recruiting
The global prevalence of coeliac disease (CD) is increasing, which contributes to the disease's significant public health care burden. Body composition and metabolic parameters of coeliac patients differ from the healthy population. Patients with non-classical CD are not necessarily lean; they usually have normal body weight but can be even overweight or obese. In coeliac patients, bodyweight tends to elevate, whereas the body composition changes unfavourably during a gluten-free diet (GFD). A reason for gaining weight is the improvement of malabsorption but an important contributor is the nutrient composition of the GFD, which generally has a high calorie density with high carbohydrate and fat content while being low in fibre. While terminating or mitigating the inflammatory process - if done without adequate dietary control - a GFD can readily lead to weight gain and unfavourably metabolic consequences (e.g., dyslipidemia, fatty liver disease, insulin resistance). The result can be an increase in cardiovascular risk in CD patients with a normal or high body weight at diagnosis. However, limited information is available on the cardiovascular (CV) risk in coeliac disease, and the data are controversial. This study examines the body composition and cardiovascular risk-related metabolic parameters at the diagnosis and on a gluten-free diet in a Hungarian cohort of CD patients. The randomised controlled trial (RCT) investigates the effect of structured, repeated, group-based dietary education on the examined metabolic parameters and body composition.
This study aims to draw attention to a new aspect of the management of CD patients: from a metabolic and cardiovascular point of view. Findings will help to identify which parameters are beneficial to optimize and re-assess during follow-up in CD.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
(applies to all subjects):
Inclusion criteria
(applies to specific cohorts of patients):
Exclusion criteria
Patients will participate in a structured, group-based dietary counseling. Consultations will be organized online (Zoom meeting) lasting approximately 60 min/occasion. The intervention will include 6 sessions for 1 year (monthly for 5 months and finally at month 9). The aim of the counseling is to maintain a GFD and to develop a healthy lifestyle, in line with the Mediterranean diet.
Patients will receive standard of care and baseline dietary education.
Anthropometric measurements (body height, body composition assessment-InBody 770), questionnaires (symptoms, quality of life, dietary adherence, diet quality, cardiovascular risk), assessment of sarcopenia (handgrip dynamometer), urine collection (dietary adherence - urine gluten immunogenic peptide detection), blood collection (immunological tests, hormone levels complemented with routine laboratory panel), transabdominal US examination to assess the extent of fatty liver disease.
Time frame: 1 year
Percent body fat in percentage measured by an InBody 770 body composition analyzer.
Time frame: 1 year
CV risk assessment will be performed by measuring waist circumference in centimeters.
Time frame: 1 year
CV risk assessment will be performed by measuring blood pressure in Hgmm.
Time frame: 1 year
Transabdominal ultrasonography will be used to assess the extent of fatty liver disease (based on non-alcoholic fatty liver disease-liver fat score (NAFLD-LFS), with a score range of 0-3).
Time frame: 1 year
CV risk assessment will be performed by the Systematic Coronary Risk Evaluation (SCORE) chart.
Time frame: 1 year
CD-related symptoms will be assessed by the Celiac Symptom Index (CSI).
Time frame: 1 year
CD-specific quality of life questionnaire will be also used (Celiac Disease Quality of Life (CD-QoL).
Time frame: 1 year
Disease activity will be estimated by tissue transglutaminase (tTG) levels.
Time frame: 1 year
Sarcopenia will be assessed based on body composition and handgrip strength via handgrip dynamometer.
Time frame: 1 year
Triglyceride level in mmol/L.
Time frame: 1 year
Cholesterol (total, HDL and LDL lipoproteins) level in mmol/L.
Time frame: 1 year
Fasting glucose level in mmol/L.
Time frame: 1 year
Fasting insulin level in mmol/L.
Time frame: 1 year
HbA1c level in percentage.
Time frame: 1 year
HOMA index
Time frame: 1 year
Bilirubin level in µmol/L.
Time frame: 1 year
Uric acid µmol/L.
Time frame: 1 year
Urea level in mmol/L.
Time frame: 1 year
Creatinine level in µmol/L.
Time frame: 1 year
Sodium level in mmol/L.
Time frame: 1 year
Potassium level in mmol/L.
Time frame: 1 year
Calcium level in mmol/L.
Time frame: 1 year
Vitamin D level in ng/mL.
Time frame: 1 year
Vitamin B12 level in pg/mL.
Time frame: 1 year
Folic acid level in µg/L.
Time frame: 1 year
Iron level in µmol/L.
Time frame: 1 year
Ferritin level in µg/L.
Time frame: 1 year
Transferrin level in g/L.
Time frame: 1 year
Transferrin saturation in percentage.
Time frame: 1 year
INR
Time frame: 1 year
Aspartate aminotransferase level in U/L.
Time frame: 1 year
Alanine aminotransferase in U/L.
Time frame: 1 year
FIB-4 Index for liver fibrosis.
Time frame: 1 year
Total protein level in g/L.
Time frame: 1 year
Albumin level in g/L.
Time frame: 1 year
Immunoglobulins in U/mL.
Time frame: 1 year
hs-CRP level in mg/L.
Time frame: 1 year
Fibrinogen level in g/L.
Time frame: 1 year
Blood counts in Giga/L.
Time frame: 1 year
Homocysteine levels in µmol/L.
Time frame: 1 year
Interleukin-6 levels in ng/L.
Time frame: 1 year
Leptin levels in ng/mL.
Time frame: 1 year
Ghrelin levels in pg/mL.
Time frame: 1 year
Adiponectin levels in µg/mL.
Time frame: 1 year
Galectin-3 levels in ng/mL.
Time frame: 1 year
Dietary adherence will be determined by dietary interview provided by an expertise dietitian.
Time frame: 1 year
Dietary adherence will be determined by the Celiac Disease Adherence Test (CDAT).
Time frame: 1 year
Dietary adherence will be determined by coeliac-specific antibodies (tissue transglutaminase (tTG) immunoglobulin (Ig) A/IgG and endomysium antibody levels (EMA) IgA) in U/mL.
Time frame: 1 year
Dietary adherence will be determined by urine gluten immunogenic peptide (GIP) measurement.
Time frame: 1 year
The composition of a GFD will be evaluated with the indicator of adherence to the Mediterranean diet, the Mediterranean Diet Score (MDS).
Time frame: 1 year
Height in centimeters measured by a stadiometer.
Time frame: 1 year
Weight in kilograms measured by an InBody 770 body composition analyzer.
Time frame: 1 year
Body mass index in kg/m2 calculated by an InBody 770 body composition analyzer.
Time frame: 1 year
Body fat mass in kilograms measured by an InBody 770 body composition analyzer.
Time frame: 1 year
Skeletal muscle mass in kilograms measured by an InBody 770 body composition analyzer.
Time frame: 1 year
Visceral fat area in cm2 measured by an InBody 770 body composition analyzer.
Time frame: 1 year
Total body water in liters measured by an InBody 770 body composition analyzer.
Contact information is provided by the study sponsor or research team.
University of Pecs
Other
Acronym: ARCTIC
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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