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NCT Number: NCT05530070

Cardiovascular Risk Factors in Coeliac Disease: a Series of Studies

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

First Department of Medicine, Medical School, University of Pécs

Pécs, Baranya, 7624, Hungary

Location status: Recruiting

Location contact

Judit Bajor, MD, PhD

CONTACT

[email protected]

+36 72 536 000

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(applies to all subjects):

  • Age should be over 18 years.
  • Blood collection must be indicated with medical conditions.
  • Signed informed consent.

Inclusion criteria

(applies to specific cohorts of patients):

  • The diagnosis of CD should be set up according to the current guidelines (based on serology and histology in adults or as per the European Society for Paediatric Gastroenterology Hepatology and Nutrition (ESPGHAN) guideline in children).
  • The newly diagnosed CD patients should be on a gluten-containing diet.
  • Patients following a GFD for at least 1 year should exhibit good dietary adherence.
  • In the randomized controlled trial (RCT), strict dietary adherence will be established based on CD-specific serology (normal level of antibodies), urine gluten immunogenic peptides (negative urine test), and dietary interview (convincing knowledge on the GFD and positive attitude towards strict adherence). Adherence to the mediterranean diet should be suboptimal (≤ 8 Medietrranean Diet Score). RCT-patients must have internet access and must be capable to attend the online sessions for 1 year.
  • Control subjects should be free from CD according to the recent guidelines and should be on a gluten-containing diet.

Exclusion criteria

  • Chronic conditions:
  • Estimated glomerular filtration rate calculated with the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) formula is <60mL/min/1.73m2 (CKD3 or more severe kidney failure).
  • Liver cirrhosis in Child-Pugh class B-C.
  • Heart failure (New York Heart Association (NYHA) III-IV).
  • Active malignant diseases.
  • Any acute diseases or acute deterioration of underlying chronic conditions.
  • Diseases that may be associated with clinically relevant malabsorption.
  • Refractory CD.
  • Pregnancy, lactation.
  • Patients unable to understand the essentials of the informed consent.
  • Lack of consent or withdrawal of consent.

Treatment and study plan

Dietary Intervention

Other

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.

Standard of care

Other

Patients will receive standard of care and baseline dietary education.

Cardiovascular risk-related parameters

Diagnostic Test

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.

Primary outcomes

  1. Percent body fat

    Time frame: 1 year

    Percent body fat in percentage measured by an InBody 770 body composition analyzer.

Secondary outcomes

  1. Waist circumference

    Time frame: 1 year

    CV risk assessment will be performed by measuring waist circumference in centimeters.

  2. Blood pressure

    Time frame: 1 year

    CV risk assessment will be performed by measuring blood pressure in Hgmm.

  3. Fatty liver disease

    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).

  4. Cardiovascular risk assessment

    Time frame: 1 year

    CV risk assessment will be performed by the Systematic Coronary Risk Evaluation (SCORE) chart.

  5. Coeliac disease-related symptoms

    Time frame: 1 year

    CD-related symptoms will be assessed by the Celiac Symptom Index (CSI).

  6. Coeliac disease-specific quality of life

    Time frame: 1 year

    CD-specific quality of life questionnaire will be also used (Celiac Disease Quality of Life (CD-QoL).

  7. Disease activity

    Time frame: 1 year

    Disease activity will be estimated by tissue transglutaminase (tTG) levels.

  8. Sarcopenia

    Time frame: 1 year

    Sarcopenia will be assessed based on body composition and handgrip strength via handgrip dynamometer.

  9. Triglyceride level

    Time frame: 1 year

    Triglyceride level in mmol/L.

  10. Cholesterol level

    Time frame: 1 year

    Cholesterol (total, HDL and LDL lipoproteins) level in mmol/L.

  11. Fasting glucose level

    Time frame: 1 year

    Fasting glucose level in mmol/L.

  12. Fasting insulin level

    Time frame: 1 year

    Fasting insulin level in mmol/L.

  13. Haemoglobin (Hb) A1c level

    Time frame: 1 year

    HbA1c level in percentage.

  14. Homeostasis Model Assessment (HOMA) index

    Time frame: 1 year

    HOMA index

  15. Bilirubin level

    Time frame: 1 year

    Bilirubin level in µmol/L.

  16. Uric acid level

    Time frame: 1 year

    Uric acid µmol/L.

  17. Urea level

    Time frame: 1 year

    Urea level in mmol/L.

  18. Creatinine level

    Time frame: 1 year

    Creatinine level in µmol/L.

  19. Sodium level

    Time frame: 1 year

    Sodium level in mmol/L.

  20. Potassium level

    Time frame: 1 year

    Potassium level in mmol/L.

  21. Calcium level

    Time frame: 1 year

    Calcium level in mmol/L.

  22. Vitamin D

    Time frame: 1 year

    Vitamin D level in ng/mL.

  23. Vitamin B12

    Time frame: 1 year

    Vitamin B12 level in pg/mL.

  24. Folic acid level

    Time frame: 1 year

    Folic acid level in µg/L.

  25. Iron level

    Time frame: 1 year

    Iron level in µmol/L.

  26. Ferritin level

    Time frame: 1 year

    Ferritin level in µg/L.

  27. Transferrin level

    Time frame: 1 year

    Transferrin level in g/L.

  28. Transferrin saturation

    Time frame: 1 year

    Transferrin saturation in percentage.

  29. International Normalized Ratio (INR)

    Time frame: 1 year

    INR

  30. Aspartate aminotransferase level

    Time frame: 1 year

    Aspartate aminotransferase level in U/L.

  31. Alanine aminotransferase level

    Time frame: 1 year

    Alanine aminotransferase in U/L.

  32. Fibrosis-4 (FIB-4) Index

    Time frame: 1 year

    FIB-4 Index for liver fibrosis.

  33. Total protein level

    Time frame: 1 year

    Total protein level in g/L.

  34. Albumin level

    Time frame: 1 year

    Albumin level in g/L.

  35. Immunoglobulins

    Time frame: 1 year

    Immunoglobulins in U/mL.

  36. High-sensitivity C-reactive protein (hs-CRP) level

    Time frame: 1 year

    hs-CRP level in mg/L.

  37. Fibrinogen level

    Time frame: 1 year

    Fibrinogen level in g/L.

  38. Blood counts

    Time frame: 1 year

    Blood counts in Giga/L.

  39. Homocysteine levels

    Time frame: 1 year

    Homocysteine levels in µmol/L.

  40. Interleukin-6 levels

    Time frame: 1 year

    Interleukin-6 levels in ng/L.

  41. Leptin levels

    Time frame: 1 year

    Leptin levels in ng/mL.

  42. Ghrelin levels

    Time frame: 1 year

    Ghrelin levels in pg/mL.

  43. Adiponectin levels

    Time frame: 1 year

    Adiponectin levels in µg/mL.

  44. Galectin-3 levels

    Time frame: 1 year

    Galectin-3 levels in ng/mL.

  45. Dietary interview

    Time frame: 1 year

    Dietary adherence will be determined by dietary interview provided by an expertise dietitian.

  46. Celiac Disease Adherence Test

    Time frame: 1 year

    Dietary adherence will be determined by the Celiac Disease Adherence Test (CDAT).

  47. Coeliac-specific antibodies

    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.

  48. Urine gluten immunogenic peptide

    Time frame: 1 year

    Dietary adherence will be determined by urine gluten immunogenic peptide (GIP) measurement.

  49. Diet composition

    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).

  50. Body height

    Time frame: 1 year

    Height in centimeters measured by a stadiometer.

  51. Body weight

    Time frame: 1 year

    Weight in kilograms measured by an InBody 770 body composition analyzer.

  52. Body mass index

    Time frame: 1 year

    Body mass index in kg/m2 calculated by an InBody 770 body composition analyzer.

  53. Body fat mass

    Time frame: 1 year

    Body fat mass in kilograms measured by an InBody 770 body composition analyzer.

  54. Skeletal muscle mass

    Time frame: 1 year

    Skeletal muscle mass in kilograms measured by an InBody 770 body composition analyzer.

  55. Visceral fat area

    Time frame: 1 year

    Visceral fat area in cm2 measured by an InBody 770 body composition analyzer.

  56. Total body water

    Time frame: 1 year

    Total body water in liters measured by an InBody 770 body composition analyzer.

Study contacts

Contact information is provided by the study sponsor or research team.

Judit Bajor, MD, PhD

CONTACT

[email protected]

+36 72 536 000

Sponsors and collaborators

Lead sponsor

University of Pecs

Other

Registry information

Acronym: ARCTIC

Important dates

Study start
2022
Primary completion
2026
Study completion
2026
First posted
Sep 7, 2022
Registry last updated
Jan 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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