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Celiac Disease and Vitamin Status: Evaluation of the Effect of Supplementation With a Probiotic (VIVOMIXX®) in a Cohoort of Celiac Patients

Celiac Disease and Vitamin Status: Evaluation of the Effect of Supplementation With a Probiotic (VIVOMIXX®) on Vitamin B6, B12, 25'OH D, Folic Acid and Omocystein Levels, Metabolic and Inflammatory Status, and Gut Microbiota Metabolomics in a Cohoort of Celiac Patients

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04160767
Acronym
VIVOMIXX
Enrollment
90
Registered
2019-11-13
Start date
2019-01-30
Completion date
2021-07-31
Last updated
2021-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Celiac Disease

Keywords

Celiac disease, Gut microbiota

Brief summary

Celiac disease is a disorder caused by a disregulation of the immune system which leads to immune response to gluten. Diet therapy is the gold standard of treatment, and the only effective one. Macronutrients and micronutrients deficiency (vitamin D, folic acid, vitamin B12, vitamin B6, iron and zinc), which is in any case far more common in patients who don't follow gluten free diet, can persist in a subset of patients who follow gluten-free diet. Supplementation of vitamins in these patients may have a beneficial role. A recent study in a murine model showed that supplementation with probiotic VIVOMIXX® leads to an increase in expression of vitamin D receptors in proximal and distal colon. This is an interventional controlled randomized double blind study, which evaluates the effect of VIVOMIXX® on vitamin status.

Detailed description

90 patients with celiac disease who follow gluten free diet will be enrolled. INCLUSION CRITERIA * Celiac disease (diagnosis made according to ESPGHAN criteria) EXCLUSION CRITERIA * Supplementation with pre/probiotics in the previous 3 months; * Antibiotic therapy in the previous 3 months; * Comorbidity with other acute (in the previous 3 months) or chronic gastrointestinal disorders * Supplementation with group B vitamins for any reason Patients enrolled will be referred to Paediatric Gastroenterology Service in San Paolo Hospital at the time of enrollement (T0) and after intervention therapy (T1, + 4 months). Patients will be randomized in one of the two arms of intervention (VIVOMIXX once a day for 4 months versus placebo once a day for 4 months). VIVOMIXX® is a probiotic containing 8 differenct strains of bacteria: Streptococcus thermophilus DSM 24731, bifidobacteria (B. breve DSM 24732, B. longum DSM 24736, B. infantis DSM 24737) lactobacilli (L. acidophilus DSM 24735, L. plantarum DSM 24730, L. paracasei DSM 24733, L. delbrueckii subsp. bulgaricus DSM 24734). Every sachet contains 450 billions of bacteria, maltose and silicon dioxide. VIVOMIXX® will be freely given by the society MENDES S.A. - Lugano Switzerland. At each time point clinic evaluation, nutritional assessment and blood testing will be made. Data collection will include: * Systemic arterial blood pressure; * Anthropometric measures (height, weight, body mass index, waist circumference, triceps skinfold) * Clinical evaluation including presence/absence of oral aphtous stomatitis * Measure of chinolinic acid, serotonin, ghrelin (analysis will be made at Istituto Malattie Infettive, Università La Sapienza, Roma). * Dosing of inflammatory markers (analysis will be made at Health Sciences Department, San Paolo Hospital). * Metabolomics on stool samples (analysis will be made at Bologna University, Dipartimento di Scienze e Tecnologie Agro-Alimentari, Cesena, with a financial fund by MENDES S.A. - Lugano Switzerland). * Routine blood testing including complete blood cell count, vitamin B6, acid folic, vitamin B12, vitamin D 25'OH, fasting glucose, fasting insulin, total cholesterol, LDL and HDL cholesterol, Apolipoprotein A1 and Apolipoprotein B, triglycerides, homocistein, auto-antibody anti endomisium and anti-transglutaminase, * Genetic testing for MTHFR gene * ESR, highly sensitive CRP, IL6, TNFalfa, fibrinogen * Fecal calprotectin.

Interventions

DRUGProbiotic Vivomixx

VIVOMIXX once a day for 4 months. VIVOMIXX® is a probiotic containing 8 differenct strains of bacteria: Streptococcus thermophilus DSM 24731, bifidobacteria (B. breve DSM 24732, B. longum DSM 24736, B. infantis DSM 24737) lactobacilli (L. acidophilus DSM 24735, L. plantarum DSM 24730, L. paracasei DSM 24733, L. delbrueckii subsp. bulgaricus DSM 24734). Every sachet contains 450 billions of bacteria, maltose and silicon dioxide. VIVOMIXX® will be freely given by the society MENDES S.A. - Lugano Switzerland.

BEHAVIORALGluten free diet

Gluten free diet will be encouraged in both arms

OTHERPlacebo

Placebo with same taste than VIVOMIXX, containing maltose and silicon dioxide once a day for 4 months.

Sponsors

University of Milan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
MALE
Age
No minimum to 14 Years
Healthy volunteers
No

Inclusion criteria

* Celiac disease (diagnosis made according to European Society for Paediatric Gastroenterology Hepatology and Nutrition)

Exclusion criteria

* Supplementation with pre/probiotics in the previous 3 months; * Antibiotic therapy in the previous 3 months; * Comorbidity with other acute (in the previous 3 months) or chronic gastrointestinal disorders * Supplementation with group B vitamins for any reason

Design outcomes

Primary

MeasureTime frame
Changes in vitamin B6, folic acid, vitamin B12 and 25'OH vitamin D levels in bloodTime point 0: day 0 Time point 1: after 4 months
Changes in homocysteine levels in bloodTime point 0: day 0 Time point 1: after 4 months
Changes in ghrelin, chinolinic acid and serotonin levelsTime point 0: day 0 Time point 1: after 4 months
Changes in fecal metabolomics (including production of short chain fatty acids verified by gas-chromatography)Time point 0: day 0 Time point 1: after 4 months
Changes in highly sensitive C reactive protein levelsTime point 0: day 0 Time point 1: after 4 months
Changes in erythrocite sedimentation rateTime point 0: day 0 Time point 1: after 4 months
Changes in fibrinogen blood levelsTime point 0: day 0 Time point 1: after 4 months
Changes in IL-6 blood levelsTime point 0: day 0 Time point 1: after 4 months
Changes in Tumor Necrosis Factor alfa blood levelsTime point 0: day 0 Time point 1: after 4 months

Secondary

MeasureTime frame
Changes in weightTime point 0: day 0 Time point 1: after 4 months
Changes in waist circumferenceTime point 0: day 0 Time point 1: after 4 months
Entity of reduction of triceps skinfold thicknessTime point 0: day 0 Time point 1: after 4 months
Changes in prevalence of aphtous stomatitisTime point 0: day 0 Time point 1: after 4 months
Changes in chinolinic acid, serotonin, ghrelin levels in bloodTime point 0: day 0 Time point 1: after 4 months
Changes in complete cell blood countTime point 0: day 0 Time point 1: after 4 months
Changes in fasting glucose levelsT0 T1 (+4 months)
Changes in HDL cholesterol levelsTime point 0: day 0 Time point 1: after 4 months
Changes in LDL cholesterol levelsTime point 0: day 0 Time point 1: after 4 months
Changes in auto-antibody anti-transglutaminase titerTime point 0: day 0 Time point 1: after 4 months
Changes in fecal calprotectin levelsTime point 0: day 0 Time point 1: after 4 months
Prevalence of wildtype allele of MTHFR gene by gene sequencingTime point 0: day 0 (at the enrollement)
Changes in total cholesterol levelsTime point 0: day 0 Time point 1: after 4 months
Changes in fasting insulin levelsTime point 0: day 0 Time point 1: after 4 months
Changes in auto-antibody anti endomisium titerTime point 0: day 0 Time point 1: after 4 months
Changes in triglycerides levelsTime point 0: day 0 Time point 1: after 4 months
Changes in Apolipoprotein A1 levelsTime point 0: day 0 Time point 1: after 4 months
Changes in Apolipoprotein B levelsTime point 0: day 0 Time point 1: after 4 months
Changes in body mass indexTime point 0: day 0 Time point 1: after 4 months
Changes in systemic arterial systolic and diastolic blood pressureTime point 0: day 0 Time point 1: after 4 months
Changes in heightTime point 0: day 0 Time point 1: after 4 months

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026