The Effects of 5-methyltetrahydrofolate Supplementation in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)
The Effect of 5-methyltetrahydrofolate Supplementation on Serum Folate and Homocysteine Level and PPARα and TNFα Gene Expression in Patients With Metabolic Dysfunction-Associated Steatotic Liver Disease: a Double-blind, Parallel Randomized Controlled Trial Study
Aperçu de l'étude
Statut
Statut
Les conditions
Les conditions
- NAFLD
- Stéatose hépatique non alcoolique
- Maladie du foie gras non alcoolique (NAFLD)
- NAFLD - Maladie du foie gras non alcoolique
- NAFLD (maladie du foie gras non alcoolique)
- NAFLD (maladie du foie gras non alcoolique)
- NAFLD - Maladie du foie gras non alcoolique
- MASLD
- Maladie hépatique stéatosique associée à un dysfonctionnement métabolique
- MASLD - Maladie hépatique stéatosique associée à un dysfonctionnement métabolique
Intervention / Traitement
Intervention / Traitement
Description détaillée
Metabolic dysfunction-associated steatotic liver disease (MASLD), formerly termed non-alcoholic fatty liver disease (NAFLD), is diagnosed via liver biopsy or imaging when steatosis is present in the absence of alcohol intake or other hepatic disorders. As the liver manifestation of metabolic syndrome, it commonly coexists with obesity, diabetes, dyslipidemia, hypertension, and related conditions. Global prevalence of MASLD continues to rise.
Evidence from an earlier systematic review and meta-analysis indicated that MASLD patients had significantly lower serum folate and higher homocysteine concentrations. Folate is an essential water-soluble B vitamin that occurs in multiple chemically related forms. Food folates are mainly reduced and polyglutamated, with 5-MTHF predominating in both the diet and systemic circulation. 5-MTHF does not require reduction by DHFR and can enter the bloodstream directly for use. Reduced folates act as methyl donors in one carbon metabolism, supporting cellular proliferation, homocysteine re-methylation to methionine, nucleic acid synthesis and methylation of DNA, RNA, proteins and phospholipids.
Experimental studies have demonstrated that diet-induced hyperhomocysteinemia promotes hepatic steatosis and liver injury and folate as a key regulator of homocysteine concentration, may exert hepatoprotective effects. Evidence suggests that folate may improve hepatic lipid metabolism by activating peroxisome proliferator-activated receptor alpha (PPARα) signaling and modulate the immune response and reduce inflammatory mediators. Nevertheless, no evidence on the effects of folate on PPARα and TNFα gene expression in MASLD patients exist. Moreover, PPARα gene expression is dysregulated in MASLD and related metabolic conditions; PPARα is highly expressed in the liver, skeletal muscle and brown adipose tissue, stimulates β-oxidation and suppresses fatty-acid synthesis. Although the effect of 5-MTHF supplementation on gene expression of PPARα and TNFα in MASLD patients has not been examined, evidence showed that folate can modulate PPARα and TNFα. As folate has been shown to affect lipid metabolism and inflammation, we hypothesized that 5-MTHF supplementation might regulate PPARα and TNFα expression in MASLD patients. This randomized, double-blind, placebo-controlled clinical trial will therefore be undertaken to determine the effects of 5-MTHF supplementation on serum levels of folate and homocysteine, and gene expression of PPARα and TNFα in MASLD patients.
Type d'étude
Type d'étude
Inscription (Estimé)
Inscription
Phase
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
Coordonnées de l'étude
- Nom: Fatemeh Tamjid, MSc, PhD student
- Numéro de téléphone: +989144755462
- E-mail: tamjid.f@tbzmed.ac.ir
Sauvegarde des contacts de l'étude
- Nom: Bahram Pourghassem Gargari, PhD. Professor at TUMS
- Numéro de téléphone: +989143165247
- E-mail: pourghassemb@tbzmed.ac.ir, bahrampg@yahoo.com
Lieux d'étude
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Tabriz, L'Iran
- Liver Clinic of Valiasr Hospital (Tabriz, Iran)
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Contact:
- Fatemeh Tamjid, MSc, PhD student
- Numéro de téléphone: +989144755462
- E-mail: tamjid.f@tbzmed.ac.ir
-
Contact:
- Bahram Pourghassem Gargari, PhD. Professor at TUMS
- Numéro de téléphone: +989143165247
- E-mail: pourghassemb@tbzmed.ac.ir, bahrampg@yahoo.com
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Critères de participation
Critère d'éligibilité
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
La description
Inclusion Criteria:
- Adult men or women (18-50 years)
- Diagnosis of MASLD (grade 1 or 2 of steatosis confirmed by ultrasound)
- Body mass index (BMI) = 25-34.9 kg/m²
- Providing written informed consent
Exclusion Criteria:
- Pregnancy, lactation, or plans to get pregnant during the next three months.
- Liver disease (viral hepatitis, autoimmune liver disease, cirrhosis, drug-induced hepatotoxicity, or alcoholic fatty liver disease), heart or renal failure, kidney stones, any neoplasia, inflammatory disease, hypothyroidism, hypercortisolism, or hypertension
- Taking drugs affecting glucose or lipid metabolism, folate supplements, anti-obesity medications, weight-loss diets, or dietary supplements
- Lifestyle factors known to impact folate status (current smoking, alcohol intake, recreational drug use)
- Pre-existing conditions affecting folate status (malabsorptive or inflammatory bowel diseases, active celiac disease, gastric bypass surgery, atrophic gastritis, epilepsy, advanced liver disease, kidney dialysis, type 1 or 2 diabetes mellitus, or sickle cell trait/anemia)
- Medications that interfere with B-vitamin metabolism (chloramphenicol, methotrexate, metformin, sulfasalazine, phenobarbital, phenytoin, primidone, triamterene, barbiturates)
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Quadruple
Nombre de bras
Armes et Interventions
Groupe de participants / BrasGroupe de participants / Bras |
Intervention / TraitementIntervention / Traitement |
|---|---|
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Comparateur placebo: Placebo
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Patients in this group will receive placebo for 90 days.
The placebo is corn starch/ cellulose and will be consumed once a day.
Placebo tablets will be manufactured by Ashbal Chemi Co. (Tehran, Iran).
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Expérimental: Intervention
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Patients in this group will receive 5-methyltetrahydrofolate tablets (800 mcg) once a day for 90 days.
Tablets will be manufactured by Ashbal Chemi pharmaceutical company (Qfol, Ashbal Chemi Co., Tehran, Iran).
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Que mesure l'étude ?
Principaux critères de jugement
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Serum folate level
Délai: 3 months
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Changes in serum folate level pre and post the 3-month intervention period.
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3 months
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Serum homocysteine level
Délai: 3 months
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Changes in serum homocysteine level pre and post the 3-month intervention period.
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3 months
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Expression of PPARα and TNFα genes
Délai: 3 months
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Changes in expression of PPARα and TNFα genes pre and post the 3-month intervention period.
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3 months
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Mesures de résultats secondaires
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Liver biochemical parameters (ALT (alanine aminotransferase), AST (aspartate aminotransferase), and GGT (gamma-glutamyl transferase)
Délai: 3 months
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Changes in ALT, AST, and GGT pre and post the 3-month intervention period.
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3 months
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The fibrosis-4 (FIB-4) index
Délai: 3 months
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Changes in FIB-4 index pre and post the 3-month intervention period.
The Fibrosis-4 (FIB-4) index will be calculated using the following formula: FIB-4 = (Age [years] × AST [U/L]) / (Platelet count [10⁹/L] × √ALT [U/L]).
FIB-4 values >1.3, indicate a greater likelihood of liver fibrosis.
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3 months
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Quality of life using SF-36 (36-Item Short Form Health Survey) questionnaires
Délai: 3 months
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Changes in quality-of-life pre and post the 3-month intervention period.
Health-related quality of life will be assessed using the validated 36-Item Short Form Health Survey (SF-36).
The questionnaire evaluates eight health domains: physical functioning, role limitations due to physical health, bodily pain, general health, vitality, social functioning, role limitations due to emotional problems, and mental health.
Scores for each domain will be transformed to a 0-100 scale according to the standard scoring algorithm, with higher scores indicating better health-related quality of life.
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3 months
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Lipid profile (triglycerides, total cholesterol, LDL-C (low-density lipoprotein cholesterol), HDL-C (high-density lipoprotein cholesterol))
Délai: 3 monhs
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Changes in lipid profile (triglycerides, total cholesterol, LDL-C, HDL-C) pre and post the 3-month intervention period.
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3 monhs
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Fasting blood glucose
Délai: 3 months
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Changes in fasting blood glucose pre and post the 3-month intervention period.
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3 months
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Fasting serum insulin
Délai: 3 months
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Changes in fasting serum insulin pre and post the 3-month intervention period.
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3 months
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QUICKI (quantitative insulin sensitivity check index)
Délai: 3 months
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Changes in QUICKI pre and post the 3-month intervention period.
The quantitative insulin sensitivity check index (QUICKI) will be calculated as 1/[log(fasting insulin [µU/mL]) + log(fasting glucose [mg/dL])], higher values indicating greater insulin sensitivity.
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3 months
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HOMA-IR (homeostatic model assessment of insulin resistance
Délai: 3 months
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Changes in HOMA-IR pre and post the 3-month intervention period.
Insulin resistance will be assessed using the homeostatic model assessment of insulin resistance (HOMA-IR), calculated as fasting insulin (µU/mL) × fasting glucose (mg/dL) / 405, higher values indicating greater insulin resistance.
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3 months
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Weight
Délai: 3 months
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Changes in weight pre and post the 3-month intervention period.
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3 months
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Body Mass Index (BMI)
Délai: 3 months
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Changes in BMI pre and post the 3-month intervention period.
Body mass index (BMI) will be calculated as weight (kg) divided by the square of height (m²) and expressed as kg/m².
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3 months
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Waist circumference
Délai: 3 months
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Changes in waist circumference pre and post the 3-month intervention period.
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3 months
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Waist-to-hip ratio (WHR)
Délai: 3 months
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Changes in WHR pre and post the 3-month intervention period.
Waist-to-hip ratio (WHR) will be calculated by dividing waist circumference by hip circumference.
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3 months
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Body composition (fat-free mass)
Délai: 3 months
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Changes in fat-free mass (%) pre and post the 3-month intervention period.
Body composition will be determined using a bioelectrical impedance analyzer.
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3 months
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Body composition (fat mass)
Délai: 3 months
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Changes in fat mass (%) pre and post the 3-month intervention period.
Body composition will be determined using a bioelectrical impedance analyzer.
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3 months
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Collaborateurs et enquêteurs
Parrainer
Parrainer
Les enquêteurs
Les enquêteurs
- Chercheur principal: Bahram Pourghassem Gargari, Tabriz University of Medical Sciences
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Début de l'étude
Achèvement primaire (Estimé)
Achèvement primaire
Achèvement de l'étude (Estimé)
Achèvement de l'étude
Dates d'inscription aux études
Première soumission
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Première publication
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour publiée
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
Autres numéros d'identification d'étude
- IRCT20100123003140N26
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
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