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
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
- NAFLD
- Enfermedad del hígado graso no alcohólico
- Enfermedad del hígado graso no alcohólico (EHGNA)
- NAFLD - Enfermedad del hígado graso no alcohólico
- NAFLD (enfermedad del hígado graso no alcohólico)
- NAFLD (enfermedad del hígado graso no alcohólico)
- NAFLD - Enfermedad del hígado graso no alcohólico
- MASLD
- Enfermedad hepática esteatósica asociada a disfunción metabólica
- MASLD: enfermedad hepática esteatósica asociada a disfunción metabólica
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
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.
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Fatemeh Tamjid, MSc, PhD student
- Número de teléfono: +989144755462
- Correo electrónico: tamjid.f@tbzmed.ac.ir
Copia de seguridad de contactos de estudio
- Nombre: Bahram Pourghassem Gargari, PhD. Professor at TUMS
- Número de teléfono: +989143165247
- Correo electrónico: pourghassemb@tbzmed.ac.ir, bahrampg@yahoo.com
Ubicaciones de estudio
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Tabriz, Irán
- Liver Clinic of Valiasr Hospital (Tabriz, Iran)
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Contacto:
- Fatemeh Tamjid, MSc, PhD student
- Número de teléfono: +989144755462
- Correo electrónico: tamjid.f@tbzmed.ac.ir
-
Contacto:
- Bahram Pourghassem Gargari, PhD. Professor at TUMS
- Número de teléfono: +989143165247
- Correo electrónico: pourghassemb@tbzmed.ac.ir, bahrampg@yahoo.com
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-
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
Acepta Voluntarios Saludables
Descripción
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 de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Cuadruplicar
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
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Comparador de placebos: 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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Experimental: Intervención
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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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¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Serum folate level
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Liver biochemical parameters (ALT (alanine aminotransferase), AST (aspartate aminotransferase), and GGT (gamma-glutamyl transferase)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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))
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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)
Periodo de tiempo: 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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Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Investigador principal: Bahram Pourghassem Gargari, Tabriz University of Medical Sciences
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
Otros números de identificación del estudio
- IRCT20100123003140N26
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
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