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
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
상세 설명
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.
연구 유형
연구 유형
등록 (추정된)
등록
단계
단계
- 해당 없음
연락처 및 위치
연구 연락처
연구 연락처
- 이름: Fatemeh Tamjid, MSc, PhD student
- 전화번호: +989144755462
- 이메일: tamjid.f@tbzmed.ac.ir
연구 연락처 백업
- 이름: Bahram Pourghassem Gargari, PhD. Professor at TUMS
- 전화번호: +989143165247
- 이메일: pourghassemb@tbzmed.ac.ir, bahrampg@yahoo.com
연구 장소
-
-
-
Tabriz, 이란
- Liver Clinic of Valiasr Hospital (Tabriz, Iran)
-
연락하다:
- Fatemeh Tamjid, MSc, PhD student
- 전화번호: +989144755462
- 이메일: tamjid.f@tbzmed.ac.ir
-
연락하다:
- Bahram Pourghassem Gargari, PhD. Professor at TUMS
- 전화번호: +989143165247
- 이메일: pourghassemb@tbzmed.ac.ir, bahrampg@yahoo.com
-
-
참여기준
자격 기준
자격 기준
공부할 수 있는 나이
- 성인
건강한 자원 봉사자를 받아들입니다
설명
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)
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
팔의 수
무기와 개입
참가자 그룹 / 팔참가자 그룹 / 팔 |
개입 / 치료개입 / 치료 |
|---|---|
|
위약 비교기: 위약
|
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).
|
|
실험적: 간섭
|
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).
|
연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Serum folate level
기간: 3 months
|
Changes in serum folate level pre and post the 3-month intervention period.
|
3 months
|
|
Serum homocysteine level
기간: 3 months
|
Changes in serum homocysteine level pre and post the 3-month intervention period.
|
3 months
|
|
Expression of PPARα and TNFα genes
기간: 3 months
|
Changes in expression of PPARα and TNFα genes pre and post the 3-month intervention period.
|
3 months
|
2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Liver biochemical parameters (ALT (alanine aminotransferase), AST (aspartate aminotransferase), and GGT (gamma-glutamyl transferase)
기간: 3 months
|
Changes in ALT, AST, and GGT pre and post the 3-month intervention period.
|
3 months
|
|
The fibrosis-4 (FIB-4) index
기간: 3 months
|
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.
|
3 months
|
|
Quality of life using SF-36 (36-Item Short Form Health Survey) questionnaires
기간: 3 months
|
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.
|
3 months
|
|
Lipid profile (triglycerides, total cholesterol, LDL-C (low-density lipoprotein cholesterol), HDL-C (high-density lipoprotein cholesterol))
기간: 3 monhs
|
Changes in lipid profile (triglycerides, total cholesterol, LDL-C, HDL-C) pre and post the 3-month intervention period.
|
3 monhs
|
|
Fasting blood glucose
기간: 3 months
|
Changes in fasting blood glucose pre and post the 3-month intervention period.
|
3 months
|
|
Fasting serum insulin
기간: 3 months
|
Changes in fasting serum insulin pre and post the 3-month intervention period.
|
3 months
|
|
QUICKI (quantitative insulin sensitivity check index)
기간: 3 months
|
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.
|
3 months
|
|
HOMA-IR (homeostatic model assessment of insulin resistance
기간: 3 months
|
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.
|
3 months
|
|
Weight
기간: 3 months
|
Changes in weight pre and post the 3-month intervention period.
|
3 months
|
|
Body Mass Index (BMI)
기간: 3 months
|
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.
|
3 months
|
|
Waist circumference
기간: 3 months
|
Changes in waist circumference pre and post the 3-month intervention period.
|
3 months
|
|
Waist-to-hip ratio (WHR)
기간: 3 months
|
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.
|
3 months
|
|
Body composition (fat-free mass)
기간: 3 months
|
Changes in fat-free mass (%) pre and post the 3-month intervention period.
Body composition will be determined using a bioelectrical impedance analyzer.
|
3 months
|
|
Body composition (fat mass)
기간: 3 months
|
Changes in fat mass (%) pre and post the 3-month intervention period.
Body composition will be determined using a bioelectrical impedance analyzer.
|
3 months
|
공동 작업자 및 조사자
수사관
수사관
- 수석 연구원: Bahram Pourghassem Gargari, Tabriz University of Medical Sciences
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
기타 연구 ID 번호
- IRCT20100123003140N26
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .