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
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
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.
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- 適用できない
連絡先と場所
研究連絡先
研究連絡先
- 名前:Fatemeh Tamjid, MSc, PhD student
- 電話番号:+989144755462
- メール:tamjid.f@tbzmed.ac.ir
研究連絡先のバックアップ
- 名前:Bahram Pourghassem Gargari, PhD. Professor at TUMS
- 電話番号:+989143165247
- メール:pourghassemb@tbzmed.ac.ir, bahrampg@yahoo.com
研究場所
-
-
-
Tabriz、イラン
- Liver Clinic of Valiasr Hospital (Tabriz, Iran)
-
コンタクト:
- Fatemeh Tamjid, MSc, PhD student
- 電話番号:+989144755462
- メール:tamjid.f@tbzmed.ac.ir
-
コンタクト:
- Bahram Pourghassem Gargari, PhD. Professor at TUMS
- 電話番号:+989143165247
- メール:pourghassemb@tbzmed.ac.ir, bahrampg@yahoo.com
-
-
参加基準
適格基準
適格基準
就学可能な年齢
- 大人
健康ボランティアの受け入れ
説明
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)
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
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プラセボコンパレーター:プラセボ
|
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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実験的:介入
|
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).
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Serum folate level
時間枠:3 months
|
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
時間枠:3 months
|
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
時間枠:3 months
|
Changes in expression of PPARα and TNFα genes pre and post the 3-month intervention period.
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3 months
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Liver biochemical parameters (ALT (alanine aminotransferase), AST (aspartate aminotransferase), and GGT (gamma-glutamyl transferase)
時間枠:3 months
|
Changes in ALT, AST, and GGT pre and post the 3-month intervention period.
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3 months
|
|
The fibrosis-4 (FIB-4) index
時間枠: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.
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3 months
|
|
Quality of life using SF-36 (36-Item Short Form Health Survey) questionnaires
時間枠: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.
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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))
時間枠: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
時間枠:3 months
|
Changes in fasting blood glucose pre and post the 3-month intervention period.
|
3 months
|
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Fasting serum insulin
時間枠:3 months
|
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)
時間枠: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.
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3 months
|
|
HOMA-IR (homeostatic model assessment of insulin resistance
時間枠: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.
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3 months
|
|
Weight
時間枠:3 months
|
Changes in weight pre and post the 3-month intervention period.
|
3 months
|
|
Body Mass Index (BMI)
時間枠: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.
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3 months
|
|
Waist circumference
時間枠:3 months
|
Changes in waist circumference pre and post the 3-month intervention period.
|
3 months
|
|
Waist-to-hip ratio (WHR)
時間枠: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.
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3 months
|
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Body composition (fat-free mass)
時間枠: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)
時間枠: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
|
協力者と研究者
捜査官
捜査官
- 主任研究者:Bahram Pourghassem Gargari、Tabriz University of Medical Sciences
研究記録日
主要日程の研究
研究開始 (推定)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
その他の研究ID番号
- IRCT20100123003140N26
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
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