成人 MASLD 患者に対するプロバイオティクス ライセート (ポストバイオティクスおよびメタバイオティクス) の補給 (DELI_MASLD 研究)
成人MASLD患者におけるプロバイオティックライセート(ポストバイオティックおよびメタバイオティック)補給の有効性と安全性
The current study aim was to conduct placebo-controlled randomize clinical trial to assess the short-term efficacy and safety of postbiotics on hepatic fat content as measured by biochemichal hepatic steatosis indeces, serum lipid profile, transaminases activity and chronic systemic inflammatory markers in MASLD patients.
The study will include 3 periods. Screening period of up to 1 weeks to assess the eligibility to inclusion/exclusion criteria. Treatment period for 3 month where the participants will receive a twice daily oral dose of postbiotics (cell lysate and DNA fragments of the probiotic strain L. rhamnosus DV - NRRLB-68023) at the assigned dose of 100mg or placebo in capsules. During this period monthly phone contacts will be done for assessment of compliance and safety concerns. Follow-up period of up to 3 month.
調査の概要
状態
詳細な説明
The scientific literature points to the beneficial properties of probiotics in the process of regulating metabolism, yet at the same time, some scientific papers question the effectiveness and the safety of probiotics. In turn, postbiotics and metabiotics are preparations of inanimate microorganisms and / or their components, which are directly identified with the safety of their use and the health benefits of the host. Due to the chemical structure of postbiotics and metabiotics, it is found that they have many health benefits; in particular, they have a local effect on certain tissues of the intestinal epithelium, and influence on many other organs and tissues. It is postbiotics metabolites and metabiotics structural cell fragments that create the appearance of a therapeutic effect of probiotics, which, in turn, limits the risk of introducing living microorganisms into a weakened immune defence. It should also be pointed out that postbiotics and metabiotics are more stable and have a longer shelf-life.
The practical use of probiotics and the study of the mechanism of their action made lately to find that a certain level of biological activity is preserved by dead probiotic cells and even their lysates, which are the natural mixes of metabiotic and postbiotic substances; a biological activity which is strongly oriented toward gut health and immune system regulation. Because probiotic lysates demonstrated biological activity without any of the potential adverse side effects associated with live bacterial cells, one of the future goal is research of the novel postbiotics and metabiotics substances, their individual structures and biological characteristics for understanding their way of communications with host cells and microbiota representatives.
Considering the high biological activity and safety of postbiotics and metabiotic substances, it can be concluded that such a treatment vector will be promising in the near future. That's why our investigation will concentrate on postbiotic, a supplement containing dry fermented cell lysate and DNA fragments of the probiotic strain L. rhamnosus DV - NRRLB-68023.
Recent scientific animal studies on the stated issues point to the benefits of some postbiotics in treating metabolic disorders. The current study aim was to conduct placebo-controlled randomize clinical trial to assess the short-term efficacy and safety of postbiotics on hepatic fat content as measured by biochemichal hepatic steatosis indeces, serum lipid profile, transaminases activity and chronic systemic inflammatory markers in MASLD patients.
The study will include 3 periods. Screening period of up to 1 weeks to assess the eligibility to inclusion/exclusion criteria. Treatment period for 3 month where the participants will receive a twice daily oral dose of postbiotics (cell lysate and DNA fragments of the probiotic strain L. rhamnosus DV - NRRLB-68023) at the assigned dose of 100mg or placebo in capsules. All capsules will be identical with similar organoleptic characteristics (e.g., taste and appearance). Follow-up period of up to 3 month.
The pre-randomization period will be designed to minimize the effects of dietary changes on metabolic markers. For this purpose, 2 weeks before the study start, after inform consent signed, patients were instructed in one-on-one sessions with a dietitian to follow a therapeutic lifestyle-change diet as classified by the NCEP. In addition, participants were instructed to continue with stable anti-hyperglycemic treatment and received standardized mild physical training for 1 hour per day.
Patients who underwent the study were instructed to take the trial medication as prescribed. Throughout the study, weekly phone follow-up visits were provided for assessment of compliance, adherence to the protocol, as well as the recording of adverse events. The effectiveness of therapy was compared and evaluated separately in the two groups.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
-
-
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Kyiv、ウクライナ、01601
- Bogomolets National Medical University
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Kyiv、ウクライナ、01601
- Taras Shevchenko National University of Kyiv
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Kyiv、ウクライナ、01601
- Kyiv City Clinical Endocrinology Center
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Kyiv、ウクライナ、02000
- Center for Innovative Medical Technologies of the National Academy of Sciences of Ukraine
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Lviv、ウクライナ、79010
- Danylo Halytsky Lviv National Medical University
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-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- adult participants (ages 18-70)
- presence of MASLD according to "A multisociety Delphi consensus statement", 2023;
- the diagnosis of fatty liver was based on the results of abdominal ultrasonography. Of 4 known criteria (hepato-renal echo contrast, liver brightness, deep attenuation, and vascular blurring), the participants were required to have hepato-renal contrast and liver brightness to be given a diagnosis of SLD
- fatty liver index (FLI) more than 60;
- BMI 25-39.9 kg/m2;
- aspartate transaminase (AST) and alanine transaminase (ALT) ≤3x upper limit of normal;
- written informed consent.
Exclusion Criteria:
- recent hepatitis, or positive screening test for hepatitis B (hepatitis B virus surface antigen) or hepatitis C (hepatitis C antibody);
- alcohol abuse (>20 g/day (2 standard drinks) in women or > 30 g/d (3 drinks) in men over a two-year period);
- drug-induced liver disease, Wilson's disease, hereditary deficiency of antitrypsin-1 and idiopathic hemochromatosis;
- history of decompensated liver disease including ascites, encephalopathy or variceal bleeding;
- regular use of an agents with gut microbiota modulation activity (antibiotic, pro-, pre-, post or synbiotics supplement etc.) within 3 months prior to enrollment;
- allergy on probiotics or their components;
- use of agents such as vitamin E, omega-3 fatty acids or medications with evidence for effects on NAFLD (pioglitazone, GLP-1 analogues, dipeptidyl peptidase IV inhibitors, ursodeoxycholic acid);
- subjects with a history of bariatric surgery or significant weight loss (> 5% body weight) or rapid weight loss (> 1.6kg/week), within 6 months prior to enrollment;
- uncontrolled cardiovascular or respiratory disease, decompensated liver disease including ascites, encephalopathy or variceal bleeding, active malignancy, or chronic infections;
- participant who had severe course of COVID-19 (extracorporeal membrane oxygenation, mechanically ventilated), and/or had a confirmed case of COVID-19 within 4 weeks prior to enrollment;
- participation in other clinical trials;
- presence of pregnancy or lactation.
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:トリプル
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
アクティブコンパレータ:Probiotic lysate (postbiotic and metabiotc) group
oral, 2 capsules per day (BID) for 3 month treatment |
Each capsule contains 100 mg of cell lysate and DNA fragments of the probiotic strain L. rhamnosus DV - NRRLB-68023 in powder |
|
プラセボコンパレーター:Placebo group
placebo, oral, 2 capsules per day (BID) for 3 month treatment |
Placebo |
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
changes in fatty liver index (FLI)
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
FLI = [e 0.953*loge (triglycerides) + 0.139*BMI + 0.718*loge (ggt) + 0.053*waist circumference - 15.745) / (1 + e 0.953*loge (triglycerides) + 0.139*BMI + 0.718*loge (ggt) + 0.053*waist circumference - 15.745)] × 100 |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
hepatic steatosis index (HSI)
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
HSI = 8 x ALT/AST + BMI(+ 2 if type 2 diabetes yes, + 2 if female) |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
TyG index
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
TyG = ln [Fasting triglyceride (mg / dl) x Fasting glucose (mg / dl)] / 2 |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Concentration of AST
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
AST in IU/L |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
Concentration of ALT
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
ALT in IU/L |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
Concentration of Gamma-glutamyl Transferase (GGT)
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
GGT in IU/L |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
Concentration of Total Cholesterol (TC)
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
TC in mmol/l |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
Concentration of Tryglicerides (TG)
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
TG in mmol/l |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
Concentration of high sensitivity CRP (hs-CRP)
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
hs-CRP in mg/L |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
waist circumferences (WC)
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
WC in cm |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
body mass index (BMI)
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
weight in kg and height in meters will be combined to report BMI in kg/m^2 |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
|
visceral fat content
時間枠:at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
visceral fat content using electronic scales-analyzers of body composition Tanita Scale BC-601 |
at 3 month (end of treatment) and 6 month (follow-up period) compared to baseline]
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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
詳しくは
本研究に関する用語
その他の研究ID番号
- DELI_MASLD
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?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
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