Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease
Pilot Study: Diabetes Prevention Program for the Treatment of Nonalcoholic Fatty Liver Disease
Nonalcoholic fatty liver disease (NAFLD) is a rapidly growing epidemic worldwide and is an increasingly important etiology of chronic liver disease and hepatocellular carcinoma. NAFLD affects approximately 90 million people in the United States (US) amounting to an annual cost of $100 billion yearly. It is projected to become the leading cause of liver transplantation in the US by 2030 and is associated with significant morbidity and mortality. NAFLD is a spectrum of liver diseases, ranging from simple steatosis (nonalcoholic fatty liver, NAFL) to hepatic steatosis associated with inflammation (nonalcoholic steatohepatitis, NASH), which can be associated with liver scarring (hepatic fibrosis) and cirrhosis. There are limited therapeutic options that have been shown to effectively reduce or reverse the progression of disease.
Lifestyle modification is the backbone of therapy, but difficult to achieve. A modest amount of weight loss of approximately 3% can reduce liver steatosis and a 10% weight loss can reduce the NASH and improve liver fibrosis. The American Association of the Study of Liver Diseases (AASLD) guidelines state that "a combination of a hypocaloric diet (daily reduction by 500-1000 kcal) and moderate intensity exercise is the best likelihood of sustaining weight loss over time." There are several barriers to adopting a healthy lifestyle involving both patient and physician limitations. The aim of this study is to engage patients in a lifestyle intervention program that has already been shown to be successful in achieving weight loss goals and adopting healthier lifestyle patterns.
The CDC Diabetes Prevention Program, (DPP) was a large (n=3,234) multicenter study aimed to evaluate the effect of lifestyle intervention or treatment with metformin on the incidence of type 2 diabetes (T2DM). Lifestyle intervention reduced the incidence of T2DM by 58% (95% CI, 48-66%) and metformin reduced the incidence by 31% (95% CI, 17-43%) as compared to placebo. To prevent one case of diabetes over three years, 6.9 persons would have to participate in the lifestyle-intervention program, and 13.9 would have to receive metformin. The CDC DPP program has been adapted and tested in the multiple different community and state-wide programs including the YMCA, WorkWellNYC and NYS DPP. In these real-world models, the life style intervention program has been delivered in a group-based format by DPP lifestyle coaches. These programs have been successful like that of the randomized trial and improvements were sustainable at 6 and 12 month follow up after completion of the program. The program is now available and reimbursable through Medicare (Medicare Diabetes Prevention Program).
In this pilot study, the researchers will enroll 20 patients with NAFLD in an adapted DPP program and follow study participants for 1 year. The rationale for the proposed research is to apply the DPP to NAFLD because of the close relationship with Diabetes and determine the real-world outcome of the DPP program on weight loss in patients with NAFLD. If the researchers illustrate that weight loss can be achieved and is sustainable in patients with NAFLD enrolled in lifestyle intervention programs, the researchers can develop innovative approaches to deliver such a program nationwide in a cost-effective and sustainable manner.
調査の概要
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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New York
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New York、New York、アメリカ、10003
- Mount Sinai Union Square
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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:
- diagnosis of NAFLD, defined by the presence of hepatic steatosis with vibration controlled transient elastography (VCTE) controlled attenuation parameter (CAP) measurement over 240dB/m, or liver biopsy showing macrovesicular steatosis in ≥ 5% of hepatocytes.
- patients were 18 years and older,
- fluent in English (the program could only be conducted in English by the DPP-certified coach),
- able to meet program scheduling requirements, and able to participate in physical activity.
Exclusion Criteria:
- additional causes of liver disease such as viral hepatitis, biliary obstruction, hepatocellular carcinoma, Wilson's disease, Budd Chiari Syndrome, autoimmune hepatitis, alcoholic liver disease or alcohol use (>20g/day women, >30g/day men),
- aspartate aminotransferase (AST) or alanine aminotransferase (ALT) values >300 U/L,
- using steatogenic medications (amiodarone, methotrexate, tamoxifen, and corticosteroids),
- pregnant,
- a history of liver transplantation.
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:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的:Treatment Arm
Patients enrolled in 1 year program
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The Diabetes Prevention Program is a 1 year validated program to prevent the development of type 2 diabetes.
Participants with NAFLD will engage will work with a CDC certified DPP certified lifestyle coach and other participants in a group setting during the study focusing on lifestyle changes to achieve weight loss and improvement in NAFLD.
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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 |
|---|---|---|
|
Number of participants in the program at the end of the study
時間枠:12 months
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Retention defined as number of patients in the program at the end of the study
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12 months
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Change in Weight
時間枠:baseline and 12 months
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Change in Weight at 12 months as compared to baseline
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baseline and 12 months
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Hepatic steatosis via Fibroscan
時間枠:Baseline
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Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.
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Baseline
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Hepatic steatosis via Fibroscan
時間枠:6 months
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Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter .
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6 months
|
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Hepatic steatosis via Fibroscan
時間枠:12 months
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Changes in hepatic steatosis measured with fibroscan using the controlled attenuated parameter.
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12 months
|
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Glycosylated A1C
時間枠:Baseline
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Glycosylated A1C in assessing metabolic comorbidity
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Baseline
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Glycosylated A1C
時間枠:6 months
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Glycosylated A1C in assessing metabolic comorbidity
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6 months
|
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Glycosylated A1C
時間枠:12 months
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Glycosylated A1C in assessing metabolic comorbidity
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12 months
|
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Lipid levels
時間枠:Baseline
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Lipid levels in assessing metabolic comorbidity
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Baseline
|
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Lipid levels
時間枠:6 months
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Lipid levels in assessing metabolic comorbidity
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6 months
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Lipid levels
時間枠:12 months
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Lipid levels in assessing metabolic comorbidity
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12 months
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Liver enzymes levels
時間枠:Baseline
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Liver enzymes levels for ALT, AST, and ALP
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Baseline
|
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Liver enzymes levels
時間枠:6 months
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Liver enzymes levels for ALT, AST, and ALP
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6 months
|
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Liver enzymes levels
時間枠:12 months
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Liver enzymes levels for ALT, AST, and ALP
|
12 months
|
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Bilirubin level
時間枠:Baseline
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Liver enzyme level for Bilirubin
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Baseline
|
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Bilirubin level
時間枠:6 months
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Liver enzyme level for Bilirubin
|
6 months
|
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Bilirubin level
時間枠:12 months
|
Liver enzyme level for Bilirubin
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12 months
|
協力者と研究者
捜査官
- 主任研究者:Amreen Dinani、Icahn School of Medicine, Division of Liver Diseases
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
追加の関連 MeSH 用語
その他の研究ID番号
- GCO 18-1283
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?
IPD プランの説明
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
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
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