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Completed

NCT Number: NCT04283942

Effect of Intermittent Calorie Restriction on MASLD Patients With Abnormal Glucose Metabolism

This study is designed to observe the effect of 5:2 intermittent calorie restriction (fasting 2 days each week) on liver fat content in MASLD patients with abnormal blood glucose.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Zhongshan Hospital, Fudan University

Shanghai, China

About this study

Intermittent caloric restriction (ICR) can effectively reduce weight and facilitate blood glucose control, but whether it can be applied for clinical treatment to metabolic dysfunction-associated steatotic liver disease (MASLD) patients remains unclear. We intend to carry out this study in MASLD patients with abnormal glucose metabolism. It is an open-labeled randomized trial designed to observe the effect of 5:2 intermittent calorie restriction (fasting 2 days each week) on liver fat content in MASLD patients with abnormal blood glucose. 60 patients will be randomly divided into ICR group and control group for 12 weeks of intervention. ICR group: during the 2-day fasting-mimicking period each week, the food based on plant ingredients will be served (4 pieces of nutrition bars / day, 1:2:1 for breakfast, lunch and dinner, 124.4kcal / piece, 497.2kcal / day in total). In the rest 5 days each week, subjects are allowed ad libitum to their usual food. Control group (continuous calorie restriction, CCR): under the guidance of nutritionist, subjects have to learn the method of food calories calculation. The daily calories intake for control group should be: 25 kcal / kg × [height (cm) - 100] kg. Daily food diary is required in both groups. During the experiment, all subjects should maintain their exercise routine. The use of drugs affecting blood glucose and fatty liver should be avoided. After 12 weeks of intervention, the changes of liver fat content were evaluated by magnetic resonance spectroscopy (MRS) and Magnetic Resonance Imaging-Proton Density Fat Fraction (MRI-PDFF). The effects of ICR on body weight, blood glucose and body fat will also be evaluated. Both groups will be followed up on their changes of weight 4 weeks after intervention.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age 18-70
  • Diagnosed as fatty liver by ultrasound or magnetic resonance imaging
  • BMI ≥ 24 kg/m2
  • abnormal glucose metabolism: (meeting at least one):
  • Impaired glucose regulation: fasting blood glucose ≥ 100 mg/dL, postprandial blood glucose ≥ 140 mg/dL or HbA1c ≥ 5.7%
  • Diabetes mellitus: diabetic symptoms + plasma glucose concentration ≥ 200 mg/dL at any time or fasting plasma glucose concentration ≥ 100 mg/dL or OGTT 2 h plasma glucose concentration ≥ 200 mg/dL

Exclusion criteria

  • Type 1 diabetes, gestational diabetes and other special types of diabetes
  • Poor blood glucose control, HbA1c > 8.5% within 3 months
  • Taking antidiabetic drugs in the past month
  • Serum ALT > 6 times of normal upper limit
  • Excessive alcohol consumption (alcohol intake: men > 140 g, women > 70 g in the past 6 months)
  • Other liver diseases: such as acute and chronic viral hepatitis, drug-induced hepatitis, immune hepatitis, liver cirrhosis, liver cancer, etc
  • Taking drugs that may affect MASLD in the past three months, such as vitamin E
  • Biliary obstructive diseases
  • Other diseases affecting glucose and lipid metabolism: hyperthyroidism, hypothyroidism, Cushing's syndrome, etc
  • Chronic kidney disease (serum creatinine ≥ 2.0 mg/dL)
  • Life expectancy of no more than 5 years
  • Already pregnant or plan to be pregnant in the near future
  • Mental illness
  • Other conditions affecting follow-up
  • Have participated in other clinical trials in the past 4 weeks
  • Absent of informed consent

Treatment and study plan

Intermittent calorie restriction (ICR)

Behavioral

Participants in ICR group were instructed to ensure 2 successive days of fasting-mimicking and 5 days of recovery per week. On fasting-mimicking days, the participants were instructed to consume approximately 500 kcal/day and they were provided with plant-based meal replacement to improve adherence and ensured adequate intake of micronutrients. In the rest 5 days of recovery per week, participants were allowed to consume their usual diet.

Participants will receive dietary counseling from experienced nutritionists and eat a balanced diet (macronutrient distribution of approximately 10-15% protein, 55-65% carbohydrate and 20-30% fat).They are required to write daily dietary log. Besides, they are required to maintain their exercise routines and record their daily steps using a unified pedometer (Redmi Smart Band, Xiaomi Corporation, China). The use of drugs affecting blood glucose and LFC will be avoided.

Other names: Intermittent fasting

Continuous calorie restriction (CCR)

Behavioral

Participants in CCR group were instructed to consume the prescribed calories (25 kcal / kg × [height (cm) - 100] kg) every day by eating conventional food without time restriction.

Participants will receive dietary counseling from experienced nutritionists and eat a balanced diet (macronutrient distribution of approximately 10-15% protein, 55-65% carbohydrate and 20-30% fat).They are required to write daily dietary log. Besides, they are required to maintain their exercise routines and record their daily steps using a unified pedometer (Redmi Smart Band, Xiaomi Corporation, China). The use of drugs affecting blood glucose and LFC will be avoided.

Other names: Daily calorie restriction

Primary outcomes

  1. Change of Liver Fat Content in %

    Time frame: From baseline to week 12

    Change of liver fat content in %.

Secondary outcomes

  1. Change of Weight

    Time frame: From baseline to week 12

    Change of weight in kilograms.

  2. Change of Blood Glucose: Fasting Blood Glucose

    Time frame: From baseline to week 12

    Change of fasting blood glucose in mg/dL.

  3. Change of Blood Glucose: 2h Postload Blood Glucose

    Time frame: From baseline to week 12

    Change of 2h postload blood glucose in mg/dL.

  4. Change of HbA1c

    Time frame: From baseline to week 12

    Change of HbA1c in %.

  5. Change of Liver Enzymes: Alanine Aminotransferase

    Time frame: From baseline to week 12

    Change of alanine aminotransferase in U/L.

  6. Change of Liver Enzymes: Aspartate Aminotransferase

    Time frame: From baseline to week 12

    Change of aspartate aminotransferase in U/L.

  7. Change of Liver Enzymes: γ-glutamyl Transpeptidase

    Time frame: From baseline to week 12

    Change of γ-glutamyl transpeptidase in U/L.

  8. Change of Lipid Profile: Total Cholesterol

    Time frame: From baseline to week 12

    Change of total cholesterol in mg/dL.

  9. Change of Lipid Profile: Triglyceride

    Time frame: From baseline to week 12

    Change of triglyceride in mg/dL.

  10. Change of Lipid Profile: High-density Lipoprotein-cholesterol

    Time frame: From baseline to week 12

    Change of high-density lipoprotein-cholesterol in mg/dL.

  11. Change of Lipid Profile: Low-density Lipoprotein-cholesterol

    Time frame: From baseline to week 12

    Change of low-density lipoprotein-cholesterol in mg/dL.

  12. Change of Lipid Profile: Free Fatty Acid

    Time frame: From baseline to week 12

    Change of free fatty acid in mg/dL.

Other outcomes

  1. Change of Fat Mass

    Time frame: From baseline to week 12

    measured by bioimpedance analyzer, fat mass in kilograms.

  2. Change of Lean Mass

    Time frame: From baseline to week 12

    measured by bioimpedance analyzer, skeletal muscle mass in kilograms.

  3. Change of Abdominal Adipose Tissue Area

    Time frame: From baseline to week 12

    measured by MRI, including visceral adipose and subcutaneous adipose, all in square centimeter.

  4. Change of Liver Stiffness Measure of Liver Transient Elastography

    Time frame: From baseline to week 12

    Change of liver stiffness measure of liver transient elastography, in kPa.

  5. Change of Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) Index

    Time frame: From baseline to week 12

    Change of HOMA-IR index from baseline to week 12. HOMA-IR index was calculated as fasting serum insulin (μU/ml) × fasting plasma glucose (mmol/l)/22.5. A HOMA-IR index higher than 75th quartile of non diabetes subjects is considered to be insulin resistance. However, due to differences in race, gender and research subjects, there is currently no recognized cut-off point. The cut-off values of HOMA-IR reported in previous studies varied greatly. A study on Caucasian non diabetes population showed that the cut-off value is 2.29. And a Chinese study proposed that the cut-off value of population over 40 years old in Shanghai was 4.31 for men and 4.51 for women.

  6. Change of Fasting Insulin

    Time frame: From baseline to week 12

    Change of fasting insulin in μU/mL.

Sponsors and collaborators

Lead sponsor

Shanghai Zhongshan Hospital

Other

Registry information

Official study title

Effect of Intermittent Calorie Restriction on Metabolic Dysfunction-Associated Steatotic Liver Disease Patients With Abnormal Glucose Metabolism

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
Feb 25, 2020
Registry last updated
Sep 23, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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