Effect of Intermittent Calorie Restriction on MASLD Patients With Abnormal Glucose Metabolism
Fatty Liver Disease, Type 2 Diabetes, Impaired Glucose Regulation
About this trial
This is an interventional treatment trial for Fatty Liver Disease focused on measuring Metabolic dysfunction-associated steatotic liver disease, Type 2 Diabetes
Eligibility Criteria
Inclusion Criteria:
- Age 18-70
- diagnosed as fatty liver
- BMI≥24 kg/m2
The diagnostic criteria for abnormal glucose metabolism are as follows (meeting at least one):
- Impaired glucose regulation: fasting blood glucose ≥ 5.6 mmol / L, postprandial blood glucose ≥ 7.8 mmol / L or HbA1c ≥ 5.7%.
- Diabetes mellitus: diabetic symptoms + plasma glucose concentration ≥ 11.1 mmol / L at any time or fasting plasma glucose concentration ≥ 7.0 mmol / L or OGTT 2 h plasma glucose concentration ≥ 11.1 mmol / L.
Exclusion Criteria:
- Type 1 diabetes, gestational diabetes and other special types of diabetes
- Poor blood glucose control, HbA1c > 8.5% within 3 months
- Had antidiabetic drugs in the past month
- Serum ALT was more than 6 times of normal upper limit
- Excessive alcohol consumption (definition: in the past 6 months, alcohol intake: men > 140g, women > 70g)
- Other liver diseases: such as acute and chronic viral hepatitis, drug-induced hepatitis, immune hepatitis, liver cirrhosis, liver cancer, etc
- Had drugs that may affect NAFLD in the past three months, such as vitamin E
- Biliary diseases: biliary obstructive diseases, etc
- Other diseases affecting glycolipid metabolism: hyperthyroidism, hypothyroidism, Cushing's syndrome, etc
- Chronic kidney disease (serum creatinine ≥ 2.0mg/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
- Participated in other clinical trials in the past 4 weeks
- Absent of informed consent
Sites / Locations
- Zhongshan Hospital, Fudan University
Arms of the Study
Arm 1
Arm 2
Experimental
Other
Intermittent Calorie Restriction (ICR)
Control (Continuous calorie restriction, CCR)
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 (ZhenBaiNian nutrition bar, Beijing Wanlaikang Nutrition and Health Food Science and Technology Research Institute Co., Ltd, China) 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 in control group were instructed to consume the prescribed calories (25 kcal / kg × [height (cm) - 100] kg) every day by eating conventional food without time restriction.