Low-calorie diets and remission of type 2 diabetes in Chinese: phenotypic changes and individual variability.

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Tác giả: Ying Dong, Xihao Du, Nannan Feng, Yang Liu, Zhenxiu Liu, Zhewei Sun, Yue Tan, Feng Tao, Jie Wang, Sujing Wang, Yaqing Xu, Victor W Zhong

Ngôn ngữ: eng

Ký hiệu phân loại: 809.008 History and description with respect to kinds of persons

Thông tin xuất bản: England : Nutrition journal , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 712462

BACKGROUND: Chinese have distinct phenotypes of type 2 diabetes (T2D) and obesity compared with people of other ethnicities, but using low-calorie diets to achieve T2D remission has never been conducted in Chinese. This study aimed to assess if T2D remission can be achieved using low-calorie formula diet (LCFD) and low-calorie real food-based diet (LCRFD) in Chinese similarly to other populations and to identify determinants of individual variability in T2D remission. METHODS: This 6-month intervention consisted of a 3-month isocaloric intensive weight loss phase (815-835 kcal/d) and a 3-month weight maintenance phase. Enrolled participants with T2D had BMI of 24-45 kg/m RESULTS: At 6 months, 29.3% of participants had ≥ 12 kg weight loss, 39.0% lost ≥ 10% weight, and 56.1% achieved T2D remission. MRI-derived liver and pancreatic fat decreased significantly. Significant improvement was also seen in insulin sensitivity, continuous glucose monitoring-derived metrics, and various other cardiometabolic risk factors but not arginine-induced insulin secretory response. There was no difference in all outcomes between LCFD and LCRFD. Compared with responders for T2D remission, nonresponders were more likely to be women, and had more fat mass, longer diabetes duration, poorer glycemic control, and lower beta-cell function. CONCLUSIONS: T2D remission rate and weight loss amount following low-calorie diet intervention in Chinese people were comparable to those reported from other populations, although individual variability existed. LCFD and LCRFD were similarly effective. TRIAL REGISTRATION: The trial was registered with ClinicalTrials.gov: NCT05472272.
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