Otto Loewi Research Center, Division of Pharmacology, Medical University of Graz, Graz, 8010, Austria.
Interdisciplinary Metabolic Medicine Trials Unit, Division of Endocrinology and Diabetology, Medical University of Graz, Graz, 8036, Austria.
Cardiovasc Diabetol. 2024 Sep 12;23(1):339. doi: 10.1186/s12933-024-02426-5.
Cardiovascular disease represents a significant risk factor for mortality in individuals with type 2 diabetes mellitus (T2DM). High-density lipoprotein (HDL) is believed to play a crucial role in maintaining cardiovascular health through its multifaceted atheroprotective effects and its capacity to enhance glycemic control. The impact of dietary interventions and intermittent fasting (IF) on HDL functionality remains uncertain. The objective of this study was to assess the effects of dietary interventions and IF as a strategy to safely improve glycemic control and reduce body weight on functional parameters of HDL in individuals with T2DM.
Before the 12-week intervention, all participants (n = 41) of the INTERFAST-2 study were standardized to a uniform basal insulin regimen and randomized to an IF or non-IF group. Additionally, all participants were advised to adhere to dietary recommendations that promoted healthy eating patterns. The IF group (n = 19) followed an alternate-day fasting routine, reducing their calorie intake by 75% on fasting days. The participants' glucose levels were continuously monitored. Other parameters were measured following the intervention: Lipoprotein composition and subclass distribution were measured by nuclear magnetic resonance spectroscopy. HDL cholesterol efflux capacity, paraoxonase 1 (PON1) activity, lecithin cholesterol acyltransferase (LCAT) activity, and cholesterol ester transfer protein (CETP) activity were assessed using cell-based assays and commercially available kits. Apolipoprotein M (apoM) levels were determined by ELISA.
Following the 12-week intervention, the IF regimen significantly elevated serum apoM levels (p = 0.0144), whereas no increase was observed in the non-IF group (p = 0.9801). ApoM levels correlated with weight loss and fasting glucose levels in the IF group. Both groups exhibited a robust enhancement in HDL cholesterol efflux capacity (p < 0.0001, p = 0.0006) after 12 weeks. Notably, only the non-IF group exhibited significantly elevated activity of PON1 (p = 0.0455) and LCAT (p = 0.0117) following the 12-week intervention. In contrast, the changes observed in the IF group did not reach statistical significance.
A balanced diet combined with meticulous insulin management improves multiple metrics of HDL function. While additional IF increases apoM levels, it does not further enhance other aspects of HDL functionality.
The study was registered at the German Clinical Trial Register (DRKS) on 3 September 2019 under the number DRKS00018070.
心血管疾病是 2 型糖尿病(T2DM)患者死亡的重要危险因素。高密度脂蛋白(HDL)被认为通过其多方面的抗动脉粥样硬化作用及其增强血糖控制的能力,在维持心血管健康方面发挥着关键作用。饮食干预和间歇性禁食(IF)对 HDL 功能的影响仍不确定。本研究旨在评估饮食干预和 IF 作为一种安全改善血糖控制和减轻体重的策略,对 T2DM 个体 HDL 功能参数的影响。
在 12 周干预之前,INTERFAST-2 研究的所有参与者(n=41)都标准化为统一的基础胰岛素方案,并随机分为 IF 或非 IF 组。此外,所有参与者都被建议遵循促进健康饮食模式的饮食建议。IF 组(n=19)遵循隔日禁食常规,在禁食日减少 75%的热量摄入。参与者的血糖水平被连续监测。干预后测量其他参数:脂蛋白组成和亚类分布通过核磁共振光谱法测量。使用基于细胞的测定法和市售试剂盒评估 HDL 胆固醇外排能力、对氧磷酶 1(PON1)活性、卵磷脂胆固醇酰基转移酶(LCAT)活性和胆固醇酯转移蛋白(CETP)活性。通过 ELISA 测定载脂蛋白 M(apoM)水平。
经过 12 周的干预,IF 方案显著提高了血清 apoM 水平(p=0.0144),而非 IF 组则没有升高(p=0.9801)。apoM 水平与 IF 组的体重减轻和空腹血糖水平相关。两组在 12 周后均表现出 HDL 胆固醇外排能力的显著增强(p<0.0001,p=0.0006)。值得注意的是,只有非 IF 组在 12 周后显示出 PON1(p=0.0455)和 LCAT(p=0.0117)活性的显著升高。相比之下,IF 组的变化没有达到统计学意义。
均衡饮食结合精细胰岛素管理可改善 HDL 功能的多项指标。虽然额外的 IF 会增加 apoM 水平,但不会进一步增强 HDL 功能的其他方面。
该研究于 2019 年 9 月 3 日在德国临床试验注册处(DRKS)注册,注册号为 DRKS00018070。