Bonham Maxine P, Leung Gloria K W, Rogers Michelle, Davis Rochelle, Clark Angela B, Davis Corinne, Phoi Yan Yin, Ware Robert S, El-Heneidy Asmaa, Kellow Nicole J, Dorrian Jillian, Banks Siobhan, Sletten Tracey L, Huggins Catherine E, Coates Alison M
Department of Nutrition, Dietetics and Food, Monash University, Notting Hill, Victoria, Australia.
Department of Nutrition, Dietetics and Food, Monash University, Notting Hill, Victoria, Australia.
EBioMedicine. 2025 Jun 18;117:105803. doi: 10.1016/j.ebiom.2025.105803.
Weight gain and an increased risk of developing type 2 diabetes are recognised consequences of night shift work. We tested the effectiveness of two modified intermittent fasting (IF) strategies compared with continuous energy restriction (CER) on weight loss and improvements in insulin resistance in night shift workers.
A parallel group, three-arm randomised superiority clinical trial (Melbourne and Adelaide) recruited night shift workers (aged ≥ 25 and ≤ 65 years) with overweight/obesity. Participants were randomised by minimisation (site, age, gender) 1:1:1 to CER or one of two modified IF strategies. For 24 weeks participants followed a diet of 2100 kJ/d for two days of the week (modified IF) either on days off/day shift (IF:2D) or whilst on night shift (IF:2N) and followed their usual diet on the remaining five days. Co-primary outcomes were body weight and insulin resistance measured by the Homeostatic Model Assessment for Insulin Resistance (HOMA-IR) at 24-weeks. Participants and those assessing weight outcomes were not blinded to group assignment. Researchers assessing biochemical outcomes and study statistician were blinded to group assignment. Between-group differences were calculated using mixed-effects regression models.
From October 2019 to February 2022, 250 participants (CER = 85; IF:2D = 83; IF:2N = 82) were randomised (mean (SD) age 46.8 (9.8) years; 133 women (53.2%)), with 170 (68%) completing. No significant difference between either modified IF strategy and CER for body weight; IF:2D vs CER (mean difference (MD) = -0.2 kg [95% CI -6.4 to 5.9]) and IF:2N vs CER (MD = -0.6 kg [95% CI -6.8 to 5.6]) and insulin resistance; IF:2D vs CER (MD = -0.1 [95% CI -1.0 to 0.8]) and IF:2N vs CER (MD = -0.3 [95% CI -0.5 to 1.2]) were observed. For secondary outcomes, those randomised to IF:2D had lower total and LDL cholesterol compared to CER ((MD = -23.2 mg/dL [95% CI -34.8 to -11.6]) and (MD = -19.3 mg/dL [95% CI -30.9 to -7.7]) respectively). In a completer's analysis, favourable changes in body weight, insulin resistance, body composition, blood pressure, and cardiometabolic markers were observed within all groups. No serious trial related adverse events were reported.
At 24 weeks, weight and HOMA-IR were not different between the modified IF groups compared with CER. Clinically significant improvements in weight and metabolic health were achieved for the majority of night shift workers who remained in the intervention at 24 weeks.
National Health and Medical Research Council (APP1159762). ANZCTR registry, ACTRN-12619001035112.
体重增加和患2型糖尿病风险上升是公认的夜班工作后果。我们比较了两种改良间歇性禁食(IF)策略与持续能量限制(CER)对夜班工作者体重减轻及胰岛素抵抗改善情况的有效性。
一项平行组、三臂随机优效性临床试验(墨尔本和阿德莱德)招募了超重/肥胖的夜班工作者(年龄≥25岁且≤65岁)。参与者按最小化法(地点、年龄、性别)以1:1:1随机分配至CER组或两种改良IF策略之一。在24周内,参与者每周两天遵循2100千焦/天的饮食(改良IF),休息日/白班(IF:2D)或夜班时(IF:2N),其余五天遵循平常饮食。共同主要结局为24周时通过胰岛素抵抗稳态模型评估(HOMA-IR)测量的体重和胰岛素抵抗。参与者及评估体重结局者未对分组设盲。评估生化结局的研究人员和研究统计学家对分组设盲。组间差异采用混合效应回归模型计算。
2019年10月至2022年2月,250名参与者(CER组 = 85名;IF:2D组 = 83名;IF:2N组 = 82名)被随机分组(平均(标准差)年龄46.8(9.8)岁;133名女性(53.2%)),170名(68%)完成试验。两种改良IF策略与CER在体重方面均无显著差异;IF:2D与CER相比(平均差值(MD)=-0.2千克[95%置信区间 -6.4至5.9]),IF:2N与CER相比(MD = -0.6千克[95%置信区间 -6.8至5.6]),胰岛素抵抗方面;IF:2D与CER相比(MD = -0.1[95%置信区间 -1.0至0.8]),IF:2N与CER相比(MD = -0.3[95%置信区间 -0.5至1.2])。对于次要结局,随机分配至IF:2D组的参与者总胆固醇和低密度脂蛋白胆固醇低于CER组(分别为(MD = -23.2毫克/分升[95%置信区间 -34.8至 -11.6])和(MD = -19.3毫克/分升[95%置信区间 -30.9至 -7.7]))。在完成者分析中,所有组内均观察到体重、胰岛素抵抗、身体成分、血压和心血管代谢标志物的有利变化。未报告与试验相关的严重不良事件。
24周时,改良IF组与CER组在体重和HOMA-IR方面无差异。24周时仍参与干预的大多数夜班工作者在体重和代谢健康方面实现了具有临床意义的改善。
国家卫生与医学研究委员会(APP1159762)。澳大利亚和新西兰临床试验注册中心,注册号:ACTRN-12619001035112。