Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Barbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Diabetes Obes Metab. 2024 Jul;26(7):2662-2672. doi: 10.1111/dom.15582. Epub 2024 Apr 8.
Type 1 diabetes (T1D) increases the risk of morbidity and mortality from cardiovascular disease, and insufficient sleep is prevalent. Emerging evidence suggests a link between sleep and cardiometabolic health, but this has not been examined across the lifespan in individuals with T1D. We aimed to examine associations between sleep and cardiometabolic health in adolescents and adults with T1D in a secondary analysis of data from a 4-week double-blind, random-order, placebo-controlled crossover trial of bromocriptine quick release (BCQR) therapy with a 4-week washout in between conditions.
Forty-two adults (19-60 years) and 42 adolescents (12-18 years) with T1D >9 months completed 1 week of home monitoring with wrist-worn actigraphy to estimate sleep duration and continuous glucose monitoring, anthropometrics, arterial stiffness, magnetic resonance imaging (adolescents only), and fasting laboratory testing at each treatment phase.
Sixty-two per cent of adolescents and 74% of adults obtained <7 h of sleep per night at baseline. After adjustment for age, sex and diabetes duration, baseline sleep <7 h per night was associated with a higher body mass index, a higher waist circumference, a higher systolic blood pressure, worse arterial stiffness and a lower estimated insulin sensitivity (all p < .05). When examined by age group, associations between sleep duration and cardiometabolic health outcomes remained significant, predominantly for adolescents. In adolescents only, wake time was significantly later (p = .027) and time in bed was significantly longer with BCQR versus placebo (p = .049).
Objectively measured sleep <7 h per night was prevalent in adolescents and adults with T1D and associated with poorer cardiometabolic health markers. Small changes in sleep were seen following BCQR treatment in adolescents only. Sleep may be an important and novel target for improving cardiometabolic health in individuals with T1D.
1 型糖尿病(T1D)会增加心血管疾病的发病率和死亡率,而睡眠不足在 T1D 患者中很常见。新出现的证据表明睡眠与心脏代谢健康之间存在联系,但在 T1D 患者的整个生命周期中,这一点尚未得到研究。我们旨在通过对一项为期 4 周的溴隐亭快速释放(BCQR)治疗的双盲、随机、交叉试验的二次分析,来研究 T1D 青少年和成人的睡眠与心脏代谢健康之间的关系,该试验在两种治疗条件之间有 4 周的洗脱期。
42 名成年(19-60 岁)和 42 名青少年(12-18 岁)T1D 患者(患病时间>9 个月)在家中佩戴腕戴式活动记录仪进行了为期 1 周的睡眠监测,以估计睡眠时间和连续血糖监测、人体测量、动脉僵硬、磁共振成像(仅适用于青少年)和空腹实验室检查,在每个治疗阶段。
62%的青少年和 74%的成年人在基线时每晚睡眠不足 7 小时。在调整年龄、性别和糖尿病持续时间后,基线时每晚睡眠不足 7 小时与较高的体重指数、较高的腰围、较高的收缩压、较差的动脉僵硬和较低的胰岛素敏感性相关(所有 p 值均<0.05)。按年龄组检查时,睡眠时间与心脏代谢健康结果之间的关联仍然显著,主要是青少年。只有在青少年中,与安慰剂相比,BCQR 治疗后清醒时间明显延迟(p=0.027),卧床时间明显延长(p=0.049)。
T1D 青少年和成人中每晚客观测量睡眠时间<7 小时很常见,并且与较差的心脏代谢健康标志物相关。在青少年中,仅在接受 BCQR 治疗后才出现睡眠的微小变化。睡眠可能是改善 T1D 患者心脏代谢健康的一个重要且新颖的目标。