Halliday Jennifer A, Russell-Green Sienna, Lam Benjamin, Trawley Steven, McAuley Sybil A, Bach Leon A, Burt Morton G, Cohen Neale D, Colman Peter G, Davis Elizabeth A, Holmes-Walker Deborah Jane, Jenkins Alicia J, Kaye Joey, Keech Anthony C, Lee Melissa H, McCallum Roland W, Paldus Barbora, Stranks Stephen N, Sundararajan Vijaya, Ward Glenn, Jones Timothy W, O'Neal David, Speight Jane, Hendrieckx Christel
Institute for Health Transformation, Deakin University, Geelong, Victoria, Australia
The Australian Centre for Behavioural Research in Diabetes, Diabetes Victoria, Carlton, Victoria, Australia.
BMJ Open Diabetes Res Care. 2024 Dec 22;12(6):e004428. doi: 10.1136/bmjdrc-2024-004428.
This analysis aimed to investigate diabetes-specific psychological outcomes among adults with type 1 diabetes (T1D) using hybrid closed-loop (HCL) versus standard therapy.
In this multicenter, open-label, randomized, controlled, parallel-group clinical trial, adults with T1D were allocated to 26 weeks of HCL (MiniMed™ 670G) or standard therapy (insulin pump or multiple daily injections without real-time continuous glucose monitoring). Psychological outcomes (awareness and fear of hypoglycemia; and diabetes-specific positive well-being, diabetes distress, diabetes treatment satisfaction, and diabetes-specific quality of life (QoL)) were measured at enrollment, mid-trial and end-trial. Linear mixed models were conducted, using restricted maximum likelihood estimation, unadjusted and adjusted (for covariates: age, sex, diabetes duration, glycated hemoglobin, recent severe hypoglycemia, pre-trial insulin delivery modality, enrollment and mid-study scores).
120 participants (mean age 44±12 years) were randomized to intervention (n=61) or standard therapy (n=59). At 13 weeks, the HCL group had better diabetes-specific positive well-being than the standard therapy group (unadjusted: Δ=1.0, p=0.025; adjusted: Δ=1.1, p=0.01), which was maintained at 26 weeks (unadjusted: Δ=0.9, p=0.042; adjusted: Δ=1.0, p=0.023). At 26 weeks, the HCL group also had less diabetes distress (adjusted: Δ=-6.4, p=0.039), fear of hypoglycemia ("maintain high": adjusted: Δ=-0.8, p=0.034; and "worry": adjusted: Δ=-1.8, p=0.048), and perceived "unacceptably high glucose levels" (unadjusted: Δ=-1.1, p<0.001; adjusted: Δ=-1.1, p<0.001). HCL did not improve diabetes treatment satisfaction, diabetes-specific QoL, hypoglycemia awareness, or perceived frequency of unacceptably low glucose levels.
These findings imply that HCL offers important psychological benefits. In particular, improvement in diabetes-specific positive well-being was observed 13 weeks after HCL initiation and maintained at 26 weeks. Reduction in the perceived frequency of hyperglycemia was also apparent by 26 weeks. Adjusted analyses showed significant reductions in diabetes distress and fear of hypoglycemia at 26 weeks, suggesting these benefits were apparent for people with particular characteristics.
Australian New Zealand Clinical Trials Registry: ACTRN12617000520336.
本分析旨在研究使用混合闭环(HCL)疗法与标准疗法的1型糖尿病(T1D)成年患者的糖尿病特异性心理结局。
在这项多中心、开放标签、随机、对照、平行组临床试验中,将T1D成年患者分配接受26周的HCL(美敦力MiniMed™ 670G)或标准疗法(胰岛素泵或每日多次注射,无实时连续血糖监测)。在入组时、试验中期和试验结束时测量心理结局(低血糖意识和恐惧;以及糖尿病特异性积极幸福感、糖尿病困扰、糖尿病治疗满意度和糖尿病特异性生活质量(QoL))。使用限制最大似然估计进行线性混合模型分析,未调整和调整(针对协变量:年龄、性别、糖尿病病程、糖化血红蛋白、近期严重低血糖、试验前胰岛素给药方式、入组和研究中期得分)。
120名参与者(平均年龄44±12岁)被随机分配至干预组(n = 61)或标准治疗组(n = 59)。在13周时,HCL组的糖尿病特异性积极幸福感优于标准治疗组(未调整:Δ = 1.0,p = 0.025;调整后:Δ = 1.1,p = 0.01),并在26周时维持(未调整:Δ = 0.9,p = 0.042;调整后:Δ = 1.0,p = 0.023)。在26周时,HCL组的糖尿病困扰也更少(调整后:Δ = -6.4,p = 0.039),低血糖恐惧(“保持高水平”:调整后:Δ = -0.8,p = 0.034;“担忧”:调整后:Δ = -1.8,p = 0.048),以及感知到的“不可接受的高血糖水平”(未调整:Δ = -1.1,p < 0.001;调整后:Δ = -1.1,p < 0.001)。HCL并未改善糖尿病治疗满意度、糖尿病特异性QoL、低血糖意识或感知到的不可接受的低血糖水平发生频率。
这些发现表明HCL具有重要的心理益处。特别是,在开始HCL治疗13周后观察到糖尿病特异性积极幸福感有所改善,并在26周时维持。到26周时,感知到的高血糖发生频率也明显降低。调整分析显示,在26周时糖尿病困扰和低血糖恐惧显著降低,表明这些益处对于具有特定特征的人群明显。
澳大利亚新西兰临床试验注册中心:ACTRN12617000520336。