间歇性扫描连续血糖监测6个月对1型糖尿病高危HbA1c青少年和青年习惯性睡眠模式和睡眠质量的影响

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Shelley Rose, B. Galland, Sara E. Styles, E. Wiltshire, James Stanley, M. D. de Bock, P. Tomlinson, Jenny A Rayns, B. Wheeler
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引用次数: 0

摘要

背景。睡眠和血糖水平之间的双向关系可能特别影响青少年和年轻人(AYA),他们更有可能经历不健康的血糖结果和更多的睡眠模式中断。迄今为止,很少有数据描述间歇性扫描连续血糖监测(isCGM)对AYA合并1型糖尿病(T1D)的习惯性睡眠模式和睡眠质量的影响。目标。评估6个月使用isCGM对T1D和HbA1c≥75 mmol/mol的年轻人习惯性睡眠和觉醒时间、睡眠持续时间、频率和夜间觉醒持续时间、睡眠效率和感知睡眠质量的影响。参与者。研究招募了64名参与者,年龄13-20岁(平均16.6±2.1),女性占48%,糖尿病病程7.5±3.8年,Māori或Pasifika占41%,平均HbA1c为96.0±18.0 mmol/mol[10.9±3.8%];33人被分配到isCGM +自我监测血糖[SMBG]干预组,31人被分配到SMBG对照组。方法。参与者在基线和6个月时完成了7天的活动记录仪测量和匹兹堡睡眠质量指数问卷。回归分析用于组间比较建模,并根据基线睡眠测量进行调整。结果。在6个月时,两组之间的总体睡眠质量、潜伏期、持续时间、效率、夜间干扰、睡眠药物使用和白天功能障碍的主观测量是相似的。活动描记仪的回归分析发现,在调整了年龄、学年和基线睡眠值后,客观测量的睡眠时间和持续时间在一周内没有显著差异。结论。在T1D、HbA1c升高和睡眠模式高度可变的AYA患者中,除手指点刺试验外,使用第一代isCGM对客观或主观睡眠测量没有影响。在这一人群中,使用替代干预措施改善血糖结局、习惯性睡眠-觉醒时间、持续时间和感知睡眠质量是有必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of 6 months’ Use of Intermittently Scanned Continuous Glucose Monitoring on Habitual Sleep Patterns and Sleep Quality in Adolescents and Young Adults with Type 1 Diabetes and High-Risk HbA1c
Background. The bidirectional relationship between sleep and blood glucose levels may particularly affect adolescents and young adults (AYA), who are more likely to experience less healthy glycemic outcomes and more disrupted sleep patterns. To date, few data exist describing the impact of intermittently scanned continuous glucose monitoring (isCGM) on habitual sleep patterns and sleep quality in AYA with type 1 diabetes (T1D). Objective. To evaluate the impact of 6-month use of isCGM on habitual sleep and wake timing, sleep duration, frequency, and duration of night-time awakenings, sleep efficiency, and perceived sleep quality in young people with T1D and HbA1c ≥ 75 mmol/mol. Participants. The study recruited 64 participants aged 13–20 years (mean 16.6 ± 2.1), 48% female, diabetes duration 7.5 ± 3.8 years, 41% Māori or Pasifika, and a mean HbA1c 96.0 ± 18.0 mmol/mol [10.9 ± 3.8%]; 33 were allocated to an isCGM plus self-monitoring blood glucose [SMBG] intervention, and 31 were allocated to the SMBG control group. Methods. Participants completed 7-day actigraphy measures and the Pittsburgh Sleep Quality Index questionnaire at the baseline and at 6 months. Regression analyses were used to model between-group comparisons, adjusted for baseline sleep measures. Results. At 6 months, subjective measures for overall sleep quality, latency, duration, efficiency, night-time disturbances, use of sleep medications, and daytime dysfunction were similar between the groups. Regression analyses of actigraphy found no significant differences in objectively measured sleep timing and duration across the week after adjusting for age, the period of the school year, and baseline sleep values. Conclusions. The use of first-generation isCGM in addition to finger-prick testing did not impact objective or subjective sleep measures in AYA with T1D, elevated HbA1c, and highly variable sleep patterns. Research using alternative interventions for improving glycemic outcomes and habitual sleep-wake timing, duration, and perceived sleep quality is warranted in this population group.
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CiteScore
7.20
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