Prolonged Use of an Automated Insulin Delivery System Improves Sleep in Long-Standing Type 1 Diabetes Complicated by Impaired Awareness of Hypoglycemia

被引:4
|
作者
Malone, Susan Kohl [1 ]
Matus, Austin M. [2 ]
Flatt, Anneliese J. [3 ]
Peleckis, Amy J. [3 ]
Grunin, Laura [1 ]
Yu, Gary [1 ]
Jang, Sooyong [4 ]
Weimer, James [4 ]
Lee, Insup [4 ]
Rickels, Michael R. [3 ]
Goel, Namni [5 ]
机构
[1] New York Univ, Rory Meyers Coll Nursing, New York, NY USA
[2] Univ Pennsylvania, Sch Nursing, Philadelphia, PA USA
[3] Univ Pennsylvania, & Inst Diabet, Perelman Sch Med, Div Endocrinol, Philadelphia, PA USA
[4] Univ Pennsylvania, Sch Engn & Appl Sci, Dept Comp & Informat Sci, PRECISE Ctr, Philadelphia, PA USA
[5] Rush Univ Med Ctr, Dept Psychiat & Behav Sci, Biol Rhythms Res Lab, Chicago, IL USA
来源
基金
美国国家航空航天局;
关键词
circadian; diabetes therapeutic technologies; sleep; type; 1; diabetes; hypoglycemia; insulin delivery; AUTONOMIC FAILURE; GLYCEMIC LABILITY; YOUNG-ADULTS; GLUCOSE; ASSOCIATIONS; RESPONSES; SEVERITY; IMPACT;
D O I
10.1177/19322968231182406
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: This study assessed changes in actigraphy-estimated sleep and glycemic outcomes after initiating automated insulin delivery (AID). Methods: Ten adults with long-standing type 1 diabetes and impaired awareness of hypoglycemia (IAH) participated in an 18-month clinical trial assessing an AID intervention on hypoglycemia and counter-regulatory mechanisms. Data from eight participants (median age = 58 years) with concurrent wrist actigraph and continuous glucose monitoring (CGM) data were used in the present analyses. Actigraphs and CGM measured sleep and glycemic control at baseline (one week) and months 3, 6, 9, 12, 15, and 18 (three weeks) following AID initiation. HypoCount software integrated actigraphy with CGM data to separate wake and sleep-associated glycemic measures. Paired sample t-tests and Cohen's d effect sizes modeled changes and their magnitude in sleep, glycemic control, IAH (Clarke score), hypoglycemia severity (HYPO score), hypoglycemia exposure (CGM), and glycemic variability (lability index [LI]; CGM coefficient-of-variation [CV]) from baseline to 18 months. Results: Sleep improved from baseline to 18 months (shorter sleep latency [P < .05, d = 1.74], later sleep offset [P < .05, d = 0.90], less wake after sleep onset [P < .01, d = 1.43]). Later sleep onset (d = 0.74) and sleep midpoint (d = 0.77) showed medium effect sizes. Sleep improvements were evident from 12 to 15 months after AID initiation and were preceded by improved hypoglycemia awareness (Clarke score [d = 1.18]), reduced hypoglycemia severity (HYPO score [d = 2.13]), reduced sleep-associated hypoglycemia (percent time glucose was < 54 mg/dL, < 60 mg/dL,< 70 mg/dL; d = 0.66-0.81), and reduced glucose variability (LI, d = 0.86; CV, d = 0.62). Conclusion: AID improved sleep initiation and maintenance. Improved awareness of hypoglycemia, reduced hypoglycemia severity, hypoglycemia exposure, and glucose variability preceded sleep improvements. This trial is registered with ClinicalTrials.gov NCT03215914 https://clinicaltrials.gov/ct2/show/NCT03215914.
引用
收藏
页码:1416 / 1423
页数:8
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