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苏沃雷生对 2 型糖尿病伴失眠患者睡眠质量和代谢参数的时间治疗疗效。

Chronotherapeutic efficacy of suvorexant on sleep quality and metabolic parameters in patients with type 2 diabetes and insomnia.

机构信息

Division of Diabetes, Metabolism, and Endocrinology, Department of Toho University Graduate School of Medicine, 6-11-1 Omori-Nishi, Ota-ku, Tokyo 143-8541, Japan.

Division of Diabetes, Metabolism, and Endocrinology, Department of Toho University Graduate School of Medicine, 6-11-1 Omori-Nishi, Ota-ku, Tokyo 143-8541, Japan.

出版信息

Diabetes Res Clin Pract. 2020 Nov;169:108412. doi: 10.1016/j.diabres.2020.108412. Epub 2020 Sep 8.

Abstract

AIMS

This study aimed to assess the chronotherapeutic efficacy of suvorexant on subjective sleep parameters and metabolic parameters in patients with type 2 diabetes and insomnia.

METHODS

Thirteen patients with type 2 diabetes who met the Pittsburg Sleep Quality index criteria for primary insomnia took suvorexant 20 mg/day (15 mg/day for ≥65 years) for 14 ± 2 weeks. The following parameters were assessed before and after the treatment: sleep diary for sleep duration and quality (i.e., sleep onset latency, waking after sleep onset, and sleep efficiency [sSE]), Insomnia Severity Index, clinical and biochemical data, continuous glucose monitoring (CGM), and validated self-administered questionnaire on food intake.

RESULTS

Suvorexant significantly improved sSE, abdominal circumference, and sucrose intake (all p < 0.05), but did not change HbA1c, CGM parameters, or body weight. Correlation analysis revealed that changes in sSE were associated with those in HbA1c and body weight (r = -0.61 and r = -0.66, respectively; both p < 0.05).

CONCLUSIONS

Suvorexant significantly improved sleep quality and obesity-associated parameters in patients with type 2 diabetes in 14 weeks. Improvements in sleep quality were associated with improvements in glycemic control. Sleep disorder treatment using suvorexant may provide metabolic benefits for patients with type 2 diabetes.

摘要

目的

本研究旨在评估苏沃雷生对 2 型糖尿病伴失眠患者主观睡眠参数和代谢参数的时间治疗效果。

方法

13 名符合匹兹堡睡眠质量指数原发性失眠标准的 2 型糖尿病患者服用苏沃雷生 20mg/天(≥65 岁者服用 15mg/天),治疗 14±2 周。在治疗前后评估以下参数:睡眠日记以评估睡眠时间和质量(即入睡潜伏期、睡眠后觉醒和睡眠效率[sSE])、失眠严重程度指数、临床和生化数据、连续血糖监测(CGM)以及经过验证的食物摄入自我管理问卷。

结果

苏沃雷生显著改善了 sSE、腹围和蔗糖摄入量(均 p<0.05),但未改变糖化血红蛋白、CGM 参数或体重。相关性分析显示,sSE 的变化与糖化血红蛋白和体重的变化相关(r=-0.61 和 r=-0.66,均 p<0.05)。

结论

苏沃雷生在 14 周内显著改善了 2 型糖尿病患者的睡眠质量和肥胖相关参数。睡眠质量的改善与血糖控制的改善相关。使用苏沃雷生治疗睡眠障碍可能为 2 型糖尿病患者带来代谢益处。

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