Evaluation of Sleep Health in Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

IF 5.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Laura Golob, Yesica Mercado-Munoz, Wenxi Liu, Anvita Singh, James S Hodges, Lianne Siegel, Helena Morero, Zan Gao, Angela Tipp, Stacey L Simon, Kyriakie Sarafoglou
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引用次数: 0

Abstract

Context: Literature on sleep health in children with congenital adrenal hyperplasia (CAH) is sparse despite the important role the hypothalamic-pituitary-adrenal axis plays in sleep onset, duration, and awakenings after sleep onset.

Objective: To evaluate sleep health in children and adolescents with CAH as measured by wrist actigraphy and validated sleep questionnaires.

Methods: Cross-sectional study at our multidisciplinary CAH clinic. Participants aged 3 to 18 years with classic CAH wore an ActiGraph GT3X+ accelerometer for 1 week. Children and parents completed sleep questionnaires, and the results were compared to published samples from the community and children with sleep disorders (clinical). Actigraphy sleep health measures were compared to consensus sleep duration recommendations and normative data in healthy children.

Results: Forty-four participants (23 male) with CAH completed the study. Actigraphy found sleep duration in children with CAH was less than recommended guidelines with significantly worse sleep efficiency and increased wake after sleep onset (P < .05) compared to healthy children. After sleep onset, the average number of awakenings increased from 1.67 per hour during the first 2 hours after the evening hydrocortisone dose to 3.12 per hour 4 to 7 hours after the dose, corresponding with washout of the evening hydrocortisone dose. Parents of 3- to 10-year-olds reported significantly worse sleep onset delay and decreased sleep duration than both the community and clinical samples, and significantly more night awakenings than the community sample.

Conclusion: Our findings suggest that sleep health is impaired in children with CAH and is an important consideration for both clinical practice and future research.

21-羟化酶缺乏所致先天性肾上腺增生儿童睡眠健康评价
背景:尽管下丘脑-垂体-肾上腺(HPA)轴在睡眠开始、持续时间和睡眠开始后醒来中起着重要作用,但关于先天性肾上腺增生(CAH)儿童睡眠健康的文献很少。目的:通过腕动仪和睡眠问卷对儿童和青少年CAH患者的睡眠健康状况进行评价。方法:在我们的多学科CAH诊所进行横断面研究。3-18岁的经典CAH患者佩戴ActiGraph GT3X+加速度计一周。儿童和家长填写睡眠问卷,并将结果与社区和睡眠障碍儿童(临床)公布的样本进行比较。将活动描记睡眠健康测量与健康儿童的一致睡眠时间建议和规范数据进行比较。结果:44名患有CAH的参与者(23名男性)完成了研究。活动图显示,CAH患儿的睡眠时间低于推荐指南,睡眠效率明显降低,睡眠后醒来增加(结论:我们的研究结果表明,CAH患儿的睡眠健康受到损害,这是临床实践和未来研究的重要考虑因素。
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来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
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