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家用唾液褪黑素初相评估测定昼夜节律相位的方案。

A Protocol to Determine Circadian Phase by At-Home Salivary Dim Light Melatonin Onset Assessment.

机构信息

School of Psychological Sciences, Monash University, Melbourne, Victoria, Australia.

Turner Institute for Brain and Mental Health, Monash University, Melbourne, Victoria, Australia.

出版信息

J Pineal Res. 2024 Aug;76(5):e12994. doi: 10.1111/jpi.12994.

Abstract

Internal circadian phase assessment is increasingly acknowledged as a critical clinical tool for the diagnosis, monitoring, and treatment of circadian rhythm sleep-wake disorders and for investigating circadian timing in other medical disorders. The widespread use of in-laboratory circadian phase assessments in routine practice has been limited, most likely because circadian phase assessment is not required by formal diagnostic nosologies, and is not generally covered by insurance. At-home assessment of salivary dim light melatonin onset (DLMO, a validated circadian phase marker) is an increasingly accepted approach to assess circadian phase. This approach may help meet the increased demand for assessments and has the advantages of lower cost and greater patient convenience. We reviewed the literature describing at-home salivary DLMO assessment methods and identified factors deemed to be important to successful implementation. Here, we provide specific protocol recommendations for conducting at-home salivary DLMO assessments to facilitate a standardized approach for clinical and research purposes. Key factors include control of lighting, sampling rate, and timing, and measures of patient compliance. We include findings from implementation of an optimization algorithm to determine the most efficient number and timing of samples in patients with Delayed Sleep-Wake Phase Disorder. We also provide recommendations for assay methods and interpretation. Providing definitive criteria for each factor, along with detailed instructions for protocol implementation, will enable more widespread adoption of at-home circadian phase assessments as a standardized clinical diagnostic, monitoring, and treatment tool.

摘要

内部生物钟相位评估越来越被认为是诊断、监测和治疗生物钟节律睡眠-觉醒障碍以及研究其他医学疾病中生物钟定时的重要临床工具。由于正式的诊断分类学不要求进行生物钟相位评估,并且通常不在保险范围内,因此在常规实践中广泛使用实验室生物钟相位评估受到限制。唾液褪黑素微光起始时间(DLMO,一种经过验证的生物钟相位标志物)的家庭评估是评估生物钟相位的一种越来越被接受的方法。这种方法可能有助于满足评估需求的增加,并且具有成本更低和患者更方便的优点。我们回顾了描述家庭唾液 DLMO 评估方法的文献,并确定了被认为对成功实施重要的因素。在这里,我们提供了进行家庭唾液 DLMO 评估的具体方案建议,以促进临床和研究目的的标准化方法。关键因素包括光照控制、采样率和时间以及患者依从性的衡量。我们包括了在延迟睡眠-觉醒时相障碍患者中确定最有效样本数量和时间的优化算法实施的结果。我们还提供了分析方法和解释的建议。为每个因素提供明确的标准,并详细说明方案实施的说明,将使家庭生物钟相位评估作为一种标准化的临床诊断、监测和治疗工具得到更广泛的采用。

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