家庭昏暗灯光下褪黑素在肥胖成人中的起效评估:可行性和程序考虑。

Francisco Romo-Nava, Helen J Burgess, Thomas J Blom, Georgi Georgiev, Jakyb Stoddard, Elly McMillan, Nicole N Mori, Christina Charnas, Anna I Guerdjikova, Robert K McNamara, Jeffrey A Welge, Carlos M Grilo, Frank A J L Scheer, Susan L McElroy
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引用次数: 0

摘要

研究目的:昏暗光线下褪黑激素的发生(DLMO)是中心昼夜节律阶段最成熟的标志,可能有助于揭示昼夜节律系统在肥胖中的作用。本研究使用基于家庭的评估来评估肥胖个体的DLMO,并探讨其临床相关性和程序差异。方法:58名女性(平均[SD]年龄40.9[7.8]岁)和体重指数(41.4 [6.6]kg/m2)完成了基于家庭的DLMO评估,测量了睡眠质量、昼夜偏好和心脏代谢参数。我们探索的程序差异包括个性化与标准化DLMO阈值,7天与3天睡眠开始时间(SOT)评估,以及基于日记、基于活动记录或“组合”方法计算SOT,以及每小时与半小时唾液样本数据点。采用相关系数和单因素方差分析模型进行统计分析。Bland-Altman图用于说明方法之间的一致性。结果:使用个性化或标准化阈值分别检测到98.2%和89.6%的参与者的DLMO。DLMO与SOT相关,但与体重指数、心脏代谢参数、睡眠质量或昼夜偏好无关。较晚的SOT和较大的夹带相位角(DLMO-SOT)与较年轻的年龄和傍晚性相关。多数替代方法与原方法吻合良好。结论:以家庭为基础的评估在肥胖女性中发现高检出率的DLMO。昼夜偏好与中心昼夜节律阶段无关,这表明其他因素(如行为、社会人口学)可能与该人群的时间型评估有关。我们为未来的研究提供了启示,包括需要考虑的程序变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Home-based dim light melatonin onset assessment among adults with obesity: feasibility and procedural considerations.

Home-based dim light melatonin onset assessment among adults with obesity: feasibility and procedural considerations.

Home-based dim light melatonin onset assessment among adults with obesity: feasibility and procedural considerations.

Study objectives: Dim light melatonin onset (DLMO) is the best-established marker of central circadian phase and may contribute to unraveling the role of the circadian system in obesity. This study evaluated DLMO among individuals with obesity using a home-based assessment and explored its clinical correlates and procedural variations.

Method: Fifty-eight women (mean [SD] age 40.9 [7.8] years) and body mass index (41.4 [6.6] kg/m2) completed a home-based DLMO assessment, measures of sleep quality, diurnal preference, and cardiometabolic parameters. Procedural variations we explored included individualized versus standardized DLMO thresholds, 7 versus 3 days assessment of sleep onset timing (SOT), as well as diary-based, actigraphy-based, or a "combined" method to calculate SOT, and hourly versus half-hourly saliva sample data points. Correlation coefficients and univariate ANOVA models were used for statistical analysis. Bland-Altman plots were used to inform agreement between methods.

Results: DLMO was detected in 98.2% and 89.6% of participants using an individualized or a standardized threshold, respectively. DLMO correlated with SOT but not with body mass index, cardiometabolic parameters, sleep quality, or diurnal preference. A later SOT and a larger phase angle of entrainment (DLMO-SOT) correlated with younger age and with eveningness. Most procedural alternatives showed good agreement with the original methods.

Conclusions: Home-based assessment yielded a high rate of detectable DLMO in women with obesity. Diurnal preference was not correlated with central circadian phase, suggesting that other factors (e.g. behavioral, sociodemographic) may be relevant in chronotype assessment in this population. We offer implications for future research including procedural variations to consider.

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