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人类循环白细胞介素-6的昼夜变化:一项荟萃分析。

Diurnal Variation of Circulating Interleukin-6 in Humans: A Meta-Analysis.

作者信息

Nilsonne Gustav, Lekander Mats, Åkerstedt Torbjörn, Axelsson John, Ingre Michael

机构信息

Stockholm University, Stress Research Institute, Stockholm, Sweden.

Karolinska Institutet, Department of Clinical Neuroscience, Stockholm, Sweden.

出版信息

PLoS One. 2016 Nov 10;11(11):e0165799. doi: 10.1371/journal.pone.0165799. eCollection 2016.

DOI:10.1371/journal.pone.0165799
PMID:27832117
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5104468/
Abstract

The pleiotropic cytokine interleukin-6 (IL-6) has been proposed to contribute to circadian regulation of sleepiness by increasing in the blood at night. Earlier studies have reported diurnal variation of IL-6, but phase estimates are conflicting. We have therefore performed a meta-analysis on the diurnal variation of circulating IL-6. Studies were included if they reported IL-6 in plasma or serum recorded at least twice within 24 hours in the same individual. A systematic search resulted in the inclusion of 43 studies with 56 datasets, for a total of 1100 participants. Individual participant data were available from 4 datasets with a total of 56 participants. Mixed-effects meta-regression modelling confirmed that IL-6 varied across the day, the most conspicuous effect being a trough in the morning. These results stand in contrast to earlier findings of a peak in the evening or night, and suggest that diurnal variation should be taken into account in order to avoid confounding by time of day in studies of IL-6 in plasma or serum.

摘要

多效性细胞因子白细胞介素-6(IL-6)被认为通过在夜间血液中水平升高而参与昼夜节律性嗜睡调节。早期研究报道了IL-6的昼夜变化,但相位估计存在冲突。因此,我们对循环IL-6的昼夜变化进行了荟萃分析。如果研究报告了同一受试者在24小时内至少两次记录的血浆或血清中的IL-6,则纳入该研究。系统检索后纳入了43项研究,共56个数据集,涉及1100名参与者。4个数据集提供了个体参与者数据,共56名参与者。混合效应荟萃回归模型证实,IL-6在一天中有所变化,最显著的效应是早晨出现低谷。这些结果与早期关于傍晚或夜间出现峰值的发现形成对比,表明在血浆或血清中IL-6的研究中,为避免昼夜时间的混杂影响,应考虑昼夜变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/9ce093986a7f/pone.0165799.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/b213d18bfd98/pone.0165799.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/c16534e51330/pone.0165799.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/32ce1326d40b/pone.0165799.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/3e5d33301d30/pone.0165799.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/2fc9d09c05dc/pone.0165799.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/26ee08f333df/pone.0165799.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/9ce093986a7f/pone.0165799.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/b213d18bfd98/pone.0165799.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/c16534e51330/pone.0165799.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/32ce1326d40b/pone.0165799.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/3e5d33301d30/pone.0165799.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/2fc9d09c05dc/pone.0165799.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/26ee08f333df/pone.0165799.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8965/5104468/9ce093986a7f/pone.0165799.g007.jpg

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