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老年感染人类免疫缺陷病毒 (HIV) 的非洲人存在昼夜节律延迟。

Delayed circadian rhythms in older Africans living with human immunodeficiency virus (HIV).

机构信息

Wits Sleep Laboratory, Brain Function Research Group, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Faculty of Health and Medical Sciences, University of Surrey, Guildford, Surrey, UK.

出版信息

J Pineal Res. 2023 Jan;74(1):e12838. doi: 10.1111/jpi.12838. Epub 2022 Nov 6.

Abstract

The increasing number of people living with human immunodeficiency virus, HIV, (PLWH) have an elevated incidence of risk for noncommunicable comorbidities, the aetiology of which remains incompletely understood. While sleep disturbances are often reported in PLWH, it is unknown to what extent they relate to changes in the circadian and/or sleep homeostatic processes. We studied the relationship between sleep characteristics, circadian phase, and HIV status in older adults from the HAALSI (Health and Ageing in Africa: a Longitudinal Study of an INDEPTH Community in South Africa) subsample of the Agincourt Health and Demographic Surveillance System in South Africa (n = 187, 36 human immunodeficiency virus positive [HIV+], age: 66.7 ± 11.5 years, range 45-93 years), where HIV prevalence is high and (in contrast to the global north) does not associate significantly with potentially confounding behavioural differences. In participants with valid actigraphy data (n = 172), regression analyses adjusted for age and sex indicated that HIV+ participants had slightly later sleep onset (β = .16, p = .039), earlier sleep offset times (β = -.16, p = .049) and shorter total sleep times (β = -.20, p = .009) compared to the HIV negative (HIV-) participants. In a subset of participants (n = 51, 11 HIV+), we observed a later dim light melatonin onset (DLMO) in HIV+ (21:16 ± 01:47) than in HIV- (20:06 ± 00:58) participants (p = .006). This substantial difference remained when adjusted for age and sex (β = 1.21; p = .006). In 36 participants (6 HIV+) with DLMO and actigraphy data, median phase angle of entrainment was -6 min in the HIV+ group and +1 h 25 min in the HIV- group. DLMO time correlated with sleep offset (ρ = 0.47, p = .005) but not sleep onset (ρ = -0.086, p = .623). Collectively, our data suggest that the sleep phase occurred earlier than what would be biologically optimal among the HIV+ participants. This is the first report of a mistimed circadian phase in PLWH, which has important potential implications for their health and well-being, especially given the well-established relationships between circadian asynchrony and sleep deprivation with poorer health outcomes.

摘要

越来越多的人感染了人类免疫缺陷病毒(HIV),他们患有非传染性合并症的风险增加,其病因仍不完全清楚。尽管 HIV 感染者常报告睡眠障碍,但尚不清楚其与昼夜节律和/或睡眠稳态过程的变化有多大关系。我们研究了睡眠特征、昼夜节律相位与南非阿格因库尔健康和人口监测系统(Agincourt Health and Demographic Surveillance System)HAALSI(非洲健康和老龄化:南非深入社区的纵向研究)子样本中老年人 HIV 状态之间的关系,该子样本包括南非(n=187,36 名人类免疫缺陷病毒阳性[HIV+],年龄:66.7±11.5 岁,范围 45-93 岁)中的成年人,HIV 感染率很高,并且(与全球北方不同)与潜在的混杂行为差异没有显著关联。在具有有效活动记录仪数据的参与者中(n=172),经年龄和性别调整的回归分析表明,与 HIV 阴性(HIV-)参与者相比,HIV+参与者的睡眠潜伏期略晚(β=0.16,p=0.039),睡眠潜伏期和总睡眠时间较短(β=0.20,p=0.009)。在参与者的一个亚组(n=51,11 名 HIV+)中,我们观察到 HIV+(21:16±01:47)的暗光褪黑素开始时间(DLMO)晚于 HIV-(20:06±00:58)参与者(p=0.006)。当调整年龄和性别时,这种显著差异仍然存在(β=1.21;p=0.006)。在 36 名(6 名 HIV+)有 DLMO 和活动记录仪数据的参与者中,HIV+组的中值趋同相位角为-6 分钟,HIV-组为+1 小时 25 分钟。DLMO 时间与睡眠终点相关(ρ=0.47,p=0.005),但与睡眠开始无关(ρ=-0.086,p=0.623)。总的来说,我们的数据表明,HIV+参与者的睡眠阶段早于生物最佳阶段。这是第一个关于 PLWH 昼夜节律相位失调的报告,这对他们的健康和福祉有重要的潜在影响,尤其是考虑到昼夜节律失谐与睡眠剥夺与较差的健康结果之间的既定关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d43/10078505/43f86cc0dc54/JPI-74-0-g001.jpg

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