Division of General Internal Medicine, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, United States of America.
Division of Cardiovascular Medicine, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
PLoS One. 2021 Feb 9;16(2):e0246073. doi: 10.1371/journal.pone.0246073. eCollection 2021.
Insomnia may be a risk factor for cardiovascular disease in HIV (HIV-CVD); however, mechanisms have yet to be elucidated.
We examined cross-sectional associations of insomnia symptoms with biological mechanisms of HIV-CVD (immune activation, systemic inflammation, and coagulation) among 1,542 people with HIV from the Veterans Aging Cohort Study (VACS) Biomarker Cohort. Past-month insomnia symptoms were assessed by the item, "Difficulty falling or staying asleep?," with the following response options: "I do not have this symptom" or "I have this symptom and…" "it doesn't bother me," "it bothers me a little," "it bothers me," "it bothers me a lot." Circulating levels of the monocyte activation marker soluble CD14 (sCD14), inflammatory marker interleukin-6 (IL-6), and coagulation marker D-dimer were determined from blood specimens. Demographic- and fully-adjusted (CVD risk factors, potential confounders, HIV-related factors) regression models were constructed, with log-transformed biomarker variables as the outcomes. We present the exponentiated regression coefficient (exp[b]) and its 95% confidence interval (CI).
We observed no significant associations between insomnia symptoms and sCD14 or IL-6. For D-dimer, veterans in the "Bothers a Lot" group had, on average, 17% higher D-dimer than veterans in the "No Difficulty Falling or Staying Asleep" group in the demographic-adjusted model (exp[b] = 1.17, 95%CI = 1.01-1.37, p = .04). This association was nonsignificant in the fully-adjusted model (exp[b] = 1.09, 95%CI = 0.94-1.26, p = .27).
We observed little evidence of relationships between insomnia symptoms and markers of biological mechanisms of HIV-CVD. Other mechanisms may be responsible for the insomnia-CVD relationship in HIV; however, future studies with comprehensive assessments of insomnia symptoms are warranted.
失眠可能是 HIV(HIV-CVD)患者发生心血管疾病的一个风险因素;然而,其机制尚未阐明。
我们检测了 1542 名来自退伍军人老龄化队列研究(VACS)生物标志物队列的 HIV 患者中失眠症状与 HIV-CVD 的生物学机制(免疫激活、全身炎症和凝血)的横断面关联。通过“入睡或保持睡眠困难?”这一项目评估过去一个月的失眠症状,回答选项为:“我没有这种症状”或“我有这种症状,并且......”“它不困扰我”“它有点困扰我”“它困扰我”“它困扰我很多”。从血液样本中测定单核细胞激活标志物可溶性 CD14(sCD14)、炎症标志物白细胞介素-6(IL-6)和凝血标志物 D-二聚体的水平。采用对数转换后的生物标志物变量作为因变量,构建了包含人口统计学和完全调整(心血管疾病风险因素、潜在混杂因素、HIV 相关因素)的回归模型。我们呈现了指数回归系数(exp[b])及其 95%置信区间(CI)。
我们未观察到失眠症状与 sCD14 或 IL-6 之间存在显著关联。对于 D-二聚体,在人口统计学调整模型中,“困扰很多”组的退伍军人的 D-二聚体平均比“无入睡或保持睡眠困难”组高 17%(exp[b] = 1.17,95%CI = 1.01-1.37,p =.04)。在完全调整模型中,该关联无统计学意义(exp[b] = 1.09,95%CI = 0.94-1.26,p =.27)。
我们几乎没有发现失眠症状与 HIV-CVD 生物学机制标志物之间存在关联。可能有其他机制导致 HIV 中失眠与 CVD 之间的关系;然而,仍需要对失眠症状进行全面评估的未来研究。