Clinical Epidemiology and Biostatistics, School of Medical Sciences, Örebro University, Örebro, Sweden.
Clinical Epidemiology and Biostatistics, School of Medical Sciences, Örebro University, Örebro, Sweden; Department of Public Health Sciences, Stockholm University, Sweden.
Psychoneuroendocrinology. 2019 Dec;110:104421. doi: 10.1016/j.psyneuen.2019.104421. Epub 2019 Aug 27.
Loneliness has been associated with adverse health outcomes, including age-related diseases with an inflammatory etiology such as cardiovascular disease. We aimed to identify potential biological pathways linking loneliness with morbidity and mortality by examining associations of loneliness with biomarkers. Participants in the English Longitudinal Study of Ageing (n = 3239) aged 50 years or older with an average age of 64 years, provided data in waves 4 (2008/2009) and 6 (2012/2013). Linear regression conditional change models had three outcomes: C reactive protein (CRP) measured in mg/L (log transformed), fibrinogen in g/L and ferritin in g/dL. In men, the onset of loneliness indicated by answering 'no' at wave 4 and 'yes' at wave 6 to question "Much of the time during the past week, you felt lonely?" was associated with a statistically significant increase in levels of CRP (β = 0.36, 95% confidence interval (0.09 to 0.62)), plasma fibrinogen (0.18 (0.04 to 0.31)) and ferritin (41.04 (6.58 to 75.50)), after full adjustment. A statistically significant increase in CRP in men was also observed for onset of loneliness assessed with the question "How often do you feel lonely?" (0.20 (0.03 to 0.38)). These associations were not mediated by depressive symptoms. Persistent loneliness (loneliness experienced at both baseline and follow-up) assessed using the University of California Los Angeles (UCLA) loneliness scale was associated with an increase in CRP (0.11 (0.004 to 0.22)) among men. Associations of the two latter loneliness measures with fibrinogen and ferritin were mainly null. Among women, the only statistically significant association was for persistent loneliness (loneliness at both waves) identified by question "Much of the time during the past week, you felt lonely?" with a reduction in levels of ferritin (-20.62 (-39.78 to -1.46)). Men may be more susceptible to loneliness-associated disease risks signaled by biological changes, including systemic inflammation. Combined social and targeted medical interventions may help to reduce health risks associated with loneliness.
孤独与不良健康结果有关,包括与炎症病因相关的年龄相关疾病,如心血管疾病。我们旨在通过检查孤独与生物标志物的关联来确定将孤独与发病率和死亡率联系起来的潜在生物学途径。参加英国老龄化纵向研究(n=3239)的参与者年龄在 50 岁或以上,平均年龄为 64 岁,在第 4 波(2008/2009 年)和第 6 波(2012/2013 年)提供了数据。线性回归条件变化模型有三个结果:以 mg/L(对数转换)测量的 C 反应蛋白(CRP)、g/L 中的纤维蛋白原和 g/dL 中的铁蛋白。在男性中,通过回答“在过去一周的大部分时间里,你感到孤独?”在第 4 波回答“否”,而在第 6 波回答“是”来表示孤独的开始,与 CRP(β=0.36,95%置信区间(0.09 至 0.62))、血浆纤维蛋白原(0.18(0.04 至 0.31))和铁蛋白(41.04(6.58 至 75.50))水平的统计学显著增加相关,经过充分调整。对于用问题“你感到孤独的频率如何?”评估的孤独开始,男性的 CRP 也观察到统计学显著增加(0.20(0.03 至 0.38))。这些关联不受抑郁症状的影响。使用加利福尼亚大学洛杉矶分校(UCLA)孤独量表评估的持续性孤独(在基线和随访时都经历孤独)与 CRP 的增加相关(男性为 0.11(0.004 至 0.22))。后两种孤独测量方法与纤维蛋白原和铁蛋白的关联主要为零。在女性中,仅对孤独的持久性(在两波中都感到孤独)有统计学意义,该问题是“在过去一周的大部分时间里,你感到孤独?”与铁蛋白水平降低相关(-20.62(-39.78 至-1.46))。男性可能更容易受到孤独相关疾病风险的影响,这些风险由生物变化提示,包括全身炎症。综合社会和有针对性的医疗干预措施可能有助于降低与孤独相关的健康风险。