Castellini Giovanni, Wu Frederick C W, Finn Joseph D, OʼNeill Terrence W, Lean Michael E J, Pendleton Neil, Rastrelli Giulia, Rutter Martin K, Gacci Mauro, Ricca Valdo, Maggi Mario
From the Sexual Medicine and Andrology Unit (Castellini, Rastrelli, Maggi), Department of Experimental, Clinical and Biomedical Sciences, and Psychiatric Unit (Castellini, Ricca), Department of Neuropsychiatric Sciences, University of Florence, Florence, Italy; Andrology Research Unit (Wu, Rutter), Endocrinology and Diabetes Research Group, Institute of Human Development, Faculty of Medical Human Sciences, The University of Manchester, Manchester, UK; Manchester Royal Infirmary (Wu, Rutter), Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK; Arthritis Research UK Epidemiology Unit (Finn, O'Neill), The University of Manchester, Manchester Academic Health Science Centre, Manchester, UK; Department of Human Nutrition (Lean), University of Glasgow, Glasgow, UK; School of Community Based Medicine (Pendleton), The University of Manchester, Salford Royal NHS Trust, Salford, UK; Manchester Diabetes Centre (Rutter), Central Manchester University Hospitals NHS Foundation Trust, Manchester Academic Health Science Centre, Manchester, UK; Department of Oncology (Gacci), Urology Unit, University Hospital Careggi (AOUC), University of Florence, Florence, Italy.
Psychosom Med. 2016 Jul-Aug;78(6):758-69. doi: 10.1097/PSY.0000000000000328.
Depression and lower urinary tract symptoms (LUTSs) have been found to co-occur among aging men. The present study attempted to clarify the nature of this relationship, considering adverse life events as potential moderators and the inflammation as an underlying biological mechanism.
The relationship between depression and LUTS was evaluated using data from the European Male Ageing Study, the largest multicenter population-based study of aging in European men. The sample included 3369 men who were assessed by means of several self-reported questionnaires, including the Beck Depression Inventory-II, the International Prostate Symptom Score, and the Adverse Life Events Scale. Participants were asked to provide information regarding general health and life-style, and medical comorbidities. Biological measures including prostate-specific antigen, testosterone, and C-reactive protein were measured.
LUTS and depressive symptoms were correlated (R = 0.32, β = .10, p < .001), even after adjusting for life-style, psychological, and medical variables. A history of adverse life events was associated with both higher LUTS and Beck Depression Inventory scores. Furthermore, adverse life events moderated the LUTS-depression association (F = 22.62, b = 0.061, p < .001), which increased as a function of the number of life events. C-reactive protein was found to mediate the LUTS-depression association. This mediation effect was moderated by number of adverse life events.
Participants with a history of adverse life events represent a vulnerable population in whom the association between somatic and depressive symptoms is stronger. One of the biological mechanisms underlying this association could be an activation of the central inflammatory signaling pathways.
研究发现,老年男性中抑郁症与下尿路症状(LUTSs)并存。本研究试图阐明这种关系的本质,将不良生活事件视为潜在的调节因素,并将炎症视为潜在的生物学机制。
使用来自欧洲男性衰老研究的数据评估抑郁症与LUTS之间的关系,该研究是欧洲男性中规模最大的基于多中心人群的衰老研究。样本包括3369名男性,他们通过几份自我报告问卷进行评估,包括贝克抑郁量表第二版、国际前列腺症状评分和不良生活事件量表。参与者被要求提供有关总体健康、生活方式和合并症的信息。测量了包括前列腺特异性抗原、睾酮和C反应蛋白在内的生物学指标。
即使在调整了生活方式、心理和医学变量后,LUTS与抑郁症状仍具有相关性(R = 0.32,β = 0.10,p < 0.001)。不良生活事件史与较高的LUTS和贝克抑郁量表评分均相关。此外,不良生活事件调节了LUTS与抑郁的关联(F = 22.62,b = 0.061,p < 0.001),且这种关联随着生活事件数量的增加而增强。发现C反应蛋白介导了LUTS与抑郁的关联。这种中介效应受不良生活事件数量的调节。
有不良生活事件史的参与者是一个易受影响的群体,其躯体症状与抑郁症状之间的关联更强。这种关联背后的生物学机制之一可能是中枢炎症信号通路的激活。