Heslin M, Desai R, Lappin J M, Donoghue K, Lomas B, Reininghaus U, Onyejiaka A, Croudace T, Jones P B, Murray R M, Fearon P, Doody G A, Dazzan P, Fisher H L, Demjaha A, Craig T, Morgan C
Institute of Psychiatry, Psychology and Neuroscience, King's College London, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK.
University of New South Wales, Sydney, Australia.
Soc Psychiatry Psychiatr Epidemiol. 2016 Feb;51(2):233-45. doi: 10.1007/s00127-015-1131-1. Epub 2015 Oct 31.
Few studies have investigated risk factors for psychotic major depression (PMD). We aimed to investigate the biological and psychosocial risk factors associated with PMD compared with other psychotic disorders.
Based on the aetiology and ethnicity in schizophrenia and other psychoses (ÆSOP) study, we used a case-control study to identify and recruit, at baseline and 10-year follow-up, all first episode cases of psychosis, presenting for the first time to specialist mental health services in defined catchment areas in the UK. Population-based controls were recruited from the same areas. Data were collected on: sociodemographics; social isolation; childhood adversity; life events; minor physical anomalies; and neurological soft signs.
Living alone (aOR = 2.26, CI = 1.21-4.23), basic level qualification (aOR = 2.89, CI = 1.08-7.74), being unemployed (aOR = 2.12, CI = 1.13-3.96), having contact with friends less than monthly (aOR = 4.24, CI = 1.62-11.14), having no close confidants (aOR = 4.71, CI = 2.08-10.68), having experienced childhood adversity (aOR = 2.57, CI = 1.02-6.44), family history of mental illness (aOR = 10.68, CI = 5.06-22.52), family history of psychosis (aOR = 12.85, CI = 5.24-31.51), and having more neurological soft signs (aOR = 1.15, CI = 1.07-1.24) were all associated with a follow-up diagnosis of PMD and schizophrenia. Few variables associated with PMD were also associated with a diagnosis of bipolar disorder. Minor physical anomalies were associated with a follow-up diagnosis of schizophrenia and bipolar disorder, but not PMD.
Risk factors associated with PMD appear to overlap with those for schizophrenia, but less so for bipolar disorder. Future work on the differential aetiology of PMD, from other psychoses is needed to find the 'specifier' between PMD and other psychoses. Future research on aetiology in PMD, and perhaps other psychoses, should account for diagnostic change.
很少有研究调查过伴有精神病性症状的重度抑郁症(PMD)的风险因素。我们旨在研究与PMD相关的生物学和社会心理风险因素,并与其他精神病性障碍进行比较。
基于精神分裂症及其他精神病的病因与种族(ÆSOP)研究,我们采用病例对照研究,在基线期和10年随访期识别并招募所有首次发作的精神病病例,这些病例首次在英国特定集水区的专科心理健康服务机构就诊。基于人群的对照从相同地区招募。收集了以下数据:社会人口统计学信息;社会隔离情况;童年逆境;生活事件;轻微身体异常;以及神经系统软体征。
独居(比值比=2.26,可信区间=1.21 - 4.23)、基础教育水平(比值比=2.89,可信区间=1.08 - 7.74)、失业(比值比=2.12,可信区间=1.13 - 3.96)、每月与朋友联系少于一次(比值比=4.24,可信区间=1.62 - 11.14)、没有亲密知己(比值比=4.71,可信区间=2.08 - 10.68)、经历过童年逆境(比值比=2.57,可信区间=1.02 - 6.44)、有精神疾病家族史(比值比=10.68,可信区间=5.06 - 22.52)、有精神病家族史(比值比=12.85,可信区间=5.24 - 31.51)以及有更多神经系统软体征(比值比=1.15,可信区间=1.07 - 1.24)均与随访诊断为PMD和精神分裂症相关。与PMD相关的变量很少也与双相情感障碍的诊断相关。轻微身体异常与随访诊断为精神分裂症和双相情感障碍相关,但与PMD无关。
与PMD相关的风险因素似乎与精神分裂症的风险因素重叠,但与双相情感障碍的重叠程度较小。需要开展关于PMD与其他精神病性障碍病因差异的未来研究,以找出PMD与其他精神病性障碍之间的“鉴别因素”。未来关于PMD以及可能其他精神病性障碍病因的研究应考虑诊断变化。