School of Psychiatry, University of New South Wales, Black Dog Institute Building, Prince of Wales Hospital, Hospital Road, Randwick, NSW 2031, Australia.
Aust N Z J Psychiatry. 2009 Nov;43(11):1070-6. doi: 10.3109/00048670903179152.
The aim of the present study was to evaluate, using serotonin transporter genotyping as an example, the preparedness of individuals from an urban general population identified with hypothetical genetic risk for a depressive disorder to moderate risk through cognitive or behavioural intervention. It also evaluated endorsement of genetic and environmental causal attributions of mental illness.
A qualitative approach using focus group methodology was selected as most appropriate because these issues are relatively unexplored. Participants (n=36) aged > or =18 years from metropolitan Sydney discussed their understanding of the role of genetic and environmental risk factors in mental illness and attitudes towards pre-symptomatic interventions based on genetic risk information.
Thirty-six participants attended four focus groups involving 8-10 participants per group. Participants predominantly viewed genetic risk factors for depression as predisposing rather than causal, with environmental risk factors acting as triggers. Hypothetical identification with a genetic variant suggesting predisposition to depression prompted strong interest in seeking further information about predictive genetic testing from medical professionals, willingness to reduce life stress, drugs and alcohol intake, willingness to increase exercise, and willingness to undertake cognitive and behavioural interventions at a pre-symptomatic stage. Mixed views prevailed as to whether stress was a modifiable risk factor. Preventive intervention at a presymptomatic stage of depression was viewed negatively in a minority of participants due to a fatalistic attitude towards a genetic predisposition and attitudes that intervention was futile in the absence of symptoms.
There is a likely public demand for preventive mental health interventions for healthy people on the basis of genetic susceptibility if predictive genetic testing becomes available in psychiatry. The findings have implications for general practitioner and public education about predictive genetic testing for susceptibility to common multifactorial disorders for at-risk groups.
本研究旨在通过 5-羟色胺转运体基因分型(例如)评估个体对抑郁障碍的假设遗传风险的准备情况,即通过认知或行为干预将其从中度风险降低至低风险。同时,本研究还评估了个体对精神疾病遗传和环境病因的归因。
选择使用焦点小组方法进行定性研究,因为这些问题尚未得到充分探索。从悉尼大都市区招募年龄大于等于 18 岁的个体(n=36),并让他们参与 4 个焦点小组,每组 8-10 人,讨论他们对精神疾病中遗传和环境风险因素作用的理解,以及对基于遗传风险信息的症状前干预的态度。
36 名参与者参加了 4 个焦点小组,每组 8-10 人。参与者普遍认为抑郁的遗传风险因素是易感性而不是病因,环境风险因素起触发作用。假设识别出一种遗传变异,提示其有抑郁倾向,这会促使参与者强烈希望从医疗专业人员那里获得更多关于预测性基因检测的信息,愿意减少生活压力、减少药物和酒精摄入、愿意增加运动,并且愿意在无症状前阶段进行认知和行为干预。大多数参与者认为压力是否可改变风险因素,存在混合看法。少数参与者对抑郁无症状前阶段的预防性干预持负面态度,这是因为他们对遗传易感性持宿命论态度,并且认为在没有症状的情况下,干预是徒劳的。
如果预测性基因检测在精神病学中得到应用,那么有健康人可能会因为遗传易感性而对基于基因的预防性心理健康干预有需求。这些研究结果对一般从业者和公众进行有关预测性基因检测的教育,以及对处于风险中的群体常见多因素疾病的遗传易感性具有重要意义。