Johnstone Eve C, Ebmeier Klaus P, Miller Patrick, Owens David G C, Lawrie Stephen M
Division of Psychiatry, University of Edinburgh, Kennedy Tower, Royal Edinburgh Hospital, Morningside Park, Edinburgh EH10 5HF, UK.
Br J Psychiatry. 2005 Jan;186:18-25. doi: 10.1192/bjp.186.1.18.
The hypothesis that schizophrenia is neurodevelopmental was investigated in a prospective study of young people with a postulated 10-15% risk for the development of schizophrenia.
To determine premorbid variables distinguishing high-risk people who will go on to develop schizophrenia from those who will not.
A high-risk sample of 163 young adults with two relatives with schizophrenia was recruited. They and 36 controls were serially examined. Baseline measures were compared between those who did develop schizophrenia, a well control group, a well high-risk group and high-risk participants with partial or isolated psychotic symptoms.
Of those at high risk, 20 developed schizophrenia within 2(1/2) years. More experienced isolated or partial psychotic symptoms. Those who developed schizophrenia differed from those who did not on social anxiety, withdrawal and other schizotypal features. The whole high-risk sample differed from the control group on developmental and neuropsychological variables.
The genetic component of schizophrenia affects many more individuals than will develop the illness, and partial impairment can be found in them. Highly significant predictors of the development of schizophrenia are detectable years before onset.
在一项针对假定有10%-15%患精神分裂症风险的年轻人的前瞻性研究中,对精神分裂症是神经发育性疾病这一假说进行了调查。
确定能区分将发展为精神分裂症的高危人群和不会发展为精神分裂症的高危人群的病前变量。
招募了一个高危样本,其中包括163名有两名精神分裂症亲属的年轻成年人。对他们以及36名对照者进行了系列检查。比较了发展为精神分裂症的人群、一个健康对照组、一个健康高危组以及有部分或孤立精神病性症状的高危参与者之间的基线测量值。
在高危人群中,20人在2.5年内发展为精神分裂症。更多人经历了孤立或部分精神病性症状。发展为精神分裂症的人群在社交焦虑、退缩及其他分裂型特征方面与未发展为精神分裂症的人群不同。整个高危样本在发育和神经心理学变量方面与对照组不同。
精神分裂症的遗传成分影响的个体比实际会患病的个体多得多,且在这些个体中可发现部分损害。在精神分裂症发病前数年就能检测到其发展的高度显著预测因素。