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[在首次精神病发作之前检测高危因素有意义吗?]

[Is there any point in detecting high risk factors prior to a first psychosis?].

作者信息

Klaassen M C, Nieman D H, Becker H E, Linszen D H

机构信息

De Rivierduinen te Leiden.

出版信息

Tijdschr Psychiatr. 2006;48(6):467-76.

Abstract

BACKGROUND

If schizophrenia and related disorders are diagnosed and treated early, symptoms will be less severe and the prognosis will be more favourable. There is little point in screening for schizophrenia in the general population because the illness has such a low incidence. However, we do need to find out whether it is meaningful to screen genetically impaired individuals (high risk group) and specific groups of psychiatric patients (ultra high risk group).

AIM

To survey the research into the (high and ultra high) risk factors for developing a first psychosis and to find out whether it makes good sense to screen certain groups of persons.

METHOD

We conducted extensive desk-research and a wide-ranging search of the literature from 1990 to 2004. The key words we used in our search were 'prodrome', 'high risk', 'ultra high risk', in conjunction with 'psychosis' and 'schizophrenia'.

RESULTS

In the genetically impaired group risk factors for developing schizophrenia seem to be transient psychiatric problems in childhood, schizotypical traits, anxiety, behavioural problems in adolescence, being brought up in an unstable environment and producing deviant results in neurocognitive tests. Among the patients referred to a psychiatrist it is possible to identify a special group of patients with an ultra high risk of developing a psychosis. Within ayear 40% of patients who had mild or short-term psychotic symptoms or who were genetically impaired adolescents with decreased functioning had developed a psychosis.

CONCLUSION

Screening all genetically vulnerable persons in the general population has no consequencesfor treatment. Early diagnosis by psychiatrists is certainly advisable. However, larger groups and longer studies are needed in order to demonstrate conclusively the preventive effect of interventions prior to a first psychosis.

摘要

背景

如果精神分裂症及相关障碍能早期诊断和治疗,症状将不那么严重,预后也会更有利。在普通人群中筛查精神分裂症意义不大,因为该疾病发病率很低。然而,我们确实需要弄清楚对基因受损个体(高危人群)和特定精神病患者群体(超高危人群)进行筛查是否有意义。

目的

调查首次发生精神病的(高和超高)危险因素的研究,并确定对某些人群进行筛查是否有意义。

方法

我们进行了广泛的案头研究,并对1990年至2004年的文献进行了广泛检索。我们检索时使用的关键词是“前驱症状”“高危”“超高危”,并结合“精神病”和“精神分裂症”。

结果

在基因受损群体中,患精神分裂症的危险因素似乎包括儿童期短暂的精神问题、分裂型特质、焦虑、青少年期行为问题、在不稳定环境中成长以及神经认知测试结果异常。在转介给精神科医生的患者中,可以识别出一组患精神病风险极高的特殊患者。在一年内,40%有轻度或短期精神病症状的患者,或功能下降的基因受损青少年患者发展成了精神病。

结论

对普通人群中所有基因易损个体进行筛查对治疗没有影响。精神科医生进行早期诊断当然是可取的。然而,需要更大规模的群体和更长时间的研究,以便最终证明首次精神病发作前干预措施的预防效果。

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