Samiotakis G, Kollias C, Lazaratou H, Anagnostopoulos D, Kontaxakis V
Psychiatric Department of Child and Adolescent Psychiatry, Sismanogleio General Hospital, Athens.
Early Psychosis Unit, 1st Department of Psychiatry, Eginition Hospital, University of Athens, Athens.
Psychiatriki. 2017 Apr-Jun;28(2):120-130. doi: 10.22365/jpsych.2017.282.120.
In recent years an increasing number of studies focus on the issue of early diagnosis and intervention. At the same time, a large number of special service units for early psychosis have been established around the world especially in Australia, USA, UK, Germany etc. Recently, similar units operate in Greece also. The Diagnostic Manual of Mental Disorders of the American Psychiatric Association in its latest edition in 2013 (DSM-5), introduced the category "Attenuated Psychosis Syndrome" (APS) for people with early psychotic experiences in the section: "Conditions for further study '. This new category has specific criteria and describes a situation, in which a person displays psychotic symptoms in an attenuated form, with quite unaffected reality testing, but not qualifying a diagnosis of schizophrenic spectrum. The clinical expression of APS should be differentiated with several well known psychiatric disorders such as: brief psychotic disorder, schizotypal personality disorder, major depression with psychotic features, adolescence adjustment disorders, drug use, etc. The "Attenuated Psychosis Syndrome" occurs mainly in adolescence and in young adulthood. The mean percentage of transition to psychosis for these individuals is estimated at 36%, three years after the onset of initial symptoms, while the risk of transition to psychosis, although smaller, seems to remain up to ten years later. For some other individuals, transition to other psychiatric disorders occurs, such as depression with psychotic elements, or bipolar disorder, while a significant number of them will not transmit to even more serious disorders. At the biological level, studies focused in brain's neuroimaging, suggest significant volumetric differences among people at high risk for psychosis who later develop psychosis compared to those who don't, while studies of psychophysiological indicators or / and genetic markers show promising results for the identification of relevant parameters indicating the transition to psychosis. Αlthough an heterogeneous population, people with APS, show significant difficulties in social, professional and cognitive level, that should be therapeutically addressed. In an attempt to improve the clinical status of these individuals, to delay or even to prevent a psychotic episode, a series of interventions have been used by psychiatrists. These interventions include: (a) administration of drugs, especially atypical antipsychotics or antidepressants in low dosage, (b) administration of non-pharmaceutical supplements (e.g. omega-3 ), (c) psychotherapeutic interventions, mainly cognitive behavior therapy and (d) a combination of the above. Many questions need to be answered such as, the period of therapeutic intervention, identification of indicators (biological or/and clinical) that may determine the most suited for the APS individuals therapeutic interventions or, that may foresee, to prevent the transition to psychosis. Thus, the continuation of research in populations of APS individuals in multiple levels is necessary.
近年来,越来越多的研究聚焦于早期诊断和干预问题。与此同时,世界各地,尤其是澳大利亚、美国、英国、德国等国,已经建立了大量针对早期精神病的特殊服务机构。最近,希腊也有类似机构在运营。美国精神病学协会2013年最新版的《精神疾病诊断手册》(DSM - 5)在“有待进一步研究的病症”部分引入了“精神病性症状衰减综合征”(APS)这一类别,用于描述有早期精神病体验的人群。这一新类别有特定标准,描述了一种情况,即一个人以衰减形式表现出精神病性症状,现实检验能力基本未受影响,但不符合精神分裂症谱系障碍的诊断标准。APS的临床表现应与几种知名的精神障碍相鉴别,如:短暂精神病性障碍、分裂型人格障碍、伴有精神病性特征的重度抑郁症、青少年适应障碍、药物使用等。“精神病性症状衰减综合征”主要发生在青少年期和青年期。这些个体在初始症状出现三年后发展为精神病的平均转变率估计为36%,而发展为精神病的风险虽然较小,但似乎在十年后仍存在。对于其他一些个体,则会转变为其他精神障碍,如伴有精神病性成分的抑郁症或双相情感障碍,而其中相当一部分人甚至不会发展为更严重的障碍。在生物学层面,聚焦于大脑神经影像学研究表明,后来发展为精神病的高危人群与未发展为精神病的人群相比,在脑容量上存在显著差异,而心理生理指标或/和基因标记的研究在识别表明向精神病转变的相关参数方面显示出有前景的结果。尽管APS患者群体具有异质性,但他们在社交、职业和认知层面都存在显著困难,需要在治疗中加以解决。为了改善这些个体的临床状况,延迟甚至预防精神病发作,精神科医生采用了一系列干预措施。这些干预措施包括:(a)药物治疗,特别是低剂量的非典型抗精神病药物或抗抑郁药物,(b)非药物补充剂(如ω-3)的使用,(c)心理治疗干预,主要是认知行为疗法,以及(d)上述方法的联合使用。许多问题需要解答,比如治疗干预的时长、确定最适合APS个体的治疗干预措施或预测预防向精神病转变的指标(生物学或/和临床指标)。因此,有必要在多个层面继续对APS个体群体进行研究。