The transdiagnostic dimension of psychosis: implications for psychiatric nosology and research

Jim VAN OS

?Commentary?

The transdiagnostic dimension of psychosis: implications for psychiatric nosology and research

Jim VAN OS

psychosis; diagnosis; nosology; epidemiology; schizophrenia; transdiagnostic

1. Introduction

Paul Bebbington’s Special Article in this issue[1]provides a fascinating perspective on the literature linking psychosis to the social world and how this relationship is impacted by emotional regulation and reasoning biases. In the last decade, this research has contributed to novel psychological treatments with exciting new results, such as the recent trial showing that a brief psychological intervention to reduce worry impacts paranoia outcomes.[2]The work discussed by Bebbington has important conceptual implications for psychiatry,as it views psychosis as a transdiagnostic dimension,the expression of which is governed by complicated underlying dynamics involving emotional and cognitive mechanisms.

Given the recent focus on transdiagnostic dimensional expression of psychopathology, during the development of DSM-5 serious consideration was given to the possible inclusion of a system of transdiagnostic dimensions, including psychosis. The introduction of transdiagnostic dimensions would have allowed for a diagnostic system combining a nomothetic groupspecific categorical diagnosis (such as schizoaffective disorder) with an idiographic person-specific set of dimensional scores – for example, scores on anxiety,depression, psychosis, mania, motivational alterations,cognition and suicidality. The advantage of such a system is that it focuses attention on the dynamic interaction of symptoms in a network of psychopathology,[3]and on how this psychopathological network is affected bythe social world.[4]Unfortunately, setting up a system of transdiagnostic dimensions proved too complicated and was not introduced in DSM-5. Nevertheless, in the transition from DSM-IV to DSM-5, psychosis became a transdiagnostic feature of several diagnostic groups,such as the psychotic variants of obsessive-compulsive disorder and body dysmorphic disorder. These shifts re flect increasing awareness that psychotic experiences are frequent not only in psychotic disorders, but also in non-psychotic disorders.

2. What is the transdiagnostic dimension of psychosis?

What have we learned about the transdiagnostic dimension of psychosis? A particularly fascinating perspective is offered by epidemiology. Conceptually and historically, psychosis has a strong association with the diagnosis of schizophrenia. As a result, psychosis has been studied predominantly in the context of a diagnosis of schizophrenia, while other disorders in the psychosis spectrum have been largely ignored. For example, a search of PUBMED on 5 April 2015 identi fied 49 979 articles with ‘schizophrenia’ in the title versus only 681 with ‘schizoaffective disorder’, 170 with‘delusional disorder’, 17 with ‘brief psychotic disorder’,and 5 with ‘psychotic disorder not otherwise speci fied(NOS)’. Thus schizophrenia is considered the dominant context for the study of psychosis. However, recent data have cast doubt on the validity of this strategy.

Methodologically comprehensive work from Finland(illustrated in Figure 1) has shown that the spectrum of psychotic disorders (including schizophrenia,schizoaffective disorder, schizophreniform disorder,delusional disorder, psychotic disorder NOS, brief psychotic disorder, psychotic depression, psychotic bipolar disorder, substance-induced psychotic disorder,psychotic disorder due to a medical condition), whilst largely ignored in research, is much broader than the diagnosis of schizophrenia alone. The total lifetime prevalence of the full spectrum of psychotic disorders is 3.5%; schizophrenia only accounts for 1% (less than one-third) of this overall prevalence. There is substantial evidence that the various disorders that make up the psychotic disorder spectrum represent different manifestations of the same underlying syndrome, sharing etiology, psychopathology, treatment approaches, and prognosis; moreover, this view is further supported by the lack of clear and consistent‘points of rarity’ between the various conditions.[5]Given the requirement of relative chronicity in the DSMIV criteria for schizophrenia (i.e., a duration of at least 6 months), the 30% fraction of the psychotic disorder spectrum meeting the criteria for schizophrenia can be considered the ‘poor outcome fraction’ of the spectrum.

3. Possible bias in psychosis research: schizophrenia

If the diagnosis of schizophrenia represents the poor outcome fraction of a much broader psychotic disorder spectrum, the interpretation of research findings about schizophrenia is not straightforward. For example, a case-control comparison between schizophrenia and healthy controls showing differences in cognition could be interpreted either as showing that (a) cognition is associated with the onset of schizophrenia, or (b)cognition predicts poor outcome within the psychotic disorder spectrum. The latter interpretation is a plausible hypothesis, given the association between cognition and universal predictors of poor outcomes in health care such as poverty[6]and education.[7]Similarly,recent research indicates strong associations between the diagnosis of schizophrenia and low social class,[8]another universal predictor of poor outcome in health care. The fact that schizophrenia research may be biased by chronicity poses a problem, as novel treatments are developed in the understanding that research findings reflect fundamental mechanisms underlying the disorder, not the mechanisms that determine the outcome of the disorder.

Figure 1. Schizophrenia represents only a fraction of the total psychotic disorder spectrum

3.1. Possible bias in psychosis research: non-psychotic disorders

As the study of psychosis as a transdiagnostic dimension has progressed, fascinating findings have emerged about psychotic experiences outside the psychotic disorder spectrum, that is, in the traditionally ‘non-psychotic’disorders of anxiety and depression. As illustrated in Figure 2, research has shown that around 30% of individuals with a diagnosis of anxiety or depression(the so-called ‘common mental disorders’) present with subtle sub-threshold psychotic experiences[9-11]and that 7% of the general population report psychoticlike experiences.[12]Importantly, the concurrent presence of subthreshold psychotic experiences in individuals with common mental disorders is related to the clinical severity of the mental disorder[9-11]and is a marker of poor response to pharmacological and psychotherapeutic treatments.[13,14]These findings indicate that current diagnostic criteria for non-psychotic disorders neglect an important psychopathological element that has a major influence on clinical severity and treatment response, an omission that may distort scienti fic findings about these conditions.

Figure 2. Transdiagnostic prevalence of psychotic symptoms and psychotic experiences

4. Towards an agnostic network model of diagnosis in psychiatry

The work presented by Bebbington is compatible with the proposition that mental disorders are reducible to sets of symptoms that are connected through systems of causal relationships[15]and that are sensitive to the social world.[16]Evidence from general population studies suggests that this conceptualization of mental disorders is particularly relevant to the earliest stages of psychopathology. One indirect indicator of the existence of this proposed network model is that the transition from a given subthreshold state to a given mental disorder is not symptom-specific; for example,subthreshold psychosis predicts both psychotic and(albeit more weakly) non-psychotic outcomes.[17]A more direct indicator of the model is that the earliest expressions of psychopathology dynamically interact with each other. For example, there is evidence that transition from subthreshold psychosis to psychotic disorder is contingent on the earlier presence of subtle indices of motivational impairment (early negative symptoms);[18]the transition from subthreshold mania to bipolar disorder is contingent on the presence of earlier subthreshold psychosis;[19]and the relationship between insomnia and paranoia may be mediated by affective dysregulation.[20]Interaction may also occur between symptoms within the same domain; for example, studies have shown that early hallucinatory states are more likely to result in transition to a clinical disorder when there is concurrent delusional ideation.[21]Similarly,subthreshold psychosis is associated with subthreshold depression and subthreshold mania in a dose-response fashion (suggesting a causal link); the stronger the association between the two domains, the greater the risk of transition to a clinical disorder.[22]Finally, many individuals with subthreshold psychosis present to clinical services with anxiety disorders or depressive disorders; in individuals with these common mental disorders the concurrent presence of subthreshold psychosis has a negative impact on the course and outcome of the disorder.[13,14]Clearly, the paradigm of subthreshold psychosis which considers these symptoms as specific predictors of psychotic disorder needs to be reconsidered; subthreshold psychosis may also be a predictor of the course and outcome of nonpsychotic disorders.[23]

5. Conclusion

The work presented by Bebbington suggests that the challenge in the years to come is to understand how the earliest expressions of psychopathology form part of a dynamic circuit of symptoms that interact with each other and gradually differentiate into more speci fic, but still largely overlapping, clinical syndromes.There is evidence that the manner in which the early stages of different psychopathological systems interact with each other over time is influenced by genetic and environmental factors.[24]Similarly, it is attractive to speculate that symptom circuits in the earliest stages of psychopathology reflect the dynamics of the neural circuits that regulate affect, assignment of salience, motivational processes, and social cognition.Of particular interest is how progressive changes in the dynamics of early psychopathology contribute to changes in functioning and personal attributions of ill-health, resulting in help-seeking behavior.Finally, assessment of the early dynamic interaction of symptoms over time facilitates person-specific diagnostic formulations, and the development of individualized treatments that target the most dominant links in the dynamic circuit of early psychopathology.[25]

Con flict of interest

The author reports no con flict of interest related to this manuscript

Funding

The preparation of this manuscript was funded by the European Community’s Seventh Framework Program under grant agreement No. HEALTH-F2-2009-241909(Project EU-GEI).

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10. Wigman JT, van Nierop M, Vollebergh WA, et al. Evidence that psychotic symptoms are prevalent in disorders of anxiety and depression, impacting on illness onset, risk,and severity--implications for diagnosis and ultra-high risk research.Schizophr Bull. 2012; 38: 247-57

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12. Linscott RJ, van Os J. An updated and conservative systematic review and meta-analysis of epidemiological evidence on psychotic experiences in children and adults: on the pathway from proneness to persistence to dimensional expression across mental disorders.Psychol Med. 2013; 43: 1133-1149

13. Wigman JT, van Os J, Abidi L, Huibers MJ, Roelofs J, Arntz A,et al. Subclinical psychotic experiences and bipolar spectrum features in depression: association with outcome of psychotherapy.Psychol Med. 2014; 44: 325-336. doi: http://dx.doi.org/10.1017/S0033291713000871

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15. Kendler KS, Zachar P, Craver C. What kinds of things are psychiatric disorders?Psychological Medicine. 2010; 41(6):1-8. doi: http://dx.doi.org/10.1017/S0033291710001844

16. Guloksuz S, van Nierop M, Lieb R, et al. Evidence that the presence of psychosis in non-psychotic disorder is environment-dependent and mediated by severity of nonpsychotic psychopathology.Psychol Med. 2015; 42(11): 1-13.http://dx.doi.org/10.1017/S0033291715000380

17. Kaymaz N, Drukker M, Lieb R, Wittchen H-U, Werbeloff N, Weiser M,et al. Do subthreshold psychotic experiences predict clinical outcomes in unselected non-help-seeking population-based samples? A systematic review and meta-analysis, enriched with new results.Psychol Med.2012; 42: 2239-2253. doi: http://dx.doi.org/10.1017/S0033291711002911

18. Dominguez MD, Saka MC, Lieb R, Wittchen HU, van Os J. Early expression of negative/disorganized symptoms predicting psychotic experiences and subsequent clinical psychosis: a 10-year study.Am J Psychiatry. 2010;167: 1075-1082. doi: http://dx.doi.org/10.1176/appi.ajp.2010.09060883

19. Kaymaz N, van Os J, de Graaf R, Ten Have M, Nolen W, Krabbendam L. The impact of subclinical psychosis on the transition from subclinicial mania to bipolar disorder.J Affect Disord. 2007; 98: 55-64

20. Freeman D, Stahl D, McManus S, Meltzer H, Brugha T, Wiles N, et al. Insomnia, worry, anxiety and depression as predictors of the occurrence and persistence of paranoid thinking.Soc Psychiatry Psychiatr Epidemiol. 2012; 47: 1195-1203. doi: http://dx.doi.org/10.1007/s00127-011-0433-1

21. Smeets F, Lataster T, Dominguez MD, Hommes J, Lieb R,Wittchen H-U, et al. Evidence that onset of psychosis in the population reflects early hallucinatory experiences that through environmental risks and affective dysregulation become complicated by delusions.Schizophre Bull. 2012; 38:531-542. doi: http://dx.doi.org/10.1093/schbul/sbq117

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23. van Os J, Murray RM. Can we identify and treat"schizophrenia light" to prevent true psychotic illness?BMJ.2013; 346: f304

24. Wigman JT, Collip D, Wichers M, Delespaul P, Derom C,Thiery E, et al. Altered transfer of momentary mental states(ATOMS) as the basic unit of psychosis liability in interaction with environment and emotions.PLoS One. 2013; 8: e54653.doi: http://dx.doi.org/10.1371/journal.pone.0054653

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, 2015-04-05; accepted, 2015-04-07)

Jim van Os trained in Psychiatry at the Institute of Psychiatry, King’s College, London (UK). After his clinical training he was awarded a three-year UK Medical Research Council Training Fellowship in Clinical Epidemiology at the London School of Hygiene and Tropical Medicine. He is on the editorial board of European and American psychiatric journals such as ‘Acta Psychiatrica Scandinavica’,‘European Psychiatry’, ‘Psychological Medicine’, ‘Schizophrenia Research’, ‘Schizophrenia Bulletin’, and‘Early Intervention in Psychiatry’. He is also an Academic Editor at ‘PLoS ONE’. In 2011, he was elected member of the Royal Netherlands Academy of Arts and Sciences (KNAW); he appears on the 2014 Thomson-Reuter Web of Science list of the world’s ‘most in fluential scienti fic minds’ of our time. Jim van Os is coordinator of a €12M EU FP7 IP project on gene-environment interactions in schizophrenia and is also active in clinical gene-environment interaction research in depression and bipolar disorder. He was a member of the Psychosis Group of the DSM-5 Task Force.

精神病的跨診斷維度：對精神疾病的分類學(xué)與研究的意義

van Os J

精神?。辉\斷；疾病分類學(xué)；流行病學(xué)調(diào)查；精神分裂癥；跨診斷的

Summary:If psychosis is a transdiagnostic dimension, the expression of which is governed by a dynamic set of contextual and emotional factors that are amenable to treatment, current approaches in psychiatric nosology and therapeutic research may need to be revised. The dominant approach to date is to clinically and conceptually situate psychotic symptoms in the construct of schizophrenia. However, schizophrenia,which has a lifetime prevalence of 1%, only represents the poor outcome fraction of a much broader spectrum of psychotic disorders which have a lifetime prevalence of 3.5%. Therefore, research findings in schizophrenia may reflect mechanisms of prognosis rather than fundamental associations with psychosis and other symptom domainsper se. Similarly, the discovery that up to 30% of individuals with non-psychotic common mental disorders have subthreshold psychotic symptoms that situate them on the transdiagnostic dimension of psychosis – and which impact clinical severity and treatment response – indicates that the rigid separation between ‘psychotic’ and ‘non-psychotic’ hampers both clinical practice and research.Diagnostic manuals in psychiatry would benefit from a system of transdiagnostic dimensions, including a transdiagnostic dimension of psychosis. Introduction of transdiagnostic dimensions allows for a system combining a nomothetic (i.e., group-specific) categorical diagnosis with an idiographic (i.e., person-specific)combination of dimensional scores. The advantage of such a system is that it encourages consideration of how symptoms dynamically interact with each other in a network of psychopathology, and of how this network is impacted by the social world.

[Shanghai Arch Psychiatry. 2015; 27(2): 82-86.

http://dx.doi.org/10.11919/j.issn.1002-0829.215041]

Maastricht University Medical Centre, South Limburg Mental Health Research and Teaching Network, EURON, Maastricht, The Netherlands King’s College London, King’s Health Partners, Department of Psychosis Studies, Institute of Psychiatry, London, United Kingdom

correspondence: vanosj@gmail.com

概述：如果精神病是一種跨診斷的維度，精神病性癥狀的出現(xiàn)受動(dòng)態(tài)變化的情境和情感因素左右，而后者又是可治療的，那么目前精神科疾病的分類學(xué)和治療研究的方法可能需要修改。迄今為止，無論在臨床工作上還是在疾病概念上，占主導(dǎo)地位的方法是將精神病性癥狀置于精神分裂癥的框架中。然而，終生患病率為1%的精神分裂癥只代表了部分預(yù)后不佳的精神病譜系障礙，而后者發(fā)生更多，終生患病率為3.5%。因此，精神分裂癥的研究結(jié)果可能反映了預(yù)后相關(guān)的機(jī)制，而非精神病和其他癥狀維度之間本質(zhì)上的相關(guān)性。同樣，常見的非精神病性精神障礙中高達(dá)30%的個(gè)體有閾下精神病性癥狀，他們會被歸于精神病的跨診斷維度之下，這些精神癥狀還會影響臨床嚴(yán)重程度和治療有效性 。上述發(fā)現(xiàn)也同樣提示武斷區(qū)分“精神病性”與“非精神病性”的做法妨礙了臨床實(shí)踐和研究。精神病學(xué)診斷手冊可以借鑒跨診斷維度（包括精神病的跨診斷維度）的體系。引入跨診斷維度，則既能根據(jù)原則進(jìn)行分類診斷（即疾病分組的特異性），又可結(jié)合個(gè)體特有的多維度綜合評分（即個(gè)體特異性）。這樣的益處在于促使人們思考在精神病理學(xué)中癥狀之間是如何動(dòng)態(tài)地交互作用的，并思考社會環(huán)境是如何影響精神病理癥狀的。

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