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Basic symptoms of schizophrenia

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Symptoms in Schizophrenia, a 1938 silent film.

Basic symptoms of schizophrenia are subjective symptoms, described as experienced from a person's perspective, which show evidence of underlying psychopathology. Basic symptoms have generally been applied to the assessment of people who may be at risk to develop psychosis. Though basic symptoms are often disturbing for the person, problems generally do not become evident to others until the person is no longer able to cope with their basic symptoms. Basic symptoms are more specific to identifying people who exhibit signs of prodromal psychosis (prodrome) and are more likely to develop schizophrenia over other disorders related to psychosis.[1] Schizophrenia is a psychotic disorder, but is not synonymous with psychosis.[1] In the prodrome to psychosis, uncharacteristic basic symptoms develop first, followed by more characteristic basic symptoms and brief and self-limited psychotic-like symptoms, and finally the onset of psychosis.[2] People who were assessed to be high risk according to the basic symptoms criteria have a 48.5% likelihood of progressing to psychosis.[3] In 2015, the European Psychiatric Association issued guidance recommending the use of a subscale of basic symptoms, called the Cognitive Disturbances scale (COGDIS), in the assessment of psychosis risk in help-seeking psychiatric patients; in a meta-analysis, COGDIS was shown to be as predictive of transition to psychosis as the Ultra High Risk (UHR) criteria up to 2 years after assessment, and significantly more predictive thereafter.[4] The basic symptoms measured by COGDIS, as well as those measured by another subscale, the Cognitive-Perceptive basic symptoms scale (COPER), are predictive of transition to schizophrenia.[5]

Course

There are several factors that interact prior to the development of basic symptoms, including predisposed vulnerability, environmental stressors, and support systems.[6] Recent work in the field of neural oscillation has demonstrated that defective excitatory and inhibitory signalling in the brain during development plays an important role in the formation of basic symptoms.[7] These signalling disturbances can lead to cognitive deficits that result in the future appearance of more complicated symptoms of the disorder.[7] The interaction of these factors increases the risk for development of basic symptoms of schizophrenia.[6] It is important to identify when a person is exposed to these factors to prevent, modify or delay the onset of basic symptoms through early intervention.[6] The recognition of these basic symptoms in the prodromal phase can lead to early intervention in psychosis that aids in the delay or prevention of schizophrenia.[8] Such early interventions include cognitive behavioural therapy (CBT) or the use of antipsychotic drugs.[8]

Basic symptoms often appear several years before the onset of psychosis, but are often preceded by the onset of self-disorders (see supplementary material at [5]). They may sometimes appear and then disappear before appearing again much later, where they occur as part of an outpost syndrome. At one point, uncharacteristic basic symptoms will appear, which comprise various disturbances of mood, emotions, drive, thought, and attention that can occur in many other disorders, followed by the characteristic basic symptoms, which comprise disturbances of thought, perception, and attention, along with minor reality distortion, that are associated with schizophrenia in particular. Afterward, attenuated symptoms of psychosis or brief periods of psychosis will appear, before culminating in the emergence of full-blown psychosis. At any stage before psychosis, the person will attempt to cope with the basic symptoms, which might conceal the problems from others; once the person reaches the limit of their ability to compensate, however, the problems will become evident to others and cause impairment.[5] Poorer long-term outcomes such as increases in relapses, increases in hospitalizations, and poorer social/occupational functioning are associated with the age of onset of these symptoms, suggesting the importance of early intervention.[9]

After the resolution of psychosis, basic symptoms may follow one of 3 courses: Psychosis and the basic symptoms may resolve completely allowing the restoration of normal functioning; they may remit but remain at an uncharacteristic level, with relapses of psychosis; or the characteristic basic symptoms may remain creating a deficit syndrome dominated by negative symptoms.[5]

Evaluation

Basic symptoms are generally evaluated using the Schizophrenia Proneness Instrument (SPI), of which there are both a child and youth version (SPI-CY) and an adult version (SPI-A) (see supplemental material at [5]); this instrument assesses basic symptoms, both those that are uncharacteristic and those characteristic of psychosis. Out of the items evaluated on the SPI-CY and the SPI-A, there can be derived 2 scales to evaluate specifically the characteristic basic symptoms: the Cognitive Disturbances scale (COGDIS) and the Cognitive-Perceptual Basic Symptoms scale (COPER).[5]

COGDIS criteria are met when at least 2 of the symptoms on the scale (see table below) are present with at least weekly occurrence in the last 3 months, and which were not present during the pre-morbid phase of the illness and do not result from drug use. The European Psychiatric Association (EPA) recommends the use of this scale, along with attenuated psychotic symptoms and brief transient psychosis, to detect at-risk mental states in help-seeking people.[4]

COPER criteria are met when at least 1 of the symptoms on the scale (see table below) is present with at least weekly occurrence in the last 3 months, and the first occurrence of symptoms was more than 12 months prior to evaluation.[5]

Below are the basic symptoms associated with psychosis, along with whether they appear on COGDIS, COPER, or both:[2][4][5]

Symptom COGDIS COPER Description
Thought interference Yes Yes Interference of unimportant, irrelevant thoughts that hinders thinking and concentration.
Thought perseveration No Yes Repetition of thoughts that have little or no salience.
Thought pressure Yes Yes Many thoughts with no common theme pop up uncontrollably.
Thought blockages Yes Yes Sudden loss of train of thought that may be accompanied by the intrusion of a new thought.
Disturbance of receptive language Yes Yes Lack of immediate comprehension of speech or text in one's native language.
Disturbance of expressive language Yes No Difficulty producing speech or text that is appropriate to one's message in one's native language.
Disturbances of abstract thinking Yes No Difficulty comprehending idioms and metaphors.
Inability to divide attention Yes No Difficulty doing something with one sense (such as vision) while simultaneously using another sense for something else (such as hearing).
Captivation of attention by details of the visual field Yes No Attention is drawn to unimportant details as if one were "spellbound".
Decreased ability to discriminate between perception and ideas, true memories and fantasies No Yes Difficulty discriminating between what one has observed and what one has imagined.
Unstable ideas of reference with insight Yes Yes Sub-psychotic referential ideation that is thereafter immediately corrected by the person.
Derealization No Yes Sense of disconnect or unreality in one's environment.
Visual or acoustic perceptual disturbances with insight No Yes Disturbances of the perception of brightness or loudness, color or sound quality, or distortions in one's perceptions that are recognized by the person as false.

The Examination of Anomalous Self-Experience (EASE) is another scale used to evaluate subjective symptoms of schizophrenia.[10][11] This is a semi-structured interview scheme that was designed to specifically assess anomalous self-experience.[10]

See also

References

  1. ^ a b Piras, S; Casu, G; Casu, MA; Orrù, A; Ruiu, S; Pilleri, A; Manca, G; Marchese, G (2014). "Prediction and prevention of the first psychotic episode: new directions and opportunities". Therapeutics and Clinical Risk Management. 10: 241–53. doi:10.2147/TCRM.S55770. PMC 3974689. PMID 24729711.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  2. ^ a b Schultze-Lutter F (January 2009). "Subjective symptoms of schizophrenia in research and the clinic: the basic symptom concept". Schizophrenia Bulletin. 35 (1): 5–8. doi:10.1093/schbul/sbn139. ISSN 0586-7614. PMC 2643966. PMID 19074497.
  3. ^ Fusar-Poli, P; Bonoldi, I; Yung, AR; Borgwardt, S; Kempton, MJ; Valmaggia, L; Barale, F; Caverzasi, E; McGuire, P (March 2012). "Predicting psychosis: meta-analysis of transition outcomes in individuals at high clinical risk". Archives of General Psychiatry. 69 (3): 220–9. doi:10.1001/archgenpsychiatry.2011.1472. PMID 22393215.
  4. ^ a b c Schultze-Lutter F, Michel C, Schmidt SJ, Schimmelmann BG, Maric NP, Salokangas RK, Riecher-Rössler A, van der Gaag M, Nordentoft M, Raballo A, Meneghelli A, Marshall M, Morrison A, Ruhrmann S, Klosterkötter J (2015). "EPA guidance on the early detection of clinical high risk states of psychoses". Eur. Psychiatry. 30 (3): 405–16. doi:10.1016/j.eurpsy.2015.01.010. PMID 25735810.
  5. ^ a b c d e f g h Schultze-Lutter F, Debbané M, Theodoridou A, Wood SJ, Raballo A, Michel C, Schmidt SJ, Kindler J, Ruhrmann S, Uhlhaas PJ (2016). "Revisiting the Basic Symptom Concept: Toward Translating Risk Symptoms for Psychosis into Neurobiological Targets". Front Psychiatry. 7: 9. doi:10.3389/fpsyt.2016.00009. PMC 4729935. PMID 26858660.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  6. ^ a b c Cheng, SC; Walsh, E; Schepp, KG (December 2016). "Vulnerability, Stress, and Support in the Disease Trajectory from Prodrome to Diagnosed Schizophrenia: Diathesis-Stress-Support Model". Archives of Psychiatric Nursing. 30 (6): 810–817. doi:10.1016/j.apnu.2016.07.008. PMID 27888978.
  7. ^ a b Uhlhaas, Peter J.; Singer, Wolf (2015-06-15). "Oscillations and neuronal dynamics in schizophrenia: the search for basic symptoms and translational opportunities". Biological Psychiatry. 77 (12): 1001–1009. doi:10.1016/j.biopsych.2014.11.019. ISSN 1873-2402. PMID 25676489.
  8. ^ a b Stafford, MR; Jackson, H; Mayo-Wilson, E; Morrison, AP; Kendall, T (18 January 2013). "Early interventions to prevent psychosis: systematic review and meta-analysis". BMJ (Clinical Research Ed.). 346: f185. doi:10.1136/bmj.f185. PMC 3548617. PMID 23335473.
  9. ^ Immonen, J; Jääskeläinen, E; Korpela, H; Miettunen, J (27 April 2017). "Age at onset and the outcomes of schizophrenia: A systematic review and meta-analysis". Early Intervention in Psychiatry. 11 (6): 453–460. doi:10.1111/eip.12412. PMC 5724698. PMID 28449199.
  10. ^ a b Parnas, J; Henriksen, MG (2014). "Disordered self in the schizophrenia spectrum: a clinical and research perspective". Harvard Review of Psychiatry. 22 (5): 251–65. doi:10.1097/HRP.0000000000000040. PMC 4219858. PMID 25126763.
  11. ^ Parnas, Josef; Møller, Paul; Kircher, Tilo; Thalbitzer, Jørgen; Jansson, Lennart; Handest, Peter; Zahavi, Dan (September 2005). "EASE: Examination of Anomalous Self-Experience". Psychopathology. 38 (5): 236–258. doi:10.1159/000088441. ISSN 0254-4962. PMID 16179811.
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