| Literature DB >> 24466189 |
Jim van Os1, Tineke Lataster2, Philippe Delespaul2, Marieke Wichers2, Inez Myin-Germeys2.
Abstract
BACKGROUND: For the purpose of diagnosis, psychopathology can be represented as categories of mental disorder, symptom dimensions or symptom networks. Also, psychopathology can be assessed at different levels of temporal resolution (monthly episodes, daily fluctuating symptoms, momentary fluctuating mental states). We tested the diagnostic value, in terms of prediction of treatment needs, of the combination of symptom networks and momentary assessment level.Entities:
Mesh:
Year: 2014 PMID: 24466189 PMCID: PMC3900579 DOI: 10.1371/journal.pone.0086652
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Figure 1Experience sampling methodology (ESM) showing the details of a single day in the ESM paradigm.
At 10 random moments during the day, mental states (eg anxiety, low mood, paranoia, being happy) and contexts (stress, company, activity, drug use) are assessed. The arrows represent examples of prospectively analysing the impact of mental states and contexts on each other over time, allowing for the construction of an ecological psychopathology interactome.
Mechanistic findings in Psychiatry with Experience Sampling Method (ESM).
| MECHANISM | EVIDENCE |
| MECHANISMS UNDERLYING TREATMENT RESPONSE AND PROGNOSIS | In depression, baseline Reward Experience (momentary positive affective response to positive events) and baseline negative affect variability (variability in momentary negative affective response to negative events) in the ESM paradigm predict outcome, independent of conventional predictors |
| In antipsychotics with tight binding to the dopamine D2 receptor, increased levels of estimated D(2) receptor occupancy is associated with decreased feelings of momentary positive affect (PA) and increased feelings of negative affect (NA) in the ESM paradigm | |
| In depression, early change in positive rather than negative emotions in the ESM paradigm best predicted response to treatment, over and above changes in traditional rating scales (eg Hamilton Depression Rating Scale) | |
| In depression, future response to treatment was associated with altered baseline dynamics between NA and PA in the ESM paradigm: daily life boosts of PA were followed by a stronger suppression of NA over subsequent hours than in other depressed groups or controls | |
| Remission criteria for schizophrenia are manifested in daily life as fewer instances of momentary aberrant salience, better momentary mood states and partial recovery of momentary reward experience (positive momentary affective response to momentary positive events) | |
| Depression treatment with Mindfulness-based Cognitive Therapy is mediated by increased experience of momentary positive emotions as well as greater appreciation of, and enhanced responsiveness to, pleasant daily-life activities in the ESM paradigm | |
| Response to antidepressant medication is mediated by increase in Reward Experience (momentary positive affective response to positive events) rather than reduction in Stress-Sensitivity (momentary negative affective response to negative events) | |
| The therapeutic effect of physical activity on mood is mediated by momentary increases in positive affect rather than reduction in negative affect in the ESM paradigm | |
| MECHANISMS UNDERLYING SYMPTOMS | Formation of clinically detectable psychotic symptoms is associated with alterations in the level of momentary transfer of momentary experience of aberrant salience in the ESM paradigm, in interaction with momentary emotional factors |
| Onset of psychotic symptoms is mediated in part by the tendency to develop momentary aberrant salience after momentary increases in negative affect in the ESM daily life paradigm | |
| Paranoid delusionality is driven by momentary negative emotions and reductions in momentary self-esteem in the ESM paradigm | |
| Onset of depressive symptoms is predicted by baseline stress sensitivity (momentary negative affective response to momentary stressful events) in the ESM paradigm | |
| The construct of negative schizotypy is associated with underlying momentary mental states and ecological interactions in the ESM paradigm, including decreased momentary positive affect and pleasure in daily life, increased momentary negative affect, and decreases in momentary social contact and interest | |
| The construct of negative symptoms in schizophrenia does not translate to altered emotional processing in the ESM paradigm: Lower rather than higher levels of negative symptoms were associated with a pattern of emotional processing in daily life which was different from healthy controls | |
| MECHANISMS UNDERLYING ENVIRONMENTAL RISK FACTORS | Exposure to early trauma increases sensitivity to stress in daily life, both in terms of emotional response (momentary negative affective response to momentary stressful events in daily life) and aberrant salience response (momentary psychotic response to momentary stressful events in daily life) |
| Growing up in an urban environment is not associated with enhanced sensitivity to stress in the flow of daily life | |
| The psychotogenic effects of cannabis are mediated by induction of momentary experiences of aberrant salience in the flow of daily life | |
| The influence of major Life Events (LE) on onset of psychotic disorder is mediated by the cumulative impact on LE on momentary stress sensitivity in the ESM paradigm (momentary negative affective response to momentary stress) | |
| MECHANISMS UNDERLYINGGENETIC RISK FACTORS | Genetic effects in depression are mediated by increased momentary negative affective responses to momentary stress in the flow of daily life |
| Momentary positive emotions in the ESM paradigm attenuate genetic effects on negative mood bias in daily life | |
| Vulnerability for psychotic disorder is associated, in the ESM paradigm, to both the momentary psychosis-inducing and the momentary mood-enhancing effects of cannabis | |
| Genetic risk for psychotic disorder is mediated in part by enhanced momentary aberrant salience in response to momentary stress in the flow of daily life | |
| Familial risk for psychotic disorder is expressed greater level of momentary transfer (or persistence) of experience of aberrant salience in the flow of daily life | |
| Individuals at genetic risk for depression and psychotic disorder have a different diurnal cortisol profile than those without, suggesting that altered hypothalamic-pituitary-adrenal axis functioning is an indicator of susceptibility to depression and psychosis | |
| MECHANISMS UNDERLYING PERSONALITY VARIATION | Borderline patients continually react stronger than patients with psychosis and healthy controls to small disturbances that continually happen in the natural flow of everyday life. Altered negative affective and aberrant salience stress reactivity may define borderline personality disorder |
| Neuroticism as measured by Eysenck questionnaire may index an environmental risk for decreased daily life levels of PA, and a genetic as well as an environmental risk for increased NA variability. Decomposing the broad measure of neuroticism into measurable persons-context interactions increases its ‘informative’ value in explaining psychopathology |
PA = positive affect; NA = negative affect.
Figure 2Prospective development (from top to bottom) of a cross-diagnostic network of momentary mental states and contexts making up an ecological psychopathology interactome.
Prospective development (from top to bottom) of a cross-diagnostic network of momentary mental states and contexts making up the ecological psychopathology interactome; the DSM diagnosis evolves (from top to bottom) with the dynamics of the network, showing qualitative changes, as the DSM system assumes that a “different disease” has manifested itself. Thickness of the arrows reflect the strength of the associations between the elements in the psychopathology interactome.
Figure 3Hypothesized relationship between Momentary Psychotic Experiences, assessed in the Experience Sampling paradigm, and Clinical Psychotic Symptoms, measured with the PANSS.
The degree to which Momentary Psychotic Experiences (Psy) are manifested as Clinical Psychotic Symptoms (i.e. their clinical relevance) is determined by interactions between Momentary Psychotic Experiences and momentary negative affect (NA – higher levels increasing clinical relevance of momentary psychosis), momentary positive affect (PA – higher levels decreasing clinical relevance of momentary psychosis) and momentary environmental stress (Env – higher levels increasing level of momentary NA and thus increasing clinical relevance of momentary psychosis). Thickness and colour of arrows indicate respectively strength and direction of association.
Degree to which Momentary Psychotic Experiences in the ESM paradigm manifest as Clinical Psychotic Symptoms at PANSS interview, contingent on momentary context and emotion variables.
| Moderating variable | Stratified association | P Interaction | P Interaction | |
| Momentary negative affect | Low NA | 0.25 (0.08–0.42) | <0.001 | <0.001 |
| High NA | 0.42 (0.25–0.59) | |||
| Momentary positive affect | Low PA | 0.38 (0.21–0.55) | 0.002 | <0.001 |
| High PA | 0.30 (0.13–0.47) | |||
| Momentary event stress | Low stress | 0.31 (0.14–0.49) | 0.008 | 0.009 |
| High stress | 0.39 (0.22–0.57) | |||
| Momentary activity stress | Low stress | 0.30 (0.13–0.47) | 0.001 | <0.001 |
| High stress | 0.39 (0.22–0.56) | |||
Interaction tests whether, for example, dichotomous NA moderates the association between Momentary Psychotic Experiences (dependent variable) and Clinical Psychotic Symptoms (independent variable).
†Sensitivity analysis tests same interaction using dichotomous measure of Momentary Psychotic Experiences (dependent variable) and dichotomous measure of Clinical Psychotic Symptoms (independent variable).
Figure 4Clinical relevance of Momentary Psychotic Experiences (expressed as association with Clinical Psychotic Symptoms) as a function of momentary ecological and emotional moderators.
Degree to which Momentary (Auditory) Hallucinatory Experiences in the ESM paradigm manifest as Clinical Psychotic Symptoms at PANSS interview, contingent on momentary paranoid ideation.
| Level of momentary paranoid ideation | Stratified association | P interaction | P Interaction | |
| Absent | 1 | 0.35 (0.17–0.53) | 0.0013 | <0.001 |
| ↓ | 2 | 0.38 (0.12–0.65) | ||
| ↓ | 3 | 0.57 (0.21–0.93) | ||
| ↓ | 4 | 0.74 (0.31–1.17) | ||
| ↓ | 5 | 0.36 (−0.20–0.92) | ||
| ↓ | 6 | 0.02 (−0.82–0.85) | ||
| Very much | 7 | 1.42 (0.56–2.28) | ||
Interaction tests whether momentary paranoid ideation moderates the association between Momentary Hallucinatory Experiences (dependent variable) and Clinical Psychotic Symptoms (independent variable).
†Sensitivity analysis tests same interaction using dichotomous measure of Momentary Hallucinatory Experiences (dependent variable) and dichotomous measure of Clinical Psychotic Symptoms (independent variable).
Figure 5Clinical relevance of Momentary (Auditory) Hallucinatory Experiences (expressed as association with Clinical Psychotic Symptoms) as a function of momentary paranoid ideation.
*expressed as association with Clinical Psychotic Symptoms.
Degree to which Momentary (Visual) Hallucinatory Experiences in the ESM paradigm manifest as Clinical Psychotic Symptoms at PANSS interview, contingent on momentary paranoid ideation.
| Level of momentary paranoid ideation | Stratified association | P interaction | P Interaction | |
| Absent | 1 | 0.17 (0.06–0.28) | <0.001 | <0.001 |
| ↓ | 2 | 0.04 (−0.13–0.21) | ||
| ↓ | 3 | 0.26 (0.02–0.50) | ||
| ↓ | 4 | 0.32 (0.03–0.61) | ||
| ↓ | 5 | 0.54 (0.15–0.93) | ||
| ↓ | 6 | 0.32 (−0.27–0.90) | ||
| Very much | 7 | 1.48 (0.88–2.08) | ||
Interaction tests whether momentary paranoid ideation moderates the association between Momentary Hallucinatory Experiences (dependent variable) and Clinical Psychotic Symptoms (independent variable).
†Sensitivity analysis tests same interaction using dichotomous measure of Momentary Hallucinatory Experiences (dependent variable) and dichotomous measure of Clinical Psychotic Symptoms (independent variable).
Figure 6Clinical relevance of Momentary (Visual) Hallucinatory Experiences (expressed as association with Clinical Psychotic Symptoms) as a function of momentary paranoid ideation.
*expressed as association with Clinical Psychotic Symptoms.
Degree to which Momentary Psychotic Experiences in the ESM paradigm are associated with Unmet Treatment Needs at CAN interview, contingent on momentary context and emotion variables, and adjusted for PANSS psychopathology (PANSS positive, negative and general factors).
| Moderating variable | Stratified association | P Interaction | P Interaction | |
| Momentary negative affect | Low NA | 0.07 (0.00–0.15) | <0.001 | <0.001 |
| High NA | 0.12 (0.05–0.20) | |||
| Momentary positive affect | Low PA | 0.12 (0.05–0.20) | <0.001 | <0.001 |
| High PA | 0.07 (0.00–0.15) | |||
| Momentary event stress | Low stress | 0.08 (0.00–0.15) | 0.002 | 0.004 |
| High stress | 0.12 (0.04–0.19) | |||
| Momentary activity stress | Low stress | 0.08 (0.01–0.16) | 0.002 | <0.001 |
| High stress | 0.12 (0.04–0.19) | |||
Interaction tests whether, for example, dichotomous NA moderates the association between Momentary Psychotic Experiences (dependent variable) and Unmet Treatment Needs (independent variable).
†Sensitivity analysis tests same interaction using dichotomous measure of Momentary Psychotic Experiences (dependent variable) and dichotomous measure of Unmet Treatment Needs (independent variable).
Figure 7Treatment relevance of Momentary Psychotic Experiences (expressed as association with Unmet Treatment Needs) as a function of momentary ecological and emotional moderators.
Degree to which Momentary (Auditory) Hallucinatory Experiences in the ESM paradigm are associated with Unmet Treatment Needs at CAN interview, contingent on momentary paranoid ideation, and adjusted for PANSS psychopathology (PANSS positive, negative and general factors).
| Level of momentary paranoid ideation | Stratified association | P interaction | P Interaction | |
| Absent | 1 | 0.04 (−0.05–0.14) | <0.001 | <0.001 |
| ↓ | 2 | 0.09 (−0.03–0.21) | ||
| ↓ | 3 | 0.11 (−0.04–0.23) | ||
| ↓ | 4 | 0.16 (−0.01–0.31) | ||
| ↓ | 5 | 0.35 (0.17–0.53) | ||
| ↓ | 6 | 0.32 (0.03–0.61) | ||
| Very much | 7 | 0.85 (0.57–1.12) | ||
Interaction tests whether momentary paranoid ideation moderates the association between Momentary Hallucinatory Experiences (dependent variable) and Unmet Treatment Needs (independent variable).
†Sensitivity analysis tests same interaction using dichotomous measure of Momentary Hallucinatory Experiences (dependent variable) and dichotomous measure of Unmet Treatment Needs (independent variable).
Figure 8Treatment relevance of Momentary (Auditory) Hallucinatory Experiences (expressed as association with Unmet Treatment Needs) as a function of momentary paranoid ideation.
*expressed as association with Clinical Psychotic Symptoms.
Degree to which Momentary (Visual) Hallucinatory Experiences in the ESM paradigm are associated with Unmet Treatment Needs at CAN interview, contingent on momentary paranoid ideation, and adjusted for PANSS psychopathology (PANSS positive, negative and general factors).
| Level of momentary paranoid ideation | Stratified association | P interaction | P Interaction | |
| Absent | 1 | 0.02 (−0.04–0.08) | <0.001 | <0.001 |
| ↓ | 2 | 0.05 (−0.02–0.13) | ||
| ↓ | 3 | 0.04 (−0.05–0.13) | ||
| ↓ | 4 | 0.07 (−0.04–0.18) | ||
| ↓ | 5 | 0.09 (−0.04–0.22) | ||
| ↓ | 6 | 0.27 (0.06–0.48) | ||
| Very much | 7 | 0.68 (0.47–0.88) | ||
Interaction tests whether momentary paranoid ideation moderates the association between Momentary Hallucinatory Experiences (dependent variable) and Unmet Treatment Needs (independent variable).
†Sensitivity analysis tests interaction using dichotomous measure of Momentary Hallucinatory Experiences (dependent variable) and dichotomous measure of Unmet Treatment Needs (independent variable).
Figure 9Treatment relevance of Momentary (Visual) Hallucinatory Experiences (expressed as association with Unmet Treatment Needs) as a function of momentary paranoid ideation.
*expressed as association with Clinical Psychotic Symptoms.