| Literature DB >> 31645228 |
Jon E Grant1, Murat Yücel2, Lucy Albertella2, Samuel R Chamberlain3,4, Mike E Le Pelley5, Lisa-Marie Greenwood2,6,7, Rico Sc Lee2, Lauren Den Ouden2, Rebecca A Segrave2.
Abstract
BACKGROUND: Compulsivity can be seen across various mental health conditions and refers to a tendency toward repetitive habitual acts that are persistent and functionally impairing. Compulsivity involves dysfunctional reward-related circuitry and is thought to be significantly heritable. Despite this, its measurement from a transdiagnostic perspective has received only scant research attention. Here we examine both the psychometric properties of a recently developed compulsivity scale, as well as its relationship with compulsive symptoms, familial risk, and reward-related attentional capture.Entities:
Keywords: Addiction; cognition.; compulsive; marker; phenotype
Year: 2019 PMID: 31645228 PMCID: PMC7115959 DOI: 10.1017/S1092852919001330
Source DB: PubMed Journal: CNS Spectr ISSN: 1092-8529 Impact factor: 3.790
Figure 1.Sequence of trial events in the visual search task. Participants responded to the orientation of the line segment (horizontal or vertical) within the diamond (target). One of the nontarget circles could be a colour singleton distractor. Fast, correct responses to the target received monetary reward, depending on the distractor colour. A distractor rendered in a high-reward colour signalled that this was a bonus trial on which a large reward could be won. If instead the search display contained a distractor rendered in a low-reward colour (or did not contain a colour singleton distractor), then the trial was a standard trial on which only a small reward was available. Slower response times (RTs) on trials with a high-reward distractor than trials with a low-reward distractor demonstrate value-modulated attentional capture (VMAC).
Figure 2.Distribution of CHI-T total scores in the sample. Left—histogram; middle—box-whisker plot (the red bracket defines the shortest half of the data ie, the densest region); and right—Normal Quantile Plot.
Correlations between CHI-T total scores and different compulsive symptom domains.
| Measure |
|
|
|---|---|---|
| IAT total score | 0.3599 | <.0001 |
| PGSI total score | 0.1777 | 0.0041 |
| OCI-R total score | 0.5234 | <0.001 |
| Compulsive Alcohol Use | 0.1627 | 0.0086 |
| Compulsive Gambling | 0.1980 | 0.0013 |
| Compulsive Eating | 0.1793 | 0.0037 |
| Contamination compulsions | 0.2820 | <.0001 |
| Checking compulsions | 0.3644 | <.0001 |
| Just right and ordering compulsions | 0.3846 | <.0001 |
| Problematic Usage of the Internet | 0.3519 | <.0001 |
| Family history of addictions | 0.200 | 0.0030 |
| Family history of OCRDs | 0.2487 | <.001 |
Abbreviations: BATCAP, Brief Assessment Tool for Compulsivity Associated Problems; IAT, Internet addiction test; PGSI, Pathological Gambling Symptoms Inventory; OCI-R, Obsessive Compulsive Inventory Revised; OCRDs, obsessive-compulsive and related disorders.
p-values are uncorrected.
Figure 3.Standardized model coefficients for PLS model, linking each explanatory (X) variable to CHI-T scores (Y). All explanatory variables were statistically significant predictors of higher CHI-T scores (p < 0.05, bootstrap) except for family history of psychotic spectrum disorder.
Figure 4.A scatterplot of VMAC score (response time for trials with a distractor that signaled high-reward minus response time for trials with a distractor that signaled low-reward) as a function of CHI-T score.