This study investigates general and specific features of self-reported depression and anxiety in adolescents. Alternative factor models to characterise the latent structure of depression and anxiety symptoms as IRT-informed dimensional phenotypes using latent trait modelling principles and methods were compared. In our large sample of British 14-year-old adolescents a three-factor model was preferred over one or two factor solutions in initial EFA. The three-factor (first-order) model contained a depressed mood factor, consisting of affective and social-cognitive symptoms of depression, a worrying factor, as well as a somatic/information processing factor including psychomotor disturbance, irritability, and thinking/decision-making difficulties. Under this model these factors can be viewed as distinct yet closely related constructs. Alternatively, a bifactor model representation also fitted the data well. This representation is in line with recent theoretical developments and offers improved insights into specific factors.
The
three-factor model reflects the view that depression and anxiety show a clearly distinguishable symptomatology. The distinct somatic/information processing factor implies that symptoms including concentration, irritability, sleeping difficulties, tiredness, and motor disturbances to be at the same hierarchical level with the depressed mood and the worrying factor, rather than being a subordinate construct. This is in line with structural studies of adult self-report depression scales which yield cognitive and somatic factors [
31]. In contrast to the tripartite model, the somatic/information processing factor in the three-factor solution in this study of adolescents contains not only arousal symptoms, but also psychomotor retardation, decision making and concentration difficulties.
Although the fit indices of the three-factor model were good, the substantial correlations of the factors suggest an alternative interpretation in terms of a common dimension for depressive, anxious, and somatic symptoms-a general factor influencing all items. Our
bifactor model formulation, which is based on the initial Mplus and FACTOR results, supports the hypothesis of a
general distress factor for depression and anxiety which accounts for a large proportion of the communality of depression and anxiety items and is consistent with an internalizing factor with depression, generalized anxiety disorder, and social anxiety [
32,
3-
5]. The bifactor model confirmed reliable variance for two domain specific factors for hopelessness-suicidality and restlessness-fatigue respectively. As expected, given the number and magnitude of item loadings, the general distress factor shows higher measurement precision and allows more precise measurement across a broader range of the population continuum than the specific factors and the three-factor (first order) model.
For these reasons, the bifactor representation proved to be more useful as a model for the structure of depression and anxiety symptoms in adolescents than the three factor model.
Our findings highlight the importance of domain specific factors which provide unique information over and above the general distress factor and reflect the distinctiveness of certain symptomatology and illness signs within depression and anxiety. The most salient features of psychopathology in the domain specific factor are hopelessness and suicidal thoughts, contrary to low positive affect or anhedonia as described by the tripartite model. Importantly, this
hopelessness-suicidality factor capturing a distinct feature of depression is associated with a higher severity on the latent distress continuum. In a similar framework applied to adult data, Simms et al. [
10] found that suicidality, panic, appetite loss, and ill temper were associated with higher levels on the underlying distress dimension. Low well-being, generalized anxiety, lassitude, and dysphoria were associated with lower levels of distress. Few studies have attempted general-specific factor separation in adolescents.
The specific restlessness-fatigue factor is analogous to somatic-endogenous constructs used clinically. It does not include items assessing other physiological symptoms such as shortness of breath or sweaty hands and is therefore distinct from the hyperarousal factor of the tripartite model.
The specific factor for generalized worrying contained only three items with factor loadings > .4, which were all similarly worded. Therefore, the relationship among these items could potentially represent a methodological artefact, able to be modelled using correlated errors rather than a specific psychopathological worrying factor. Thus, in a school-based community sample of adolescents, anxious symptoms seem more to be associated with general distress than reflecting a specific psychopathological construct. This view makes the bifactor representation more parsimonious, since it suggests only two specific factors.
A limitation of these results is that only self-report data were included in our cross-sectional analysis of the baseline phase of an ongoing longitudinal study. Longitudinal data are essential to further examine stability in the general and the specific factors over time. External correlates may help to elucidate potential aetiological factors. In addition, the anxiety self-report measure used is relatively weak on ascertaining fear based items and contains relatively few items specific for obsessional and compulsive acts that can be correlated with anxiety. This may account for the lack of validity in the specific worry factor. A further limitation is the relatively low response rate to initial recruitment within schools. This could be due to the ethically approved recruitment strategy which required participants to actively "opt in" rather than "opt out". We were aware that highly dysfunctional families could form a higher proportion of families that did not actively opt in to the study. Finally, factor structures and gender effects might differ according to the degree of psychopathology. This possibility needs to be explored in suitably large clinical samples.