| Literature DB >> 33986245 |
Jacob J Crouse1, Nicholas Ho2, Jan Scott2,3,4,5, Nicholas G Martin6, Baptiste Couvy-Duchesne6,7,8, Daniel F Hermens9, Richard Parker6, Nathan A Gillespie10, Sarah E Medland6, Ian B Hickie2.
Abstract
Improving our understanding of the causes of functional impairment in young people is a major global challenge. Here, we investigated the relationships between self-reported days out of role and the total quantity and different patterns of self-reported somatic, anxious-depressive, psychotic-like, and hypomanic symptoms in a community-based cohort of young adults. We examined self-ratings of 23 symptoms ranging across the four dimensions and days out of role in >1900 young adult twins and non-twin siblings participating in the "19Up" wave of the Brisbane Longitudinal Twin Study. Adjusted prevalence ratios (APR) and 95% confidence intervals (95% CI) quantified associations between impairment and different symptom patterns. Three individual symptoms showed significant associations with days out of role, with the largest association for impaired concentration. When impairment was assessed according to each symptom dimension, there was a clear stepwise relationship between the total number of somatic symptoms and the likelihood of impairment, while individuals reporting ≥4 anxious-depressive symptoms or five hypomanic symptoms had greater likelihood of reporting days out of role. Furthermore, there was a stepwise relationship between the total number of undifferentiated symptoms and the likelihood of reporting days out of role. There was some suggestion of differences in the magnitude and significance of associations when the cohort was stratified according to sex, but not for age or twin status. Our findings reinforce the development of early intervention mental health frameworks and, if confirmed, support the need to consider interventions for subthreshold and/or undifferentiated syndromes for reducing disability among young people.Entities:
Mesh:
Year: 2021 PMID: 33986245 PMCID: PMC8119948 DOI: 10.1038/s41398-021-01390-y
Source DB: PubMed Journal: Transl Psychiatry ISSN: 2158-3188 Impact factor: 6.222
Fig. 1Prevalence of self-rated somatic, anxious-depressive, hypomanic, and psychotic-like symptoms in a community-based cohort of young adults.
Percentages are reported to the nearest whole number.
Sociodemographic characteristics of sample (N = 1904).
| Age, years | 26.3 (3.9) |
| Sex (female) | 1113 (58.5%) |
| Married | 466 (24.5) |
| Separated, divorced, and widowed | 41 (2.2) |
| Never married | 1395 (73.3) |
| Full-time | 1184 (62.3) |
| Part-time | 238 (12.5) |
| Studying | 252 (13.2) |
| Home duties | 106 (5.6) |
| Employed, not working (e.g., illness) | 28 (1.5) |
| Receiving sickness/disability benefits | 16 (0.8) |
| Volunteer | 10 (0.5) |
| Unemployed | 62 (3.3) |
| Prefer not to answer/don’t know | 6 (0.3) |
| Postgraduate degree | 275 (14.5) |
| Undergraduate degree | 840 (44.2) |
| Certificate/diploma | 484 (25.4) |
| Junior/senior high school | 299 (15.7) |
| No formal education | 1 (0.1) |
| Prefer not to answer/don’t know | 3 (0.2) |
aMissing for N = 2.
Fig. 2Relationships between days out of role and the number of somatic, anxious-depressive, hypo-manic, and psychotic-like symptoms in a community-based cohort of young adults.
A Model for total sample; B separate models stratified by sex. SOMA somatic symptoms, ANX-DEP = anxious-depressive symptoms, HMLE hypomanic, PLE psychotic-like symptoms.
Relationships between somatic, anxious-depressive hypo-manic, and psychotic-like, symptoms and “days out of role” in a community sample of young adults.
| Symptom dimension | APR Whole samplea,b,c | Raw | FDR-adjusted |
|---|---|---|---|
| 0 | 1.00 | ||
| 1 | 1.90 (1.37–2.63) | *** | *** |
| 2 | 2.07 (1.50–2.88) | *** | *** |
| 3 | 2.34 (1.65–3.32) | *** | *** |
| 4 | 2.72 (1.89–3.91) | *** | *** |
| 5 | 3.18 (2.15–4.72) | *** | *** |
| 6 | 3.67 (2.40–5.61) | *** | *** |
| 0 | 1.00 | ||
| 1 | 1.11 (0.83–1.49) | NS | NS |
| 2 | 1.39 (1.03–1.89) | * | NS |
| 3 | 1.09 (0.76–1.56) | NS | NS |
| 4 | 1.89 (1.30–2.75) | *** | ** |
| 5 | 2.60 (1.77–3.83) | *** | *** |
| 6 | 2.83 (1.92–4.19) | *** | *** |
| 0 | 1.00 | ||
| 1 | 1.32 (0.96–1.83) | NS | NS |
| 2 | 1.46 (1.08–1.96) | * | * |
| 3 | 1.21 (0.87–1.68) | NS | NS |
| 4 | 1.34 (0.97–1.86) | NS | NS |
| 5 | 1.71 (1.28–2.29) | *** | *** |
| 0 | 1.00 | ||
| 1 | 1.13 (0.84–1.54) | NS | NS |
| 2+ | 1.54 (1.04–2.29) | * | NS |
| Age | 0.99 (0.97–1.02) | NS | NS |
| Female | 1.00 | ||
| Male | 0.64 (0.52–0.79) | *** | *** |
| Not a twin | 1.00 | ||
| Monozygotic | 1.24 (0.96–1.59) | NS | NS |
| Dizygotic | 1.21 (0.94–1.55) | NS | NS |
APR adjusted prevalence ratio, NS non-significant (p > 0.05).
*p < 0.05.
**p < 0.01.
***p < 0.001.
aAdjusted for age.
bAdjusted for zygosity.
cAdjusted for sex.
Fig. 3Relationships between days out of role and the total number of undifferentiated symptoms in a community-based cohort of young adults.
A Model for total sample. B Separate models stratified by sex.
Relationships between number of “undifferentiated” symptoms and “days out of role” in a community sample of young adults.
| APR whole samplea,b,c | Raw | FDR-adjusted | |
|---|---|---|---|
| 0 | 1.00 | ||
| 1 | 1.51 (0.89–2.57) | NS | NS |
| 2 | 1.94 (1.20–3.13) | ** | * |
| 3 | 2.11 (1.30–3.42) | ** | ** |
| 4 | 2.58 (1.63–4.08) | *** | *** |
| 5 | 1.91 (1.17–3.13) | ** | * |
| 6 | 2.98 (1.87–4.75) | *** | *** |
| 7 | 3.22 (2.00–5.18) | *** | *** |
| 8 | 3.76 (2.27–6.22) | *** | *** |
| 9 | 4.22 (2.52–7.06) | *** | *** |
| 10 | 4.34 (2.58–7.33) | *** | *** |
| 11 | 5.03 (2.86–8.86) | *** | *** |
| 12 | 4.33 (2.50–7.49) | *** | *** |
| 13 | 5.44 (2.98–9.94) | *** | *** |
| 14 | 6.18 (3.29–11.61) | *** | *** |
| 15+ | 7.41 (3.70–14.84) | *** | *** |
| 0.99 (0.97–1.02) | NS | NS | |
| Female | 1.00 | ||
| Male | 0.62 (0.50–0.77) | *** | *** |
| Not a twin | 1.00 | ||
| Monozygotic | 1.20 (0.93–1.54) | NS | NS |
| Dizygotic | 1.19 (0.93–1.52) | NS | NS |
APR adjusted prevalence ratio, NS non-significant (p > 0.05).
*p < 0.05
**p < 0.01
***p < 0.001
aAdjusted for age.
bAdjusted for zygosity.
cAdjusted for sex.