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Validity of the Center for Epidemiological Studies Depression scale in Type 2 diabetes
Jasmine Carter1, Hugo Cogo-Moreira2, Nathan Herrmann3
1University of Toronto, Department of Pharmacology and Toxicology, Canada; Sunnybrook Research Institute, Hurvitz Brain Sciences Centre, Canada; University Health Network Toronto Rehabilitation Institute, Cardiac Rehabilitation Program, Canada.
Objective:
Depressive symptoms are common among people with Type 2 diabetes mellitus (T2DM). This study aimed to validate the 3-factor structure of the 14-item Center for Epidemiological Studies Depression (CES-D) scale proposed by Carleton et al. (2013) in a T2DM population.
Methods:
The CES-D was administered to consecutive patients with T2DM entering a rehabilitation program. Construct validity was assessed using confirmatory factor analysis. Subscale viability, differential item functioning, and associations with clinical characteristics were tested in bifactor models.
Results:
Among adults with T2DM (n=305, age 56.9±11.1, 44.9% male, duration of diabetes 7.8±7.9years, HbA1c 0.076±0.014%), the construct validity of Carleton's 3-factor solution (negative affective, positive affective and somatic symptoms) was confirmed, although negative affective and somatic symptoms were highly correlated (r=0.926). The CES-D items can be summed to arrive at a total score (ωH=0.869), but not subscale scores (ωS>0.7). Differential item functioning was not found based on age or body mass index (BMI), but Item 1 ("I was bothered by things that don't usually bother me") was inflated in women and Item 7 ("I felt that everything I did was an effort") was inflated in those with higher glycosylated haemoglobin (HbA1c). The general depression factor decreased with age (β=-0.247, p<0.001) and increased with BMI (β=0.102, p=0.041) but not HbA1c (β=0.065, p=0.461). Negative affective symptoms (β=0.743, p=0.001), but not other depressive symptoms, were higher in women.
Conclusions:
The 14-item CES-D retained construct validity in adults with T2DM. Depressive symptoms were associated with younger age, female gender and BMI, but not with glycemic control.
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