Measurement invariance of the Center for Epidemiological Studies-Depression scale and associations with genetic risk in older adults

PLoS One. 2024 Oct 28;19(10):e0312194. doi: 10.1371/journal.pone.0312194. eCollection 2024.

Abstract

Background: As populations are aging, it needs to be ensured that valid depression rating scales are available across old adulthood. Center for Epidemiological Studies-Depression scale (CES-D) is a common depression rating scale, however, few studies have assessed its validity in individuals with age over 90 and/or cognitive impairment. We examined the factor structures of 20-, 15-, and 8-item CES-D scales, their measurement invariance for age and cognition, and associations with genetic risk of depression.

Methods: Participants were from a population-based older Finnish Twin Cohort study including 71-79-year-olds from the MEMTWIN II (n = 1034 for exploratory and n = 664 for confirmatory factor analyses) and 90+ year-olds from the NONAGINTA (n = 134, confirmatory factor analyses) sub-studies. Associations of polygenic risk score of major depressive disorder (MDD-PRS) with CES-D scales were examined in MEMTWIN II.

Results: Exploratory factor analyses (n = 1034) suggested four- (CES-D 20) and three-factor (CES-D 8) structures and these models fit well in confirmatory analyses (n = 664). Unidimensional models had good (CES-D 15 & 20) or fair fit (CES-D 8). Results supported scalar invariance of all CES-D versions for age and cognitive status. Higher MDD-PRS was associated with more depressive symptoms in different CES-D versions.

Conclusions: Different CES-D versions are adequate for measuring depressive symptoms across age groups and cognitive spectrum in old age. Genetic risk of depression predicts depressive symptoms even in old age.

Publication types

  • Twin Study

MeSH terms

  • Aged
  • Aged, 80 and over
  • Cohort Studies
  • Depression / epidemiology
  • Depression / genetics
  • Depressive Disorder, Major / epidemiology
  • Depressive Disorder, Major / genetics
  • Factor Analysis, Statistical
  • Female
  • Finland / epidemiology
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Psychiatric Status Rating Scales
  • Risk Factors

Grants and funding

Data collection and analyses in the Finnish Twin Cohort have been supported by the Academy of Finland (grants to JK: 312073, 336823, 352792). MEMTWIN II data collection was supported by the Sigrid Juselius foundation, The Academy of Finland (grants 133193 and 310962) and Finnish Governmental Research Funding (VTR). NONAGINTA study was funded by the Academy of Finland grants (320109 and 345988 to EV). EV was supported by the Academy Research Fellow grant 314639 and the Sigrid Jusélius Foundation. Open access funded by Helsinki University Library.