TY - JOUR
T1 - Depression prevalence of the Geriatric Depression Scale-15 was compared to Structured Clinical Interview for DSM using individual participant data meta-analysis
AU - the DEPRESsion Screening Data (DEPRESSD) GDS Group
AU - Parsons, Marc
AU - Qiu, Lu
AU - Levis, Brooke
AU - Fan, Suiqiong
AU - Sun, Ying
AU - Amiri, Lara S.N.
AU - Harel, Daphna
AU - Markham, Sarah
AU - Vigod, Simone N.
AU - Ziegelstein, Roy C.
AU - Wu, Yin
AU - Boruff, Jill T.
AU - Cuijpers, Pim
AU - Gilbody, Simon
AU - Patten, Scott B.
AU - Benedetti, Andrea
AU - Thombs, Brett D.
AU - Krishnan, Ankur
AU - He, Chen
AU - Santo, Tiffany Dal
AU - Neupane, Dipika
AU - Domínguez, Nadia González
AU - Brehaut, Eliana
AU - Bhandari, Parash M.
AU - Qiu, Xia
AU - Li, Letong
AU - Imran, Mahrukh
AU - Nassar, Elsa Lynn
AU - Ioannidis, John P.A.
AU - Allgaier, Antje Kathrin
AU - Chagas, Marcos H.N.
AU - Isik, Ahmet Turan
AU - Jetté, Nathalie
AU - König, Hans Helmut
AU - Löbner, Margrit
AU - Marsh, Laura
AU - Michopoulos, Ioannis
AU - Mougias, Antonis A.
AU - Nelson, Christian J.
AU - Pabst, Alexander
AU - Quinn, Terence J.
AU - Riedel-Heller, Steffi G.
AU - Saracino, Rebecca
AU - Scherer, Martin
AU - Taylor-Rowan, Martin
AU - Volz, Matthias
AU - Werheid, Katja
AU - Weyerer, Siegfried B.
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024/12
Y1 - 2024/12
N2 - Depression questionnaire cutoffs are calibrated for screening accuracy and not to assess prevalence, but the Geriatric Depression Scale (GDS-15) is often used to estimate diagnostic prevalence among older adults, most commonly with scores of ≥ 5. We conducted an individual participant data meta-analysis to compare depression prevalence based on GDS-15 ≥ 5 to Structured Clinical Interview for Diagnostic and Statistical Manual (SCID) diagnoses and assessed whether an alternative cutoff could be more accurate. We used generalized linear mixed models to estimate prevalence. Data from 14 studies (3602 participants, 434 SCID major depression) were included. Pooled GDS-15 ≥ 5 prevalence was 34.2% (95% confidence interval [CI] 27.5–41.6%), and pooled SCID prevalence was 14.8% (95% CI 10.0–21.5%; difference of 17.6%, 95% CI 11.6–23.6%). GDS-15 ≥ 8 provided the closest estimate to SCID with mean difference of − 0.3% (95% prediction interval − 17.0–16.5%). Prevalence estimate differences were not associated with study or participant characteristics. In sum, GDS-15 ≥ 5 substantially overestimated depression prevalence. A cutoff of ≥ 8 was accurate overall, but heterogeneity was too high for implementation in practice. Validated diagnostic interviews should be used to estimate major depression prevalence among older adults.
AB - Depression questionnaire cutoffs are calibrated for screening accuracy and not to assess prevalence, but the Geriatric Depression Scale (GDS-15) is often used to estimate diagnostic prevalence among older adults, most commonly with scores of ≥ 5. We conducted an individual participant data meta-analysis to compare depression prevalence based on GDS-15 ≥ 5 to Structured Clinical Interview for Diagnostic and Statistical Manual (SCID) diagnoses and assessed whether an alternative cutoff could be more accurate. We used generalized linear mixed models to estimate prevalence. Data from 14 studies (3602 participants, 434 SCID major depression) were included. Pooled GDS-15 ≥ 5 prevalence was 34.2% (95% confidence interval [CI] 27.5–41.6%), and pooled SCID prevalence was 14.8% (95% CI 10.0–21.5%; difference of 17.6%, 95% CI 11.6–23.6%). GDS-15 ≥ 8 provided the closest estimate to SCID with mean difference of − 0.3% (95% prediction interval − 17.0–16.5%). Prevalence estimate differences were not associated with study or participant characteristics. In sum, GDS-15 ≥ 5 substantially overestimated depression prevalence. A cutoff of ≥ 8 was accurate overall, but heterogeneity was too high for implementation in practice. Validated diagnostic interviews should be used to estimate major depression prevalence among older adults.
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U2 - 10.1038/s41598-024-68496-3
DO - 10.1038/s41598-024-68496-3
M3 - Article
C2 - 39075146
AN - SCOPUS:85199990162
SN - 2045-2322
VL - 14
JO - Scientific reports
JF - Scientific reports
IS - 1
M1 - 17430
ER -