Estimating prevalence of subjective cognitive decline in and across international cohort studies of aging: A COSMIC study
By
Susanne Roehr,
Alexander Pabst,
Steffi Riedel-Heller,
Frank Jessen,
Yuda Turana,
Yvonne S. Handajani,
Carol Brayne,
Fiona E. Matthews,
Blosso C.M. Stephan,
Richard B. Lipton,
Mindy J. Katz,
Cuiling Wang,
Maëlenn Guerchet,
Pierre-Marie Preux,
Pascal Mbelesso,
Karen Ritchie,
Marie-Laure Ancelin,
Isabelle Carrière,
Antonio Guaita,
Annalisa Davin,
Roberta Vaccaro,
Ki Woong Kim,
Ji Won Han,
Seung Wan Suh,
Suzana Shahar,
Normah C. Din,
Divya Vanoh,
Martin van Boxtel,
Sebastian Köhler,
Mary Ganguli,
Erin P. Jacobsen,
Beth E Snitz,
Kaaren J. Anstey,
Nicolas Cherbuin,
Shuzo Kumagai,
Sanmei Chen,
Kenji Narazaki,
Tze Pin Ng,
Qi Gao,
Xin Yi Gwee,
Henry Brodaty,
Nicole A Kochan,
Julian Trollor,
Antonio Lobo,
Raúl López-Antón,
Javier Santabárbara,
John D. Crawford,
Darren M. Lipnicki,
Perminder S. Sachdev
Posted 26 May 2020
medRxiv DOI: 10.1101/2020.05.20.20106526
Subjective cognitive decline (SCD) is recognized as a risk stage for Alzheimer`s disease (AD) and other dementias, but its prevalence is not well known. We aimed to use uniform criteria to better estimate SCD prevalence across international cohorts. Therefore, we combined individual participant data for 16 cohorts from 15 countries (members of the COSMIC consortium) and used qualitative and quantitative (Item Response Theory/IRT) harmonization techniques to estimate SCD prevalence. The sample comprised 39,387 cognitively unimpaired individuals above age 60. The prevalence of SCD across studies was around one quarter with both qualitative harmonization/QH (23.8%, 95%CI=23.3%-24.4%) and IRT (25.6%, 95%CI=25.1%-26.1%); however, prevalence estimates varied largely between studies (QH: 6.1%, 95%CI=5.1%-7.0%, to 52.7%, 95%CI=47.4%-58.0%; IRT: 7.8%, 95%%CI=6.8%-8.9%, to 52.7%, 95%CI = 47.4%-58.0%). Across studies, SCD prevalence was higher in men than women, in lower levels of education, in individuals with Asian and African ancestry compared to European ancestry, in lower- and middle-income countries compared to high-income countries, and in studies conducted in later decades. Data harmonization and application of uniform criteria across diverse cohorts yielded more accurate estimates of SCD prevalence. Having a quarter of older individuals with SCD warrants further investigation of its significance, as a risk stage for AD and other dementias, and of ways to help individuals with SCD who seek medical advice.
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