TY - JOUR
T1 - Risk factors for mild cognitive impairment, dementia and mortality
T2 - the Sydney memory and ageing study
AU - Lipnicki, Darren M.
AU - Crawford, John
AU - Kochan, Nicole A.
AU - Trollor, Julian N.
AU - Draper, Brian
AU - Reppermund, Simone
AU - Maston, Kate
AU - Mather, Karen A.
AU - Brodaty, Henry
AU - Sachdev, Perminder S.
AU - Sydney Memory and Ageing Study Team
AU - Bowman, Allison
AU - Burns, Kim
AU - Broe, Anthony
AU - Dekker, Joula
AU - Dooley, Louise
AU - de Permentier, Michele
AU - Fairjones, Sarah
AU - Fletcher, Janelle
AU - French, Therese
AU - Foster, Cathy
AU - Nugent-Cleary-Fox, Emma
AU - Gooi, Chien
AU - Harvey, Evelyn
AU - Helyer, Rebecca
AU - Hsieh, Sharpley
AU - Hughes, Laura
AU - Jacek, Sarah
AU - Johnston, Mary
AU - Kang, Kristan
AU - McCade, Donna
AU - Meeth, Samantha
AU - Milne, Eveline
AU - Moir, Angharad
AU - O'Grady, Ros
AU - Pfaeffli, Kia
AU - Pose, Carine
AU - Reuser, Laura
AU - Rose, Amanda
AU - Schofield, Peter
AU - Shahnawaz, Zeeshan
AU - Sharpley, Amanda
AU - Slavin, Melissa
AU - Thompson, Claire
AU - Queisser, Wiebke
AU - Wong, Sam
PY - 2017/5/1
Y1 - 2017/5/1
N2 - Background: The nature and commonality of late-life risk factors for mild cognitive impairment (MCI), dementia, and mortality remain unclear. Our aim was to investigate potential risk factors, simultaneously in a single cohort including many individuals initially with normal cognition and followed for 6 years. Methods: We classified 873 community-dwelling individuals (70–90 years old and without dementia at baseline) from the Sydney Memory and Ageing Study as cognitively normal (CN), having MCI or dementia, or deceased 6 years after baseline. Associations with baseline demographic, lifestyle, health, and medical factors were investigated, including apolipoprotein (APOE) genotype, MCI at baseline, and reversion from MCI to CN within 2 years of baseline. Results: Eighty-three (9.5%) participants developed dementia and 114 (13%) died within 6 years; nearly 33% had MCI at baseline, of whom 28% reverted to CN within 2 years. A core set of baseline factors was associated with MCI and dementia at 6 years, including older age (per year: odds ratios and 95% confidence intervals = 1.08, 1.01–1.14 for MCI; 1.19, 1.09–1.31 for dementia), MCI at baseline (5.75, 3.49–9.49; 8.23, 3.93–17.22), poorer smelling ability (per extra test point: 0.89, 0.79–1.02; 0.80, 0.68–0.94), slower walking speed (per second: 1.12, 1.00–1.25; 1.21, 1.05–1.39), and being an APOE ε4 carrier (1.84, 1.07–3.14; 3.63, 1.68–7.82). All except APOE genotype were also associated with mortality (age: 1.11, 1.03–1.20; MCI: 3.87, 1.97–7.59; smelling ability: 0.83, 0.70–0.97; walking speed: 1.18, 1.03–1.34). Compared with stable CN participants, individuals reverting from MCI to CN after 2 years were at greater risk of future MCI (3.06, 1.63–5.72). Those who reverted exhibited some different associations between baseline risk factors and 6-year outcomes than individuals with stable MCI. Conclusion: A core group of late-life risk factors indicative of physical and mental frailty are associated with each of dementia, MCI, and mortality after 6 years. Tests for slower walking speed and poorer smelling ability may help screen for cognitive decline. Individuals with normal cognition are at greater risk of future cognitive impairment if they have a history of MCI.
AB - Background: The nature and commonality of late-life risk factors for mild cognitive impairment (MCI), dementia, and mortality remain unclear. Our aim was to investigate potential risk factors, simultaneously in a single cohort including many individuals initially with normal cognition and followed for 6 years. Methods: We classified 873 community-dwelling individuals (70–90 years old and without dementia at baseline) from the Sydney Memory and Ageing Study as cognitively normal (CN), having MCI or dementia, or deceased 6 years after baseline. Associations with baseline demographic, lifestyle, health, and medical factors were investigated, including apolipoprotein (APOE) genotype, MCI at baseline, and reversion from MCI to CN within 2 years of baseline. Results: Eighty-three (9.5%) participants developed dementia and 114 (13%) died within 6 years; nearly 33% had MCI at baseline, of whom 28% reverted to CN within 2 years. A core set of baseline factors was associated with MCI and dementia at 6 years, including older age (per year: odds ratios and 95% confidence intervals = 1.08, 1.01–1.14 for MCI; 1.19, 1.09–1.31 for dementia), MCI at baseline (5.75, 3.49–9.49; 8.23, 3.93–17.22), poorer smelling ability (per extra test point: 0.89, 0.79–1.02; 0.80, 0.68–0.94), slower walking speed (per second: 1.12, 1.00–1.25; 1.21, 1.05–1.39), and being an APOE ε4 carrier (1.84, 1.07–3.14; 3.63, 1.68–7.82). All except APOE genotype were also associated with mortality (age: 1.11, 1.03–1.20; MCI: 3.87, 1.97–7.59; smelling ability: 0.83, 0.70–0.97; walking speed: 1.18, 1.03–1.34). Compared with stable CN participants, individuals reverting from MCI to CN after 2 years were at greater risk of future MCI (3.06, 1.63–5.72). Those who reverted exhibited some different associations between baseline risk factors and 6-year outcomes than individuals with stable MCI. Conclusion: A core group of late-life risk factors indicative of physical and mental frailty are associated with each of dementia, MCI, and mortality after 6 years. Tests for slower walking speed and poorer smelling ability may help screen for cognitive decline. Individuals with normal cognition are at greater risk of future cognitive impairment if they have a history of MCI.
KW - mild cognitive impairment
KW - dementia
KW - mortality
KW - risk factors
KW - reversion to normal
UR - https://www.scopus.com/pages/publications/85009267009
UR - http://purl.org/au-research/grants/nhmrc/350833
UR - http://purl.org/au-research/grants/nhmrc/568940
U2 - 10.1016/j.jamda.2016.10.014
DO - 10.1016/j.jamda.2016.10.014
M3 - Article
C2 - 28043804
AN - SCOPUS:85009267009
SN - 1525-8610
VL - 18
SP - 388
EP - 395
JO - Journal of the American Medical Directors Association
JF - Journal of the American Medical Directors Association
IS - 5
ER -