What Determines Cognitive Functioning in the Oldest-Old? The EMIF-AD 90+Study

被引:14
作者
Legdeur, Nienke [1 ]
Badissi, Maryam [1 ]
Yaqub, Maqsood [2 ]
Beker, Nina [1 ]
Sudre, Carole H. [3 ,4 ]
ten Kate, Mara [1 ,2 ]
Gordon, Mark Forrest [5 ]
Novak, Gerald [6 ]
Barkhof, Frederik [2 ,7 ]
van Berckel, Bart N. M. [2 ]
Holstege, Henne [1 ,8 ]
Muller, Majon [9 ]
Scheltens, Philip [1 ]
Maier, Andrea B. [10 ,11 ]
Visser, Pieter Jelle [1 ,12 ]
机构
[1] Vrije Univ Amsterdam, Alzheimer Ctr Amsterdam, Dept Neurol, Amsterdam UMC,Amsterdam Neurosci, POB 7057, NL-1007 MB Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Dept Radiol & Nucl Med, Amsterdam UMC, Amsterdam Neurosci, Amsterdam, Netherlands
[3] Kings Coll London, Sch Biomed Engn & Imaging Sci, London, England
[4] UCL, Dementia Res Ctr, Inst Neurol, London, England
[5] Teva Pharmaceut, Frazer, PA USA
[6] Janssen Pharmaceut Res & Dev, Titusville, NJ USA
[7] UCL, Inst Neurol, London, England
[8] Vrije Univ Amsterdam, Dept Clin Genet, Amsterdam UMC, Amsterdam Neurosci, Amsterdam, Netherlands
[9] Amsterdam UMC, Dept Internal Med, Amsterdam, Netherlands
[10] Univ Melbourne, Royal Melbourne Hosp, Dept Med & Aged Care, AgeMelbourne, Melbourne, Vic, Australia
[11] Vrije Univ Amsterdam, Res Inst Amsterdam Movement Sci, Dept Human Movement Sci, AgeAmsterdam, Amsterdam, Netherlands
[12] Maastricht Univ, Sch Mental Hlth & Neurosci, Dept Psychiat & Neuropsychol, Maastricht, Netherlands
来源
JOURNALS OF GERONTOLOGY SERIES B-PSYCHOLOGICAL SCIENCES AND SOCIAL SCIENCES | 2021年 / 76卷 / 08期
关键词
Alzheimer's disease; Brain pathology biomarkers; Cognitive aging; Oldest-old; Risk factors; WHITE-MATTER HYPERINTENSITIES; HANDGRIP STRENGTH; ALZHEIMERS-DISEASE; RISK; AGE; DEMENTIA; DECLINE; ASSOCIATION; BETA; BURDEN;
D O I
10.1093/geronb/gbaa152
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Objectives: Determinants of cognitive functioning in individuals aged 90 years and older, the oldest-old, remain poorly understood. We aimed to establish the association of risk factors, white matter hyperintensities (WMHs), hippocampal atrophy, and amyloid aggregation with cognition in the oldest-old. Method: We included 84 individuals without cognitive impairment and 38 individuals with cognitive impairment from the EMIF-AD 90+ Study (mean age 92.4 years) and tested cross-sectional associations between risk factors (cognitive activity, physical parameters, nutritional status, inflammatory markers, and cardiovascular risk factors), brain pathology biomarkers (WMH and hippocampal volume on magnetic resonance imaging, and amyloid binding measured with positron emission tomography), and cognition. Additionally, we tested whether the brain pathology biomarkers were independently associated with cognition. When applicable, we tested whether the effect of risk factors on cognition was mediated by brain pathology. Results: Lower values for handgrip strength, Short Physical Performance Battery (SPPB), nutritional status, HbA1c, and hippocampal volume, and higher values for WMH volume and amyloid binding were associated with worse cognition. Higher past cognitive activity and lower body mass index were associated with increased amyloid binding, lower muscle mass with more WMH, and lower SPPB scores with more WMH and hippocampal atrophy. The brain pathology markers were independently associated with cognition. The association of SPPB with cognition was partially mediated by hippocampal volume. Discussion: In the oldest-old, physical parameters, nutritional status, HbA1c, WMH, hippocampal atrophy, and amyloid binding are associated with cognitive impairment. Physical performance may affect cognition through hippocampal atrophy. This study highlights the importance to consider multiple factors when assessing cognition in the oldest-old.
引用
收藏
页码:1499 / 1511
页数:13
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