TY - JOUR
T1 - Glycemia but not the Metabolic Syndrome is Associated with Cognitive Decline
T2 - Findings from the European Male Ageing Study
AU - Overman, Margot J.
AU - Pendleton, Neil
AU - O'Neill, Terence W.
AU - Bartfai, Gyorgy
AU - Casanueva, Felipe
AU - Forti, Gianni
AU - Rastrelli, Giulia
AU - Giwercman, Aleksander
AU - Han, Thang S
AU - Huhtaniemi, Ilpo T.
AU - Kula, Krzysztof
AU - Lean, Michael E J
AU - Punab, Margus
AU - Lee, David M.
AU - Correa, Elon S.
AU - Ahern, Tomas
AU - Laurent, Michaël R
AU - Verschueren, Sabine M P
AU - Antonio, Leen
AU - Gielen, Evelien
AU - Rutter, Martin K.
AU - Vanderschueren, Dirk
AU - Wu, Frederick C. W.
AU - Tournoy, Jos
PY - 2017
Y1 - 2017
N2 - Objective: Previous research has indicated that components of the metabolic syndrome (MetS), such as hyperglycemia and hypertension, are negatively associated with cognition. However, evidence that MetS itself is related to cognitive performance has been inconsistent. This longitudinal study investigates whether MetS or its components affect cognitive decline in aging men and whether any interaction with inflammation exists. Methods: Over a mean of 4.4 years (SD ± 0.3), men aged 40-79 years from the multicenter European Male Ageing Study were recruited. Cognitive functioning was assessed using the Rey-Osterrieth Complex Figure (ROCF), the Camden Topographical Recognition Memory (CTRM) task, and the Digit Symbol Substitution Test (DSST). High-sensitivity C-reactive protein (hs-CRP) levels were measured using a chemiluminescent immunometric assay. Results: Overall, 1,913 participants contributed data to the ROCF analyses and 1,965 subjects contributed to the CTRM and DSST analyses. In multiple regression models the presence of baseline MetS was not associated with cognitive decline over time (p > 0.05). However, logistic ordinal regressions indicated that high glucose levels were related to a greater risk of decline on the ROCF Copy (β = -0.42, p < 0.05) and the DSST (β = -0.39, p < 0.001). There was neither a main effect of hs-CRP levels nor an interaction effect of hs-CRP and MetS at baseline on cognitive decline. Conclusion: No evidence was found for a relationship between MetS or inflammation and cognitive decline in this sample of aging men. However, glycemia was negatively associated with visuoconstructional abilities and processing speed.
AB - Objective: Previous research has indicated that components of the metabolic syndrome (MetS), such as hyperglycemia and hypertension, are negatively associated with cognition. However, evidence that MetS itself is related to cognitive performance has been inconsistent. This longitudinal study investigates whether MetS or its components affect cognitive decline in aging men and whether any interaction with inflammation exists. Methods: Over a mean of 4.4 years (SD ± 0.3), men aged 40-79 years from the multicenter European Male Ageing Study were recruited. Cognitive functioning was assessed using the Rey-Osterrieth Complex Figure (ROCF), the Camden Topographical Recognition Memory (CTRM) task, and the Digit Symbol Substitution Test (DSST). High-sensitivity C-reactive protein (hs-CRP) levels were measured using a chemiluminescent immunometric assay. Results: Overall, 1,913 participants contributed data to the ROCF analyses and 1,965 subjects contributed to the CTRM and DSST analyses. In multiple regression models the presence of baseline MetS was not associated with cognitive decline over time (p > 0.05). However, logistic ordinal regressions indicated that high glucose levels were related to a greater risk of decline on the ROCF Copy (β = -0.42, p < 0.05) and the DSST (β = -0.39, p < 0.001). There was neither a main effect of hs-CRP levels nor an interaction effect of hs-CRP and MetS at baseline on cognitive decline. Conclusion: No evidence was found for a relationship between MetS or inflammation and cognitive decline in this sample of aging men. However, glycemia was negatively associated with visuoconstructional abilities and processing speed.
KW - Aging
KW - Cognition
KW - Male health
KW - Metabolic syndrome
KW - Multicenter study
UR - http://www.scopus.com/inward/record.url?scp=85014102091&partnerID=8YFLogxK
U2 - 10.1016/j.jagp.2017.02.004
DO - 10.1016/j.jagp.2017.02.004
M3 - Article
C2 - 28259698
AN - SCOPUS:85014102091
SN - 1064-7481
VL - 25
SP - 662
EP - 671
JO - American Journal of Geriatric Psychiatry
JF - American Journal of Geriatric Psychiatry
IS - 6
ER -