Albuminuria and Microalbuminuria as Predictors of Cognitive Performance in a General Population: An 11-Year Follow-Up Study

• Published in: Journal of Alzheimer's disease Vol. 62; no. 2; p. 635
• Main Authors: Ekblad, Laura L, Toppala, Sini, Johansson, Jouni K, Koskinen, Seppo, Sundvall, Jouko, Rinne, Juha O, Puukka, Pauli, Viitanen, Matti, Jula, Antti
• Format: Journal Article
• Language: English
• Published: Netherlands 01.01.2018
• Subjects: Adult; Aged; Albuminuria - epidemiology; Cognition; Cognitive Dysfunction - epidemiology; Creatinine - urine; Cross-Sectional Studies; Female; Finland - epidemiology; Follow-Up Studies; Humans; Kidney - physiopathology; Linear Models; Male; Middle Aged; Multivariate Analysis; Neuropsychological Tests; Risk Factors; Finland; microalbuminuria; longitudinal study; Albuminuria; cognition; cognitive decline
• ISSN: 1875-8908
• DOI: 10.3233/JAD-170972

Microalbuminuria, defined as urine albumin-to-creatinine ratio (UACR)>3.0 mg/mmol and ≤ 30 mg/mmol, is an early marker of endothelial damage of the renal glomeruli. Recent research suggests an association among microalbuminuria, albuminuria (UACR > 3.0 mg/mmol), and cognitive impairment. Previous studies on microalbuminuria, albuminuria, and cognition in the middle-aged have not provided repeated cognitive testing at different time-points. We hypothesized that albuminuria (micro- plus macroalbuminuria) and microalbuminuria would predict cognitive decline independently of previously reported risk factors for cognitive decline, including cardiovascular risk factors. In addition, we hypothesized that UACR levels even below the cut-off for microalbuminuria might be associated with cognitive functioning. These hypotheses were tested in the Finnish nationwide, population-based Health 2000 Survey (n = 5,921, mean age 52.6, 55.0% women), and its follow-up, Health 2011 (n = 3,687, mean age at baseline 49.3, 55.6% women). Linear regression analysis was used to determine the associations between measures of albuminuria and cognitive performance. Cognitive functions were assessed with verbal fluency, word-list learning, word-list delayed recall (at baseline and at follow-up), and with simple and visual choice reaction time tests (at baseline only). Here, we show that micro- plus macroalbuminuria associated with poorer word-list learning and a slower reaction time at baseline, with poorer word-list learning at follow-up, and with a steeper decline in word-list learning during 11 years after multivariate adjustments. Also, higher continuous UACR consistently associated with poorer verbal fluency at levels below microalbuminuria. These results suggest that UACR might have value in evaluating the risk for cognitive decline.