For Manuscript Submission, Check or Review Login please go to Submission Websites List.
For the academic login, please select your country in the dropdown list. You will be redirected to verify your credentials.
Metabolic Syndrome and Dementia Risk in a Multiethnic Elderly CohortMuller M.a, i · Tang M.-X.a, b · Schupf N.c-e, h · Manly J.J.a, c, f · Mayeux R.a, c-f · Luchsinger J.A.a, c, d, g
aGertrude H. Sergievsky Center, bDivision of Biostatistics, Joseph P. Mailman School of Public Health, cTaub Institute for Research of Alzheimer’s Disease and the Aging Brain, and dDepartment of Epidemiology, Joseph P. Mailman School of Public Health, Columbia University, eDepartment of Psychiatry, fDepartment of Neurology, and gDivision of General Medicine, Department of Medicine, Columbia University College of Physicians and Surgeons, New York, N.Y., and hLaboratory of Epidemiology, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, N.Y., USA; iDepartment of Geriatric Medicine, University Medical Center, Utrecht, The Netherlands Corresponding Author
José A. Luchsinger
Division of General Medicine
PH9East-105, 630 West 168th Street
New York, NY 10032 (USA)
Tel. +1 212 305 4730, Fax +1 212 305 9349, E-Mail email@example.com
Background/Aims: The metabolic syndrome (MeSy) may be related to Alzheimer’s disease (AD). Our aims were to investigate the association of the MeSy with incident dementia in a multiethnic elderly cohort in the United States. Methods: We conducted cross-sectional and prospective analyses in 2,476 men and women aged 65 years and older and with data available on the MeSy and dementia diagnosis in Northern New York City. MeSy was defined by the National Cholesterol Education Program Adult Treatment Program III and the European Group for the Study of Insulin Resistance criteria. Dementia was diagnosed using standard criteria. Results: No association was found between MeSy and prevalent dementia. After 4.4 years of follow-up, 236 individuals of the 1,833 without prevalent dementia developed dementia. MeSy was not associated with incident dementia. Of the components of the MeSy, diabetes and hyperinsulinemia were associated with an increased risk of incident AD [hazard ratio 1.4 (95% CI 1.0–2.1), and hazard ratio 1.4 (95% CI 0.9–2.7), respectively] and dementia associated with stroke [hazard ratio 1.9 (95% CI 1.1–3.1), and hazard ratio 2.3 (95% CI 1.1–4.7), respectively]. Conclusions: The MeSy was not associated with an increased dementia risk in a multiethnic elderly cohort, but diabetes and hyperinsulinemia were. In the elderly, examining diabetes and hyperinsulinemia separately may be preferable to using the MeSy as a risk factor.
© 2007 S. Karger AG, Basel