Several research studies suggest a secular decline in AD trends. However factors influencing negative secular trend in AD are unknown. Besides, racial differences in these secular trends also need to be established for African American minorities. To address these issues, we propose to use a large population-based study with cognitive tests of executive functioning, episodic memory, and overall global cognition and orientation in 10,801 participants, and clinical diagnosis of AD in 2,839 participants of African American and European American ethnicity to study age, race, and sex-specific decline in AD trends between 1993 and 2012, and reasons for a negative secular trend in AD. More specifically, the five objectives of this proposal are: (1) Demographic differences in AD trends aim: evaluate age-, sex-, and race-specific trends in AD using composite and individual tests of cognition, ADLS, and clinical diagnosis in prevalent and incident Alzheimer?s AD from 1993 to 2012; (2) Risk factors aim: understand the association of demographic characteristics, hypertension, stroke, diabetes, Body Mass Index (BMI), perceived stress, and depressive symptoms on AD trends using composite and individual tests of cognition, ADLS, and clinical diagnosis of prevalent and incident AD between 1993 and 2012. (3) Protective factors aim: examine the association of educational attainment, income, social engagement, neuroticism, extraversion, physical activity, and cognition enriching activities on AD trends using composite and individual tests of cognition, ADLS, and clinical diagnosis of prevalent and incident AD between 1993 and 2012. (4) Medications use aim: Examine how anti-hypertensive, statin, and diabetes medication, and multi-vitamin supplement use may be associated with incident AD, and how change in hypertension, statin, and diabetes medication use may be associated with AD trends using composite and individual tests of cognition, ADLS, and clinical diagnosis of AD between 1993 and 2012. In this proposal, we use a newly developed AD likelihood score (ADLS) to translate clinical diagnosis of AD in clinical sample that uses 19 neuropsychological tests to likelihood of AD in our population sample that uses 4 short-battery neuropsychological tests. Such an approach will drastically improve our power to detect potential reasons for secular decline in AD trends. In addition, our proposal examines demographic differences in AD trends, and putative risk factors and preventive factors that might influence AD trends. This proposal has the potential to make a large public health impact in potentially identifying factors that could be influencing AD trends leading to intervention studies that could be geared towards improving the identified factors in the general population.

Public Health Relevance

Description: This proposal aims to examine the decline in age-, sex-, and race-specific AD trends using a biracial population sample between 1993 and 2012. The decline in AD trends will be assessed using clinical diagnosis of AD, as well as Alzheimer?s disease likelihood score (ADLS), and composite and individuals tests of cognitive function in the population sample. In addition to examining the decline in AD trends, we will assess the relationship of risk and protective factors on the decline in AD trends. Potential changes in hypertension, diabetes, and statin medication use will also be examined as reasons for decline in AD trends between 1993 and 2012. This proposal is based on a longitudinal cohort of 10,801 older adults with recurrent cognitive assessments and risk factors identified over the long duration of the study. The clinical diagnosis of AD was performed in 2,945, however, the ADLS score is available on the entire study sample (N=10,801) making it easier and efficient to trace the change in population estimate of AD over time.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Multi-Year Funded Research Project Grant (RF1)
Project #
1RF1AG057532-01
Application #
9422107
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Anderson, Dallas
Project Start
2017-09-15
Project End
2021-06-30
Budget Start
2017-09-15
Budget End
2021-06-30
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Rush University Medical Center
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
068610245
City
Chicago
State
IL
Country
United States
Zip Code
60612
Rajan, Kumar B; Weuve, Jennifer; Barnes, Lisa L et al. (2018) Prevalence and incidence of clinically diagnosed Alzheimer's disease dementia from 1994 to 2012 in a population study. Alzheimers Dement :
Ali, Talha; Nilsson, Charlotte Juul; Weuve, Jennifer et al. (2018) Effects of social network diversity on mortality, cognition and physical function in the elderly: a longitudinal analysis of the Chicago Health and Aging Project (CHAP). J Epidemiol Community Health 72:990-996
Rajan, Kumar B; Barnes, Lisa L; Wilson, Robert S et al. (2018) Blood pressure and risk of incident Alzheimer's disease dementia by antihypertensive medications and APOE ?4 allele. Ann Neurol 83:935-944
McAninch, Elizabeth A; Rajan, Kumar B; Miller, Corinne H et al. (2018) Systemic Thyroid Hormone Status During Levothyroxine Therapy In Hypothyroidism: A Systematic Review and Meta-Analysis. J Clin Endocrinol Metab :
Wilson, Robert S; Barnes, Lisa L; Rajan, Kumar B et al. (2018) Antecedents and consequences of unawareness of memory impairment in dementia. Neuropsychology 32:931-940
Weuve, Jennifer; Rajan, Kumar B; Barnes, Lisa L et al. (2018) Secular Trends in Cognitive Performance in Older Black and White U.S. Adults, 1993-2012: Findings From the Chicago Health and Aging Project. J Gerontol B Psychol Sci Soc Sci 73:S73-S81
McAninch, Elizabeth A; Rajan, Kumar B; Evans, Denis A et al. (2018) A Common DIO2 Polymorphism and Alzheimer Disease Dementia in African and European Americans. J Clin Endocrinol Metab 103:1818-1826
Rajan, Kumar B; Barnes, Lisa L; Wilson, Robert S et al. (2017) Racial Differences in the Association Between Apolipoprotein E Risk Alleles and Overall and Total Cardiovascular Mortality Over 18 Years. J Am Geriatr Soc 65:2425-2430