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The literature on Alzheimer’s disease (AD) provides little data about long-term cognitive course trajectories. We identify global cognitive outcome trajectories and associated predictor variables that may inform clinical research and care.
Design:
Data derived from the National Alzheimer’s Coordinating Center (NACC) Uniform Data Set were used to examine the cognitive course of persons with possible or probable AD, a Mini-Mental State Examination (MMSE) of ≥10, and complete annual assessments for 5 years.
Setting:
Thirty-six Alzheimer’s Disease Research Centers.
Participants:
Four hundred and fourteen persons.
Measurements:
We used a hybrid approach comprising qualitative analysis of MMSE trajectory graphs that were operationalized empirically and binary logistic regression analyses to assess 19 variables’ associations with each trajectory. MMSE scores of ±3 points or greater were considered clinically meaningful.
Results:
Five distinct cognitive trajectories were identified: fast decliners (32.6%), slow decliners (30.7%), zigzag stable (15.9%), stable (15.9%), and improvers (4.8%). The decliner groups had three subtypes: curvilinear, zigzag, and late decline. The fast decliners were associated with female gender, lower baseline MMSE scores, a shorter illness duration, or receiving a cognitive enhancer. An early MMSE decline of ≥3 points predicted a worse outcome. A higher rate of traumatic brain injury, the absence of an ApoE ϵ4 allele, and male gender were the strongest predictors of favorable outcomes.
Conclusions:
Our hybrid approach revealed five distinct cognitive trajectories and a variegated pattern within the decliners and stable/improvers that was more consistent with real-world clinical experience than prior statistically modeled studies. Future investigations need to determine the consistency of the distribution of these categories across settings.
Self-rated health is one of the most widely used measures in gerontology, but it has not been evaluated systematically in older adults with schizophrenia (OAS). Therefore, the aim of this study was to determine the utility of self-rated health in OAS by examining its influencing factors and contrasting these findings with a community comparison (CC) group.
Method:
We compared 249 community-dwelling persons aged 55 years and older having a Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision, diagnosis of schizophrenia arising before age 45 years with a demographically similar group of 113 older adults in the general community. Using a modified version of Ocampo’s model of self-rated health, we identified 12 predictor variables within 5 dimensions.
Results:
There were no significant differences in self-health ratings between the OAS and the CC groups. Six of the 12 variables in the model significantly correlated with self-rated health in both groups. In linear regression analysis, three variables were significantly associated with self-rated health in both groups: Center for Epidemiological Studies−Depression score, number of physical disorders, and perception of self-health versus others. Self-rated health assessment was not associated with positive or negative symptoms or lack of awareness of mental illness.
Conclusion:
There was a striking similarity in the factors influencing self-rated health in the two groups. The findings were consistent with results of previous gerontological studies that self-rated health reflects elements of psychiatric and physical well-being, as well as perceptions of their age peers. Our results support the use of self-rated health as a legitimate clinical and research measure in OAS.
This chapter discusses many of the key themes presented in this volume. Some of the principal issues include: (1) concerns about the diagnostic complexities of rendering a diagnosis of psychoses in later life and which outcome criteria should be used, (2) diagnostic challenges of new-onset psychotic disorders with respect to dementia, (3) the evolution and classification of cognitive disorders arising in older adults with schizophrenia (OAS), (4) factors influencing the diverse trajectories in the course and outcome of schizophrenia in later life, (5) the extent to which OAS show accelerated aging, (6) the lack of controlled studies in the use of antipsychotic agents in OAS and the potential for some persons to discontinue medication in later life, (7) the need for more controlled studies on non-pharmacological interventions in OAS, (8) the desirability for more qualitative studies of how OAS perceive their illness over their lifespan and how they view their current circumstances, (9) the recognition of the complementary roles for subjective and objective appraisals of daily needs and life quality, (10) the needs of caregivers of OAS, (11) the extent to which geographic differences influenced by national health systems and culture affect outcome and treatment strategies of OAS, (11) the elements comprising an individualized care model for OAS.
This chapter reviews epidemiological findings concerning medical comorbidity and mortality in older adults with schizophrenia (OAS). Several key points emerged from this review: (1) There are inconsistencies in the prevalence of various medical disorders among OAS. (2) There is a 2.0 to 2.5 times increase in all-cause mortality in OAS compared to their age peers, although it is lower than their younger counterparts. (3) The risk of suicide trends downward in OAS patients after the age of 60. (4) A higher prevalence of respiratory diseases has not been demonstrated consistently; however, there is increased mortality for respiratory disease versus age peers, but reduced compared to younger counterparts. (5) There has been no demonstrated increase in mortality or prevalence of diabetes in OAS versus age peers. (6) OAS have declining mortality rates from cardiovascular disease compared to younger counterparts, but still elevated compared to age peers. (7) There have been inconsistent findings regarding the incidence of cancer compared to age peers; however, the cancer mortality rate is higher. (8) A healthcare utilization gap exists for OAS. Novel care strategies include self-management, peer support groups, integrated care models, and greater use of telehealth and mobile technologies.
Outcome is an unsettled area of debate in psychiatry that has varied historically and across investigative sites. It has included symptoms as well as social indices. This chapter examines various outcome dimensions in older adults with schizophrenia (OAS) as well as the associations between them and various predictor variables. Based on cross-sectional and longitudinal data from a community sample of OAS living in New York City, contrary to earlier views of a quiescent end stage in later life, heterogeneity in course persists into later life. Because of the fluidity of outcome and the various combinations of favorable outcomes, “recovering” remains a viable conceptual framework in later life. Although the outcome indices are largely independent of each other, provisional data suggest that, over time, alleviation of depressive symptoms is associated with improved community integration, which in turn is associated with higher rates of remission; improved cognitive function may also augment remission. There were few other predictors of the various outcome indices suggesting that clinical strategies need to target the specific clinical or social domain. Because of the various combinations of outcome and the high independence among outcome dimensions, an individualized care approach can achieve the optimal outcome.