Somatic chronic diseases and 6-year change in cognitive functioning among older persons
Introduction
Aging is generally associated with an increasing prevalence of somatic chronic diseases as well as cognitive decline. Understanding the influence of chronic diseases in the context of its co-morbidity on cognitive functioning is important, because in old age, cognitive deficits may easily be misattributed to an early stage of dementia. Previously, the association between several specific chronic diseases and cognitive decline has been investigated extensively. Although this research has occasionally produced equivocal findings, most studies indicate a positive association between cognitive decline and cardiovascular (Di Carlo et al., 2000, Elwood et al., 2002, Van Exel et al., 2002), peripheral vascular (Elwood et al., 2002) and cerebro-vascular diseases (Jelicic and Kempen, 1997, Kase et al., 1998, Di Carlo et al., 2000, Dik et al., 2000), diabetes mellitus (Elias et al., 1997, Van Boxtel et al., 1998, Gregg et al., 2000, Arvanitakis et al., 2004, Logroscino et al., 2004), chronic obstructive pulmonary disease (COPD) (Jelicic and Kempen, 1997, Incalzi et al., 1998, Kozora and Make, 2000) and cancer (Meyers et al., 2000, Sjogren et al., 2000, Schagen et al., 2001). Most of these studies have been performed from an etiological or mechanistic viewpoint. Therefore, persons with co-morbid diseases are excluded from participation in order to investigate the association between a specific disease and cognitive decline. However, in old age, 50% of persons suffer from two or more chronic diseases (Haley, 1996), therefore investigating chronic diseases in persons with only one disease does not provide a realistic picture (Patrick et al., 2002). The relevance of this issue has been demonstrated in two studies that have shown that co-morbid diseases were associated with more serious cognitive decline than single diseases (Patrick et al., 2002, Hassing et al., 2004). Furthermore, most of the studies, which did take into account co-morbidity, used a cross-sectional study design, despite the fact that the influence of chronic disease on cognitive decline is best studied using a longitudinal design. Finally, in studying the association between somatic chronic diseases and cognitive decline in older persons, it is also important to take into consideration other concomitant risk factors for cognitive decline, such as old age, depression, vision or hearing impairment and the use of benzodiazepines.
Therefore, in the present study the association between specific chronic diseases and cognitive decline is investigated in the context of co-morbidity with other diseases. A longitudinal study design is employed, taking into account other concomitant risk factors for cognitive decline.
Section snippets
Methods
The data were collected as part of LASA (Deeg et al., 2002), an ongoing longitudinal study on predictors and consequences of changes in physical, cognitive, emotional and social functioning in older persons.
Results
Characteristics of the study sample are presented in Table 1. The sample size differed between the three measurements, because we included persons with at least two measurements. This resulted in a sample of n = 1294 at T1, n = 1296 at T2 and n = 1016 at T3. At baseline, 48.4% of the respondents were male, their average age was 72.1 years and their mean level of education was 9.0 years. At baseline (T1) 29.9% of the sample had two or more chronic diseases, while at the last measurement (T3) this
Discussion
This study has provided insights into the influence of somatic chronic diseases on changes in cognitive functioning in the context of co-morbidity. Therefore we examined the longitudinal association between specific chronic diseases and cognitive functioning in a population-based sample in multivariate analyses. It was found that diabetes mellitus was negatively associated with general cognitive functioning, fluid intelligence and speed of information processing. Furthermore, the rate of
Acknowledgements
The authors thank Douglas A. Hershey for his valuable comments on the paper.
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