Neuropsychological Contributions to the Early Identification of Alzheimer’s Disease

Abstract

Introduction

The search for antecedent markers of Alzheimer’s disease (AD), whether clinical or biological, is predicated on the notion that significant neural dysfunction and cell death occurs well in advance of the clinical diagnosis. From a treatment perspective, it is imperative to reliably identify individuals during the disease prodrome (i.e., prior to the development of significant clinical symptoms) in order to have a maximum impact on cognitive function and quality of life. A wealth of studies has identified neuropsychological and neuroimaging changes in older adults during this prodromal period. The focus of much of this research has been on the study of higher risk groups (e.g., those of advanced age, termed the Very-Old; those with genetic susceptibility such as carriers of the apolipoprotein E epsilon-4 [APOE ε4] allele; and those with mild cognitive impairments but relatively normal daily function), as well as the prospective tracking of individuals who progress to AD over time.

In this review, we will highlight and discuss important neuropsychological differences by age and genetic risk in the expression of cognitive and brain changes during the clinical and prodromal periods of AD. For a more specific review of neuroimaging changes in the prodromal period of AD, we refer the reader to another recent critical review (see Wierenga and Bondi 2007). However, much remains to be done in characterizing the progression to AD in the Very-Old, and further clarification of the evolution of these brain and behavioral differences through the use of emerging neuropsychological (e.g., cognitive discrepancy measures) and neuroimaging (e.g., functional magnetic resonance imaging [fMRI]) techniques is needed. Critical examination of another risk factor for progression to AD, Mild Cognitive Impairment (MCI; Petersen et al. 1999), is also needed, given its recent definitional modifications (see Petersen and Morris 2005). We will argue in this review for more rigorous criteria and knowledge of clinical outcomes to better characterize MCI as a risk factor of AD. Finally, the oft-neglected impact of cerebrovascular disease (CVD) and CVD risk on the prodromal period of AD will also be discussed. Overall, this exciting area of research will undoubtedly continue to lead to better and more cost-effective methods for early detection as well as to provide a better understanding of the underlying brain substrata and risk factors related to the earliest cognitive declines in AD.

Clinical And Neuropathologic Features Of Alzheimer’s Disease

Alzheimer’s disease is a progressive and degenerative brain disease that results in dementia. Of the more than 70 known causes of dementia (Cummings and Benson 1992), AD is the most common and accounts for roughly half of all dementias. Alzheimer’s disease is characterized by brain atrophy and the microscopic appearance of diffuse and neuritic plaques and neurofibrillary tangles (Alzheimer 1907). These neuropathologic accumulations are thought to begin primarily in the medial temporal lobes (e.g., entorhinal cortex, hippocampus) and then progress to the association cortices of the temporal, parietal and frontal lobes (Braak and Braak 1991). Primary sensory and motor cortices, and most subcortical structures are relatively spared (see Fig. 1). Degeneration in the basal forebrain results in a major reduction of acetylcholine (Whitehouse et al. 1982). Consistent with these widespread neuropathologic changes, the primary clinical manifestation of AD is a progressive dementia syndrome that usually begins in later life. Typically, the dementia syndrome is characterized by prominent amnesia with additional deficits in language and semantic knowledge, executive functions, attention, and constructional and visuospatial abilities (Salmon and Bondi 1999). These cognitive deficits and the decline in everyday function they produce are the core features of the AD dementia syndrome.

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Fig. 1

Evolution of neurofibrillary tangle pathology as originally conceived by Braak and Braak (1991). Prior to the appearance of significant clinical symptoms, neurofibrillary changes begin to accumulate in entorhinal and transentorhinal cortex (stages I and II) and may appear surprisingly early in life (e.g., in one’s thirties or forties). Increasing involvement of the medial temporal lobe and surrounding association cortices are then thought to coincide with the appearance of mild clinical symptoms (stages III and IV), followed by clinically apparent Alzheimer’s disease and correspondingly severe involvement of medial temporal and cortical association areas (stages V and VI; adapted from Braak and Braak 1991, 1995; Braak et al. 1998)

Risk Factors

Advancing age is the single most important risk factor for AD, and the prevalence of the disease rises in an approximately exponential fashion between the ages of 65 and 85. With respect to the Oldest-Old (age 85 and above), the fastest growing segment of our population, prevalence rates for dementia are high, ranging between 40% and 60%. A number of studies suggest that women have a slightly greater risk for AD than men (Zhang et al. 1990), although the increased prevalence of AD in women may be attributable to differential survival after the onset of dementia due to their longer life expectancy. For example, although the Framingham study of AD showed about a 3:1 prevalence ratio of women to men with AD (Bachman et al. 1992), no gender difference was found in the incidence of dementia or AD (Bachman et al. 1993). However, more recent incidence rates from the Cache County epidemiological study of dementia, a study that includes the very old, reveal that the incidence among women increases after age 80 and exceeds the risk among men by more than twofold in late old age (Miech et al. 2002).

Regarding environmental factors, numerous epidemiological and biological studies show that higher education, occupational work complexity, as well as a mentally and socially integrated lifestyle in late life postpones the onset of clinical dementia and AD (see also Kawas and Katzman 1999; Fratiglioni and Wang 2007, for reviews). Long-term benefits of exercise and cardiorespiratory fitness on cognition have also been established, and clinical trials of fitness training interventions show a positive impact on cognition (Barnes et al. 2003). Indeed, physical activity has been shown to reduce the risk for dementia and improve cognition (see Kramer & Erickson 2007, for review). Moreover, head injury has been identified as an important risk factor for AD (Jellinger 2004). Specifically, the risk of AD is doubled for individuals with a history of a single head injury that led to loss of consciousness or hospitalization (Mortimer et al. 1991). Similarly, retired professional football players with histories of recurrent concussions show greater cognitive impairments in late life than do retired players without concussion histories (Guskiewicz et al. 2005).

With respect to genetic risk, AD development is increased by a positive family history in a first-degree relative (van Duijn et al. 1991), and specific point mutations on the amyloid precursor protein gene of chromosome 21 as well as presenilin gene mutations on chromosomes’ 1 and 14 are deterministic gene mutations for AD. In addition, the APOE ε4 allele located on chromosome 19 is over-represented in AD and has been identified as the single most important susceptibility gene for the disease (Corder et al. 1993; Saunders et al. 1993; Strittmatter et al. 1993). Gene-environment interactions may also be evident. For example, when Mayeux et al. (1995) examined the interaction between the APOE ε4 allele and head injury, they found a tenfold increase in the risk of developing AD in people with both risk factors. In high-exposure professional boxers, Jordan et al. (1997) also found that possession of an APOE ε4 allele was associated with increased severity of chronic neurologic deficits.

Our understanding of the risk factors for AD is growing rapidly and now includes not only those risk factors imparted in late life but also those present across the entire lifespan. For example, perinatal conditions, brain development, body growth, socioeconomic conditions, environmental enrichment, and cognitive reserve have all been suggested as early life factors that influence the onset of AD (see Borenstein et al. 2006). To summarize, the literature suggests that risk for AD is not likely to be determined in any single time period but results from a complex interplay between genetic and environmental exposures throughout one’s life (Borenstein et al. 2006).

Neuropsychological Characteristics of Alzheimer’s Disease

Neuropsychological Studies of the Prodromal Period of Alzheimer’s Disease

One of the most active areas of clinical research on AD is the attempt to identify cognitive changes that occur during the prodromal phase that precedes the manifestation of the overt dementia syndrome. Evidence consistently suggests that subtle declines in episodic memory in the older adult presages the development of the dementia syndrome associated with AD (Jacobs et al. 1995; Grober and Kawas 1997; Bondi et al. 1999; Collie and Maruff 2000; Smith et al. 2007). In addition, recent work also highlights that an episodic memory deficit need not be the only affected cognitive domain during the AD prodrome (see Twamley et al. 2006, for review), a finding also emphasized in recent re-characterizations of the concept of Mild Cognitive Impairment (Petersen and Morris 2005).

The ability to identify cognitive declines prior to overt dementia has led to the adoption of the designation Mild Cognitive Impairment (MCI; Petersen et al. 1999, 2001) for those with impaired performance on objective memory tests, but with intact general cognition and daily functioning. As Petersen and Morris (2005) more recently noted, MCI can be characterized more broadly in terms of the specific profile of impairment (e.g., amnestic vs. non-amnestic). The MCI condition (particularly the amnestic type) is a risk factor for the development of AD. Unfortunately, the practice of defining MCI is idiosyncratic and has varied widely across studies in the decade since its inception. Moreover, we have argued (see Twamley et al. 2006) that much of the literature’s formulations of MCI might well be re-cast as early AD but for the use of antiquated psychometric cutoffs (e.g., MMSE≥24 constituting “preserved general cognitive function”; see Salmon et al. 2002) and poor cognitive and functional (e.g., activities of daily living) characterizations. Thus, more rigorous criteria and knowledge of clinical outcomes are needed to better characterize this risk factor. We will address this further in the section on MCI below.

Another approach to identifying potential cognitive markers of AD during its prodromal phase has been to compare the neuropsychological changes of nondemented older adults who have an increased risk for developing the disease to that of individuals who do not have an increased risk. This approach assumes that a group of individuals with the risk factor will be more likely than one without this factor to contain individuals who are in the prodromal phase of the disease. These prodromal AD subjects will contribute to poor group performance on those tests that are particularly sensitive to early AD pathology. Studies that have adopted this approach to the search for cognitive markers of early AD, for the most part, have focused on increased risk due to a positive history of AD in a first degree relative (e.g., mother, father, or sibling) or the presence of a genetic marker for the disease, most commonly the ε4 allele type of apolipoprotein E (APOE), a low density lipoprotein cholesterol carrier.

A number of studies have shown that nondemented older adults with a positive family history for AD perform significantly worse than those with a negative family history on tests of episodic memory (Bondi et al. 1994; Caselli et al. 2004; La Rue et al. 1992; Levy et al. 2004). Our neuropsychological studies have also demonstrated that nondemented older adults who are at risk for developing AD by virtue of the APOE ε4 allele perform more poorly than those without this risk factor on tests of episodic memory, and that episodic memory measures are more effective for differentiating between these groups than are other cognitive measures of executive functions, attention, constructional ability, or psychomotor speed (Bondi et al. 1995, 1999; Lange et al. 2002; Mickes et al. 2007). Our research group has also shown that risk groups and those who convert to AD might be better characterized in terms of cognitive discrepancies between pairs of tests (see below), rather than through traditional methods of analyzing overall group means on individual cognitive tasks (Jacobson et al. 2002, 2005a, b; Houston et al. 2005; Wetter et al. 2005, 2006).

Course of Cognitive Decline in Prodromal Alzheimer’s Disease

As is now evident, a subtle decline in episodic memory often occurs prior to the emergence of frank dementia (Bondi et al. 1999). The course of episodic memory change during the prodromal phase of AD has been the focus of a number of studies (Bäckman et al. 2001; Chen et al. 2001; Lange et al. 2002; Rubin et al. 1998; Small et al. 2000; Storandt et al. 2002). These studies suggest that memory performance may be poor but stable a number of years prior to the development of the dementia syndrome in those with AD, and then decline rapidly in the year or two immediately preceding the dementia diagnosis. For example, both Small et al. (2000) and Bäckman et al. (2001) found that episodic memory was mildly impaired 6 years prior to dementia onset, but changed little over the next 3 years. In contrast, Chen et al. (2001) and Lange et al. (2002) showed a significant and steady decline in episodic memory beginning about 2 to 3 years prior to the dementia diagnosis in individuals with prodromal AD. Taken together, findings suggest a plateau effect in the course of decline in episodic memory rather than a monotonic or linear course of decline. Such a plateau model (i.e., mild but stable episodic memory decline followed by more abrupt decline in the years proximal to diagnosis) was validated in a large-scale study by Smith et al. (2007) who found that a plateau was evident on tests of episodic memory but not for the other cognitive domains examined (see Fig. 2).

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Fig. 2

Linear versus plateau trajectories of episodic memory decline prior to a diagnosis of Alzheimer’s disease. The solid line (—) represents a linear trajectory of cognitive decline, whereas the dashed line (– –) represents individuals with an initial mild decline, then a period of stabilization, followed by a more abrupt decline in the year or two preceding an AD diagnosis. Evidence suggests that episodic memory may reflect a plateau model of decline, whereas other cognitive functions may not (adapted from Smith et al. 2007 and Twamley et al. 2006)

These results indicate that an abrupt decline in memory in an elderly individual might better predict the imminent onset of dementia than poor but stable memory ability. Also, the mild but stable episodic memory decrements in an early preclinical period, followed by more abrupt and severe declines during a late preclinical period, suggest the operation of compensatory brain changes in response to increasing neuropathologic encroachments. A variety of studies examining functional neuroimaging (Bookheimer et al. 2000; Bondi et al. 2005; Han et al. 2007), neurochemical (DeKosky et al. 2002) and neurotrophic (Durany et al. 2000; Egan et al. 2003) factors, support this notion.

Although the search for cognitive changes in prodromal AD has largely focused on episodic memory, several recent reviews and meta-analyses suggest that there is largely nonspecific cognitive decline in the few years prior to a dementia diagnosis. Although a decline in episodic memory is consistently found in these studies, they also often reveal additional deficits in executive functions, perceptual speed, verbal ability, visuospatial skill, and attention during the prodromal phase of AD (Bäckman et al. 2005; Storandt et al. 2006; Twamley et al. 2006). This widespread decline in cognitive abilities mirrors evidence that multiple brain regions (e.g., medial and lateral temporal lobes, frontal lobes, anterior cingulate cortex) or connectivity between these regions are impaired in prodromal AD (Albert et al. 2001; Andrews-Hanna et al. 2007; Small et al. 2003) (see Table 1).

Table 1

Summary of specific cognitive domains affected in 90 older adults diagnosed with Mild Cognitive Impairment according to Petersen and Morris’ (2005) revised criteria (adapted from Storandt et al. 2006)

Neuropsychological domain	Percentage of patients with affected domain
Memory	30
Visuospatial skills	11
Executive functions	19
Memory and visuospatial skills	14
Memory and executive functions	7
Visuospatial skills and executive  functions	9
Memory, visuospatial, and  executive functions	10

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Consistent with this broader view, measures of semantic knowledge show significant declines during prodromal AD (Mickes et al. 2007; see also Cuetos et al. 2007; Powell et al. 2006), and this may be relatively independent of episodic memory deficits (Koenig et al. 2007). For example, Mickes et al. (2007) have shown in a detailed neuropsychological study of prodromal AD that both semantic memory and episodic memory functions declined rapidly in a 3-year period progressing to AD, whereas executive function deficits were not especially prominent (see Fig. 3). From these findings, the authors suggest that cognitive abilities thought to be subserved by the medial and lateral temporal lobes (episodic memory and semantic knowledge, respectively) may be substantially more impaired than cognitive functions subserved by the frontal lobes (executive functions). These findings map nicely onto the known neuropathologic encroachments of AD early on in the disease process (Braak and Braak 1991) and are also consistent with recent reports of decreased semantic access in nondemented APOE ε4 older adults (Rosen et al. 2005) and the ability of language tasks to predict pathologic AD 6 years later (Powell et al. 2006).

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Fig. 3

Control-referenced standard scores for prodromal AD patients on tests of episodic memory, semantic memory, and executive functions. Their neuropsychological profiles were examined 1 year (−1) and 2 years (−2) prior to the first year of their non-normal diagnosis (adapted from Mickes et al. 2007)

Cognitive Discrepancy Studies

The likelihood of a long prodromal period preceding the onset of AD is now well established. Although cognitive changes like those noted above appear to be the most common neuropsychological deficits prior to diagnosis, given the wide variability in domains initially affected it is unlikely that a single test or domain will be sufficient to accurately predict who will develop AD or to detect its earliest onset (Albert et al. 2007). A combination of methods that include a cognitive profile may prove more useful in defining a prodromal period in AD. Recent studies suggest that an asymmetric cognitive profile could improve our ability to characterize the earliest cognitive changes in AD.

Asymmetric cognitive profiles can capture relative intraindividual differences by comparing performance on dissimilar neuropsychological tests or domains such as verbal relative to visuospatial abilities. Infrequent or atypical performance discrepancies may signal a neurodegenerative process and are frequently used in both clinical and research settings to identify potential changes from premorbid levels of cognitive functioning (Dori and Chelune 2004; Lange and Chelune 2006; Wilde et al. 2001). Thus, asymmetric cognitive profiles may have utility for detecting a prodromal phase of AD for a number of reasons. Because AD has such a heterogeneous clinical presentation, there is a strong possibility that distinct cognitive subgroups exist within the larger at-risk population (Martin 1990). By averaging performance with a single test score across subjects, we may inadvertently obscure potential subgroups that exist within a larger group (Mitrushina et al. 1995). For example, an older adult subgroup with preserved verbal memory skills could mask the presence of a second subgroup with a subtle decline in verbal memory (see Demadura et al. 2001).

There is considerable evidence for cognitive asymmetry in the early stages of AD. EEG and SPECT studies show structural and functional asymmetries in early AD (Celsis et al. 1997). Studies using PET, MRI perfusion, and MRI morphometry also document increased left-right asymmetry associated with aging, cognitive decline, and early AD (Celsis et al. 1997; Small et al. 1995a, 1995b; Franceschi et al. 1995). Right versus left hemisphere reductions in glucose metabolism show correspondence with lateralized functional deficits in spatial and verbal skills, respectively (Haxby et al. 1985, 1990). Case studies describe unilateral neglect syndrome in AD patients and frequent asymmetric cerebral atrophy (Bugiani et al. 1991; Venneri et al. 1998). Interestingly, MRI brain morphometry studies suggest that a reduction of normal, structural asymmetry in hippocampal volume is a consequence of a neurodegenerative process in higher-risk older adults with APOE-ε4 genotype (Geroldi et al. 2000) and in older adults with increased cognitive dysfunction (Wolf et al. 2001). Bigler et al. (2002) found that, in general, significant hippocampal and parahippocampal asymmetries (i.e., greater volume in right versus left hemisphere) were associated with relatively more preserved cognitive functions in AD patients.

Many studies of asymmetric brain structure and function in early AD document lateralized cognitive changes with composite measures of language and visuospatial abilities. However, more detailed studies using cognitive neuroscience paradigms have further refined our knowledge of the component processes involved in cognitive asymmetry. Delis et al. (1992) suggested that the traditional verbal/spatial dichotomy could mask a more primary impairment in processing large, global forms relative to detailed, local stimuli. Subsequent studies using computerized global/local (Navon-type) visual stimuli identified specific impairments in disengaging and shifting attention (Filoteo et al. 1992) in early AD, possibly resulting from disconnection of posterior temporoparietal regions (Parasuraman et al. 1992).

Consequently, asymmetric cognitive profiles in early AD can be more discrete than a verbal/spatial dichotomy. For example, Cherry et al. (1996) proposed that the phonological loop and visuospatial scratchpad could be independently affected in AD, resulting in discrete deficits in auditory or visuospatial span, or discrepancies between memory span and supraspan ability (also see Collette et al. 1997). Although subgroups with relatively preserved “verbal” or “spatial” profiles have been confirmed in early stages of AD, a corresponding advantage does not always extend to more specific cognitive functions like verbal or visuospatial memory (Demadura et al. 2001) and may differ between genetic risk groups (Finton et al. 2003). Effects of handedness and motor asymmetry have also been documented in AD (Doody et al. 1999; Strite et al. 1997). Given this substantial evidence for cognitive asymmetry in the early stages of AD, it is likely that these profiles may exist in a more subtle form in a prodromal phase.

To directly investigate the possibility of cognitive asymmetry in a prodromal phase of AD, Jacobson et al. (2002) conducted a retrospective study of performance discrepancies between naming and visuoconstructive ability in cognitively intact, community dwelling older adults. A prodromal group was identified by a subsequent change in clinical diagnosis to AD approximately 2 years after the assessment. The control group consisted of age- and education-matched individuals with no subsequent cognitive decline (for a minimum of 4 years). Cognitive asymmetry was calculated as the difference (standardized-scores) between Boston Naming Test (BNT) and Block Design subtest (BD) scores. Although the groups showed comparable mean performance on the individual measures, an analysis of performance discrepancies revealed that the prodromal AD group had a significantly larger discrepancy between BNT and BD scores relative to those with no cognitive decline or change in diagnosis. Consistent with our predictions, the prodromal group had a significantly greater frequency of asymmetric profiles (greater than 1 SD discrepancy) compared to the control group (see Fig. 4).

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Fig. 4

Distribution of standard score differences between naming and visuospatial skills for each participant. Note that 50% of the prodromal AD patients demonstrated an asymmetry score greater than 1 SD, whereas only 25% of the normal control participants demonstrated an asymmetry 1 SD or more. (Adapted from Jacobson et al. 2002)

The stability of asymmetric cognitive profiles in the face of declining cognitive abilities has been questioned (Rasmusson and Brandt 1995). Many neuropsychological tests are subject to floor effects, and the probability of global cognitive decline would seem to predict decreasing frequency of asymmetric profiles over time. However, in a large sample of subjects with a range of cognitive deficits, distinct verbal and visuospatial subgroups were confirmed in mild through severe dementia severity levels based on neuropsychological deficits (Strite et al. 1997). Some models of normal aging suggest that reduction of functional asymmetry is a compensatory mechanism that preserves cognitive abilities (see Cabeza et al. 2002), rather than a sign of neurodegeneration. Other theories suggest that correlations between cognitive domains tend to be relatively symmetrical, and disruption of brain systems supporting cognition would actually increase measures of cognitive asymmetry (Andrews-Hanna et al. 2007). The debate surrounding “atypical” asymmetry is complicated by whether a given brain structure or function is symmetrical in normal, younger individuals without neurologic disease. Structural neuroimaging findings are also equivocal. Some investigations showing relatively little structural asymmetry in non-demented older adults (Mu et al. 1999; Raz et al. 2004), whereas other investigations using meta-analysis and multi-site legacy datasets confirm hippocampal asymmetry (right greater than left) in healthy older adults and possible reduction of asymmetry in prodromal AD (Pedraza et al. 2004; Fennema-Notestine et al. 2007).

To investigate the longitudinal course of cognitive asymmetry, Jacobson et al. (2002) examined six consecutive years of neuropsychological test scores for an individual in her eighties who ultimately received a clinical AD diagnosis. During the study period, however, she had intact learning and memory skills and no initial evidence of overall cognitive or functional decline. Cognitive asymmetry was examined with a discrepancy-score method, calculating age-adjusted z-score differences between opposing verbal and spatial tasks. Over 6 years, a pattern of increasing cognitive asymmetry was apparent with relatively preserved performance on non-verbal/visuospatial tests relative to declining scores on verbally mediated tasks (see Fig. 5). Her neuropsychological test scores revealed significant cognitive discrepancies on four verbal/spatial contrasts (tasks of memory, fluency, attention/memory span, naming/visuoconstruction) for all six assessments even while her individual test scores remained within normal limits for her age. In addition, there were significant discrepancies between higher-level cognitive skills and baseline skills (e.g., letter number sequencing/shifting relative to simple sequencing). Results from this case study (Jacobson et al. 2002) suggest that cognitive discrepancies can be a sensitive marker of prodromal neuropsychological changes, and they are apparent prior to changes in either memory or overall cognitive ability.

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Fig. 5

Six consecutive years of scores of an individual who progressed to a clinical diagnosis of AD at year 7. The graph depicts the discrepancy between verbal and visual recall measures (solid line), and the discrepancy between tests of naming and visuospatial skills (dashed line). Note the general increase in discrepancies between measures over time (adapted from Jacobson et al. 2002)

Other work in this area has focused on differences in cognitive discrepancies between genetic risk groups. Although only a subgroup of individuals who carry the APOE-ε4 allele go on to develop AD, this genotype has often served as a possible surrogate marker for prodromal AD when evaluating asymmetric cognitive profiles. For example, cognitively intact older adults with and without the APOE-ε4 allele were administered verbal and spatial tasks of working memory and attention span (Jacobson et al. 2005a). The APOE-ε4 genotype group showed significantly increased cognitive discrepancies between verbal and spatial attention span relative to the non-ε4 group despite comparable mean performance on the individual span tasks. In a follow-up study by Jacobson et al. (2005b), hierarchical (global/local) visual stimuli with documented sensitivity to lateralized hemispheric dysfunction (Delis et al. 1988) were used to investigate cognitive asymmetry. Despite similar levels of overall recall ability in normal elderly APOE-ε4 and non-ε4 groups, the APOE-ε4 group showed a significantly larger discrepancy between recall of global relative to local components. Houston et al. (2005) also found larger cognitive discrepancies in a normal elderly APOE-ε4 group compared to a non-ε4 group, but only when contrasting performance on a switching condition with baseline skills of verbal versus design fluency (Delis-Kaplan Executive Function Scale [D-KEFS]; Delis and Kaplan 2001). In addition, Wetter et al. (2005) found that, compared to non-ε4 elderly, the cognitively intact APOE-ε4 elderly group showed increased error-rate variance on a higher-level Stroop switching condition relative to baseline conditions. Wetter et al. (2006) also used a cognitive discrepancy approach to identify evidence of greater heterogeneity of variance in a non-demented APOE-ε4 group relative to a non-ε4 group on complex verbal memory measures, but not on fundamental verbal skills such as vocabulary.

Overall, recurring findings of structural and functional asymmetry in early AD have led to the confirmation of asymmetric cognitive profiles in a prodromal phase of the disease, as well as in cognitively intact older adults at genetic risk for AD. It is not yet clear whether these functional asymmetries reflect compensatory responses to aging, specific neuroanatomic changes related to the neurodegenerative process, or a more general loss of functional connectivity between brain regions. Nevertheless, it is evident that cognitive asymmetries are not restricted to verbal/spatial deficits but may include discrepancies between complex cognitive abilities and more basic skills, or discrepancies between component processes within a single domain. There is a growing consensus that accurate detection of prodromal AD may require combinations of neuropsychological tests and cognitive profiles, and the presence of atypical functional asymmetries could contribute to our ability to identify AD at its earliest stages.

Vascular Contributions to Alzheimer’s Disease and its Prodrome

The role of vascular risk factors such as stroke, heart disease, and hypertension in the development of cognitive impairments and vascular dementia (VaD) has been well established. By definition, vascular conditions are associated with VaD, and in general the relationship between various vascular risk factors and subsequent VaD are typically additive in nature (Hayden et al. 2006; Kivipelto et al. 2005). In contrast to VaD, the role of vascular risk factors in the development and progression of AD is much less clear, and historically there has been considerable debate and controversy surrounding this issue. For more than three decades AD has been characterized as primarily a neurodegenerative disorder with little to no vascular underpinnings (Blessed et al. 1968; American Psychiatric Association, Diagnostic and Statistical Manual of Mental Disorders, 4th edition [DSM-IV]). However, within recent years, studies investigating the relationship between vascular risk and AD have burgeoned dramatically. Although the debate is certainly not a new one (see de la Torre 2002, for review), the pathophysiological links between vascular disease and AD is widely acknowledged and, increasingly, vascular risk factors are being implicated in the pathogenesis of MCI and AD.

There is a growing body of research to suggest that the relationship between vascular disease and AD is more complex than previously believed. For example, vascular risk factors have been associated with cerebral atrophy (Swan et al. 2000), and it has been suggested that brain atrophy can result from an ischemic process (Mentis et al. 1994). In addition, population-based postmortem studies have shown that the incidence of “pure” AD is much lower than once thought, perhaps below 50% (Snowdon et al. 1997; Etiene et al. 1998), although others suggest that significant vascular contributions are present in about 30–40% of AD cases (Knopman et al. 2001). Moreover, it is striking that, at autopsy, the vast majority of patients with AD demonstrate microvascular degeneration, and roughly a third of AD patients show frank stroke (Helbecque and Amouyel 2004). Finally, studies have shown that white matter lesion pathology appears to be associated with AD (Barber et al. 2000; Hirono et al. 2000), vascular factors predict rate of progression in AD (Mielke et al. 2007), and we have shown a particularly strong relationship between white matter lesions and MCI-related cognitive dysfunction (Delano-Wood et al. 2008). Given little clarity in the pathogenesis and treatment of AD, research has begun to focus more heavily on the identification of risk factors to both elucidate the pathophysiology of AD and provide new potential avenues for its prevention and treatment. With regard to the latter, vascular risk factors are quite modifiable and treatable (Bowler and Hachinski 2003), and thus it is plausible that secondary prevention of vascular risk factors may be helpful in delaying disease onset or progression in AD. Indeed, postponing the onset of clinical AD by 5 years would lead to a decrease in the prevalence of the disease by an astounding 50% (Brookmeyer et al. 1998).

Within the past decade, numerous population-based longitudinal studies have demonstrated links between several vascular factors and increased risk for the development of AD, including atherosclerosis (Hofman et al. 1997), atrial fibrillation (Ott et al. 1997), diabetes (Ott et al. 1999), hyperlipidemia (Jick et al. 2000), and stroke (Honig et al. 2003). Particularly strong longitudinal associations have been found between elevated blood pressure in midlife and higher risk for the development of AD in later life (Launer et al. 2000). Interestingly, Petrovich et al. (2000) showed that hypertension measured in midlife was related to significantly greater AD neuropathology (e.g., higher density of hippocampal neurofibrillary tangles) almost four decades later. Similarly, hypertension has been shown to be related to an increased risk for MCI, and this risk appears to be as strong as that imparted by the presence of the APOE ε4 genotype (DeCarli et al. 2001; Margaglione et al. 1998). Among the vascular risk factors, diabetes appears to provide strong evidence for a direct role in AD (Luchsinger and Mayeux 2004; Luchsinger et al. 2004, 2007) given its relationship to both cerebrovascular disease and hyperinsulinemia, which is thought to impair ß-amyloid clearance in the brain (Farris et al. 2003, 2004).

The possibility that reduced cerebral perfusion may be a marker for early AD is a current focus of investigation as well. In MCI patients who later progressed to AD, for example, hypoperfusion has been identified in several brain regions, including the temporoparietal cortex (Kogure et al. 2000), hippocampal and parahippocampal regions (Okamura et al. 2000), and the posterior cingulate (Rodriguez et al. 2000). Often a direct result of lowered cerebral perfusion, PET imaging studies have shown reduced cerebral glucose metabolism in the hippocampus of MCI patients (De Santi et al. 2001; Arnaiz et al. 2001). Similarly, this association has been detected in normally aging older adults who later converted to MCI (de Leon et al. 2001). Bangen et al. (2007) have also shown robust associations between resting cerebral blood flow in the medial temporal lobe and CVD risk in cognitively intact healthy older adults. Silvestrini et al. (2006) have also demonstrated that altered cerebrovascular hemodynamics (i.e., elevated cerebral vasomotor reactivity to hypercapnia) was associated with hastened cognitive decline in AD patients over 1 year. Indeed, although much research is required to enhance our understanding of the pathogenesis and pathophysiology of AD, the use of advanced neuroimaging techniques has shown promise in helping to reliably detect prodromal clinical features predictive of AD-related cognitive losses.

The interplay between vascular disease and AD neurodegenerative pathology is unclear, although many theories have been put forth touting a relationship. Perhaps the most commonly held view is that vascular pathology may exert an additive effect on the brain, increasing the overall burden of pathology as well as the rate of AD progression. In support of this theory, studies have shown that AD patients with concomitant stroke demonstrate more severe dementia (Snowdon et al. 1997; Honig et al. 2003), and the risk appears to be highest for those with other established vascular risk factors (e.g., hypertension, diabetes, heart disease; Honig et al. 2003; Luchsinger et al. 2005). Given brain tissue necrosis associated with stroke, Honig et al. (2003) suggested that this theory explains why a lesser amount of AD-related neuropathologic change may be necessary to produce dementia in patients who have suffered stroke. Another study supporting the vascular additive effects model showed that patients with low vascular risk do not decline cognitively or functionally over an 18-month period, whereas those with higher vascular burden demonstrate significantly greater AD-associated deterioration (Regan et al. 2006). The authors concluded that, although vascular risk factors are likely not part of the underlying etiologic process of AD, they contribute to the expression of the disease process in its very early stages.

A related prevalent theory states that pathogenic factors of AD and vascular disease may interact to produce synergistic effects on the brain and thus increase the likelihood of expressing cognitive impairment (Iadecola and Gorelick 2003; Bowler 2003; Chui et al. 2006). Proponents of this view argue that accumulation of ß-amyloid (an important mechanism implicated in neurodegeneration) may be both the cause and the consequence of cerebrovascular impairment. Indeed, as stated earlier, vascular risk factors have been shown to be associated with cerebral atrophy (Swan et al. 2000). In addition, animal studies have demonstrated that elevated cholesterol intake increases the deposition of ß-amyloid in the brains of transgenic mice expressing human amyloid precursor protein (Refolo et al. 2000). However, others argue that, at least in the case of stroke, only an additive effect on neurodegeneration appears to exist (Schneider et al. 2004; Silvestrini et al. 2006).

Some investigators have posited that a cerebrovascular component is seen in some AD brains as a consequence of incorrect diagnosis. For instance, these associations may stem from a misclassification of VaD as AD. Alternatively, given that vascular disease and AD pathology appears to exist co-morbidly in many cases, it has been argued that “mixed dementia” represents a separate clinical entity from that of “pure” dementia forms in which only neurodegeneration (AD) or cerebrovascular disease (VaD) are present. However, a number of studies show that vascular risk factors such as atherosclerosis, cardiac disease, and diabetes appear to be involved in progression to VaD just as often as AD (Breteler 1998, 2000; Ott et al. 1998, 1999; Tyas et al. 2001; Polvikoski et al. 2001).

Perhaps the most provocative and controversial theory holds that AD may itself be considered a vascular disorder. Along this vein, de la Torre (2002) put forth the term “vasculopathic complex” to describe how vascular-related factors negatively impact cerebral perfusion to a “critical level of dysfunction” (pg. 1157). de la Torre (2002) argues that there is mounting evidence to support this contention, including the observation that (1) epidemiological studies have demonstrated that known risk factors for AD have a vascular basis; (2) shared risk factors exist for both AD and VaD (e.g., APOE); (3) medications used to slow the development of AD improve cerebral perfusion; (4) regional cerebral perfusion deficits can predict preclinical AD; (5) there is often similar clinical symptomatology in AD and VaD; (6) cerebrovascular pathological lesions frequently overlap in AD and VaD; and (7) cerebral hypoperfusion may precede AD-related hypometabolic, neuropsychological, and neurodegenerative pathology. Clearly, additional research is needed to better characterize the cascade of neuropathologic events that precede and promote the development of AD.

Given the expected continued growth of the aging population, the prevalence of AD is projected to grow to 14 million or more by 2050 (Brookmeyer et al. 1998). Because of the possibility that vascular risk factors may increase the risk and promote the development of the disease process, greater emphasis is being placed on the detection of early, preclinical features that may be predictive of AD-related changes. Future work is needed to help elucidate whether vascular disease exerts an additive or synergistic effect with respect to AD, or whether vascular pathology is itself intrinsic to the pathogenesis of AD. Identification of the etiologic mechanisms underlying this disorder will greatly help delineate the pathophysiological underpinnings responsible for progressive cognitive and functional decline.

Summary

The identification of prodromal neuropsychological markers of Alzheimer’s disease is predicated on the notion that significant neural losses accrue well in advance of the clinical diagnosis. It is important that we reliably identify individuals while in this early stage of disease expression in order to treat them during a period that will have maximal impact in maintaining cognitive and functional abilities. The early diagnosis of AD in a prodromal stage remains an extremely important goal given the likelihood that this stage will be amenable to treatments designed either to halt or slow disease progression or treat cerebrovascular disease, if present. To identify and verify the accuracy of subtle neuropsychological abnormalities (e.g., poor delayed recall, cognitive asymmetry) in those non-demented older adults who are destined to develop dementia in the relatively near future will help maximize intervention efforts and ultimately preserve quality of life. Finally, the characterization of MCI and its subtypes will require better reliability and standardization of methods if it is to improve its applicability for accurate identification of the AD prodrome.

Acknowledgements

Contributor Information

Mark W. Bondi, Department of Psychiatry, University of California San Diego, La Jolla, CA, USA; Psychology Service, San Diego VA Healthcare System, San Diego, CA, USA.

Amy J. Jak, Department of Psychiatry, University of California San Diego, La Jolla, CA, USA; Research Service, San Diego VA Healthcare System, San Diego, CA, USA.

Lisa Delano-Wood, Department of Psychiatry, University of California San Diego, La Jolla, CA, USA.

Mark W. Jacobson, Department of Psychiatry, University of California San Diego, La Jolla, CA, USA; Research Service, San Diego VA Healthcare System, San Diego, CA, USA.

Dean C. Delis, Department of Psychiatry, University of California San Diego, La Jolla, CA, USA; Psychology Service, San Diego VA Healthcare System, San Diego, CA, USA.

David P. Salmon, Department of Neurosciences, University of California San Diego, La Jolla, CA, USA.

References