Longitudinal SPECT study in Alzheimer’s disease: relation to apolipoprotein E polymorphism
- M Lehtovirtaa,
- J Kuikkab,
- S Helisalmic,
- P Hartikainena,
- A Mannermaac,
- M Ryynänenc,
- P Sr Riekkinena,
- H Soininena
- aDepartment of Neurology, bDepartment of Clinical Physiology, cUnit of Clinical Genetics of the Department of Gynecology, Kuopio University Hospital and University of Kuopio, Finland
- Dr Maarit Lehtovirta, Department of Neurology, Kuopio University Hospital, FIN 70211 Kuopio, Finland. Fax 00358 17 173019.
- Received 2 June 1997
- Revised 27 October 1997
- Accepted 29 October 1997
OBJECTIVES In mild Alzheimer’s disease, SPECT imaging of regional cerebral blood flow has highlighted deficits in the posterior association cortex, and later in the disease process, the deficit spreads to involve the frontal cortex. The ε4 allele of apolipoprotein E is a risk factor for Alzheimer’s disease. The effect of apolipoprotein E polymorphism on cerebral perfusion was studied. The hypothesis was that those patients with Alzheimer’s disease who carry the ε4 allele would have more severe cerebral hypoperfusion.
METHODS Thirty one patients with Alzheimer’s disease and eight age and sex matched control subjects were examined in a three year longitudinal study. Patients with Alzheimer’s disease were divided into subgroups according to their number of ε4 alleles. Regional cerebral blood flow ratios referred to the cerebellum were examined by 99mTc-HMPAO SPECT. Apolipoprotein E genotypes were determined by digestion of polymerase chain reaction products with the restriction enzyme Hha1.
RESULTS All patients with Alzheimer’s disease had bilateral temporoparietal hypoperfusion compared with control subjects. The two ε4 allele subgroups had the lowest ratios at the baseline assessment in the parietal and occipital cortices, and at the follow up in the temporal, parietal, and occipital cortices. They had the highest reduction in percentage terms in the temporal and occipital cortices compared with the other subgroups. However, the global clinical severity did not differ at the baseline or follow up examinations between the subgroups.
CONCLUSION Apolipoprotein E polymorphism is involved in the pathogenesis and heterogeneity of Alzheimer’s disease as the most severe cerebral hypoperfusion was found in the ε4 allele subgroups. This might have implications for therapeutic approaches in Alzheimer’s disease.
Clinical, neurochemical, pathological, and genetic studies suggest that Alzheimer’s disease is a heterogeneous entity.1-4 The ε4 allele of apolipoprotein E is a risk factor for Alzheimer’s disease and accelerates the onset of dementia.5-8 The apolipoprotein E gene, located on chromosome 19, has three major alleles: ε2, ε3, and ε4. Apolipoprotein E is present in senile plaques, neurofibrillary tangles, and cerebrovascular amyloid, the major neuropathological changes seen in Alzheimer’s disease. Different binding properties of the apolipoprotein isoforms to β-amyloid and tau protein also suggests that it is involved in the pathogenesis of Alzheimer’s disease.9 In addition, the extent of the deficit of acetylcholine containing neurons in brains of patients with Alzheimer‘s disease is related to the number of ε4 alleles present.10 11
Changes in the cerebral metabolism and perfusion can be detected by single photon emission computed tomography (SPECT). The decreased metabolism and reduced cerebral perfusion in Alzheimer’s disease are known to occur predominantly in temporal and parietal areas,12-14 regions which show the greatest neurochemical postmortem abnormalities.15 It has been suggested that mildly affected patients show temporoparietal and some frontal changes, whereas more severely demented patients also show decreased blood flow in other regions—for example, the occipital areas.14 16In a recent PET study, subjects with age associated memory impairment, one ε4 allele, and a family history of Alzheimer’s disease had abnormally low and asymmetric rates of glucose metabolism in a preselected parietal region even before the onset of dementia.17 Another PET study on cognitively normal subjects, with a family history of Alzheimer’s disease reported that the ε4 homozygotes had significantly reduced rates of glucose metabolism in the same posterior cingulate, parietal, temporal, and prefrontal regions as seen in patients with probable Alzheimer’s disease.18
This study attempted to examine the role of apolipoprotein E polymorphism in Alzheimer’s disease with perfusion SPECT included in a three year longitudinal follow up. Our hypothesis was that those patients with Alzheimer’s disease carrying the ε4 allele of apolipoprotein E would have more severe deficits in their cerebral perfusion compared with patients without any ε4 alleles.
Patients and methods
We studied 31 patients fulfilling the NINCDS-ADRDA criteria of probable Alzheimer’s disease19 and eight age and sex matched cognitively intact control subjects in a longitudinal study, in which the follow up examination was three years after the baseline assessment. Table 1 presents their clinical characteristics. The patients with Alzheimer’s disease were at the baseline either undergoing diagnostic examination or had been recently diagnosed. The ethics committee of the Kuopio University Hospital approved the study and all the subjects and caregivers of demented patients gave informed consent for participation in the study.
The patients with Alzheimer’s disease underwent the following examinations: general physical and clinical neurological examination, assessment of clinical severity with mini mental state examination (MMSE)20 and brief cognitive rating scale (BCRS),21 assessment of extrapyramidal signs with the Webster scale,22 assessment of depressive symptoms by the Hamilton scale,23 neuropsychological tests, laboratory tests to exclude secondary causes of dementia, brain MRI and SPECT, conventional and quantitative EEG, and event related potentials. All patients with Alzheimer’s disease scored less than 4 on the modified ischaemic scale.24
SINGLE PHOTON EMISSION COMPUTED TOMOGRAPHY
A dose of 370 to 555 MBq 99m Tc-HMPAO (Amersham International, London, UK) was intravenously injected into a subject’s vein in a dark and quiet room. High resolution SPECT was carried out with a three head Siemens MultiSPECT 3 gamma camera equipped with high resolution collimators.25 Ten minutes after injection of the tracer, the radioactivity distribution of the brain was acquired in a 128×128 matrix mode. Data sets were acquired at 3° intervals for 35 seconds each, with a total of 40 sets (120° per camera head). Three and a half millimeter thick transaxial (oriented in orbitomeatal line), sagittal, and coronal slices were reconstructed using a Butterworth filter (a cut off frequency of 0.5 cm−1) and a uniform attenuation correction of 0.12 cm−1. The imaging resolution was 8–9 mm.25 Two consecutive slices were summed to obtain a slice thickness of 7 mm and visually surveyed on a TV screen. A semiautomatic brain quantification program of Siemens Gammsonics Inc (Hofman, IL, USA) was used to analyse the regions of interest. Firstly, the slices were rotated and realigned so that transaxial (x direction), sagittal (y direction), and coronal (z direction) ones were in 90° angles to each other. Secondly, the regions of interest were drawn on to aligned transaxial slices on the right and then mirrored on the left. The method has been described earlier in detail.26 Regional count densities (regional cerebral blood flow) were calculated for frontal, temporal, parietal, and occipital cortices. The regional counts were related to the cerebellar counts and regional cerebral blood flow is expressed as this ratio for each region. Cerebellum was used to normalise the other cortical areas, because it is generally spared by major pathological involvement.27 The rater was not aware of the clinical data of the subjects.
DETERMINATION OF APOLIPOPROTEIN E GENOTYPE
DNA was prepared from blood leucocytes of patients with Alzheimer’s disease by standard procedures. Apolipoprotein E genotypes were analysed using the polymerase chain reaction (PCR) described earlier28 29 with minor modifications.30Apolipoprotein E genotypes were identified through HhaIdigestion. Digested DNA fragments were analysed via polyacrylamide gel electrophoresis and separated fragments of DNA were visualised by staining with ethidium bromide.
STATISTICAL ANALYSIS OF DATA
The data were analysed using SPSS for Windows version 6.1.3. software. We used analysis of variance (ANOVA) to detect differences in means over the study groups at the baseline and the follow up examination. The Duncan method was applied in post hoc analysis when appropriate. Multivariate analysis for repeated measures (MANOVA) with Bonferroni’s correction was used to detect the change in perfusion ratios over time between the study groups. Patients with Alzheimer’s disease were divided into three subgroups according to the number of apolipoprotein E alleles; two ε4 alleles, one ε4 allele, and no ε4 alleles. A χ2 test was used for evaluation of the categorical data. The level of significance was set at p<0.05.
Patients with Alzheimer’s disease and control subjects did not differ in age, education, or sex. Alzheimer’s disease subgroups had a similar duration of dementia and equal clinical severity as assessed with MMSE at the baseline and follow up, the decline in MMSE was about six points in three years. However, the homozygous ε4 allele subgroup had an earlier onset of the disease and was younger than the other subgroups (table 1).
Cerebral perfusion ratios measured with SPECT for all patients with Alzheimer’s disease were significantly reduced in temporoparietal regions compared with control subjects. Moreover, some differences were evident in the perfusion ratios for subgroups of Alzheimer’s disease. The homozygous ε4 allele subgroup had the lowest ratios at the baseline in the parietal and occipital cortices, and at the follow up in the temporal, parietal, and occipital cortices. The difference was significant at the follow up in the right and left occipital cortices compared with the no ε4 allele subgroup and control subjects. Also, at the follow up, the one ε4 allele subgroup had a significantly reduced perfusion ratio in the left occipital cortex compared with the no ε4 allele subgroup (table2).
Multivariate analysis of variance for repeated tests showed a significant effect of the three year follow up time on all regions studied. A significant interaction effect of time and different apolipoprotein E groups was found in the right occipital cortex and the left parietal cortex. In the right occipital cortex, the perfusion ratio was significantly reduced in the homozygous ε4 allele subgroup compared with the no ε4 allele subgroup and in the left parietal cortex in the one ε4 allele subgroup compared with the control subjects (figure). The figure 1 shows, in percentage terms, the change between the baseline and follow up examination in the different study groups. The homozygous ε4 allele subgroup had the highest reduction in the perfusion ratios in the temporal and the occipital cortices compared with the other subgroups.
Patients with Alzheimer’s disease show cerebral hypoperfusion, mainly in the temporal and parietal cortices,12-14 but 15%-20% of patients also show hypoperfusion in the frontal cortices.31 32 Occipital areas have been used as reference regions for normalising perfusion values, although PET and a few SPECT studies have also shown occipital changes in patients with Alzheimer’s disease.14 33 34 In our three year longitudinal study, patients with Alzheimer’s disease had decreased perfusion ratios in the parietal and temporal regions compared with the control subjects. When patients with dementia were divided into subgroups according to the ε4 allele, the homozygous ε4 allele subgroup had the lowest perfusion ratios in the parietal and occipital cortices at the baseline, and at the follow up this was evident also in the temporal cortices. The ε4 allele of apolipoprotein E is a well established risk factor for Alzheimer’s disease. In both patients with Alzheimer’s disease and non-demented elderly subjects, memory functions and medial temporal lobe structures, such as the hippocampus, seem to be particularly vulnerable to the deleterious effects of the ε4 allele of apolipoprotein E.29 35-37 Two PET studies in non-demented relatives at risk for familial dementia showed reduced rates of glucose metabolism in the same regions where this occurs in patients with Alzheimer’s disease.17 18 These findings suggest that identification of ε4 homozygous subjects with memory impairment might help to identify those at highest risk for dementia, and locate a possible group for treatment strategies to prevent the disease.
The homozygous ε4 subgroup had the greatest reduction in percentage terms in the follow up in the temporal and occipital cortices compared with other subgroups (figure). An earlier two year longitudinal SPECT study reported that the decreases in regional cerebral function, compared with control values varied from 1% to 4.2% in the different regions.38 In our three year follow up study, the perfusion values for all patients with Alzheimer’s disease compared with controls, decreased on average, between 2.4% and 9%. In our study, at the baseline and follow up examinations, the extent of global disease was equally severe in the Alzheimer subgroups. Moreover, the homozygous ε4 allele subgroup did not differ from other subgroups in visuospatial functions as examined with a copy a cube and clock setting test39 and the block design subtest of the Wechsler adult intelligence scale.40 However, the homozygous ε4 allele subgroup had the lowest scores on immediate and delayed tests assessing verbal and visual memory. Verbal memory was examined with a list learning test using shopping items41 and the Wechsler logical memory test using one story.42 Visual memory was examined with the Heaton visual reproduction test.43 The delayed recall of the story and the figures and a yes/no recognition of the words in the list were asked after a 30 minute delay filled with other psychometric tests. Occipital hypoperfusion is only occasionally found in most studies of Alzheimer’s disease. Recently, a PET study of three patients with pathologically verified pure diffuse Lewy body disease and three patients with combined Lewy body and Alzheimer’s disease pathology disclosed pronounced declines in association and primary somatomotor cortices in both groups. However, the patients with pure Lewy body disease also exhibited hypometabolism in the occipital association and primary visual cortex.44 Patients with Lewy body disease are thought to have a more severe cholinergic deficit than patients with Alzheimer’s disease.45 Also, recent data suggest that the magnitude of the cholinergic depletion is greater in ε4 homozygous patients with Alzheimer’s disease.10 11 The cerebral blood flow is regulated by cholinergic, noradrenergic, and serotonergic pathways.46As the density of cholinergic innervation is lower in the primary sensory areas—such as the occipital cortex—than in associative cortical regions and limbic structures,47 it is possible that the more severe cholinergic depletion in the ε4 homozygotes may be reflected in early phases as hypoperfusion in those regions with reduced cholinergic innervation.
In conclusion, we found that the homozygous ε4 patients with Alzheimer’s disease had the lowest cerebral perfusion in the temporal, parietal, and occipital cortices compared with those patients with Alzheimer’s with one or no ε4 alleles. Apolipoprotein E polymorphism seems to be a major contributor to the heterogeneity of Alzheimer’s disease, and this might have implications for therapeutic approaches in this disorder.
This study was supported by grant from the Health Research Council of the Academy of Finland and the North Savo Regional Fund of the Finnish Cultural Foundation.