Abstract
Objective: To investigate the association between white matter damage, as evidenced by myelin loss (ML), the extent of cerebral amyloid angiopathy (CAA), or arteriosclerosis (Art), and apolipoprotein E (ApoE) e4 allele in Alzheimer's disease (AD), in order to understand the causes of damage to white matter in AD and its contribution to the pathogenesis of the disorder.
Materials and methods: Brain tissues were obtained from 94 patients with AD confirmed by autopsy. ApoE genotyping was performed by PCR on DNA extracted from frontal cortex or cerebellum. CAA and Art were assessed on Weigert's haematoxylin and eosin stained sections in frontal, temporal, parietal, and occipital cortices; the extent of ML was scored on Luxol fast blue stained sections of these regions.
Results: The ApoE e4 allele frequency in the 61 patients with ML was not significantly different from that in the 33 patients without ML, nor did this differ in the 84 patients with Art from that in the 10 patients without Art. There were no significant differences in the proportions of patients with genotypes containing 0, 1, or 2 ApoE e4 alleles in the presence or absence of ML or Art. The mean ML, Art, or CAA scores within each region, and the total scores summed across all four brain regions, did not differ between patients with 0, 1, or 2 ApoE e4 alleles. However, the mean ML severity score in the occipital cortex was significantly greater than that in the frontal or temporal cortices in patients with 1 or 2 ApoE e4 alleles. The severity of CAA in the occipital cortex was significantly higher than that in other areas of cortex in patients with 0 or 2 ApoE e4 alleles. The mean Art score in the occipital cortex was greater than that in the temporal cortex in patients with two ApoE e4 alleles and was higher than that in the frontal cortex in patients with one ApoE e4 allele.
Conclusions: The likelihood of patients with AD suffering from CAA, Art, or ML is not influenced by ApoE e4 allele, nor is the overall burden of these pathological changes in the brain. However, the distribution of ML, CAA, and Art within the brain is at least partly influenced by genotype and dosage of ApoE e4 allele, with the occipital cortex being more severely affected by all of these pathological changes in e4 allele bearers, particularly when two ApoE e4 alleles are present.
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Selected References
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- Barber R., Gholkar A., Scheltens P., Ballard C., McKeith I. G., Morris C. M., O'Brien J. T. Apolipoprotein E epsilon4 allele, temporal lobe atrophy, and white matter lesions in late-life dementias. Arch Neurol. 1999 Aug;56(8):961–965. doi: 10.1001/archneur.56.8.961. [DOI] [PubMed] [Google Scholar]
- Bronge L., Fernaeus S. E., Blomberg M., Ingelson M., Lannfelt L., Isberg B., Wahlund L. O. White matter lesions in Alzheimer patients are influenced by apolipoprotein E genotype. Dement Geriatr Cogn Disord. 1999 Mar-Apr;10(2):89–96. doi: 10.1159/000017107. [DOI] [PubMed] [Google Scholar]
- Brun A., Englund E. A white matter disorder in dementia of the Alzheimer type: a pathoanatomical study. Ann Neurol. 1986 Mar;19(3):253–262. doi: 10.1002/ana.410190306. [DOI] [PubMed] [Google Scholar]
- Chalmers K., Wilcock G. K., Love S. APOE epsilon 4 influences the pathological phenotype of Alzheimer's disease by favouring cerebrovascular over parenchymal accumulation of A beta protein. Neuropathol Appl Neurobiol. 2003 Jun;29(3):231–238. doi: 10.1046/j.1365-2990.2003.00457.x. [DOI] [PubMed] [Google Scholar]
- Doody R. S., Azher S. N., Haykal H. A., Dunn J. K., Liao T., Schneider L. Does APO epsilon4 correlate with MRI changes in Alzheimer's disease? J Neurol Neurosurg Psychiatry. 2000 Nov;69(5):668–671. doi: 10.1136/jnnp.69.5.668. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ferrer I., Bella R., Serrano M. T., Martí E., Guionnet N. Arteriolosclerotic leucoencephalopathy in the elderly and its relation to white matter lesions in Binswanger's disease, multi-infarct encephalopathy and Alzheimer's disease. J Neurol Sci. 1990 Aug;98(1):37–50. doi: 10.1016/0022-510x(90)90180-u. [DOI] [PubMed] [Google Scholar]
- Furuta A., Ishii N., Nishihara Y., Horie A. Medullary arteries in aging and dementia. Stroke. 1991 Apr;22(4):442–446. doi: 10.1161/01.str.22.4.442. [DOI] [PubMed] [Google Scholar]
- Gearing M., Mori H., Mirra S. S. Abeta-peptide length and apolipoprotein E genotype in Alzheimer's disease. Ann Neurol. 1996 Mar;39(3):395–399. doi: 10.1002/ana.410390320. [DOI] [PubMed] [Google Scholar]
- Goulding J. M., Signorini D. F., Chatterjee S., Nicoll J. A., Stewart J., Morris R., Lammie G. A. Inverse relation between Braak stage and cerebrovascular pathology in Alzheimer predominant dementia. J Neurol Neurosurg Psychiatry. 1999 Nov;67(5):654–657. doi: 10.1136/jnnp.67.5.654. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gray F., Dubas F., Roullet E., Escourolle R. Leukoencephalopathy in diffuse hemorrhagic cerebral amyloid angiopathy. Ann Neurol. 1985 Jul;18(1):54–59. doi: 10.1002/ana.410180110. [DOI] [PubMed] [Google Scholar]
- Greenberg S. M., Briggs M. E., Hyman B. T., Kokoris G. J., Takis C., Kanter D. S., Kase C. S., Pessin M. S. Apolipoprotein E epsilon 4 is associated with the presence and earlier onset of hemorrhage in cerebral amyloid angiopathy. Stroke. 1996 Aug;27(8):1333–1337. doi: 10.1161/01.str.27.8.1333. [DOI] [PubMed] [Google Scholar]
- Heinonen O., Lehtovirta M., Soininen H., Helisalmi S., Mannermaa A., Sorvari H., Kosunen O., Paljärvi L., Ryynänen M., Riekkinen P. J., Sr Alzheimer pathology of patients carrying apolipoprotein E epsilon 4 allele. Neurobiol Aging. 1995 Jul-Aug;16(4):505–513. doi: 10.1016/0197-4580(95)00076-q. [DOI] [PubMed] [Google Scholar]
- Itoh Y., Yamada M., Suematsu N., Matsushita M., Otomo E. Influence of apolipoprotein E genotype on cerebral amyloid angiopathy in the elderly. Stroke. 1996 Feb;27(2):216–218. doi: 10.1161/01.str.27.2.216. [DOI] [PubMed] [Google Scholar]
- Jellinger K. A. Alzheimer disease and cerebrovascular pathology: an update. J Neural Transm (Vienna) 2002 May;109(5-6):813–836. doi: 10.1007/s007020200068. [DOI] [PubMed] [Google Scholar]
- Jellinger K. Inverse relation between Braak stage and cerebrovascular pathology in Alzheimer predominant dementia. J Neurol Neurosurg Psychiatry. 2000 Jun;68(6):799–800. doi: 10.1136/jnnp.68.6.799a. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Leys D., Scheltens P., Steinling M. White-matter lesions on CT in Alzheimer patients. Acta Neurol Scand. 1991 Sep;84(3):264–265. doi: 10.1111/j.1600-0404.1991.tb04949.x. [DOI] [PubMed] [Google Scholar]
- Mann D. M., Iwatsubo T., Pickering-Brown S. M., Owen F., Saido T. C., Perry R. H. Preferential deposition of amyloid beta protein (Abeta) in the form Abeta40 in Alzheimer's disease is associated with a gene dosage effect of the apolipoprotein E E4 allele. Neurosci Lett. 1997 Jan 17;221(2-3):81–84. doi: 10.1016/s0304-3940(96)13294-8. [DOI] [PubMed] [Google Scholar]
- Mirra S. S., Heyman A., McKeel D., Sumi S. M., Crain B. J., Brownlee L. M., Vogel F. S., Hughes J. P., van Belle G., Berg L. The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part II. Standardization of the neuropathologic assessment of Alzheimer's disease. Neurology. 1991 Apr;41(4):479–486. doi: 10.1212/wnl.41.4.479. [DOI] [PubMed] [Google Scholar]
- Nagy Z., Esiri M. M., Jobst K. A., Johnston C., Litchfield S., Sim E., Smith A. D. Influence of the apolipoprotein E genotype on amyloid deposition and neurofibrillary tangle formation in Alzheimer's disease. Neuroscience. 1995 Dec;69(3):757–761. doi: 10.1016/0306-4522(95)00331-c. [DOI] [PubMed] [Google Scholar]
- Ohm T. G., Kirca M., Bohl J., Scharnagl H., Gross W., März W. Apolipoprotein E polymorphism influences not only cerebral senile plaque load but also Alzheimer-type neurofibrillary tangle formation. Neuroscience. 1995 Jun;66(3):583–587. doi: 10.1016/0306-4522(94)00596-w. [DOI] [PubMed] [Google Scholar]
- Olichney J. M., Hansen L. A., Galasko D., Saitoh T., Hofstetter C. R., Katzman R., Thal L. J. The apolipoprotein E epsilon 4 allele is associated with increased neuritic plaques and cerebral amyloid angiopathy in Alzheimer's disease and Lewy body variant. Neurology. 1996 Jul;47(1):190–196. doi: 10.1212/wnl.47.1.190. [DOI] [PubMed] [Google Scholar]
- Pantoni L., Garcia J. H., Gutierrez J. A. Cerebral white matter is highly vulnerable to ischemia. Stroke. 1996 Sep;27(9):1641–1647. doi: 10.1161/01.str.27.9.1641. [DOI] [PubMed] [Google Scholar]
- Pantoni L., Garcia J. H. Pathogenesis of leukoaraiosis: a review. Stroke. 1997 Mar;28(3):652–659. doi: 10.1161/01.str.28.3.652. [DOI] [PubMed] [Google Scholar]
- Pfeifer L. A., White L. R., Ross G. W., Petrovitch H., Launer L. J. Cerebral amyloid angiopathy and cognitive function: the HAAS autopsy study. Neurology. 2002 Jun 11;58(11):1629–1634. doi: 10.1212/wnl.58.11.1629. [DOI] [PubMed] [Google Scholar]
- Premkumar D. R., Cohen D. L., Hedera P., Friedland R. P., Kalaria R. N. Apolipoprotein E-epsilon4 alleles in cerebral amyloid angiopathy and cerebrovascular pathology associated with Alzheimer's disease. Am J Pathol. 1996 Jun;148(6):2083–2095. [PMC free article] [PubMed] [Google Scholar]
- Sawada H., Udaka F., Izumi Y., Nishinaka K., Kawakami H., Nakamura S., Kameyama M. Cerebral white matter lesions are not associated with apoE genotype but with age and female sex in Alzheimer's disease. J Neurol Neurosurg Psychiatry. 2000 May;68(5):653–656. doi: 10.1136/jnnp.68.5.653. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Scheltens P., Barkhof F., Valk J., Algra P. R., van der Hoop R. G., Nauta J., Wolters E. C. White matter lesions on magnetic resonance imaging in clinically diagnosed Alzheimer's disease. Evidence for heterogeneity. Brain. 1992 Jun;115(Pt 3):735–748. doi: 10.1093/brain/115.3.735. [DOI] [PubMed] [Google Scholar]
- Skoog I., Hesse C., Aevarsson O., Landahl S., Wahlström J., Fredman P., Blennow K. A population study of apoE genotype at the age of 85: relation to dementia, cerebrovascular disease, and mortality. J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):37–43. doi: 10.1136/jnnp.64.1.37. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thaker U., McDonagh A. M., Iwatsubo T., Lendon C. L., Pickering-Brown S. M., Mann D. M. A. Tau load is associated with apolipoprotein E genotype and the amount of amyloid beta protein, Abeta40, in sporadic and familial Alzheimer's disease. Neuropathol Appl Neurobiol. 2003 Feb;29(1):35–44. doi: 10.1046/j.1365-2990.2003.00425.x. [DOI] [PubMed] [Google Scholar]
- Tian J., Shi J., Bailey K., Mann D. M. A. Relationships between arteriosclerosis, cerebral amyloid angiopathy and myelin loss from cerebral cortical white matter in Alzheimer's disease. Neuropathol Appl Neurobiol. 2004 Feb;30(1):46–56. doi: 10.1046/j.0305-1846.2003.00510.x. [DOI] [PubMed] [Google Scholar]
- Tomimoto H., Akiguchi I., Akiyama H., Ikeda K., Wakita H., Lin J. X., Budka H. Vascular changes in white matter lesions of Alzheimer's disease. Acta Neuropathol. 1999 Jun;97(6):629–634. doi: 10.1007/s004010051039. [DOI] [PubMed] [Google Scholar]
- Vinters H. V., Ellis W. G., Zarow C., Zaias B. W., Jagust W. J., Mack W. J., Chui H. C. Neuropathologic substrates of ischemic vascular dementia. J Neuropathol Exp Neurol. 2000 Nov;59(11):931–945. doi: 10.1093/jnen/59.11.931. [DOI] [PubMed] [Google Scholar]
- Wenham P. R., Price W. H., Blandell G. Apolipoprotein E genotyping by one-stage PCR. Lancet. 1991 May 11;337(8750):1158–1159. doi: 10.1016/0140-6736(91)92823-k. [DOI] [PubMed] [Google Scholar]
- Zarow C., Zaias B., Lyness S. A., Chui H. Cerebral amyloid angiopathy in Alzheimer disease is associated with apolipoprotein E4 and cortical neuron loss. Alzheimer Dis Assoc Disord. 1999 Jan;13(1):1–8. doi: 10.1097/00002093-199903000-00001. [DOI] [PubMed] [Google Scholar]