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(Stroke. 1995;26:743-748.)
© 1995 American Heart Association, Inc.


Articles

Relation of Coronary Atherosclerosis and Apolipoprotein E Genotypes in Alzheimer Patients

O. Kosunen, MD; S. Talasniemi, MD; M. Lehtovirta, MD; O. Heinonen, PhD; S. Helisalmi, MSci; A. Mannermaa, MSci; L. Paljärvi, MD, PhD; M. Ryynänen, MD, PhD; P.J. Riekkinen, Sr, MD, PhD H. Soininen, MD, PhD

From the Departments of Pathology (O.K., L.P.) and Neurology (M.L., O.H., P.J.R., H.S.) and the Unit of Clinical Genetics (S.H., A.M, M.R.) of the Department of Gynecology and Obstetrics, Kuopio University Hospital, University of Kuopio; and the Harjula Hospital (S.T.), Kuopio, Finland.

Correspondence to Dr Hilkka Soininen, MD, PhD, Department of Neurology, University of Kuopio, PO Box 1627, 70 211 Kuopio, Finland.

Background and Purpose Apolipoprotein E (apoE) {varepsilon}4 allele has been associated with a high risk for coronary heart disease. Increased frequency of the {varepsilon}4 allele has also been reported in patients with late-onset familial and sporadic Alzheimer's disease (AD). The aim of this study was to investigate the degree of coronary and cerebral atherosclerosis in a neuropathologically verified series of AD patients with different apoE genotypes. In addition, we studied the relationship between the degree of coronary and cerebral atherosclerosis and the extent of ß-amyloid (Aß) accumulation.

Methods We studied 38 subjects (32 patients with definite AD and 6 age-matched control subjects) for whom postmortem autopsy delay was less than 8 hours. ApoE genotypes were identified through Hha I digestion of the polymerase chain reaction–amplified samples. We used Aß immunohistochemistry to detect diffuse and neuritic plaques as well as cerebrovascular amyloid. The degree of coronary and cerebral atherosclerosis was rated as none, mild, moderate, or severe.

Results The apoE genotypes of the AD patients were {varepsilon}4/4 2, {varepsilon}3/4 19, {varepsilon}3/3 9, and {varepsilon}3/2 2. We found more severe atherosclerosis of the coronary vessels among AD patients with the apoE {varepsilon}4 allele compared with those AD patients without the {varepsilon}4 allele ({chi}2=4.1, df=1, P<.05). The extent of cerebral atherosclerosis did not differ among AD subgroups with and without the {varepsilon}4 allele. The degree of coronary or cerebral atherosclerosis was not related to the amount of amyloid accumulation in the frontal and temporal cortices or in the hippocampal structures.

Conclusions This study confirms the association of apoE {varepsilon}4 allele with coronary atherosclerosis in AD patients.


Key Words: Alzheimer's disease • apolipoproteins • atherosclerosis




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