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Neurology 2001;56:655-659
© 2001 American Academy of Neurology


Articles

APOE-{varepsilon}4 is associated with weight loss in women with AD

A population-based study

M. Vanhanen, PhD;, M. Kivipelto, MD;, K. Koivisto, MD, PhD;, J. Kuusisto, MD, PhD;, L. Mykkänen, MD, PhD;, E.-L. Helkala, PhD;, T. Hänninen, PhD;, K. Kervinen, MD, PhD;, Y.A. Kesäniemi, MD, PhD;, M.P. Laakso, MD, PhD;, H. Soininen, MD, PhD; and M. Laakso, MD, PhD

From the Departments of Neurology and Neuroscience of the Kuopio University Hospital (Drs. Vanhanen, Koivisto, Hänninen, and Soininen) and the University of Kuopio (Drs. Kivipelto, M.P. Laakso, and Soininen); the Department of Medicine of the Kuopio University Hospital (Drs. Kuusisto and M. Laakso) and the University of Kuopio (Drs. Mykkänen and M. Laakso); the Department of Community Health and General Practice of the University of Kuopio (Dr. Helkala); and the Department of Internal Medicine (Drs. Kervinen and Kesäniemi) and Biocenter Oulu (Dr. Kervinen) of the University of Oulu, Finland.

Address correspondence and reprint requests to Dr. Matti Vanhanen, Department of Neurology, Kuopio University Hospital, POB 1777, 70211 Kuopio, Finland; e-mail: matti.vanhanen{at}kuh.fi

OBJECTIVE: To investigate whether the APOE-{varepsilon}4 allele is associated with weight loss in patients with AD or in nondemented elderly subjects. Background: Weight loss has been considered a typical feature of AD. APOE-{varepsilon}4 is a risk factor for AD and was recently proposed to be associated with weight loss in elderly women. It is not known whether APOE-{varepsilon}4 is associated with weight loss in patients with AD or in the general population.

METHODS: Weight and BMI measurements at an average interval of 3.5 years and APOE phenotype determination were performed in an elderly population (n = 980), including 46 patients with AD and 911 control subjects at the end of the follow-up.

RESULTS: On average, patients with AD with the {varepsilon}4 allele lost 1.9 ± 4.0 kg (BMI 0.8 ± 1.8 kg/m2) whereas {varepsilon}4 noncarriers gained 1.2 ± 3.8 kg (BMI 0.4 ± 1.5 kg/m2) (both p < 0.05), after controlling for diabetes and exercise. However, when men and women were analyzed separately, weight loss was observed only in those women with AD with the {varepsilon}4 allele. Clinically significant weight loss, defined as loss of >=5% of body weight, occurred more frequently in both patients with AD (30% versus 6%; p < 0.05) and control subjects (28% versus 18%; p < 0.001) carrying the {varepsilon}4 allele.

CONCLUSIONS: The APOE-{varepsilon}4 allele may contribute to the unexplained weight loss in AD, especially in women.




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