4.7 Article

Nonmelanoma skin cancer is associated with reduced Alzheimer disease risk

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NEUROLOGY
卷 80, 期 21, 页码 1966-1972

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LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e3182941990

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  1. National Institute of Aging, the Einstein Aging Study [2P01AG003949]
  2. National Cancer Institute, the Albert Einstein Cancer Center [5P50CA013330]

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Objective: To explore the association of nonmelanoma skin cancer (NMSC) and Alzheimer disease (AD) in the Einstein Aging Study, an epidemiologic study of aging in New York City. Methods: Community-residing volunteers aged 70 years or older were assessed annually, followed by multidisciplinary diagnostic consensus. Cancer status and type was obtained by self-report. Cox proportional hazards models were used to test associations between NMSC and subsequent risk of developing a neurocognitive disorder. To deduce a biologically specific association between AD and NMSC, we considered 3 nested outcomes groups: only AD (probable or possible AD as the sole diagnosis), any AD (probable AD or possible AD, as well as mixed AD/vascular dementia), and all-cause dementia. Results: We followed 1,102 adults with a mean age of 79 years at enrollment. Prevalent NMSC was associated with reduced risk of only AD (hazard ratio = 0.21; 95% confidence interval = 0.051-0.87; p = 0.031) among subjects after adjustment for demographics, hypertension, diabetes, and coronary heart disease. APOE epsilon 4 genotypes were available in 769 individuals. The association was similar in magnitude, but nonsignificant, when the number of APOE epsilon 4 alleles was included in the model. No significant association was found between NMSC and subsequent development of any AD or all-cause dementia. Conclusions: This population-based longitudinal study shows that individuals older than 70 years with NMSC have a significantly reduced risk of developing AD compared with individuals without NMSC. We deduce Alzheimer-specific neuroprotection, because the effect is attenuated or eliminated when considering less-specific diagnoses such as AD with another diagnosis (any AD) or all-cause dementia. Neurology (R) 2013;80:1966-1972

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