Saul B. Korey Department of Neurology, Albert Einstein College of Medicine, Bronx, NY, USA.
Neurology. 2013 May 21;80(21):1966-72. doi: 10.1212/WNL.0b013e3182941990. Epub 2013 May 15.
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.
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.
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 ε4 genotypes were available in 769 individuals. The association was similar in magnitude, but nonsignificant, when the number of APOE ε4 alleles was included in the model. No significant association was found between NMSC and subsequent development of any AD or all-cause dementia.
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.
在爱因斯坦老龄化研究中探索非黑色素瘤皮肤癌 (NMSC) 和阿尔茨海默病 (AD) 的关联,这是一项针对纽约市老龄化的流行病学研究。
每年评估居住在社区中的 70 岁或以上的志愿者,然后进行多学科诊断共识。通过自我报告获得癌症状况和类型。使用 Cox 比例风险模型来测试 NMSC 与随后发生神经认知障碍的风险之间的关联。为了推断 AD 和 NMSC 之间存在生物学特异性关联,我们考虑了 3 个嵌套结果组:仅 AD(唯一诊断为可能或可能 AD)、任何 AD(可能 AD 或可能 AD,以及混合 AD/血管性痴呆)和所有原因痴呆。
我们随访了 1102 名平均年龄为 79 岁的成年人,在登记时患有常见的 NMSC。在调整人口统计学、高血压、糖尿病和冠心病后,患有 NMSC 的患者发生仅 AD 的风险降低(风险比 = 0.21;95%置信区间 = 0.051-0.87;p = 0.031)。在 769 名个体中可获得 APOE ε4 基因型。当在模型中包含 APOE ε4 等位基因数量时,该关联的大小相似,但无统计学意义。未发现 NMSC 与随后发生任何 AD 或所有原因痴呆之间存在显著关联。
这项基于人群的纵向研究表明,与没有 NMSC 的个体相比,年龄超过 70 岁且患有 NMSC 的个体发生 AD 的风险显著降低。我们推断出阿尔茨海默病特异性神经保护,因为当考虑不太特异性的诊断(如伴有其他诊断的 AD[任何 AD]或所有原因痴呆)时,这种效应会减弱或消除。