Department of Neurology, Loma Linda University Health, Loma Linda.
Department of Neurology, Weill Cornell Medical College, New York, NY.
Alzheimer Dis Assoc Disord. 2020 Apr-Jun;34(2):122-127. doi: 10.1097/WAD.0000000000000369.
Studies have demonstrated an inverse relationship between Alzheimer dementia (AD) and cancer. This inverse relationship was further explored. In addition, Pin1 expression has been implicated in the cell cycle regulation of both disease processes. The relationship of Pin1 expression in 10 cancer types and secondary diagnosis of AD was examined.
A cross-sectional analysis was performed using discharge data from the National Inpatient Sample from 1999 to 2008. Cancer was defined as the primary discharge diagnosis and AD was defined as the secondary discharge diagnosis. Cancer types were grouped according to their Pin1 expression to examine its relationship with AD. Analysis was performed by logistic regression.
Of ∼3 million cancer discharge diagnoses, 1.0% had a secondary diagnosis of AD. Discharge data of all 10 cancer types revealed a lower likelihood of secondary AD diagnosis. Prostate [crude odds ratios (OR): 0.26 (0.24 to 0.29), multivariate OR: 0.39 (0.35 to 0.43)], ovarian [crude OR: 0.38 (0.32 to 0.44), multivariate OR: 0.35 (0.30 to 0.41)], and lung cancer [crude OR: 0.39 (0.36 to 0.41), multivariate OR: 0.41 (0.39 to 0.44)] demonstrated the lowest odds of secondary AD diagnosis. When cancer types were grouped per Pin1 expression, cancer types with Pin1 underexpression were more likely to be associated with secondary diagnosis of AD than cancer types with Pin1 overexpression [crude OR: 1.4 (1.3 to 1.4), multivariate OR: 1.08 (1.02 to 1.14)].
This secondary data analysis further demonstrated an inverse relationship between AD and 10 cancer types, with prostate, ovarian, and lung cancers displaying the greatest inverse relationship. Pin1 underexpressing cancer types had a significantly higher likelihood of secondary diagnosis of AD than Pin1 overexpressing cancer types.
研究表明,阿尔茨海默病(AD)与癌症之间存在反比关系。本研究进一步探讨了这种反比关系。此外,Pin1 表达已被牵连到这两种疾病过程的细胞周期调节中。本研究检测了 10 种癌症类型中 Pin1 表达与 AD 二次诊断之间的关系。
使用 1999 年至 2008 年国家住院患者样本的出院数据进行横断面分析。癌症定义为主要出院诊断,AD 定义为次要出院诊断。根据 Pin1 表达将癌症类型分组,以检查其与 AD 的关系。分析采用逻辑回归进行。
在约 300 万例癌症出院诊断中,有 1.0%的患者有 AD 的二次诊断。所有 10 种癌症类型的出院数据显示,AD 二次诊断的可能性较低。前列腺癌[粗比值比(OR):0.26(0.24 至 0.29),多变量 OR:0.39(0.35 至 0.43)]、卵巢癌[粗 OR:0.38(0.32 至 0.44),多变量 OR:0.35(0.30 至 0.41)]和肺癌[粗 OR:0.39(0.36 至 0.41),多变量 OR:0.41(0.39 至 0.44)]显示出 AD 二次诊断的最低可能性。当根据 Pin1 表达对癌症类型进行分组时,Pin1 低表达的癌症类型比 Pin1 高表达的癌症类型更有可能与 AD 的二次诊断相关[粗 OR:1.4(1.3 至 1.4),多变量 OR:1.08(1.02 至 1.14)]。
本二次数据分析进一步表明,AD 与 10 种癌症之间存在反比关系,其中前列腺癌、卵巢癌和肺癌的反比关系最大。Pin1 低表达的癌症类型比 Pin1 高表达的癌症类型更有可能被诊断为 AD。