The overexpression of microglia can result in a significant increase in the production and expression of proinflammatory cytokines (e.g., TNF-α, IL-1β) and neurotoxic substances (e.g., reactive oxygen species, nitric oxide) (Singhal and Baune 2017), subsequently leading to cognitive dysfunction and psychiatric illnesses, such as depression (Patel 2013) and AD (Mrak 2012). This evidence concerns the gene TNF and depressive symptom measurement.