Gender differences in the associations of psychosocial trauma and acute medical stressors with immune system activation and dementia risk.
Erin LogueRobin C HilsabeckEsther MelamedPublished in: The Clinical neuropsychologist (2024)
Objective: The purpose of this article is to provide a narrative review synthesizing the literature on differences between women and men in relationships among certain stressors associated with immune system activation and their relationship to cognitive dysfunction and dementia. Method: We review the cycle of stress leading to neuroinflammation via cortisol and neurochemical alterations, cell-mediated immune system activation, and pro-inflammatory cytokines, and how this is implicated in the development of dementia. We follow this by discussing sex differences in stress physiology and immune function. We then review the work on early life adversity (ELA) and adverse childhood experiences (ACEs), post-traumatic stress disorder, acute medical stressors, and their associations with cognitive dysfunction and dementia. Throughout, we emphasize women's presentations and issues unique to women (e.g. trauma disorder prevalence). Conclusions: There is a need for more mechanistic and longitudinal studies that consider trauma accumulation, both physical and emotional, as well as a greater focus on traumas more likely to occur in women (e.g. sexual abuse), and their relationship to early cognitive decline and dementia.
Keyphrases
- mild cognitive impairment
- cognitive decline
- early life
- polycystic ovary syndrome
- cognitive impairment
- pregnancy outcomes
- mental health
- cervical cancer screening
- liver failure
- breast cancer risk
- respiratory failure
- physical activity
- type diabetes
- systematic review
- insulin resistance
- traumatic brain injury
- risk factors
- single cell
- aortic dissection
- metabolic syndrome
- adipose tissue
- lipopolysaccharide induced
- cross sectional
- inflammatory response
- intensive care unit
- blood brain barrier
- hepatitis b virus
- depressive symptoms
- mesenchymal stem cells
- skeletal muscle
- bone marrow