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Neuropsychiatric disorders and cognitive dysfunction in patients with Cushing's disease
Yu-fan Chen1, Yun-feng Li, Xiao Chen
1Department of Neurosurgery, Ruijin Hospital, Affiliated Hospital of Shanghai Jiaotong University, Shanghai, China.
Insights
Cushing's disease (CD) causes neuropsychiatric and cognitive issues due to excess cortisol. Glucocorticoid excess leads to brain atrophy and hippocampal changes, impacting mood and cognition.
Area of Science:
- Neuroendocrinology
- Neuropsychiatry
- Cognitive Neuroscience
Background:
- Cushing's disease (CD) is characterized by excessive cortisol secretion.
- Patients with CD often exhibit significant neuropsychiatric and cognitive deficits.
Purpose of the Study:
- To review the neuropsychiatric disorders and cognitive deficits in Cushing's disease.
- To explore the pathophysiological mechanisms underlying these impairments.
- To inform potential prevention and treatment strategies.
Main Methods:
- Literature search of PubMed for studies on psychiatric and cognitive complications in CD.
- Keywords included: Cushing's disease, cognitive, hippocampal, glucocorticoids.
- Focus on papers published in English within the last 20 years, referencing recent reviews.
Main Results:
- Active CD is associated with emotional instability, depression, anxiety, impulsivity, and cognitive impairment.
- Excess glucocorticoids (GCs) cause structural and functional changes in the hippocampus and basal ganglia.
- Hippocampal volume loss, reduced neurogenesis, and impaired long-term potentiation are observed, contributing to brain atrophy.
Conclusions:
- Excess cortisol-induced brain atrophy and hippocampal changes are key in the pathophysiology of cognitive and psychiatric disturbances in CD.
- The precise mechanisms of GC-induced hippocampal volume loss require further investigation.
- Further research is essential to understand GC effects on the brain and develop effective interventions.
Objective:
To review the main neuropsychiatric disorders and cognitive deficits in patients with Cushing's disease (CD) and the associated pathophysiological mechanisms underlying CD. These mechanistic details may provide recommendations for preventing or treating the cognitive impairments and mood disorders in patients with CD.
Data Sources:
Data were obtained from papers on psychiatric and cognitive complications in CD published in English within the last 20 years. To perform the PubMed literature search, the following keywords were input: cushing's disease, cognitive, hippocampal, or glucocorticoids.
Study Selection:
Studies were selected if they contained data relevant to the topic addressed in the particular section. Because of the limited length of this article, we have frequently referenced recent reviews that contain a comprehensive amalgamation of literature rather than the actual source papers.
Results:
Patients with active CD not only suffer from many characteristic clinical features, but also show some neuropsychiatric disorders and cognitive impairments. Among the psychiatric manifestations, the common ones are emotional instability, depressive disorder, anxious symptoms, impulsivity, and cognitive impairment. Irreversible effects of previous glucocorticoid (GC) excess on the central nervous system, such as hippocampal and the basal ganglia, is the most reasonable reason. Excess secretion of cortisol brings much structural and functional changes in hippocampal, such as changes in neurogenesis and morphology, signaling pathway, gene expression, and glutamate accumulation. Hippocampal volume loss can be found in most patients with CD, and decreased glucose utilization caused by GCs may lead to brain atrophy, neurogenesis impairment, inhibition of long-term potentiation, and decreased neurotrophic factors; these may also explain the mechanisms of GC-induced brain atrophy and hippocampal changes.
Conclusions:
Brain atrophy and hippocampal changes caused by excess secretion of cortisol are thought to play a significant pathophysiological role in the etiology of changes in cognitive function and psychiatric disturbances. The exact mechanisms by which GCs induce hippocampal volume loss are not very clear till now. So, further investigations into the mechanisms by which GCs affect the brain and the effective coping strategy are essential.
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