Blood DNA methylation of CRF and its association with amygdala volume and mood in Cushing’s syndrome

Objective The impact of chronic exposure to stress or glucocorticoids on psychiatric symptoms has been exemplified by cases of iatrogenic or endogenous hypercortisolism such as Cushing’s syndrome (CS). The amygdala plays an important role in mediating both stress and affective responses, and one of the key factors that link stress response and psychiatric symptoms is the corticotropin-releasing factor (CRF). Epigenetic changes, especially those occurring on CpG dinucleotides in DNA of glucocorticoid target genes in blood, have been previously implicated as potential predictors of glucocorticoid-related events in the central nervous system (CNS). In this study, we examined amygdala volume and mood symptoms in CS patients and aimed at evaluating whether these parameters were associated with blood DNA methylation of CRF . Methods In this cross-sectional study, 32 CS patients and 32 healthy controls matched for age, sex, and years of education underwent an MRI scan, a Beck Depression Inventory-II, and a State-Trait Anxiety Inventory. Genomic DNA extracted from total leukocytes were used for DNA methylation analysis of several CpG dinucleotides at the CRF promoter region. Results Significant associations between CRF methylation vs. amygdala volume (CpG-1, P = 0.006) and depression scores (CpG-2, P = 0.01) were found. To assess whether the promoter CpG methylation has functional consequences, we examined RNA and DNA extracted from non-CS, postmortem amygdala tissues. A significant association between CpG methylation and gene expression (CpG-1, P = 0.004) was observed. Conclusion These results demonstrate that methylation levels of the CRF promoter CpGs are associated with amygdala volume in CS and related mood symptoms. Methylation levels may also be associated with CRF expression. This finding supports the feasibility of using epigenetic patterns in blood as a surrogate for assessing GC-related pathologies in the brain.

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Publication Details

Journal
Frontiers in Epigenetics and Epigenomics
Published
2024-10-02
DOI
https://doi.org/10.3389/freae.2024.1435634
Primary Topic
Pituitary Gland Disorders and Treatments
Type
article
Field-Weighted Citation Impact
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article

Blood DNA methylation of CRF and its association with amygdala volume and mood in Cushing’s syndrome

Alicia Santos, Anna Aulinas, Yolanda Vives‐Gilabert, Susan M. Webb et al.
Frontiers in Epigenetics and Epigenomics
Pituitary Gland Disorders and Treatments
article

Blood DNA methylation of CRF and its association with amygdala volume and mood in Cushing’s syndrome

Alicia Santos, Anna Aulinas, Yolanda Vives‐Gilabert, Susan M. Webb, Henri M. Garrison‐Desany, Eugenia Resmini, Olivia Cox, Jenny L. Carey, Richard S. Lee, Gabriel Cuilan
article en

Abstract

Objective The impact of chronic exposure to stress or glucocorticoids on psychiatric symptoms has been exemplified by cases of iatrogenic or endogenous hypercortisolism such as Cushing’s syndrome (CS). The amygdala plays an important role in mediating both stress and affective responses, and one of the key factors that link stress response and psychiatric symptoms is the corticotropin-releasing factor (CRF). Epigenetic changes, especially those occurring on CpG dinucleotides in DNA of glucocorticoid target genes in blood, have been previously implicated as potential predictors of glucocorticoid-related events in the central nervous system (CNS). In this study, we examined amygdala volume and mood symptoms in CS patients and aimed at evaluating whether these parameters were associated with blood DNA methylation of CRF . Methods In this cross-sectional study, 32 CS patients and 32 healthy controls matched for age, sex, and years of education underwent an MRI scan, a Beck Depression Inventory-II, and a State-Trait Anxiety Inventory. Genomic DNA extracted from total leukocytes were used for DNA methylation analysis of several CpG dinucleotides at the CRF promoter region. Results Significant associations between CRF methylation vs. amygdala volume (CpG-1, P = 0.006) and depression scores (CpG-2, P = 0.01) were found. To assess whether the promoter CpG methylation has functional consequences, we examined RNA and DNA extracted from non-CS, postmortem amygdala tissues. A significant association between CpG methylation and gene expression (CpG-1, P = 0.004) was observed. Conclusion These results demonstrate that methylation levels of the CRF promoter CpGs are associated with amygdala volume in CS and related mood symptoms. Methylation levels may also be associated with CRF expression. This finding supports the feasibility of using epigenetic patterns in blood as a surrogate for assessing GC-related pathologies in the brain.

Frontiers in Epigenetics and EpigenomicsVol. 2
Universitat de Vic - Universitat Central de Catalunya (ES), Universitat Autònoma de Barcelona (ES), Johns Hopkins University (US), Johns Hopkins Medicine (US), Hospital de Sant Pau (ES), Universitat Politècnica de València (ES)
Baker Foundation, European Commission, Ministerio de Ciencia e Innovación, Instituto de Salud Carlos III
Openalex Percentile: Top 74%
Pituitary Gland Disorders and Treatments
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