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Depressive disorders are associated with increased peripheral blood cell deformability: a cross-sectional
Andreas Walther1,2, Anne Mackens-Kiani3, Julian Eder3
1Biopsychology, TU Dresden, Dresden, Germany. a.walther@psychologie.uzh.ch.
Translational Psychiatry
|April 9, 2022
Summary
Depressive disorders are linked to increased blood cell flexibility. This study found that immune cells like lymphocytes, monocytes, and neutrophils show altered mechanical properties, potentially indicating persistent immune responses.
Area of Science:
- Immunology
- Cell Biology
- Psychiatry
Background:
- Depressive disorders are characterized by inflammation and elevated glucocorticoids.
- These factors may alter cell mechanics, including deformability.
- Previous research has not extensively explored blood cell morpho-rheological properties in depression.
Purpose of the Study:
- To investigate morpho-rheological properties of blood cells in individuals at high risk for depressive disorders.
- To compare cell deformability and size between patients with depressive disorders and healthy controls.
- To identify specific blood cell types associated with depressive disorder phenotypes.
Main Methods:
- Cross-sectional case-control study design.
- Real-time deformability cytometry (RT-DC) for blood cell analysis.
- Deep learning for cell classification and quantification of morpho-rheological parameters.
Main Results:
- Peripheral blood cells were more deformable in patients with depressive disorders.
- Increased cell deformability was observed in monocytes and neutrophils in lifetime persistent depressive disorder.
- Erythrocytes showed increased deformability in 12-month persistent depressive disorder, and lymphocytes in 12-month major depressive disorder.
Conclusions:
- This is the first study to link depressive disorders, particularly persistent forms, with increased blood cell deformability.
- Immune cells, including lymphocytes, monocytes, and neutrophils, are significantly affected.
- Altered immune cell mechanics in depression may serve as a predictive marker for persistent immune responses.
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