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Retinal Microvascular Abnormalities in Major Depression

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Abstract

Background: The aim of our study was to find a possible association between retinal microvascular abnormality and major depression in a non-geriatric population.

Method: The participants with major depression were hospitalised at the University Hospital in Hradec Kralove, Department of Psychiatry. Retinal images were obtained using a stationary Fundus camera FF450 by Zeiss and a hand-held camera by oDocs.

Results: Fifty patients (men n=18, women n=32) aged 16 to 55 (men's average age 33.7±9.9 years, women's average age 37.9±11.5 years) were compared with fifty mentally healthy subjects (men n=28, women n=22) aged 18 to 61 (men's average age 35.3±9.2 years, women's average age 36.6±10.6 years) in a cross-sectional design. The patients were diagnosed with a single depressive episode (n=26) or a recurrent depressive disorder (n=24) according to the ICD-10 classification. Our results confirmed significant microvascular changes in the retina in patients with depressive disorder in comparison to the control group of mentally healthy subjects, with significantly larger arteriolar (P<0.0001) as well as venular (P<0.001-0.0001) calibres in major depression.

Conclusion: According to the literature, acute and chronic neuroinflammation is associated with changes in microvascular form and function. The endothelium becomes a major participant in the inflammatory response damaging the surrounding tissue and its function. Because the retina and brain tissue share a common embryonic origin, we suspect similar microvascular pathology in the retina and in the brain in major depression. Our results may contribute to a better understanding of depression etiopathogenesis and to its personalized treatment.

References
1.
Firk C, Markus C . Review: Serotonin by stress interaction: a susceptibility factor for the development of depression?. J Psychopharmacol. 2007; 21(5):538-44. DOI: 10.1177/0269881106075588. View

2.
Dinan T . Glucocorticoids and the genesis of depressive illness. A psychobiological model. Br J Psychiatry. 1994; 164(3):365-71. DOI: 10.1192/bjp.164.3.365. View

3.
Smith R . The macrophage theory of depression. Med Hypotheses. 1991; 35(4):298-306. DOI: 10.1016/0306-9877(91)90272-z. View

4.
Schiepers O, Wichers M, Maes M . Cytokines and major depression. Prog Neuropsychopharmacol Biol Psychiatry. 2005; 29(2):201-17. DOI: 10.1016/j.pnpbp.2004.11.003. View

5.
Pasco J, Nicholson G, Williams L, Jacka F, Henry M, Kotowicz M . Association of high-sensitivity C-reactive protein with de novo major depression. Br J Psychiatry. 2010; 197(5):372-7. DOI: 10.1192/bjp.bp.109.076430. View