Key result
Larger baseline CRVE is linked to ~10% higher risk of incident depressive symptoms per SD.
Why the study?
Cerebral microvascular dysfunction may contribute to depression via disruption of mood-regulating brain structures, but evidence is limited.
Does larger baseline retinal microvascular caliber increase the risk of incident depressive symptoms in middle-aged and older adults?
Cohort (n=4,366)
Yes
Does larger baseline retinal microvascular caliber increase the risk of incident depressive symptoms in middle-aged and older adults?
Hazard Ratio: 1.1 (95% CI 1.02–1.17)
Retinal venular widening, a marker of cerebral microvascular dysfunction, may identify patients at elevated risk for developing incident depressive symptoms.
Larger baseline CRVE may flag higher depressive symptom risk in older adults; leaves open whether retinal venular caliber aids prediction beyond established factors.
Cerebral microvascular dysfunction may contribute to depression via disruption of brain structures involved in mood regulation, but evidence is limited. The retina allows for visualization of a microvascular bed that shares similarities with the cerebral microvasculature. We investigated the associations between baseline retinal arteriolar and venular calibers (central retinal arteriolar equivalent (CRAE) and central retinal venular equivalent (CRVE), respectively) and incident depressive symptoms in the Multi-Ethnic Study of Atherosclerosis (MESA). We used longitudinal data on 4,366 participants (mean age = 63.2 years; 48.5% women, 28.4% Black) without baseline depressive symptoms. Depressive symptoms, defined as Center for Epidemiologic Studies Depression Scale score ≥16 and/or use of antidepressant medication, were determined between 2002 and 2004 (baseline; MESA visit 2) and at 3 follow-up examinations conducted every 1.5-2 years thereafter. Fundus photography was performed at baseline. After a mean follow-up period of 6.1 years, 21.9% (n = 958) had incident depressive symptoms. After adjustment for sociodemographic, lifestyle, and cardiovascular factors, a 1-standard-deviation larger baseline CRVE was associated with a higher risk of depressive symptoms (hazard ratio = 1.10, 95% confidence interval: 1.02, 1.17), and a 1-standard-deviation larger baseline CRAE was not statistically significantly associated with incident depressive symptoms (hazard ratio = 1.04, 95% confidence interval: 0.97, 1.11). In this study, larger baseline CRVE, but not CRAE, was associated with a higher incidence of depressive symptoms.
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Gennip et al. (2021) conducted a cohort in Incident depressive symptoms (n=4,366). Central retinal venular equivalent (CRVE) and central retinal arteriolar equivalent (CRAE) vs. Lower retinal microvascular caliber was evaluated on Incident depressive symptoms (CES-D score ≥16 and/or use of antidepressant medication) (HR 1.10, 95% CI 1.02, 1.17). A 1-standard-deviation larger baseline central retinal venular equivalent (CRVE) was associated with a higher risk of incident depressive symptoms (HR 1.10), whereas CRAE was not (HR 1.04).
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