Evaluating SSRI/SNRI Use and Amyloid-Related Imaging Abnormalities in Anti-Amyloid Therapy in a Real WorldCohort
Background:
•Amyloid-related imaging abnormalities (ARIA) are a common and clinically significant adverse effect of anti-amyloid monoclonal antibody therapies (Fox et al. 2025; Sims et al. 2023; van Dyck et al. 2022)
•Selective serotonin and serotonin-norepinephrine reuptake inhibitors (SSRIs/SNRIs) are frequently prescribed in patients with Alzheimer’s Disease (Mo et al. 2025)
•SSRI/SNRI’s have been shown to reduce platelet aggregation (Kaye et al. 2025) and have been linked with increased risk of abnormal bleeding, particularly upper GI bleeding (Andrede et al. 2010)
• Hypothesis: SSRI or SNRI use may be associated with increased ARIA risk in individuals receiving anti-amyloid therapies
Methods:
•Retrospective chart review of 57 patients receiving lecanemab or donanemab infusions at University Hospitals (January 1, 2024- August 31, 2025)
•ARIA incidence was compared between:
Individuals on SSRI’s or SNRI’s and those not receiving these medications
•Secondary analyses: ARIA rates were compared between:
Antidepressant class (SSRI vs. SNRI)
Antidepressant dose (low vs. medium dose)
Results:
•There was no statistically significant difference in ARIA rates with vs. without antidepressant use:
SSRI/SNRI vs. ARIA → χ² p = 0.68
•Descriptively, higher ARIA rates were observed among individuals on SNRI’s (50%) compared to SSRI’s (28.6%), though the sample size was insufficient to allow meaningful statistical comparison
SSRI vs. ARIA → Fisher’s p = 0.53 (NS)
SNRI vs. ARIA → Fisher’s p = n too low
•Sample size was too low to draw conclusions about SSRI/SNRI dose (low vs. medium doses) and ARIA
ARIA vs. Low/Medium dose SSRI/SNRI → n too low
Conclusions:
•Summary: This provides an initial evaluation of the relationship between antidepressant use and ARIA risk in patients receiving anti-amyloid monoclonal antibody therapies.
•We did not identify a statistically significant association between SSRI or SNRI use or dose and ARIA rate.
•Limitations: Analyses were limited by small sample size and were retrospective.
•Future directions: Larger, prospective studies are needed to further evaluate this relationship and to account for other relevant confounders, including vascular risk factors such as blood pressure.