• Five immune cell phenotypes were causally associated with atrial fibrillation risk, including CD11c on monocytes and CX3CR1 on monocyte subsets.
• Three immune phenotypes (CD19 on switched memory B cells, CD25++CD8+ T cells, and their absolute count) were protective against hypertension.
• No significant heterogeneity or horizontal pleiotropy was detected in sensitivity analyses, supporting the robustness of the causal estimates.
• The findings suggest that immune cell phenotypes may serve as potential targets for monitoring and treating atrial fibrillation and hypertension.
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