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combined single-cell RNA sequencing and population-level genetic analyses to reveal two key chondrocyte subpopulations, inflammatory and fibrocartilage chondrocytes, that are expanded in hand OA and enriched for ferroptosis-related and inflammatory pathways, with elevated expression of FTH1, implicating iron overload in OA pathogenesis ( + T cells in the synovium as drivers of cartilage degeneration and subchondral bone damage through interactions with chondrocytes, offering mechanistic insight into immune-mediated OA progression (Sun et al., 2024)