Composition of Gut Microbiota and Renal Transcriptome Fluctuate with Age: Midlife Represents a Key Transitional Point

Human aging is associated with declining renal function, potentially worsened by gut microbiota-derived uremic toxins. Although the gut-kidney axis is implicated in disease, its dynamic role in physiological aging remains unclear. Through integrated 16S rDNA and transcriptomic analyses in young (3-month), middle (12-month), and old-aged (24-month) mice, we identified age-dependent shifts in gut microbiota and renal gene expression. The shifts are non-linear, with midlife (12 months) representing a key transitional point. The gut microbiota shifts from a commensal metabolic partner in youth to a driver of a pro-inflammatory microenvironment in old age. Concurrently, the kidney shows enhanced inflammatory, pro-fibrotic, and pro-coagulant transcriptional signatures. These changes are synchronized, revealing a stage-specific gut-kidney interplay: an adaptive peak in midlife precedes a coordinated functional shift toward a pro-aging microenvironment in late life. Our findings introduce the concepts of "stage-specific aging" and aging changes in both gut microbiota and kidney transcriptome are non-linear, midlife is an important stage for gut-kidney aging transit.