Glomerular Haematopoietic Prostaglandin D Synthase-Prostaglandin D2 Axis Contributes to the Periodontitis-Related Exacerbation of Diabetic Nephropathy in KK-A(y) Mice.

AIMS: Recent clinical studies have proposed a potential association between chronic kidney diseases, including diabetic nephropathy (DN) and periodontitis. Nevertheless, the causal relationship of periodontitis with DN and the underlying molecular mechanisms remain unclear. MATERIALS AND METHODS: Ligature-induced experimental periodontitis (LIP) was induced in KK-A(y) mice to investigate the molecular mechanisms underlying the LIP-mediated aggravation of glomerular pathology in DN. Outpatients with type 2 diabetes (T2D) at Kyushu University Hospital were recruited to confirm the association of renal dysfunction and periodontitis with a urinary factor identified by RNA sequencing (RNA-seq) in the mouse glomeruli. RESULTS: LIP aggravated renal dysfunction and glomerular pathologies in KK-A(y) mice. RNA-seq in the glomeruli revealed haematopoietic prostaglandin D synthase (HPGDS) as the possible factor bridging periodontitis with DN progression. Glomerular PGD2 levels in KK-Ay mice were significantly elevated by LIP. Oral administration of an HPGDS inhibitor, HQL-79, successfully prevented LIP-mediated DN progression in KK-A(y) mice by lowering glomerular PGD2 levels. Urinary HPGDS-to-creatinine ratio could be associated with renal dysfunction and periodontitis in outpatients with T2D. CONCLUSION: Periodontitis may contribute to DN progression via the glomerular HPGDS-PGD2 axis. These results suggest a novel mechanism in periodontitis-related DN progression.