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Porphyromonas gingivalis infection in the oral cavity is associated with elevated galactose-deficient IgA1 and increased nephritis severity in IgA nephropathy. | LitMetric

AI Article Synopsis

  • The study investigates the link between the bacterial pathogen Porphyromonas gingivalis and the development of IgA nephropathy (IgAN) in patients, particularly focusing on the role of galactose-deficient IgA1 (Gd-IgA1).
  • Saliva samples from IgAN patients showed higher levels of Gd-IgA1 compared to chronic kidney disease (CKD) patients, indicating a potential connection to P. gingivalis presence.
  • IgAN patients with detectable P. gingivalis also exhibited significantly increased Gd-IgA1 and protein levels in urine, and more severe kidney damage as evident from renal biopsy findings, suggesting that P. gingivalis may contribute to IgAN

Article Abstract

Background: The relationship between the major periodontal bacteria, Porphyromonas gingivalis, and the pathogenesis of IgA nephropathy (IgAN)-particularly with respect to galactose-deficient IgA1 (Gd-IgA1)-has not been fully elucidated.

Methods: Saliva samples from 30 IgAN patients and 44 patients with chronic kidney disease (CKD) were subjected to analysis of P. gingivalis status via polymerase chain reaction using a set of P. gingivalis-specific primers. The associations between P. gingivalis presence and clinical parameters, including plasma Gd-IgA1, were analyzed in each group.

Results: Compared with the CKD group, the IgAN group demonstrated significantly higher plasma Gd-IgA1 levels (p < 0.05). Compared with the P. gingivalis-negative subgroup, the P. gingivalis-positive subgroup exhibited significantly higher plasma Gd-IgA1 levels in both IgAN and CKD patients (p < 0.05). Additionally, among IgAN patients, the P. gingivalis-positive subgroup displayed significantly higher plasma Gd-IgA1 and urine protein levels, compared with the P. gingivalis-negative subgroup (p < 0.05). With respect to renal biopsy findings, the frequencies of segmental glomerulosclerosis and tubular atrophy/interstitial fibrosis were significantly greater in the P. gingivalis-positive subgroup than in the P. gingivalis-negative subgroup, according to the Oxford classification of IgAN (p < 0.05).

Conclusion: Our findings suggest an association between the presence of P. gingivalis in the oral cavity and the pathogenesis of IgAN, mediated by increased levels of Gd-IgA1.

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Source
http://dx.doi.org/10.1007/s10157-023-02411-4DOI Listing

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