4.6 Article

Structural modeling for Oxford histological classifications of immunoglobulin A nephropathy

Journal

PLOS ONE
Volume 17, Issue 9, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0268731

Keywords

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Funding

  1. Ministry of Health, Labour and Welfare of Japan [20FC1045]
  2. AMED [JP19ek0109261]

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This study used structural equation modeling (SEM) to analyze the direct and indirect effects of histological variables on renal functional decline in patients with immunoglobulin A nephropathy (IgAN). The results showed that tubular atrophy/interstitial fibrosis had a direct promoting effect on renal functional decline, while endocapillary hypercellularity and active crescent had an indirect weakening effect via steroid therapy with/without tonsillectomy. Segmental sclerosis had an indirect weakening effect via estimated glomerular filtration rate, and mesangial hypercellularity had an accelerating indirect effect on renal functional decline via proteinuria.
In immunoglobulin A nephropathy (IgAN), Cox regression analysis can select independent prognostic variables for renal functional decline (RFD). However, the correlation of the selected histological variables with clinical and/or treatment variables is unknown, thereby making histology-based treatment decisions unreliable. We prospectively followed 946 Japanese patients with IgAN for a median of 66 mo. and applied structural equation modeling (SEM) to identify direct and indirect effects of histological variables on RFD as a regression line of estimated glomerular filtration rate (eGFR) via clinical variables including amount of proteinuria, eGFR, mean arterial pressure (MAP) at biopsy, and treatment variables such as steroid therapy with/without tonsillectomy (ST) and renin-angiotensin system blocker (RASB). Multi-layered correlations between the variables and RFD were identified by multi-variate linear regression analysis and the model's goodness of fit was confirmed. Only tubular atrophy/interstitial fibrosis CO had an accelerative direct effect on RFD, while endocapillary hypercellularity and active crescent (C) had an attenuating indirect effect via ST. Segmental sclerosis (S) had an attenuating indirect effect via eGFR and mesangial hypercellularity (M) had accelerative indirect effect for RFD via proteinuria. Moreover, M and C had accelerative indirect effect via proteinuria, which can be controlled by ST. However, both T and S had additional indirect accelerative effects via eGFR or MAP at biopsy, which cannot be controlled by ST. SEM identified a systemic path links between histological variables and RFD via dependent clinical and/or treatment variables. These findings lead to clinically applicable novel methodologies that can contribute to predict treatment outcomes using the Oxford classifications.

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