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August 22, 2026Lupus

Interstitial palladin is associated with tubulointerstitial chronicity and adverse outcomes in patients with lupus nephritis

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Authors

NYNaoki YamamotoKanazawa UniversityNSNorihiko SakaiKanazawa UniversitySNShiori NakagawaKanazawa University

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Implication

Retrospective study finds interstitial palladin expression correlates with tubulointerstitial chronicity in lupus nephritis, suggesting its potential role in disease progression.

Key Points

  • To evaluate whether interstitial expression of the actin-associated protein palladin is associated with histopathological chronicity indices and long-term clinical prognosis in lupus nephritis.
  • Retrospectively analyzed 34 Japanese patients with biopsy-proven lupus nephritis evaluated at Kanazawa University Hospital between 1990 and 2018.
  • Quantified interstitial palladin area using immunohistochemistry (log2-transformed) and examined its colocalization with α-smooth muscle actin (αSMA) via immunofluorescence.
  • Correlated expression levels with modified NIH activity and chronicity indices, and evaluated event-free survival for renal replacement therapy initiation or all-cause death over a median follow-up of 10.1 years (IQR, 3.3–17.5).
  • Palladin was predominantly expressed in the interstitium, colocalized with αSMA-positive cells, and log2 palladin correlated significantly with the modified NIH chronicity index (ρ = 0.61, p < 0.01), tubular atrophy (ρ = 0.53, p < 0.01), interstitial fibrosis (ρ = 0.56, p < 0.01), and interstitial inflammation (ρ = 0.55, p < 0.01).
  • Log2 palladin showed no significant correlation with the total activity index (ρ = 0.24, p = 0.16).
  • Seven patients reached the composite endpoint (five in the high-palladin group vs. two in the low-palladin group), with high palladin expression significantly associated with poorer event-free survival (log-rank p = 0.04).

Cite This Study

Yamamoto et al. (2026) studied this question.

synapsesocial.com/papers/6a895f9cca7ade938187e5dahttps://doi.org/10.1177/09612033261479120
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