Tonsillar histomorphometry in IgA nephropathy: a cross-sectional study of correlations between clinical and renal histopathological findings

Author:

Ueda Hiroyuki1,Joh Kensuke1,Ueda Yoshimi1,Marumoto Hirokazu1,Isaka Nao1,Tsuboi Nobuo1,Kojima Hiromi1,Miyazaki Yoichi1,Yokoo Takashi1,Okabe Masahiro1

Affiliation:

1. The Jikei University School of Medicine

Abstract

Abstract There is insufficient evidence to confirm the involvement of tonsillar immune disorders in the pathogenesis of IgA nephropathy (IgAN). This cross-sectional study investigated the association between histological changes in the palatine tonsil, its clinical presentation, and renal histopathological findings in IgAN. Eighty-seven patients with IgAN who underwent tonsillectomy within one year of undergoing renal biopsy were compared with 27 age-matched patients with recurrent tonsillitis (RT). The mean lymphoid follicle and germinal center sizes in patients with IgAN were significantly smaller than in those with RT (P < 0.001). The relative areas of lymphoid follicles (%LFA) and germinal centers in the total tonsillar tissue were smaller in IgAN than in RT (P < 0.001). The mean interfollicular area was larger in patients with IgAN than those with RT. Crypt epithelia in IgAN showed more expanded non-reticular areas lacking lymphoepithelial symbiosis than those observed in RT (P = 0.003). Lower %LFA was associated with higher urinary protein excretion (P = 0.01) and a longer period from the onset of urinary abnormalities to renal biopsy. A lower %LFA was associated with S and C lesions in the Oxford classification. The frequency of glomeruli with sclerotic lesions showed a close inverse correlation with %LFA (ρ = -0.46, P < 0.001). Reduced size of lymphoid follicles and germinal centers, enlarged interfollicular areas, and expanded non-reticular crypt epithelia in the palatine tonsils were prominent IgAN features. Reduced %LFA showed a significant correlation with IgAN renal histopathological severity, supporting the concept of accelerated involution of secondary lymphoid follicles during IgAN progression.

Publisher

Research Square Platform LLC

Reference19 articles.

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