Development of angiogenic periglomerular microvessels after acute glomerular lesions in IgA nephropathy

Author:

Kamano Chisako1,Mii Akiko2ORCID,Osono Eiichi3,Kunugi Shinobu1,Igarashi Toru4,Yanagihara Takeshi5,Kaneko Tomohiro6,Terasaki Mika1ORCID,Shimizu Akira1

Affiliation:

1. Department of Analytic Human Pathology Nippon Medical School Tokyo Japan

2. Department of Endocrinology, Metabolism and Nephrology Nippon Medical School Tokyo Japan

3. Department of Nephrology Koshigaya Obukuro Clinic Saitama Japan

4. Department of Pediatrics Nippon Medical School Musashi Kosugi Hospital Kawasaki Kanagawa Japan

5. Department of Pediatrics Nippon Medical School Hospital Tokyo Japan

6. Department of Nephrology Nippon Medical School Tama Nagayama Hospital Tokyo Japan

Abstract

AimTo clarify the clinicopathological characteristics and role of periglomerular angiogenesis in IgA nephropathy.Methods and ResultsThe renal biopsy specimens of 114 patients with IgA nephropathy were examined. Among them, 46 (40%) showed periglomerular angiogenesis around the glomeruli. CD34 and α‐smooth muscle actin (α‐SMA) staining in serial sections revealed that these vessels contained CD34+ α‐SMA+ microarterioles along with CD34+ α‐SMA− capillaries. We termed these “periglomerular microvessels (PGMVs)”. Patients with PGMVs (PGMV group) had clinically and histologically more severe disease than those without PGMVs (non‐PGMV group) at the time of biopsy. Even after adjusting for age, there were significant differences in the degree of proteinuria and estimated glomerular filtration rate reduction between the PGMV and non‐PGMV groups. The PGMV group showed a higher incidence of segmental and global glomerulosclerosis and crescentic lesions than the non‐PGMV group (P < 0.01). Here, PGMVs were undetectable in the acute and active inflammation phase, but were observed in the acute to chronic or chronic glomerular remodelling phase. PGMVs mainly developed around glomerular adherent lesions to the Bowman's capsule with small or minimal glomerular sclerotic lesions. Conversely, they were rarely observed in segmental sclerosis areas.ConclusionThe PGMV group is clinically and pathologically more severe than the non‐PGMV group; however, they were undetectable in segmental sclerosis with mesangial matrix accumulation. PGMVs might occur after acute/active glomerular lesions, suggesting that PGMVs may inhibit segmental glomerulosclerosis progression and could be a marker for good repair response after acute/active glomerular injury in severe IgA nephropathy cases.

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

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