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Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
by
Tokola Heikki
, Nuutinen Matti
, Ylinen Elisa
, Koskela Mikael
, Jalanko Hannu
, Lohi Jouko
, Jahnukainen Timo
, Heikkilä Päivi
, Autio-Harmainen Helena
in
Actin
/ Biopsy
/ Inflammation
/ Kidney diseases
/ Nephritis
/ P-selectin
/ Proteinuria
/ Renal function
/ Risk factors
/ Schonlein-Henoch purpura
/ Smooth muscle
/ Vimentin
2020
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Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
by
Tokola Heikki
, Nuutinen Matti
, Ylinen Elisa
, Koskela Mikael
, Jalanko Hannu
, Lohi Jouko
, Jahnukainen Timo
, Heikkilä Päivi
, Autio-Harmainen Helena
in
Actin
/ Biopsy
/ Inflammation
/ Kidney diseases
/ Nephritis
/ P-selectin
/ Proteinuria
/ Renal function
/ Risk factors
/ Schonlein-Henoch purpura
/ Smooth muscle
/ Vimentin
2020
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Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
by
Tokola Heikki
, Nuutinen Matti
, Ylinen Elisa
, Koskela Mikael
, Jalanko Hannu
, Lohi Jouko
, Jahnukainen Timo
, Heikkilä Päivi
, Autio-Harmainen Helena
in
Actin
/ Biopsy
/ Inflammation
/ Kidney diseases
/ Nephritis
/ P-selectin
/ Proteinuria
/ Renal function
/ Risk factors
/ Schonlein-Henoch purpura
/ Smooth muscle
/ Vimentin
2020
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Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
Journal Article
Prediction of renal outcome in Henoch–Schönlein nephritis based on biopsy findings
2020
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Overview
BackgroundIn Henoch–Schönlein nephritis (HSN), a risk factor for unfavorable outcome is prolonged proteinuria, but the value of renal biopsies in prognosis assessment is debatable.MethodsWe evaluated serial renal biopsies from 26 HSN patients. Follow-up biopsy occurred at median 2.1 years after diagnostic biopsy. Patients formed two groups at the follow-up biopsy: patients without proteinuria (group I; n = 11) and with proteinuria (group II; n = 15). Biopsies underwent evaluation according to three classifications: International Study of Kidney Disease in Children (ISKDC), Oxford (MEST-C), and semiquantitative classification (SQC) including an activity and chronicity score. Analysis also included expression of pro-fibrotic (alpha-smooth muscle actin and vimentin) and inflammatory (P-selectin glycoprotein ligand-1) molecules in the diagnostic biopsy specimens. Definition of unfavorable outcome was active renal disease or reduced renal function at last follow-up.ResultsBetween the biopsies, SQC chronicity score increased in 22 (85%) patients, whereas activity score and ISKDC grade decreased in 21 (81%) and 17 (65%), respectively. Of the MEST-C parameters, endocapillary proliferation (from 83 to 13%; p < 0.001) and crescents (from 63 to 25%; p = 0.022) showed significant reduction, and segmental glomerulosclerosis (from 38 to 79%; p = 0.006) significant increment. These changes occurred similarly in groups I and II. Expression of the pro-fibrotic and inflammatory molecules showed no clinically significant differences between groups I and II. None in group I and five (33%) patients in group II had unfavorable outcome (p = 0.053).ConclusionsOur results suggest that follow-up biopsies provide limited additional information to clinical symptoms in HSN outcome prediction.
Publisher
Springer Nature B.V
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