Abstract.
We investigated the onset of renal scarring in 62 males (aged 4 – 26 years) with Alport syndrome by measuring cortical interstitial volume fraction [Vv (interstitium/cortex)] and percentage global glomerular sclerosis in kidney biopsies. Male pediatric (n = 9) and adult (n = 7) donor kidneys served as controls. Creatinine clearance at the time of biopsy was available for 43 Alport patients. A statistically insignificant correlation between age and Vv (interstitium/cortex) was observed in normal subjects (r = +0.47, slope = 0.0009, P = 0.07). In the Alport patients, age was significantly correlated with Vv (interstitium/cortex (r = +0.49, slope = 0.01, P = 0.001) and global glomerular sclerosis (r = +0.41, P = 0.01), and inversely correlated with creatinine clearance (r = –0.33, P = 0.04). Creatinine clearance was inversely correlated with Vv (interstitium/cortex) (r = –0.78, P = 0.001) and global glomerular sclerosis (r = –0.74, P = 0.001). The correlation with creatinine clearance was especially strong for Vv (interstitium/cortex) values above the normal range, i. e., >0.2 (r = –0.82, P = 0.001), and was absent for Vv (interstitium/cortex) <0.2 (r = –0.119, P = 0.55). Creatinine clearance values less than 80 ml/min per 1.73 m2 occurred more frequently in patients with Vv (interstitium/cortex) values >0.2 (P <0.0001) and in patients with >10% globally sclerosed glomeruli (P <0.001). Patients ≤ or >10 years of age differed in Vv (interstitium/cortex) [0.13±0.09 (mean ±SD) vs. 0.24±0.026, P <0.001], the frequency of Vv (interstitium/cortex) >0.2 (3/32 vs. 15/31, P <0.0001), the frequency of >10% globally sclerosed glomeruli (3/33 vs. 11/30, P <0.05), mean creatinine clearance (113±7 vs. 84±10 ml/min per 1.73 m2, P = 0.057), and the frequency of creatinine clearance <80 ml/min per 1.73 m2 (1/20 vs. 11/23, P <0.01). Thus, reduced creatinine clearance in males with Alport syndrome is associated with Vv (interstitium/cortex) >0.2 and >10% globally sclerosed glomeruli. These are frequently detectable in the 2nd decade. We hypothesize that most Alport males will require intervention during the 1st decade for optimal preservation of kidney function.
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Received July 7, 1997; received in revised form October 23, 1997; accepted October 26, 1997
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Kashtan, C., Gubler, MC., Sisson-Ross, S. et al. Chronology of renal scarring in males with Alport syndrome. Pediatr Nephrol 12, 269–274 (1998). https://doi.org/10.1007/s004670050451
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DOI: https://doi.org/10.1007/s004670050451