Towards a Translatable Model for Studying Therapeutic Efficacy in Alport Syndrome

Background: Reducing GFR loss is the primary outcome for studying therapeutic effectiveness in Alport syndrome (AS). Unlike humans, standard dose ACE inhibition (ramipril 10 mg/kg) almost completely normalizes the kidney in the Col4a3 KO (AS) mouse. We sought to establish a model with more similarity to its human counterpart by (1) comparing the reliability of GFR methods, and (2) using GFR as the primary outcome to establish a model for testing agents on top of ACE inhibition. Methods: Study 1 GFR was measured (mGFR) in wild type and Col4a3 KO mice comparing the gold standard of fluorescein-labeled sinistrin (inulin analogue) with plasma creatinine, BUN and cystatin C. In Study 2, having established cystatin C as a preferred method, we assessed the ACE inhibitor dose-response relationship, aiming for an approximate 50% improvement in GFR, akin to human disease. Urinary ACR, glomerulosclerosis and interstitial fibrosis were also assessed. Results: Study 1. At 8 weeks of age, the between group difference between WT and Col4a3 KO was 11-fold for sinistrin-GFR, 4.9 fold for plasma creatinine, 2.6 fold for BUN and 6.9 fold for cystatin C. All comparisons p <0.001. Study 2 (Table 1). In comparison with untreated Col4a3 KO mice, ramipril induced dose-dependent reductions in cystatin C. ACR, glomerulosclerosis and interstitial fibrosis while near-normalized by ramipril 10 mg/kg were unaffected by lower doses. Conclusion: Changes in cystatin C most closely resemble sinistrin-based mGFR. ACE inhibition with ramipril provided dose-dependent improvements in cystatin C with an approximate 50% reduction at 1 mg/kg, akin to findings of standard of care in humans. Accordingly, 1 mg/kg may be an appropriate dose to use in studies testing the efficacy of new additive agents. The dynamic range for UACR, GSI and IF may be too narrow to allow for such testing. Funding: Government Support – Non-U.S. Renal function parametres and histologic analysis - WT RO water ramipril 0.1 ramipril 1 ramipril 10 cystatin C mmol/l 306 ± 21 2360 ± 158 1450 ± 168† 1129 ± 191†‡ 502 ± 52†‡§ UACR (mg/mmol) 3.1 (2.9 – 7.9) 423 (292 – 635 484 (325 – 807) 303 (187 – 474) 15 (7 – 126)† GSI 0.2 (0.2 – 0.7) 3.8 (3.3 – 3.9) 3.7 (2.4 – 3.9) 3.7 (2.9 – 3.9) 0.5 (0.4 – 1.0)† IF (%) 1.2 ± 0.3 11 ± 2.5 10 ± 4.6 6.9 ± 2.6 2.2 ± 1.0* * p<0.05 versus RO water ; † p≤0.001 versus RO water; ‡ p<0.01 versus 0.1 ramipril; § p<0.01 versus 1 ramipril WT, wild type; RO, reverse osmosis water. RO water and ramipril-treated mice were all studied in Col4a3 KO mice.

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Journal
Journal of the American Society of Nephrology
Published
2024-10-01
DOI
https://doi.org/10.1681/asn.2024e5rj5pgm
Primary Topic
Cell Adhesion Molecules Research
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article
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article

Towards a Translatable Model for Studying Therapeutic Efficacy in Alport Syndrome

Carlos E. Sales de Oliveira, Richard E. Gilbert, Linda Nghiem, Yanling Zhang et al.
Journal of the American Society of Nephrology
Cell Adhesion Molecules Research
article

Towards a Translatable Model for Studying Therapeutic Efficacy in Alport Syndrome

Carlos E. Sales de Oliveira, Richard E. Gilbert, Linda Nghiem, Yanling Zhang, Kerri Thai, Hai Wang
article en

Abstract

Background: Reducing GFR loss is the primary outcome for studying therapeutic effectiveness in Alport syndrome (AS). Unlike humans, standard dose ACE inhibition (ramipril 10 mg/kg) almost completely normalizes the kidney in the Col4a3 KO (AS) mouse. We sought to establish a model with more similarity to its human counterpart by (1) comparing the reliability of GFR methods, and (2) using GFR as the primary outcome to establish a model for testing agents on top of ACE inhibition. Methods: Study 1 GFR was measured (mGFR) in wild type and Col4a3 KO mice comparing the gold standard of fluorescein-labeled sinistrin (inulin analogue) with plasma creatinine, BUN and cystatin C. In Study 2, having established cystatin C as a preferred method, we assessed the ACE inhibitor dose-response relationship, aiming for an approximate 50% improvement in GFR, akin to human disease. Urinary ACR, glomerulosclerosis and interstitial fibrosis were also assessed. Results: Study 1. At 8 weeks of age, the between group difference between WT and Col4a3 KO was 11-fold for sinistrin-GFR, 4.9 fold for plasma creatinine, 2.6 fold for BUN and 6.9 fold for cystatin C. All comparisons p <0.001. Study 2 (Table 1). In comparison with untreated Col4a3 KO mice, ramipril induced dose-dependent reductions in cystatin C. ACR, glomerulosclerosis and interstitial fibrosis while near-normalized by ramipril 10 mg/kg were unaffected by lower doses. Conclusion: Changes in cystatin C most closely resemble sinistrin-based mGFR. ACE inhibition with ramipril provided dose-dependent improvements in cystatin C with an approximate 50% reduction at 1 mg/kg, akin to findings of standard of care in humans. Accordingly, 1 mg/kg may be an appropriate dose to use in studies testing the efficacy of new additive agents. The dynamic range for UACR, GSI and IF may be too narrow to allow for such testing. Funding: Government Support – Non-U.S. Renal function parametres and histologic analysis - WT RO water ramipril 0.1 ramipril 1 ramipril 10 cystatin C mmol/l 306 ± 21 2360 ± 158 1450 ± 168† 1129 ± 191†‡ 502 ± 52†‡§ UACR (mg/mmol) 3.1 (2.9 – 7.9) 423 (292 – 635 484 (325 – 807) 303 (187 – 474) 15 (7 – 126)† GSI 0.2 (0.2 – 0.7) 3.8 (3.3 – 3.9) 3.7 (2.4 – 3.9) 3.7 (2.9 – 3.9) 0.5 (0.4 – 1.0)† IF (%) 1.2 ± 0.3 11 ± 2.5 10 ± 4.6 6.9 ± 2.6 2.2 ± 1.0* * p<0.05 versus RO water ; † p≤0.001 versus RO water; ‡ p<0.01 versus 0.1 ramipril; § p<0.01 versus 1 ramipril WT, wild type; RO, reverse osmosis water. RO water and ramipril-treated mice were all studied in Col4a3 KO mice.

Journal of the American Society of NephrologyVol. 35(10S)
Unity Health Toronto
Openalex Percentile: Top 72%
Cell Adhesion Molecules Research
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