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Solidified Glomerulosclerosis, Identified Using Single Glomerular Proteomics, Predicts End-stage Renal Disease in Chinese Patients with Type 2 Diabetes

Abstract

Few histological prognostic indicators for end-stage renal disease (ESRD) have been validated in diabetic patients. This biopsy-based study aimed to identify nephropathological risk factors for ESRD in Chinese patients with type 2 diabetes. Histological features of 322 Chinese type 2 diabetic patients with biopsy-confirmed diabetic nephropathy (DN) were retrospectively analysed. Cox proportional hazards analysis was used to estimate the hazard ratio (HR) for ESRD. Single glomerular proteomics and immunohistochemistry were used to identify differentially expressed proteins and enriched pathways in glomeruli. During the median follow-up period of 24 months, 144 (45%) patients progressed to ESRD. In multivariable models, the Renal Pathology Society classification failed to predict ESRD, although the solidified glomerulosclerosis (score 1: HR 1.65, 95% confidence interval [CI] 1.04-2.60; score 2: HR 2.48, 95% CI 1.40-4.37) and extracapillary hypercellularity (HR 2.68, 95% CI 1.55-4.62) were identified as independent risk factors. Additionally, single glomerular proteomics, combined with immunohistochemistry, revealed that complement C9 and apolipoprotein E were highly expressed in solidified glomerulosclerosis. Therefore, solidified glomerulosclerosis and extracapillary hypercellularity predict diabetic ESRD in Chinese patients. Single glomerular proteomics identified solidified glomerulosclerosis as a unique pathological change that may be associated with complement overactivation and abnormal lipid metabolism.

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References
1.
Pinsker J, Shank T, Dassau E, Kerr D . Comment on American Diabetes Association. Approaches to glycemic treatment. Sec. 7. In Standards of Medical Care in Diabetes-2015. Diabetes Care 2015;38(Suppl. 1):S41-S48. Diabetes Care. 2015; 38(10):e174. DOI: 10.2337/dc15-0839. View

2.
Zhao L, Zou Y, Zhang J, Zhang R, Ren H, Li L . Serum transferrin predicts end-stage Renal Disease in Type 2 Diabetes Mellitus patients. Int J Med Sci. 2020; 17(14):2113-2124. PMC: 7484672. DOI: 10.7150/ijms.46259. View

3.
Saito A, Komatsuda A, Saito M, Kaga H, Abe F, Sawamura M . Clinicopathological features and outcomes of diabetic kidney disease with extracapillary hypercellularity: a Japanese single-center experience. Clin Exp Nephrol. 2020; 24(6):509-517. DOI: 10.1007/s10157-020-01859-y. View

4.
Aoki M, Kang D, Katayama A, Kuwahara N, Nagasaka S, Endo Y . Optimal conditions and the advantages of using laser microdissection and liquid chromatography tandem mass spectrometry for diagnosing renal amyloidosis. Clin Exp Nephrol. 2018; 22(4):871-880. DOI: 10.1007/s10157-018-1533-y. View

5.
Mottl A, Gasim A, Schober F, Hu Y, Dunnon A, Hogan S . Segmental Sclerosis and Extracapillary Hypercellularity Predict Diabetic ESRD. J Am Soc Nephrol. 2017; 29(2):694-703. PMC: 5791055. DOI: 10.1681/ASN.2017020192. View