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      Call for Papers: Digital Platforms and Artificial Intelligence in Dementia

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      About Dementia and Geriatric Cognitive Disorders: 2.2 Impact Factor I 4.7 CiteScore I 0.809 Scimago Journal & Country Rank (SJR)

      Call for Papers: Epidemiology of CKD and its Complications

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      About Kidney and Blood Pressure Research: 2.3 Impact Factor I 4.8 CiteScore I 0.674 Scimago Journal & Country Rank (SJR)

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      Develop and Validate a Risk Score in Predicting Renal Failure in Focal Segmental Glomerulosclerosis

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          Abstract

          Introduction

          The aim of this study was to develop and validate a risk score (RS) for end-stage kidney disease (ESKD) in patients with focal segmental glomerulosclerosis (FSGS).

          Methods

          Patient with biopsy-proven FSGS was enrolled. All the patients were allocated 1:1 to the two groups according to their baseline gender, age, and baseline creatinine level by using a stratified randomization method. ESKD was the primary endpoint.

          Results

          We recruited 359 FSGS patients, and 177 subjects were assigned to group 1 and 182 to group 2. The clinicopathological variables were similar between two groups. There were 23 (13%) subjects reached to ESKD in group 1 and 22 (12.1%) in group 2. By multivariate Cox regression analyses, we established RS 1 and RS 2 in groups 1 and 2, respectively. RS 1 consists of five parameters including lower eGFR, higher urine protein, MAP, IgG level, and tubulointerstitial lesion (TIL) score; RS 2 also consists of five predictors including lower C3, higher MAP, IgG level, hemoglobin, and TIL score. RS 1 and RS 2 were cross-validated between these two groups, showing RS 1 had better performance in predicting 5-year ESKD in group 1 (c statics, 0.86 [0.74–0.98] vs. 0.82 [0.69–0.95]) and group 2 (c statics, 0.91 [0.83–0.99] vs. 0.89 [0.79–0.99]) compared to RS 2. We then stratified the risk factors into four groups, and Kaplan-Meier survival curve revealed that patients progressed to ESKD increased as risk levels increased.

          Conclusions

          A predictive model incorporated clinicopathological feature was developed and validated for the prediction of ESKD in FSGS patients.

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          Most cited references49

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          Association of trypanolytic ApoL1 variants with kidney disease in African Americans.

          African Americans have higher rates of kidney disease than European Americans. Here, we show that, in African Americans, focal segmental glomerulosclerosis (FSGS) and hypertension-attributed end-stage kidney disease (H-ESKD) are associated with two independent sequence variants in the APOL1 gene on chromosome 22 {FSGS odds ratio = 10.5 [95% confidence interval (CI) 6.0 to 18.4]; H-ESKD odds ratio = 7.3 (95% CI 5.6 to 9.5)}. The two APOL1 variants are common in African chromosomes but absent from European chromosomes, and both reside within haplotypes that harbor signatures of positive selection. ApoL1 (apolipoprotein L-1) is a serum factor that lyses trypanosomes. In vitro assays revealed that only the kidney disease-associated ApoL1 variants lysed Trypanosoma brucei rhodesiense. We speculate that evolution of a critical survival factor in Africa may have contributed to the high rates of renal disease in African Americans.
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            A predictive model for progression of chronic kidney disease to kidney failure.

            Chronic kidney disease (CKD) is common. Kidney disease severity can be classified by estimated glomerular filtration rate (GFR) and albuminuria, but more accurate information regarding risk for progression to kidney failure is required for clinical decisions about testing, treatment, and referral. To develop and validate predictive models for progression of CKD. Development and validation of prediction models using demographic, clinical, and laboratory data from 2 independent Canadian cohorts of patients with CKD stages 3 to 5 (estimated GFR, 10-59 mL/min/1.73 m(2)) who were referred to nephrologists between April 1, 2001, and December 31, 2008. Models were developed using Cox proportional hazards regression methods and evaluated using C statistics and integrated discrimination improvement for discrimination, calibration plots and Akaike Information Criterion for goodness of fit, and net reclassification improvement (NRI) at 1, 3, and 5 years. Kidney failure, defined as need for dialysis or preemptive kidney transplantation. The development and validation cohorts included 3449 patients (386 with kidney failure [11%]) and 4942 patients (1177 with kidney failure [24%]), respectively. The most accurate model included age, sex, estimated GFR, albuminuria, serum calcium, serum phosphate, serum bicarbonate, and serum albumin (C statistic, 0.917; 95% confidence interval [CI], 0.901-0.933 in the development cohort and 0.841; 95% CI, 0.825-0.857 in the validation cohort). In the validation cohort, this model was more accurate than a simpler model that included age, sex, estimated GFR, and albuminuria (integrated discrimination improvement, 3.2%; 95% CI, 2.4%-4.2%; calibration [Nam and D'Agostino χ(2) statistic, 19 vs 32]; and reclassification for CKD stage 3 [NRI, 8.0%; 95% CI, 2.1%-13.9%] and for CKD stage 4 [NRI, 4.1%; 95% CI, -0.5% to 8.8%]). A model using routinely obtained laboratory tests can accurately predict progression to kidney failure in patients with CKD stages 3 to 5.
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              Executive summary of the KDIGO 2021 Guideline for the Management of Glomerular Diseases

                Author and article information

                Journal
                Kidney Dis (Basel)
                Kidney Dis (Basel)
                KDD
                KDD
                Kidney Diseases
                S. Karger AG (Basel, Switzerland )
                2296-9381
                2296-9357
                28 March 2023
                August 2023
                : 9
                : 4
                : 285-297
                Affiliations
                [1]Department of Nephrology, Institute of Nephrology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
                Author notes
                Correspondence to: Hong Ren, renhong66@ 123456126.com or Jingyuan Xie, nephroxie@ 123456163.com

                Yikai Cai, Yunzi Liu, and Jun Tong have contributed equally to this work.

                Article
                529773
                10.1159/000529773
                10601954
                adef94c1-580e-46b0-bb2f-af6185c77376
                © 2023 The Author(s). Published by S. Karger AG, Basel

                This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) ( http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.

                History
                : 17 November 2022
                : 8 February 2023
                : 2023
                Page count
                Figures: 4, Tables: 4, References: 49, Pages: 13
                Funding
                This work was supported by grants from the Major International (Regional) Joint Research Program of National Natural Science Foundation of China (No. 82120108007), the National Natural Science Foundation of China (No. 81870460, 81570598, 81370015), Program of Shanghai Academic/Technology Research Leader (No. 21XD1402000), Science and Technology Innovation Action Plan of Shanghai Science and Technology Committee (No. 22140904000, 17441902200), Shanghai Municipal Education Commission Gaofeng Clinical Medicine Grant (No. 20152207), Shanghai Shenkang Hospital Development Center “Three-year Action Plan for Promoting Clinical Skills and Clinical Innovation in Municipal Hospitals” (No. SHDC2020CR6017), and Shanghai Jiaotong University “Jiaotong Star” Plan Medical Engineering Cross Research Key Project (No. YG2019ZDA18). The funding bodies had no role in the design of the study, collection, analysis, and interpretation of data, or the writing of the manuscript.
                Categories
                Research Article

                focal segmental glomerulosclerosis,clinicopathological features,survival analysis,predictive model

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