Cardiovascular, Kidney Failure, and All-Cause Mortality Events in Patients with FSGS in a US Real-World Database

Author:

Velez Juan Carlos Q.12ORCID,Thakker Kamlesh M.3ORCID,Bensink Mark E.4ORCID,Lerma Edgar V.5ORCID,Lieblich Richard6ORCID,Bunke C. Martin7,Gong Wu4ORCID,Wang Kaijun4ORCID,Rava Andrew R.8ORCID,Amari Diana T.8,Oliveri David8,Murphy Michael V.8,Cork David M.W.9ORCID

Affiliation:

1. Department of Nephrology, Ochsner Health, New Orleans, Louisiana

2. Ochsner Clinical School, The University of Queensland, Brisbane, Queensland, Australia

3. Notting Hill Consulting LLC, Celebration, Florida

4. Travere Therapeutics, Inc., San Diego, California

5. University of Illinois Chicago/Advocate Christ Medical Center, Oak Lawn, Illinois

6. VJA Consulting, Walnut Creek, California

7. CM Bunke Consulting, Mt. Pleasant, South Carolina

8. Genesis Research Group, Hoboken, New Jersey

9. Genesis Research Group, Newcastle upon Tyne, United Kingdom

Abstract

Key Points In our patients with FSGS, elevated proteinuria and progression to kidney failure (KF) were associated with a higher risk of cardiovascular disease/all-cause mortality events.In addition, elevated pre-KF proteinuria was associated with KF/all-cause mortality events.CKD stage, nephrotic syndrome, and cardiovascular disease event rates, as well as the incremental costs of these events, were high. Background FSGS leads to proteinuria and progressive decline in GFR, which correlates with kidney failure (KF) and increased cardiovascular risk. The purpose of this study was to estimate the effects of proteinuria on KF status/all-cause mortality and cardiovascular disease (CVD) events/all-cause mortality, as well as the relationship between progression to KF and occurrence of CVD/mortality events among adult patients (18 years or older) with FSGS. Methods This was an observational, retrospective cohort study utilizing Optum deidentified Market Clarity Data and proprietary Natural Language Processing data. The study period was from January 1, 2007, through March 31, 2021, with patients in the overall cohort being identified from July 1, 2007, through March 31, 2021. The index date was the first FSGS ICD-10 diagnosis code or FSGS-related natural language processing term within the identification period. Results Elevated proteinuria >1.5 and ≥3.5 g/g increased the risk of KF/all-cause mortality (adjusted hazard ratio [HR] [95% confidence interval (CI)], 2.34 [1.99 to 2.74] and 2.44 [2.09 to 2.84], respectively) and CVD/all-cause mortality (adjusted HR [95% CI], 2.11 [1.38 to 3.22] and 2.27 [1.44 to 3.58], respectively). Progression to KF was also associated with a higher risk of CVD/all-cause mortality (adjusted HR [95% CI], 3.04 [2.66 to 3.48]). Conclusions A significant proportion of patients with FSGS experience KF and CVD events. Elevated proteinuria and progression to KF were associated with a higher risk of CVD/all-cause mortality events, and elevated pre-KF proteinuria was associated with progression to KF/all-cause mortality events. Treatments that meaningfully reduce proteinuria and slow the decline in GFR have the potential to reduce the risk of CVD, KF, and early mortality in patients with FSGS.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference20 articles.

1. How does proteinuria cause progressive renal damage?;Abbate;J Am Soc Nephrol.,2006

2. Differentiating primary, genetic, and secondary FSGS in adults: a clinicopathologic approach;De Vriese;J Am Soc Nephrol.,2018

3. Focal segmental glomerulosclerosis;Rosenberg;Clin J Am Soc Nephrol.,2017

4. KDIGO 2021 clinical practice guideline for the management of glomerular diseases;Kidney Int.,2021

5. Secondary focal segmental glomerulosclerosis: from podocyte injury to glomerulosclerosis;Kim;Biomed Res Int.,2016

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