Persistent albuminuria and chronic kidney disease in adults with sickle cell anaemia: Results from a multicenter natural history study

Author:

Zhou Laura Y.1,Derebail Vimal K.2ORCID,Desai Payal C.3,Elsherif Laila4ORCID,Patillo Kammie L.5,McCune Paula5,Wichlan David6,Landes Kristina7,Ogu Ugochi O.4ORCID,Nelson Marquita4,Loehr Laura R.8,Cronin Robert M.9,Tang Yihan10,Cai Jianwen10,Ataga Kenneth I.4ORCID

Affiliation:

1. Department of Biostatistics and Health Data Science Indiana University School of Medicine Indianapolis Indiana USA

2. Division of Nephrology and Hypertension University of North Carolina Chapel Hill North Carolina USA

3. Department of Hematology Levine Cancer Institute—Atrium Health Charlotte North Carolina USA

4. Center for Sickle Cell Disease University of Tennessee Health Science Center Memphis Tennessee USA

5. Office of Clinical Trials University of Tennessee Health Science Center Memphis Tennessee USA

6. Division of Hematology University of North Carolina Chapel Hill North Carolina USA

7. Division of Hematology The Ohio State University Columbus Ohio USA

8. Division of General Medicine and Epidemiology University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

9. Department of Internal Medicine The Ohio State University Columbus Ohio USA

10. Department of Biostatistics University of North Carolina at Chapel Hill Chapel Hill North Carolina USA

Abstract

SummaryClinical and laboratory correlates of chronic kidney disease (CKD) in sickle cell anaemia remain incompletely defined. In a multicenter cohort study, we evaluated the prevalence of persistent albuminuria (PA) and characteristics associated with PA, albumin–creatinine ratio (ACR) and decreased estimated glomerular filtration rate (eGFR) using logistic, linear and multinomial regression models, respectively. Of 269 participants (median age: 30 years; 57.2% females), the prevalence of PA was 35.7%. Using baseline ACR values of <100 and ≥100 mg/g, the probabilities of PA were 30.0% and 94.6%, respectively. In multivariable logistic regression analyses, male sex (β = 0.80 [SE = 0.36], p = 0.024) and ACE inhibitors/ARBs use (β = 1.54 [SE = 0.43], p < 0.001) were associated with higher likelihoods of PA, while higher haemoglobin (β = −0.33 [SE = 0.13], p = 0.009) and HbF (β = −0.04 [SE = 0.02], p = 0.041) were associated with lower likelihoods of PA. In multivariable multinomial regression analyses, older age (β = 0.06 [SE = 0.02], p = 0.004) and higher alkaline phosphatase (β = 0.01 [SE = 0.00], p = 0.004) were associated with higher odds of having eGFR 60–90 versus eGFR>90 mL/min/1.73 m2 using the cystatin C‐based CKD‐EPI‐2012 equation. Additionally, higher systolic blood pressure (β = 0.11 [SE = 0.03], p = 0.001) and blood urea nitrogen (β = 0.45 [SE = 0.12], p < 0.001) were associated with higher odds, while higher haemoglobin (β = −1.22 [SE = 0.43], p = 0.004) was associated with lower odds of having eGFR<60 versus eGFR>90 mL/min/1.73 m2. PA and decreased eGFR are associated with measures of disease severity and comorbid conditions (Clinicaltrials.gov Identifier: NCT03277547).

Funder

U.S. Food and Drug Administration

Publisher

Wiley

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