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Lipid profile of patients treated with evolocumab in Spanish hospital nephrology units (RETOSS NEFRO). | LitMetric

AI Article Synopsis

  • The study focused on the use of evolocumab in patients treated in Nephrology Units in Spain, analyzing their clinical characteristics and treatment effects from February 2016 to August 2018.
  • Of the 60 enrolled patients, many had familial hypercholesterolemia or atherosclerotic cardiovascular disease, with high LDL-c levels at treatment initiation, and a significant portion exhibited chronic kidney disease.
  • After 12 weeks of treatment with evolocumab, patients achieved substantial LDL-c reductions, reaching optimal cholesterol levels while maintaining stable kidney function and ongoing statin therapy.

Article Abstract

Background And Objective: To describe the clinical characteristics, the reasons for initiating therapy and the effects of treatment in the initial phase of evolocumab availability in the Nephrology Units of Spain.

Material And Methods: Retrospective, observational and multicentric study that included patients initiating treatment with evolocumab (from February 2016 to August 2018), in 15 Nephrology Units in Spain. The demographic and clinical characteristics of the patients, the lipid lowering treatment and the evolution of the lipid profiles between 24 weeks pre-initiation and 12±4 weeks post-initiation of evolocumab were reviewed.

Results: 60 patients were enrolled: 53.3% women; mean (SD) age, 56.9 (12.8) years, 45.0% with familial hypercholesterolemia (FH) (5.0% homozygous and 40.0% heterozygous) and 65.0% with atherosclerotic cardiovascular disease. The mean (SD) eGFR was 62.6 (30.0) ml/min/1.73m (51.7% of patients had eGFR <60ml/min/1.73m [CKD stage>2]), 50.0% had proteinuria (>300mg/g) and 10.0% had nephrotic syndrome. Other CV risk factors were hypertension (75.0%), diabetes (25.0%), and smoking (21.7%). A 40.0% of patients were statin intolerant. At evolocumab initiation, 41.7% of patients were on a high intensity statin, 18.3% on moderate intensity statin and 50.0% were receiving ezetimibe. Mean (SD) LDL-c at evolocumab initiation was 179.7 (62.9) mg/dL (53.4% of patients with LDL-c ≥160mg/dL and 29.3% ≥190mg/dL). After 12 weeks, evolocumab resulted in LDL-c reductions of 60.1%. At week 12, 90.0% of patients reached LDL-c levels <100mg/dL, 70.0% <70mg/dL, and 55.0% <55mg/dL, while mean eGFR levels and statin use remained stable.

Conclusion: In Nephrology Units of Spain, evolocumab was predominantly prescribed in patients with FH, chronic renal disease (CRD>2) and secondary prevention, with LDL-c levels above those recommended by the guidelines. Evolocumab used in clinical practice significantly reduced the LDL-c levels in all patients included in the study.

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Source
http://dx.doi.org/10.1016/j.nefroe.2022.05.005DOI Listing

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