Evolocumab safety and efficacy in hypercholesteremia patients with or without diabetes: a retrospective real-world analysis

Abstract Background Proprotein convertase subtilisin/kexin type 9 inhibitors effectively reduce LDL cholesterol and adverse cardiovascular events with a safety profile comparable to a placebo. Limited real-world data exists on their effectiveness in different patient groups. This study evaluated evo...

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Main Authors: Sultan Ibrahim Alraddadi, Hind Almodaimegh, Abdullah Kharbosh, Hadeel Alharbi, Ahmed Ibrahim Fathelrahman, Mona Yaser Alsheikh, Lama Alfehaid
Format: Article
Language:English
Published: BMC 2025-01-01
Series:Diabetology & Metabolic Syndrome
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Online Access:https://doi.org/10.1186/s13098-025-01587-x
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author Sultan Ibrahim Alraddadi
Hind Almodaimegh
Abdullah Kharbosh
Hadeel Alharbi
Ahmed Ibrahim Fathelrahman
Mona Yaser Alsheikh
Lama Alfehaid
author_facet Sultan Ibrahim Alraddadi
Hind Almodaimegh
Abdullah Kharbosh
Hadeel Alharbi
Ahmed Ibrahim Fathelrahman
Mona Yaser Alsheikh
Lama Alfehaid
author_sort Sultan Ibrahim Alraddadi
collection DOAJ
description Abstract Background Proprotein convertase subtilisin/kexin type 9 inhibitors effectively reduce LDL cholesterol and adverse cardiovascular events with a safety profile comparable to a placebo. Limited real-world data exists on their effectiveness in different patient groups. This study evaluated evolocumab’s efficacy and safety in hypercholesteremia patients with and without diabetes. Method In a large tertiary hospital in Saudi Arabia, patients aged 18 and above who initiated evolocumab therapy were screened for eligibility between January 2017 and July 2023. All patients who had been on maximally tolerated statin and ezetimibe therapy for at least 4 months before starting evolocumab were included. The included participants were then divided into diabetic and non-diabetic groups and assessed for evolocumab’s efficacy and safety. Efficacy was measured by LDL-C reduction and target achievement, while safety was assessed by examining glycemic control changes, new-onset diabetes (NOD) and hepatic enzyme levels. Data analysis included descriptive and comparative methods, with significance set at p < 0.05. Results A total of 151 patients were included, with an average age of 51.77 years. The majority of patients were male (67.6%) and obese (81.5%). Around 55% had diabetes, and 63% had established atherosclerotic cardiovascular disease at baseline. During a mean follow-up period of 13.17 months, the average reduction in LDL-C from baseline was − 34.21, − 28.66, and − 39.61% for the overall cohort, non-diabetic patients, and diabetic patients, respectively. In the overall cohort, 34.4 and 24.5% reached the target LDL-C levels of less than 1.4 mmol/L (55 mg/dL) and less than 1.8 mmol/L (70 mg/dL), respectively. Worsening of glycemic control (HbA1C increase > 0.5) was observed in 25.83% of the overall cohort, 16.18% of non-diabetics, and 33.74% of diabetics. An HbA1C increase > 1 was observed in 13.25% of the overall cohort, 2.94% in non-diabetics and 21.69% in diabetics. Five patients (3.3%) developed NOD. Conclusion The study demonstrated that the addition of evolocumab to maximally tolerated statin and ezetimibe therapy reduced LDL-C levels but with a smaller average reduction and a lower proportion of patients achieving recommended LDL-C targets than in landmark clinical trials. Additionally, there was a potential negative effect on glycemic control, warranting further investigation.
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spelling doaj-art-3ced5112f55246ab9915c3e7757c72e22025-02-02T12:35:10ZengBMCDiabetology & Metabolic Syndrome1758-59962025-01-0117111210.1186/s13098-025-01587-xEvolocumab safety and efficacy in hypercholesteremia patients with or without diabetes: a retrospective real-world analysisSultan Ibrahim Alraddadi0Hind Almodaimegh1Abdullah Kharbosh2Hadeel Alharbi3Ahmed Ibrahim Fathelrahman4Mona Yaser Alsheikh5Lama Alfehaid6Pharmaceutical Care Department, King Abdulaziz Medical CityPharmaceutical Care Department, King Abdulaziz Medical CityDepartment of Clinical Pharmacy, College of Pharmacy, Taif UniversityPharmaceutical Care Department, King Abdulaziz Medical CityDepartment of Clinical Pharmacy, College of Pharmacy, Taif UniversityDepartment of Pharmacy Practice, Faculty of Pharmacy, King Abdulaziz UniversityPharmaceutical Care Department, King Abdulaziz Medical CityAbstract Background Proprotein convertase subtilisin/kexin type 9 inhibitors effectively reduce LDL cholesterol and adverse cardiovascular events with a safety profile comparable to a placebo. Limited real-world data exists on their effectiveness in different patient groups. This study evaluated evolocumab’s efficacy and safety in hypercholesteremia patients with and without diabetes. Method In a large tertiary hospital in Saudi Arabia, patients aged 18 and above who initiated evolocumab therapy were screened for eligibility between January 2017 and July 2023. All patients who had been on maximally tolerated statin and ezetimibe therapy for at least 4 months before starting evolocumab were included. The included participants were then divided into diabetic and non-diabetic groups and assessed for evolocumab’s efficacy and safety. Efficacy was measured by LDL-C reduction and target achievement, while safety was assessed by examining glycemic control changes, new-onset diabetes (NOD) and hepatic enzyme levels. Data analysis included descriptive and comparative methods, with significance set at p < 0.05. Results A total of 151 patients were included, with an average age of 51.77 years. The majority of patients were male (67.6%) and obese (81.5%). Around 55% had diabetes, and 63% had established atherosclerotic cardiovascular disease at baseline. During a mean follow-up period of 13.17 months, the average reduction in LDL-C from baseline was − 34.21, − 28.66, and − 39.61% for the overall cohort, non-diabetic patients, and diabetic patients, respectively. In the overall cohort, 34.4 and 24.5% reached the target LDL-C levels of less than 1.4 mmol/L (55 mg/dL) and less than 1.8 mmol/L (70 mg/dL), respectively. Worsening of glycemic control (HbA1C increase > 0.5) was observed in 25.83% of the overall cohort, 16.18% of non-diabetics, and 33.74% of diabetics. An HbA1C increase > 1 was observed in 13.25% of the overall cohort, 2.94% in non-diabetics and 21.69% in diabetics. Five patients (3.3%) developed NOD. Conclusion The study demonstrated that the addition of evolocumab to maximally tolerated statin and ezetimibe therapy reduced LDL-C levels but with a smaller average reduction and a lower proportion of patients achieving recommended LDL-C targets than in landmark clinical trials. Additionally, there was a potential negative effect on glycemic control, warranting further investigation.https://doi.org/10.1186/s13098-025-01587-xLDL-CHypercholesterolemiaEvolocumabStatinEzetimibeGlycemic control
spellingShingle Sultan Ibrahim Alraddadi
Hind Almodaimegh
Abdullah Kharbosh
Hadeel Alharbi
Ahmed Ibrahim Fathelrahman
Mona Yaser Alsheikh
Lama Alfehaid
Evolocumab safety and efficacy in hypercholesteremia patients with or without diabetes: a retrospective real-world analysis
Diabetology & Metabolic Syndrome
LDL-C
Hypercholesterolemia
Evolocumab
Statin
Ezetimibe
Glycemic control
title Evolocumab safety and efficacy in hypercholesteremia patients with or without diabetes: a retrospective real-world analysis
title_full Evolocumab safety and efficacy in hypercholesteremia patients with or without diabetes: a retrospective real-world analysis
title_fullStr Evolocumab safety and efficacy in hypercholesteremia patients with or without diabetes: a retrospective real-world analysis
title_full_unstemmed Evolocumab safety and efficacy in hypercholesteremia patients with or without diabetes: a retrospective real-world analysis
title_short Evolocumab safety and efficacy in hypercholesteremia patients with or without diabetes: a retrospective real-world analysis
title_sort evolocumab safety and efficacy in hypercholesteremia patients with or without diabetes a retrospective real world analysis
topic LDL-C
Hypercholesterolemia
Evolocumab
Statin
Ezetimibe
Glycemic control
url https://doi.org/10.1186/s13098-025-01587-x
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