The therapeutic effect of PCSK9 inhibitors on dyslipidemia: one-year follow up

被引:0
作者
Farahani, Maryam Moshkani [1 ]
Nasiri, Alireza [1 ]
Salari, Mahdi [2 ]
Shamsedini, Ali [1 ]
机构
[1] Baqiyatallah Univ Med Sci, Atherosclerosis Res Ctr, Tehran, Iran
[2] Kerman Univ Med Sci, Shafa Cardiovasc Med & Res Ctr, Kemran, Iran
关键词
dyslipidemia; hypercholesterolemia; PCSK9; inhibitors; lipid profile; cardiovascular disease; FAMILIAL HYPERCHOLESTEROLEMIA; LDL-C; EFFICACY; SAFETY; ALIROCUMAB; EVOLOCUMAB; MANAGEMENT;
D O I
10.4081/ejtm.2024.12937
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Despite the availability of statins and lifestyle modifications, many patients with Dyslipidemia struggle to achieve optimal low-density lipoprotein cholesterol (LDL-C) control. PCSK9 inhibitors offer a promising new therapeutic option with superior LDL-C lowering efficacy compared to statins. However, data on their real-world use, particularly in Iran, is limited. This study aims to address this gap by investigating the one-year effects of evolocumab on lipid profiles and potential cardiovascular outcomes in Iranian patients with Familial Hypercholesterolemia (FH).This single- center, prospective study evaluated evolocumab effectiveness in lowering LDL-C in 50 Iranian adults with FH. Participants with a documented LDL-C >190 mg/dL on existing cholesterol medications (excluding PCSK9 inhibitors) and a clinical FH diagnosis was included. After baseline assessments (medical history, demographics, lipid profile), evolocumab was administered subcutaneously every two weeks for one year. Follow-up assessments at year one measured changes in LDL-C, high-density lipoprotein cholesterol (HDL-C), and triglycerides. The study enrolled 50 participants with an average age of 55 years old (range 35-80 years). Treatment with evolocumab led to significant improvements in lipid profiles at all follow-up points compared to baseline. On average, LDL-C levels decreased by 105.24 mg/dL, triglycerides decreased by 59.20 mg/dL, and HDL-C levels increased by a modest but significant 4.5 mg/dL after one year(p<0.001). Subgroup analysis revealed no statistically significant interactions between baseline demographics (age, sex, BMI) or lifestyle habits (smoking, alcohol) and changes in lipid levels(p>0.05). However, a significant interaction emerged between baseline lipid levels and their corresponding reductions, suggesting greater improvement in patients with higher baseline values(p<0.05). It is noteworthy that no new cardiovascular events were reported during the study period. This study demonstrates the effectiveness of evolocumab in improving lipid profiles in Iranian patients with FH. The observed reductions in LDL-C and triglycerides, along with a modest increase in HDL-C, suggest potential benefits for cardiovascular risk reduction. The absence of new cardiovascular events during the study is encouraging, but further research with larger and longer-term follow-up is needed to confirm these findings and assess the long-term safety and impact on quality of life.
引用
收藏
页码:113 / 121
页数:9
相关论文
共 27 条
[1]  
AlHajri L, 2017, THER ADV CARDIO DIS, V11, P155, DOI 10.1177/1753944717698925
[2]  
Azimi M, 2022, Evid Based Complement Alternat Med, V2022
[3]   Optimizing Dyslipidemia Management for the Prevention of Cardiovascular Disease: a Focus on Risk Assessment and Therapeutic Options [J].
Berman, Adam N. ;
Blankstein, Ron .
CURRENT CARDIOLOGY REPORTS, 2019, 21 (09)
[4]   Efficacy and Safety of Alirocumab in Adults With Homozygous Familial Hypercholesterolemia The ODYSSEY HoFH Trial [J].
Blom, Dirk J. ;
Harada-Shiba, Mariko ;
Rubba, Paolo ;
Gaudet, Daniel ;
Kastelein, John J. P. ;
Charng, Min-Ji ;
Pordy, Robert ;
Donahue, Stephen ;
Ali, Shazia ;
Dong, Yuping ;
Khilla, Nagwa ;
Banerjee, Poulabi ;
Baccara-Dinet, Marie ;
Rosenson, Robert S. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2020, 76 (02) :131-142
[5]   Efficacy and Safety of Alirocumab in Patients with Heterozygous Familial Hypercholesterolemia and LDL-C of 160 mg/dl or Higher [J].
Ginsberg, Henry N. ;
Rader, Daniel J. ;
Raal, Frederick J. ;
Guyton, John R. ;
Baccara-Dinet, Marie T. ;
Lorenzato, Christelle ;
Pordy, Robert ;
Stroes, Erik .
CARDIOVASCULAR DRUGS AND THERAPY, 2016, 30 (05) :473-483
[6]   PCSK9 Inhibitors: Mechanisms of Action, Metabolic Effects, and Clinical Outcomes [J].
Hess, Connie N. ;
Wang, Cecilia C. Low ;
Hiatt, William R. .
ANNUAL REVIEW OF MEDICINE, VOL 69, 2018, 69 :133-145
[7]   Long-term safety, tolerability, and efficacy of evolocumab in patients with heterozygous familial hypercholesterolemia [J].
Hovingh, G. Kees ;
Raal, Frederick J. ;
Dent, Ricardo ;
Stefanutti, Claudia ;
Descamps, Olivier ;
Masana, Luis ;
Lira, Armando ;
Bridges, Ian ;
Coll, Blai ;
Sullivan, David .
JOURNAL OF CLINICAL LIPIDOLOGY, 2017, 11 (06) :1448-1457
[8]   Current and future therapies for addressing the effects of inflammation on HDL cholesterol metabolism [J].
Iqbal, Fatima ;
Baker, Wendy S. ;
Khan, Madiha I. ;
Thukuntla, Shwetha ;
McKinney, Kevin H. ;
Abate, Nicola ;
Tuvdendorj, Demidmaa .
BRITISH JOURNAL OF PHARMACOLOGY, 2017, 174 (22) :3986-4006
[9]   Harmine Mitigates Liver Injury Induced by Mercuric Chloride via the Inhibition of Oxidative Stress [J].
Jalili, Cyrus ;
Darakhshan, Sara ;
Azimi, Mohammadreza ;
Ghanbari, Ali .
RESEARCH JOURNAL OF PHARMACOGNOSY, 2021, 8 (03) :13-23
[10]   Dyslipidemia Management in 2020: An Update on Diagnosis and Therapeutic Perspectives [J].
Karantas, Ioannis D. ;
Okur, Mehmet Evren ;
Okur, Neslihan U. ;
Siafaka, Panoraia, I .
ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS, 2021, 21 (05) :815-834