Real-world use of PCSK9 inhibitors: A single-center experience

Autor: Marcel Zughaib, Sinan Sarsam, George Degheim, Abeer Berry, Robby Singh
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Oncology
Male
Medicine (General)
Clinical Research Reports
Gene Expression
030204 cardiovascular system & hematology
Single Center
Biochemistry
0302 clinical medicine
Risk Factors
PCSK9 Inhibitors
Hypolipidemic Agents
lipid-lowering therapy
Atherosclerotic cardiovascular disease
atherosclerotic cardiovascular disease
General Medicine
Middle Aged
Treatment Outcome
030220 oncology & carcinogenesis
LDL cholesterol
Drug Therapy
Combination

Female
lipids (amino acids
peptides
and proteins)

Proprotein Convertase 9
medicine.medical_specialty
Heterozygote
Statin
medicine.drug_class
PCSK9 inhibitor
Hypercholesterolemia
03 medical and health sciences
R5-920
Internal medicine
medicine
Humans
Protease Inhibitors
Risk factor
Triglycerides
Aged
Retrospective Studies
Ldl cholesterol
business.industry
Biochemistry (medical)
Cholesterol
HDL

statin
Cell Biology
Cholesterol
LDL

medicine.disease
Proprotein convertase
Atherosclerosis
Dyslipidemia
Hydroxymethylglutaryl-CoA Reductase Inhibitors
business
Zdroj: Journal of International Medical Research, Vol 47 (2019)
The Journal of International Medical Research
ISSN: 1473-2300
0300-0605
Popis: Objective Hyperlipidemia is an important risk factor for atherosclerotic cardiovascular disease. Many patients are intolerant to or have limited benefit from statins. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have been approved for treating hyperlipidemia in these patients. We sought to investigate the impact of these medications in a real-world cardiology practice. Methods This was a retrospective study of 17 patients with either heterozygous familial hypercholesterolemia or established atherosclerotic cardiovascular disease with low-density lipoprotein cholesterol (LDL-C) levels above the treatment target despite maximally tolerated statins. Baseline lipid profile was compared with a repeat lipid profile obtained 4 to 6 weeks after initiating treatment with a PCSK9 inhibitor. Results The average duration of PCSK9 inhibitor treatment was 10.7 months. Lipid profile comparison showed that total cholesterol decreased from 243 ± 72 to 148 ± 39 (mg/dL) (39% reduction), triglycerides decreased from 185 ± 86 to 149 ± 62 (mg/dL) (19.5% reduction), high-density lipoprotein cholesterol increased from 56 ± 20 to 62 ± 26 (mg/dL) (10.7% increase), and LDL-C decreased from 154 ± 30 to 57 ± 32 (mg/dL) (63% reduction) from baseline. Conclusions PCSK9 inhibitors as add-on therapy to maximally tolerated statins resulted in an approximately 63% reduction in LDL-C.
Databáze: OpenAIRE