Effect of PCSK9 inhibitors on pulse wave velocity and monocyte-to-HDL-cholesterol ratio in familial hypercholesterolemia subjects: results from a single-lipid-unit real-life setting
Autor: | Agata Maria Rabuazzo, Roberto Scicali, Francesco Purrello, Antonino Di Pino, Salvatore Piro, Viviana Ferrara |
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Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Male
Endocrinology Diabetes and Metabolism Familial hypercholesterolemia 030204 cardiovascular system & hematology Monocytes Cohort Studies Leukocyte Count 0302 clinical medicine Endocrinology 030212 general & internal medicine Prospective Studies Pulse wave velocity Innate immunity Anticholesteremic Agents PCSK9 Inhibitors General Medicine Middle Aged Inflammatory profile Italy Cohort Absolute neutrophil count Cardiology lipids (amino acids peptides and proteins) Original Article Drug Therapy Combination Female Blood Flow Velocity medicine.drug medicine.medical_specialty Pulse Wave Analysis Hyperlipoproteinemia Type II 03 medical and health sciences Ezetimibe Internal medicine Diabetes mellitus Internal Medicine medicine Humans Aged business.industry PCSK9 Cholesterol HDL medicine.disease Cardiovascular risk Lipid Metabolism Hydroxymethylglutaryl-CoA Reductase Inhibitors business Lipoprotein |
Zdroj: | Acta Diabetologica |
ISSN: | 1432-5233 0940-5429 |
Popis: | Aims Subjects with familial hypercholesterolemia (FH) are characterized by an increased amount of low-density lipoprotein cholesterol (LDL-C) that promotes a continuous inflammatory stimulus. Our aim was to evaluate the effect of PCSK9-i on inflammatory biomarkers, neutrophil-to-lymphocyte ratio, monocyte-to-high-density lipoprotein ratio (MHR), and on early atherosclerosis damage analyzed by pulse wave velocity (PWV) in a cohort of FH subjects. Methods In this prospective observational study, we evaluated 56 FH subjects on high-intensity statins plus ezetimibe and with an off-target LDL-C. All subjects were placed on PCSK9-i therapy and obtained biochemical analysis as well as PWV evaluation at baseline and after six months of PCSK9-i therapy. Results After six months of add-on PCSK9-i therapy, only 42.9% of FH subjects attained LDL-C targets. As expected, a significant reduction of LDL-C (− 49.61%, p p value for both p p p value for both Conclusions In conclusion, PCSK9-i therapy significantly improved lipid and inflammatory profiles and PWV values in FH subjects; our results support the positive effect of PCSK9-i in clinical practice. |
Databáze: | OpenAIRE |
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