Atherogenic Lipoproteins for the Statin Residual Cardiovascular Disease Risk
Yanai H, Adachi H, Hakoshima M, Katsuyama H
International journal of molecular sciences · 28 citas
Cómo se estudió
- Diseño
- Metaanálisis (indexado por PubMed)
- Estudiado en
- Personas
- Resultado principal
- Eventos clínicos como enfermedad o muerte
Quién lo pagó
- Financiación
- Financiación independiente
Según la declaración de financiación del texto completo.
Publicación
- Publicado
- 2022-11-04 · Int J Mol Sci · vol. 23 · número 21 · pág. 13499
- Editorial
- Multidisciplinary Digital Publishing Institute
- Citado
- 34 citas · más que el 97% de estudios similares · 5.5× el promedio de su campo
- Impacto
- Entre el 10 % más citado de su campo
- Referencias
- 166 trabajos
- Acceso
- Acceso abierto (revista) · CC-BY
- Áreas de investigación
- Lipoproteins and Cardiovascular Health · Diabetes, Cardiovascular Risks, and Lipoproteins · Cholesterol and Lipid Metabolism
- Palabras clave
- atherogenic lipoproteins, lipoprotein(a), remnant lipoproteins, small dense LDL, malondialdehyde-modified LDL, oxidized LDL, triglycerides, HDL cholesterol, obesity, insulin resistance, diabetes mellitus, atherosclerosis, LDL cholesterol lowering
- MeSH
- humans, cardiovascular diseases, diabetes mellitus, insulin resistance, obesity, lipoproteins, hydroxymethylglutaryl-coa reductase inhibitors, risk factors, atherosclerosis, cholesterol, ldl
4 autores
- Hidekatsu Yanai🇯🇵 · autor de correspondenciaNational Center for Global Health and Medicine; Kohnodai Hospital, National Center for Global Health and Medicine
- Hiroki Adachi🇯🇵National Center for Global Health and Medicine; Kohnodai Hospital, National Center for Global Health and Medicine
- Mariko Hakoshima🇯🇵National Center for Global Health and Medicine; Kohnodai Hospital, National Center for Global Health and Medicine
- Hisayuki Katsuyama🇯🇵National Center for Global Health and Medicine; Kohnodai Hospital, National Center for Global Health and Medicine
Resumen
El texto original del estudio, en el idioma en que se publicó.
Randomized controlled trials (RCTs) show that decreases in low-density lipoprotein cholesterol (LDL-C) by the use of statins cause a significant reduction in the development of cardiovascular disease (CVD). However, one of our previous studies showed that, among eight RCTs that investigated the effect of statins vs. a placebo on CVD development, 56-79% of patients had residual CVD risk after the trials. In three RCTs that investigated the effect of a high dose vs. a usual dose of statins on CVD development, 78-87% of patients in the high-dose statin arms still had residual CVD risk. The risk of CVD development remains even when statins are used to strongly reduce LDL-C, and this type of risk is now regarded as statin residual CVD risk. Our study shows that elevated triglyceride (TG) levels, reduced high-density lipoprotein cholesterol (HDL-C), and the existence of obesity/insulin resistance and diabetes may be important metabolic factors that determine statin residual CVD risk. Here, we discuss atherogenic lipoproteins that were not investigated in such RCTs, such as lipoprotein (a) (Lp(a)), remnant lipoproteins, malondialdehyde-modified LDL (MDA-LDL), and small-dense LDL (Sd-LDL). Lp(a) is under strong genetic control by apolipoprotein (a), which is an LPA gene locus. Variations in the LPA gene account for 91% of the variability in the plasma concentration of Lp(a). A meta-analysis showed that genetic variations at the LPA locus are associated with CVD events during statin therapy, independent of the extent of LDL lowering, providing support for exploring strategies targeting circulating concentrations of Lp(a) to reduce CVD events in patients receiving statins. Remnant lipoproteins and small-dense LDL are highly associated with high TG levels, low HDL-C, and obesity/insulin resistance. MDA-LDL is a representative form of oxidized LDL and plays important roles in the formation and development of the primary lesions of atherosclerosis. MDA-LDL levels were higher in CVD patients and diabetic patients than in the control subjects. Furthermore, we demonstrated the atherogenic properties of such lipoproteins and their association with CVD as well as therapeutic approaches.
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