Effects of High Intensity Statin Therapy in the Treatment of Diabetic Dyslipidemia in Patients with Coronary Artery Disease

2018 ◽  
Vol 24 (4) ◽  
pp. 427-441 ◽  
Author(s):  
Marija Vavlukis ◽  
Sasko Kedev

Background: Diabetic dyslipidemia has specifics that differ from dyslipidemia in patients without diabetes, which contributes to accelerated atherosclerosis equally as dysglycemia. The aim of this study was to deduce the interdependence of diabetic dyslipidemia and cardiovascular diseases (CVD), therapeutic strategies and the risk of diabetes development with statin therapy. Method: We conducted a literature review of English articles through PubMed, PubMed Central and Cochrane, on the role of diabetic dyslipidemia in atherosclerosis, the antilipemic treatment with statins, and the role of statin therapy in newly developed diabetes, by using key words: atherosclerosis, diabetes mellitus, diabetic dyslipidemia, CVD, statins, nicotinic acid, fibrates, PCSK9 inhibitors. Results: hyperglycemia and dyslipidemia cannot be treated separately in patients with diabetes. It seems that dyslipidemia plays one of the key roles in the development of atherosclerosis. High levels of TG, decreased levels of HDL-C and increased levels of small dense LDL- C particles in the systemic circulation are the most specific attributes of diabetic dyslipidemia, all of which originate from an inflated flux of free fatty acids occurring due to the preceding resistance to insulin, and exacerbated by elevated levels of inflammatory adipokines. Statins are a fundamental treatment for diabetic dyslipidemia, both for dyslipidemia and for CVD prevention. The use of statin treatment with high intensity is endorsed for all diabetes-and-CVD patients, while a moderate - intensity treatment can be applied to patients with diabetes, having additional risk factors for CVD. Statins alone are thought to possess a small, although of statistical significance, risk of incident diabetes, outweighed by their benefits. Conclusion: As important as hyperglycemia and glycoregulation are in CVD development in patients with diabetes, diabetic dyslipidemia plays an even more important role. Statins remain the cornerstone of antilipemic treatment in diabetic dyslipidemia, and their protective effects in CVD progression overcome the risk of statin- associated incident diabetes.

2020 ◽  
Vol 6 (4) ◽  
pp. 323-331
Author(s):  
Jonas Banefelt ◽  
Maria Lindh ◽  
Maria K Svensson ◽  
Björn Eliasson ◽  
Ming-Hui Tai

Abstract Aims Clinical studies have demonstrated the efficacy of intensive statin therapy in lowering low-density lipoprotein cholesterol and cardiovascular (CV) events. Our objective was to examine statin titration patterns and the association between titration patterns and subsequent CV events in very high-risk patients. Methods and results Using Swedish national population-based registry data, we identified 192 435 patients with very high risk of atherosclerotic CV disease initiated on moderate-intensity statin therapy between 2006 and 2013. Outcomes of interest were titration to high-intensity therapy and the major adverse cardiovascular events (MACE) composite (myocardial infarction, ischaemic stroke, and CV death) outcome. Cumulative incidence of MACE was assessed by titration status 1-year post-treatment initiation in patients adherent to treatment during the first year, using a 12-week cut-off from initiation to define early, delayed and no up-titration to high-intensity statins. Cox regression analysis was used to estimate adjusted hazard ratios (HRs). In 144 498 eligible patients, early titration was associated with significantly lower risk of MACE in the subsequent 2 years compared to no up-titration (HR 0.76, P < 0.01]. Delayed up-titration was associated with a smaller reduction (HR 0.88, P = 0.08). The majority of patients did not up-titrate. Conclusion Early up-titration to high-intensity statins was independently associated with lower risk of subsequent CV events compared to no up-titration. Delayed up-titration was not associated with the same benefit. Despite the higher risk associated with no up-titration, few patients at very high CV risk who started treatment on moderate-intensity up-titrated to high intensity, indicating a potential need for more aggressive lipid management of these patients in clinical practice.


2010 ◽  
Vol 7 (2) ◽  
pp. 92
Author(s):  
Alberico L Catapano ◽  
Liliana Grigore ◽  
Angela Pirillo ◽  
◽  
◽  
...  

Diabetes increases the risk of developing cardiovascular disease (CVD), and several guidelines suggest that subjects with diabetes are at high risk of developing CVD. The increased risk can be attributed, at least in part, to associated risk factors, including hypertension and dyslipidaemia. The role of statins in primary and secondary prevention of CVD is well established, and the positive effect has been clearly demonstrated also in patients with type 2 diabetes. A number of studies have evaluated the effect of statin therapy on incident CVD and shown that statin therapy produces a great reduction in cardiovascular risk, but a recent meta-analysis revealed a slight increase in the risk of developing diabetes. Such risk is, however, low, especially when compared with the reduction in cardiovascular events and should not interfere with the choice of treating diabetic patients with a cholesterol-lowering therapy.


2018 ◽  
Vol 24 (7) ◽  
pp. 1095-1101 ◽  
Author(s):  
Hee Sue Park ◽  
Ja-Yoon Gu ◽  
Hyun Ju Yoo ◽  
Se Eun Han ◽  
Chan Ho Park ◽  
...  

Statins not only have a lipid-lowering effect but also reduce inflammation and have an antithrombotic effect. Since hypercoagulability assessed by thrombin generation assay (TGA) and increased formation of neutrophil extracellular traps (NET) were demonstrated in diabetes, we investigated whether statin therapy in diabetes modifies coagulation status and NET formation. Twenty-five consecutive patients with diabetes were recruited. Global coagulation assays (prothrombin time [PT], activated partial thromboplastin time [aPTT], and TGA) and NET markers (DNA–histone complex, cell-free DNA, and neutrophil elastase) were measured before and after 3-month moderate-intensity statin therapy. In addition, all coagulation factors and 3 anticoagulation factors were measured. Statin therapy significantly reduced endogenous thrombin potential (ETP) value and blood lipids but did not change the PT and aPTT values or NET formation markers. Statin significantly decreased not only coagulation factors (II, V, VIII, IX, and X) but also the anticoagulation factor antithrombin. Statin-induced reduction of factor V and X significantly contributed to the reduction of ETP value. The extent of reduction in coagulation factors correlated with that of anticoagulation factors, but not that of cholesterol. It is possible to use TGA as a global coagulation assay that can detect coagulation status modified by statin therapy. Additional studies are needed to evaluate the clinical implications of statin-induced simultaneous reduction of coagulation and anticoagulation factors.


2020 ◽  
pp. 317-319
Author(s):  
V.O. Shumakov

Background. Computed tomography studies of ancient mummies have shown that the representatives of all ancient civilizations had atherosclerosis. It is now known that the severity of atherosclerosis depends on the content of non-high density lipoprotein cholesterol (nHDL-C) and age. A detailed analysis of global statistics on mortality from cardiovascular disease (CVD) found that the mortality of Ukrainian men and women is 14 and 23 times higher than the French counterparts. However, since the beginning of the 21st century, almost all European middle-income countries have reached a decline in mortality, probably due to the implementation of programs to combat hypertension and dyslipidemia. Objective. To describe modern pharmacotherapy of coro- nary heart disease. Materials and methods. Analysis of the literature on this topic. Results and discussion. A significant proportion of deaths are due to acute coronary heart disease. Long-term treat- ment of patients after myocardial infarction should include control of risk factors and lifestyle changes, antithrombotic therapy, use of b-blockers, angiotensin-converting enzyme inhibitors, mineralocorticoid receptor inhibitors, lipid-lowering therapy. Serial intravascular ultrasound studies have shown that high-intensity statin therapy has reduced the burden of atherosclerotic plaques in non-infarct-dependent arteries (from 67.5 to 58.5 %). In addition to slowing atherosclerosis, statins also increase plaque calcification and improve its stability. Medium-intensity statin therapy reduces low-density lipoprotein cholesterol (LDL-C) by 30 %, high-intensity statin therapy – by 50 %, high-intensity statin therapy in combination with ezetimibe – by 65 %, PCSK9 inhibitors – by 60 %, high-intensity statin and PCSK9 inhibitors – by 75 %, highintensity statin therapy in combination with PCSK9 inhibitors and ezetimibe – by 85 %. The FOURIER study confirmed the high efficacy of PCSK9 inhibitors in reducing LDL-C in high-risk patients. The hazard ratio for the composite endpoint (cardiovascular death, myocardial infarction, CVD hospitaliza- tion, need for revascularization) for evolocumab compared to placebo was 0.85 (p<0.0001). The ODYSSEY OUTCOMES study found similar results for alirocumab. In general, statin therapy with a decrease in LDL-C of more than 50 % and/or to a level <1.4 mmol/L is recommended for all patients with acute coro- nary syndrome without ST segment elevation. If maximal dose of statins does not allow to reach such results in 4-6 weeks, it is recommended to add ezetimibe. In the absence of effect on the background of treatment with this combination, it is necessary to add PCSK9 inhibitors. In the context of the COVID-19 pandemic, it is necessary to continue taking all cardiac drugs, including statins. There is evidence that statins help to reduce the severity of viral pneumonia and to decrease the mortality from acute respiratory viral infections. Statins have a number of pleiotropic effects: anti-inflammatory, immunomodulatory, antioxidant, and antithrombotic. All of them are favorable for coronavirus infection. In addition to statins, in coronary heart disease it is advisable to prescribe metabolic therapy. Tivorel (“Yuria-Pharm”) is indicated for coronary heart disease, acute myocardial infarction and after a heart attack. Already on the third day of treatment of acute coronary syn- drome, the effectiveness of basic therapy in combination with Tivorel (100 ml per day) exceeds the effectiveness of basic therapy only in reducing the incidence of anginal pain by 35 % and the use of opioid analgesics in case of pain by 38 % (Vakaliuk I.P., 2015). Foreign studies confirm that L-arginine reduces the symptoms of angina and improves the quality of life of patients, reduces blood pressure and pulmonary artery pressure in patients with pulmonary hypertension. Apart from that, L-carnitine helps to increase the ejection fraction and re- duce the area of myocardial infarction, eliminate arrhythmias, reduce cardiovascular mortality. Tivorel has a beneficial effect on left ventricular remodeling. After 10 days of basic therapy in combination with Tivorel, the end systolic volume of the left ventricle in post-infarction patients is reduced by 16 %, and in the group of basic therapy – by 3 %. 32-80 % of CVD patients have mental disorders that increase the risk of death. Lodixem (“Yuria-Pharm”) is a specialized cardioprotector with a daytime tranquilizer effect. The effectiveness of Lodixem in the combined therapy of stable angina, hypertension, heart failure, acute coronary syndrome has been proven. Conclusions. 1. Long-term therapy of patients after myo- cardial infarction should include control of risk factors and lifestyle changes, antithrombotic therapy, use of b-blockers, angiotensin-converting enzyme inhibitors, mineralocorticoid receptor inhibitors, and lipid-lowering therapy. 2. All patients with acute coronary syndrome without ST segment elevation are recommended statin therapy with a decrease in LDL-C by more than 50 % and/or to a level <1.4 mmol/L. 3. In the context of the COVID-19 pandemic, it is necessary to continue taking all cardiac drugs, including statins. 4. Tivorel reduces the incidence of anginal pain, the use of opioid analgesics for pain, and has a beneficial effect on left ventricular remodeling. 5. Lodixem (a specialized cardioprotector with the effect of a daytime tranquilizer) is effective in the treatment of stable angina, hypertension, heart failure, acute coronary syndrome.


2019 ◽  
Vol 14 (6) ◽  
pp. 922-934 ◽  
Author(s):  
Yu. A. Karpov

The aim of this review was to present the recently published results of ODYSSEY OUTCOMES trial and discuss the clinical perspective of these data. Patients with acute coronary syndrome are at very high risk of recurrent ischemic cardiovascular complications, especially during the first year after the event. The use of high-intensity statin therapy in this group of patients does not always lead to the achievement of target levels of atherogenic lipoproteins. PCSK9 inhibitors, administered in addition to statins, can provide additional reduction of low-density lipoprotein cholesterol, which leads to further improvements of outcomes in patients with atherosclerotic cardiovascular disease. According to the latest results from ODYSSEY OUTCOMES trial, among patients with recent acute coronary syndrome, who were receiving high-intensity statin therapy, the risk of recurrent ischemic cardiovascular events was lower among those who were treated with alirocumab then among those who received placebo. The treatment with alirocumab in patients with recent acute coronary syndrome was associated with reduction in death from any causes. The absolute risk reduction with alirocumab was the most prominent in the subpopulation of patients with low-density lipoprotein cholesterol ≥2,6 mmol/l at baseline. These results have implication for clinical practice and may play an important role for the improvement of outcomes in patients at highest cardiovascular risk after acute cardiovascular syndrome.


Stroke ◽  
2015 ◽  
Vol 46 (suppl_1) ◽  
Author(s):  
Melissa A Greiner ◽  
Emily O'Brien ◽  
Ying Xian ◽  
Deepak L Bhatt ◽  
Lesley Maisch ◽  
...  

Background: Current treatment guidelines recommend high-intensity statin therapy for patients with a history of stroke. However, older patients with higher comorbidity were under-represented in trials and dosing varies in clinical practice. We compared the effectiveness of high vs moderate-intensity statins on clinical outcomes in older patients from the GWTG-Stroke registry. Methods: We studied statin-naïve ischemic stroke patients ≥65 years from GWTG-Stroke linked to Medicare claims from 2008-2011 who were discharged on statins. Outcomes included home time days (days alive and not in acute or post-acute care facility), major adverse cardiovascular events (MACE), mortality, all-cause, stroke and CV readmission within 2 years of discharge. We estimated unadjusted and adjusted associations between statin intensity and outcomes using negative binomial and Cox proportional hazards models. Inverse-weighted estimates of the probability of high-intensity statin (IPW) were used to adjust for treatment selection. Results: Of 29,631 ischemic stroke patients discharged on statins, 9,145 (31%) received high-intensity statins. Patients receiving high-intensity statins were younger and had higher LDL-C compared with patients on moderate-intensity statins. The high-intensity statin group had 5 fewer home time days and higher all-cause readmission within 2 years, but other observed outcomes were similar (Table). Except for a slightly higher hazard of all-cause readmission with high-intensity statin use, there were no significant differences in MACE, hemorrhagic stroke, or other outcomes after IPW adjustment (Table). Conclusions: We found no differences in MACE or home time days within 2 years of initiation of high vs. moderate-intensity statin therapy following ischemic stroke. These findings can inform patients and clinicians regarding the risk-benefit associated with statin dosing after ischemic stroke.


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