Pharmacological Management of Cardiac Disease in Patients with Type 2 Diabetes: Insights into Clinical Practice

被引:9
作者
Patoulias, Dimitrios [1 ]
Stavropoulos, Konstantinos [1 ]
Imprialos, Konstantinos [1 ]
Athyros, Vasilios [1 ]
Doumas, Michael [1 ,2 ,3 ]
Karagiannis, Asterios [1 ]
机构
[1] Aristotle Univ Thessaloniki, Gen Hosp Hippokrat, Propedeut Dept Internal Med 2, Thessaloniki, Greece
[2] VA Med Ctr, 50 Irving St NW, Washington, DC 20422 USA
[3] George Washington Univ, Washington, DC USA
关键词
Type; 2; diabetes; cardiovascular disease; mortality; prevention; insulin; glycemic control; ALL-CAUSE MORTALITY; GLUCOSE COTRANSPORTER-2 INHIBITORS; CONTROL CARDIOVASCULAR RISK; CORONARY-ARTERY-DISEASE; PEPTIDASE; INHIBITORS; BLOOD-PRESSURE CONTROL; PRIMARY PREVENTION; HEART-FAILURE; ANTIPLATELET THERAPY; GLYCEMIC CONTROL;
D O I
10.2174/1570161117666190426162746
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Type 2 Diabetes Mellitus (T2DM) has emerged as a growing pandemic. Cardiovascular disease (CVD) constitutes another major health problem, with coronary heart disease being the leading cause of cardiovascular death. Patients with T2DM require a multilevel therapeutic approach, both for primary and secondary prevention of CVD. Objective: To present and summarize the most recent, highest level evidence retrieved from literature, relevant to the pharmaceutical management of CVD in T2DM. Methods: We conducted a comprehensive search of the literature on MEDLINE from its inception till today, primarily for relevant systematic reviews, meta-analyses and randomized controlled trials. Results: There is a trend towards more intensified therapeutic interventions in T2DM, concerning glycemic, lipid and blood pressure control. New drugs, such as sodium-glucose co-transporter 2 (SGLT-2) inhibitors, glucagon-like peptide-1 receptor agonists (GLP-1RAs) and proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors might evolve as key players in the management of diabetes and its complications within the next years. Classic drugs, such as those targeting the renin-angiotensin-aldosterone system, statins and aspirin remain first-line treatment options, both for primary and secondary prevention of CVD. Lifestyle interventions should always be integrated into a complete therapeutic strategy in diabetic patients. Novel drugs, such as finerenone and LCZ696 have provided significant results in cardiovascular outcome studies; however, their role in T2DM has to be further elucidated. Conclusion: Pharmaceutical approach of CVD in T2DM is multilevel and complex. Drug classes featuring pleiotropic effects may boost our armamentarium in the fight against CVD.
引用
收藏
页码:125 / 138
页数:14
相关论文
共 127 条
[1]   Cardiovascular and non-cardiovascular safety of dipeptidyl peptidase-4 inhibition: a meta-analysis of randomized controlled cardiovascular outcome trials [J].
Abbas, A. S. ;
Dehbi, H. -M. ;
Ray, K. K. .
DIABETES OBESITY & METABOLISM, 2016, 18 (03) :295-299
[2]  
Achimastos A, 2016, HORM-INT J ENDOCRINO, V15, P8, DOI [10.14310/horm.2002.1659, 10.1007/BF03401398]
[3]   Systematic review and meta-analysis of different dietary approaches to the management of type 2 diabetes [J].
Ajala, Olubukola ;
English, Patrick ;
Pinkney, Jonathan .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2013, 97 (03) :505-516
[5]   Antiplatelet Therapy in Diabetes: Efficacy and Limitations of Current Treatment Strategies and Future Directions [J].
Angiolillo, Dominick J. .
DIABETES CARE, 2009, 32 (04) :531-540
[6]  
[Anonymous], 2018, DIABETES CARE S1, DOI DOI 10.2337/DC18-S008
[7]  
[Anonymous], 2016, PLOS MED
[8]  
[Anonymous], 2017, COCHRANE DATABASE SY
[9]   Comparison of cardiovascular and metabolic outcomes in people with type 2 diabetes on insulin versus non-insulin glucose-lowering therapies (GLTs): A systematic review and meta-analysis of clinical trials [J].
Anyanwagu, U. ;
Mamza, J. ;
Donnelly, R. ;
Idris, I. .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2016, 121 :69-85
[10]   Efficacy and safety of more intensive lowering of LDL cholesterol: a meta-analysis of data from 170 000 participants in 26 randomised trials [J].
Baigent, C. ;
Blackwell, L. ;
Emberson, J. ;
Holland, L. E. ;
Reith, C. ;
Bhala, N. ;
Peto, R. ;
Barnes, E. H. ;
Keech, A. ;
Simes, J. ;
Collins, R. .
LANCET, 2010, 376 (9753) :1670-1681