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Glycemic Control: A Combination of Lifestyle Management and the Use of Drugs

机译:血糖控制:生活方式管理和药物使用的结合

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Some 30% of contemporary cardiology patients have coexisting known diabetes, and another 40% have either undiagnosed diabetes or prediabetes. There is still no final conclusive evidence of cardiovascular benefit by good glycemic control in type 2 diabetes, although studies like the United Kingdom Prospective Diabetes Study (UKPDS) and the Prospective Pioglitazone Clinical Trial in Macrovascular Events, and meta-analyses based on these and other randomized controlled trials of blood glucose-lowering therapies have been encouraging. On the other hand, microvascular disease is clearly reduced by good glycemic control. Structured education has remained a mandatory prerequisite of any successful treatment. Not only is appropriate weight management by diet and exercise able to revert new onset diabetes to normal, but it is also the foundation of any successful pharmacotherapy of diabetes. Aiming at normal fasting plasma glucose concentrations of 5.3?mmol/L or 95?mg/dL appears to be safe since publication of the long-term outcome results of the Outcome Reduction with an Initial Glargine INtervention trial. Individualized target glycosylated hemoglobin levels as near to normal as safely possible (i.e., American Diabetes Association /European Association for the Study of Diabetes position statement mentions five options as step two of the treatment algorithm for combination with metformin: sulfonylureas, pioglitazone, dipeptidyl peptidase-4 inhibitors, glucagon-like peptide-1 agonists, and basal insulin.
机译:当代心脏病患者中约30%患有已知的糖尿病,另外40%患有未诊断的糖尿病或糖尿病前期。尽管有英国前瞻性糖尿病研究(UKPDS)和大血管事件前瞻性吡格列酮临床试验以及基于这些和其他方法的荟萃分析等研究,但尚无最终结论性证据表明良好的血糖控制可有效控制2型糖尿病对心血管的益处。降低血糖治疗的随机对照试验令人鼓舞。另一方面,良好的血糖控制可明显减少微血管疾病。结构化教育仍然是任何成功治疗的强制性先决条件。通过饮食和锻炼进行适当的体重管理不仅可以使新发病的糖尿病恢复正常,而且还是成功进行糖尿病药物治疗的基础。自从最初的甘精胰岛素干预试验公布了降低结果的长期结果以来,针对正常的空腹血糖浓度为5.3?mmol / L或95?mg / dL似乎是安全的。个体化的目标糖基化血红蛋白水平应尽可能安全地接近正常水平(即,美国糖尿病协会/欧洲糖尿病研究协会的立场声明提到与二甲双胍联合治疗的第二步治疗方案有五个选择:磺酰脲类,吡格列酮,二肽基肽酶- 4种抑制剂,胰高血糖素样肽1激动剂和基础胰岛素。

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