Scirica Benjamin M
TIMI Study Group, Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Clin Chem. 2017 Jan;63(1):186-195. doi: 10.1373/clinchem.2016.255539.
As the worldwide prevalence of type 2 diabetes mellitus (T2DM) increases, it is even more important to develop cost-effective methods to predict and diagnose the onset of diabetes, monitor progression, and risk stratify patients in terms of subsequent cardiovascular and diabetes complications.
Nonlaboratory clinical risk scores based on risk factors and anthropomorphic data can help identify patients at greatest risk of developing diabetes, but glycemic indices (hemoglobin A, fasting plasma glucose, and oral glucose tolerance tests) are the cornerstones for diagnosis, and the basis for monitoring therapy. Although family history is a strong predictor of T2DM, only small populations of patients carry clearly identifiable genetic mutations. Better modalities for detection of insulin resistance would improve earlier identification of dysglycemia and guide effective therapy based on therapeutic mechanisms of action, but improved standardization of insulin assays will be required. Although clinical risk models can stratify patients for subsequent cardiovascular risk, the addition of cardiac biomarkers, in particular, high-sensitivity troponin and natriuretic peptide provide, significantly improves model performance and risk stratification.
Much more research, prospectively planned and with clear treatment implications, is needed to define novel biomarkers that better identify the underlying pathogenic etiologies of dysglycemia. When compared with traditional risk features, biomarkers provide greater discrimination of future risk, and the integration of cardiac biomarkers should be considered part of standard risk stratification in patients with T2DM.
随着2型糖尿病(T2DM)在全球的患病率上升,开发具有成本效益的方法来预测和诊断糖尿病的发病、监测病情进展以及根据后续心血管和糖尿病并发症对患者进行风险分层变得更加重要。
基于风险因素和人体测量数据的非实验室临床风险评分有助于识别患糖尿病风险最高的患者,但血糖指标(糖化血红蛋白、空腹血糖和口服葡萄糖耐量试验)是诊断的基石以及监测治疗的基础。虽然家族史是T2DM的有力预测指标,但只有一小部分患者携带可明确识别的基因突变。更好地检测胰岛素抵抗的方法将有助于更早地识别血糖异常,并根据治疗作用机制指导有效治疗,但需要改进胰岛素检测的标准化。虽然临床风险模型可以对患者的后续心血管风险进行分层,但加入心脏生物标志物,特别是高敏肌钙蛋白和利钠肽,可显著提高模型性能和风险分层。
需要开展更多前瞻性规划且具有明确治疗意义的研究,以确定能更好地识别血糖异常潜在致病病因的新型生物标志物。与传统风险特征相比,生物标志物能更准确地判别未来风险,应考虑将心脏生物标志物纳入T2DM患者标准风险分层的一部分。