Cardiology Division, Massachusetts General Hospital, Boston, Massachusetts, USA; Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, Massachusetts, USA; Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA; Harvard Medical School, Boston, Massachusetts, USA.
Program in Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, Massachusetts, USA; Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA; Computational Biology and Bioinformatics Program, Yale University, New Haven, Connecticut, USA. Electronic address: https://twitter.com/zekavatm.
J Am Coll Cardiol. 2021 Aug 3;78(5):453-464. doi: 10.1016/j.jacc.2021.05.004. Epub 2021 May 17.
Treatment guidelines for prediabetes primarily focus on glycemic control and lifestyle management. Few evidence-based cardiovascular and kidney risk-reduction strategies are available in this population.
This study sought to characterize cardiovascular and kidney outcomes across the glycemic spectrum.
Among participants in the UK Biobank without prevalent type 1 diabetes, cardiovascular disease, or kidney disease, Cox models tested the association of glycemic exposures (type 2 diabetes [T2D], prediabetes, normoglycemia) with outcomes (atherosclerotic cardiovascular disease [ASCVD], chronic kidney disease [CKD], and heart failure), adjusting for demographic, lifestyle, and cardiometabolic risk factors.
Among 336,709 individuals (mean age: 56.3 years, 55.4% female), 46,911 (13.9%) had prediabetes and 12,717 (3.8%) had T2D. Over median follow-up of 11.1 years, 6,476 (13.8%) individuals with prediabetes developed ≥1 incident outcome, of whom only 802 (12.4%) developed T2D prior to an incident diagnosis. Prediabetes and T2D were independently associated with ASCVD (prediabetes: adjusted HR [aHR]: 1.11; 95% CI: 1.08-1.15; P < 0.001; T2D: aHR: 1.44; 95% CI: 1.37-1.51; P < 0.001), CKD (prediabetes: aHR: 1.08; 95% CI: 1.02-1.14; P < 0.001; T2D: aHR: 1.57; 95% CI: 1.46-1.69; P < 0.001), and heart failure (prediabetes: aHR: 1.07; 95% CI: 1.01-1.14; P = 0.03; T2D: aHR: 1.25; 95% CI: 1.14-1.37; P < 0.001). Compared with hemoglobin A1c (HbA1c) <5.0%, covariate-adjusted risks increased significantly for ASCVD above HbA1c of 5.4%, CKD above HbA1c of 6.2%, and heart failure above HbA1c of 7.0%.
Prediabetes and T2D were associated with ASCVD, CKD, and heart failure, but a substantial gradient of risk was observed across HbA levels below the threshold for diabetes. These findings highlight the need to design risk-reduction strategies across the glycemic spectrum.
针对糖尿病前期的治疗指南主要侧重于血糖控制和生活方式管理。在这一人群中,很少有基于证据的心血管和肾脏风险降低策略。
本研究旨在描述整个血糖谱中的心血管和肾脏结局。
在英国生物银行中没有现患 1 型糖尿病、心血管疾病或肾脏疾病的参与者中,Cox 模型测试了血糖暴露(2 型糖尿病 [T2D]、糖尿病前期、正常血糖)与结局(动脉粥样硬化性心血管疾病 [ASCVD]、慢性肾脏病 [CKD] 和心力衰竭)之间的关联,调整了人口统计学、生活方式和心血管代谢危险因素。
在 336709 名参与者(平均年龄:56.3 岁,55.4%为女性)中,46911 名(13.9%)患有糖尿病前期,12717 名(3.8%)患有 T2D。在中位随访 11.1 年后,6476 名(13.8%)患有糖尿病前期的患者发生了≥1 次的事件结局,其中只有 802 名(12.4%)在发生事件诊断前患有 T2D。糖尿病前期和 T2D 与 ASCVD(糖尿病前期:调整后的 HR [aHR]:1.11;95%置信区间:1.08-1.15;P<0.001;T2D:aHR:1.44;95%置信区间:1.37-1.51;P<0.001)、CKD(糖尿病前期:aHR:1.08;95%置信区间:1.02-1.14;P<0.001;T2D:aHR:1.57;95%置信区间:1.46-1.69;P<0.001)和心力衰竭(糖尿病前期:aHR:1.07;95%置信区间:1.01-1.14;P=0.03;T2D:aHR:1.25;95%置信区间:1.14-1.37;P<0.001)独立相关。与血红蛋白 A1c(HbA1c)<5.0%相比,ASCVD 在 HbA1c 高于 5.4%、CKD 在 HbA1c 高于 6.2%以及心力衰竭在 HbA1c 高于 7.0%时,经协变量调整的风险显著增加。
糖尿病前期和 T2D 与 ASCVD、CKD 和心力衰竭相关,但在低于糖尿病阈值的 HbA 水平下,风险呈显著梯度。这些发现强调了在整个血糖谱中设计降低风险策略的必要性。