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血糖谱范围内的心血管和肾脏结局:来自英国生物库的见解。

Cardiovascular and Kidney Outcomes Across the Glycemic Spectrum: Insights From the UK Biobank.

机构信息

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.

出版信息

J Am Coll Cardiol. 2021 Aug 3;78(5):453-464. doi: 10.1016/j.jacc.2021.05.004. Epub 2021 May 17.

Abstract

BACKGROUND

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.

OBJECTIVES

This study sought to characterize cardiovascular and kidney outcomes across the glycemic spectrum.

METHODS

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.

RESULTS

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%.

CONCLUSIONS

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.

摘要

背景

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。

目的

本研究旨在描述整个血糖谱中的心血管和肾脏结局。

方法

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。

结果

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。

结论

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。

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