Association of long-term insulin variability before the onset of diabetes with cardiovascular outcomes in later life: Findings from the coronary artery risk development in young adults (CARDIA) study

IF 4.3 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS American journal of preventive cardiology Pub Date : 2025-03-08 DOI:10.1016/j.ajpc.2025.100952
Kun Zhang , Chunlan Huang , Junping Li , Peibiao Mai , Shuwan Xu , Feifei Huang , Wanbing He , Huanji Zhang , Yang Liu , Weijing Feng
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Abstract

Background

The important effects of variability of some physiological/biological characteristics (such as LDL cholesterol, blood pressure) on cardiovascular outcomes have been elucidated, while the role of insulin variability is undefined.

Objectives

To investigate the associations of long-term fasting insulin variability during young adulthood before the onset of diabetes with subsequent cardiovascular outcomes in middle age.

Methods

We included 3,983 CARDIA (Coronary Artery Risk Development Study in Young Adults) participants aged 18 to 30 years with at least three fasting insulin measurements. Intra-individual fasting insulin variability was defined by the average real variability (ARV) of insulin and standard deviation (SD) of insulin during 30-year follow-up. The presence and the degree of coronary artery calcification (CAC) were assessed by computed tomography at year 25. Incident cardiovascular disease (CVD) and all-cause mortality were adjudicated.

Results

After multivariable adjustment, comparing high versus low tertile of insulin ARV, the hazard of CVD increased by 65 % (HR, 1.65; 95 % CI, 1.13–2.39) and all-cause mortality by 97 % (HR, 1.97; 95 % CI, 1.38–2.82). Higher tertile of insulin ARV was associated with significantly worse degree of CAC (β =0.1; 95 % CI, 0.03–0.18) but not with the presence of CAC (P = 0.197). Similar results were also observed in insulin SD.

Conclusion

High long-term insulin variability in young adulthood before the onset of diabetes was associated with an increased risk of CVD and all-cause mortality in later life, independent of average FG, HOMA-IR and other established cardiovascular risk factors. Long-term insulin variability was associated with the degree but not the presence of CAC.

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背景一些生理/生物特征(如低密度脂蛋白胆固醇、血压)的变化对心血管预后的重要影响已被阐明,而胰岛素变化的作用尚未明确。方法 我们纳入了 3,983 名年龄在 18-30 岁之间、至少进行过三次空腹胰岛素测量的 CARDIA(年轻人冠状动脉风险发展研究)参与者。个体内空腹胰岛素变异性由 30 年随访期间的胰岛素平均实际变异性 (ARV) 和胰岛素标准偏差 (SD) 来定义。冠状动脉钙化(CAC)的存在和程度在第 25 年时通过计算机断层扫描进行评估。结果经多变量调整后,比较胰岛素ARV的高三分位数与低三分位数,心血管疾病的风险增加了65%(HR,1.65;95% CI,1.13-2.39),全因死亡率增加了97%(HR,1.97;95% CI,1.38-2.82)。胰岛素抗逆转录病毒药物的三等分值越高,CAC程度越严重(β =0.1; 95 % CI, 0.03-0.18),但与是否存在CAC无关(P = 0.197)。结论糖尿病发病前青壮年时期胰岛素的长期高变异性与晚年心血管疾病和全因死亡风险的增加有关,与平均 FG、HOMA-IR 和其他已确定的心血管风险因素无关。长期胰岛素变化与CAC的程度有关,但与CAC的存在无关。
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来源期刊
American journal of preventive cardiology
American journal of preventive cardiology Cardiology and Cardiovascular Medicine
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6.60
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76 days
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