Department of Health Outcomes and Policy, College of Medicine, University of Florida, Gainesville, FL, USA.
Department of Medicine, Johns Hopkins University, Baltimore, MD, USA.
Diabetologia. 2017 Jul;60(7):1261-1270. doi: 10.1007/s00125-017-4267-6. Epub 2017 Apr 4.
AIMS/HYPOTHESIS: The study aimed to assess for an association between the degree of severity of the metabolic syndrome and risk of type 2 diabetes beyond that conferred by the individual components of the metabolic syndrome.
We assessed HRs for an Adult Treatment Panel III (ATP-III) metabolic syndrome score (ATP-III MetS) and a sex- and race-specific continuous metabolic syndrome severity z score related to incident diabetes over a median of 7.8 years of follow-up among participants of two observational cohorts, the Atherosclerosis Risk in Communities study (n = 10,957) and the Jackson Heart Study (n = 2137).
The ATP-III MetS had an HR for incident diabetes of 4.36 (95% CI 3.83, 4.97), which was attenuated in models that included the individual metabolic syndrome components. By contrast, participants in the fourth quartile of metabolic syndrome severity (compared with the first quartile) had an HR of 17.4 (95% CI 12.6, 24.1) for future diabetes; in models that also included the individual metabolic syndrome components, this remained significant, with an HR of 3.69 (95% CI 2.42, 5.64). There was a race × metabolic syndrome interaction in these models such that HR was greater for black participants (5.30) than white participants (2.24). When the change in metabolic syndrome severity score was included in the hazard models, this conferred a further association, with changes in metabolic syndrome severity score of ≥0.5 having a HR of 2.66 compared with changes in metabolic syndrome severity score of ≤0.
CONCLUSIONS/INTERPRETATION: Use of a continuous sex- and race-specific metabolic syndrome severity z score provided an additional prediction of risk of diabetes beyond that of the individual metabolic syndrome components, suggesting an added risk conferred by the processes underlying the metabolic syndrome. Increases in this score over time were associated with further risk, supporting the potential clinical utility of following metabolic syndrome severity over time.
目的/假设:本研究旨在评估代谢综合征严重程度与 2 型糖尿病风险之间的关联,这种关联超出了代谢综合征各组成部分所赋予的关联。
我们评估了成人治疗小组 III(ATP-III)代谢综合征评分(ATP-III MetS)和与性别和种族相关的连续代谢综合征严重程度 z 评分与两个观察队列参与者中发生糖尿病的风险之间的 HR,中位随访时间为 7.8 年。该队列包括动脉粥样硬化风险社区研究(n=10957)和杰克逊心脏研究(n=2137)。
ATP-III MetS 发生糖尿病的 HR 为 4.36(95%CI 3.83,4.97),在纳入单个代谢综合征成分的模型中,这种 HR 会减弱。相比之下,代谢综合征严重程度第四四分位数(与第一四分位相比)的参与者未来患糖尿病的 HR 为 17.4(95%CI 12.6,24.1);在也包括单个代谢综合征成分的模型中,这仍然显著,HR 为 3.69(95%CI 2.42,5.64)。在这些模型中存在种族与代谢综合征的相互作用,使得黑人参与者(5.30)的 HR 大于白人参与者(2.24)。当代谢综合征严重程度评分的变化被纳入危险模型时,这进一步产生了关联,与代谢综合征严重程度评分变化≥0.5 相比,代谢综合征严重程度评分变化≤0 的 HR 为 2.66。
结论/解释:使用连续的性别和种族特异性代谢综合征严重程度 z 评分提供了一种预测糖尿病风险的方法,这种方法超出了代谢综合征各组成部分所赋予的预测方法,这表明代谢综合征潜在的过程赋予了额外的风险。随着时间的推移,该评分的增加与更高的风险相关,支持随着时间的推移跟踪代谢综合征严重程度的潜在临床效用。