Non-diabetes status after diagnosis of impaired glucose tolerance and risk of long-term death and vascular complications: A post hoc analysis of the Da Qing Diabetes Prevention Outcome Study.

IF 15.8 1区 医学 Q1 Medicine PLoS Medicine Pub Date : 2024-07-09 eCollection Date: 2024-07-01 DOI:10.1371/journal.pmed.1004419
Xin Qian, Jinping Wang, Qiuhong Gong, Yali An, Xinxing Feng, Siyao He, Xiaoping Chen, Wenjuan Wang, Lihong Zhang, Yuanchi Hui, Xiuwei Zhai, Bo Zhang, Yanyan Chen, Guangwei Li
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Abstract

Background: The association between years of non-diabetes status after diagnosis of impaired glucose tolerance (IGT) and the risk of long-term death and cardiovascular outcomes needed to be clarified.

Methods and findings: In this post hoc analysis, we included 540 individuals with IGT who participated in the original Da Qing Diabetes Prevention Study (DQDPS). In the DQDPS, all participants were diagnosed with IGT by a 75 g oral glucose tolerance test and randomized to intervention or control groups with a 6-year lifestyle intervention trial. After the completion of the trial, death, cardiovascular events, and microvascular complications were monitored over a 30-year follow-up. In this post hoc analysis, the Cox analysis assessed the extended risk of these outcomes in individuals who either remained non-diabetes status or progressed to diabetes at the end of 2, 4, and 6 years after diagnosis of IGT. In all participants, the difference in the cumulative incidence rate of the outcomes between the diabetes and non-diabetes group gradually increased over 30 years. Compared with the diabetes group, a significantly lower risk of all-cause death (hazard ratio [HR]: 0.74; 95% confidence interval [CI]: 0.57 to 0.97, p = 0.026), cardiovascular events (HR: 0.63; 95% CI: 0.49 to 0.82, p < 0.001), and microvascular complications (HR: 0.62; 95% CI: 0.45 to 0.86, p = 0.004) first emerged in individuals who remained non-diabetes at the 4 years visit, whereas the significant risk reduction in cardiovascular death was first observed at the end of 6 years (HR: 0.56; 95% CI: 0.39 to 0.81, p = 0.002) after adjustment for age, sex, smoking status, BMI, systolic blood pressure, blood glucose, total cholesterol, intervention, and medications (including insulin plus oral hypoglycaemics, antihypertensives, and lipid-lowering agents). The results in the original intervention group alone were similar to the whole group. The main limitations of our study are the limited number of participants and the sole ethnicity of the Chinese population.

Conclusions: In this study, we observed that maintaining several years of non-diabetes status after IGT diagnosis was associated with a significant reduction in long-term risk of death and vascular complications, and for most of these outcomes, maintaining at least 4 years of non-diabetes status may be needed to achieve a significant risk reduction.

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确诊糖耐量受损后的非糖尿病状态与长期死亡和血管并发症的风险:大庆糖尿病预防结果研究的事后分析。
背景:糖耐量减低症(IGT)确诊后未患糖尿病的年数与长期死亡和心血管疾病风险之间的关系需要明确:糖耐量减低症(IGT)确诊后的非糖尿病状态年限与长期死亡和心血管疾病风险之间的关系需要明确:在这项事后分析中,我们纳入了参与最初的大庆糖尿病预防研究(DQDPS)的540名IGT患者。在大庆糖尿病预防研究中,所有参与者均通过 75 克口服葡萄糖耐量试验确诊为 IGT,并随机分为干预组和对照组,进行为期 6 年的生活方式干预试验。试验结束后,对死亡、心血管事件和微血管并发症进行了长达30年的随访监测。在这项事后分析中,Cox 分析评估了在确诊 IGT 后 2 年、4 年和 6 年末,保持非糖尿病状态或发展为糖尿病的个体发生这些结果的扩展风险。在所有参与者中,糖尿病组和非糖尿病组之间的结果累积发生率差异在30年内逐渐增大。与糖尿病组相比,全因死亡风险明显降低(危险比 [HR]:0.74; 95% 置信区间 [CI]:与糖尿病组相比,全因死亡风险(危险比 [HR]:0.74;95% 置信区间 [CI]:0.57 至 0.97,p = 0.026)、心血管事件(HR:0.63;95% CI:0.49 至 0.82,p < 0.001)和微血管并发症(HR:0.62;95% CI:0.45 至 0.86,p = 0.004)的显著降低首先出现在 4 年访视时仍未患糖尿病的人群中,而心血管死亡风险的显著降低则首次出现在 6 年末(HR:0.56; 95% CI: 0.39 to 0.81, p = 0.002),这是在调整了年龄、性别、吸烟状况、体重指数、收缩压、血糖、总胆固醇、干预措施和药物(包括胰岛素加口服降糖药、降压药和降脂药)之后得出的结果。原干预组的结果与全组相似。我们研究的主要局限性在于参与者人数有限,而且只有中国人:在这项研究中,我们观察到在确诊 IGT 后维持数年的非糖尿病状态与显著降低死亡和血管并发症的长期风险有关。
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来源期刊
PLoS Medicine
PLoS Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
17.60
自引率
0.60%
发文量
227
审稿时长
4-8 weeks
期刊介绍: PLOS Medicine is a prominent platform for discussing and researching global health challenges. The journal covers a wide range of topics, including biomedical, environmental, social, and political factors affecting health. It prioritizes articles that contribute to clinical practice, health policy, or a better understanding of pathophysiology, ultimately aiming to improve health outcomes across different settings. The journal is unwavering in its commitment to uphold the highest ethical standards in medical publishing. This includes actively managing and disclosing any conflicts of interest related to reporting, reviewing, and publishing. PLOS Medicine promotes transparency in the entire review and publication process. The journal also encourages data sharing and encourages the reuse of published work. Additionally, authors retain copyright for their work, and the publication is made accessible through Open Access with no restrictions on availability and dissemination. PLOS Medicine takes measures to avoid conflicts of interest associated with advertising drugs and medical devices or engaging in the exclusive sale of reprints.
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