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在低收入和中等收入国家引入钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂和胰高血糖素样肽1(GLP1)受体激动剂后胰岛素使用量减少及糖尿病并发症减少:一项微观模拟研究

Reduced insulin use and diabetes complications upon introduction of SGLT-2 inhibitors and GLP1-receptor agonists in low- and middle-income countries: A microsimulation.

出版信息

PLoS Med. 2025 Apr 17;22(4):e1004559. doi: 10.1371/journal.pmed.1004559. eCollection 2025 Apr.

Abstract

BACKGROUND

Diabetes mellitus, particularly type 2 diabetes, is a growing health concern in low- and middle-income countries (LMICs). The potential impact of newer diabetes medications, such as glucagon-like peptide 1 (GLP-1) receptor agonists and sodium-glucose co-transporter-2 (SGLT-2) inhibitors, on insulin dosage and health outcomes in these settings is not well understood.

METHODS AND FINDINGS

We developed a microsimulation model to estimate the impact of treating patients with type 2 diabetes who use insulin with GLP-1 receptor agonists or SGLT-2 inhibitors in LMICs. The model utilized data from the Global Health and Population Project on Access to Care for Cardiometabolic Diseases (HPACC) dataset, encompassing surveys from 79 countries and clinical trial data to estimate insulin dose reduction. We incorporated weight-based insulin dosing formulas and hazard ratios for severe hypoglycemia, cardiovascular and renal outcomes, side effects of new therapies, and mortality. The primary outcome was the change in insulin dosage, and secondary outcomes were disability-adjusted life years (DALYs) lost per 1,000 person-years by diabetes complication (micro- and macro-vascular). Our results indicate that the addition of GLP-1 receptor agonists or SGLT-2 inhibitors could reduce insulin dosage by 8.2 IU/day (IQR: 6.9, 9.5) and 5.3 IU/day (IQR: 4.5, 6.2), respectively. The median DALYs lost per 1,000 person-years decreased from 2.20 (IQR: 1.49, 4.02) to 1.01 (IQR: 0.61, 1.86) with GLP-1 receptor agonists and 1.25 (IQR: 0.81, 2.29) with SGLT-2 inhibitors. Primary benefits arose from weight loss, decreased cardiorenal disease, and decreased mortality, with smaller DALY benefits from the prevention of severe hypoglycemia. Key limitations include the inability to differentiate between type 1 and type 2 diabetes in some datasets and reliance on assumptions from clinical trials conducted primarily in high-income countries.

CONCLUSIONS

The introduction of GLP-1 receptor agonists and SGLT-2 inhibitors for managing type 2 diabetes in LMICs could significantly reduce insulin dosage and associated health risks, leading to improved outcomes and reduced disability. These findings suggest that expanding access to these newer diabetes medications in LMICs could have substantial public health benefits.

摘要

背景

糖尿病,尤其是2型糖尿病,在低收入和中等收入国家(LMICs)正成为一个日益严重的健康问题。新型糖尿病药物,如胰高血糖素样肽1(GLP-1)受体激动剂和钠-葡萄糖协同转运蛋白2(SGLT-2)抑制剂,在这些环境中对胰岛素剂量和健康结果的潜在影响尚不清楚。

方法与结果

我们开发了一个微观模拟模型,以估计在低收入和中等收入国家用GLP-1受体激动剂或SGLT-2抑制剂治疗使用胰岛素的2型糖尿病患者的影响。该模型利用了全球心血管代谢疾病医疗可及性健康与人口项目(HPACC)数据集的数据,包括来自79个国家的调查和临床试验数据,以估计胰岛素剂量的减少。我们纳入了基于体重的胰岛素给药公式以及严重低血糖、心血管和肾脏结局、新疗法的副作用和死亡率的风险比。主要结局是胰岛素剂量的变化,次要结局是每1000人年因糖尿病并发症(微血管和大血管)损失的伤残调整生命年(DALYs)。我们的结果表明,添加GLP-1受体激动剂或SGLT-2抑制剂可分别将胰岛素剂量降低8.2 IU/天(IQR:6.9,9.5)和5.3 IU/天(IQR:4.5,6.2)。使用GLP-1受体激动剂时,每1000人年损失的DALYs中位数从2.20(IQR:1.49,4.02)降至1.01(IQR:0.61,1.86),使用SGLT-2抑制剂时降至1.25(IQR:0.81,2.29)。主要益处来自体重减轻、心脏和肾脏疾病减少以及死亡率降低,预防严重低血糖带来的DALY益处较小。主要局限性包括在某些数据集中无法区分1型和2型糖尿病,以及依赖主要在高收入国家进行的临床试验的假设。

结论

在低收入和中等收入国家引入GLP-1受体激动剂和SGLT-2抑制剂来管理2型糖尿病可显著降低胰岛素剂量及相关健康风险,从而改善结局并减少残疾。这些发现表明,在低收入和中等收入国家扩大获得这些新型糖尿病药物的机会可能会带来重大的公共卫生益处。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/987d/12005516/821cabad80f2/pmed.1004559.g001.jpg

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