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起始常见抗 HIV 逆转录病毒药物后发生 2 型糖尿病。

Incident type 2 diabetes mellitus after initiation of common HIV antiretroviral drugs.

机构信息

NYU Langone Medical Center.

AIDS Healthcare Foundation, New York City, New York.

出版信息

AIDS. 2021 Jan 1;35(1):81-90. doi: 10.1097/QAD.0000000000002718.

Abstract

OBJECTIVES

To describe the prevalence and incidence of prediabetes and type 2 diabetes mellitus (T2DM) among people living with HIV (PLHIV) and evaluate the association between antiretroviral therapy (ART) initiation with dolutegravir (DTG), elvitegravir/cobicistat (EVG/c), raltegravir (RAL), or boosted darunavir (bDRV) and incident T2DM.

DESIGN

Longitudinal study based on electronic health records of 29 674 PLHIV from the Observational Pharmaco-Epidemiology Research and Analysis (OPERA) cohort.

METHODS

Calculate prevalence of prediabetes and T2DM at regimen initiation. Among PLHIV without prevalent disease, estimate prediabetes and T2DM incidence (Poisson regression) and association between regimen and incident T2DM (multivariate Cox proportional hazards regression). Analyses stratified by ART experience.

RESULTS

Among ART-naive and ART-experienced/suppressed PLHIV, the estimated prevalence of prediabetes was 8 and 11%; that of T2DM was 4 and 10%, respectively. The T2DM incidence rate was 9 per 1000 person-years [95% confidence interval (CI): 8-11] among ART-naive and 13 per 1000 person-years (95% CI: 12-15) among ART-experienced/suppressed PLHIV, with no statistically significant differences between regimens. Compared with DTG, no statistically significant association between T2DM risk and regimen was observed among ART-naive on EVG/c [adjusted hazard ratios: 0.70 (95% CI: 0.47-1.05)] or bDRV [0.53 (0.26-1.04)] and ART-experienced/suppressed on EVG/c [0.96 (0.70-1.33)], RAL [1.17 (0.70-1.96)] or bDRV [0.90 (0.57-1.42)].

CONCLUSION

No increased risk of T2DM was observed with EVG/c, RAL or bDRV compared with DTG in ART-naive and experienced PLHIV. However, despite a large cohort, there was a small number of events and differential risk cannot be excluded.

摘要

目的

描述艾滋病毒感染者(PLHIV)中糖尿病前期和 2 型糖尿病(T2DM)的患病率和发病率,并评估以多替拉韦(DTG)、艾维雷格/考比司他(EVG/c)、拉替拉韦(RAL)或增效达芦那韦(bDRV)起始抗逆转录病毒治疗(ART)与 T2DM 发病之间的关系。

设计

基于 29674 名来自观察性药物流行病学研究和分析(OPERA)队列的 PLHIV 的电子健康记录的纵向研究。

方法

计算方案起始时糖尿病前期和 T2DM 的患病率。在无现有疾病的 PLHIV 中,估计糖尿病前期和 T2DM 的发病率(泊松回归)以及方案与 T2DM 发病之间的关系(多变量 Cox 比例风险回归)。按 ART 经验进行分层分析。

结果

在初治和经治/抑制的 PLHIV 中,糖尿病前期的估计患病率分别为 8%和 11%;T2DM 的患病率分别为 4%和 10%。初治 PLHIV 的 T2DM 发病率为每 1000 人年 9 例[95%置信区间(CI):8-11],经治/抑制 PLHIV 的发病率为每 1000 人年 13 例[95%CI:12-15],不同方案之间无统计学显著差异。与 DTG 相比,在初治的 EVG/c 组[调整后的危害比:0.70(95%CI:0.47-1.05)]或 bDRV 组[0.53(0.26-1.04)],以及经治/抑制的 EVG/c 组[0.96(0.70-1.33)]、RAL 组[1.17(0.70-1.96)]或 bDRV 组[0.90(0.57-1.42)]中,T2DM 风险与方案之间未见统计学显著关联。

结论

在初治和经治的 PLHIV 中,与 DTG 相比,EVG/c、RAL 或 bDRV 并未增加 T2DM 的风险。然而,尽管队列规模较大,但事件数量较少,不能排除差异风险。

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