Risks of metabolic syndrome and diabetes with integrase inhibitor-based therapy

被引:18
作者
Shah, Shahini [1 ]
Hill, Andrew [2 ]
机构
[1] Imperial Coll London, Fac Med, London, England
[2] Univ Liverpool, Dept Translat Med, Pharmacol, Liverpool, Merseyside, England
关键词
diabetes; HIV; insulin resistance; integrase strand transfer inhibitors; metabolic syndrome; obesity; weight gain; TENOFOVIR DISOPROXIL FUMARATE; HIV-1; INFECTION; DOUBLE-BLIND; ANTIRETROVIRAL THERAPY; TREATMENT-NAIVE; RALTEGRAVIR; DOLUTEGRAVIR; EFAVIRENZ; ADULTS; EMTRICITABINE;
D O I
10.1097/QCO.0000000000000695
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose of review A growing body of evidence suggests that integrase inhibitors (INSTIs) are significantly associated with weight gain and obesity. Obesity is a significant risk factor for metabolic syndrome and diabetes. This article comprehensively reviews recent available evidence weight gain and the risks of metabolic syndrome and diabetes associated with INSTIs. Recent findings Recent evidence continues to contribute to the evidence for weight gain associated with INSTIs, especially when used with newer nucleoside reverse transcriptase inhibitor, tenofovir alafenamide (TAF). Although the literature suggests a neutral effect on lipids, there is evidence that INSTIs are associated with metabolic syndrome due to treatment-emergent obesity. The literature for short-term treatment-emergent diabetes and insulin resistance remains inconsistent, but there is some evidence that weight gain could lead to an increased risk of developing diabetes in the future. Summary Longer term studies are required to understand the metabolic impact of INSTIs, secondary to weight gain. Evidence suggests that INSTIs, when used with TAF, contribute to metabolic syndrome and may have long-term risks of diabetes. INSTIs, when used with tenofovir disoproxil fumarate, have fewer metabolic implications. Clinicians must monitor for weight gain and metabolic effects, especially in those with underlying risk factors.
引用
收藏
页码:16 / 24
页数:9
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