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Metabolic Complications Associated with Use of Integrase Strand Transfer Inhibitors (InSTI) for the Treatment of HIV-1 Infection: Focus on Weight Changes, Lipids, Glucose and Bone Metabolism
被引:0
|作者:
Savinelli, Stefano
[1
,2
]
Newman, Ellen
[1
]
Mallon, Patrick W. G.
[1
,2
]
机构:
[1] St Vincents Univ Hosp, Dept Infect Dis, Dublin, Ireland
[2] Univ Coll Dublin, UCD Ctr Expt Pathogen Host Res CEPHR, Sch Med, Dublin, Ireland
关键词:
HIV;
InSTI;
Weight gain;
Lipids;
Glucose;
Bone health;
TENOFOVIR DISOPROXIL FUMARATE;
GAIN FOLLOWING SWITCH;
ANTIRETROVIRAL THERAPY;
INITIAL TREATMENT;
DOLUTEGRAVIR;
EFAVIRENZ;
MULTICENTER;
ALAFENAMIDE;
PHASE-3;
EMTRICITABINE;
D O I:
10.1007/s11904-024-00708-x
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Purpose of ReviewThis review aims to summarize recently published peer reviewed papers on the influence of treatment with Integrase Strand Transfer Inhibitors (InSTI) in people with HIV (HIV) on metabolic health, including weight gain, lipid parameters, glucose homeostasis, and bone health.Recent FindingsInSTI have a mild/moderate effect on weight gain in both antiretroviral (ART) na & iuml;ve and ART experienced PWH, which is more pronounced in certain groups (i.e. women, people of Black African ethnicity, those with lower socioeconomic status, and older people). The effect on weight is also driven by other components of the ART regimen as well as previous exposure to certain ART. InSTI have a relatively safe profile in terms of lipid parameters and bone health, compared to other ART classes, although some studies suggest a greater risk of insulin resistance and diabetes in PWH using InSTI, especially 2nd generation InSTI.SummaryWhile there is some evidence suggesting a negative impact of InSTI on some aspects of metabolic health (weight gain and glucose homeostasis), they remain the preferred treatment option for most PWH, due to their high efficacy and tolerability. However, an individualised approach to ART choice in PWH should be used in order to avoid negative outcomes in populations at higher risks of metabolic complications.
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页码:293 / 308
页数:16
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