Hester E Kelly, Greenlee Sage, Durham Spencer H
Department of Pharmacy Practice, Auburn University Harrison School of Pharmacy, Auburn, AL, USA.
Department of Pharmacy, Houston Methodist Hospital, Houston, TX, USA.
Ann Pharmacother. 2022 Feb 8:10600280211073321. doi: 10.1177/10600280211073321.
To describe weight changes with integrase strand transfer inhibitor (INSTI) therapy.
A literature search was performed (through December 15, 2021) using the PubMed and CINAHL databases using the search terms: "integrase inhibitors," "integrase strand transfer inhibitors," and "weight."
Studies were included that provided relevant information on weight or body mass index (BMI) changes on INSTI therapy. Controlled or observational studies comparing different INSTI therapies or compared INSTI therapy to another class of antiretroviral therapy were included.
Forty-three articles met criteria for inclusion, and data are presented. Although some trials have observed similar weight gains between INSTI, protease inhibitor, and non-nucleoside inhibitor therapies, the increase appears to be greater with INSTI therapy, particularly during initiation of therapy. Risk factors for weight gain with INSTI therapy include female gender, lower CD4 count, and combined use of tenofovir alafenamide. Within the INSTI class, dolutegravir and bictegravir appear to have the greatest propensity for weight gain.
INSTI-based therapies are the preferred initial management of HIV infection. Discerning the factors contributing to weight changes on INSTI therapy and risks of associated health-related outcomes is important to both the management of weight gain and HIV medical management.
Within the INSTI class, dolutegravir and bictegravir may be associated with the greatest risk for weight gain particularly when combined with tenofovir alafenamide. Further research is needed to determine mechanisms for observed weight changes and any contributions to clinically significant metabolic and cardiovascular adverse outcomes associated with INSTI therapy.
描述整合酶链转移抑制剂(INSTI)治疗过程中的体重变化情况。
通过使用PubMed和CINAHL数据库进行文献检索(截至2021年12月15日),检索词为:“整合酶抑制剂”、“整合酶链转移抑制剂”和“体重”。
纳入的研究需提供有关INSTI治疗过程中体重或体重指数(BMI)变化的相关信息。纳入了比较不同INSTI治疗方法或将INSTI治疗与另一类抗逆转录病毒治疗进行比较的对照研究或观察性研究。
43篇文章符合纳入标准,并呈现了相关数据。尽管一些试验观察到INSTI、蛋白酶抑制剂和非核苷抑制剂治疗之间体重增加情况相似,但INSTI治疗导致的体重增加似乎更大,尤其是在治疗开始阶段。INSTI治疗导致体重增加的风险因素包括女性、较低的CD4计数以及替诺福韦艾拉酚胺的联合使用。在INSTI类别中,多替拉韦和比克替拉韦似乎体重增加倾向最大。
基于INSTI的治疗方法是HIV感染初始管理的首选。识别导致INSTI治疗过程中体重变化的因素以及相关健康相关结局的风险,对于体重增加的管理和HIV医疗管理都很重要。
在INSTI类别中,多替拉韦和比克替拉韦可能与体重增加的最大风险相关,特别是与替诺福韦艾拉酚胺联合使用时。需要进一步研究以确定观察到的体重变化机制以及与INSTI治疗相关的任何对临床显著代谢和心血管不良结局的影响。