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评估人类免疫缺陷病毒患者起始蛋白酶或整合酶核苷转移抑制剂治疗后体重的变化。

An assessment of weight change associated with the initiation of a protease or integrase strand transfer inhibitor in patients with human immunodeficiency virus.

机构信息

Janssen Scientific Affairs, LLC, Titusville, NJ, USA.

Analysis Group, Inc, Montréal, QC, Canada.

出版信息

Curr Med Res Opin. 2020 Aug;36(8):1313-1323. doi: 10.1080/03007995.2020.1775074. Epub 2020 Jun 17.

DOI:10.1080/03007995.2020.1775074
PMID:32459155
Abstract

OBJECTIVE

Evidence suggests that integrase strand transfer inhibitors (INSTIs) are associated with greater weight gain than other antiretrovirals. This real-world study compares weight/body mass index (BMI) change between insured US patients with human immunodeficiency virus (HIV-1) initiating a protease inhibitor (PI) or INSTI.

METHODS

A retrospective longitudinal study was conducted using Decision Resources Group's Real World Data Repository (7/17/2017-6/1/2019). Adult patients with HIV-1 who initiated a new PI or INSTI on or after 7/17/2018 (index date) and had ≥12 months of continuous pre-index clinical activity were included. Baseline characteristics were balanced using inverse probability of treatment weighting. The proportion of patients with ≥5% weight/BMI increases and mean weight/BMI change from pre- to post-index were compared using odds ratios (ORs) and mean differences (MDs).

RESULTS

20,367 patients (9993 PI, 10,374 INSTI) were included (mean age = 50 years; ∼30% females). Pre- and post-index weight and BMI measurements were available in 429 and 430 PI patients, and 397 and 383 INSTI patients, respectively (mean time between index and post-index measurements: ∼7 months). The PI cohort was 39%/49% less likely to experience ≥5% weight/BMI increase than the INSTI cohort, respectively (OR [≥5% weight gain] = 0.61; = .014; OR [≥5% BMI gain] = 0.51; < .001). Mean weight/BMI gain was significantly lower in the PI cohort than the INSTI cohort (weight MD = -1.90 kg [-4.19 lbs], BMI MD = -0.61kg/m; both < .001).

CONCLUSIONS

Relative to INSTI, patients initiating a new PI were less likely to experience ≥5% weight/BMI gain post-index. Additionally, mean weight/BMI gain was lower in the PI than in the INSTI cohort.

摘要

目的

有证据表明,整合酶链转移抑制剂(INSTIs)比其他抗逆转录病毒药物更易导致体重增加。本项真实世界研究比较了开始使用蛋白酶抑制剂(PI)或 INSTIs 的艾滋病毒(HIV-1)感染者的保险患者的体重/体重指数(BMI)变化。

方法

本项回顾性纵向研究使用了 Decision Resources Group 的真实世界数据仓库(2017 年 7 月 17 日至 2019 年 6 月 1 日)进行。纳入于 2018 年 7 月 17 日(索引日期)或之后开始使用新的 PI 或 INSTI 且具有≥12 个月连续预索引临床活动的成年 HIV-1 患者。通过逆概率治疗加权来平衡基线特征。使用优势比(OR)和平均差值(MD)比较体重/BMI 增加≥5%的患者比例和从预索引到后索引的平均体重/BMI 变化。

结果

共纳入 20367 例患者(PI 组 9993 例,INSTI 组 10374 例;平均年龄 50 岁;约 30%为女性)。PI 组和 INSTI 组分别有 429 例和 430 例患者具有预索引和后索引体重和 BMI 测量值,分别有 397 例和 383 例患者具有索引和后索引测量值(索引与后索引测量值之间的平均时间:约 7 个月)。PI 组分别有 39%和 49%的患者发生体重/BMI 增加≥5%的可能性低于 INSTI 组(体重增加≥5%的 OR = 0.61; =.014;体重指数增加≥5%的 OR = 0.51; <.001)。PI 组的平均体重/BMI 增加显著低于 INSTI 组(体重 MD = -1.90kg [-4.19 磅],BMI MD = -0.61kg/m;均 <.001)。

结论

与 INSTIs 相比,开始使用新 PI 的患者在索引后发生体重/BMI 增加≥5%的可能性更低。此外,PI 组的平均体重/BMI 增加低于 INSTI 组。

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