Lang Jingjing, Xin Xin, Chen Panpan, Ning Zhen, Xiao Shaotan
School of Public Health, Fudan University, Shanghai, China.
Pudong New Area Center for Disease Control and Prevention, Shanghai, China.
Front Med (Lausanne). 2023 Jan 17;9:1071431. doi: 10.3389/fmed.2022.1071431. eCollection 2022.
This study sought to identify potential change patterns and predictors of fasting plasma glucose (FPG) and lipid levels after initiating highly active antiretroviral therapy (HAART).
A retrospective cohort study was conducted on 1,572 patients tested positive for HIV who initiated HAART between January 2010 and October 2020 in Shanghai, China. The growth mixture models (GMM) were used for capturing subgroups of FPG trajectories as well as triglyceride (TG) and total cholesterol (TC) dual-trajectories. Multinomial logistic regression models identified correlates of given trajectories.
The median follow-up time was 2.0 years (IQR 1.0-4.7). Three FPG trajectory subgroups were identified as FPG low-stable (62.3%), medium-stable (30.5%), and high-increasing (7.2%). Furthermore, three subgroups of TG and TC dual-trajectories were identified as TG and TC high-slight increasing (13.7%), low-rapid increasing (27.6%), and a subgroup of medium-stable TC and slight-decreasing TG (58.7%). Older age, high TG, FPG, BMI, CD4 count of <200 at baseline, and initial use of zidovudine (AZT) and protease inhibitors (PIs) helped to identify the class with increasing glucose or lipid metabolism trajectories.
The change patterns of plasma glucose and lipid in patients tested positive for HIV were heterogeneous and tailored interventions should be considered in specific subgroups.
本研究旨在确定开始高效抗逆转录病毒治疗(HAART)后空腹血糖(FPG)和血脂水平的潜在变化模式及预测因素。
对2010年1月至2020年10月在中国上海开始接受HAART治疗的1572例HIV检测呈阳性的患者进行了一项回顾性队列研究。生长混合模型(GMM)用于捕捉FPG轨迹亚组以及甘油三酯(TG)和总胆固醇(TC)双轨迹。多项逻辑回归模型确定了给定轨迹的相关因素。
中位随访时间为2.0年(四分位间距1.0 - 4.7)。确定了三个FPG轨迹亚组,分别为FPG低稳定组(62.3%)、中稳定组(30.5%)和高增长组(7.2%)。此外,确定了TG和TC双轨迹的三个亚组,分别为TG和TC高轻度增长组(13.7%)、低快速增长组(27.6%)以及TC中稳定和TG轻度下降亚组(58.7%)。年龄较大、TG高、FPG高、BMI高、基线CD4计数<200以及初始使用齐多夫定(AZT)和蛋白酶抑制剂(PIs)有助于识别血糖或脂质代谢轨迹增加的类别。
HIV检测呈阳性患者的血糖和血脂变化模式存在异质性,应在特定亚组中考虑针对性干预措施。