Evidence map›Paper›PMID 41530701›Full record

ArticleBMC infectious diseases2026

Longitudinal analysis of metabolic changes in people with HIV on integrase inhibitor-based versus efavirenz-based therapy: a prospective real-world cohort study in China.

Mingzhu Tao, Muye Xia, Tao Yu, Bing Li, Jie Peng, Shaohang Cai, Xuwen Xu

Abstract read
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Mingzhu TaoDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Muye XiaDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Tao YuDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Bing LiDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Jie PengDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Shaohang CaiDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Xuwen XuDepartment of Infectious Diseases, Nanfang Hospital, Southern Medical University, Guangzhou, China. xuxuwen95@126.com.

Funding

National Key Research and Development Program of China 2022YFC2304800
6 · The paper itself

Abstract

backgroundIntegrase strand transfer inhibitor (INSTI)-based antiretroviral therapy (ART) is recommended for HIV treatment but has been associated with metabolic adverse effects. However, real-world longitudinal data on these metabolic changes remain limited. This study aimed to characterize weight gain, dyslipidemia, and hepatic steatosis in ART-naïve people living with HIV (PLWH) initiating INSTI-based versus efavirenz (EFV)-based therapy.

methodsThis prospective cohort study enrolled 772 participants at Nanfang Hospital, Southern Medical University from 2020 to 2023. Participants were categorized into 3 groups: EFV/tenofovir disoproxil fumarate (TDF)/lamivudine (3TC) (n = 389); elvitegravir/cobicistat (EVG/c)/tenofovir alafenamide (TAF)/emtricitabine (FTC) or bictegravir (BIC)/TAF/FTC (n = 168); and dolutegravir (DTG)/3TC or DTG/3TC/TDF (n = 215). Metabolic parameters-including body mass index (BMI), lipids, and hepatic steatosis assessed via controlled attenuation parameter (CAP)-were evaluated at baseline, 6, 12, and 24 months using generalized estimating equations.

resultsAt 24 months, INSTI-based regimens were associated with significantly higher BMI compared to EFV/TDF/3TC (all P < 0.001), with no difference between INSTI subtypes. All groups showed early increases in triglycerides (TG) and total cholesterol (TC) that stabilized after 12 months; TG and TC levels at 24 months did not differ significantly between TAF-containing INSTI regimens and other groups. The prevalence of hepatic steatosis (CAP ≥ 238 dB/m) peaked at 31.2% at year 1 and declined to 28.8% at year 2. Multivariate analysis identified higher BMI (OR 1.55, 95% CI 1.44-1.67; p < 0.001), elevated TG (OR 1.44, 95% CI 1.22-1.70; p < 0.001), and elevated LDL-C (OR 1.90, 95% CI 1.21-2.98; p = 0.005) as independent risk factors.

conclusionINSTI-based ART was associated with sustained weight gain but did not worsen long-term dyslipidemia compared to an EFV-based regimen in a real-world setting. Hepatic steatosis correlated with metabolic parameters rather than INSTI exposure.

Indexed as

AlkynesAnti-HIV AgentsBenzoxazinesCyclopropanesHIV InfectionsHIV Integrase InhibitorsAdultChinaDyslipidemiasFatty LiverFemaleHumansLongitudinal StudiesMaleMiddle AgedProspective StudiesAlkynesAnti-HIV AgentsBenzoxazinesCyclopropanesefavirenzHIV Integrase InhibitorsAntiretroviral therapyDyslipidemiaHepatic steatosisHIVIntegrase strand transfer inhibitorWeight gain

Identifiers

PMID41530701
PMCPMC12888376

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.