Evidence map›Paper›PMID 32571409›Full record

ArticleInfectious diseases of poverty2020

Very high baseline HIV viremia impairs efficacy of non-nucleoside reverse transcriptase inhibitor-based ART: a long-term observation in treatment-naïve patients.

Shuai Chen, Yang Han, Xiao-Jing Song, Yan-Ling Li, Ting Zhu, Hong-Zhou Lu, Xiao-Ping Tang, Tong Zhang, Min Zhao, Yun He and 8 more

Open access · goldAbstract read
In one paragraph

Article in Infectious diseases of poverty, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.2field-weighted citation impact, top 35% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

10 citing papers in PubMed, 17 citations in OpenAlex.

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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

18 authors at 11 institutions in 1 country.

Shuai ChenDepartment of Infectious Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Wangfujing Street, Beijing, 100730, China.
Yang HanDepartment of Infectious Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Wangfujing Street, Beijing, 100730, China.
Xiao-Jing SongDepartment of Infectious Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Wangfujing Street, Beijing, 100730, China.
Yan-Ling LiDepartment of Infectious Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Wangfujing Street, Beijing, 100730, China.
Ting ZhuDepartment of Infectious Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Wangfujing Street, Beijing, 100730, China.
Hong-Zhou LuShanghai Public Health Clinical Center affiliated with Fudan University, Shanghai, China.
Xiao-Ping TangGuangzhou Eighth People's Hospital, Guangzhou, China.
Tong ZhangBeijing You'an Hospital, Capital Medical University, Beijing, China.
Min ZhaoFifth Medical Center of Chinese PLA General Hospital, Beijing, China.
Yun HeThe Infectious Disease Hospital of Henan Province, Zhengzhou, China.
Sheng-Hua HeChengdu Infectious Diseases Hospital, Chengdu, China.
Min WangThe First Hospital of Changsha, Changsha, China.
Yong-Zhen LiThe Center for Disease Prevention and Control of Guangxi province, Nanning, China.
Shao-Biao HuangNanning No.4 People's Hospital, Nanning, China.
Yong LiThe Longtan Hospital, Liuzhou, China.
Jing LiuThe hospital affiliated with the Chinese Medical University, Hangzhou, China.
Wei CaoDepartment of Infectious Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Wangfujing Street, Beijing, 100730, China. wcao_pumch@163.com.
Tai-Sheng LiDepartment of Infectious Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No.1 Shuaifuyuan, Wangfujing Street, Beijing, 100730, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNPeking Union Medical College Hospital · CNBeijing YouAn Hospital · CNChinese PLA General Hospital · CNGuangxi Longtan Hospital · CNGuangzhou Eighth People's Hospital · CNShanghai Public Health Clinical Center · CNThe First Hospital of Changsha · CNThe Second Nanning People's Hospital · CNThe Sixth People's Hospital of Zhengzhou · CNZhejiang Chinese Medical University · CN

Funding

National Key Technologies R&D Program for the 13th Five-Year Plan 2017ZX10202101the CAMS Initiative for Innovative Medicine CAMS-I2M: 2017-I2M-1-014the National Key Technologies R&D Program for the 11th Five-Year Plan 2008ZX10001006-001the National Key Technologies R&D Program for the 12th Five-Year Plan 2012ZX10001003-001
6 · The paper itself

Abstract

backgroundIt is not completely clear whether a very high pre-therapy viral load (≥ 500 000 copies/ml) can impair the virological response. The aim of this study was to examine the influence of very high baseline HIV-RNA levels on long-term virological responses under one type of regimen.

methodsA retrospective study was performed based on data from two multicenter cohorts in China from January to November 2009, and from May 2013 to December 2015. Untreated HIV infected adults between 18 and 65 years old were recruited before receiving non-nucleoside reverse transcriptase inhibitor-based regimen. All patients had baseline HIV-RNA levels over 500 copies/ml, good adherence, and were followed for at least 24 weeks. Virological suppression was defined as the first HIV-RNA < 50 copies/ml. Virological failure was defined as any of incomplete viral suppression (HIV-RNA ≥ 200 copies/ml without virological suppression within 24 weeks of treatment) and viral rebound (confirmed HIV-RNA level ≥ 50 copies/ml after virological suppression). Chi-square test, Kaplan-Meier analysis, Cox proportional hazards model and Logistic regression were used to compare virological response between each pretreated viral load stratum.

resultsA total of 758 treatment-naïve HIV patients in China were enlisted. Median follow-up time (IQR) was 144 (108-276) weeks. By week 48, rates of virological suppression in three groups (< 100 000, 100 000-500 000 and ≥ 500 000 copies/ml) were 94.1, 85.0, and 63.8%, respectively (P < 0.001). Very high baseline HIV viremia over 500 000 copies/ml were found to be associated with delayed virological suppression (≥ 500 000 vs <  100 000, adjusted relative hazard = 0.455, 95% CI: 0.32-0.65; P < 0.001) as well as incomplete viral suppression (≥ 500 000 vs < 100 000, adjusted odds ratio [aOR] = 6.084, 95% CI: 2.761-13.407; P < 0.001) and viral rebound (≥ 50 000 vs < 100 000, aOR = 3.671, 95% CI: 1.009-13.355, P = 0.048).

conclusionsVery high levels of pre-treatment HIV-RNA were related with delayed efficacy of NNRTI-based ART and increased risk of treatment failure. More potent initial regimens should be considered for those with this clinical character.

Indexed as

AdultAgedAnti-HIV AgentsChinaCohort StudiesFemaleHIV InfectionsHumansMaleMiddle AgedRetrospective StudiesRNA-Directed DNA PolymeraseViral LoadViremiaAnti-HIV AgentsRNA-Directed DNA PolymeraseAntiretroviral therapyBaseline RNAHIVTreatment outcomeViral loadVirologic response

Identifiers

PMID32571409
PMCPMC7310120
OpenAlexW3035783590

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LicenceCC BY
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Registered trials

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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.