Evidence map›Paper›PMID 37846087›Full record

Observational studyJMIR public health and surveillance2024

CD4/CD8 Ratio Recovered as a Predictor of Decreased Liver Damage in Adults Infected With HIV: 16-Year Observational Cohort Study.

Bingyu Liang, Rujing Sun, Yanyan Liao, Aidan Nong, Jinfeng He, Fengxiang Qin, Yanyun Ou, Jianhua Che, Zhenxian Wu, Yuan Yang and 5 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in JMIR public health and surveillance, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 72% 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

2 citing papers in PubMed, 0 citations in OpenAlex.

  1. Article
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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

15 authors at 3 institutions in 2 countries.

Bingyu Liang *Guangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, China.ORCID 0000-0001-9788-5826
Rujing Sun *Guangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, China.ORCID 0009-0000-7152-4854
Yanyan Liao *Guangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, China.ORCID 0000-0003-1789-8091
Aidan NongHIV/AIDS prevention department, Chongzuo Center for Disease Control and Prevention, Chongzuo, China.ORCID 0009-0000-9667-4381
Jinfeng HeGuangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, China.ORCID 0009-0002-6606-5950
Fengxiang QinGuangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, China.ORCID 0000-0003-1459-4826
Yanyun OuHIV/AIDS prevention department, Chongzuo Center for Disease Control and Prevention, Chongzuo, China.ORCID 0009-0008-4344-9170
Jianhua CheHIV/AIDS prevention department, Chongzuo Center for Disease Control and Prevention, Chongzuo, China.ORCID 0009-0001-7711-1548
Zhenxian WuHIV/AIDS prevention department, Chongzuo Center for Disease Control and Prevention, Chongzuo, China.ORCID 0009-0000-6761-0522
Yuan YangGuangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, China.ORCID 0009-0004-0117-9396
Jiao QinHIV/AIDS prevention department, Chongzuo Center for Disease Control and Prevention, Chongzuo, China.ORCID 0009-0001-0816-8081
Jie CaiHIV/AIDS prevention department, Chongzuo Center for Disease Control and Prevention, Chongzuo, China.ORCID 0009-0002-7310-5439
Lijuan BaoHIV/AIDS prevention department, Chongzuo Center for Disease Control and Prevention, Chongzuo, China.ORCID 0009-0004-7113-1486
Li YeGuangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, China.ORCID 0000-0001-7688-4867
Hao LiangGuangxi Key Laboratory of AIDS Prevention and Treatment, School of Public Health, Guangxi Medical University, Nanning, China.ORCID 0000-0001-7534-5124
Guangxi Medical University · CNChongqing Dazu District People's Hospital · CNTaiwan Centers for Disease Control · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs the life expectancy of individuals infected with HIV continues to increase, vigilant monitoring of non-AIDS-related events becomes imperative, particularly those pertaining to liver diseases. In comparison to the general population, patients infected with HIV experience a higher frequency of liver-related deaths. The CD4/CD8 ratio is emerging as a potential biomarker for non-AIDS-related events. However, few existing studies have been specially designed to explore the relationship between the CD4/CD8 ratio and specific types of non-AIDS-related events, notably liver damage.

objectiveThis study aimed to investigate the potential association between the CD4/CD8 ratio and the development of liver damage in a sizable cohort of patients infected with HIV receiving antiretroviral treatment (ART). Additionally, the study sought to assess the effectiveness of 3 antiretroviral drugs in recovering the CD4/CD8 ratio and reducing the occurrence of liver damage in this population.

methodsWe conducted an observational cohort study among adults infected with HIV receiving ART from 2004 to 2020 in Guangxi, China. Propensity score matching, multivariable Cox proportional hazard, and Fine-Gray competing risk regression models were used to determine the relationship between the CD4/CD8 ratio recovered and liver damage.

resultsThe incidence of liver damage was 20.12% among 2440 eligible individuals during a median follow-up period of 4 person-years. Patients whose CD4/CD8 ratio did not recover to 1.0 exhibited a higher incidence of liver damage compared to patients with a CD4/CD8 ratio recovered (adjusted hazard ratio 7.90, 95% CI 4.39-14.21; P<.001; subdistribution hazard ratio 6.80, 95% CI 3.83-12.11; P<.001), findings consistent with the propensity score matching analysis (adjusted hazard ratio 6.94, 95% CI 3.41-14.12; P<.001; subdistribution hazard ratio 5.67, 95% CI 2.74-11.73; P<.001). The Efavirenz-based regimen exhibited the shortest time for CD4/CD8 ratio recovery (median 71, IQR 49-88 months) and demonstrated a lower prevalence of liver damage (4.18/100 person-years).

conclusionsRecovery of the CD4/CD8 ratio was associated with a decreased risk of liver damage in patients infected with HIV receiving ART, adding evidence for considering the CD4/CD8 ratio as a potential marker for identifying individuals at risk of non-AIDS-related diseases. An efavirenz-based regimen emerged as a recommended choice for recovering the CD4/CD8 ratio and mitigating the risk of liver damage.

Indexed as

HIV InfectionsLiver DiseasesAdultAlkynesBenzoxazinesCD8-Positive T-LymphocytesChinaCohort StudiesCyclopropanesHumansAlkynesBenzoxazinesCyclopropanesefavirenzAIDSantiretroviral therapyCD4/CD8efavirenzHIVliver damagelopinavirnevirapine

Identifiers

PMID37846087
PMCPMC10806443
OpenAlexW4387691720

What OpenQuestion holds

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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.