Evidence map›Paper›PMID 35658835›Full record

ArticleBMC gastroenterology2022

Risk factors of severe hepatotoxicity among HIV-1 infected individuals initiated on highly active antiretroviral therapy in the Northwest Region of Cameroon.

Lem Edith Abongwa, Anthony Kebira Nyamache, Fokunang Charles, Judith Torimiro, Nshom Emmanuel, Irénée Domkam, Mbu Eyongetah, Beriyuy Jude, Fung Holgar Mua, Sama Bella and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 15 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

14 authors at 6 institutions in 2 countries.

Lem Edith AbongwaDepartment of Biological Sciences, Faculty of Science, University of Bamenda, BP 39, Bamenda, North West Region, Cameroon. lemedith@gmail.com.
Anthony Kebira NyamacheDepartment of Microbiology, School of Pure and Applied Sciences, Kenyatta University, Nairobi, Kenya.
Fokunang CharlesFaculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon.
Judith TorimiroChantal Biya International Center for Research on the Prevention and Management of HIV/AIDS (CIRCB), Yaoundé, Cameroon.
Nshom EmmanuelBaptist Convention Health Board, Mbingo Baptist Hospital, Bamenda, North West Region, Cameroon.
Irénée DomkamChantal Biya International Center for Research on the Prevention and Management of HIV/AIDS (CIRCB), Yaoundé, Cameroon.
Mbu EyongetahBamenda Regional Hospital, Bamenda, North West Region, Cameroon.
Beriyuy JudeSanta district health centre, Santa, North West Region, Cameroon.
Fung Holgar MuaNdop district health centre, Ndop, North West Region, Cameroon.
Sama BellaNdop district health centre, Ndop, North West Region, Cameroon.
Tankou Colman TambohBali District Health Centre, Bali, North West Region, Cameroon.
Erna Charlene MoungangBafut District Hospitals, Bafut, North West Region, Cameroon.
Victorine NgumBafut District Hospitals, Bafut, North West Region, Cameroon.
Paul OkemoDepartment of Microbiology, School of Pure and Applied Sciences, Kenyatta University, Nairobi, Kenya.
Kenyatta University · KEUniversité de Yaoundé I · CMBamenda University of Science and Technology · CMCameroon Baptist Convention Health Services · CMCentre International De Reference Chantal Biya · CMUniversity of Bamenda · CM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatotoxicity due to highly active antiretroviral therapy (HAART) has gained prominent attention since it can be affected by many factors. The aim of this study was to determine the prevalence of hepatotoxicity and related risk factors of severe hepatotoxicity following HAART initiation.

methodsA total of 100 drug-naive patients aged between 18 and 61 years were recruited. They were put on Tenofovir/Lamivudine/Efavirenz [TDF/3TC/EFV] (64), Zidovudine/ Lamivudine/Efavirenz [AZT/3TC/EFV] (22), and Zidovudine/Lamivudine/Nevirapine AZT/3TC/NVP (14) and monitored for 6months and blood samples drawn.Alanine aminotransferases (ALT), aspartate aminotransferases (AST), and alkaline phosphatase (ALP) wereanalyzed by enzymatic methods and used to classify levels of hepatotoxicity.

resultsA total of 37(37%) and 49(49%) patients presented with hepatotoxicity while 15% and 28% had severe hepatotoxicity at 4 and 24 weeks respectively. Serum levels of all enzymes increased significantly (p = 0.001) with increased treatment duration. Univariate analysis revealed that the risk factor of developing severe hepatotoxicity was significantly greater in patients < 30years (p = 0.02), males(p = 0.04), low BMI (p = 0.02), low monthly income (p = 0.01) earners, and patients on AZT + 3TC + NVP regimen (p = 0.01). While multivariate analysis at p < 0.09 showed that age 30-40 years, low BMI, low monthly income, and the use of AZT + 3TC + NVP regimen were independent risk factors.

conclusionsLow BMI, age group of 30-40years, low monthly income, and the use of AZT + 3TC + NVP regimen identified as risk factors for the development of severe hepatotoxicity should be considered as an important strategy by clinicians in preventing the hepatotoxicity.

Indexed as

Anti-HIV AgentsChemical and Drug Induced Liver InjuryHIV-1HIV InfectionsAdolescentAdultAntiretroviral Therapy, Highly ActiveCameroonHumansLamivudineMaleMiddle AgedRisk FactorsYoung AdultZidovudineAnti-HIV AgentsLamivudineZidovudineHAARTHepatotoxicityHIV-1Liver enzymesRisk factors

Identifiers

PMID35658835
PMCPMC9166462
OpenAlexW4281678383

What OpenQuestion holds

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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.