Evidence map›Paper›PMID 27560968›Full record

Observational studyPloS one2016

Renal Dysfunction during Tenofovir Use in a Regional Cohort of HIV-Infected Individuals in the Asia-Pacific.

Junko Tanuma, Awachana Jiamsakul, Abhimanyu Makane, Anchalee Avihingsanon, Oon Tek Ng, Sasisopin Kiertiburanakul, Romanee Chaiwarith, Nagalingeswaran Kumarasamy, Kinh Van Nguyen, Thuy Thanh Pham and 16 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 23 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

26 authors at 20 institutions in 12 countries.

Junko TanumaAIDS Clinical Center, National Center for Global Health and Medicine, Tokyo, Japan.
Awachana JiamsakulThe Kirby Institute, UNSW Australia, Sydney, Australia.
Abhimanyu MakaneInstitute of Infectious Diseases, Pune, India.
Anchalee AvihingsanonThe Netherland Australia Thailand Research Collaboration/Thai Red Cross AIDS Research Centre, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Oon Tek NgDepartment of Infectious Disease and Communicable Disease Centre, Tan Tock Seng Hospital, Singapore, Singapore.
Sasisopin KiertiburanakulFaculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Romanee ChaiwarithResearch Institute for Health Sciences, Chiang Mai, Thailand.
Nagalingeswaran KumarasamyChennai Antiviral Research and Treatment Clinical Research Site, Y.R. Gaitonde Centre for AIDS Research and Education, Chennai, India.
Kinh Van NguyenNational Hospital of Tropical Diseases, Hanoi, Vietnam.
Thuy Thanh PhamInfectious Disease Department, Bach Mai Hospital, Hanoi, Vietnam.
Man Po LeeDepartment of Medicine, Queen Elizabeth Hospital, Hong Kong, China.
Rossana DitangcoDepartment of Health, Research Institute for Tropical Medicine, Manila, Philippines.
Tuti Parwati MeratiFaculty of Medicine, Udayana University & Sanglah Hospital, Bali, Indonesia.
Jun Yong ChoiDivision of Infectious Diseases, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, South Korea.
Wing Wai WongInfectious Diseases and AIDS Unit, Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.
Adeeba KamarulzamanFaculty of Medicine, University Malaya Medical Centre, Kuala Lumpur, Malaysia.
Evy YunihastutiFaculty of Medicine, University of Indonesia, Cipto Mangunkusumo Hospital, Jakarta, Indonesia.
Benedict Lh SimDepartment of Medicine, Hospital Sungai Buloh, Sungai Buloh, Malaysia.
Winai RatanasuwanFaculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Pacharee KantipongDepartment of Medicine, Chiangrai Prachanukroh Hospital, Chiang Rai, Thailand.
Fujie ZhangBeijing Ditan Hospital, Capital Medical University, Beijing, China.
Mahiran MustafaMedical Department, Hospital Raja Perempuan Zainab II, Kota Bharu, Malaysia.
Vonthanak SaphonnNational Center for HIV/AIDS, Dermatology & STDs, University of Health Sciences, Phnom Penh, Cambodia.
Sanjay PujariInstitute of Infectious Diseases, Pune, India.
Annette H SohnTREAT Asia, amfAR - The Foundation for AIDS Research, Bangkok, Thailand.
TREAT Asia HIV Observational Databases (TAHOD)
Bạch Mai Hospital · VNCapital Medical University · CNChiangRai Prachanukroh Hospital · THDepartment of Health · PHHIV Netherlands Australia Thailand Research Collaboration · THHospital for Tropical Diseases · VNHospital Raja Perempuan Zainab II · MYHospital Sungai Buloh · MYMahidol University · THNational Center for Global Health and Medicine · JPNational Center for HIV/AIDS, Dermatology and STD · KHQueen Elizabeth Hospital · CNRumah Sakit Umum Pusat Nasional Dr. Cipto Mangunkusumo · IDSiriraj Hospital · THTaipei Veterans General Hospital · TWTan Tock Seng Hospital · SGUdayana University · IDUniversity Malaya Medical Centre · MYYonsei University · KRYR Gaitonde Centre for AIDS Research and Education · IN

Funding

The Asia-Pacific HIV Research CollaborationU01AI069907 · NIAID · FOUNDATION FOR AIDS RESEARCH · PI ANNETTE H SOHN · 2006 to 2026
$44.8M
NIAID NIH HHS U01 AI069907
6 · The paper itself

Abstract

backgroundIn resource-limited settings, routine monitoring of renal function during antiretroviral therapy (ART) has not been recommended. However, concerns for tenofovir disoproxil fumarate (TDF)-related nephrotoxicity persist with increased use.

methodsWe investigated serum creatinine (S-Cr) monitoring rates before and during ART and the incidence and prevalence of renal dysfunction after starting TDF by using data from a regional cohort of HIV-infected individuals in the Asia-Pacific. Time to renal dysfunction was defined as time from TDF initiation to the decline in estimated glomerular filtration rate (eGFR) to <60 ml/min/1.73m2 with >30% reduction from baseline using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation or the decision to stop TDF for reported TDF-nephrotoxicity. Predictors of S-Cr monitoring rates were assessed by Poisson regression and risk factors for developing renal dysfunction were assessed by Cox regression.

resultsAmong 2,425 patients who received TDF, S-Cr monitoring rates increased from 1.01 to 1.84 per person per year after starting TDF (incidence rate ratio 1.68, 95%CI 1.62-1.74, p <0.001). Renal dysfunction on TDF occurred in 103 patients over 5,368 person-years of TDF use (4.2%; incidence 1.75 per 100 person-years). Risk factors for developing renal dysfunction included older age (>50 vs. ≤30, hazard ratio [HR] 5.39, 95%CI 2.52-11.50, p <0.001; and using PI-based regimen (HR 1.93, 95%CI 1.22-3.07, p = 0.005). Having an eGFR prior to TDF (pre-TDF eGFR) of ≥60 ml/min/1.73m2 showed a protective effect (HR 0.38, 95%CI, 0.17-0.85, p = 0.018).

conclusionsRenal dysfunction on commencing TDF use was not common, however, older age, lower baseline eGFR and PI-based ART were associated with higher risk of renal dysfunction during TDF use in adult HIV-infected individuals in the Asia-Pacific region.

Indexed as

AdultAnti-HIV AgentsCreatinineDatabases, FactualFemaleGlomerular Filtration RateHIV InfectionsHumansKidneyKidney DiseasesMaleMiddle AgedPoisson DistributionProportional Hazards ModelsProspective StudiesRisk FactorsAnti-HIV AgentsCreatinineTenofovir

Identifiers

PMID27560968
PMCPMC4999237
OpenAlexW2507860931

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.