Evidence map›Paper›PMID 38419093›Full record

ArticleJournal of pharmaceutical health care and sciences2024

Renal function and lipid metabolism in Japanese HIV-1-positive individuals 288 weeks after switching from tenofovir disoproxil fumarate to tenofovir alafenamide fumarate: a single-center, retrospective cohort study.

Kensuke Abe, Junji Imamura, Akiko Sasaki, Tomoko Suzuki, Satomi Kamio, Taku Obara, Toshihiro Ito

Open access · goldAbstract read
In one paragraph

Article in Journal of pharmaceutical health care and sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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 at 3 institutions in 1 country.

Kensuke AbeDepartment of Pharmacy, National Hospital Organization Morioka Medical Center, 1-25-1 Aoyama, Morioka, Iwate, 020-0133, Japan. abe.kensuke.rc@mail.hosp.go.jp.ORCID http://orcid.org/0000-0003-3832-605X
Junji ImamuraHIV/AIDS Comprehensive Medical Center, National Hospital Organization Sendai Medical Center, 983-8520, Miyagino 2-11-12, Sendai, Japan.
Akiko SasakiHIV/AIDS Comprehensive Medical Center, National Hospital Organization Sendai Medical Center, 983-8520, Miyagino 2-11-12, Sendai, Japan.
Tomoko SuzukiHIV/AIDS Comprehensive Medical Center, National Hospital Organization Sendai Medical Center, 983-8520, Miyagino 2-11-12, Sendai, Japan.
Satomi KamioDepartment of Pharmacy, National Hospital Organization Shibukawa Medical Center, 377-0280, Shirai 383, Shibukawa, Japan.
Taku ObaraDepartment of Pharmaceutical Scienses, Tohoku University Hospital, 980-8574, Seiryomachi 1-1, Sendai, Japan.
Toshihiro ItoHIV/AIDS Comprehensive Medical Center, National Hospital Organization Sendai Medical Center, 983-8520, Miyagino 2-11-12, Sendai, Japan.
Sendai Medical Center · JPNational Hospital Organization · JPTohoku University Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundContinued use of tenofovir disoproxil fumarate (TDF), an antiretroviral drug, causes renal function decline and tubular damage in individuals with HIV. While tenofovir alafenamide fumarate (TAF) may have less damaging effects, it causes weight gain and abnormal lipid metabolism.

methodsThis single-center, retrospective cohort study used medical records from the National Hospital Organization Sendai Medical Center to investigate renal function of Japanese HIV-1-positive individuals who switched from TDF to antiretroviral therapy including TAF by 2017. The endpoints were: estimated glomerular filtration rate (eGFR), urinary β2 microglobulin (Uβ2MG), weight, and lipid metabolism parameters at 288 weeks after switching. Possible correlation between eGFR and Uβ2MG and factors affecting eGFR decline were examined.

resultsSixty patients switched from TDF to TAF and continued therapy for 288 weeks. eGFR showed a significant decline after 144 weeks, although it was controlled from the time of change until 96 weeks. In the renal impairment group, the decline was suppressed until week 288. Uβ2MG continued to decrease significantly after 48 weeks. However, the suggested correlation between eGFR and Uβ2MG disappeared when patients switched from TDF to TAF. Weight and lipid metabolic parameters increased significantly at 48 weeks and were maintained. Factors associated with decreased eGFR were: history of acquired immune deficiency syndrome (AIDS) and Uβ2MG. However, considering the odds ratio, the switch from TDF to TAF suppressed the eGFR decline in the group with a history of AIDS, and Uβ2MG had no effect on the eGFR decline.

conclusionsSwitching from TDF to TAF for the long term slows eGFR decline, decreases Uβ2MG levels, and reduces worsening of renal function. Weight gain and abnormal lipid metabolism may occur in the short term but are controllable.

Indexed as

HIVLipid metabolismRenal functionTenofovir alafenamide fumarateTenofovir disoproxil fumarate

Identifiers

PMID38419093
PMCPMC10900624
OpenAlexW4392238325

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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.