Evidence map›Paper›PMID 30995263›Full record

Trial reportPloS one2019

Chronic kidney disease in patients infected with human immunodeficiency virus (HIV) in an urban cohort.

Rosbel M Brito, Duc T Nguyen, Justine R Johnson, Eric J Lai, Rochelle E Castro, Angelina M Albert, Ann S Barnes, Edward A Graviss, Wadi N Suki

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Observational
  2. Article
  3. Sequelae of Immunocompromised Host Pneumonia.Clinics in chest medicine · 2025
    Review
  4. Article
  5. 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

9 authors at 3 institutions in 1 country.

Rosbel M BritoOffice of Graduate Medical Education, Houston Methodist Research Institute, Houston, Texas, United States of America.
Duc T NguyenHouston Methodist Research Institute, Houston, Texas, United States of America.
Justine R JohnsonDepartment of Obstetrics and Gynecology, Houston Methodist Hospital, Houston, Texas, United States of America.
Eric J LaiNephrology Fellowship Training Program, Houston Methodist Hospital, Houston, Texas, United States of America.
Rochelle E CastroLegacy Community Healthcare Center, Houston, Texas, United States of America.
Angelina M AlbertCommunity Education at Methodist Hospital, Houston, Texas, United States of America.ORCID 0000-0002-5059-4404
Ann S BarnesLegacy Community Healthcare Center, Houston, Texas, United States of America.
Edward A GravissHouston Methodist Research Institute, Houston, Texas, United States of America.
Wadi N SukiNephrology Training Program at Houston Methodist Hospital, Houston, Texas, United States of America.
Houston Methodist · USLegacy Community Health Services · USMethodist Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesHIV-infected patients are at risk for developing chronic kidney disease (CKD), defined by estimated glomerular filtration rate (eGFR) <60 ml/min/1.73m2. Our purpose was to understand the genesis of CKD in HIV patients from a large urban clinic in Houston, Texas, USA, and to characterize progression of CKD in the cohort. DESIGN, SETTING, PARTICIPANTS AND MEASUREMENTS: A retrospective cohort study (2012-2016) was conducted in all HIV-infected patients seen in a federally qualified community health center in Houston, Texas. CKD prevalence and its association with HIV viral load and CD4 count were determined. The association of the change in eGFR over time and comorbidities was assessed using linear mixed models.

resultsOf 3714 HIV-infected patients analyzed, 153 (4.1%) had CKD. The prevalence of CKD in the different racial groups was 5.4% White, 4.0% African American, 2.8% Hispanic/Latino and 3.2% Asian. There was no difference in the rate of decline in kidney function in White vs. African American HIV infected patients with CKD. Compared with non-CKD patients, CKD patients were older, had lived longer with HIV infection, had lower CD4 cell counts, higher proportions of hypertension, hyperlipidemia, and cerebrovascular disease, and had significantly higher rates of eGFR deterioration represented by a median decrease of 26.5% from first to last follow-up eGFR (versus 0% change). Linear mixed modeling identified older age, male gender, White race, longer time with HIV infection, hypertension, history of kidney stones, cerebrovascular disease, autoimmune disease, increased potassium and total cholesterol levels, and being treated with combination ART as associated with a worsening eGFR over time.

conclusionThis study demonstrates a prevalence of CKD in HIV-infected patients of 4.1% and points to an important role for HIV medications and other common comorbidities in the genesis and progression of kidney disease. Importantly, CKD was not more prevalent in African Americans than in Whites, perhaps due to a low prevalence of IV drug abuse as inferred from the lower prevalence of HCV infection in this cohort.

Indexed as

HIV-1HIV InfectionsRenal Insufficiency, ChronicAdultAgedCD4 Lymphocyte CountCerebrovascular DisordersFemaleHumansHyperlipidemiasHypertensionMaleMiddle AgedPrevalenceRisk FactorsTexas

Identifiers

PMID30995263
PMCPMC6469809
OpenAlexW2937374032

What OpenQuestion holds

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LicenceCC BY
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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.