Evidence map›Paper›PMID 27007656›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2016

Multiple facets of HIV-associated renal disease.

D R da Silva, I C Gluz, J Kurz, G G Thomé, R Zancan, R N Bringhenti, P G Schaefer, M Dos Santos, E J G Barros, F V Veronese

Open access · goldAbstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Observational
  6. Article
  7. Review
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

10 authors at 1 institution in 1 country.

D R da SilvaServiço de Nefrologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
I C GluzServiço de Nefrologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
J KurzServiço de Nefrologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
G G ThoméServiço de Nefrologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
R ZancanServiço de Nefrologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
R N BringhentiServiço de Patologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
P G SchaeferServiço de Patologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
M Dos SantosServiço de Nefrologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
E J G BarrosServiço de Nefrologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
F V VeroneseServiço de Nefrologia, Hospital de Clínicas de Porto Alegre, RS, Porto Alegre, Brasil.
Hospital de Clínicas de Porto Alegre · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

HIV infection has a broad spectrum of renal manifestations. This study examined the clinical and histological manifestations of HIV-associated renal disease, and predictors of renal outcomes. Sixty-one (64% male, mean age 45 years) HIV patients were retrospectively evaluated. Clinical presentation and renal histopathology were assessed, as well as CD4 T-cell count and viral load. The predictive value of histological lesion, baseline CD4 cell count and viral load for end-stage renal disease (ESRD) or death were determined using the Cox regression model. The outcomes of chronic kidney disease (CKD) and ESRD or death were evaluated by baseline CD4 cell count. The percent distribution at initial clinical presentation was non-nephrotic proteinuria (54%), acute kidney injury (28%), nephrotic syndrome (23%), and chronic kidney disease (22%). Focal segmental glomerulosclerosis (28%), mainly the collapsing form (HIVAN), acute interstitial nephritis (AIN) (26%), and immune complex-mediated glomerulonephritis (ICGN) (25%) were the predominant renal histology. Baseline CD4 cell count ≥ 200 cells/mm3 was a protective factor against CKD (hazard ratio=0.997; 95%CI=0.994-0.999; P=0.012). At last follow-up, 64% of patients with baseline CD4 ≥ 200 cells/mm3 had eGFR >60 mL·min-1·(1.73 m2)-1 compared to the other 35% of patients who presented with CD4 <200 cells/mm3 (log rank=9.043, P=0.003). In conclusion, the main histological lesion of HIV-associated renal disease was HIVAN, followed by AIN and ICGN. These findings reinforce the need to biopsy HIV patients with kidney impairment and/or proteinuria. Baseline CD4 cell count ≥ 200 cells/mm3 was associated with better renal function after 2 years of follow-up.

Indexed as

AIDS-Associated NephropathyBiopsyCD4 Lymphocyte CountDisease ProgressionFemaleGlomerular Filtration RateGlomerulonephritisHIV InfectionsHumansMaleMiddle AgedPredictive Value of TestsProportional Hazards ModelsProteinuriaRenal Insufficiency, ChronicRetrospective StudiesSerum Albumin

Identifiers

PMID27007656
PMCPMC4819412
OpenAlexW2305347692

What OpenQuestion holds

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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.