Evidence map›Paper›PMID 30052698›Full record

ReviewJornal brasileiro de nefrologia

APOL1 risk variants and kidney disease: what we know so far.

Tobias August Siemens, Miguel Carlos Riella, Thyago Proença de Moraes, Cristian Vidal Riella

Open access · diamondAbstract readReview
In one paragraph

Review in Jornal brasileiro de nefrologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. ADAR regulates APOL1 via A-to-I RNA editing by inhibition of MDA5 activation in a paradoxical biological circuit.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Arteriosclerosis, thrombosis, and vascular biology · 2021
    Article
  13. A focus on the association of Apol1 with kidney disease in children.Pediatric nephrology (Berlin, Germany) · 2021
    Review
  14. Article
  15. Podocytopathies.Nature reviews. Disease primers · 2020
    Review
  16. Review
  17. Article
  18. APOL1-Associated Kidney Disease in Brazil.Kidney international reports · 2019
    Article
  19. Review
  20. 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

4 authors at 4 institutions in 3 countries.

Tobias August SiemensHospital Universitário Cajuru, Curitiba, PR, Brasil.ORCID http://orcid.org/0000-0003-0643-6668
Miguel Carlos RiellaFundação Pró-Renal, Curitiba, PR, Brasil.
Thyago Proença de MoraesPontificia Universidade Católica do Paraná, Departamento de Medicina, Curitiba, PR, Brasil.
Cristian Vidal RiellaBeth Israel Deaconess Medical Center, Boston, MA, United States.
Beth Israel Deaconess Medical Center · USHospital Universitário Cajuru · BRPontifícia Universidade Católica do Paraná · BRRenal Association · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There are striking differences in chronic kidney disease between Caucasians and African descendants. It was widely accepted that this occurred due to socioeconomic factors, but recent studies show that apolipoprotein L-1 (APOL1) gene variants are strongly associated with focal segmental glomerulosclerosis, HIV-associated nephropathy, hypertensive nephrosclerosis, and lupus nephritis in the African American population. These variants made their way to South America trough intercontinental slave traffic and conferred an evolutionary advantage to the carries by protecting against forms of trypanosomiasis, but at the expense of an increased risk of kidney disease. The effect of the variants does not seem to be related to their serum concentration, but rather to local action on the podocytes. Risk variants are also important in renal transplantation, since grafts from donors with risk variants present worse survival.

Indexed as

Apolipoprotein L1Black or African AmericanCardiovascular DiseasesGenetic VariationHumansPodocytesPolymorphism, GeneticPrevalenceRenal Insufficiency, ChronicRisk FactorsAPOL1 protein, humanApolipoprotein L1

Identifiers

PMID30052698
PMCPMC6533999
OpenAlexW2884891358

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.