Evidence map›Paper›PMID 29652635›Full record

ArticlePhysiological genomics2018

FAR2 is associated with kidney disease in mice and humans.

Grant Backer, Sean Eddy, Susan M Sheehan, Yuka Takemon, Anna Reznichenko, Holly S Savage, Matthias Kretzler, Ron Korstanje

Open access · hybridAbstract read
In one paragraph

Article in Physiological genomics, 2018. 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
0.6field-weighted citation impact, top 32% 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, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. 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

8 authors at 2 institutions in 1 country.

Grant BackerThe Jackson Laboratory , Bar Harbor, Maine.
Sean EddyDepartment of Internal Medicine, the Division of Nephrology, University of Michigan , Ann Arbor, Michigan.
Susan M SheehanThe Jackson Laboratory , Bar Harbor, Maine.
Yuka TakemonThe Jackson Laboratory , Bar Harbor, Maine.
Anna ReznichenkoThe Jackson Laboratory , Bar Harbor, Maine.
Holly S SavageThe Jackson Laboratory , Bar Harbor, Maine.
Matthias KretzlerDepartment of Internal Medicine, the Division of Nephrology, University of Michigan , Ann Arbor, Michigan.
Ron KorstanjeThe Jackson Laboratory , Bar Harbor, Maine.ORCID 0000-0002-2808-1610
Jackson Laboratory · USUniversity of Michigan · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
Translational CoreP30AG038070 · NIA · JACKSON LABORATORY · PI John Matthew Mahoney · 2010 to 2026
$19.3M
The Jackson Laboratory Center for Precision Genetics: From New Models to Novel TherapeuticsU54OD020351 · OD · JACKSON LABORATORY · PI NISHINA, PATSY M · 2015 to 2019
$10.2M
NCI NIH HHS P30 CA034196NIA NIH HHS P30 AG038070NIH HHS U54 OD020351
6 · The paper itself

Abstract

Mesangial matrix expansion is an important process in the initiation of chronic kidney disease, yet the genetic factors driving its development are unknown. Our previous studies have implicated Far2 as a candidate gene associated with differences in mesangial matrix expansion between mouse inbred strains. Consistent with the hypothesis that increased expression of Far2 leads to mesangial matrix expansion through increased production of platelet-activating factor precursors, we show that FAR2 is capable of mediating de novo platelet-activating factor synthesis in vitro and driven by the transcription factor NKX3.2. We demonstrate that knockdown of Far2 in mice delays the progression of mesangial matrix expansion with at least six months (equivalent to ~15 yr in human). Furthermore, we show that increased FAR2 expression in human patients is associated with diabetic nephropathy, lupus nephritis, and IgA nephropathy. Taken together, these results highlight FAR2's role in the development of mesangial matrix expansion and chronic kidney disease.

Indexed as

AdultAgedAldehyde OxidoreductasesAnimalsDiabetic NephropathiesFemaleGlomerular MesangiumHomeodomain ProteinsHumansMaleMice, Inbred C3HMice, Inbred C57BLMice, KnockoutMiddle AgedTranscription FactorsYoung AdultAldehyde OxidoreductasesFAR2 protein, humanFAR2 protein, mouseHomeodomain ProteinsNKX3-2 protein, humanTranscription Factorsagingkidneymesangial matrixmouse

Identifiers

PMID29652635
PMCPMC6139637
OpenAlexW2797826654

What OpenQuestion holds

Textmetadata
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.