Evidence map›Paper›PMID 23503162›Full record

ArticleCurrent hypertension reviews2012

Impact of Mast Cell Chymase on Renal Disease Progression.

Haimanot Wasse, Nawazish Naqvi, Ahsan Husain

Abstract read
In one paragraph

Article in Current hypertension reviews, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

21 citing papers in PubMed, 38 citations in OpenAlex.

  1. Article
  2. Article
  3. Role of Mast Cells and Their Mediators in Chronic Kidney Diseases.International journal of molecular sciences · 2025
    Review
  4. Article
  5. The mast cell: A Janus in kidney transplants.Frontiers in immunology · 2023
    Review
  6. Review
  7. Review
  8. Review
  9. Impact of fossil fuel emissions and particulate matter on pulmonary health.Proceedings (Baylor University. Medical Center) · 2019
    Article
  10. Article
  11. Mast cell chymase: morphofunctional characteristics.Histochemistry and cell biology · 2019
    Review
  12. Proteases in Pemphigoid Diseases.Frontiers in immunology · 2019
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. 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

3 authors at 1 institution in 1 country.

Haimanot WasseDivision of Nephrology, Department of Medicine, School of Medicine, Emory University, Atlanta, GA, USA.
Nawazish Naqvi
Ahsan Husain
Emory University · US

Funding

The Vascular Chymase-Angiotensin II SystemR01HL079040 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI HUSAIN, AHSAN · 2006 to 2014
$3.0M
Atlanta Clinical and Translational Science Institute (KL2)KL2RR025009 · NCRR · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2007 to 2011
$2.9M
Atlanta Clinical and Translational Science Institute (TL1)TL1RR025010 · NCRR · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2007 to 2011
$1.1M
Predictors of Hemodialysis Access DysfunctionK23DK065634 · NIDDK · EMORY UNIVERSITY · PI WASSE, HAIMANOT · 2006 to 2010
$637k
NCRR NIH HHS KL2 RR025009NCRR NIH HHS TL1 RR025010NHLBI NIH HHS R01 HL079040NIDDK NIH HHS K23 DK065634
6 · The paper itself

Abstract

Chymase, a serine protease found in mast cell granules, is released into the interstitium following injury or inflammation. Chymase is the primary ACE-independent pathway of angiotensin II formation, and also functions to activate TGF-beta and other promoters of extracellular matrix degradation, thereby playing a role in tissue remodeling. In the diseased kidney, chymase-containing mast cells markedly increase and their density correlates with tubulointerstitial fibrosis severity. Studies in humans support the pathologic role of chymase in diabetic nephropathy, while animal studies form the basis for the importance of increased chymase-dependent angiotensin II formation in progressive hypertensive, diabetic and inflammatory nephropathies. Moreover, humans with kidney disease express chymase in diseased blood vessels in concordance with significantly elevated plasma chymase levels. Conversely, specific chymase inhibitors attenuate angiotensin II production and renal fibrosis in animal models, suggesting their potential therapeutic benefit in human nephropathy, where chymase-containing mast cells accumulate and contribute to progressive disease.

Indexed as

angiotensin IIChymasekidney diseasemast cellstransforming growth factor-β

Identifiers

PMID23503162
PMCPMC3596835
OpenAlexW2113066517

What OpenQuestion holds

Textmetadata
LicenceTDM
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.