Evidence map›Paper›PMID 23584425›Full record

ReviewCardiology in review

20-HETE and blood pressure regulation: clinical implications.

Cheng-Chia Wu, Tanush Gupta, Victor Garcia, Yan Ding, Michal L Schwartzman

Abstract readReview
In one paragraph

Review in Cardiology in review. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
7.7field-weighted citation impact, top 2% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 133 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Bioactive lipids in hypertension.Advances in pharmacology (San Diego, Calif.) · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Pleiotropic Effects of Ticagrelor: Influence onDrug design, development and therapy · 2022
    Article
  18. The CYP/20-HETE/GPR75 axis in hypertension.Advances in pharmacology (San Diego, Calif.) · 2022
    Review
  19. Circadian Control of Sodium and Blood Pressure Regulation.American journal of hypertension · 2021
    Review
  20. Article

18 more citing papers are in PubMed but not listed here.

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

5 authors at 1 institution in 1 country.

Cheng-Chia WuFrom the *Department of Pharmacology and Department of Medicine, New York Medical College, Valhalla, NY; †Department of Medicine, Greenwich Hospital, Greenwich, CT; and ‡Department of Medicine, New York Medical College, Valhalla, NY.
Tanush Gupta
Victor Garcia
Yan Ding
Michal L Schwartzman
New York Medical College · US

Funding

Vasoregulatory Function of CYP2E1-Derived EicosanoidsP01HL034300 · NHLBI · NEW YORK MEDICAL COLLEGE · PI SCHWARTZMAN, MICHAL LANIADO · 1985 to 2015
$33.4M
20-HETE regulation of androgen-induced hypertensionF30HL097402 · NHLBI · NEW YORK MEDICAL COLLEGE · PI WU, CHENG-CHIA · 2009 to 2012
$146k
NHLBI NIH HHS F30 HL097402NHLBI NIH HHS HL034300NHLBI NIH HHS HL34300NHLBI NIH HHS P01 HL034300
6 · The paper itself

Abstract

20-Hydroxy-5, 8, 11, 14-eicosatetraenoic acid (20-HETE) is a cytochrome P450 (CYP)-derived omega-hydroxylation metabolite of arachidonic acid. 20-HETE has been shown to play a complex role in blood pressure regulation. In the kidney tubules, 20-HETE inhibits sodium reabsorption and promotes natriuresis, thus, contributing to antihypertensive mechanisms. In contrast, in the microvasculature, 20-HETE has been shown to play a pressor role by sensitizing smooth muscle cells to constrictor stimuli and increasing myogenic tone, and by acting on the endothelium to further promote endothelial dysfunction and endothelial activation. In addition, 20-HETE induces endothelial angiotensin-converting enzyme, thus, setting forth a potential feed forward prohypertensive mechanism by stimulating the renin-angiotensin-aldosterone system. With the advancement of gene sequencing technology, numerous polymorphisms in the regulatory coding and noncoding regions of 20-HETE-producing enzymes, CYP4A11 and CYP4F2, have been associated with hypertension. This in-depth review article discusses the biosynthesis and function of 20-HETE in the cardiovascular system, the pharmacological agents that affect 20-HETE action, and polymorphisms of CYP enzymes that produce 20-HETE and are associated with systemic hypertension in humans.

Indexed as

Blood PressureCytochrome P-450 CYP4ACytochrome P-450 Enzyme SystemCytochrome P450 Family 4Endothelium, VascularHumansHydroxyeicosatetraenoic AcidsHypertensionKidney TubulesPeptidyl-Dipeptidase APolymorphism, GeneticRenin-Angiotensin System20-hydroxy-5,8,11,14-eicosatetraenoic acidCYP4A11 protein, humanCYP4F2 protein, humanCytochrome P-450 CYP4ACytochrome P-450 Enzyme SystemCytochrome P450 Family 4Hydroxyeicosatetraenoic AcidsPeptidyl-Dipeptidase A

Identifiers

PMID23584425
PMCPMC4292790
OpenAlexW2319299237

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.