Evidence map›Paper›PMID 19042039›Full record

ReviewTrends in pharmacological sciences2009

Vascular protection by tetrahydrobiopterin: progress and therapeutic prospects.

Zvonimir S Katusic, Livius V d'Uscio, Karl A Nath

Abstract readReview
In one paragraph

Review in Trends in pharmacological sciences, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
–field-weighted citation impact
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

73 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
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  9. Review
  10. Review
  11. Article
  12. Article
  13. Inactivation of BACE1 increases expression of endothelial nitric oxide synthase in cerebrovascular endothelium.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2022
    Article
  14. Article
  15. Review
  16. Sapropterin (BH4) Aggravates Autoimmune Encephalomyelitis in Mice.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2021
    Observational
  17. Nitric oxide and sickle cell disease-Is there a painful connection?Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
  18. Neuronal Nitric Oxide Synthase (nNOS) in Neutrophils: An Insight.Reviews of physiology, biochemistry and pharmacology · 2021
    Review
  19. Article
  20. Article

13 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

3 authors.

Zvonimir S KatusicDepartment of Anesthesiology, Mayo Clinic College of Medicine, Rochester, MN 55905, USA. katusic.zvonimir@mayo.edu
Livius V d'Uscio
Karl A Nath

Funding

VASCULAR PATHOBIOLOGY OF SICKLE CELL DISEASEP01HL055552 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI VERCELLOTTI, GREGORY M · 1995 to 2011
$17.3M
Vascular gene transfer using a novel cellular stentP01HL066958 · NHLBI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI RUSSELL, STEPHEN J · 2001 to 2005
$8.2M
Mechanism of Dialysis Arteriovenous Fistula DysfunctionR01DK070124 · NIDDK · MAYO CLINIC ROCHESTER · PI NATH, KARL A. · 2005 to 2015
$3.4M
TETRAHYDROBIOPTERIN--REGULATOR OF ENDOTHELIAL FUNCTIONR01HL053524 · NHLBI · MAYO CLINIC ROCHESTER · PI KATUSIC, ZVONIMIR S · 1995 to 2009
$2.3M
NITRIC OXIDE/SUPEROXIDE IN LIPID VASCULAR DISEASER01HL058080 · NHLBI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI KATUSIC, ZVONIMIR S · 2001 to 2005
$1.5M
NITRIC OXIDE/SUPEROXIDE IN LIPID VASCULAR DISEASER29HL058080 · NHLBI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI O'BRIEN, TIMOTHY · 1998 to 2000
$100k
NHLBI NIH HHS HL-53524NHLBI NIH HHS HL-55552NHLBI NIH HHS HL-58080NHLBI NIH HHS HL-66958NHLBI NIH HHS P01 HL055552NHLBI NIH HHS P01 HL066958NHLBI NIH HHS R01 HL053524NHLBI NIH HHS R01 HL058080NHLBI NIH HHS R29 HL058080NIDDK NIH HHS DK-70124NIDDK NIH HHS R01 DK070124
6 · The paper itself

Abstract

Tetrahydrobiopterin (BH4) is an essential cofactor required for the activity of endothelial nitric oxide (NO) synthase. Suboptimal concentrations of BH4 in the endothelium reduce the biosynthesis of NO, thus contributing to the pathogenesis of vascular endothelial dysfunction. Supplementation with exogenous BH4 or therapeutic approaches that increase endogenous amounts of BH4 can reduce or reverse endothelial dysfunction by restoring production of NO. Improvements in formulations of BH4 for oral delivery have stimulated clinical trials that test the efficacy of BH4 in the treatment of systemic hypertension, peripheral arterial disease, coronary artery disease, pulmonary arterial hypertension, and sickle cell disease. This review discusses ongoing progress in the translation of knowledge, accumulated in preclinical studies, into the clinical application of BH4 in the treatment of vascular diseases. This review also addresses the emerging roles of BH4 in the regulation of endothelial function and their therapeutic implications.

Indexed as

AnimalsBiopterinsBlood VesselsClinical Trials as TopicDrug Evaluation, PreclinicalEndotheliumHumansModels, TheoreticalVascular DiseasesBiopterinssapropterin

Identifiers

PMID19042039
PMCPMC2637534

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.