Evidence map›Paper›PMID 14569381›Full record

ArticleDer Urologe. Ausg. A2003

[Therapy of erectile dysfunction in 2005].

H Porst

Abstract read
PubMed Publisher
In one paragraph

Article in Der Urologe. Ausg. A, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

1 author at 1 institution in 1 country.

H PorstHamburg. Porst20354@aol.com
Hamburg Institut (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Erectile dysfunction (ED) management in the following 3-5 years will be dominated by substances targeting the L-arginine-NO-guanylate cyclase-cGMP-PDE-5 pathway, resulting in an intracellular elevation of the cGMP concentrations. Promising alternatives to the PDE-5 inhibitors, such as guanylate cyclase activators and Rho-kinase inhibitors, may also effectively compliment a PDE-5 inhibitor. Intranasal application of the melanocortin agonist PT 141 (Melanotan II) seems to be promising. As scheduled sexual activities are not preferred by the majority of couples, the future of ED-therapy will focus on drugs with a 1-2 day long efficacy window, or a daily bedtime application of low dosage agents which result in nocturnal reoxygenation of the cavernous bodies and in turn in functional improvement. Elevation of the cGMP levels and improvement of endothelial function as a result of this approach also promises benefits in cardiovascular diseases and in LUTS.

Indexed as

3',5'-Cyclic-GMP PhosphodiesterasesAnimalsArginineCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5Drugs, InvestigationalEnzyme ActivationErectile DysfunctionForecastingGuanylate CyclaseHumansIntracellular Signaling Peptides and ProteinsMalePhosphodiesterase InhibitorsPhosphoric Diester HydrolasesProtein Serine-Threonine Kinases3',5'-Cyclic-GMP PhosphodiesterasesArginineCyclic GMPCyclic Nucleotide Phosphodiesterases, Type 5Drugs, InvestigationalGuanylate CyclaseIntracellular Signaling Peptides and ProteinsPDE5A protein, humanPhosphodiesterase InhibitorsPhosphoric Diester HydrolasesProtein Serine-Threonine Kinasesrho-Associated Kinases

Identifiers

PMID14569381
OpenAlexW2411556799

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.