Evidence map›Paper›PMID 31506747›Full record

ReviewWorld journal of urology2020

Emerging drugs to target lower urinary tract symptomatology (LUTS)/benign prostatic hyperplasia (BPH): focus on the prostate.

Stefan Ückert, George T Kedia, Dimitrios Tsikas, Annika Simon, Andreas Bannowsky, Markus A Kuczyk

Abstract readReview
PubMed Publisher
In one paragraph

Review in World journal of urology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 11% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

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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

6 authors at 2 institutions in 1 country.

Stefan ÜckertDivision of Surgery, Department of Urology and Urological Oncology, Hannover Medical School, 30623, Hannover, Germany. sue_de_99@yahoo.de.ORCID http://orcid.org/0000-0001-7169-0385
George T KediaDivision of Surgery, Department of Urology and Urological Oncology, Hannover Medical School, 30623, Hannover, Germany.
Dimitrios TsikasCore Unit Proteomics, Center of Pharmacology and Toxicology, Hannover Medical School, Hannover, Germany.
Annika SimonDepartment of Internal Medicine, Hannover Medical School, Hannover, Germany.
Andreas BannowskyDepartment of Urology, Imland Klinik GmbH, Rendsburg, Germany.
Markus A KuczykDivision of Surgery, Department of Urology and Urological Oncology, Hannover Medical School, 30623, Hannover, Germany.
Medizinische Hochschule Hannover · DEInstitut für Berufliche Aus- und Fortbildung · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe benign prostatic syndrome, comprising lower urinary tract symptomatology secondary to benign prostatic hyperplasia/enlargement, represents a major health care issue in westernized countries. The pharmacological management involves alpha-adrenoceptor antagonists, intervention into the hormonal control of prostate growth using inhibitors of the enzyme 5-alpha-reductase, and stimulation of the nitric oxide/cyclic GMP pathway by tadalafil, an inhibitor of the phosphodiesterase type 5.

methodsThis review summarizes the achievements which have been made in the development of drug candidates assumed to offer opportunities as beneficial treatment options in the management of the benign prostatic syndrome.

resultsA review of the literature has revealed that the line of development is focusing on drugs interfering with peripheral neuromuscular/neuronal mechanisms (nitric oxide donor drugs, agonists/antagonists of endogenous peptides, botulinum toxin, NX-1207), the steroidal axis (cetrorelix) or the metabolic turn-over (lonidamine), as well as the combination of drugs already established in the treatment of lower urinary tract symptomatology/benign prostatic hyperplasia (phosphodiesterase 5 inhibitor plus alpha-adrenoceptor antagonist).

conclusionMany research efforts have provided the basis for the development of new therapeutic modalities for the management of lower urinary tract dysfunctions, some of which might be offered to the patients in the near future.

Indexed as

Adrenergic alpha-AntagonistsBotulinum ToxinsHumansLower Urinary Tract SymptomsMaleNitric OxideProstatic HyperplasiaSignal TransductionAdrenergic alpha-AntagonistsBotulinum ToxinsNitric OxideBenign prostatic hyperplasia (BPH)Lower urinary tract symptoms (LUTS)Pharmacotherapy

Identifiers

PMID31506747
OpenAlexW2972454727

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.