Evidence map›Paper›PMID 31533264›Full record

ReviewInternational journal of molecular sciences2019

The Second Life of Methylarginines as Cardiovascular Targets.

Natalia Jarzebska, Arduino A Mangoni, Jens Martens-Lobenhoffer, Stefanie M Bode-Böger, Roman N Rodionov

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
3.9field-weighted citation impact, top 6% 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

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 61 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

5 authors at 3 institutions in 2 countries.

Natalia JarzebskaDivision of Angiology, Department of Internal Medicine III, University Center for Vascular Medicine, Technische Universität Dresden, 01307 Dresden, Germany. natalia.jarzebska@uniklinikum-dresden.de.
Arduino A MangoniDepartment of Clinical Pharmacology, College of Medicine and Public Health, Flinders University and Flinders Medical Centre, Bedford Park 5042, Adelaide, Australia. arduino.mangoni@flinders.edu.au.ORCID 0000-0001-8699-1412
Jens Martens-LobenhofferInstitute of Clinical Pharmacology, Otto-von-Guericke University, 39120 Magdeburg, Germany. jens.martens-lobenhoffer@med.ovgu.de.
Stefanie M Bode-BögerInstitute of Clinical Pharmacology, Otto-von-Guericke University, 39120 Magdeburg, Germany. stefanie.bode-boeger@med.ovgu.de.
Roman N RodionovDivision of Angiology, Department of Internal Medicine III, University Center for Vascular Medicine, Technische Universität Dresden, 01307 Dresden, Germany. Roman.Rodionov@uniklinikum-dresden.de.
Klinik und Poliklinik für Psychotherapie und Psychosomatik · DEOtto-von-Guericke-Universität Magdeburg · DEFlinders University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endogenous methylarginines were proposed as cardiovascular risk factors more than two decades ago, however, so far, this knowledge has not led to the development of novel therapeutic approaches. The initial studies were primarily focused on the endogenous inhibitors of nitric oxide synthases asymmetric dimethylarginine (ADMA) and monomethylarginine (MMA) and the main enzyme regulating their clearance dimethylarginine dimethylaminohydrolase 1 (DDAH1). To date, all the screens for DDAH1 activators performed with the purified recombinant DDAH1 enzyme have not yielded any promising hits, which is probably the main reason why interest towards this research field has started to fade. The relative contribution of the second DDAH isoenzyme DDAH2 towards ADMA and MMA clearance is still a matter of controversy. ADMA, MMA and symmetric dimethylarginine (SDMA) are also metabolized by alanine: glyoxylate aminotransferase 2 (AGXT2), however, in addition to methylarginines, this enzyme also has several cardiovascular protective substrates, so the net effect of possible therapeutic targeting of AGXT2 is currently unclear. Recent studies on regulation and functions of the enzymes metabolizing methylarginines have given a second life to this research direction. Our review discusses the latest discoveries and controversies in the field and proposes novel directions for targeting methylarginines in clinical settings.

Indexed as

AmidohydrolasesAnimalsArginineBiological TransportBiomarkersCardiovascular DiseasesCardiovascular SystemDisease SusceptibilityEnergy MetabolismHumansMolecular Targeted TherapyAmidohydrolasesArginineBiomarkersdimethylargininaseN,N-dimethylargininesymmetric dimethylarginine6-guanidino-2-oxocaproic acid (GOCA)alanine:glyoxylate aminotransferase 2 (AGXT2)asymmetric dimethylarginine (ADMA)asymmetric α-keto-dimethylguanidinovaleric acid (ADGV)beta-aminoisobutyric acid (BAIBA)dimethylarginine dimethylaminohydrolase (DDAH)Homoargininesymmetric dimethylarginine (SDMA)symmetric α-keto-dimethylguanidinovaleric acid (SDGV)

Identifiers

PMID31533264
PMCPMC6769906
OpenAlexW2973975811

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.