Evidence map›Paper›PMID 30071927›Full record

ArticleEuropean journal of rheumatology2018

Higher levels of SDMA and not ADMA are associated with poorer survival of trial patients with systemic ANCA-associated vasculitis.

Uta Erdbrügger, Jan T Kielstein, Kerstin Westman, Jennie Z Ma, Wenjun Xin, Stephanie M Bode-Böger, Mȧrten Segelmark, Niels Rasmussen, Kirsten De Groot

Abstract read
In one paragraph

Article in European journal of rheumatology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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

9 authors.

Uta ErdbrüggerDivision of Nephrology, Department of Medicine, University of Virginia Health System, Virginia, USA.ORCID http://orcid.org/0000-0002-6829-6624
Jan T KielsteinDepartment of Hypertension and Nephrology, Medical Clinic V, Klinikum Braunschweig, Braunschweig, Germany.ORCID http://orcid.org/0000-0001-8110-9064
Kerstin WestmanDepartment of Nephrology, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0002-2930-998X
Jennie Z MaDepartment of Biostatistics, University of Virginia Health System, Virginia, USA.ORCID http://orcid.org/0000-0002-5839-2882
Wenjun XinDepartment of Biostatistics, University of Virginia Health System, Virginia, USA.ORCID http://orcid.org/0000-0002-3172-1017
Stephanie M Bode-BögerOtto-von-Guericke University, Institute of Clinical Pharmacology, Magdeburg, Germany.ORCID http://orcid.org/0000-0002-5132-6591
Mȧrten SegelmarkDivision of Drug Research, Department of Medical Health Sciences, Linköping University, Linköping, Sweden.ORCID http://orcid.org/0000-0002-1221-0772
Niels RasmussenDepartment of Biochemistry and Immunology, Statens Seruminstitut, Copenhagen, Denmark.ORCID http://orcid.org/0000-0003-2496-4368
Kirsten De GrootDepartment of Nephrology and Rheumatology, Medical Clinic III, Sana Klinikum, Offenbach, Germany.ORCID http://orcid.org/0000-0001-6100-2403

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveEndothelial dysfunction, increased cardiovascular events (CVE), and accelerated atherosclerosis have been described in patients with small vessel vasculitis and collagen vascular disease. Identifying predictors of cardiovascular risk will help to optimize short- and long-term care of patients with vasculitis. The present study investigates the predictive role of the endogenous nitric oxide synthase (NOS) inhibitor asymmetric dimethylarginine (ADMA) and its stereoisomer symmetric dimethylarginine (SDMA) for cardiovascular risk, all-cause mortality, and renal function in patients with anti-neutrophil-cytoplasmic antibodies-associated small vessel vasculitis (AASV) subjected to standardized treatment regimens in four European Vasculitis Study Group trials representing all stages of renal disease.

methodsSera from 89 patients with AASV were available for measuring SDMA, ADMA, and arginine using liquid chromatography/mass spectrometry at the time of active disease and remission. Clinical data on disease activity, remission, relapse rate, and 5-year follow-up data for CVE and renal outcome were collected.

resultsSymmetric dimethylarginine and ADMA levels were not predictive of CVE at 5 years of follow-up. The overall CVE rate was low in the present cohort of AASV (8%). However, SDMA, and not ADMA, levels were significantly associated with poorer survival (death/ESRD) independent of entry glomerular filtration rate.

conclusionThis novel outcome in a well-defined group of patients with AASV might indicate a different mechanism of endothelial response in AASV as compared with atherosclerosis. This should be further explored in a larger cohort of AASV patients with a higher CVE rate and/or a longer follow-up. Moreover, these findings should be correlated to other markers of vascular damage.

Identifiers

PMID30071927
PMCPMC6116852

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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.