Evidence map›Paper›PMID 40642321›Full record

ArticleClinical kidney journal2025

Asymmetric dimethylarginine and citrulline are risk factors for cardiovascular disease independently of both estimated and measured GFR.

Nikoline B Rinde, Toralf Melsom, Ole Martin Fuskevåg, Bjørn O Eriksen, Jon Viljar Norvik

Abstract read
In one paragraph

Article in Clinical kidney journal, 2025. 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
–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

1 citing paper in PubMed.

  1. 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

5 authors.

Nikoline B RindeMetabolic and Renal Research Group, UiT The Arctic University of Norway, Tromsø, Norway.ORCID https://orcid.org/0000-0003-1652-4864
Toralf MelsomMetabolic and Renal Research Group, UiT The Arctic University of Norway, Tromsø, Norway.
Ole Martin FuskevågDivision of Diagnostic Services, Department of Laboratory Medicine, University Hospital of North Norway, Tromsø, Norway.
Bjørn O EriksenMetabolic and Renal Research Group, UiT The Arctic University of Norway, Tromsø, Norway.ORCID https://orcid.org/0000-0002-5837-2806
Jon Viljar NorvikMetabolic and Renal Research Group, UiT The Arctic University of Norway, Tromsø, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nitric oxide (NO) is crucial for endothelial dysfunction and its deficiency is linked to cardiovascular disease (CVD) and impaired kidney function. While research has explored NO metabolism in individuals with kidney disease, diabetes mellitus (DM) or CVD, the relationship in healthy individuals remains unclear. Studies using estimated glomerular filtration rate (eGFR) for kidney function may introduce non-GFR-related factors, confounding the results. We investigated the association between NO-related biomarkers and CVD outcomes in a healthy population, comparing adjustments using eGFR and measured GFR (mGFR). Methods: This 14-year longitudinal study evaluated 1575 healthy, middle-aged participants without pre-existing DM, CVD or kidney disease in the Renal Iohexol Clearance Survey (RENIS). Cox regression models assessed the effects of asymmetric dimethylarginine (ADMA), symmetric dimethylarginine (SDMA), arginine, citrulline and ornithine levels on CVD incidence and all-cause mortality. Analyses were adjusted for GFR using mGFR by iohexol clearance or eGFR based on serum creatinine (eGFR Results: Elevated ADMA levels were associated with incident CVD across all GFR adjustment methods, with a hazard ratio (HR) of 1.21 [95% confidence interval (CI) 1.06-1.38] for mGFR. SDMA was associated with CVD when adjusting for eGFR Conclusions: In a healthy population, ADMA and citrulline were associated with incident CVD, regardless of the GFR adjustment method, while the association of SDMA depended on the method used.

Indexed as

ADMAcardiovascular diseasecitrullineglomerular filtration rateSDMA

Identifiers

PMID40642321
PMCPMC12241856

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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.