Impaired vascular function in patients with chronic kidney disease who have elevated symmetric dimethylarginine but not asymmetric dimethylarginine

Chronic kidney disease (CKD) is associated with heightened cardiovascular disease (CVD) risk, partly due to impaired peripheral vascular function. Symmetric dimethylarginine (SDMA) and asymmetric dimethylarginine (ADMA) are emerging biomarkers implicated in nitric oxide (NO) regulation and vascular health. Although ADMA is a well-established inhibitor of NO synthesis, recent evidence suggests that SDMA may also play a critical role in vascular health, especially in CKD before end-stage. Thus, in 23 stages 3 and 4 patients with CKD (66 ± 9 yr) and 32 age-matched controls (64 ± 8 yr), we compared serum SDMA and ADMA levels and examined their associations with vascular function, including flow-mediated dilation (FMD), peak blood velocity to reactive hyperemia, and carotid-femoral pulse wave velocity (cfPWV). SDMA was significantly elevated in patients with CKD (163 ± 37 vs. 100 ± 15 ng/mL, <i>P</i> < 0.0001), while ADMA did not differ significantly between groups (111 ± 22 vs. 103 ± 12 ng/mL, <i>P</i> = 0.083). Patients with CKD had lower FMD (3.66 ± 2.45 vs. 4.47 ± 2.45%, <i>P</i> = 0.048) and peak blood velocity (47.43 ± 16.67 vs. 60.18 ± 16.88 cm/s, <i>P</i> = 0.009), but higher cfPWV (8.82 ± 1.53 vs. 7.69 ± 1.35 m/s, <i>P</i> = 0.004) than controls. Pooled analysis revealed that SDMA correlated inversely with eGFR (<i>r</i> = -0.86, <i>P</i> < 0.0001), FMD (<i>r</i><sub>s</sub> = -0.28, <i>P</i> = 0.039), and peak blood velocity (<i>r</i><sub>s</sub> = -0.40, <i>P</i> = 0.001) but not cfPWV (<i>r</i> = 0.14, <i>P</i> = 0.338). ADMA correlated inversely with peak blood velocity (<i>r</i><sub>s</sub> = -0.28, <i>P</i> = 0.042) but not eGFR (<i>r</i> = -0.25, <i>P</i> = 0.063), FMD (<i>r</i><sub>s</sub> = -0.06, <i>P</i> = 0.664), or cfPWV (<i>r</i> = 0.21, <i>P</i> = 0.146). Collectively, these findings suggest that SDMA, relative to ADMA, may be a stronger marker of vascular dysfunction in stages 3 and 4 CKD. However, the predictive value of SDMA for vascular function was modest, which may limit its overall potential as a biomarker for vascular function in CKD.<b>NEW & NOTEWORTHY</b> The associations between symmetric dimethylarginine (SDMA) and asymmetric dimethylarginine (ADMA) and measures of vascular function were investigated in patients with stage 3-4 chronic kidney disease (CKD). We found that SDMA exhibited stronger relationships with vascular function than ADMA. However, the strength of associations was modest, potentially limiting their role as standalone predictors of vascular dysfunction. Nonetheless, these data support emerging evidence of a differential impact of SDMA and ADMA in patients with CKD.

Authors

Institutions

Publication Details

Journal
American Journal of Physiology-Renal Physiology
Published
2025-08-14
DOI
https://doi.org/10.1152/ajprenal.00158.2025
Citations
1
Primary Topic
Nitric Oxide and Endothelin Effects
Type
article
Field-Weighted Citation Impact
1.16

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Impaired vascular function in patients with chronic kidney disease who have elevated symmetric dimethylarginine but not asymmetric dimethylarginine

Damsara Nandadeva, Benjamin E. Young, Rachel J. Skow, Taha Alhalimi et al.
1 citations
American Journal of Physiology-Renal Physiology
Nitric Oxide and Endothelin Effects
1.16
article

Impaired vascular function in patients with chronic kidney disease who have elevated symmetric dimethylarginine but not asymmetric dimethylarginine

Damsara Nandadeva, Benjamin E. Young, Rachel J. Skow, Taha Alhalimi, Paul J. Fadel, Brandi Y. Stephens, Ann‐Katrin Grotle, Jasdeep Kaur, P.F. Mohan
article en
1 citations

Abstract

Chronic kidney disease (CKD) is associated with heightened cardiovascular disease (CVD) risk, partly due to impaired peripheral vascular function. Symmetric dimethylarginine (SDMA) and asymmetric dimethylarginine (ADMA) are emerging biomarkers implicated in nitric oxide (NO) regulation and vascular health. Although ADMA is a well-established inhibitor of NO synthesis, recent evidence suggests that SDMA may also play a critical role in vascular health, especially in CKD before end-stage. Thus, in 23 stages 3 and 4 patients with CKD (66 ± 9 yr) and 32 age-matched controls (64 ± 8 yr), we compared serum SDMA and ADMA levels and examined their associations with vascular function, including flow-mediated dilation (FMD), peak blood velocity to reactive hyperemia, and carotid-femoral pulse wave velocity (cfPWV). SDMA was significantly elevated in patients with CKD (163 ± 37 vs. 100 ± 15 ng/mL, <i>P</i> < 0.0001), while ADMA did not differ significantly between groups (111 ± 22 vs. 103 ± 12 ng/mL, <i>P</i> = 0.083). Patients with CKD had lower FMD (3.66 ± 2.45 vs. 4.47 ± 2.45%, <i>P</i> = 0.048) and peak blood velocity (47.43 ± 16.67 vs. 60.18 ± 16.88 cm/s, <i>P</i> = 0.009), but higher cfPWV (8.82 ± 1.53 vs. 7.69 ± 1.35 m/s, <i>P</i> = 0.004) than controls. Pooled analysis revealed that SDMA correlated inversely with eGFR (<i>r</i> = -0.86, <i>P</i> < 0.0001), FMD (<i>r</i><sub>s</sub> = -0.28, <i>P</i> = 0.039), and peak blood velocity (<i>r</i><sub>s</sub> = -0.40, <i>P</i> = 0.001) but not cfPWV (<i>r</i> = 0.14, <i>P</i> = 0.338). ADMA correlated inversely with peak blood velocity (<i>r</i><sub>s</sub> = -0.28, <i>P</i> = 0.042) but not eGFR (<i>r</i> = -0.25, <i>P</i> = 0.063), FMD (<i>r</i><sub>s</sub> = -0.06, <i>P</i> = 0.664), or cfPWV (<i>r</i> = 0.21, <i>P</i> = 0.146). Collectively, these findings suggest that SDMA, relative to ADMA, may be a stronger marker of vascular dysfunction in stages 3 and 4 CKD. However, the predictive value of SDMA for vascular function was modest, which may limit its overall potential as a biomarker for vascular function in CKD.<b>NEW & NOTEWORTHY</b> The associations between symmetric dimethylarginine (SDMA) and asymmetric dimethylarginine (ADMA) and measures of vascular function were investigated in patients with stage 3-4 chronic kidney disease (CKD). We found that SDMA exhibited stronger relationships with vascular function than ADMA. However, the strength of associations was modest, potentially limiting their role as standalone predictors of vascular dysfunction. Nonetheless, these data support emerging evidence of a differential impact of SDMA and ADMA in patients with CKD.

American Journal of Physiology-Renal PhysiologyVol. 329(3)
University of Peradeniya (LK), University of North Texas (US), University of Alberta (CA), University of North Texas Health Science Center (US), Western Norway University of Applied Sciences (NO), The University of Texas at Arlington (US), Dermatology Specialists (US), Southwestern Medical Center (US), The University of Texas at Austin (US), The University of Texas Southwestern Medical Center (US)
National Heart, Lung, and Blood Institute
Good health and well-being
Openalex Percentile: Top 19%
Nitric Oxide and Endothelin Effects
1.16
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.