Key result
In a pediatric cohort, plasma concentrations of homoarginine, SDMA, and ADMA were highest in neonates, while children with chronic kidney disease had 1.92-fold higher SDMA levels than controls independent of GFR.
Why the study?
High ADMA and SDMA but low L-hArg concentrations are linked to cardio- and cerebrovascular events in adults, but their role in paediatric patients remains less clear.
Cross-Sectional (n=198)
No
Answers are grounded in this paper and cite their sources.
This study provides the first comprehensive dataset of guanidino compound levels across all pediatric age groups, demonstrating distinct developmental dynamics and confirming SDMA as a marker for CKD in children.
Guanidino compounds such as dimethylarginines (SDMA, ADMA) and L-homoarginine ((L-)hArg) can interfere with bioavailability and function of the main NO-donor L-arginine (L-Arg). High ADMA and SDMA but low L-hArg concentrations have been associated with cardio- and cerebrovascular events and mortality in adults. The role of guanidino compounds in paediatric patients remains less clear. We, therefore, compared guanidino compound levels in plasma samples of 57 individuals with chronic kidney disease (CKD) and 141 individuals without CKD from the age of 0 to 17 years, including patients with different comorbidities by correlation and regression analyses. We found highest hArg, SDMA and ADMA concentrations in neonates (Kruskal-Wallis, p < 0.001 for all). From the age of 1 year on, hArg levels increased, whereas SDMA und ADMA levels further decreased in children. SDMA and ADMA are higher in children with CKD independent of GFR (mean factor 1.92 and 1.38, respectively, p < 0.001 for both), and SDMA is strongly correlated with creatinine concentration in children with CKD (Spearman's rho 0.74, p < 0.001). We provide guanidino compound levels in a large sample covering all paediatric age groups for the first time. Our data can be used to assess the role of guanidino compounds such as hArg in disease states, i.e. cerebro- and cardiovascular disorders in childhood and adolescence.
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Baach et al. (2023) conducted a cross-sectional in Chronic kidney disease (n=198). Chronic kidney disease vs. Children without chronic kidney disease was evaluated on SDMA plasma levels (mean factor 1.92, 95% CI 1.56-2.37, p=<0.001). In a pediatric cohort, plasma concentrations of homoarginine, SDMA, and ADMA were highest in neonates, while children with chronic kidney disease had 1.92-fold higher SDMA levels than controls independent of GFR.
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