Key result
Plasma calmodulin levels were significantly associated with early markers of cardiovascular disease in pediatric chronic kidney disease (all r > 0.2; p < 0.05).
Why the study?
Calmodulin is implicated in cardiac remodeling and was identified as differentially expressed in hypertensive pediatric CKD, prompting assessment of plasma calmodulin as a CVD biomarker compared with traditional risk markers.
Does plasma calmodulin correlate with early markers of cardiovascular disease in pediatric patients with chronic kidney disease?
Cross-Sectional (n=81)
Does plasma calmodulin correlate with early markers of cardiovascular disease in pediatric patients with chronic kidney disease?
Plasma calmodulin may serve as a sensitive early biomarker for subclinical cardiovascular disease in pediatric patients with chronic kidney disease.
Plasma calmodulin was associated with subclinical CVD markers in pediatric CKD; leaves open its utility as a complementary biomarker pending prospective validation.
Background: Calmodulin is a calcium-signaling protein implicated in cardiac remodeling and could be released extracellularly. It was previously identified as differentially expressed in hypertensive pediatric chronic kidney disease (CKD). This study assessed plasma calmodulin as a cardiovascular disease (CVD) biomarker in pediatric CKD and compared it with traditional risk markers. Methods: We conducted a cross-sectional study of 81 children with CKD aged 3–18 years. All underwent clinical assessments and echocardiography; 44 had carotid ultrasound, and 38 completed ambulatory blood pressure monitoring (ABPM). Results: Most participants had preserved renal function (median eGFR, 104.4 mL/min/1.73 m2). Plasma calmodulin levels were significantly associated with early markers of CVD, including interventricular septal thickness, left ventricular mass, carotid intima–media thickness, and ABPM systolic measures (all r > 0.2; p < 0.05). In multivariable analysis, only calmodulin and office systolic blood pressure (BP) independently predicted abnormal BP profiles. Conclusions: Plasma calmodulin may serve as a sensitive, though non-specific, early CVD biomarker in pediatric CKD and could complement conventional screening tools.
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Lee et al. (2025) conducted a cross-sectional in pediatric chronic kidney disease (n=81). Plasma calmodulin was evaluated on early markers of cardiovascular disease including interventricular septal thickness, left ventricular mass, carotid intima-media thickness, and ABPM systolic measures (r > 0.2, p=< 0.05). Plasma calmodulin levels were significantly associated with early markers of cardiovascular disease in pediatric chronic kidney disease (all r > 0.2; p < 0.05).
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