Association Between Acylcarnitine Metabolism and Cardiovascular Disease in Patients with CKD

Background: Acylcarnitines have emerged as important biomarkers in various diseases, including metabolic disorders, neuropsychiatric conditions, and cardiovascular diseases (CVD). However, research on the relationship between acylcarnitine metabolism and CVD in chronic kidney disease (CKD) patients is limited. This study aims to investigate the association between serum acylcarnitine profiles and the presence of CVD in patients with CKD. Methods: A total of 451 CKD patients were included in this cross-sectional study. Serum levels of 34 acylcarnitine species were measured using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Patients were divided into two groups based on the presence or absence of CVD, and clinical characteristics and serum acylcarnitine levels were compared. Univariate and multivariate logistic regression analyses were performed to identify factors associated with CVD in these patients. Additionally, a predictive risk model was established. Results: Among the patients, 285 (63.2%) were male, with a median estimated glomerular filtration rate (eGFR) of 51.1 (26.56, 75.94) mL/min/1.73 m2. A total of 87 patients (19.3%) had concurrent CVD. Compared to those without CVD, patients with CVD were older, had lower eGFR, and exhibited lower levels of hemoglobin, total cholesterol, triglycerides, and low-density lipoprotein cholesterol (P < 0.05). Of the 34 acylcarnitine species measured, 16 were significantly elevated in the CVD group. C4, C10:1, C4DC, C8, eGFR, and triglycerides (TG) were identified as independent factors associated with CVD in CKD patients, with increased serum levels of C4 and C10:1 positively correlating with CVD. The composite model exhibited strong performance, with an area under the curve (AUC) of 0.862 (95% CI: 0.790–0.930), demonstrating high sensitivity (80.6%) and specificity (81.2%). Conclusion: Patients with CKD and CVD exhibit significantly higher serum levels of 16 acylcarnitine species compared to those without CVD. C4, C10:1, C4DC, C8, eGFR, and TG are independently associated with the presence of CVD in CKD patients. The composite prediction model may effectively identifiy high-risk CVD populations among CKD patients. Funding: Government Support – Non-U.S.

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Journal
Journal of the American Society of Nephrology
Published
2025-10-01
DOI
https://doi.org/10.1681/asn.20250zdp51z8
Primary Topic
Metabolism and Genetic Disorders
Type
article
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article

Association Between Acylcarnitine Metabolism and Cardiovascular Disease in Patients with CKD

Lei Jiang, Chunsun Dai, Lulu Wang, Lingling Xu
Journal of the American Society of Nephrology
Metabolism and Genetic Disorders
article

Association Between Acylcarnitine Metabolism and Cardiovascular Disease in Patients with CKD

Lei Jiang, Chunsun Dai, Lulu Wang, Lingling Xu
article en

Abstract

Background: Acylcarnitines have emerged as important biomarkers in various diseases, including metabolic disorders, neuropsychiatric conditions, and cardiovascular diseases (CVD). However, research on the relationship between acylcarnitine metabolism and CVD in chronic kidney disease (CKD) patients is limited. This study aims to investigate the association between serum acylcarnitine profiles and the presence of CVD in patients with CKD. Methods: A total of 451 CKD patients were included in this cross-sectional study. Serum levels of 34 acylcarnitine species were measured using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Patients were divided into two groups based on the presence or absence of CVD, and clinical characteristics and serum acylcarnitine levels were compared. Univariate and multivariate logistic regression analyses were performed to identify factors associated with CVD in these patients. Additionally, a predictive risk model was established. Results: Among the patients, 285 (63.2%) were male, with a median estimated glomerular filtration rate (eGFR) of 51.1 (26.56, 75.94) mL/min/1.73 m2. A total of 87 patients (19.3%) had concurrent CVD. Compared to those without CVD, patients with CVD were older, had lower eGFR, and exhibited lower levels of hemoglobin, total cholesterol, triglycerides, and low-density lipoprotein cholesterol (P < 0.05). Of the 34 acylcarnitine species measured, 16 were significantly elevated in the CVD group. C4, C10:1, C4DC, C8, eGFR, and triglycerides (TG) were identified as independent factors associated with CVD in CKD patients, with increased serum levels of C4 and C10:1 positively correlating with CVD. The composite model exhibited strong performance, with an area under the curve (AUC) of 0.862 (95% CI: 0.790–0.930), demonstrating high sensitivity (80.6%) and specificity (81.2%). Conclusion: Patients with CKD and CVD exhibit significantly higher serum levels of 16 acylcarnitine species compared to those without CVD. C4, C10:1, C4DC, C8, eGFR, and TG are independently associated with the presence of CVD in CKD patients. The composite prediction model may effectively identifiy high-risk CVD populations among CKD patients. Funding: Government Support – Non-U.S.

Journal of the American Society of NephrologyVol. 36(10S)
Second Affiliated Hospital of Nanjing Medical University (CN)
Openalex Percentile: Top 59%
Metabolism and Genetic Disorders
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