Abstract: FR-PO997
Homocysteine Is Associated with Kidney Injury and Increased Arterial Stiffness
Session Information
- CKD Mechanisms: From Mendel to Mars
November 03, 2023 | Location: Exhibit Hall, Pennsylvania Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: CKD (Non-Dialysis)
- 2303 CKD (Non-Dialysis): Mechanisms
Authors
- Piko, Nejc, Univerzitetni Klinicni Center Maribor, Maribor, Maribor, Slovenia
- Bevc, Sebastjan, Univerzitetni Klinicni Center Maribor, Maribor, Maribor, Slovenia
- Hojs, Radovan, Univerzitetni Klinicni Center Maribor, Maribor, Maribor, Slovenia
- Petreski, Tadej, Univerzitetni Klinicni Center Maribor, Maribor, Maribor, Slovenia
- Varda, Luka, Univerzitetni Klinicni Center Maribor, Maribor, Maribor, Slovenia
- Ekart, Robert, Univerzitetni Klinicni Center Maribor, Maribor, Maribor, Slovenia
Background
Homocysteine (Hcy) promotes atherogenesis and is elevated in chronic kidney disease (CKD). Few studies addressed the association between Hcy, different markers of kidney injury and arterial stiffness (AS).
Methods
127 patients (70.9% male, mean age 65.0±9.2 years, 78.7% hypertensive, and 20.5% diabetics) were admitted due to elective coronarography. The immunoassay method was used to measure serum Hcy (mmol/L) and cystatin C (CysC, mg/L). Hyperhomocysteinemia was defined by Hcy≥15 (Group 1, n=37), and patients with Hcy<15 were included in Group 2 (n=90). Albuminuria was expressed as UACR (mg/g). The glomerular filtration rate was estimated (eGFR) by the CKD-EPI 2009 equation (ml/min/1.73 m2). Carotid-femoral pulse wave velocity (cfPWV, m/s) was used as a marker of AS (SphygmoCor®, Atcor, Australia). SPSS® (version 22) was used for statistical analysis.
Results
Mean Hcy was 14.1±5.7, eGFR 75.5±17.2, CysC 1.1±0.7, UACR 25.9±35.7 and cfPWV 10.3±2.7. Spearman's test showed a significant correlation between Hcy and CysC (rs=0.608, p<0.001), UACR (rs=0.264, p=0.004), eGFR (rs=-0.485, p<0.001) and between Hcy and cfPWV (rs=0.328, p<0.001). Group 1 had lower eGFR (62.4±21.5 vs 80.3±12.2, p<0.001), higher cysC (1.5±1.2 vs 0.9±0.2, p<0.001), higher UACR (49.6±57.5 vs 16.5±13.7, p<0.001), and higher cfPWV (11.5±3.3 vs 9.6±2.1, p<0.001). No difference was observed in comorbidities or medications. Multiple regression analysis (independent variables gender, age, diabetes, hypertension) confirmed a correlation between Hcy and eGFR (β=-0.535, p<0.001), UACR (β=0.331, p<0.001) and cysC (β=0.561, p<0.001). Hcy was higher in patients with lower eGFR (Figure 1). An independent correlation was also found between Hcy and cfPWV (β=0.238, p=0.005) and age and cfPWV (β=0.407, p<0.001). No association was found between cfPWV/Hcy and coronary artery disease (CAD).
Conclusion
Serum Hcy is associated with decreased eGFR, increased UACR, increased cysC and increased AS, but not CAD.