Abstract: FR-PO0279
Higher Serum Angiopoietin-Like Protein 2 Is Associated with Subsequent eGFR Decline but Not Albuminuria
Session Information
- CKD: Omics, Systemic Stressors, and Targeted Pharmacotherapy
October 23, 2026 | Location: Exhibit Hall A, Convention Center
Abstract Time: 10:00 AM - 12:00 PM
Category: CKD (Non-Dialysis)
- 2201 CKD (Non-Dialysis): Epidemiology, Risk Factors, and Prevention
Authors
- Kim, Chae-Been, Tsukuba Daigaku, Tsukuba, Ibaraki Prefecture, Japan
- Yoshikoshi, Shun, Tsukuba Daigaku, Tsukuba, Ibaraki Prefecture, Japan
- Kosaki, Keisei, Tsukuba Daigaku, Tsukuba, Ibaraki Prefecture, Japan
- Mori, Shoya, Tokyo Nogyo Daigaku, Setagaya, Tokyo, Japan
- Maeda, Seiji, Waseda Daigaku Sports Kagaku Gakujutsuin, Tokorozawa, Saitama Prefecture, Japan
- Kuro-o, Makoto, Jichi Ika Daigaku, Shimotsuke, Tochigi Prefecture, Japan
- Yamagata, Kunihiro, Tsukuba Daigaku, Tsukuba, Ibaraki Prefecture, Japan
Background
Angiopoietin-like protein 2 (ANGPTL2) is a circulating protein associated with chronic inflammation and metabolic dysfunction, both implicated in age-related kidney function decline. However, the longitudinal association of serum ANGPTL2 with changes in kidney function and albuminuria remains unclear.
Methods
We conducted a prospective cohort study of 294 community-dwelling adults (mean age, 62.5 years; 64% women) followed for 5 years. Linear mixed-effects models were used to examine associations of baseline ANGPTL2 with longitudinal changes in estimated glomerular filtration rate (eGFR) and urinary albumin-to-creatinine ratio (UACR). Cox proportional hazards models evaluated associations of ANGPTL2 with a ≥20% eGFR decline and doubling of UACR. ANGPTL2 was log-transformed and standardized before analysis. Models were adjusted for demographic, metabolic, and clinical covariates, including baseline kidney measures.
Results
Higher standardized log-transformed ANGPTL2 was associated with greater decline in eGFR over time (β for ANGPTL2 × time interaction = −0.19; 95% confidence interval [CI], −0.33 to −0.049). In contrast, ANGPTL2 was not significantly associated with the trajectory of UACR (β = 0.005; 95% CI, −0.003 to 0.012). In time-to-event analyses, higher ANGPTL2 levels were associated with an increased risk of ≥20% eGFR decline (hazard ratio [HR] = 1.48; 95% CI, 1.04 to 2.11) but not with doubling of UACR (HR = 1.09; 95% CI, 0.87 to 1.37).
Conclusion
Higher circulating ANGPTL2 levels were associated with subsequent eGFR decline but not with UACR changes in a community-based population. These findings support further investigation of ANGPTL2 as a potential marker of early kidney function decline.
Figure 1. Restricted cubic spline analyses of the associations of baseline ANGPTL2 with the risk of (A) ≥20% decline in eGFR and (B) ≥2-fold increase in UACR. Hazard ratios are expressed per 1 SD increase in log-transformed ANGPTL2. Shaded areas indicate 95% CI.
Funding
- Government Support – Non-U.S.