Circulating angiopoietin-like protein 2 levels and mortality risk in patients receiving maintenance hemodialysis: a prospective cohort study

Author:

Morinaga Jun1234,Kakuma Tatsuyuki4,Fukami Hirotaka12,Hayata Manabu1,Uchimura Kohei5,Mizumoto Teruhiko1,Kakizoe Yutaka1,Miyoshi Taku1,Shiraishi Naoki1,Adachi Masataka1,Izumi Yuichiro1,Kuwabara Takashige1,Okadome Yusuke2,Sato Michio2,Horiguchi Haruki2,Sugizaki Taichi2,Kadomatsu Tsuyoshi2,Miyata Keishi2,Tajiri Saeko6,Tajiri Tetsuya6,Tomita Kimio1,Kitamura Kenichiro5,Oike Yuichi2,Mukoyama Masashi1

Affiliation:

1. Department of Nephrology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

2. Department of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan

3. Department of Clinical Investigation, Kumamoto University Hospital, Kumamoto, Japan

4. Biostatistics Center, Kurume University, Fukuoka, Japan

5. Third Department of Internal Medicine, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan

6. Medical Corporation, Jinseikai, Kumamoto, Japan

Abstract

Abstract Background Patients undergoing hemodialysis treatment have a poor prognosis, as many develop premature aging. Systemic inflammatory conditions often underlie premature aging phenotypes in uremic patients. We investigated whether angiopoietin-like protein 2 (ANGPTL 2), a factor that accelerates the progression of aging-related and noninfectious inflammatory diseases, was associated with increased mortality risk in hemodialysis patients. Methods We conducted a multicenter prospective cohort study of 412 patients receiving maintenance hemodialysis and evaluated the relationship between circulating ANGPTL2 levels and the risk for all-cause mortality. Circulating ANGPTL2 levels were log-transformed to correct for skewed distribution and analyzed as a continuous variable. Results Of 412 patients, 395 were included for statistical analysis. Time-to-event data analysis showed high circulating ANGPTL2 levels were associated with an increased risk for all-cause mortality after adjustment for age, sex, hemodialysis vintage, nutritional status, metabolic parameters and circulating high-sensitivity C-reactive protein levels {hazard ratio [HR] 2.04 [95% confidence interval (CI) 1.10–3.77]}. High circulating ANGPTL2 levels were also strongly associated with an increased mortality risk, particularly in patients with a relatively benign prognostic profile [HR 3.06 (95% CI 1.86–5.03)]. Furthermore, the relationship between circulating ANGPTL2 levels and mortality risk was particularly strong in patients showing few aging-related phenotypes, such as younger patients [HR 7.99 (95% CI 3.55–18.01)], patients with a short hemodialysis vintage [HR 3.99 (95% CI 2.85–5.58)] and nondiabetic patients [HR 5.15 (95% CI 3.19–8.32)]. Conclusion We conclude that circulating ANGPTL2 levels are positively associated with mortality risk in patients receiving maintenance hemodialysis and that ANGPTL2 could be a unique marker for the progression of premature aging and subsequent mortality risk in uremic patients, except those with significant aging-related phenotypes.

Funder

JSPS KAKENHI

Publisher

Oxford University Press (OUP)

Subject

Transplantation,Nephrology

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