Differential associations of fetuin-A and calcification propensity with cardiovascular events and subsequent mortality in patients undergoing hemodialysis

Author:

Mori Katsuhito1,Shoji Tetsuo23ORCID,Nakatani Shinya4,Uedono Hideki4,Ochi Akinobu4,Yoshida Hisako5,Imanishi Yasuo4,Morioka Tomoaki4,Tsujimoto Yoshihiro6,Kuro-o Makoto7,Emoto Masanori124

Affiliation:

1. Department of Nephrology, Osaka Metropolitan University Graduate School of Medicine , Osaka , Japan

2. Department of Vascular Medicine, Osaka Metropolitan University Graduate School of Medicine , Osaka , Japan

3. Vascular Science Center for Translational Research, Osaka Metropolitan University Graduate School of Medicine , Osaka , Japan

4. Department of Metabolism, Endocrinology and Molecular Medicine, Osaka Metropolitan University Graduate School of Medicine , Osaka , Japan

5. Department of Medical Statistics, Osaka Metropolitan University Graduate School of Medicine , Osaka , Japan

6. Division of Internal Medicine, Inoue Hospital , Suita, Osaka , Japan

7. Center for Molecular Medicine, Jichi Medical University , Shimotsuke, Tochigi , Japan

Abstract

ABSTRACT Background Fetuin-A inhibits precipitation of calcium-phosphate crystals by forming calciprotein particles (CPP). A novel T50 test, which measures transformation time from primary to secondary CPP, is an index for calcification propensity. Both lower fetuin-A and shorter T50 levels were associated with cardiovascular disease (CVD) risk in patients with chronic kidney disease (CKD). Extremely high risk for CVD death in advanced CKD patients consists of high-incidental CVD event and high mortality after CVD event. To date, it is unclear whether fetuin-A and/or T50 can equally predict each CVD outcome. Methods This prospective cohort study examined patients undergoing maintenance hemodialysis. The exposures were fetuin-A and T50. The outcomes of interests were new CVD events and subsequent deaths. The patients were categorized into tertiles of fetuin-A or T50 (T1 to T3). Results We identified 190 new CVD events during the 5-year follow-up of the 513 patients and 59 deaths subsequent to the CVD events during 2.5-year follow-up. A lower fetuin-A but not T50 was significantly associated with new CVD events [subdistribution hazard ratio (HR) 1.73, 95% confidence interval (CI) 1.15–2.61, P = .009 for T1 vs T3]. In contrast, a shorter T50 but not fetuin-A was a significant predictor of deaths after CVD events (HR 3.31, 95% CI 1.42–7.74, P = .006 for T1 + T2 vs T3). A lower fetuin-A was predictive of new CVD events, whereas a shorter T50 was more preferentially associated with subsequent death. Conclusion These results indicate that fetuin-A and T50 are involved in cardiovascular risk in different manners.

Funder

JSPS

Publisher

Oxford University Press (OUP)

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