Serum S100A12 and Progression of Coronary Artery Calcification Over 4 Years in Hemodialysis Patients

被引:17
作者
Wang, Yin-na [1 ]
Sun, Yi [1 ]
Wang, Ying [1 ]
Jia, Yan-li [1 ]
机构
[1] Capital Med Univ, Fu Xing Hosp, Div Nephrol, Beijing 100038, Peoples R China
关键词
S100A12; Vascular calcification; Coronary artery calcification; Hemodialysis; CHRONIC-KIDNEY-DISEASE; GLYCATION END-PRODUCTS; CIRCULATING SOLUBLE RECEPTOR; STAGE RENAL-DISEASE; VASCULAR CALCIFICATION; CARDIOVASCULAR MORTALITY; MYOCARDIAL-INFARCTION; PROTEIN S100A12; PLASMA S100A12; RAGE LEVELS;
D O I
10.1159/000438869
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background/Aim: Vascular calcification is common and contributes to increased cardiovascular mortality in hemodialysis (HD) patients. In this prospective study, we aimed to investigate the associations of serum S100A12 in the presence of severe coronary artery calcification (CAC) and the progression of CAC in HD patients. Methods: Sixty maintenance HD patients and 30 controls were enrolled. Serum S100A12 levels were measured using ELISA. CAC scores (CACs) were measured twice at a 4-year interval using multislice spiral CT. The HD patients were classified as rapid progressors or slow progressors according to the change in the CACs across these 2 measurements (Delta CACs). Results: The incidences of rapid progression of CAC in patients with baseline CACs <= 10, CACs > 10 and CACs > 400 were 12.5, 40.0 and 64.3%, respectively. Both baseline and 4-year serum S100A12 levels were significantly higher in the rapid progressors than in the slow progressors (medians of 45.6 vs. 30.2 ng/ml, p < 0.001 and 62.3 vs. 39.4 ng/ml, p = 0.002, respectively). The serum S100A12 levels were significantly correlated with baseline CACs (r = 0.466, p < 0.001), 4-year CACs (r = 0.440, p < 0.001) and Delta CACs (r = 0.392, p < 0.001). Importantly, the Delta CACs were significantly correlated with Delta S100A12 levels (r = 0.396, p < 0.001). Logistic regression analysis revealed that the serum S100A12 level was as an independent determinant of the presence of severe CAC and that the increment in the serum S100A12 level was a factor that was significantly independently associated with the progression of CAC. Conclusions: Serum S100A12 levels were significantly associated with the presence of severe CAC, and the increment in serum S100A12 levels was an independent determinant of the progression of CAC. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:4 / 13
页数:10
相关论文
共 32 条
[1]   QUANTIFICATION OF CORONARY-ARTERY CALCIUM USING ULTRAFAST COMPUTED-TOMOGRAPHY [J].
AGATSTON, AS ;
JANOWITZ, WR ;
HILDNER, FJ ;
ZUSMER, NR ;
VIAMONTE, M ;
DETRANO, R .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1990, 15 (04) :827-832
[2]   Circulating soluble receptor for advanced glycation end products is inversely associated with glycemic control and S100A12 protein [J].
Basta, Giuseppina ;
Sironi, Anna Maria ;
Lazzerini, Guido ;
Del Turco, Serena ;
Buzzigoli, Emma ;
Casolaro, Arturo ;
Natali, Andrea ;
Ferrannini, Ele ;
Gastaldelli, Amalia .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (11) :4628-4634
[3]   Effects of sevelamer and calcium on coronary artery calcification in patients new to hemodialysis [J].
Block, GA ;
Spiegel, DM ;
Ehrlich, J ;
Mehta, R ;
Lindbergh, J ;
Dreisbach, A ;
Raggi, P .
KIDNEY INTERNATIONAL, 2005, 68 (04) :1815-1824
[4]   S100A12 in Vascular Smooth Muscle Accelerates Vascular Calcification in Apolipoprotein E-Null Mice by Activating an Osteogenic Gene Regulatory Program [J].
Bowman, Marion A. Hofmann ;
Gawdzik, Joseph ;
Bukhari, Usama ;
Husain, Aliya N. ;
Toth, Peter T. ;
Kim, Gene ;
Earley, Judy ;
McNally, Elizabeth M. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2011, 31 (02) :337-U243
[5]   Cardiovascular mortality in end-stage renal disease [J].
Collins, AJ .
AMERICAN JOURNAL OF THE MEDICAL SCIENCES, 2003, 325 (04) :163-167
[6]   Expression of the pro-inflammatory protein S100A12 (EN-RAGE) in rheumatoid and psoriatic arthritis [J].
Foell, D ;
Kane, D ;
Bresnihan, B ;
Vogl, T ;
Nacken, W ;
Sorg, C ;
FitzGerald, O ;
Roth, J .
RHEUMATOLOGY, 2003, 42 (11) :1383-1389
[7]   Neutrophil derived human S100A12 (EN-RAGE) is strongly expressed during chronic active inflammatory bowel disease [J].
Foell, D ;
Kucharzik, T ;
Kraft, M ;
Vogl, T ;
Sorg, C ;
Domschke, W ;
Roth, J .
GUT, 2003, 52 (06) :847-853
[8]   S100A12 (EN-RAGE) in monitoring Kawasaki disease [J].
Foell, D ;
Ichida, F ;
Vogl, T ;
Yu, XY ;
Chen, R ;
Miyawaki, T ;
Sorg, C ;
Roth, J .
LANCET, 2003, 361 (9365) :1270-1272
[9]   Vascular Remodeling and Arterial Calcification Are Directly Mediated by S100A12 (EN-RAGE) in Chronic Kidney Disease [J].
Gawdzik, Joseph ;
Mathew, Liby ;
Kim, Gene ;
Puri, Tipu S. ;
Bowman, Marion A. Hofmann .
AMERICAN JOURNAL OF NEPHROLOGY, 2011, 33 (03) :250-259
[10]   S100A12 Gene Expression Is Increased in Peripheral Leukocytes in Chronic Kidney Disease Stage 4-5 Patients with Cardiovascular Disease [J].
Hara, Masaki ;
Ando, Minoru ;
Morito, Taku ;
Nokiba, Hirohiko ;
Iwasa, Yuko ;
Tsuchiya, Ken ;
Nitta, Kosaku .
NEPHRON CLINICAL PRACTICE, 2013, 123 (3-4) :202-208