scholarly journals Decreased level of serum carnitine might lead to arteriosclerosis progression via the accumulation of advanced glycation end products in maintenance hemodialysis patients

2017 ◽  
Vol 3 (1) ◽  
Author(s):  
Yumi Kamada ◽  
Takashi Masuda ◽  
Kazuhiko Kotani ◽  
Shinya Tanaka ◽  
Takeshi Nakamura ◽  
...  
2011 ◽  
Vol 44 (10) ◽  
pp. 1015-1021
Author(s):  
Hiroaki Muramoto ◽  
Kin-ya Kitada ◽  
Hisao Mutoh ◽  
Masayoshi Takeuchi

2021 ◽  
Vol 52 (1) ◽  
pp. 8-16
Author(s):  
Jianping Jiang ◽  
Yuanyuan Zhang ◽  
Jianghua Chen ◽  
Xiaobing Yang ◽  
Changlin Mei ◽  
...  

Background: The relation of tissue and circulating advanced glycation end products (AGEs) with mortality in hemodialysis (HD) patients remains inconclusive. We aimed to investigate the association of serum AGEs (CML) and tissue AGEs estimated by skin autofluorescence (SAF) with all-cause and cardiovascular disease (CVD) mortality, and examine the possible modifiers for the association in HD patients with by far the largest sample size in any similar studies. Methods: A total of 1,634 HD patients were included from the China Cooperative Study on Dialysis (CCSD), a multicenter prospective cohort study. The primary and secondary outcomes were all-cause mortality and CVD mortality, respectively. Results: The median follow-up duration was 5.2 years. Overall, there was a positive relation of baseline SAF levels with the risk of all-cause mortality (per 1 AU increment, adjusted hazard ratio (HR), 1.30; 95% confidence interval (CI): 1.12, 1.50) and CVD mortality (per 1 AU increment, adjusted HR, 1.36; 95% CI: 1.14, 1.62). Moreover, a stronger positive association between baseline SAF (per 1 AU increment) and all-cause mortality was found in participants with shorter dialysis vintage, or lower C-reactive protein levels (Both p interactions <0.05). Nevertheless, there was no significant association between serum CML and the risk of mortality. Conclusions: In patients undergoing long-term HD, baseline SAF, but not serum CML, was significantly associated with the risk of all-cause and CVD death.


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