Effects of levocarnitine on brachial-ankle pulse wave velocity in hemodialysis patients: a randomized controlled trial.
Effects of levocarnitine on brachial-ankle pulse wave velocity in hemodialysis patients: a randomized controlled trial.
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DOI:
10.3390/nu6125992
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发表时间:
2014-12-22
期刊:
影响因子:
5.9
通讯作者:
Soma M
中科院分区:
文献类型:
--
作者:
Higuchi T;Abe M;Yamazaki T;Mizuno M;Okawa E;Ando H;Oikawa O;Okada K;Kikuchi F;Soma M
Background and Aims: Atherosclerotic cardiovascular disease is the most common cause of mortality in patients with end-stage kidney disease. Chronic kidney disease patients often exhibit a deficiency in l-carnitine due to loss during hemodialysis (HD). We studied the effects of l-carnitine supplementation on brachial-ankle pulse wave velocity (baPWV), a marker of atherosclerosis, in HD patients. Methods: This was a prospective, open-label, randomized, parallel controlled, multi-center trial testing the anti-atherosclerotic efficacy of oral l-carnitine administration (20 mg/kg/day). HD patients (n = 176, mean age, 67.2 ± 10.3 years old; mean duration of HD, 54 ± 51 months) with plasma free l-carnitine deficiency (<40 μmol/L) were randomly assigned to the oral l-carnitine group (n = 88) or control group (n = 88) and monitored during 12 months of treatment. Results: There were no significant differences in baseline clinical variables between the l-carnitine and control groups. l-carnitine supplementation for 12 months significantly increased total, free, and acyl carnitine levels, and reduced the acyl/free carnitine ratio. The baPWV value decreased from 2085 ± 478 cm/s at baseline to 1972 ± 440 cm/s after six months (p < 0.05) to 1933 ± 363 cm/s after 12 months (p < 0.001) of l-carnitine administration, while no significant changes in baPWV were observed in the control group. Baseline baPWV was the only factor significantly correlated with the decrease in baPWV. Conclusions: l-carnitine supplementation significantly reduced baPWV in HD patients. l-carnitine may be a novel therapeutic strategy for preventing the progression of atherosclerotic cardiovascular disease.
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影响因子:
1.7
作者:
Abe, Masanori;Okada, Kazuyoshi;Soma, Masayoshi
通讯作者:
Soma, Masayoshi
影响因子:
13.2
作者:
Kitahara, T;Ono, K;Nojima, Y
通讯作者:
Nojima, Y
影响因子:
13.2
作者:
Barrett, BJ;Parfrey, PS;Richardson, RMA
通讯作者:
Richardson, RMA
影响因子:
6.1
作者:
Bueno, R;de Sotomayor, MA;Herrera, MD
通讯作者:
Herrera, MD
影响因子:
--
作者:
Aulivola, B;Hile, CN;Pomposelli, FB
通讯作者:
Pomposelli, FB