Literature DB >> 18786751

Randomized placebo-controlled trial assessing a treatment strategy consisting of pravastatin, vitamin E, and homocysteine lowering on plasma asymmetric dimethylarginine concentration in mild to moderate CKD.

Prabath W B Nanayakkara1, Jessica C Kiefte-de Jong, Piet M ter Wee, Coen D A Stehouwer, Frans J van Ittersum, Margreet R Olthof, Tom Teerlink, Jos W R Twisk, Coen van Guldener, Yvo M Smulders.   

Abstract

BACKGROUND: Chronic kidney disease (CKD) is associated with an increased incidence of cardiovascular disease (CVD). The Anti-oxidant Therapy In Chronic Renal Insufficiency (ATIC) Study showed that a multistep treatment strategy improved carotid intima-media thickness, endothelial function, and microalbuminuria in patients with stages 2 to 4 CKD. Increased plasma concentrations of asymmetric dimethylarginine (ADMA), an endogenous inhibitor of nitric oxide synthase, have been linked to greater CVD risk in patients with CKD. The aim of this study is to assess effects of the multistep intervention on plasma ADMA concentrations in the ATIC Study. STUDY
DESIGN: Secondary analysis of a randomized double-blind placebo-controlled trial. SETTING & PARTICIPANTS: 93 patients with creatinine clearance of 15 to 70 mL/min/1.73 m(2) (according to the Cockcroft-Gault equation) from 7 outpatient clinics in Amsterdam, The Netherlands. INTERVENTION: The treatment group received sequential treatment consisting of pravastatin, 40 mg/d. After 6 months, vitamin E, 300 mg/d, was added, and after another 6 months, homocysteine-lowering therapy (folic acid, 5 mg/d; pyridoxine, 100 mg/d; and vitamin B(12), 1 mg/d, all in 1 tablet) were added and continued for another year. The control group received matching placebos. OUTCOME & MEASURES: Plasma ADMA levels.
RESULTS: 36 participants (77%) in the treatment group and 38 (83%) in the placebo group completed the study. Mean ADMA and symmetric dimethylarginine concentrations in the total study population were 0.53 +/- 0.07 (SD) and 1.14 +/- 0.46 mumol/L, respectively. After 24 months, there was no overall effect of the treatment strategy on ADMA concentrations (beta = -0.006; P = 0.27). Analysis of separate treatment effects suggested that vitamin E significantly decreased ADMA levels by 4% in the treatment group compared with the placebo group (multiple adjusted P = 0.02). LIMITATIONS: The study was a secondary analysis, power calculation was based on the primary end point of carotid intima-media thickness, mean plasma ADMA levels were relatively low.
CONCLUSION: Overall, a multistep treatment strategy consisting of pravastatin, vitamin E, and B vitamins had no effect on plasma ADMA levels in a stage 2 to 4 CKD population. This suggests that the beneficial effects of the intervention were not mediated by changes in ADMA levels. Possible ADMA-lowering effects of vitamin E deserve further attention.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18786751     DOI: 10.1053/j.ajkd.2008.06.016

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  8 in total

1.  MicroRNA-21 promotes fibrosis of the kidney by silencing metabolic pathways.

Authors:  B Nelson Chau; Cuiyan Xin; Jochen Hartner; Shuyu Ren; Ana P Castano; Geoffrey Linn; Jian Li; Phong T Tran; Vivek Kaimal; Xinqiang Huang; Aaron N Chang; Shenyang Li; Aarti Kalra; Monica Grafals; Didier Portilla; Deidre A MacKenna; Stuart H Orkin; Jeremy S Duffield
Journal:  Sci Transl Med       Date:  2012-02-15       Impact factor: 17.956

2.  Circulating vitamin E and cardiometabolic measures: a Mendelian randomization analysis.

Authors:  Chuanlong Fan; Tao Huang; Xuejun Kong; Xiaohong Zhang; Zuquan Zou; Jing Xiao
Journal:  J Clin Biochem Nutr       Date:  2019-08-09       Impact factor: 3.114

3.  Effect of supplementation with B vitamins and antioxidants on levels of asymmetric dimethylarginine (ADMA) and C-reactive protein (CRP): a double-blind, randomised, factorial design, placebo-controlled trial.

Authors:  Mark G O'Doherty; Sarah E C M Gilchrist; Ian S Young; Michelle C McKinley; John W G Yarnell; K Fred Gey; Alun Evans; Paula M L Skidmore; Jayne V Woodside
Journal:  Eur J Nutr       Date:  2010-04-18       Impact factor: 5.614

Review 4.  Atherosclerosis in chronic kidney disease: the role of macrophages.

Authors:  Valentina Kon; MacRae F Linton; Sergio Fazio
Journal:  Nat Rev Nephrol       Date:  2010-11-23       Impact factor: 28.314

Review 5.  Hypertensive encephalopathy in patients with chronic renal failure caused by stopping antihypertensive agents: a report of two cases.

Authors:  Mari Nakabou; Tatsuya Kai; Tetsuya Maeshima; Ken Kanamasa
Journal:  Clin Exp Nephrol       Date:  2009-12-15       Impact factor: 2.801

Review 6.  Statins as regulators of redox state in the vascular endothelium: beyond lipid lowering.

Authors:  Marios Margaritis; Keith M Channon; Charalambos Antoniades
Journal:  Antioxid Redox Signal       Date:  2014-01-03       Impact factor: 8.401

Review 7.  A systematic review and meta-analysis of the effect of statins on plasma asymmetric dimethylarginine concentrations.

Authors:  Corina Serban; Amirhossein Sahebkar; Sorin Ursoniu; Dimitri P Mikhailidis; Manfredi Rizzo; Gregory Y H Lip; G Kees Hovingh; John J P Kastelein; Leszek Kalinowski; Jacek Rysz; Maciej Banach
Journal:  Sci Rep       Date:  2015-05-13       Impact factor: 4.379

Review 8.  Asymmetric dimethylarginine, endothelial dysfunction and renal disease.

Authors:  Luis Aldámiz-Echevarría; Fernando Andrade
Journal:  Int J Mol Sci       Date:  2012-09-10       Impact factor: 6.208

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.