Randomized trial of folic acid for prevention of cardiovascular events in end-stage renal disease

被引:194
作者
Wrone, EM
Hornberger, JM
Zehnder, JL
McCann, LM
Coplon, NS
Fortmann, SP
机构
[1] Satellite Res, Redwood City, CA USA
[2] Stanford Univ, Sch Med, Stanford Ctr Res Dis Prevent, Stanford, CA 94305 USA
[3] Acumen LLC, Burlingame, CA USA
[4] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2004年 / 15卷 / 02期
关键词
D O I
10.1097/01.ASN.0000110181.64655.6C
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
High serum total homocysteine (tHcy) is gaining scrutiny as a risk factor for cardiovascular disease in the general population. The relationship between tHcy and mortality and cardiovascular events in patients with end-stage renal disease (ESRD) is unsettled. This randomized trial evaluates the efficacy of high-dose folic acid in preventing events in ESRD. A total of 510 patients on chronic dialysis were randomized to 1, 5, or 15 mg of folic acid contained in a renal multivitamin with a median follow-up of 24 mo. Mortality, cardiovascular events, and homocysteine levels were assessed. There were 189 deaths, and 121 patients experienced at least one cardiovascular event. Composite rates of mortality and cardiovascular events among the folic acid groups did not differ (at 24 mo: 43.7% in 1 mg group, 38.6% in 5 mg group, 47.1% in 15 mg group; log-rank P = 0.47). Unexpectedly, high baseline tHcy was associated with lower event rates. From lowest to highest quartile, event rates at 24 mo were 54.5% for Q1, 41.8% for Q2, 41.2% for Q3, and 34.7% for Q4 (log-rank P = 0.033). In contrast to some studies describing tHcy as a risk factor for mortality and cardiovascular events, this study found a reverse relationship between tHcy and events in ESRD patients. Administration of high-dose folic acid did not affect event rates.
引用
收藏
页码:420 / 426
页数:7
相关论文
共 27 条
[1]   RELATION OF SERUM HOMOCYSTEINE AND LIPOPROTEIN(A) CONCENTRATIONS TO ATHEROSCLEROTIC DISEASE IN A PROSPECTIVE FINNISH POPULATION-BASED STUDY [J].
ALFTHAN, G ;
PEKKANEN, J ;
JAUHIAINEN, M ;
PITKANIEMI, J ;
KARVONEN, M ;
TUOMILEHTO, J ;
SALONEN, JT ;
EHNHOLM, C .
ATHEROSCLEROSIS, 1994, 106 (01) :9-19
[2]   Malnutrition, cardiac disease, and mortality:: An integrated point of view [J].
Bergström, J ;
Lindholm, B .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 32 (05) :834-841
[3]  
Bostom AG, 1999, J AM SOC NEPHROL, V10, P891
[4]   Treatment of mild hyperhomocysteinemia in renal transplant recipients versus hemodialysis patients [J].
Bostom, AG ;
Shemin, D ;
Gohh, RY ;
Beaulieu, AJ ;
Jacques, PF ;
Dworkin, L ;
Selhub, J .
TRANSPLANTATION, 2000, 69 (10) :2128-2131
[5]   High dose B-vitamin treatment of hyperhomocysteinemia in dialysis patients [J].
Bostom, AG ;
Shemin, D ;
Lapane, KL ;
Hume, AL ;
Yoburn, D ;
Nadeau, MR ;
Bendich, A ;
Selhub, J ;
Rosenberg, IH .
KIDNEY INTERNATIONAL, 1996, 49 (01) :147-152
[6]   Elevated fasting total plasma homocysteine levels and cardiovascular disease outcomes in maintenance dialysis patients - A prospective study [J].
Bostom, AG ;
Shemin, D ;
Verhoef, P ;
Nadeau, MR ;
Jacques, PF ;
Selhub, J ;
Dworkin, L ;
Rosenberg, IH .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (11) :2554-2558
[7]  
Bostom AG, 2001, KIDNEY INT, V59, pS246, DOI 10.1046/j.1523-1755.2001.07855.x
[8]   Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease -: The result of a meta-analysis [J].
Brattström, L ;
Wilcken, DEL ;
Öhrvik, J ;
Brudin, L .
CIRCULATION, 1998, 98 (23) :2520-2526
[9]   The impact of an amino acid-based peritoneal dialysis fluid on plasma total homocysteine levels, lipid profile and body fat mass [J].
Brulez, HFH ;
van Guldener, C ;
Donker, AJM ;
ter Wee, PM .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 1999, 14 (01) :154-159
[10]  
Coresh J, 1998, J Am Soc Nephrol, V9, pS24