Home |
Current Issue |
Past Issues |
In the Clinic |
ACP Journal Club |
CME |
Collections |
Audio/Video |
Mobile |
Subscribe |
Tools |
Help |
ACP Online
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
17 July 2001 | Volume 135 Issue 2 | Pages 133-137
Large randomized, controlled trials of total homocysteine-lowering therapy for the potential reduction of cardiovascular disease outcomes are ongoing in the United States and Canada. These trials are the Vitamin Intervention for Stroke Prevention (VISP) trial, the Women's Antioxidant Cardiovascular Disease Study (WACS), and the Heart Outcomes Prevention Evaluation (HOPE-2). However, the dramatic effect of policies mandating fortification of cereal grain flour products with folic acid may reduce the statistical power of these trials. All three trials assume that the active treatment groups will achieve the same mean effects of total homocysteine-lowering therapy as those reported in the absence of folic acid-fortified cereal grain flour. This paper examines this assumption using data from studies of total homocysteine-lowering therapy in U.S. and Canadian patients with cardiovascular disease who were exposed to products made with folic acid-fortified cereal grain flour. These data showed that the VISP trial, HOPE-2, and WACS will probably achieve only approximately 20% to 25% of the projected treatment effects of mean total homocysteine-lowering therapy (1.0 to 1.5 µmol/L vs. 4.0 to 6.0 µmol/L). As a result, all three trials will be substantially underpowered to test the specific hypotheses of total homocysteine-lowering therapy identified a priori. In contrast, renal transplant recipients have a persistent excess prevalence of hyperhomocysteinemia in the era of fortification but remain very responsive to supraphysiologic doses of folic acid-based supplementation (mean reduction in total homocysteine level, 5.0 to 6.0 µmol/L). Therefore, unlike other populations with normal renal function that are at high risk for cardiovascular disease but are profoundly affected by fortification efforts, renal transplant recipients continue to merit serious consideration for a controlled trial of the "homocysteine hypothesis."
Author and Article Information
From the Memorial Hospital of Rhode Island, Providence, Rhode Island, and the Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging at Tufts University, Boston, Massachusetts.
Requests for Single Reprints: Andrew G. Bostom, MD, MS, Division of Renal Diseases, Rhode Island Hospital, 593 Eddy Street, Providence, RI 02903; e-mail, abostom{at}loa.com.
Current Author Addresses: Dr. Bostom: Division of Renal Diseases, Rhode Island Hospital, 593 Eddy Street, Providence, RI 02903.
Drs. Selhub, Jacques, and Rosenberg: Jean Mayer United States Department of Agriculture Human Nutrition Research Center on Aging at Tufts University, 711 Washington Street, Boston, MA 02111. PERSPECTIVE
Power Shortage: Clinical Trials Testing the "Homocysteine Hypothesis" against a Background of Folic AcidFortified Cereal Grain Flour
![]()
Related articles in Annals:
This article has been cited by other articles:
![]() |
C. M. Albert, N. R. Cook, J. M. Gaziano, E. Zaharris, J. MacFadyen, E. Danielson, J. E. Buring, and J. E. Manson Effect of Folic Acid and B Vitamins on Risk of Cardiovascular Events and Total Mortality Among Women at High Risk for Cardiovascular Disease: A Randomized Trial JAMA, May 7, 2008; 299(17): 2027 - 2036. [Abstract] [Full Text] [PDF] |
||||
![]() |
N. Akhtar Is Homocysteine a Risk Factor for Atherothrombotic Cardiovascular Disease? J. Am. Coll. Cardiol., March 27, 2007; 49(12): 1370 - 1371. [Full Text] [PDF] |
||||
![]() |
L. A. Bazzano, K. Reynolds, K. N. Holder, and J. He Effect of Folic Acid Supplementation on Risk of Cardiovascular Diseases: A Meta-analysis of Randomized Controlled Trials JAMA, December 13, 2006; 296(22): 2720 - 2726. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. H. Rosenberg and C. D. Mulrow Trials that matter: should we routinely measure homocysteine levels and "treat" mild hyperhomocysteinemia? Ann Intern Med, August 1, 2006; 145(3): 226 - 227. [Full Text] [PDF] |
||||
![]() |
J. Loscalzo Homocysteine Trials -- Clear Outcomes for Complex Reasons N. Engl. J. Med., April 13, 2006; 354(15): 1629 - 1632. [Full Text] [PDF] |
||||
![]() |
C. O'DONNELL and T. STEPHENS The Significance of Homocysteine Levels in Schizophrenia Am J Psychiatry, July 1, 2005; 162(7): 1387 - 1388. [Full Text] [PDF] |
||||
![]() |
G. J. Hankey and J. W. Eikelboom Folic Acid-Based Multivitamin Therapy to Prevent Stroke: The Jury Is Still Out Stroke, August 1, 2004; 35(8): 1995 - 1998. [Full Text] [PDF] |
||||
![]() |
S. J. Moat, S. N. Doshi, D. Lang, I. F. W. McDowell, M. J. Lewis, and J. Goodfellow Treatment of coronary heart disease with folic acid: is there a future? Am J Physiol Heart Circ Physiol, July 1, 2004; 287(1): H1 - H7. [Full Text] [PDF] |
||||
![]() |
S. Friso, D. Girelli, N. Martinelli, O. Olivieri, V. Lotto, C. Bozzini, F. Pizzolo, G. Faccini, F. Beltrame, and R. Corrocher Low plasma vitamin B-6 concentrations and modulation of coronary artery disease risk Am. J. Clinical Nutrition, June 1, 2004; 79(6): 992 - 998. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Refsum, A. D. Smith, P. M. Ueland, E. Nexo, R. Clarke, J. McPartlin, C. Johnston, F. Engbaek, J. Schneede, C. McPartlin, et al. Facts and Recommendations about Total Homocysteine Determinations: An Expert Opinion Clin. Chem., January 1, 2004; 50(1): 3 - 32. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. G. Hackam and S. S. Anand Emerging Risk Factors for Atherosclerotic Vascular Disease: A Critical Review of the Evidence JAMA, August 20, 2003; 290(7): 932 - 940. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. B. Bailey, G. C. Rampersaud, and G. P. A. Kauwell Folic Acid Supplements and Fortification Affect the Risk for Neural Tube Defects, Vascular Disease and Cancer: Evolving Science, J. Nutr., June 1, 2003; 133(6): 1961S - 1968. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. De Bree, W. M. M. Verschuren, D. Kromhout, L. A. J. Kluijtmans, and H. J. Blom Homocysteine Determinants and the Evidence to What Extent Homocysteine Determines the Risk of Coronary Heart Disease Pharmacol. Rev., December 1, 2002; 54(4): 599 - 618. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. B. Hu and W. C. Willett Optimal Diets for Prevention of Coronary Heart Disease JAMA, November 27, 2002; 288(20): 2569 - 2578. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. W. F. Wilson Homocysteine and Coronary Heart Disease: How Great Is the Hazard? JAMA, October 23, 2002; 288(16): 2042 - 2043. [Full Text] [PDF] |
||||
![]() |
C. M. Carlsson and J. H. Stein Clinical Trials Testing the Homocysteine Hypothesis Ann Intern Med, August 20, 2002; 137(4): 295 - 296. [Full Text] [PDF] |
||||
![]() |
L. A. Bazzano, J. He, L. G. Ogden, C. Loria, S. Vupputuri, L. Myers, P. K. Whelton, and S. E. Kasner Dietary Intake of Folate and Risk of Stroke in US Men and Women: NHANES I Epidemiologic Follow-Up Study * Editorial Comment: NHANES I Epidemiologic Follow-Up Study Stroke, May 1, 2002; 33(5): 1183 - 1189. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. G. Bostom, G. Sunder-Plassmann, M. Fodinger, L. Pogach, J. A. Tice, L. Goldman, P. G. Coxson, E. Ross, I. Rosenberg, M. C. Weinstein, et al. Cost-effectiveness of Homocysteine-Lowering Therapy to Prevent Coronary Heart Disease JAMA, January 9, 2002; 287(2): 190 - 192. [Full Text] [PDF] |
||||