Power shortage: Clinical trials testing the "homocysteine hypothesis" against a background of folic acid-fortified cereal grain flour

被引:77
作者
Bostom, AG
Selhub, J
Jacques, PF
Rosenberg, IH
机构
[1] Univ Colorado, Hlth Sci Ctr, Denver, CO 80262 USA
[2] Denver Hlth, Denver, CO 80204 USA
关键词
D O I
10.7326/0003-4819-135-2-200107170-00014
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 mu mol/L vs. 4.0 to 6.0 mu mol/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 mu mol/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.".
引用
收藏
页码:133 / 139
页数:7
相关论文
共 9 条
  • [1] GANSEVOORT RT, 1995, NEPHROL DIAL TRANSPL, V10, P1963
  • [2] Angiotensin-converting enzyme inhibitors and progression of nondiabetic renal disease - A meta-analysis of patient-level data
    Jafar, TH
    Schmid, CH
    Landa, M
    Giatras, I
    Toto, R
    Remuzzi, G
    Maschio, G
    Brenner, BM
    Kamper, A
    Zucchelli, P
    Becker, G
    Himmelmann, A
    Bannister, K
    Landais, P
    Shahinfar, S
    de Jong, PE
    de Zeeuw, D
    Lau, J
    Levey, AS
    [J]. ANNALS OF INTERNAL MEDICINE, 2001, 135 (02) : 73 - 87
  • [3] EFFECT OF ANTIHYPERTENSIVE THERAPY ON THE KIDNEY IN PATIENTS WITH DIABETES - A METAREGRESSION ANALYSIS
    KASISKE, BL
    KALIL, RSN
    MA, JZ
    LIAO, MJ
    KEANE, WF
    [J]. ANNALS OF INTERNAL MEDICINE, 1993, 118 (02) : 129 - 138
  • [4] THE EFFECT OF ANGIOTENSIN-CONVERTING ENZYME-INHIBITION ON DIABETIC NEPHROPATHY
    LEWIS, EJ
    HUNSICKER, LG
    BAIN, RP
    ROHDE, RD
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (20) : 1456 - 1462
  • [5] Mosconi L, 1996, KIDNEY INT, pS91
  • [6] Long-term renoprotective effect of angiotensin-converting enzyme inhibition in non-insulin-dependent diabetes mellitus - A 7-year follow-up study
    Ravid, M
    Lang, R
    Rachmani, R
    Lishner, M
    [J]. ARCHIVES OF INTERNAL MEDICINE, 1996, 156 (03) : 286 - 289
  • [7] THE EFFECT OF INTENSIVE TREATMENT OF DIABETES ON THE DEVELOPMENT AND PROGRESSION OF LONG-TERM COMPLICATIONS IN INSULIN-DEPENDENT DIABETES-MELLITUS
    SHAMOON, H
    DUFFY, H
    FLEISCHER, N
    ENGEL, S
    SAENGER, P
    STRELZYN, M
    LITWAK, M
    WYLIEROSETT, J
    FARKASH, A
    GEIGER, D
    ENGEL, H
    FLEISCHMAN, J
    POMPI, D
    GINSBERG, N
    GLOVER, M
    BRISMAN, M
    WALKER, E
    THOMASHUNIS, A
    GONZALEZ, J
    GENUTH, S
    BROWN, E
    DAHMS, W
    PUGSLEY, P
    MAYER, L
    KERR, D
    LANDAU, B
    SINGERMAN, L
    RICE, T
    NOVAK, M
    SMITHBREWER, S
    MCCONNELL, J
    DROTAR, D
    WOODS, D
    KATIRGI, B
    LITVENE, M
    BROWN, C
    LUSK, M
    CAMPBELL, R
    LACKAYE, M
    RICHARDSON, M
    LEVY, B
    CHANG, S
    HEINHEINEMANN, M
    BARRON, S
    ASTOR, L
    LEBECK, D
    BRILLON, D
    DIAMOND, B
    VASILASDWOSKIN, A
    LAURENZI, B
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1993, 329 (14) : 977 - 986
  • [8] Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33)
    Turner, RC
    Holman, RR
    Cull, CA
    Stratton, IM
    Matthews, DR
    Frighi, V
    Manley, SE
    Neil, A
    McElroy, K
    Wright, D
    Kohner, E
    Fox, C
    Hadden, D
    Mehta, Z
    Smith, A
    Nugent, Z
    Peto, R
    Adlel, AI
    Mann, JI
    Bassett, PA
    Oakes, SF
    Dornan, TL
    Aldington, S
    Lipinski, H
    Collum, R
    Harrison, K
    MacIntyre, C
    Skinner, S
    Mortemore, A
    Nelson, D
    Cockley, S
    Levien, S
    Bodsworth, L
    Willox, R
    Biggs, T
    Dove, S
    Beattie, E
    Gradwell, M
    Staples, S
    Lam, R
    Taylor, F
    Leung, L
    Carter, RD
    Brownlee, SM
    Fisher, KE
    Islam, K
    Jelfs, R
    Williams, PA
    Williams, FA
    Sutton, PJ
    [J]. LANCET, 1998, 352 (9131) : 837 - 853
  • [9] WEIDMANN P, 1995, NEPHROL DIAL TRANSPL, V10, P39