SELENIUM and CARDIOVASCULAR DISEASE
See other papers of antioxidants and CV disease for Vitamin E; Vitamin A; Vitamin C;, papers of antioxidants and cancer for Vitamin E; Vitamin A; Vitamin C; and Selenium, and Antioxidants, Death from All Causes and Antioxidants, a Global Analysis..
Life Ahead includes Selenium as one of four antioxidants taken in sum as a group that benefit all cardiovascular diseases. See the Antioxidant Model. In accord with the BioChemical mechanism of atherosclerosis the benefits of antioxidants are taken as a duration of exposure related risk, with a recognized limit of both maximum benefit and duration of exposure. A usual US diet includes about 80-90 mg of Selenium per day. Life Ahead credits a benefit for up to 100 mg of supplemental use beyond that usual in diet. But this benefit accrues via the antioxidant model only gradually over a 20 year period, and is usually reduced further by presence of accompanying amounts of other antioxidants. If substantial amounts of Vitamin E and other antioxidants are present in diet and supplements, the addition of selenium may produce no added computed benefit for cardiovascular diseases. The antioxidant model for heart disease includes the benefits of selenium at a % per year of duration of use. Thus the total above benefit would not be achieved via Life Ahead until selenium had been used for 20 years.
But Selenium also appears to have a substantial benefit by reducing risk of cancer. Thus the taking a of a Selenium supplement of 100 mg per day would appear to be a prudent action for any health-interested person.
TABLE S
RESEARCH on CARDIOVASCULAR DISEASE and SELENIUM
|
No |
Study |
Population |
Sex |
RR
|
Error Margin |
Amt Diff, Vit E IU |
Avg Yrs |
ratio per yr |
Notes |
| OBSERVATION STUDIES | |||||||||
| For ALL CORONARY or CARDIOVASCULAR DISEASE | |||||||||
| Salolen JT, Lancet 1982, 2:175 | 95 cases vs 95 controls rom population of 11,000 age 35-59 in Finland | M&W | 0.45 | 0.25-0.83 | 7 | all CVD in population having <=45 mcg/l vs avg of 55.3 mcg/l | |||
| Virtama J, Am J Epidemiol 1985, 122:276 | 1,110 population age 55-74 in Finland, 30 cases vs 591 controls | M&W | 0.63 | 0.43-0.91 | 5 | all CVD in population having < 45 mcg/l in blood | |||
| Salonen JT, Am J Cardiol 1985, 56:226 | 92 cases vs 92 controls in Eastern Finland | M&W | 0.71 | 0.14-3.3 | 5 | having <45 mcg/l vs. avg | |||
| Ringstad J, Acta Pharmacol Toxicol 1986, 59 suppl :336 | 99 cases and 99 controls from Norway population of 9300 | M | 0.77 | 0.28-2.13 | 8 | ||||
| Kok FJ, Am J Clin Nutr 1987, 45:462 | 84 cases and 186 controls in Netherlands | M&W | 0.63 | 0.31-1.25 | 6+ | quintiles of selenium in blood | |||
| Beaglehole, R, Int J Epidemiol 1990, 19:918 |
252 cases, 88 controls in New Zealand |
M W |
0.63 0.59 |
0.45-0.91 0.29-1.11 |
below and above medium selenium, blood |
||||
|
Sandicani P, Athero-sclerosis 1992, 06:33 |
107 cases of 3400 in Denmark |
M |
0.59 |
0.39-0.88 |
3 |
tertiles of selenium in blood |
|||
|
Salvini, S, Am J Cardiol 1995, 76:1218 |
251 cases and 251 controls in Physicians Health Study |
M |
1.27 |
0.77-2.29 |
. |
10+ |
. |
quintiles of selenium in blood |
|
|
Marniemi J, Int J Epidemiol 1998, 27:799 |
142 cases vs 202 controls, age 65+ in Finland |
M&W |
1.08 |
0.68-1.72 |
13+ |
tertiles of selenium in blood |
|||
|
Kilander L, Int J Epidemiol 2001, 30:1119 |
2300 50 yr olds in Sweden |
M |
0.88 |
0.78-1.0 p=0.06 |
25 |
n/a |
|||
| Yoshizawa K, Am J epidemiol 2003, 158:852 |
470 cases and controls in Health Professionals Study |
M |
0.86 0.54 0.79 |
0.55-1.32 0.31-0.93 0.39-1.60 |
All CHD from toenail vals Heart Atttack, MI fatal coronary disease |
||||
| Wei WQ, Am J Clin Nutr 2004, 79:80 |
516 deaths from 1103 selenium measurements in China |
M&W |
0.66 0.89 p=0.05 |
0.41-1.08 0.88-1.07 |
15 |
quartile of selenium continuous risk |
|||
| Akbarely NT, Clin Chem 2005, 51:2117 | 101 cases of 1389 population ub France, age 61-73 | M&W | 0.61 | 0.36-1.03 | 9 | incr of 0.2 micromol/l selenium in blood | |||
|
Flores-Mateo G, Am J Clin Nutr 2006, 84:762 |
Meta Analysis of 25 Studies |
M&W |
0.85 0.43 0.76 |
0.74-0.99 0.29-0.66 0.62-0.93 |
Prospective studies case control studies for 50% incr in selenium, all observation studies |
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|
CLINICAL RANDOMIZED STUDIES |
|||||||||
|
For HEALTHY PEOPLE |
|||||||||
| Hercberg, S, Ach Int Med 2004, 164:2335 | Radomized trial of 13,000 French adults age 45-60 |
M W |
(0.82) (1.17) |
0.71-1.20 0.67-2.05 |
120 mg Vit C 45 IU Vit E,6 mg Beta C, 100 mg Sel, 20 mg zinc |
7.5 |
|
Not a study of selenium. seleium in blood was not reduced in women |
|
| Stranges S, Am J Epidemiol 2006,163:694 | 500 treated vs 504 placebo in SE US, 199 events | M&W | 1.03 | 0.78-1.37 | 200 mcg/day | 13 | 1.00 | similar results on different types of CVD. | |
| For PATIENTS of CARDIOVASCULAR DISEASE | |||||||||
| Korpela H, Res Commun Chem Pathol Pharmacol 1989, 65:249 | 81 patients in double blind study in Finland | M&W | 0.17 | 0.02=1.35 | 100 | 0.5 | 100 mcg selenium rich yeast | ||
| Kuklinski B, Mol Aspects Med 1994, 15:S143 | 32 cases vs 29 controls | n/a | 0.07 | 0.01-1.19 | 1 | 100 mcg selenium plus 100 mg COQ10 | |||
| Brown BG, N Engl J 2001, 345:1583 | 160 patients of coronary disease given very large dose of multiple antioxidants and Placebo | M&W | (0.6) | 0.28-1.28 | 3 | 100 mcg selenium + 800 Vit E +1000 mg Vit C + 25 mg Beta C Not a selenium measurement | |||
| You WC, Eur J Cancer Prev 2001, 10:257 | 9 events for 12 in placebo | M&W | (0.75) | 0.32-1.77 | 3.3 | 75 mcg selenium with 200 IU Vit E, 500 Vit C,25mg beta C Not a selenium study | |||
| For STROKE | |||||||||
| Virtama J, Am J Epidemiol 1985, 122:276 | 95 cases vs 95 controls 11,000 age 35-59 in Finland | M&W | 0.27 | 0.08-1.0 | 5 | all CVD in population having < 45 mcg/l in blood | |||
| Kok FJ, Am J Clin Nutr 1987, 45:462 | 84 cases and 186 controls in Netherlands | M&W | 0.31 | 0.08-1.25 | 6+ | quintiles of selenium in blood | |||