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1 may be too well-nourished to benefit from a multivitamin.
2 entrations were lower in subjects who used a multivitamin.
3 .15 [0.93 to 1.43]) compared to the low-dose multivitamin.
4 er by supplementation with folic acid plus a multivitamin.
5 le evidence supporting the prescription of a multivitamin.
6 y vitamin D (2000 IU), calcium (600 mg), and multivitamins.
7 (95% CI, 0.77 to 1.15) for patients who used multivitamins.
8 telomere length among women who did not take multivitamins.
9 actors, such as physical activity and use of multivitamins.
10 roidal anti-inflammatory drugs, statins, and multivitamins.
11 upplements and 26% to 77% reported using any multivitamins.
12 Ninety-one percent of participants consumed multivitamins.
13 ts not taking Centrum (Pfizer, New York, NY) multivitamins.
14 into 1) no current use and 2) current use of multivitamins.
18 .0 [9.0] years in those receiving the active multivitamin and 64.0 [9.1] years in those receiving the
19 intake over the past year and 10-year use of multivitamin and individual vitamin D supplements on a b
21 itive performance did not differ between the multivitamin and placebo groups on the secondary outcome
22 mean cognitive change over time between the multivitamin and placebo groups or in the mean level of
23 5% CI, 0.88-1.09; P=.76), colorectal cancer (multivitamin and placebo groups, 1.2 and 1.4 events, res
24 reduction in the incidence of total cancer (multivitamin and placebo groups, 17.0 and 18.3 events, r
25 difference in the risk of cancer mortality (multivitamin and placebo groups, 4.9 and 5.6 events, res
26 of a daily multivitamin on prostate cancer (multivitamin and placebo groups, 9.1 and 9.2 events, res
32 entation with a single supplement containing multivitamins and selenium was safe and significantly re
36 one therapy, alcohol use, physical activity, multivitamins, and calcium supplements, and negatively a
37 supplements, such as vitamin B6, vitamin A, multivitamins, antioxidants, and iron and dietary interv
46 study was to evaluate the effect of VA/BC or multivitamin (B complex, vitamin C, and vitamin E) suppl
47 l trial of supplementation with either daily multivitamins (B vitamins and vitamins C and E), seleniu
48 , placebo-controlled trial of a common daily multivitamin, began in 1997 with continued treatment and
49 or ascorbic acid determination in samples of multivitamin beverages, milk, fermented milk, and milk c
50 Na, P and Zn) determination in multimineral/multivitamins by atomic emission spectrometry in a mediu
51 o-controlled trial testing multivitamin use (multivitamin [Centrum Silver] or placebo daily) among US
52 results for the effects of periconceptional multivitamins containing folic acid and of folic acid fo
54 lation of US male physicians, taking a daily multivitamin did not reduce major cardiovascular events,
57 or age, smoking, physical activity, alcohol, multivitamins, family history, diet quality, energy inta
58 After adjustment for confounders, including multivitamins, family history, high triglycerides at bas
60 assess the balance of benefits and harms of multivitamins for the prevention of cardiovascular disea
63 disease prevention is stronger than that for multivitamins, formulations that cry out for greater sta
64 supplements of either single or multiple RDA multivitamins from enrollment until 6 wk after delivery.
66 significant AMD, there were 152 cases in the multivitamin group and 129 cases in the placebo group (H
67 The rates of prematurity were 16.9% in the multivitamin group and 16.7% in the placebo group (relat
68 rth weight was 7.8% among the infants in the multivitamin group and 9.4% among those in the placebo g
70 tational age (<10th percentile; 10.7% in the multivitamin group vs. 13.6% in the placebo group; relat
73 Compared with placebo, men taking a daily multivitamin had a statistically significant reduction i
77 ent with a high-dose folic acid, B6, and B12 multivitamin in kidney transplant recipients did not red
78 ge who consumed a folic acid (FA)-containing multivitamin in the era of FA fortification are lacking.
80 odeficiency virus infection to receive daily multivitamins (including multiples of the recommended di
81 4 y at enrollment, with complete dietary and multivitamin information, 162 men and 104 women develope
83 iated with offspring BP after confounding by multivitamin intake was accounted for, and no associatio
84 ion with vitamin C, lutein, zeaxanthin, or a multivitamin may help certain populations, but is unlike
86 neral deficiency, there is a perception that multivitamins may prevent cardiovascular disease (CVD).
87 ed dietary supplements, 31% of subjects used multivitamin mineral (MVM) products exclusively, 4% of s
89 to better policy in the field of vitamin and multivitamin-mineral supplement use should occupy our at
91 ers, counseling by experts in nutrition, and multivitamin/mineral supplement after ITx could be of be
93 porated supplements to their diets (10% used multivitamin/mineral supplements), despite the restricti
98 plementation with iron and folate-containing multivitamin multimineral supplements versus iron and fo
109 n of one or a combination of components in a multivitamin/multimineral may accelerate cancer progress
113 omes included use of any supplements; use of multivitamins/multiminerals (MVMM; defined as a product
114 l porridge and a separate dose of an aqueous multivitamin (MV) supplement between meals (control grou
116 3 HIV-infected adults enrolled in a trial of multivitamins (not including vitamin D) in Tanzania.
117 , there was no significant effect of a daily multivitamin on major cardiovascular events (11.0 and 10
119 There was no significant effect of a daily multivitamin on prostate cancer (multivitamin and placeb
123 h National Birth Cohort (1997-2003) reported multivitamin or folate-only supplement use during a 12-w
124 formation is summarized for periconceptional multivitamin or folic acid intake, which may reduce the
126 STF reviewed the evidence on the efficacy of multivitamin or mineral supplements in the general adult
129 ndazole twice daily for 3 d or 90 d of daily multivitamins or both using a 2 x 2 factorial design.
130 posure during the periconceptional period to multivitamins or liver consumption would decrease cleft
131 tene, vitamin C, vitamin D plus calcium, and multivitamins or multi-ingredient supplements was either
133 roups were as follows: lt 150 microg/d (low; multivitamins or no supplement), 150-999 microg/d (middl
139 cipants receiving the combined supplement of multivitamins plus selenium had a significantly lower ri
141 ins and vitamins C and E, selenium alone, or multivitamins plus selenium, compared with placebo.
143 reparation with ferrous sulfate) or placebo (multivitamin preparation without iron) was given from 1
144 nation of major, minor and trace elements in multivitamin preparations and dietary supplements and, b
146 was applied to their assay in 13 commercial multivitamin preparations, revealing mostly higher amoun
150 method is applicable for stability testing, multivitamin products shelf-life determination as well a
152 c enzymes and antioxidants (a combination of multivitamins, selenium, and methionine) can control sym
155 ancer at randomization, enrolled in a common multivitamin study that began in 1997 with treatment and
156 he authors evaluated the association between multivitamin supplement use and breast cancer risk in a
161 rient adequacy from food only was higher for multivitamin supplement users (n = 21,056) than for nonu
163 Ps in DNMT3A were associated with risk among multivitamin supplement users: 3' untranslated region (U
164 ly stomach cancer, for participants taking a multivitamin supplement, but this was in a borderline-de
167 +MV group, daily zinc supplementation alone, multivitamin supplementation alone, and the combined Zn+
168 evere deficiencies are prevented by standard multivitamin supplementation and what parameters are inf
169 ntrolled trial of high-dose vs standard-dose multivitamin supplementation for 24 months in 3418 patie
170 ch provides further support for the value of multivitamin supplementation in HIV-infected adults.
171 e prevention trial of male physicians, daily multivitamin supplementation modestly but significantly
179 ritional deficits occurred despite long-term multivitamin supplementation, including vitamins B1, B12
180 The results of most large-scale trials of multivitamin supplements (combinations of > or = 2 vitam
182 men without chronic diseases reported use of multivitamin supplements at least weekly over the past y
184 In adults receiving HAART, use of high-dose multivitamin supplements compared with standard-dose mul
185 Approximately 20-30% of Americans consume multivitamin supplements daily, indicating high public i
186 amin supplements compared with standard-dose multivitamin supplements did not result in a decrease in
187 omen received prenatal iron, folic acid, and multivitamin supplements irrespective of experimental as
189 a small, borderline-significant benefit from multivitamin supplements on cancer in men only and no ef
191 -year average daily dose from individual and multivitamin supplements were the exposures of primary i
197 e for the templates and can detect them from multivitamin tablets, corn flakes, energy drinks, cerebr
198 110 stable kidney transplant recipients to a multivitamin that included either a high dose (n=2056) o
199 eted villages, 951 (74.3%) of 1280 available multivitamin tickets were redeemed compared with 940 (66
201 Na(+)-coupled I(-) uptake by the human Na(+)/multivitamin transporter (hSMVT), a related protein isol
203 anzanian adults initiating ART enrolled in a multivitamin trial was followed at monthly clinic visits
204 uble-blind, placebo-controlled trial testing multivitamin use (multivitamin [Centrum Silver] or place
207 vitamin B(6), vitamin B(12), methionine) and multivitamin use among 497 Hodgkin lymphoma patients and
208 data indicate no overall association between multivitamin use and breast cancer risk but suggest that
209 e, no long-term clinical trials have studied multivitamin use and cognitive decline in older persons.
210 wn inconsistent associations between regular multivitamin use and CVD, with no long-term clinical tri
211 se association was observed between baseline multivitamin use and major CVD events among women aged >
212 founders, no associations were found between multivitamin use and mortality from all causes (for user
214 as used to estimate the relation between any multivitamin use and PTBs (<37 wk) or SGA births (birth
215 The association between periconceptional multivitamin use and PTBs varied according to prepregnan
216 ermine the relation between periconceptional multivitamin use and the risk of small-for-gestational-a
217 tamin D intake on CVD mortality, and between multivitamin use and vitamin B12 intake on CVD mortality
218 nt interaction effects were observed between multivitamin use and vitamin B6 intake on myocardial inf
219 B6 intake on myocardial infarction, between multivitamin use and vitamin D intake on CVD mortality,
229 thers received antiretroviral (ARV) therapy, multivitamin use had no effect on mortality but was asso
231 ii who answered an open-ended question about multivitamin use in 1999-2001 reported using 1246 differ
233 Regular preconception and postconception multivitamin use in women with a prepregnancy BMI (in kg
235 In this study, we evaluated whether diet and multivitamin use influenced the prevalence of gene promo
236 ovides the first epidemiologic evidence that multivitamin use is associated with longer telomere leng
240 The timing and frequency of periconceptional multivitamin use may be related to the risk of preeclamp
241 use and breast cancer risk but suggest that multivitamin use might reduce risk for women consuming a
242 ale physicians indicate that long-term daily multivitamin use modestly and significantly decreased th
243 dest suggestive inverse association (current multivitamin use of >/=6 times per week vs nonuse multiv
244 rsons who had a 10-year average frequency of multivitamin use of 6-7 days per week with nonusers was
251 the timing and frequency of periconceptional multivitamin use to SGA births and PTBs and its clinical
253 age, and household density, periconceptional multivitamin use was associated with a reduced risk of p
255 her potential confounders were adjusted for, multivitamin use was associated with longer telomeres.
257 There also was no evidence indicating that multivitamin use was associated with risk of cancer, ove
258 rly women, neither baseline nor time-varying multivitamin use was associated with the long-term risk
266 provided evidence regarding associations of multivitamin use with total and site-specific cancer inc
268 smoking (never compared with ever smokers), multivitamin use, season of BMD measurement (for cross-s
274 ssociated with greater breast cancer risk in multivitamin users (51.2% of the study population) with
275 end = 0.05; P for interaction = 0.01] and in multivitamin users (OR for highest compared with the low
277 adjusted risk of an SGA birth was reduced in multivitamin users regardless of their prepregnancy BMI
278 ith a body mass index of 22 kg/m(2), regular multivitamin users with the same body mass index had a 2
281 ncy and throughout the first 2 y postpartum: multivitamin, VA/BC, multivitamin including VA/BC, or pl
282 reviously reported that supplementation with multivitamins (vitamin B complex, vitamin C, and vitamin
283 he authors evaluated how supplemental use of multivitamins, vitamin C, and vitamin E over a 10-year p
285 to receive 3 mg/kg/day of elemental iron and multivitamins (vitamins A, C, and D) or multivitamins al
286 ts of preformed vitamin A and beta-carotene, multivitamins (vitamins B, C, and E), preformed vitamin
287 .0 and 10.8 events per 1000 person-years for multivitamin vs placebo, respectively; hazard ratio [HR]
289 individual supplement sources, but not from multivitamins, was associated with a 30% to 40% increase
291 obin concentrations among women who received multivitamins were 0.33 g/dL higher than among women who
293 er, coffee, beer, liquor, total alcohol, and multivitamins were each correlated with at least one met
296 mized, placebo-controlled clinical trials of multivitamins with cancer as the primary endpoint have b
297 ns and vitamins C and E), selenium alone, or multivitamins with selenium vs placebo in a factorial de
298 supplements of vitamins C and E and low-dose multivitamins with the risk of age-related cataract amon
299 (vitamins C, E, and B-complex), and zinc and multivitamin (Zn+MV) supplementation on growth in infant
300 ants were randomly assigned to receive zinc, multivitamins, Zn+MVs, or a placebo at 6 wk of age and w