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2 nce = 29.6 ml) of coffee per week (including decaffeinated) at the last menstrual period; and were en
3 demiologic studies link caffeinated (but not decaffeinated) beverage intake with significant decrease
4 tea, decaffeinated green tea plus caffeine, decaffeinated black tea plus caffeine, or caffeine alone
9 udy, we associated intake of caffeinated and decaffeinated coffee after diagnosis of CRC with lower r
13 arts and that the neuroprotective effects of decaffeinated coffee and nicotine-free tobacco are also
15 e report that the neuroprotective effects of decaffeinated coffee and nicotine-free tobacco require t
16 completely abstain from both caffeinated and decaffeinated coffee and other caffeine-containing produ
17 ation between consumption of caffeinated and decaffeinated coffee and risk of mortality remains incon
20 association between consumption of coffee or decaffeinated coffee and the risk of rheumatoid arthriti
22 concluded that ingestion of caffeinated and decaffeinated coffee can reduce the risk of diabetes.
23 variate model using only baseline reports of decaffeinated coffee consumption (RR 1.0, 95% CI 0.6-1.7
24 s of RA onset with the highest categories of decaffeinated coffee consumption (RR 3.10, 95% CI 1.75-5
25 ociation was observed between caffeinated or decaffeinated coffee consumption and risk of falls with
26 d not find a significant association between decaffeinated coffee consumption of >/=4 cups/day (compa
31 nsumption of >/=4 cups/day (compared with no decaffeinated coffee consumption) and subsequent risk of
32 and 14 site-specific cancers associated with decaffeinated coffee consumption, adjusted for regular c
36 as associated with a greater odds of being a decaffeinated coffee drinker (MREggr OR: 1.71; 95% CI: 1
37 caffeinated coffee and to be non-habitual or decaffeinated coffee drinkers compared with those who di
41 ted coffee high in chlorogenic acid (C-HCA), decaffeinated coffee high in chlorogenic acid, or decaff
42 o examine the consumption of caffeinated and decaffeinated coffee in relation to cardiovascular disea
44 [RR per serving: 8% for both caffeinated and decaffeinated coffee in the NHS (P < 0.0001) and 4% for
46 Similar inverse associations were found with decaffeinated coffee intake and abnormal levels of ALT (
47 and cognitive function among men or between decaffeinated coffee intake and cognitive function in ei
49 lly, few studies have considered exclusively decaffeinated coffee intake or use of coffee additives.
50 an systolic or diastolic blood pressure, but decaffeinated coffee intake was associated with a small
54 An inverse association for >2 cups/day of decaffeinated coffee intake was suggested (relative risk
55 s, 0.1-0.9, 1-1.9, 2-2.9 and >=3 cups/day of decaffeinated coffee intake were associated with HRs of
56 examined the association of caffeinated and decaffeinated coffee intake with cognitive function in a
59 products (caffeinated soda, caffeinated tea, decaffeinated coffee or chocolate) and risk of EG/EGS (P
60 in a double-blind design, 40 mL of either a decaffeinated coffee preparation plus 3 mg caffeine/kg (
63 The odds ratio for drinking > 1 cup/day of decaffeinated coffee versus nondrinkers was 1.25 (95% CI
64 nversely, the consumption of caffeinated and decaffeinated coffee was associated with a lower risk of
66 ion of total coffee, caffeinated coffee, and decaffeinated coffee was associated with lower risk of t
68 affeine from sources other than coffee or of decaffeinated coffee was not associated with reduced liv
71 o use, subjects drinking > or =4 cups/day of decaffeinated coffee were at increased risk of RA (RR 2.
75 feinated coffee high in chlorogenic acid, or decaffeinated coffee with regular amounts of chlorogenic
76 ns of consumption of total, caffeinated, and decaffeinated coffee with risk of subsequent total and c
77 coffee, 10% (95% confidence interval 4-15%); decaffeinated coffee, 10% (3-16%); tea, 14% (5-22%); bee
78 r caffeinated coffee, 9% (CI, 2% to 15%) for decaffeinated coffee, 8% (CI, 1% to 15%) for tea, and 59
80 se findings suggest that caffeinated coffee, decaffeinated coffee, and caffeine are not risk factors
83 s of baseline intakes of caffeinated coffee, decaffeinated coffee, and caffeine with measured systoli
85 examined associations of caffeinated coffee, decaffeinated coffee, and tea intake with fatal oral/pha
86 gated the association of caffeinated coffee, decaffeinated coffee, and tea with myocardial infarction
87 VD was elevated for nondrinkers, drinkers of decaffeinated coffee, and those who reported drinking >6
88 ongitudinal relations of caffeinated coffee, decaffeinated coffee, and total caffeine intakes with me
89 e evidence of an association between coffee, decaffeinated coffee, or tea consumption and the risk of
98 ving of sugar-sweetened soda/d, 1 serving of decaffeinated coffee/d was associated with a 10% (95% CI
99 sumption categories (0, 1-237, and >/=237 mL decaffeinated coffee/d) were 1.00, 1.02, and 0.77 (95% C
100 nated coffee/mo and 75% consumed > or =1 cup decaffeinated coffee/mo; the corresponding intakes for w
102 ndomly assigned to consumption of either the decaffeinated energy drink or a placebo drink on testing
104 different characteristics (soluble, ground, decaffeinated, etc) were evaluated for antioxidant capac
105 e relation between long-term caffeinated and decaffeinated filtered coffee consumption and markers of
106 esults indicate that neither caffeinated nor decaffeinated filtered coffee has a detrimental effect o
107 to test the effect of acute consumption of a decaffeinated green coffee extract (DGCE), rich in CGAs,
109 caffeinated beverages (green tea, black tea, decaffeinated green tea plus caffeine, decaffeinated bla
110 0.77; 95% CI: 0.63, 0.94; P-trend 0.009) and decaffeinated (HR: 0.70; 95% CI: 0.46, 1.06; P-trend: 0.
111 affeinated (HR: 0.94; 95% CI: 0.84, 1.05) or decaffeinated (HR: 1.05; 95% CI: 0.84, 1.31) coffee cons
112 ated coffee and tea intakes (caffeinated and decaffeinated) in relation to colon (proximal and distal
113 (FDIT), spray-dried instant tea (SDIT), and decaffeinated instant tea (DCIT)], were compared for the
114 tives.Drinking coffee, either caffeinated or decaffeinated, may lower the risk of CVD and IHD mortali
115 aximum intensity, intermediate intensity and decaffeinated) prepared from coffee capsules, using gas
116 , administration of a high-dose level of the decaffeinated teas enhanced the tumorigenic effect of UV
118 d carcinogenesis, and adding caffeine to the decaffeinated teas restored the inhibitory effects of th
119 nt to the amount in the regular teas) to the decaffeinated teas restored their inhibitory effects.