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Journal of Epidemiology logoLink to Journal of Epidemiology
. 2005 Aug 18;15(Suppl II):S98–S108. doi: 10.2188/jea.15.S98

Dietary Habits and Stomach Cancer Risk in the JACC Study

Noritaka Tokui 1, Takesumi Yoshimura 2, Yoshihisa Fujino 1,3, Tetsuya Mizoue 4, Yoshiharu Hoshiyama 5, Hiroshi Yatsuya 6, Kiyomi Sakata 7, Takaaki Kondo 8, Shogo Kikuchi 9, Hideaki Toyoshima 6, Norihiko Hayakawa 10, Tatsuhiko Kubo 1, Akiko Tamakoshi 11, for the JACC Study Group12
PMCID: PMC8639040  PMID: 16127240

Abstract

BACKGROUND: Despite a declining incidence, stomach cancer is still a dominant cancer in Japan. The association between dietary habits and stomach cancer risk was investigated in a large prospective study in Japan.

METHODS: Data were obtained using a self-administered questionnaire from 1988 through 1990. Food frequency questionnaire was used to evaluate the consumption of 33 selected food items. Proportional hazard model was used to determine the hazard ratios (HRs) and their 95% confidence intervals (CIs) of stomach cancer for different levels of the dietary intakes.

RESULTS: A western style breakfast showed an inverse association with stomach cancer risk in males (HR=0.49, 95% CI: 0.35-0.70). Women who consumed liver three to four times per week and more than once per day had a significant increased risk, respectively (HR=2.02, 95% CI: 1.12-3.63, HR=3.16, 95% CI: 1.16-8.62 ). A clear dose-response relationship between the intake of liver and stomach cancer risk was observed. We found no association between stomach cancer mortality and the consumption of fruit such as mandarin orange, and vegetables such as carrots and spinach in both men and women. The consumption of high salt foods such as miso soup and pickles was also not significantly associated with the mortality of stomach cancer in both sexes.

CONCLUSION: This prospective study suggested that a western-style breakfast is associated with a lower risk of stomach cancer, although some differences in the association were seen between men and women.

Key words: Diet, Prospective Studies, Stomach Neoplasms, Risk Factors, the JACC Study


Steady declines in incidence and mortality rates of stomach cancer have been found worldwide in recent decades.1 Despite a declining incidence, stomach cancer is still a dominant cancer in Japan.2 Previous studies indicated that environmental factors, particularly diet, play an important role in the etiology of this cancer.3,4 An increased risk of stomach cancer has been linked to low dietary intake of fresh fruit and vegetables and a high consumption of starch foods.5-10 Other reports have suggested that the risk of stomach cancer increased in a population who consumed cured or preserved fish and meat in salt or smoked.11-13 However, most of this epidemiologic evidence was based on studies with a case-control design. The results from case-control studies can be biased by differential recall of dietary intake due to stomach disorders. Recall of dietary intake could also have been influenced by current dietary habits. Prospective studies are less susceptible to recall bias because dietary intake is measured before the presence of a disease in known. Unfortunately, there have been a limited number of prospective studies in Japan.14-16 In addition, these studies have less information on lifestyle and the number of subjects was small.

Monbusho cohort study, a large-scale prospective cohort study on life style including dietary habits and cancer, began in 1988 with about 125,000 men and women. This cohort study was conducted by more than twenty universities and research institutes that were located throughout Japan. Therefore, data in this cohort would be representative of the Japanese population. We have investigated the relation between dietary intakes and mortality of stomach cancer.

METHODS

JACC study

The Japan Collaborative Cohort Study (JACC Study) for Evaluation of Cancer Risk sponsored by the Ministry of Education, Science, Sports and Culture of Japan (Monbusho) was established from 1988 through 1990 to investigate the relationship between various lifestyle variables and cancer mortality and incidence. The study methods have been described in detail elsewhere.17 In brief, this cohort consisted of 110,792 persons aged 40 -79 years who lived 52 cities, towns and villages in Japan at the beginning of the study. At baseline, the cohort members completed a self-administered questionnaire on dietary habits, smoking, alcohol use, medical history, personal and family history of cancer and demographic data. We followed the subjects from 1988 through 1999. Information on deaths among the study subjects was annually collected by examination of death certificates with permission of the Management and Coordination Agency of the Japanese Government. All baseline data and follow up data including death data were reported to the central committee office. The underlying causes of death were coded according to International Classification of Disease Revision 9 from 1988 through 1994 and after 1995, Revision 10. Stomach cancer was determined by the coding 151.0-159.0 for ICD-9 and C16.0-C16.9 for ICD-10. Informed consent was obtained from each subject.

To participate in the study, an individual’s informed consent was obtained in 36 out of 45 areas (written consent in 35 areas and oral consent in 1 area), though in 9 areas, group consent from head of the area was obtained.

Dietary questionnaire

The dietary section of the questionnaire was a 33 item food frequency questionnaire dealing with on the usual consumption of food and beverages. Frequency consumption of 33 foods was classified into five categories (almost never, less than once or twice per month, once or twice per week, three or four times per week, or almost daily). Food items of vegetables and fruits include spinach, carrot/pumpkin, tomato, cabbage, Chinese cabbage, edible wild plants, fried vegetables, mandarin orange, fresh fruit juice, and others fruits. Regarding four beverages (coffee, black tea, green tea, and oolong tea), participants were asked to choose one of five categories (almost never, 1 to 2 cups per month, 1 to 2 cups per week, 3 to 4 cups per week, or almost daily). Additionally, if they take these beverages almost daily, they were also asked to report the number of cups. For miso soup, the frequency of consumption (almost never, several times per month, every other day, or almost daily) was asked, and the number of cups per day was obtained if subjects chose the category of ‘almost daily’. Alcohol intake was based on the usual weekly intake of Japanese sake, beer, wine, whiskey and distilled spirits among current drinkers. In the above described foods, data of some food items were not collected in a few study areas because a different questionnaire was used there.

Data analysis

Proportional hazard model was used to determine hazard ratios (HRs) and their 95% confidence intervals (CIs) of stomach cancer for different levels of the dietary intakes. Analyses were conducted separately for males and females. Statistical significance (two sided) was based on the ratio of the regression coefficient and its standard error. Statistical analysis (PHREG procedure) was performed by the Statistical Analysis System® (SAS institute, 1983).

RESULTS

During the follow up period, a total of 859 stomach cancer deaths (574 males and 285 females) were obtained. The results of age adjusted analyses are presented in Table 1. There was a non-significant inverse association between the intake of vegetables such as carrots, tomatoes and spinach, and stomach cancer risk in both sexes. There was a weak non-significant association between the intake of cabbage and Chinese cabbage, and mortality among females. The relative risk of fruit consumption such as mandarin orange and pure fruit juice also did not decrease among men and women. In contrast to these results, the consumption of mushroom was associated with the increased risk of stomach cancer in females (HR=1.54, 95% CI: 1.03-2.28).

Table 1. Age adjusted hazard ratios of stomach cancer for intake of vegetables, fruit, and other foods by sex.

Male Female


No. of death Hazard ratio 95% confidence interval p for trend No. of death Hazard ratio 95% confidence interval p for trend
Spinach
1-2/month or less 34 1.00 (reference) 10 1.00 (reference)
1-2/week 121 1.16 0.79 - 1.69 50 1.29 0.65 - 2.55
3-4/week 119 1.10 0.75 - 1.62 67 1.51 0.78 - 2.93
1+/day 162 1.29 0.89 - 1.87 0.16 79 1.40 0.72 - 2.70 0.38
 
Carrot • pumpkin
1-2/month or less 71 1.00 (reference) 24 1.00 (reference)
1-2/week 150 1.28 0.96 - 1.69 56 0.86 0.54 - 1.39
3-4/week 98 1.19 0.88 - 1.61 64 1.04 0.65 - 1.67
1+/day 59 1.14 0.80 - 1.61 0.60 54 1.15 0.71 - 1.86 0.24
 
Tomato
1-2/month or less 145 1.00 (reference) 72 1.00 (reference)
1-2/week 127 1.05 0.83 - 1.33 52 0.80 0.56 - 1.15
3-4/week 82 1.06 0.81 - 1.39 43 0.91 0.62 - 1.32
1+/day 62 1.19 0.88 - 1.61 0.29 44 1.10 0.76 - 1.60 0.66
 
Cabbage
1-2/month or less 53 1.00 (reference) 15 1.00 (reference)
1-2/week 116 0.81 0.59 - 1.12 49 1.01 0.57 - 1.81
3-4/week 113 0.90 0.65 - 1.25 56 1.16 0.65 - 2.04
1+/day 111 1.11 0.80 - 1.54 0.15 71 1.49 0.85 - 2.60 0.03
 
Chinese cabbage
1-2/month or less 67 1.00 (reference) 33 1.00 (reference)
1-2/week 122 0.99 0.73 - 1.33 58 1.03 0.67 - 1.58
3-4/week 86 0.94 0.68 - 1.30 41 0.94 0.60 - 1.49
1+/day 77 1.18 0.85 - 1.64 0.39 47 1.30 0.83 - 2.03 0.31
 
Edible wild plants
None 137 1.00 (reference) 71 1.00 (reference)
1-2/month 151 1.16 0.92 - 1.46 75 1.26 0.91 - 1.74
1-2/week 51 1.02 0.74 - 1.41 26 1.05 0.67 - 1.65
3-4/week or more 48 1.37 0.98 - 1.90 0.16 22 1.22 0.75 - 2.96 0.87
 
Mandarin orange
1-2/month or less 94 1.00 (reference) 23 1.00 (reference)
1-2/week 87 0.77 0.57 - 1.03 33 0.90 0.53 - 1.53
3-4/week 84 0.79 0.59 - 1.06 43 1.00 0.60 - 1.66
1+/day 124 0.92 0.71 - 1.21 0.80 93 1.03 0.65 - 1.63 0.65
 
Pure fruit juice
None 90 1.00 (reference) 48 1.00 (reference)
1-2/month 60 0.91 0.66 - 1.26 19 0.68 0.40 - 1.17
1-2/week 69 0.77 0.56 - 1.06 38 1.03 0.67 - 1.58
3-4/week 54 0.85 0.61 - 1.20 34 1.20 0.77 - 1.86
1+/day 67 1.23 0.89 - 1.68 0.51 31 0.95 0.60 - 1.49 0.59
 
Bean curd
1-2/month or less 31 1.00 (reference) 11 1.00 (reference)
1-2/week 140 1.12 0.76 - 1.65 60 1.24 0.65 - 2.36
3-4/week 162 1.09 0.74 - 1.60 88 1.38 0.74 - 2.59
1+/day 139 1.07 0.73 - 1.58 0.97 85 1.41 0.75 - 2.64 0.25
 
Mushroom
1-2/month or less 152 1.00 (reference) 46 1.00 (reference)
1-2/week 123 0.88 0.69 - 1.11 67 1.15 0.79 - 1.67
3-4/week 66 0.97 0.72 - 1.29 53 1.54 1.03 - 2.28
1+/day 26 0.89 0.59 - 1.35 0.57 17 1.11 0.64 - 1.94 0.16

The consumption of high salt foods such as miso soup, pickles, and dried fish was not significantly associated with the mortality of stomach cancer in males (Table 2). The relative risks of these foods were close to one. In females, the intake of pickles, fish boiled in soy sauce and strong taste of salty food elevated the risk of stomach cancer, but not significantly.

Table 2. Age-adjusted hazard ratios of stomach cancer for intake of salty foods by sex.

Male Female


No. of death Hazard ratio 95% confidence interval p for trend No. of death Hazard ratio 95% confidence interval p for trend
Pickles
1-2/month or less 52 1.00 (reference) 18 1.00 (reference)
1-2/week 60 1.04 0.72 - 1.51 30 1.56 0.87 - 2.81
3-4/week 74 1.00 0.70 - 1.42 32 1.32 0.74 - 2.36
1+/day 330 1.09 0.82 - 1.47 0.48 175 1.47 0.90 - 2.39 0.26
 
Fish boiled in soy sauce
None 96 1.00 (reference) 46 1.00 (reference)
1-2/month 100 0.86 0.65 - 1.13 46 0.99 0.66 - 1.49
1-2/week 104 0.88 0.67 - 1.17 50 1.09 0.73 - 1.63
3-4/week 66 1.08 0.79 - 1.48 25 0.99 0.61 - 1.61
1+/day 30 0.92 0.61 - 1.38 0.87 24 1.57 0.95 - 2.57 0.18
 
Boiled beans
None 80 1.00 (reference) 29 1.00 (reference)
1-2/month 141 0.86 0.65 - 1.13 70 0.84 0.54 - 1.29
1-2/week 93 0.77 0.57 - 1.05 48 0.79 0.50 - 1.26
3-4/week 73 1.19 0.86 - 1.63 34 0.97 0.59 - 1.60
1+/day 27 0.93 0.60 - 1.44 0.61 16 0.84 0.46 - 1.56 0.88
 
Dried or salty fish
None 36 1.00 (reference) 29 1.00 (reference)
1-2/month 83 0.89 0.60 - 1.32 39 0.64 0.40 - 1.04
1-2/week 141 0.93 0.65 - 1.34 63 0.66 0.42 - 1.02
3-4/week 66 0.85 0.57 - 1.28 33 0.69 0.42 - 1.13
1+/day 48 1.14 0.74 - 1.76 0.64 24 0.92 0.53 - 1.58 0.86
 
Miso soup
None 15 1.00 (reference) 12 1.00 (reference)
Several times/month 43 1.42 0.79 - 2.56 25 1.38 0.69 - 2.74
Several times/week 57 1.50 0.85 - 2.65 28 1.18 0.60 - 2.31
Everyday 415 1.44 0.86 - 2.42 0.36 201 1.46 0.81 - 2.61 0.19
 
Miso soup(cup)
less than 1/day 115 1.00 (reference) 65 1.00 (reference)
1/day 93 0.90 0.69 - 1.19 65 1.21 0.86 - 1.72
2/day 114 0.99 0.76 - 1.28 62 1.24 0.87 - 1.77
3+/day 140 1.17 0.91 - 1.50 0.16 41 1.24 0.84 - 1.84 0.23
 
Preference for salty foods
No 9 1.00 (reference) 4 1.00 (reference)
A little 39 0.90 0.43 - 1.85 30 1.56 0.55 - 4.42
Fair 210 1.14 0.58 - 2.21 115 1.80 0.66 - 4.88
Pretty 119 1.11 0.56 - 2.18 35 1.51 0.54 - 4.26
Very much 51 1.36 0.67 - 2.78 0.12 13 1.89 0.62 - 5.79 0.57

Table 3 shows the relationship between intake of meat, fish and marine foods, and stomach cancer. In males, those who had beef once or twice a week showed a significant decreased risk compared to those who hardly ever consumed beef (HR=0.73, 95% CI: 0.55-0.96). Regarding the intake of chicken, the relative risk of eating it once or twice a month was also significantly reduced (HR=0.62, 95% CI: 0.45-0.86). However, the association of meat, which included sausage and liver, with stomach cancer was not observed in males. On the other hand, those who consumed liver three to four times per week and more than once a day had a increased risk among females, respectively (RR=2.02,95% CI:1.12-3.63, RR=3.16,95% CI:1.16-8.62). The non-significantly higher risk for stomach cancer was found in the third highest consumption of fish (HR=1.62, 95% CI: 0.95-2.75). No clear association was found between the intake of other meat and fish and the risk of stomach cancer in females.

Table 3. Age-adjusted hazard ratios of stomach cancer for intake of meat, fish, and marine foods by sex.

Male Female


No. of death Hazard ratio 95% confidence interval p for trend No. of death Hazard ratio 95% confidence interval p for trend
Beef
None 100 1.00 (reference) 48 1.00 (reference)
1-2/month 119 0.79 0.61 - 1.04 52 1.02 0.69 - 1.51
1-2/week 92 0.73 0.55 - 0.96 51 1.09 0.74 - 1.62
3-4/week 34 1.00 0.67 - 1.47 13 0.92 0.50 - 1.69
1+/day 6 0.90 0.39 - 2.05 0.30 4 2.05 0.74 - 5.68 0.60
 
Pork
None 40 1.00 (reference) 26 1.00 (reference)
1-2/month 84 0.96 0.66 - 1.41 40 1.13 0.69 - 1.85
1-2/week 173 1.10 0.78 - 1.55 78 1.16 0.74 - 1.82
3-4/week 66 1.10 0.74 - 1.62 34 1.35 0.81 - 2.26
1+/day 14 1.05 0.57 - 1.93 0.45 7 1.50 0.65 - 3.48 0.21
 
Sausage
None 108 1.00 (reference) 54 1.00 (reference)
1-2/month 101 0.93 0.71 - 1.22 54 1.31 0.90 - 1.91
1-2/week 139 1.00 0.77 - 1.28 62 1.13 0.78 - 1.64
3-4/week 71 1.24 0.92 - 1.67 26 1.18 0.74 - 1.89
1+/day 20 1.36 0.85 - 2.20 0.10 9 1.82 0.90 - 3.70 0.27
 
Chicken
None 54 1.00 (reference) 18 1.00 (reference)
1-2/month 99 0.62 0.45 - 0.86 50 1.12 0.66 - 1.93
1-2/week 179 0.71 0.52 - 0.96 92 1.09 0.66 - 1.81
3-4/week 81 0.84 0.59 - 1.18 46 1.30 0.76 - 2.25
1+/day 12 0.73 0.39 - 1.37 0.98 7 1.33 0.55 - 3.17 0.33
 
Liver
None 173 1.00 (reference) 81 1.00 (reference)
1-2/month 114 0.84 0.66 - 1.06 56 1.26 0.90 - 1.78
1-2/week 67 1.06 0.80 - 1.41 32 1.39 0.92 - 2.11
3-4/week 22 1.27 0.82 - 1.99 13 2.02 1.12 - 3.63
1+/day 2 0.56 0.14 - 2.28 0.75 4 3.16 1.16 - 8.62 0.00
 
Fish
1-2/month or less 45 1.00 (reference) 16 1.00 (reference)
1-2/week 144 0.85 0.61 - 1.19 65 1.22 0.71 - 2.11
3-4/week 154 0.90 0.65 - 1.26 94 1.62 0.95 - 2.75
1+/day 136 0.95 0.68 - 1.33 0.73 63 1.41 0.82 - 2.45 0.13
 
Boiled fish paste
None 75 1.00 (reference) 32 1.00 (reference)
1-2/month 107 1.03 0.77 - 1.38 43 0.91 0.58 - 1.44
1-2/week 116 1.27 0.95 - 1.69 70 1.47 0.97 - 2.24
3-4/week or more 58 1.21 0.86 - 1.71 0.10 30 1.25 0.76 - 2.06 0.06
 
Seaweed
1-2/month or less 59 1.00 (reference) 22 1.00 (reference)
1-2/week 133 0.90 0.66 - 1.22 53 0.75 0.46 - 1.24
3-4/week 176 1.15 0.86 - 1.55 79 0.90 0.56 - 1.44
1+/day 158 1.04 0.77 - 1.40 0.29 103 0.97 0.61 - 1.54 0.38

Men who had consumed yogurt once or twice a month showed a significant decreased risk compared to those who had hardly ever consumed yogurt (HR=0.69, 95% CI: 0.49-0.98) (Table 4). Daily products such as eggs and milk were not associated with stomach cancer in males. The relative risks for the second to quintile were close to null value. For intake of eggs among females, the relative risks for third and quartile significantly increased (HR=2.11, 95% CI: 1.09-4.09, HR=2.32, 95% CI: 1.22-4.42, respectively). Meantime, butter intake had a non-significant inverse association with stomach cancer risk (HR=0.37, 95% CI: 0.14-1.01).

Table 4. Age adjusted hazard ratios of stomach cancer for intake of daily products by sex.

Male Female


No. of death Hazard ratio 95% confidence interval p for trend No. of death Hazard ratio 95% confidence interval p for trend
Egg
1-2/month or less 34 1.00 (reference) 10 1.00 (reference)
1-2/week 119 1.16 0.79 - 1.69 52 1.80 0.91 - 3.53
3-4/week 118 0.90 0.62 - 1.32 76 2.11 1.09 - 4.09
1+/day 260 1.13 0.79 - 1.62 0.64 124 2.32 1.22 - 4.42 0.01
 
Milk
None 100 1.00 (reference) 60 1.00 (reference)
1-2/month 41 1.13 0.79 - 1.63 11 0.62 0.33 - 1.18
1-2/week 75 1.17 0.87 - 1.58 32 0.90 0.58 - 1.38
3-4/week 66 1.08 0.79 - 1.48 30 0.78 0.50 - 1.21
1+/day 223 1.06 0.84 - 1.35 0.81 115 0.83 0.60 - 1.13 0.34
 
Yogurt
None 247 1.00 (reference) 100 1.00 (reference)
1-2/month 35 0.69 0.49 - 0.98 29 0.95 0.63 - 1.43
1-2/week 28 0.86 0.58 - 1.28 33 1.38 0.93 - 2.05
3-4/week 18 1.22 0.76 - 1.97 10 0.85 0.44 - 1.63
1+/day 16 0.82 0.50 - 1.37 0.47 11 0.88 0.47 - 1.64 0.93
 
Cheese
None 191 1.00 (reference) 106 1.00 (reference)
1-2/month 82 0.93 0.72 - 1.20 47 1.31 0.92 - 1.85
1-2/week 51 1.08 0.80 - 1.48 19 0.93 0.57 - 1.52
3-4/week 23 1.32 0.86 - 2.04 5 0.60 0.24 - 1.46
1+/day 8 0.79 0.39 - 1.61 0.64 6 1.18 0.52 - 2.69 0.80
 
Butter
None 190 1.00 (reference) 104 1.00 (reference)
1-2/month 78 0.97 0.75 - 1.27 27 0.76 0.50 - 1.17
1-2/week 47 0.96 0.70 - 1.33 31 1.27 0.85 - 1.90
3-4/week 19 0.92 0.57 - 1.47 4 0.37 0.14 - 1.01
1+/day 11 0.70 0.38 - 1.29 0.33 11 1.22 0.65 - 2.26 0.89
 
Margarine
None 195 1.00 (reference) 89 1.00 (reference)
1-2/month 54 0.83 0.61 - 1.12 29 0.98 0.64 - 1.50
1-2/week 71 1.14 0.87 - 1.49 39 1.09 0.74 - 1.59
3-4/week 29 0.92 0.62 - 1.36 14 0.69 0.39 - 1.22
1+/day 25 0.72 0.48 - 1.10 0.36 20 0.82 0.50 - 1.33 0.30

Table 5 presented the relative risk of stomach cancer for starch food and style of breakfast. No significant association of rice intake with stomach cancer at present or in the thirties was observed in both males and females. Regarding the intake of potatoes once or twice a week in females, the relative risk significantly decreased (HR=0.66, 95% CI: 0.44-0.98). A western style breakfast showed a preventive association with stomach cancer in males (HR=0.49, 95% CI: 0.35-0.70). In contrast, tea gruel significantly elevated the risk of stomach cancer in males (HR=1.50, 95% CI: 1.03-2.18).

Table 5. Age adjusted hazard ratios of stomach cancer for intake of starch food and style of breakfast by sex.

Male Female


No. of death Hazard ratio 95% confidence interval p for trend No. of death Hazard ratio 95% confidence interval p for trend
Rice (cup)
1/day or less 47 0.93 0.68 - 1.28 36 1.25 0.86 - 1.80
2/day 96 1.09 0.85 - 1.39 52 0.96 0.70 - 1.32
3/day 198 1.00 (reference) 132 1.00 (reference)
4/day 60 0.93 0.69 - 1.24 18 0.96 0.58 - 1.57
5/day 69 1.05 0.80 - 1.38 18 1.31 0.80 - 2.15
6+/day 69 0.97 0.74 - 1.28 0.87 8 0.75 0.37 - 1.54 0.54
 
Rice (cup) (thirties)
1/day or less 7 1.38 0.63 - 3.01 8 1.91 0.89 - 4.08
2/day 36 0.87 0.58 - 1.32 26 1.09 0.66 - 1.79
3/day 59 1.00 (reference) 39 1.00 (reference)
4/day 35 1.15 0.76 - 1.75 23 1.21 0.72 - 2.03
5/day 54 1.09 0.75 - 1.57 26 0.96 0.58 - 1.58
6+/day 215 1.08 0.81 - 1.44 0.42 87 1.18 0.80 - 1.72 0.99
 
Potato
1-2/month or less 96 1.00 (reference) 36 1.00 (reference)
1-2/week 181 1.08 0.84 - 1.38 67 0.66 0.44 - 0.98
3-4/week 146 1.06 0.82 - 1.38 91 0.85 0.58 - 1.26
1+/day 94 1.08 0.81 - 1.44 0.65 61 0.86 0.57 - 1.29 0.74
 
Japanese style breakfast
No 55 1.00 (reference) 36 1.00 (reference)
Yes 397 1.30 0.98 - 1.72 184 1.24 0.87 - 1.77
 
Western style breakfast
No 418 1.00 (reference) 182 1.00 (reference)
Yes 34 0.49 0.35 - 0.70 38 0.82 0.58 - 1.17
 
Tea gruel for breakfast
No 396 1.00 (reference) 198 1.00 (reference)
Yes 29 1.50 1.03 - 2.18 5 0.50 0.21 - 1.22

Coffee consumption showed a significant inverse association with the risk of stomach cancer in age-adjusted analysis among males, with a relative risk of 0.81 for the fifth intake category (more than one cup per day) (Table 6). However, the relative risk for the consumption of three or four cups of coffee per day was statistical significant in comparison with non-drinkers in females (HR=1.70, 95% CI: 1.09-2.67). Compared to those who drank less than two cups of coffee per week, women who drank three cups or more of coffee per week had an increased risk of stomach cancer(HR=1.66, 95% CI: 1.09-2.54). There was no clear association between levels of consumption of coffee and the risk of stomach cancer among male.

Table 6. Age adjusted hazard ratios of stomach cancer for intake of coffee and tea by sex.

Male Female


No. of death Hazard ratio 95% confidence interval p for trend No. of death Hazard ratio 95% confidence interval p for trend
Coffee (cup)
None 151 1.00 (reference) 74 1.00 (reference)
1-2/month 33 0.82 0.57 - 1.20 17 1.04 0.62 - 1.77
1-2/week 84 0.92 0.70 - 1.20 36 0.99 0.66 - 1.48
3-4/week 46 1.00 0.72 - 1.40 26 1.70 1.09 - 2.67
1+/day 222 0.81 0.65 - 0.99 0.07 105 1.00 0.74 - 1.35 0.81
 
Coffee (cup)
2/week or less 268 1.00 (reference) 127 1.00 (reference)
less than 1/day 46 1.05 0.77 - 1.44 26 1.66 1.09 - 2.54
1/day 45 0.82 0.60 - 1.12 30 1.03 0.69 - 1.54
2/day 22 0.55 0.36 - 0.86 16 1.09 0.64 - 1.84
3+/day 26 1.00 0.66 - 1.50 0.06 3 0.47 0.15 - 1.50 0.79
 
Black tea (cup)
None 308 1.00 (reference) 154 1.00 (reference)
1-2/month 48 0.98 0.72 - 1.33 20 0.75 0.47 - 1.20
1-2/week 20 0.75 0.48 - 1.18 13 0.82 0.46 - 1.44
3-4/week or more 32 1.41 0.98 - 2.03 0.29 14 1.03 0.60 - 1.79 0.84
 
China tea
less than 1/day 350 1.00 (reference) 174 1.00 (reference)
1+/day 11 0.70 0.38 - 1.27 0.72 8 0.58 0.28 - 1.17 0.18

DISCUSSION

In this study, we found no association between stomach cancer mortality and the consumption of fruits and vegetables. The protective effect against stomach cancer of the consumption of a wide range of fruits and vegetables has been examined in epidemiological studies. Many case control studies have shown a decreased risk with fruits and vegetables,5-8 although there are exceptions.11,18 This protective effect might be due to food rich in vitamin C, such as oranges, tomatoes, citrus fruits. Vitamin C can prevent the formation of N-nitroso compounds.19,20 In some studies, dietary intakes of micronutrients have been estimated. These studies have shown a consistent negative association of dietary intakes of vitamin C and carotenoids with stomach cancer.21-23 In contrast, a negative association between the intakes of vegetables and fruits and stomach cancer has been less pronounced in limited cohort studies.24 In some cohort studies, the intakes of micronutrients such as vitamin C, β-carotene, and other carotenes have been examined.16,25,26 There was no significant difference in any micronutrients between men developing stomach cancer and those without stomach cancer. A meta-analytic approach to examine the evidence from cohort studies on total vegetable and fruit intake showed no significant protective effects.27 In the meantime, an intervention trial using supplementation with β-carotene, vitamin E, and selenium showed reductions in stomach cancer mortality.28 These results are difficult to generalize for populations who do not take supplements everyday.24 In this study, consumption of liver was related to the high risk of stomach cancer in females. The reason for this association might be that women who often consume liver have suffered from anemia due to a stomach disorder including stomach cancer.

No salty food such as miso soup, pickled vegetable, and salted or dried fish was associated with the risk of stomach cancer. It has been suggested that salt intake is strongly associated with intestinal metaplasia and potentiates the effects of carcinogens.29 In support of this hypothesis, several epidemiological studies have reported significant association between salt intake or salt attitude and stomach cancer,10,12,22 but these are not universal findings.25,30,31 Part of the reason for these discrepant results is that the intake of sodium is difficult to quantify.4 To obtain a valid estimation of salt intake, rigorous dietary intake methodology, including information on discretionary use of table salt and soy sauce or direct measures of salt metabolism should be used. In this study, a food frequency questionnaire without portion size was used. Therefore, the relation between salt intake and stomach cancer risk may not be adequately appraised by this method.

Previous case control studies have not found any significant associations between the consumption of coffee with stomach cancer risk.7,31-34 Coffee consumption showed a significant inverse association with the risk of stomach cancer in males. Men who had a western style breakfast have a significant lower risk of stomach cancer. Coffee consumption is considered to be a westernized dietary habit. Mutagenic substances have been found in coffee,35-37 although caffeine is not thought to be carcinogenic in humans when consumed in normal amounts.7 However, we failed to observe a clear dose-response relationship between coffee consumption and stomach cancer risk. In addition, the intake of coffee increased the risk of stomach cancer in females. Therefore, this contradictious association between coffee consumption and stomach cancer in males and females needs further investigation.

Intakes of beef, chicken and yogurt in males, and potatoes in females showed a significantly decreased risk. However, this trend did not indicate a significant association. Frequencies of intakes of these foods were rather low, once or twice per week or month. These results suggested the necessity of further epidemiological studies to verify the association between these foods and risk of stomach cancer.

It is not certain why the present study did not find a significant association between the intake of foods and stomach cancer, as shown in the past cohort studies. The possibility exists that the food frequency questionnaire used in this study was not sensitive enough to detect meaningful differences in dietary intake due to the small number of food items (33 foods). The present study did not specifically include a number of other food items that have been positively related to stomach cancer in past studies, such as foods rich in nitrate-related compounds. We were not able to adjust for total calories, because a quantitative estimate of food consumption was not available. In addition, even if some foods showed the association with stomach cancer risk in this study, most of the association did not indicate a dose-response relationship. Therefore, it is important to carefully consider the results.

We have studied the association between the consumption of different foods and stomach cancer deaths. Subjects with subclinical stomach cancer may have changed their diet because of symptoms. We should also consider the possibility that the results of the present study based on mortality data reflected not causal factors, but prognostic factors of stomach cancer.

In conclusion, no clear association with individual food consumption was observed, although the results from this prospective study indicate that some foods were associated with stomach cancer risk. We also collected incidence cases of stomach cancer in this cohort. Further study will be required to use these data.

MEMBER LIST OF THE JACC STUDY GROUP

The present investigators involved, with the co-authorship of this paper, in the JACC Study and their affiliations are as follows: Dr. Akiko Tamakoshi (present chairman of the study group), Nagoya University Graduate School of Medicine; Dr. Mitsuru Mori, Sapporo Medical University School of Medicine; Dr. Yutaka Motohashi, Akita University School of Medicine; Dr. Ichiro Tsuji, Tohoku University Graduate School of Medicine; Dr. Yosikazu Nakamura, Jichi Medical School; Dr. Hiroyasu Iso, Institute of Community Medicine, University of Tsukuba; Dr. Haruo Mikami, Chiba Cancer Center; Dr. Yutaka Inaba, Juntendo University School of Medicine; Dr. Yoshiharu Hoshiyama, University of Human Arts and Sciences; Dr. Hiroshi Suzuki, Niigata University School of Medicine; Dr. Hiroyuki Shimizu, Gifu University School of Medicine; Dr. Hideaki Toyoshima, Nagoya University Graduate School of Medicine; Dr. Kenji Wakai, Aichi Cancer Center Research Institute; Dr. Shinkan Tokudome, Nagoya City University Graduate School of Medical Sciences; Dr. Yoshinori Ito, Fujita Health University School of Health Sciences; Dr. Shuji Hashimoto, Fujita Health University School of Medicine; Dr. Shogo Kikuchi, Aichi Medical University School of Medicine; Dr. Akio Koizumi, Graduate School of Medicine and Faculty of Medicine, Kyoto University; Dr. Takashi Kawamura, Kyoto University Center for Student Health; Dr. Yoshiyuki Watanabe, Kyoto Prefectural University of Medicine Graduate School of Medical Science; Dr. Tsuneharu Miki, Graduate School of Medical Science, Kyoto Prefectural University of Medicine; Dr. Chigusa Date, Faculty of Human Environmental Sciences, Mukogawa Women’s University ; Dr. Kiyomi Sakata, Wakayama Medical University; Dr. Takayuki Nose, Tottori University Faculty of Medicine; Dr. Norihiko Hayakawa, Research Institute for Radiation Biology and Medicine, Hiroshima University; Dr. Takesumi Yoshimura, Fukuoka Institute of Health and Environmental Sciences; Dr. Akira Shibata, Kurume University School of Medicine; Dr. Naoyuki Okamoto, Kanagawa Cancer Center; Dr. Hideo Shio, Moriyama Municipal Hospital; Dr. Yoshiyuki Ohno, Asahi Rosai Hospital; Dr. Tomoyuki Kitagawa, Cancer Institute of the Japanese Foundation for Cancer Research; Dr. Toshio Kuroki, Gifu University; and Dr. Kazuo Tajima, Aichi Cancer Center Research Institute.

ACKNOWLEDGMENTS

The authors sincerely express their appreciation to Dr. Kunio Aoki, Professor Emeritus, Nagoya University School of Medicine and the former chairman of the JACC Study, and Dr. Haruo Sugano, the former Director, Cancer Institute, Tokyo, who greatly contributed to the initiation of the JACC Study, and Dr. Yoshiyuki Ohno, Professor Emeritus, Nagoya University School of Medicine, who was the past chairman of the study. The authors also wish to thank Dr. Tomoyuki Kitagawa, Cancer Institute of the Japanese Foundation for Cancer Research and the former chairman of Grant-in-Aid for Scientific Research on Priority Area ‘Cancer’, for his full support of this study.

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