1. Background
Cancer is one of the major causes of deaths in developing countries and its prevalence is rising by changing their lifestyle toward the westernized [1]. Esophageal squamous cell carcinoma (ESCC) is the eighth common cancer (among the ten common cancers in the world) and the sixth cause of cancer death in the worldwide. Despite the recent increased detection of disease, the mortality rate is still at a high level. According to statistical data of 2008, approximately 400,000 people had died due to esophageal cancer all over the world, which 80% of the mortality happened in developing countries [2]. Iran is one of the high risk areas of esophageal cancer prevalence, so that in some regions such as Golestan province, the incidence of this disease is higher than the global average. Esophageal cancer has estimated the seventh common cancer between men (7.4 cases per 100,000 persons) and the forth common cancer between women (6.3 cases per 100,000 persons) in our country.
The major risk factors of ESCC are: age, inheritance, job, smoking and alcohol, obesity, refluxes, achalasia, human papillomavirus (HPV) and helicobacter pylori, hot drinks intake, consumption of foods that consist of nitrosamines and aromatic hydrocarbon, low intake of fruit and fresh vegetables and lack of some vitamins and minerals such as C, A and E vitamins [3]. Although, recently the researchers paid more attention to the role of diet in the appearance of cancer and considered the various aspects of diet in relation to that, but there was a little attention to the role and relationship of micronutrients in the prevalence of different cancers. Also, there have been a very limited number of studies on this field in Iran and only a small number of studies have investigated the relationship between micronutrients intake and esophageal cancer [4-6]. Furthermore, there is no study in this field in Kurdistan province.
2. Objectives
The aim of the present case-control study is therefore, to evaluate the relation of antioxidant vitamins intake such as C, A and E and cancer of ESCC in Kurdistan province.
3. Patients and Methods
In this case-control study, the samples were selected among people who referred to the major hospitals of Kurdistan province by systematic sampling method. First of all newly diagnosed patients with ESCC in Kurdistan province were identified during the study and those who had entrance criteria, were enrolled. Controls were frequency-matched with cases according to sex and age (5 year’s groups). Cases were patients age 40 - 75 years, who visited major general hospitals and had incident histologically-confirmed ESCC. Cases did not have history of carcinoma of other sites and were interviewed within 6 months after their ESCC was diagnosed. Controls were chosen from individuals admitted to the same hospitals as the cases for neurosurgery, corrective surgery and appendix surgery or orthopedic, ears and throat and nose problems. Controls had no history of each type of cancer and they did not follow a special diet. Generally, 50 patients with ESCC and 100 hospital controls were interviewed face to face by professionally trained interviewers using questionnaires which evaluated socio-demographic characteristics (age, sex, education, and smoking). Additionally, weight and height of the participants were measured. Also, the usual dietary intakes of each person during the last year (for cases, 1 year before diagnosis of the disease and for the controls, 1 year before interview) were collected by a validated semi-quantitive food frequency questionnaire (FFQ) through the interview. Participants were asked to report their consumption frequency on daily, weekly, monthly basis [7]. The FFQ were consisted of 125 Iranian food items. Relative reliability and validity of the questionnaires were evaluated in Tehran province before and the results of previous studies showed a good relative reliability and validity (between 39.6% and 68.3% in men and between 39.6% and 54.1% in women) for evaluation of food intakes [8, 9].
Then by using the collected data through FFQ, the nutritional value of dietary patterns intake was determined in the two groups. In this way, consumption value was calculated for each reported time. Since the consumption value was reported based on serving size or scale of household consumption, first, grams of per serving was determined using the book (scale of household) and then was multiplied in frequency of consumption. In the present study, the consumption frequency on daily basis was considered as the compare unit and the consumption frequency based on week, month and year was converted to day. The consumption gram for each food item was entered into Excel program. N4 (nutritionist IV) software was used to determine the nutritional value of dietary patterns intake. Each food item was coded and entered to N4. So the nutritional value of dietary patterns intake was calculated for every individual.
The Statistical data analysis was performed using SPSS-16. The mean and standard deviation were used to describe the quantitative variables. Also, Klomogrov-Smirnov test was used to assess the normalization of the quantitative data and independent t-test was used to consider the relationship between quantitative and qualitative variables. Also χ2 and Fisher tests were used to compare the distribution of qualitative variables between the groups. The logistic regression was used to find the relationship between nutrient intakes and risk of esophageal cancer after controlling disturbing factors of cooking method, reflux signs, family background, eating speed, food preference, job, and BMI. Finally, the odds ratio (OR) and 95% confidence intervals (CI) for the risk of ESCC were estimated in relation with nutrient intakes. Also residual method was used to consider the effect of energy.
4. Results
The distribution of the cases and controls by socio-demographics and selected risk factors are shown in Table 1. By design, age and sex distributions were similar among cases and controls. The mean age was 58 years and the total number of samples was 143 (87 females and 56 males). The male to female ratio was obtained 6/1.
Variable | Case (n = 47) | Control (n = 96) | P Value |
---|---|---|---|
0.89 | |||
Female | 29 (62) | 58 (60) | |
Male | 18 (38) | 38 (40) | |
58 ± 10.1 | 58 ± 10.4 | 0.97 | |
20.5 ± 3.2 | 25.3 ± 4.2 | 0.00 | |
37.4 ± 7.1 | 35.2 ± 7.8 | 0.10 | |
0.34 | |||
Illiterate | 42 (89) | 80 (83) | |
Literate | 5 (11) | 16 (17) | |
0.02 | |||
Housewife | 19 (41) | 5 (52) | |
Unemployed | 1 (2) | 12 (13) | |
Employed | 27 (57) | 34 (35) | |
0.01 | |||
Yes | 16 (34) | 9 (9) | |
No | 31(66) | 87 (91) | |
0.01 | |||
Yes | 4 (9) | 0 (0) | |
No | 43 (91) | 96 (100) | |
0.002 | |||
Slow | 24 (51) | 74 (77) | |
Fast | 23 (49) | 22 (23) | |
0.01 | |||
Hot | 32 (68) | 15 (16) | |
Cold | 15 (32) | 81 (84) | |
0.01 | |||
Fried | 13 (27) | 6 (6) | |
Boiled | 18 (39) | 70 (73) | |
Both | 16 (34) | 20 (21) | |
0.10 | |||
Salty and spicy | 3 (6) | 1 (1) | |
Non salty and spicy | 44 (94) | 95 (99) | |
0.04 | |||
Yes | 22 (47) | 28 (29) | |
No | 25 (53) | 68 (71) | |
1.00 | |||
Yes | 1 (2) | 4 (4) | |
No | 46(98) | 92 (96) | |
0.26 | |||
Never | 28 (60) | 69 (71) | |
Before | 11 (23) | 13 (14) | |
Current | 8 (17) | 14 (15) | |
1.00 | |||
Yes | 3 (6) | 7 (7) | |
No | 44 (94) | 89 (93) | |
0.41 | |||
Standing | 20 (43) | 34 (35) | |
Non standing | 27 (57) | 62 (65) |
Distribution of the Cases and Controls by Demographics and Selected Risk Factors
The results showed that, there was a significant relationship between job, reflux, family back ground, cooking method, eating speed, food preference, BMI and pepper consumption variables and risk of ESCC. Also, the controls had a higher BMI and 34% of cases and 9% of controls had reflux signs and only 9% of cases had history of esophageal cancer in their family.
The mean of antioxidant vitamins intake in cases and controls is shown in Table 2. Cases consumed lower level of vitamin A, β-carotene, vitamin E (consist of all isomers) and vitamin C compared to the controls. However, the average intake of α-tocopherol (the most active isomer of vitamin E), were similar in the two groups.
Micronutrients | Case (n = 47) | Control (n = 96) | P Value |
---|---|---|---|
1124 ± 598 | 1339 ± 741 | 0.09 | |
697 ± 480 | 836 ± 562 | 0.15 | |
6 ± 6 | 11 ± 9 | 0.00 | |
8 ± 4 | 8 ± 4 | 0.80 | |
109 ± 63 | 142 ± 79 | 0.01 |
The mean of Antioxidant Vitamins Intake in Cases and Controls a
The regression analysis was done separately between esophageal cancer as a dependent variable and every single nutriment as independent variables and then the nutriments were analyzed simultaneously in a model along with disturbing factors. Table 3 shows the results indicates that, in relation to vitamin A, the risk of ESCC in the third tertile (mean intake of 1.36 μgRE) compared to the first tertile (mean intake of 1.12 μgRE) was significantly reduced in base model (P = 0.02), which was not significant in the fully-adjusted model.
Variable | Number of Case Control | Mean ± SD | Model 1 OR (95%CI) | Model 2 OR (95%CI) |
---|---|---|---|---|
Tertile 1 | 23.25 | 576 ± 1123 | 1.00 | 1.00 |
Tertile 2 | 12.36 | 698 ± 1327 | 0.36 (0.15 - 0.68) | 041 (0.10 - 1.67) |
Tertile 3 | 12.35 | 809 ± 1357 | 0.37 (0.16 - 0.89) | 0.65 (0.14 - 2.97) |
P-trend | 0.02 | 0.47 | ||
Tertile 1 | 24.23 | 586 ± 739 | 1.00 | 1.00 |
Tertile 2 | 10.39 | 475 ± 829 | 0.25 (0.01 - 0.60) | 0.38 (0.09 - 1.58) |
Tertile 3 | 13.34 | 559 ± 801 | 0.37 (0.16 - 0.86) | 0.69 (0.16 - 3.08) |
P-trend | 0.01 | 0.52 | ||
Tertile 1 | 27.20 | 7 ± 8 | 1.00 | 1.00 |
Tertile 2 | 16.33 | 7 ± 8 | 0.36 (0.16 - 0.83) | 0.25 (0.06 - 1.04) |
Tertile 3 | 4.43 | 9 ± 11 | 0.07 (0.02 - 0.22) | 0.11 (0.02 - 0.59) |
P-trend | 0.01 | 0.00 | ||
Tertile 1 | 14.33 | 4 ± 8 | 1.00 | 1.00 |
Tertile 2 | 15.34 | 4 ± 9 | 1.04 (0.44 - 2.49) | 0.42 (0.09 - 1.89) |
Tertile 3 | 18.29 | 3 ± 8 | 1.46 (0.62 - 3.45) | 0.85 (0.20 - 3.65) |
P-trend | 0.38 | 0.80 | ||
Tertile 1 | 29.18 | 80 ± 125 | 1.00 | 1.00 |
Tertile 2 | 11.38 | 69 ± 128 | 0.18 (0.07 - 0.44) | 0.02 (0.002 - 0.17) |
Tertile 3 | 7.40 | 77 ± 141 | 0.11 (0.04 - 0.29) | 0.02 (0.002 - 0.30) |
P-trend | 0.01 | 0.00 |
Relationship Between Antioxidant Vitamins Intake and Risk of Esophageal Squamous Cell Carcinoma in Case and Control Groups
There was no relation between α-tocopherol and risk of ESCC, but a significant inverse relationship between ESCC risk and higher intakes of vitamin E observed in both base and fully-adjusted models (base P = 0.01 and fully-adjusted P = 0.005). Also being in the highest tertile of β-carotene (8.01 μgRE) reduced the risk of ESCC by 37% in the base model (P = 0.01). Although no significant association was observe in the fully-adjusted model. In addition to that, the mean intake of 1.41 mg vitamin C in comparison with the mean intake of 1.25 mg reduced the risk of ESCC in both base and fully-adjusted models (base P = 0.01 and fully-adjusted P = 0.01).
5. Discussion
The results of this study showed reduced risk of ESCC according to high intake of antioxidant vitamins. Since these nutrients reflect the general dietary pattern and can be linked together and depend largely, so judgment in protective effects of a special food or a combination of them is a little difficult
By using multifactorial analysis, we could determine that vitamin E and C have a strong relation with the risk of ESCC, while no relation was founded between vitamin A, β-carotene, α-tocopherol and the risk of ESCC.
It is known that diets rich in vegetables, fruits, vitamins and antioxidants are generally protective against development of digestive tract cancers [10]. These food groups supply micro nutrients such as vitamin A, C, E carotenoids, antioxidants and fiber which prevent cancer [11]. A recent research in Sudan evaluated the relationship of antioxidants (vitamin C, vitamin E and β-carotene) intake and esophageal cancer, which reported these nutriments have an inverse relation to the risk of both types of ESCC and EAC (esophageal adenocarcinoma) [10]. Franceschi et al. [12] examined the effect of vitamins and minerals on risk of ESCC and found an inverse relation between β-carotene, vitamin C, E and the risk of this cancer. Other observational studies also report that these antioxidant nutrients are inversely associated with the risk of esophageal cancer [13]. The results of a prospective study suggest that vitamin E may have different effects on different subtypes of esophageal cancer. Dietary α-tocopherol had a significant inverse association with ESCC and GCA (Gastric cardia adenocarcinoma) risk in age and sex adjusted model but this was substantially attenuated in fully adjusted model [13]. Also, the results of our study showed no relation between dietary α-tocopherol and the risk of ESCC. Results of case-control and prospective studies confirmed the different effect of α-tocopherol against esophageal cancer [14]. It seems that the major function of vitamin E is prevention of lipid peroxidation in cell membrane, lipoproteins and fat stores [15]. In Wolfgarten et al. [16] research, vitamin E significantly reduced the risk of esophageal cancer. In our study higher intake of vitamin E was associated with reduction in risk of ESCC.
A case-control study showed that receiving more than 13 mg/day vitamin E and more than 100 mg/day vitamin C reduce the risk of ESCC [17]. The German Nutritional Society’s recommended daily allowance of vitamin E is 12 mg and higher doses are recommended to avoid peroxide formation [15].
In our study, the daily intake was less than recommended values in both groups and this deficiency was higher in the case group. Other studies in very high incidence areas of EC (Esophageal cancer), such as north of Iran, Linxian, China, north and east of Siberria and Hungary showed that dietary intake of vitamin C through fruits and vegetables inversely associated with EC [18]. A significant risk reduction was reported between monthly consumption of vitamin C and esophageal cancer among white men in NewYork [19]. Five times reduction in risk has been shown in the highest tertile intake of fruits and vegetables too [20].
In our study, vitamin C was inversely associated with risk of ESCC. Most researchers believe that vitamin C has a preventive role in cancer cells development. The opinion that there are mechanisms by which the vitamin C may act by protecting against carcinogenesis is controversial, and several hypotheses are raised. The main mechanism and action of vitamin C in the prevention of cancerous cells formation can be due to the capacity of this nutrient in decreasing nitrous acid and preventing the formation of nitrosamines in stomach [21]. Based on measures of the ascorbic acid in the gastric juice and gastric pH, Schorah et al. [22], observed that the nitrosation depends on the gastric acid secretion, of the pH and the bacterial synthesis at high pH. They demonstrated that the 300 mol/L is the ideal concentration of ascorbic acid to inhibit nitrosation, which occurs in humans with a daily oral ingestion of 200 mg of vitamin C. The Committee on Diet, Nutrition, and Cancer of the National Academy of Sciences showed in 1982, that the vitamin C inhibits the formation of some carcinogens and also the consumption of foods rich in vitamin C would be associated with low risk of esophageal carcinoma [15]. There are many soundings about recommended allowable values of vitamin C. Authors, such as Levine et al. [23] suggest a daily ingestion of 100 - 120 mg/day, through the daily consumption 5 portions of fruits and vegetables, and a maximum of 1 g/day, as a safe measure to avoid adverse effects of excessive Ingestion [24]. In our study, the mean intake of vitamin C was 109 mg/day for the cases and 142 mg/day for the controls which is more than RDA (Recommended Dietary Allowances). Free radicals can react in carcinogenesis, causing DNA oxidative lesions or cell wall damage, facilitating the entrance and action of carcinogens, such as the nitrosamines, which are very important in the formation of tumors and considering that vitamin C is an antioxidant, it would act by supplying electrons for neutralization of the free radicals [25, 26]. A large intervention trial in China, however, has failed thus far to see a reduction in the incidence of esophageal or gastric cancer in persons given supplemental vitamin C (120 mg/day) along with molybdenum (30 mg/day) for 5.25 years, which suggests that the protective effect of vitamin C, if real, occurs early in the carcinogenic process [27].
In comparison with vitamin C, a weaker inverse but clear relationship was observed with the intake of vitamin A [20]. Most of researches showed a protective effect of vitamin A [28-31]. Subsequently, a lot of studies showed an obvious relation between β-carotene intake and risk of ESCC [28, 30, 31]. However, a number of studies did not report any relation between β-carotene intake and risk reduction [32-34]. In our study, β-carotene reduced the risk of ESCC to 37%, only in base model. Even though, no information is available as the daily requirements of β-carotene in Germany, 2 - 4 mg of β-carotene are recommended as the daily dose for adults. The German Nutritional Society recommends 1 µgE daily intake of vitamin A for adults [15]. Which in our study the daily intake in both case and control groups was more than this value. Although, we could control the effect of many disturbing variables relating to the life style in this study, but we cannot ignore the possible effect of the rest disturbing factors (residual confounding), also there is the probability of recall bias due to the type of study too. So it is better to perform studies with more samples to increase the power of the study. Also the nutrients association with esophageal cancer should consider in prospective studies to evaluate and prove a powerful causal relation. Generally, the results of this study suggest that antioxidant vitamins can possibly play a protective role in preventing risk of squamous cell carcinoma.