Background
Gastric cancer, including gastric adeno-carcinoma and gastric cardia adeno-carcinoma, was the third leading cause of death in the world which accounting for 8.8% of the total cancer death, according to GLOBOCAN 2012 [
1]. It is estimated that there were 951,600 new gastric cancer cases and 723,100 deaths occurred in 2012.
Epidemiological studies have suggested that high fruits and vegetables intake are inversely associated with the risk of gastric cancer [
2,
3]. Isoflavones, the second metabolites during the growth of soybeans, are a group of bioactive polyphenols, which have a variety of physiological functions to human body [
4]. Several epidemiological studies have investigated the relationship between dietary isoflavones intake and the risk of gastric cancer, but the results are conflicting. Therefore, we conducted the current meta-analysis to further identify the effect of dietary isoflavones intake on the risk of gastric cancer.
Methods
Data sources and search strategy
We searched all relevant literature from May 1992 to May 2017 using electronic databases PubMed and Web of Science, with the search terms: (“isoflavones” or “soy isoflavones” or “phytoestrogen” or “genistein” or “daidzein”) and (“gastric cancer” or “gastric tumor” or “stomach cancer” or “stomach tumor”). Additional articles were identified from the reference lists of relevant review articles.
Inclusion criteria and exclusion criterion
Studies were selected for analysis according to the following inclusion criteria: (1) investigated the relationship of dietary isoflavones intake and gastric cancer risk; (2) the studies were either cohort or case-control studies; (3) articles reported the estimated RR/OR with their 95% CI or the indexes could be calculated. (4) articles were published in English literature. If two or more studies shared same data sets, the one with the largest sample size or the longest follow-up period was selected in the meta-analysis.
Studies were excluded if they are: (1) cell studies and animal studies; (2) reviews articles, letters to the editor and case reports; (3) isoflavones were measured with the levels in blood/urinary; (4) the RR/OR with 95% CI could not be estimated from the data in the articles.
Two reviewers (Jie You and Yafei Sun) extracted the following information independently: (1) the last name of first author; (2) year publication; (3) country; (4) study design; (5) geographic area; (6) source of control; (7) participants’ characteristics (including the range of age, gender, the total number of participants, the number of cases and controls); (8) isoflavones assessment method; (9) the RRs/ORs and their 95% CIs indicating the highest versus the lowest categories of dietary isoflavones intake; (10) adjustment for covariates. Any discrepancies were definitely resolved by a third senior professor (Quanjun Lu). The quality of the selected papers was assessed by use of the Newcastle–Ottawa scale before pooled into the analysis [
5]. The scores of 0–3, 4–6, and 7–9 were considered as low, moderate, and high quality, respectively. Finally, data extraction from included studies was shown in Additional file
1.
Statistical analysis
The association between the dietary isoflavones intake and the risk of gastric cancer was calculated with the pooled ORs together with their 95% CIs. If P < 0.05 and/or I2 > 50%, the random-effects model was conducted. Otherwise, a fixed-effects model was used. Chi-square test and the I2 test were used to quantify the heterogeneity of the studies. Subgroup analyses by study design (the type of case-control or cohort study), gender, geographic area, source of control (based on population or hospital), sample size, dietary assessment, adjustments (family history and dietary energy intake) were also performed to find potential confounder/modifier.
Egger’s test and Funnel plots were conducted to assess the potential publication bias, and a value of P < 0.05 was considered as a significant difference. All statistical analyses were conducted with the software STATA version 12.0 (Stata Corporation, College Station, TX, USA).
Discussion
In this meta-analysis, no significant association between dietary isoflavones intake and the risk of gastric cancer was detected. The subgroup analysis was also performed to further explore the relationship, which yield the similar result.
The incidence of gastric cancer has been shown to be associated with many dietary factors [
13‐
19]. Previous studies found that higher intake of vegetables and fruits is a protective factor against gastric cancer [
3,
20]. Isoflavones, act as the role of estrogenic hormone, are rich in leguminous plants [
21,
22]. Some studies showed an inverse association between dietary isoflavone intake and gastric cancer [
6], however, some other studies demonstrated there is no effect of dietary isoflavone intake on gastric cancer [
21,
22]. Previous studies had inconsistent findings regarding the association between isoflavones and gastric cancer risk. Therefore, it is necessary to perform a meta-analysis to further identify the associations.
Some epidemiological studies reported an inverse association between soy products and gastric risk [
23,
24]. Sarah and Kweon revealed that consuming unfermented soy foods could decreased the risk of gastric cancer [
25,
26]. A meta-analysis also reported that a high intake of unfermented soy foods is associated with a decreased gastric cancer risk [
27]. Those findings are not agreement with our study which might be ascribed to the possible confounding effects such as salt, vegetable, fruit, and other dietary factors. After adjusting for these dietary factors, Hara [
6] found no association between soy food intake and gastric cancer risk, which is consistent with our study.
In the 12 studies we selected, an inverse association between dietary isoflavones and the risk of gastric cancer was only shown in a female cohort study. This may attribute to the insufficient possible confounders adjustment. Moreover, numerous animal studies and cytology experiments have widely demonstrated the anticancer property of isoflavones [
28‐
30] for its antioxidant and antipromotional effects [
31], however, our study did not detected any protective effect of isoflavones against gastric cancer. The inconsistency might be attributed to the following reasons: first, the exposure dose and concentrations of isoflavones used in vitro and in vivo studies is precise, which is difficult to obtain through habitual dietary intake by humans [
32]. Second, the composition of the gut microflora, such as
Helicobacter pylori, may influence isoflavones absorption and metabolism and production of specific intestinal microbial catabolites which may in turn mediate their biological activities. Third, potential small existing effect may be affect by uncontrolled variability that is difficult to quantify between human beings [
33].
The meta-analysis study has several advantages. First, the potential confounding factors were adjusted in all individual studies (e.g. age, BMI, smoking status and alcohol drinking). In addition, the subgroup analysis was conducted to further explore the association and strengthened the results. Moreover, the pooled results might be unbiased because no publication bias was observed.
The potential limitations of our meta-analysis should be acknowledged. First, Helicobacter pylori infection which is a risk factor for gastric cancer is only reported in one case-control study. Second, the dose levels of dietary isoflavones are not well defined, so the effect of dietary isoflavones intake may be masked.