Nutrient-Wide Association Study of 92 Foods and Nutrients and Breast Cancer Risk

Alicia K. Heath; David C. Muller; Piet A. van den Brandt; Nikos Papadimitriou; Elena Critselis; Marc Gunter; Paolo Vineis; Elisabete Weiderpass; Guy Fagherazzi; Heiner Boeing; Pietro Ferrari; Anja Olsen; Anne Tjønneland; Patrick Arveux; Marie-Christine Boutron-Ruault; Francesca Romana Mancini; Tilman Kühn; Renée Turzanski-Fortner; Matthias B. Schulze; Anna Karakatsani; Paschalis Thriskos; Antonia Trichopoulou; Giovanna Masala; Paolo Contiero; Fulvio Ricceri; Salvatore Panico; Bas Bueno-de-Mesquita; Marije F. Bakker; Carla H. van Gils; Karina Standahl Olsen; Guri Skeie; Cristina Lasheras; Antonio Agudo; Miguel Rodríguez-Barranco; Maria-José Sánchez; Pilar Amiano; María-Dolores Chirlaque; Aurelio Barricarte; Isabel Drake; Ulrika Ericson; Ingegerd Johansson; Anna Winkvist; Tim Key; Heinz Freisling; Mathilde His; Inge Huybrechts; Sofia Christakoudi; Merete Ellingjord-Dale; Elio Riboli; Konstantinos K. Tsilidis; Ioanna Tzoulaki

Disclosures

Breast Cancer Res. 2020;22(5) 

In This Article

Discussion

We used the NWAS approach to evaluate dietary intakes of 92 foods and nutrients in the EPIC study and identified three dietary factors (alcohol, beer/cider, wine) for which higher consumption was associated with higher risk, and three dietary factors (fibre, apple/pear, carbohydrates) for which higher intake was associated with lower risk of breast cancer (FDR < 0.05). The positive association of alcohol, and inverse associations of fibre, apple/pear, and carbohydrate intake with breast cancer risk were confirmed in the NLCS.

In the EPIC study, associations of the identified foods and nutrients with breast cancer risk did not differ substantially by hormone receptor status, but intakes of apple/pear and carbohydrates appeared to have no association with risk of ER/PR-negative tumours. Our analyses stratified by menopausal status showed that results for postmenopausal women alone were very similar to the overall results. No foods or nutrients met the FDR threshold when analysis was restricted to premenopausal women. More research is needed to verify the lack of findings for premenopausal breast cancer and to evaluate underlying mechanisms.

Advantages of this study include its large size and long duration of follow-up, and the NWAS approach which involved a comprehensive assessment of foods and nutrients whilst accounting for multiplicity of tests, and replication of findings in an external cohort. Possible explanations for the lack of consistent associations between dietary factors and breast cancer in epidemiological studies include measurement error arising from the dietary assessment method, and inadequate dietary variation or narrow range of intakes in individual studies. Moreover, associations for dietary factors, if they do exist, may be of a small magnitude for which many studies have had inadequate statistical power to detect. A strength of the EPIC study is the variation in diet. The wide range of dietary intakes of foods and nutrients in this heterogeneous population, a key aspect of the study design,[14,25] and large number of cases provided sufficient statistical power to detect weak to moderate associations. The primary limitation of our study is that it relied on a single assessment of dietary intake during adulthood. In addition, there was no mutual adjustment for other dietary factors (except for the model mutually adjusted for fibre, apple/pear, and carbohydrate intakes), and intercorrelations and overall dietary patterns were not accounted for in these analyses. This was merely an exploratory investigation to identify which dietary factors are associated with breast cancer, so that these factors can subsequently be evaluated in-depth in focused analyses with adjustment for other dietary confounders and to evaluate interrelationships between these foods and nutrients in greater detail. Further, whilst the analogy to GWAS is somewhat appropriate, especially in terms of the approach to statistical analysis, it is far from perfect. The variants typed on a genome-wide array are typically not chosen because of any hypothesised association, but rather to provide adequate coverage of genetic variation in the whole genome. On the other hand, the 92 foods and nutrients in our study were assessed and derived and made available in the EPIC database because of prior plausibility of their association with disease outcomes. Further, the food and nutrient intakes are not independent. Thus, the NWAS approach is more closely aligned to a systematic analysis of candidate genes than it is to the hypothesis-agnostic approach of GWAS.

This study reaffirms the well-established positive association between alcohol intake and breast cancer risk[1,26–28] and, in particular, adds to the strong, convincing evidence that alcohol consumption increases the risk of postmenopausal breast cancer.[1,28,29] In the EPIC study there was a positive association between alcohol intake and ER−/PR− and ER+/PR+ breast cancer. The association for ER+/PR− breast cancer was of similar magnitude and in the same direction. In a pooled analysis of 20 prospective cohort studies (as part of the Pooling Project of Prospective Studies of Diet and Cancer), alcohol consumption was positively associated with all three of these subtypes.[28] The positive association between beer/cider intake and breast cancer risk in the EPIC study was not replicated in the NLCS, perhaps due to the low beer consumption of this elderly female Dutch cohort.[30] Overall, there is compelling evidence that alcohol intake increases the risk of breast cancer.

In this NWAS, inverse associations between dietary fibre and carbohydrate intake and breast cancer risk were identified and confirmed in the independent NLCS cohort. The 2017 WCRF/AICR Continuous Update Project report concluded that there is only limited evidence, for which no conclusions can be drawn, for associations of dietary fibre and carbohydrate intake with risk of breast cancer.[1] For fibre intake, findings from epidemiological studies have thus far been inconsistent, but recent meta-analyses have found inverse associations of small magnitude, that did not differ by menopausal status or geographical region.[31–33]

The inverse association between total dietary fibre intake and breast cancer risk in the EPIC study has been reported previously;[34] however when considering sources of fibre, this association was largely driven by an inverse association with fibre from vegetables, and possibly fruit, but not fibre from cereals or other dietary sources.[34] Dietary fibre intake was inversely associated with breast cancer risk in the Million Women Study in the UK (29,005 breast cancer cases in 691,571 postmenopausal women; relative risk (RR) per 5 g/day higher intake = 0.91, 99% CI 0.87–0.96); the association was evident for intake of fibre from fruit but not from vegetables or cereals.[29] In a meta-analysis of 16 prospective studies including 26,523 breast cancer cases in 999,271 participants, higher total dietary fibre intake was associated with a slightly lower risk of breast cancer (summary RR for high versus low intake = 0.93, 95% CI 0.89–0.98), but when considering source of fibre, the inverse association was apparent for soluble fibre but not for insoluble, vegetable, fruit, or cereal fibre.[31] It has not been established whether fibre from specific food sources is more beneficial than other sources, although it is possible that fibre intake in general is protective, irrespective of the specific food source. Few studies have investigated the association of dietary fibre with breast cancer risk by hormone receptor status, and results have been inconsistent.[29,31,35,36] Similar to a previous analysis in the EPIC study,[34] we found little variation in the association of dietary fibre intake with breast cancer risk by hormone receptor status.

The inverse association for apple/pear intake found in the current analysis could be reflecting fibre intake but might not be solely due to the fibre content of these fruits. Indeed, the association was slightly weaker but persisted after adjustment for fibre and carbohydrate intake. We speculate that it is possible that apple/pear intake is indicative of fruit intake in general since these are commonly consumed fruits in Western populations, and thus, their intake may be well captured in dietary questionnaires. In the EPIC study, apples and pears made the greatest contribution to total fruit intake.[37] In a meta-analysis of 10 prospective cohort studies, higher fruit intake was associated with a slightly lower risk of breast cancer (summary RR for highest versus lowest intake = 0.92, 95% CI 0.86–0.98).[38] Fruit intake was also inversely associated with breast cancer risk in the Million Women Study (RR per 100 g/day higher intake = 0.94, 99% CI 0.92–0.97).[29] Despite this, we found no strong evidence that total fruit intake was associated with breast cancer risk, which is consistent with previous analyses of EPIC data.[37] The converse scenario is therefore possible: that intake of apples and pears themselves may be associated with risk of breast cancer and that the observed associations for total fruit intake in some studies could be reflecting apple/pear intake. In a pooled analysis of 20 prospective cohort studies, total fruit intake was not associated with breast cancer risk (pooled RR for highest versus lowest quintile = 0.99, 95% CI 0.95–1.03), but intake of apples/pears was inversely associated with risk of ER− breast cancer (pooled RR per serving (138 g)/day = 0.92, 95% CI 0.85–0.99).[8] In our study, the inverse association of apple/pear intake was most apparent for ER+/PR+ breast cancer. The potential mechanism by which specifically apple/pear intake might be associated with breast cancer risk is unclear.

The inverse association of carbohydrate intake with breast cancer risk in this NWAS could be, at least in part, due to total carbohydrate intake capturing fibre and fruit consumption. Notably, the magnitude of the association for carbohydrates was identical to that for fibre and apple/pear intake. In addition, in the EPIC study, fruit was the second biggest food group source of carbohydrates (contributing 13%).[39] Nevertheless, after adjusting for intakes of apple/pear and fibre, the association for carbohydrate intake was weaker but did not disappear. Total carbohydrates also comprise other foods including bread (which contributed the highest proportion of carbohydrates in EPIC[39,40]), grains, cereals, dairy products, legumes, and vegetables, but none of these dietary factors were associated with risk of breast cancer in our study. Total carbohydrate intake is also reflective of overall dietary pattern, which might be more pertinent than individual foods/nutrients for breast cancer risk.

Vegetables have garnered interest due to their rich phytochemical content and have been widely investigated for possible associations with breast cancer. In our study, no individual vegetables nor vegetable groups were associated with risk of breast cancer. Consistent with our results, a meta-analysis of 10 prospective studies,[38] and a pooled analysis of 20 cohort studies,[8] did not find any association between total vegetable intake and overall breast cancer risk, and likewise, no clear association was found in the Million Women Study.[29] Several studies, including a previous analysis of EPIC data,[37] have found an inverse association of total vegetable intake with breast cancer risk, which was most apparent for ER−/PR− tumours.[9] The 2017 WCRF/AICR report concluded that there is suggestive but limited evidence that intake of non-starchy vegetables might decrease the risk of ER− breast cancer.[1] The report also stated there is limited suggestive evidence that consumption of foods (i.e. some fruits and vegetables) containing carotenoids decreases the risk of breast cancer.[1] Given the inconsistencies in the literature regarding the role of fruit and vegetable intake in prevention of breast cancer, no firm conclusions can be drawn at present. Nevertheless, fruits and vegetables contain numerous nutrients, as well as fibre, which might collectively protect against cancer, rather than conferring a protective effect in isolation.[3]

Previous analyses in the EPIC study have found a weak association between saturated fat intake and breast cancer risk,[41,42] whereas no associations for total dietary fat intake or subtypes of fat intake were found in the present analysis. The lack of associations using this systematic NWAS approach, and in several other cohort studies,[2,29] suggests that dietary fat is unlikely to play an important role in breast cancer aetiology. However, a limitation of observational studies is that dietary questionnaires are limited in assessing eating out behaviours, and high fat processed foods consumed out of home might not be fully captured.

The fact that few foods and nutrients were found to be associated with breast cancer risk in this study, and other studies,[1,6,29] could support suggestions that diet in middle-age, or relatively recent diet, might not play an important role in the development of breast cancer.[26] It remains unclear whether diet throughout the life course or potential windows of susceptibility, for example during childhood and adolescence, is associated with breast cancer risk. However, it is worth noting that consistent with the dietary factors identified in this study, fibre intake and apple intake during adolescence and early adulthood were inversely associated with breast cancer risk in the Nurses' Health Study II.[43,44]

The associations identified in this study are supported by biologically plausible mechanisms. In particular, it is thought that dietary fibre intake may exert a beneficial effect for prevention of breast cancer by decreasing circulating oestrogen levels via inhibition of intestinal reabsorption of oestrogens excreted in bile and concomitant increased faecal excretion of oestrogens.[45–48] Alcohol has been shown to increase circulating concentrations of sex steroids, particularly oestrogens,[49–51] and thus, the effect of alcohol on breast cancer risk is also thought to be at least partially mediated by an effect on endogenous sex hormone levels.[27,50] Nevertheless, the mechanisms by which alcohol consumption increases breast cancer risk are poorly understood, and other potential pathways include the effect of alcohol on folate absorption,[2] acetaldehyde production, oxidative stress, and epigenetic alterations.[27]

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