Literature DB >> 28741383

Adherence to Mediterranean Diet and Metabolic Syndrome in BRCA Mutation Carriers.

Eleonora Bruno1,2, Siranoush Manoukian1, Elisabetta Venturelli1, Andreina Oliverio1, Francesca Rovera3, Giovanna Iula4, Daniele Morelli1, Bernard Peissel1, Jacopo Azzolini1, Eliana Roveda2, Patrizia Pasanisi1.   

Abstract

BACKGROUND: Insulin resistance is associated with higher breast cancer (BC) penetrance in BRCA mutation carriers. Metabolic syndrome (MetS), an insulin resistance syndrome, can be reversed by adhering to the Mediterranean diet (MedDiet). In a dietary intervention trial on BRCA mutation carriers, we evaluated adherence to the MedDiet, and the association with the MetS, by analyzing data from the Mediterranean Diet Adherence Screener (MEDAS).
METHODS: BRCA mutation carriers, with or without BC, aged 18 to 70 years, were eligible for the trial. After the baseline examinations, women were randomized to a dietary intervention or to a control group. Both groups completed the MEDAS at baseline and at the end of the dietary intervention.
RESULTS: A total of 163 women completed the 6 months of dietary intervention. Compared with controls, the women in the intervention group significantly reduced their consumption of red meat ( P < .01) and commercial sweets ( P < .01) and their MEDAS score rose significantly (+1.3 vs +0.55, P = .02). The number of MetS parameters decreased with increasing points of adherence to the MEDAS score ( P = .01). In the intervention group, there was a significant association with the greater reduction of MetS.
CONCLUSION: BRCA mutation carriers in the intervention group experienced greater improvement in their MedDiet and MetS parameters.

Entities:  

Keywords:  BRCA mutation carriers; Mediterranean diet; breast cancer; dietary intervention trial; metabolic syndrome

Mesh:

Year:  2017        PMID: 28741383      PMCID: PMC5950953          DOI: 10.1177/1534735417721015

Source DB:  PubMed          Journal:  Integr Cancer Ther        ISSN: 1534-7354            Impact factor:   3.279


Introduction

Lifestyle factors linked to insulin resistance such as high serum levels of insulin and IGF-I (insulin-like growth factor–I), abdominal adiposity, high energy intake, milk consumption, and low levels of physical activity have been associated with higher penetrance of breast cancer (BC) in BRCA mutation carriers.[1,2] The metabolic syndrome (MetS), an insulin resistance syndrome, is defined as a clustering of risk factors of metabolic origin, such as abdominal obesity, high blood pressure, dyslipidemia, and high fasting glycemia.[3] The etiology of MetS is considered to involve a complex interaction between genetic, metabolic, and environmental factors.[4-6] MetS increases the risk of type 2 diabetes, cardiovascular diseases[7-9] and several cancers, including BC.[10] Postmenopausal status is associated with a 60% increase in the risk of MetS.[6] Antihormonal treatments for BC and/or risk-reducing surgery (prophylactic adnexectomy) may affect the risk of MetS in BRCA mutation carriers. Dorum and colleagues[11] found that patients with bilateral oophorectomy before 50 years of age had a higher prevalence of MetS than age-matched controls. Similarly, a controlled observational study showed that bilateral oophorectomy for breast and ovarian cancer prevention was significantly associated with MetS in BRCA mutation carriers.[12] The Mediterranean Diet (MedDiet) is a low-protein diet involving high consumption of unrefined cereal products (in Italy mainly bread and pasta made with durum wheat), pulses, vegetables, olive oil, nuts, fruit, moderate amounts of wine, occasionally fish and cheese, and rarely other animal products. The MedDiet has recently emerged as a healthy dietary pattern that reduces insulin resistance.[13] Prospective studies have shown an inverse relationship between adherence to the MedDiet and MetS.[14,15] Randomized intervention trials showed that MetS can be reversed by following the MedDiet, with a reduction of MetS prevalence of up to 69% after 2 years of diet.[16-18] As part of a demonstration project on BRCA mutation carriers, we are conducting a randomized controlled trial to test whether a dietary intervention based on the MedDiet and macrobiotic recipes significantly reduces IGF-I and other markers of insulin resistance (IRm).[2] Preliminary results suggest that women in the intervention arm significantly lost weight, with lower hip circumference, triglycerides, and IGF-I than control women (unpublished data). We investigated whether the BRCA mutation carriers increased their adherence to the MedDiet by analyzing the data from the Mediterranean Diet Adherence Screener (MEDAS).[19] Another aim was to study the relation between adherence to the MedDiet and MetS.

Subjects and Methods

This study is part of a more comprehensive project on 600 BRCA mutation carriers aimed at (1) whether a dietary intervention significantly reduced IGF-I and other IRm (randomized trial); (2) whether carriers with a diagnosis of BC had higher IGF-I than carriers without BC (case-control study); (3) whether IGF-I and its changes over time affected the subsequent BC incidence and prognosis (cohort follow-up). The study was approved by the Ethics Committee of the Fondazione IRCCS Istituto Nazionale dei Tumori, Milan. The study is ongoing and recruitment is still open. The trial component of the study has been previously described.[2] Eligible subjects were women aged 18 to 70 years, either unaffected or affected with BC, without metastases or previous ovarian cancer, who underwent genetic counseling and fulfilled high-risk selection criteria for genetic testing based on personal and/or family history and resulted carriers of deleterious BRCA mutations (BRCA1, BRCA2, or both). Unaffected BRCA mutation carriers with bilateral prophylactic mastectomy were not included. Women were fully informed about the study and gave signed informed consent. At baseline, all women provided a copy of their clinical notes, gave a postprandial blood sample (to measure IGF-I, IGFI-BP3, insulin, and metabolic parameters) and completed questionnaires on BC risk factors. Height and body weight were measured without shoes and heavy clothes, waist circumference was recorded with a measuring tape at the midpoint between the lowest rib and the iliac crest in expiration. Blood pressure was taken using an electronic device. The same measurements were repeated at the end of the 6 months of dietary intervention. All participants received general recommendations for the dietary prevention of cancer.[20] After the baseline examinations, women were randomized to an active dietary intervention or to a control group that continued observing the baseline recommendations. Women in the intervention group were invited to participate in 6 full days of lifestyle intervention activities over the subsequent 6 months. These activities included 6 cookery courses followed by lunch, 6 physical activity sessions (walking for 45 minutes) and 6 conferences. Since the main objective of the trial was to reduce serum levels of IGF-I and insulin resistance the recommendations for women in the intervention group included reducing protein intake, mainly milk and animal protein (except fish), down to 10% to 12% of total calorie intake; reducing calorie intake, through the preferred consumptions of highly satiating foods, such as unrefined cereals, legumes, and vegetables; reducing high–glycemic index food, such as refined flours, potatoes, white rice, corn flakes, and high-insulinemic foods, such as sugar and milk, preferring instead whole grain rice, barley, millet, oat, spelt, quinoa and buckwheat, legumes, vegetables (any type except potatoes); reducing sources of saturated fat (red and processed meat, milk and dairy products), preferring instead unrefined vegetable fats, such as olive oil, nuts, and oleaginous seeds; eating mostly food of plant origin, with a wide variety of seasonal products. These recommendations are basically those of the MedDiet.

MEDAS Questionnaire

The intervention and control groups both completed the validated 14-point MEDAS[19] at baseline and at the end of the 6 months of dietary intervention. MEDAS consists of 12 questions on food consumption frequency and 2 on eating habits: Do you use olive oil as the main source of fat for cooking? Do you prefer chicken, turkey, or rabbit instead of beef, pork, hamburgers, or sausages?—considered characteristics of the Mediterranean diet. Each question is scored 0 or 1. One point is given for using olive oil as the principal source of fat for cooking, preferring white meat over red meat, or for consuming: (1) 4 or more tablespoons (1 tablespoon = 13.5 g) of olive oil/day (including that used in frying, salads, meals eaten away from home, etc); (2) 2 or more servings of vegetables/day; (3) 3 or more pieces of fruit/day; (4) less than one serving of red meat or sausages/day; (5) less than one serving of animal fat/day; (6) less than one cup (1 cup = 100 mL) of sugar-sweetened beverages/day; (7) 7 or more servings of red wine/week; (8) 3 or more servings of pulses/week; (9) 3 or more servings of fish/week; 10) fewer than 2 commercial pastries/week; (11) 3 or more servings of nuts/week; or (12) 2 or more servings/week of a dish with a traditional sauce of tomatoes, garlic, onion, or leeks sautéed in olive oil.

Definition of the MetS

Various investigators have used different definitions of MetS. In the present study, we defined MetS on the basis of the presence of at least 3 components out of 5, according to the threshold proposed by the International Diabetic Federation[21]: systolic blood pressure ≥130 mm Hg or diastolic blood pressure ≥85 mm Hg, triglycerides ≥150 mg/100 mL, high-density lipoprotein (HDL) <50 mg/100 mL, waist circumference ≥80 cm. The exception was blood glucose for which we used the threshold of 120 mg/100 mL or more instead of 100 mg/100 mL or less, because blood was sampled an hour and a half after a standard meal.

Laboratory Methods

Blood samples were collected at baseline and after the 6-month intervention 90 minutes after a standard meal (miso soup, brown rice seasoned with sesame seeds and salt, vegetables and legumes, 50 g uncooked). Women were asked to give 20 mL of blood; we prepared 8 samples of serum (4), plasma (2), red blood cells (1), and buffy coat (1). Serum samples were aliquoted and stored at −80°C. Plasma glucose, triglycerides, total, low-density lipoprotein (LDL), and HDL cholesterol were measured using routine laboratory techniques. The technicians analyzing the serum samples were blinded to the intervention or control status of the patients.

Statistical Analysis

The distributions of each parameter, tested for normality by a graphic method, were normally distributed. The data were expressed as mean ± standard deviation (SD) or percentage. Body mass index (BMI) was defined as body weight in kilograms/height in meters squared (BMI = kg/m2). The MEDAS score depended on the answer to each item., each scored 0 or 1. If the condition is not met, 0 points are recorded for the category. The final MEDAS score, ranging from 0 to 14, was the sum of all the points. At baseline, the means of continuous metabolic variables in the intervention group were compared with the control group using Student’s t test. A χ2 test was used to compare frequencies. The Wilcoxon rank-sum test was used to compare food consumption in the intervention and control group at baseline. Statistical analysis focused on changes in food intake and the metabolic parameters under study, calculated for each woman as the difference between values at the end of the study (sixth month) and baseline. We used the nonparametric Wilcoxon rank-sum test to compare baseline and 6-month food consumptions in the 2 groups. Analysis of variance for repeated measures (RM-ANOVA) was used to check for interactions between the 2 independent variables (group and time) and the dependent variable (factors under study). The model took into account time as the within-subjects factor and group as between-subjects factor. We analyzed the magnitude of changes in food consumption and metabolic variables using the difference (delta, Δ) between the end of the study and baseline for each woman in the two groups, and controlled for age (quintiles), BMI at baseline (quintiles), weight change (quartiles) and education (none or primary school, high school, degree or more). The association between MetS and the MEDAS score was studied with a regression model. The reduction of the MetS parameters associated with the improvement of the MEDAS score was calculated using a multiple regression model including age (quintiles), BMI at baseline (quintiles), education (none or primary school, high school, degree or more), menopausal status and randomization group as model covariates. A P value <.05 was taken as significant. All statistical tests were 2-sided. All analyses were done with the STATA 12 statistical package.

Results

At the time of writing 219 women had been properly randomized, 115 in the intervention and 104 in the control group. After randomization 2 women relapsed and 2 became pregnant so they did not start the active dietary intervention. Two others decided to drop out at the beginning of the dietary intervention, by choice. Therefore, data for 213 participants were available for this analysis, 122 women with a BRCA1 mutation, 87 with a BRCA2 mutation and 2 with both. At baseline, the 2 groups were fairly homogeneous for anthropometric, hormonal, and metabolic variables (Table 1); 73.6% of women in the intervention arm and 65.5% in the control arm were menopausal at the time of recruitment (P = .19), but only 11% (in the intervention group) and 7% (controls) had a natural menopause. Two-thirds of the women (73/110) in the intervention arm and 64/103 controls had developed a BC (P = .91).
Table 1.

Baseline Characteristics of the Study Population.[a]

Intervention (n = 110)Control (n = 103)
Age, y46.9 ± 1.144.6 ± 9.7
Education
 First level12.813.8
 Second level45.043.1
 Third level42.243.1
Menopause65.473.6
Natural menopause11.07.0
Metabolic syndrome
 1-2 factors53.049.0
 ≥3 factors14.07.0
Body mass index, kg/m223.8 ± 4.523.9 ± 4.8
Waist circumference, cm75.9 ± 9.977.2 ± 11.7
Hip circumference, cm100.2 ± 11.4110.2 ± 89.3
Systolic blood pressure, mm Hg128.6 ± 18.7126.9 ± 14.5
Diastolic blood pressure, mm Hg81.0 ± 11.781.2 ± 9.6
Glycemia, mg/dL112.1 ± 21.2109.1 ± 23.1
Total cholesterol, mg/dL199.8 ± 38.8205.9 ± 36.4
High-density lipoprotein cholesterol, mg/dL67.9 ± 15.973.3 ± 18.7
Low-density liprotein cholesterol, mg/dL110.3 ± 33.1115.4 ± 34.6
Triglycerides, mg/dL107.2 ± 82.991.4 ± 47.1
IGF-I, ng/mL171.3 ± 72.8167.3± 62.4
Insulin, mU/mL30.8 ± 19.426.2 ± 17.5

Data are presented as mean ± or as percentages.

Baseline Characteristics of the Study Population.[a] Data are presented as mean ± or as percentages. Food consumption was substantially similar in the 2 groups (Table 2). Intervention and control women both used olive oil as main cooking fat, in moderate quantities (about 5 teaspoons/day) and consumed about 2 portions of vegetables per day. At baseline, intervention women ate slightly more fruit (P = .38), red meat (P = .23), legumes (P = .11), and fish (P = .29), and white meat rather than red meat (P = .35) than controls. Control women consumed slightly more pasta and wine than those in the intervention arm (Table 2). At baseline, both groups had good scores for adherence to the MedDiet (average MEDAS scores 7.9 and 7.4, P = .13). No significant differences in baseline foods consumption or in the MEDAS score emerged by comparing women with and without BC.
Table 2.

Mediterranean Diet Adherence Screener (MEDAS) Food Consumption at Baseline.

Criterion[a]Intervention (n = 110)Control (n = 103) P [b]
Do you use olive oil as main cooking fat?Yes98.7%96.4%.33
How much olive oil do you consume in a day (including oil for frying, on salads)?≥4 tablespoons4.69 ± 2.534.66 ± 2.56.92
How many vegetable servings do you eat per day? (1 serving ~ 200 g)≥21.90 ± 0.861.91 ± 0.90.97
How many fruit units do you eat per day? (1 serving ~ 100-150g)≥32.04 ± 1.331.86 ± 1.61.38
How many servings of red meat, hamburger, or meat products do you eat per day?<10.71 ± 1.010.57 ± 0.72.23
How many servings of butter, margarine, or cream do you eat per day? (1 serving = 12 g)<10.16 ± 0.450.12 ± 0.32.48
How many sweet beverages do you drink per day?<10.35 ± 0.880.33 ± 0.69.82
How much wine do you drink per week? (glass)≥71.30 ± 2.221.94 ± 2.76.07
How many servings of legumes do you eat per week? (1 portion = 150 g)≥32.54 ± 2.272.11 ± 1.50.11
How many servings of fish or shellfish do you eat per week? (1 portion = 150 /200 g)≥31.91 ± 1.1.201.67 ± 1.12.14
How many times per week do you eat commercial sweets or pastries (not homemade)?<23.27 ± 2.633.81 ± 2.75.16
How many servings of nuts do you eat per week? (1 portion = 30 g)≥32.88 ± 2.652.76 ± 2.75.76
Do you preferentially eat chicken, turkey, or rabbit meat instead of veal, pork, hamburger, or sausage?Yes77.5%71.1.35
How many times per week do you eat pasta?≥23.47 ± 2.183.77 ± 2.20.33
MEDAS score7.9 ± 2.17.4 ± 2.0.16

Criterion to score 1 point. Otherwise, 0 recorded.

P of Wilcoxon rank-sum test.

Mediterranean Diet Adherence Screener (MEDAS) Food Consumption at Baseline. Criterion to score 1 point. Otherwise, 0 recorded. P of Wilcoxon rank-sum test. So far, 163 women (80 in the intervention and 83 in control group) have completed the 6 months of dietary intervention. The before/after analysis of MEDAS indicated that in both groups most of the indicators of the MedDiet improved but the intervention women made changes with greater impact on health. They significantly reduced their consumption of red meat (P < .001), butter (P = .04) and commercial sweets (P < .001) and significantly increased the consumption of legumes (P < .001) and nuts (P < .001). They also significantly reduced their consumption of pasta (P = .01). The control women significantly improved their consumption of legumes (P = .02), fish (P = .01), and nuts (P = .02) and significantly reduced the consumption of commercial sweets (P = .04). Both groups had nonsignificant increases in vegetable and fruit consumption. Both BC affected and unaffected women improved the indicators of the MedDiet in a similar way. After the 6 months of dietary intervention, the MEDAS score increased by 1.3 in the intervention (P < .001) and 0.55 in controls (P = .01). The “delta” analysis of differences (intention to treat analysis) in food consumption between the 2 groups (Table 3) showed that intervention women reduced their consumption of red meat and commercial sweets significantly more than controls. Intervention women also had a significantly larger increase in consumption of legumes than controls and a borderline significant increase of nuts. Controlling the analysis for age, BMI at baseline, weight change, and education (ANOVA), the differences remained significant for the consumption of red meat and commercial sweets. Comparing the 2 groups, the difference in the MEDAS score improvements was borderline significant (P = .05). Controlling the analysis for age, BMI at baseline, weight change, and education, the results became significant (P = .02).
Table 3.

“Delta, Δ” Analysis of Differences (Intention to Treat Analysis) in Food Consumption Between the 2 Groups.

Intervention (n = 80)Control (n = 83) P [a] P [b]
How much olive oil do you consume in a day (including oil used for frying, or salads)?+0.94+0.62.99.79
How many vegetable servings do you eat per day? (1 serving ~ 200 g)+0.05+0.05.91.87
How many fruit units do you eat per day? (1 serving ~ 100-150 g)−0.16+0.04.65.27
How many servings of red meat, hamburger, or meat products do you eat per day?−0.54+0.05 <.01 <.01
How many servings of butter, margarine or cream do you eat per day? (1 serving = 12 g)−0.06−0.02.93.59
How many sweet beverages do you drink per day?−0.180.04.62.31
How much wine do you drink per week? (glass)−0.180.40.69.08
How many servings of legumes do you eat per week? (1 portion = 150 g)+1.19+0.66 .01 .41
How many servings of fish or shellfish do you eat per week? (1 portion = 150/200 g)+0.16+0.39.38.38
How many times per week do you eat commercial sweets, or pastries (not homemade), such as cakes, cookies, biscuits, or custard?−1.83−0.43 <.01 <.01
How many servings of nuts do you eat per week? (1 portion = 30 g)+1.63+0.96.05.06
How many times per week do you eat pasta?−0.08−0.42.18.43
MEDAS score+1.3+0.55.05 .02

Abbreviations: MEDAS, Mediterranean Diet Adherence Screener.

P of Wilcoxon rank-sum test (values in boldface indicate statistical significance).

P of analysis of variance controlling for age (quintiles), body mass index at baseline (quintiles), weight change (quartiles), and education (values in boldface indicate statistical significance).

“Delta, Δ” Analysis of Differences (Intention to Treat Analysis) in Food Consumption Between the 2 Groups. Abbreviations: MEDAS, Mediterranean Diet Adherence Screener. P of Wilcoxon rank-sum test (values in boldface indicate statistical significance). P of analysis of variance controlling for age (quintiles), body mass index at baseline (quintiles), weight change (quartiles), and education (values in boldface indicate statistical significance). Stratifying the analysis for the presence or the absence of a previous BC, the “delta” analysis of differences showed that affected women increased slightly more the consumption of legumes compared with the unaffected (P = .04). Controlling the analysis for randomization group, age, BMI at baseline, weight change, and education (ANOVA), this result remained significant. Comparing affected and unaffected women, the difference in the MEDAS score improvements was not significant either in the crude or in the adjusted analysis. As regards the metabolic pattern of the 163 BRCA mutation carriers, only 12% (13% in the intervention and 9% in the control group) had a MetS at baseline. However, 37% of the intervention arm and 30% of controls had at least 2 or more factors of the MetS (P = .56). Among these women, 89% were menopausal (15% natural menopause, 73% induced by BC treatment, and 12% due to bilateral prophylactic adnexectomy). After the 6 months of dietary intervention, most of the metabolic and anthropometric parameters significantly improved in both groups, but women in the intervention group significantly lost weight, with lower BMI, hip circumference, and triglycerides (unpublished data). Women in the intervention group had significantly less MetS (P = .01) and significantly fewer MetS factors (P < .001) while controls achieved only small changes (P for comparison = .02). The MetS and adherence to the MedDiet were inversely correlated. The multiple regression model reported a significant association between reduction of the MetS parameters and improvements in the MEDAS score. The number of MetS parameters fell slightly on increasing the points of adherence of the MEDAS score (P = .01), controlling for age, BMI, menopausal status, education, and randomization group. Menopausal status appeared to have no significant effect. Belonging to the dietary intervention group was significantly associated with a greater reduction of the MetS.

Discussion

Women with highly penetrant BRCA mutations have a 55% to 60% risk for BC.[22-24] However, since penetrance rates are not 100%, it can be postulated that some risk-modulating factors do exist. The MetS considerably influences sporadic BC risk and prognosis[25] and rare retrospective data suggest that lifestyle factors linked to insulin resistance and IGF-I might be important for BRCA mutation carriers.[1] However, there are no prospective studies in this context. We therefore designed a demonstration project to examine whether a dietary intervention, emphasizing the Mediterranean diet, leads to a reduction of IGF-I and other markers of insulin resistance (randomized trial) and to investigate whether the intervention leads to a reduction of BC incidence and BC mortality in BRCA1 and BRCA2 mutation carriers (prospective cohort study). The preliminary findings from the MEDAS questionnaires suggest that women in the intervention group showed substantial improvement in most of the indicators of the MedDiet and significantly raised their MEDAS score, by 1.3. Compared with controls, the women in the intervention group had a significantly greater reduction of consumption of red meat and commercial sweets. The control group also showed some improvement in the indicators of the MedDiet. The public awareness and the easy access to information about the benefits of the MedDiet led to the control group making some adjustments just to be on the safe side (the drop-in effect). Furthermore, this “contamination” was expected by design, because at baseline all women received the World Cancer Research Fund/American Institute for Cancer Research (WCRF/AICR0 recommendations for cancer prevention[20] and the central recommendation of the WCRF/AICR is also the basic characteristic of the MedDiet (“Eat mostly food of plant origin, with a variety of non-starchy vegetables and of fruit every day and with unprocessed cereals and/or pulses within every meal”). These recommendations and the participants’ vigorous motivation probably resulted in changes in the dietary habits of control women too and reduced the potential overall result. MetS is an insulin resistance syndrome. A recent study showed that BRCA mutation carriers with BC more frequently develop type-2 diabetes.[26] This is an interesting point because it suggests that the prediabetic condition, when insulin is typically very high, facilitates the development of mammary tumors in carriers of the BRCA mutation. MetS can be reversed by adhering to the MedDiet, with a reduction in its prevalence of up to 69% after 2 years of diet.[16-18] Our diet and androgen (DIANA) randomized controlled trials showed that an insulin-lowering diet based on traditional Mediterranean and macrobiotic recipes significantly reduced the main factors defining the MetS, body weight, and the bioavailability of sex hormones and IGF-I, in healthy postmenopausal[27,28] and in women with BC.[29] This is the first dietary intervention trial based on the MedDiet and macrobiotic recipes in BRCA mutation carriers. We previously showed that women in the intervention group had significantly lower serum levels of IGF-I and a better IGF-I/IGFBP3 ratio (unpublished data). These results also suggest an inverse relation between the MetS parameters and adherence to the MedDiet. Compared with women whose MEDAS score did not change or got worse, women whose score improved achieved a greater reduction of the MetS factors. This reduction slightly increased on increasing the points of adherence to the MEDAS score. In our population, the prevalence of MetS at baseline was fairly low (12%) and, as expected, the metabolic disorders were more prevalent in women in menopause. However, the reduction of the number of MetS factors was not influenced by menopausal status but was significantly related to the randomization group (dietary intervention) and to improvement of the MEDAS score. These findings, though encouraging, are still based on small numbers. Another prospective randomized controlled trial in BRCA mutation carriers is currently running, to demonstrate improvements in nutritional behavior (adherence to the Mediterranean diet), BMI, and physical fitness in the mutation carriers in the intervention group.[30] Both studies will assess the role of a lifestyle intervention program in a cohort of BRCA mutation carriers. A recent prospective study evaluated the impact of adherence to the prevention recommendations of the American Cancer Society on overall mortality in a high genetic risk population. Adherence to all 3 prevention recommendations (do at least 150 minutes of moderate-vigorous exercise/week, do not drink or drink at most one glass of alcoholic drink/day, keep your body mass index lower than 25 kg/m2) was associated with a 44% reduction of mortality in high-risk healthy women and 53% in women already suffering from BC.[31] Therefore, although one cannot overstate the importance of surgery and/or chemoprevention, along with surveillance for BRCA mutation carriers, we think that there is a need to be able to offer recommendations to women regarding lifestyle choices. It is conceivable that interventions to control body weight and insulin resistance or increase physical activity may help decrease cancer risk particularly among women who are not opting to undergo prophylactic surgery or who are delaying surgery. This is particularly relevant in the context of genetic counselling, where the counsellor has the potential to significantly affect women’s prevention options, specifically among those who opt to not undergo surgery or chemoprevention. With structured exercise and dietary adaptations, mutation carriers will be able to play an independent role in cancer prevention, which will help reinforce their self-management.

Conclusions

This is the first dietary intervention trial based on the MedDiet and macrobiotic recipes in BRCA mutation carriers. The results are encouraging and open a new way of thinking about prevention in high-risk families. With structured exercise and dietary adaptations, mutation carriers will be able to play an independent role in cancer prevention, which will help reinforce their self-management.
  30 in total

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Review 3.  The metabolic syndrome and cardiovascular risk a systematic review and meta-analysis.

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Authors:  Nasim Mavaddat; Susan Peock; Debra Frost; Steve Ellis; Radka Platte; Elena Fineberg; D Gareth Evans; Louise Izatt; Rosalind A Eeles; Julian Adlard; Rosemarie Davidson; Diana Eccles; Trevor Cole; Jackie Cook; Carole Brewer; Marc Tischkowitz; Fiona Douglas; Shirley Hodgson; Lisa Walker; Mary E Porteous; Patrick J Morrison; Lucy E Side; M John Kennedy; Catherine Houghton; Alan Donaldson; Mark T Rogers; Huw Dorkins; Zosia Miedzybrodzka; Helen Gregory; Jacqueline Eason; Julian Barwell; Emma McCann; Alex Murray; Antonis C Antoniou; Douglas F Easton
Journal:  J Natl Cancer Inst       Date:  2013-04-29       Impact factor: 13.506

5.  Effect of a mediterranean-style diet on endothelial dysfunction and markers of vascular inflammation in the metabolic syndrome: a randomized trial.

Authors:  Katherine Esposito; Raffaele Marfella; Miryam Ciotola; Carmen Di Palo; Francesco Giugliano; Giovanni Giugliano; Massimo D'Armiento; Francesco D'Andrea; Dario Giugliano
Journal:  JAMA       Date:  2004-09-22       Impact factor: 56.272

6.  Serum testosterone levels and breast cancer recurrence.

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Journal:  Int J Cancer       Date:  2005-01-20       Impact factor: 7.396

7.  Sociodemographic risk factors associated with metabolic syndrome in a Mediterranean population.

Authors:  Genevieve Buckland; Jordi Salas-Salvadó; Eulàlia Roure; Mònica Bulló; Lluís Serra-Majem
Journal:  Public Health Nutr       Date:  2008-08-15       Impact factor: 4.022

8.  Components of the "metabolic syndrome" and incidence of type 2 diabetes.

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Journal:  Diabetes       Date:  2002-10       Impact factor: 9.461

9.  The impact of cancer prevention guideline adherence on overall mortality in a high-risk cohort of women from the New York site of the Breast Cancer Family Registry.

Authors:  Ann J Cloud; Ashley Thai; Yuyan Liao; Mary Beth Terry
Journal:  Breast Cancer Res Treat       Date:  2015-01-21       Impact factor: 4.872

10.  Prediction of breast cancer risk based on profiling with common genetic variants.

Authors:  Nasim Mavaddat; Paul D P Pharoah; Kyriaki Michailidou; Jonathan Tyrer; Mark N Brook; Manjeet K Bolla; Qin Wang; Joe Dennis; Alison M Dunning; Mitul Shah; Robert Luben; Judith Brown; Stig E Bojesen; Børge G Nordestgaard; Sune F Nielsen; Henrik Flyger; Kamila Czene; Hatef Darabi; Mikael Eriksson; Julian Peto; Isabel Dos-Santos-Silva; Frank Dudbridge; Nichola Johnson; Marjanka K Schmidt; Annegien Broeks; Senno Verhoef; Emiel J Rutgers; Anthony Swerdlow; Alan Ashworth; Nick Orr; Minouk J Schoemaker; Jonine Figueroa; Stephen J Chanock; Louise Brinton; Jolanta Lissowska; Fergus J Couch; Janet E Olson; Celine Vachon; Vernon S Pankratz; Diether Lambrechts; Hans Wildiers; Chantal Van Ongeval; Erik van Limbergen; Vessela Kristensen; Grethe Grenaker Alnæs; Silje Nord; Anne-Lise Borresen-Dale; Heli Nevanlinna; Taru A Muranen; Kristiina Aittomäki; Carl Blomqvist; Jenny Chang-Claude; Anja Rudolph; Petra Seibold; Dieter Flesch-Janys; Peter A Fasching; Lothar Haeberle; Arif B Ekici; Matthias W Beckmann; Barbara Burwinkel; Frederik Marme; Andreas Schneeweiss; Christof Sohn; Amy Trentham-Dietz; Polly Newcomb; Linda Titus; Kathleen M Egan; David J Hunter; Sara Lindstrom; Rulla M Tamimi; Peter Kraft; Nazneen Rahman; Clare Turnbull; Anthony Renwick; Sheila Seal; Jingmei Li; Jianjun Liu; Keith Humphreys; Javier Benitez; M Pilar Zamora; Jose Ignacio Arias Perez; Primitiva Menéndez; Anna Jakubowska; Jan Lubinski; Katarzyna Jaworska-Bieniek; Katarzyna Durda; Natalia V Bogdanova; Natalia N Antonenkova; Thilo Dörk; Hoda Anton-Culver; Susan L Neuhausen; Argyrios Ziogas; Leslie Bernstein; Peter Devilee; Robert A E M Tollenaar; Caroline Seynaeve; Christi J van Asperen; Angela Cox; Simon S Cross; Malcolm W R Reed; Elza Khusnutdinova; Marina Bermisheva; Darya Prokofyeva; Zalina Takhirova; Alfons Meindl; Rita K Schmutzler; Christian Sutter; Rongxi Yang; Peter Schürmann; Michael Bremer; Hans Christiansen; Tjoung-Won Park-Simon; Peter Hillemanns; Pascal Guénel; Thérèse Truong; Florence Menegaux; Marie Sanchez; Paolo Radice; Paolo Peterlongo; Siranoush Manoukian; Valeria Pensotti; John L Hopper; Helen Tsimiklis; Carmel Apicella; Melissa C Southey; Hiltrud Brauch; Thomas Brüning; Yon-Dschun Ko; Alice J Sigurdson; Michele M Doody; Ute Hamann; Diana Torres; Hans-Ulrich Ulmer; Asta Försti; Elinor J Sawyer; Ian Tomlinson; Michael J Kerin; Nicola Miller; Irene L Andrulis; Julia A Knight; Gord Glendon; Anna Marie Mulligan; Georgia Chenevix-Trench; Rosemary Balleine; Graham G Giles; Roger L Milne; Catriona McLean; Annika Lindblom; Sara Margolin; Christopher A Haiman; Brian E Henderson; Fredrick Schumacher; Loic Le Marchand; Ursula Eilber; Shan Wang-Gohrke; Maartje J Hooning; Antoinette Hollestelle; Ans M W van den Ouweland; Linetta B Koppert; Jane Carpenter; Christine Clarke; Rodney Scott; Arto Mannermaa; Vesa Kataja; Veli-Matti Kosma; Jaana M Hartikainen; Hermann Brenner; Volker Arndt; Christa Stegmaier; Aida Karina Dieffenbach; Robert Winqvist; Katri Pylkäs; Arja Jukkola-Vuorinen; Mervi Grip; Kenneth Offit; Joseph Vijai; Mark Robson; Rohini Rau-Murthy; Miriam Dwek; Ruth Swann; Katherine Annie Perkins; Mark S Goldberg; France Labrèche; Martine Dumont; Diana M Eccles; William J Tapper; Sajjad Rafiq; Esther M John; Alice S Whittemore; Susan Slager; Drakoulis Yannoukakos; Amanda E Toland; Song Yao; Wei Zheng; Sandra L Halverson; Anna González-Neira; Guillermo Pita; M Rosario Alonso; Nuria Álvarez; Daniel Herrero; Daniel C Tessier; Daniel Vincent; Francois Bacot; Craig Luccarini; Caroline Baynes; Shahana Ahmed; Mel Maranian; Catherine S Healey; Jacques Simard; Per Hall; Douglas F Easton; Montserrat Garcia-Closas
Journal:  J Natl Cancer Inst       Date:  2015-04-08       Impact factor: 13.506

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  14 in total

1.  The Role of Circulating Adiponectin and SNP276G>T at ADIPOQ Gene in BRCA-mutant Women.

Authors:  Antonella Daniele; Angelo Virgilio Paradiso; Rosa Divella; Maria Digennaro; Margherita Patruno; Stefania Tommasi; Brunella Pilato; Antonio Tufaro; Michele Barone; Carla Minoia; Donatella Colangelo; Eufemia Savino; Porzia Casamassima; Eleonora Bruno; Andreina Oliverio; Patrizia Pasanisi
Journal:  Cancer Genomics Proteomics       Date:  2020 May-Jun       Impact factor: 4.069

2.  Mediterranean-style diet for the primary and secondary prevention of cardiovascular disease.

Authors:  Karen Rees; Andrea Takeda; Nicole Martin; Leila Ellis; Dilini Wijesekara; Abhinav Vepa; Archik Das; Louise Hartley; Saverio Stranges
Journal:  Cochrane Database Syst Rev       Date:  2019-03-13

3.  Association between diet quality and obesity indicators among the working-age adults in Inner Mongolia, Northern China: a cross-sectional study.

Authors:  Lu Jia; Haiwen Lu; Jing Wu; Xuemei Wang; Wenrui Wang; Maolin Du; Peiyu Wang; Sha Du; Yuenan Su; Nan Zhang
Journal:  BMC Public Health       Date:  2020-07-25       Impact factor: 3.295

4.  Identification of predictive factors of the degree of adherence to the Mediterranean diet through machine-learning techniques.

Authors:  Alba Arceo-Vilas; Carlos Fernandez-Lozano; Salvador Pita; Sonia Pértega-Díaz; Alejandro Pazos
Journal:  PeerJ Comput Sci       Date:  2020-07-27

5.  A Mediterranean Dietary Intervention in Female Carriers of BRCA Mutations: Results from an Italian Prospective Randomized Controlled Trial.

Authors:  Eleonora Bruno; Andreina Oliverio; Angelo Virgilio Paradiso; Antonella Daniele; Stefania Tommasi; Antonio Tufaro; Daniela Andreina Terribile; Stefano Magno; Alessio Filippone; Elisabetta Venturelli; Daniele Morelli; Ivan Baldassari; Maria Luisa Cravana; Siranoush Manoukian; Patrizia Pasanisi
Journal:  Cancers (Basel)       Date:  2020-12-11       Impact factor: 6.639

6.  The Role of Health Literacy among Outpatient Caregivers during the COVID-19 Pandemic.

Authors:  Elisabeth Rohwer; Natascha Mojtahedzadeh; Felix Alexander Neumann; Albert Nienhaus; Matthias Augustin; Volker Harth; Birgit-Christiane Zyriax; Stefanie Mache
Journal:  Int J Environ Res Public Health       Date:  2021-11-09       Impact factor: 3.390

7.  A Dietary Intervention to Lower Serum Levels of IGF-I in BRCA Mutation Carriers.

Authors:  Patrizia Pasanisi; Eleonora Bruno; Elisabetta Venturelli; Daniele Morelli; Andreina Oliverio; Ivan Baldassari; Francesca Rovera; Giovanna Iula; Monica Taborelli; Bernard Peissel; Jacopo Azzolini; Siranoush Manoukian
Journal:  Cancers (Basel)       Date:  2018-09-04       Impact factor: 6.639

8.  Association of serum lipids and severity of epithelial ovarian cancer: an observational cohort study of 349 Chinese patients.

Authors:  Yi Zhang; Jing Wu; Jun-Ya Liang; Xing Huang; Lei Xia; Da-Wei Ma; Xin-Yu Xu; Ping-Ping Wu
Journal:  J Biomed Res       Date:  2018-09-29

9.  A Pilot Low-Inflammatory Dietary Intervention to Reduce Inflammation and Improve Quality of Life in Patients With Familial Adenomatous Polyposis: Protocol Description and Preliminary Results.

Authors:  Patrizia Pasanisi; Manuela Gariboldi; Paolo Verderio; Stefano Signoroni; Andrea Mancini; Licia Rivoltini; Massimo Milione; Enzo Masci; Chiara Maura Ciniselli; Eleonora Bruno; Alessandra Macciotta; Antonino Belfiore; Maria Teresa Ricci; Giuliana Gargano; Daniele Morelli; Giovanni Apolone; Marco Vitellaro
Journal:  Integr Cancer Ther       Date:  2019 Jan-Dec       Impact factor: 3.279

10.  Physical activity and Mediterranean diet as potential modulators of osteoprotegerin and soluble RANKL in gBRCA1/2 mutation carriers: results of the lifestyle intervention pilot study LIBRE-1.

Authors:  Leonie Neirich; Maryam Yahiaoui-Doktor; Jacqueline Lammert; Maryam Basrai; Benjamin Seethaler; Anika Berling-Ernst; Juliane Ramser; Anne S Quante; Thorsten Schmidt; Uwe Niederberger; Kerstin Rhiem; Rita Schmutzler; Christoph Engel; Stephan C Bischoff; Martin Halle; Marion Kiechle; Sabine Grill
Journal:  Breast Cancer Res Treat       Date:  2021-09-27       Impact factor: 4.872

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