- Open Access
Association of body composition with odds of breast cancer by molecular subtype: analysis of the Mechanisms for Established and Novel Risk Factors for Breast Cancer in Nigerian Women (MEND) study
BMC Cancer volume 21, Article number: 1051 (2021)
The association between obesity and breast cancer (BC) has been extensively studied among US, European and Asian study populations, with often conflicting evidence. However, despite the increasing prevalence of obesity and associated conditions in Africa, the continent with the highest age-standardized BC mortality rate globally, few studies have evaluated this association, and none has examined in relation to molecular subtypes among African women. The current analysis examines the association between body composition, defined by body mass index (BMI), height, and weight, and BC by molecular subtype among African women.
We estimated odds ratios (ORs) and 95% confidence intervals (95% CI) for the association between measures of body composition and BC and molecular subtypes among 419 histologically confirmed cases of BC and 286 healthy controls from the Mechanisms for Established and Novel Risk Factors for Breast Cancer in Women of Nigerian Descent (MEND) case-control study.
Higher BMI (aOR: 0.79; 95% CI: 0.67, 0.95) and weight (aOR: 0.83; 95% CI: 0.69, 0.98) were associated with reduced odds of BC in adjusted models, while height was associated with non-statistically significant increased odds of BC (aOR: 1.07, 95% CI: 0.90, 1.28). In pre/peri-menopausal, but not post-menopausal women, both higher BMI and weight were significantly associated with reduced odds of BC. Further, higher BMI was associated with reduced odds of Luminal A, Luminal B, and HER2-enriched BC among pre/peri-menopausal women, and reduced odds of triple-negative BC among post-menopausal women.
Higher BMI and weight were associated with reduced odds of BC overall and by molecular subtype among West African women. Larger studies of women of African descent are needed to definitively characterize these associations and inform cancer prevention strategies.
Breast cancer (BC) poses a significant global challenge, with an estimated 2.1 million new cases and over 0.6 million deaths occurring in 2018 . The African continent has the highest age-standardized BC mortality rate globally, with Nigeria, the most populous African nation, experiencing the highest rate within the continent . In addition, the past few decades have been characterized by rapid increases in BC incidence rates among African women . This increase is thought to be partly attributable to an epidemiological transition—a trend characterized by a decline in infectious diseases and an increase in non-communicable diseases, including obesity, obesity-associated conditions, as well as cancer [4, 5]. Women of African descent are also more likely to experience disproportionately high rates of aggressive BC tumors with poorer prognosis [6,7,8]. Specifically, women of African descent, including African-American women in the United States  and Nigerian women, are more likely to be diagnosed with BC over-represented by the triple-negative (TN) subtypes, characterized by estrogen (ER), progesterone (PR), and human epidermal growth factor-2 (HER2) receptor negativity [7, 8].
Non-communicable disease risk factors, such as high body mass index (BMI), have been shown to influence BC risk. Several studies have found that higher BMI, an indicator of excess adiposity, is associated with increased risk of post-menopausal BC, but reduced risk of pre-menopausal BC [10, 11]. This association has been observed among diverse populations, including European , Latin American , and Asian  women. However, the few studies in Nigeria, where obesity rates are rapidly increasing , are mixed. Two studies have noted no significant associations between BMI and BC risk [16, 17], while studies assessing other measures of excess adiposity, such as waist circumference and waist-to-hip ratio, observed an association with increased risk of BC in Nigerian women [17, 18]. These measures of excess adiposity have been associated with metabolic dysregulation, including insulin resistance and hyperlipidemia , which have separately been shown to increase BC risk . Additionally, studies considering body height have found a positive association between height and BC risk [21, 22], including two studies among Nigerian women [16, 23]. Molecular BC subtype has been shown to modify the association between excess adiposity and BC risk. Obese women were found to have a higher risk of TN and Luminal A BC than normal-weight women, whereas normal-weight women were more likely to present with HER2+ BC in a population from the United States . Another United States study found that elevated waist-to-hip ratio was associated with increased risk of Luminal A BC among post-menopausal women, and increased risk of basal-like (TN) BC in both pre- and post-menopausal women . However, no study to date has examined the link between BMI and BC molecular subtypes in West African women.
Improved understanding of the impact of obesity on BC and molecular subtypes in West African women will add to the growing literature that can help inform locally relevant BC prevention strategies and contribute to enhancing existing risk prediction and prognostic models. Findings will also contribute to improved understanding of the biological mechanisms underlying aggressive tumor subtypes in women of African descent. The purpose of the current study was to evaluate the association between BMI, height, and weight with odds of BC among West African women, and to examine differences across molecular subtypes.
The Mechanisms for Established and Novel Risk Factors for Breast Cancer in Women of Nigerian Descent (MEND) study has been previously described in detail . Briefly, newly diagnosed BC patients from four tertiary hospitals in southwestern Nigeria were recruited into the research study. A trained research nurse at each site introduced the study and explained study requirements in detail to potential participants during clinical visits, and interested participants were assessed for eligibility. Exclusion criteria included other medical conditions that could interfere with participation in the study, mental impairment, or not being able to communicate in English themselves or through a family member to complete the survey. Written and verbal informed consent was obtained from all study participants. A comprehensive study questionnaire was administered to obtain information on sociodemographic characteristics, reproductive history, and self and family history of cancer. Anthropometric measurements were obtained by the research nurse, followed by blood sample collection, and tumor and adjacent normal tissue biopsy sample collection. All biospecimen were collected prior to any chemotherapy or surgical treatment. Tissue samples were processed at the clinic and stored in − 80 °C freezers until shipment to the United States for further analysis. Participants received a N500 telephone recharge card (approximately US $1.50) as well as supplies needed for their clinical biopsy (biopsy needle and ancillary items). Data on healthy controls without BC were obtained from the Human Heredity and Health Africa (H3A) Chronic Kidney Disease (CKD) case-control study; methodology for the H3A CKD study has been described elsewhere . Briefly, H3A recruitment occurred between 2015 and 2017, overlapping with case recruitment and included the recruitment of healthy, community-based adult women in southwestern Nigeria and Ghana. Extensive socio-demographic, clinical, family history and behavioral risk factor data was collected from all control participants; those with history of cancer or missing data on cancer history were excluded from analysis. Overall, 419 BC cases and 286 healthy controls were included in the current analysis (Fig. 1). All study procedures were approved by Duke University and the participating hospitals’ Institutional Review Boards.
Breast cancer cases and subtyping
BC diagnosis was confirmed in one of two ways: 1) pathology reports based on clinical tumor biopsy samples from the diagnosing hospital in Nigeria and reviewed by a trained pathologist, or 2) research tumor biopsy samples collected at recruitment (same time as clinical biopsy) and shipped to the United States for review by a pathologist. Participants were considered a confirmed cancer case if either report indicated a cancer diagnosis. Confirmed BC tumor samples were subjected to immunohistochemistry (IHC) either at the diagnosing hospital in Nigeria following standard protocol, or at the Duke University BioRepository and Precision Pathology Center. When both Nigeria and Duke IHC results were available, the Duke typing was used because it constituted the majority of IHC data on cases. Estrogen receptor and progesterone receptor status were scored using the Allred method [28, 29]. The proportion of nuclear positivity was scored as 0 (0%), 1 (< 1%), 2 (1–10%), 3 (11–33%), 4 (34–66%) or 5 (67–100%); intensity of the staining was scored as 0 (none), 1 (mild), 2 (moderate), or 3 (strong). These two scores were summed into positive (3–8) or negative (0–2). HER2 was scored as negative (scores 0, 1), equivocal (score = 2), positive (score = 3) . Cancer subtype was then classified as Luminal A (ER+ and/or PR+ / HER2-), Luminal B (ER+ and/or PR+ / HER2+), TN (ER−/PR−/HER2-), or HER2 (ER−/PR−/HER2+). In total, 169 cases had available data on ER/PR/HER2 status for molecular subtype classification.
Anthropometric measurements for cases and controls were collected by trained research staff at enrollment, and included height, weight, and blood pressure. BMI was calculated from height and weight as kg/m2. BMI, height, and weight were categorized into quartiles as well as continuous standardized variables by subtracting the sample mean and dividing by the sample standard deviation (SD). Quartiles were used rather than World Health Organization BMI categories (< 18.5 kg/m2 underweight, 18.5 - < 25 normal weight, 25 - < 30 overweight, and 30+ obese) because it has been documented that these categories may not accurately capture risk in populations of African descent . Reproductive and clinical history were self-reported by participants, and study covariates included age at menarche, parity, gravidity, menopausal status, and prior hypertension diagnosis. Participants also self-reported whether they had a history of other types of cancer; those with a positive history of cancer (< 1% of cases and controls) or missing personal cancer history data (15% of controls) were excluded from the analysis. Missing data for all measures were tabulated by case/control status. Variables with < 10% missing for both cases and controls were replaced with the median or modal value of the cases or controls, respectively, while variables with > 10% missing were not imputed.
Descriptive statistics of proportions and frequencies for categorical variables and means (SD) or medians (first quartile, third quartile) for continuous variables were used to characterize the sample by case/control status and BMI quartile. Differences in characteristics were tested using χ2 tests for categorical variables and Wilcoxon rank-sum or Kruskal-Wallis nonparametric tests for continuous variables. The distribution of BMI was evaluated by case/control status and stratified by menopausal status and age group, respectively. The associations between body composition measures (BMI, height, and weight) and BC were tested using logistic regression models. Each body composition measure was assessed separately in a series of models: unadjusted, adjusted for age only, and adjusted for age, age at menarche, number of pregnancies, number of births, menopausal status, and prior hypertension diagnosis. A final model adjusted for BMI, height, and weight simultaneously in addition to all previous covariates. The primary models assessed quartiles as a categorical variable, with the lowest quartile set as the reference group. To test for trend across quartiles, the main exposure was analyzed as a continuous variable [1,2,3,4]. Finally, the standardized values for BMI, height, and weight were examined to determine the association per unit standard deviation (SD) increase in the measure with the odds of being a cancer case. These models were repeated with stratification for menopausal status. The subset of cases with molecular subtyping was analyzed using multinomial logistic regression models, specifying control status as the outcome reference group. The previous models were repeated to assess the odds of Luminal A, Luminal B, TN, or HER2 cancer subtypes. We assessed whether H3A control participants recruited from Nigeria and Ghana were significantly different in relation to key body composition measures; there were no significant difference between the groups, and in sensitivity analysis examining the analytical models using Nigerian controls only, results from the overall analysis were consistent, therefore analysis with the entire cohort of controls is presented. SAS v9.4 (SAS Institute, Cary, NC) was used for all analyses and significance was set at α = 0.05.
A total of 419 BC cases and 286 healthy controls were included in the analysis (Fig. 1). Median age at diagnosis or enrollment (48 years vs. 47 years), median age at menarche (15 years vs. 15 years), number of pregnancies (5 vs. 4) and number of births (4 vs. 4) was similar among cases and controls (Table 1). However, cases were less likely to report any prior use of hormone replacement therapy compared with controls. Approximately half (54%) of cases and 60% of controls were overweight or obese, and controls were more likely to report a prior diagnosis of diabetes or hypertension. Among cases, the most common subtype was triple-negative (31%), and 38% of cases were diagnosed at advanced grade (grade 3). Across BMI quartiles (Table 2), those in the highest quartile were older (p < 0.001), more likely to have a prior diagnosis of hypertension (p < 0.001), report ever use of HRT (p = 0.009) and be ever pregnant (p = 0.01). Furthermore, the distribution of BMI by case/control status stratified by menopausal status and age group (Fig. 2) indicated that the proportion of cases compared to controls in the lowest BMI quartile was higher across categories of menopausal status and age.
In multivariable regression models (Table 3), BMI in the highest versus lowest quartile (BMI > 29.8 kg/m2 vs. < 22.5 kg/m2) was associated with reduced odds of BC in adjusted models (aOR: 0.56; 95% CI: 0.33, 0.92; p-trend: 0.02). However, after additionally adjusting for height and weight, the estimate was no longer statistically significant (aOR: 0.32, 95% CI: 0.10, 1.09; p-trend 0.06). Each SD increase in BMI was significantly associated with 21% reduced odds of BC (aOR: 0.79; 95% CI: 0.67, 0.95) in adjusted models but was no longer significant in models additionally adjusting for height and weight (aOR: 0.75, 95% CI: 0.15, 3.72). Weight (kg) in the highest quartile was associated with 37% reduced odds of BC (aOR: 0.63, 95% CI: 0.38, 1.04) in adjusted models, however this was not statistically significant, although each SD increase in weight was associated with significantly reduced odds of BC (aOR: 0.83; 95% CI: 0.69, 0.98). Increased height was not significantly associated with odds of BC in fully adjusted models or in weight and height adjusted models. In sub-group analyses stratified by menopausal status, BMI and weight were significantly associated with reduced odds of BC only among pre/peri-menopausal women (Fig. 3).
In multinomial logistic regression models evaluating BC molecular subtypes compared with controls (Table 4), highest versus lowest quartiles of BMI was associated with reduced but not statistically significant odds of each BC subtype, although the association of each SD increase in BMI with reduced odds of Luminal B subtype was statistically significant (aOR: 0.63; 95% CI: 0.42, 0.95). When we stratified by menopausal status, each unit SD increase in BMI was significantly associated with reduced odds of Luminal A (aOR 0.59; 95% CI: 0.35, 0.99), Luminal B (aOR: 0.48; 95% CI: 0.26, 0.90), and HER2-enriched (aOR: 0.49; 95% CI: 0.27, 0.90) BC among pre/peri-menopausal women, and reduced odds of TNBC (aOR: 0.55; 95% CI: 0.32, 0.95) among post-menopausal women. Height in the highest quartile was associated with 78% reduced odds of HER2-enriched BC (aOR: 0.22; 95% CI: 0.06, 0.83). Additionally, each unit SD increase in weight was significantly associated with 55% reduced odds of HER2-enriched BC (aOR: 0.45; 95% CI: 0.24, 0.84) only among pre/per-menopausal women.
In the first contemporary cohort of newly diagnosed African BC cases and healthy controls, increasing BMI and weight were significantly associated with reduced odds of BC overall, but no statistically significant association was noted with respect to height. Similar associations were observed among both pre/peri-menopausal and post-menopausal women, but only reached statistical significance among pre/peri-menopausal women. In our analysis of BC subtypes, higher BMI was significantly associated with reduced odds of Luminal A, Luminal B, and HER2-enriched BC among pre/peri-menopausal women, and reduced odds of TNBC among post-menopausal women.
Previous studies have evaluated the association between measures of body composition and BC in various patient populations, with results suggesting a positive association of BMI with BC risk among post-menopausal women, and inverse association among pre-menopausal women [10,11,12,13,14]. This is consistent with our findings of significant inverse associations with BMI and weight for pre-menopausal women. A few studies have evaluated these associations among Nigerian women, although most were published over a decade ago prior to the accelerated increase in obesity rates in the region. Specifically, two separate studies observed that a higher waist-to-hip ratio was associated with significantly increased risk of BC [17, 18], and three studies showed that height was associated with significantly increased risk of BC [16, 17, 23]. Additionally, obesity (defined as BMI ≥ 30) was found to be associated with increased odds of BC, although the results were not statistically significant overall or among pre- or post-menopausal women .
For the first time, we present results on the association between measures of body composition and BC subtypes compared to controls among West African women. We found reduced odds of Luminal A, Luminal B, and HER2-enriched BC among pre/peri-menopausal women, and reduced odds of TNBC among post-menopausal women with increased BMI. Prior studies on this topic are conflicting, and suggest that the associations between body composition and BC subtypes vary by menopausal status. A case-control study among Black and White women in the United States documented a positive association between elevated waist-to-hip ratio and Luminal A BC among post-menopausal women . Another analysis, which included studies in the Breast Cancer Association Consortium, a primarily European population, found that elevated BMI in younger women was more strongly associated with hormone receptor positive tumors (Luminal subtypes) , and another study from the United States noted that among post-menopausal women, BMI was associated with an increased odds of ER+/PR+ BC . In contrast, a meta-analysis of studies from the US, Europe, and Asia found that ER+/PR+ tumors were less likely to develop among higher weight pre-menopausal women, but more likely to develop among higher weight post-menopausal women . Our findings are consistent with a prior study that found an inverse association between BMI and risk of TNBC . However, our findings are inconsistent with other past studies showing positive associations between obesity and TNBC [24, 25, 36], most of which were conducted in study populations from the United States, Europe, and Asia, and may not be representative of the BC phenotypes observed in Nigeria.
Despite the documented inverse association between BMI and BC risk among pre-menopausal women, the underlying biological mechanisms remain an active area of research. For instance, lower levels of progesterone among pre-menopausal obese women may lead to a lower risk of BC because progesterone is thought to have a primarily pro-proliferative role in the adult breast . However, further research is needed to better explain how excess adiposity contributes to BC risk across different subtypes. While our findings may suggest lower BC risk among obese patients relative to lean patients, it is well-established that BC survival is negatively impacted by obesity . These seemingly paradoxical observations, dubbed the obesity paradox, may be a consequence of differences in treatment response among differently weighted patients . Additionally, biological mechanisms that explain the higher risk of TNBC in women of West African descent are not well-understood. We urge additional research among African populations to elucidate population-specific risk factors that may contribute to these outcomes.
Several considerations are relevant for our study. Given the predominance of the aggressive phenotype (high grade and TN subtype) of BC in Nigeria, also reflected in the current study population, it is possible for cases to have experienced disease associated weight loss prior to recruitment. It is worth noting that TNBCs grow quickly and are more likely to be clinically apparent compared with ER+/PR+ cancers, which are more likely to be detected by screening mammography . The low prevalence of mammogram screening in Nigeria , reflected in our sample with less than 19% of cases having had a previous mammogram screening, may contribute to the high prevalence of TNBC. However, it is important to note that studies among African American women, with similar BC morphological features to Nigerian women , have been inconsistent, with some suggesting positive associations between excess adiposity and BC risk [42, 43], while others have reported no significant associations [44, 45]. The exact relationship between BMI and BC risk remains conflicting for women of African descent, indicating a need for further study in a larger cohort, especially given the context in which BC disease is distinctly more aggressive [6,7,8].
There are several strengths and limitations of this study relevant to the interpretation of these results. Since covariate data were self-reported at diagnosis, we cannot exclude the possibility of recall bias. However, our main exposures of interest, measures of excess adiposity, were obtained consistently across study participants by trained study personnel. Furthermore, because BMI, height, and weight were recorded at the time of diagnosis, we are unable to rule out the possibility of reverse causality. Additionally, we note the limitation of relying purely on BMI (height and weight) as a measure of excess adiposity. Individuals with the same BMI can have different body fat distributions . Nevertheless, our study has important strengths, including the use of histologically confirmed cases of BC from multiple tertiary institutions in Nigeria where the majority of cancer patients receive treatment, and a vital contribution of diverse patient populations to the BC literature. Our study is the first to characterize the association between measures of body composition and BC risk among West African women by molecular subtype.
In conclusion, measures of body composition were associated with BC and these associations varied by molecular subtypes. Larger studies of women of African descent are needed to better characterize these associations and enhance population-specific BC prevention strategies.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Body mass index
Chronic kidney disease
Human epidermal growth factor-2
Human Heredity and Health Africa
Mechanisms for Established and Novel Risk Factors for Breast Cancer in Women of Nigerian Descent
Progesterone receptor (PR)
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We acknowledge the role of the H3Africa Consortium in making this research possible though the sharing of data. The National Institutes of Health (USA) and Wellcome Trust (UK) have provided the core funding for the H3Africa Consortium. We thank the many MEND investigators who contributed substantially to the inception and design of the study, and the patients and families who participated in the MEND study for their vital contribution in advancing the science of cancer in Nigeria and globally. We acknowledge the important contribution of the MEND research nurses: Cordelia Ibeneme, Peju Olabanji, Rebecca Israel, Esther Akinwale, Deborah Awodeyi, and Shukurat Oduola.
H3 Africa Kidney Research Network
Cheryl A. Winkler18
Ernestine Kubi Amos-Abanyie27
Priscilla Abena Akyaw27
Paul L. Kimmel28
Babatunde L. Salako14
Rulan S. Parekh29
Frank (Chip) Brosius19
Elliot Koranteng Tannor22
14Department of Medicine, Pediatrics and Institute of Child Health, University of Ibadan, Ibadan, Nigeria
15University of Ilorin, Ilorin, Nigeria
16University of Ghana Medical School, Accra, Ghana
17University of Nigeria, Enugu State, Nigeria
18Basic Research Laboratory, Frederick National Laboratory for Cancer Research, National Cancer Institute, Frederick, Maryland, USA
19Departments of Human Genetics, Internal Medicine and Pathology, University of Michigan, Ann Arbor, Michigan, USA
20Obafemi Awolowo University, Ile- Ife, Nigeria
21University of Cape Coast, Cape Coast, Ghana
22Kwame Nkrumah University of Science and Technology, Kumasi, Ghana
23University of Abuja, Abuja, Nigeria
24Parkinson School of Health Sciences and Public Health, Loyola University, Chicago, Illinois, USA
25Centre for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA
26Division of Nephrology, Boston Medical Center, Boston University School of Medicine, Boston, Massachusetts, USA
27Noguchi Memorial Institute for Medical Research, University of Ghana, Ghana
28National Institute of Diabetes and Digestive and Kidney Disease, Bethesda, Maryland, USA
29Department of Pediatrics, University of Toronto, Toronto, Canada
30Department of Pediatrics, Duke University Medical Center, Durham, North Carolina, USA
31University of Western Cape, Cape Town, South Africa
32Harvard Medical School, Harvard University, Boston, Massachusetts, USA
33Nnamdi Azikiwe University Teaching Hospital, Nnewi, Nigeria
34Aminu Kano Teaching Hospital, Kano, Nigeria
35Delta State University Teaching Hospital, Warri, Nigeria
36Lagos State University Teaching Hospital, Lagos, Nigeria
37Usmanu Danfodiyo University Teaching Hospital, Sokoto, Nigeria
38University of Illinois at Chicago, Chicago Illinois, USA
39University of Yaoundé, Yaoundé, Cameroon
40University of Cape Town, Cape Town, South Africa
41New York University, New York City, New York, USA
42Duke University, Durham, North Carolina, USA
43Technion-Israel Institute of Technology, Haifa, Israel
44University of Kansas School of Medicine, Kansas City, Kansas, USA
This research was specifically funded by National Institutes of Health, National Cancer Institute, Fogarty International Center (K01TW010271, T.A.). The views expressed in this paper do not represent the views of the National Institutes of Health, H3Africa Consortium or their funders.
Ethics approval and consent to participate
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The study was approved by the Institutional Review Board of Duke University (Pro00102004). This article does not contain any studies with animals performed by any of the authors. Informed consent was obtained from all individual participants included in the study.
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The authors declare that they have no competing interests.
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Akinyemiju, T., Jones, K., Gupta, A. et al. Association of body composition with odds of breast cancer by molecular subtype: analysis of the Mechanisms for Established and Novel Risk Factors for Breast Cancer in Nigerian Women (MEND) study. BMC Cancer 21, 1051 (2021). https://doi.org/10.1186/s12885-021-08775-8
- Body composition
- Breast cancer
- Molecular subtype
- Hormone receptor