Skip to main content
Archives of Medical Sciences. Atherosclerotic Diseases logoLink to Archives of Medical Sciences. Atherosclerotic Diseases
. 2019 Jul 18;4:e134–e140. doi: 10.5114/amsad.2019.86749

Stroke and breast cancer in the United States during 2007–2017

Irene Rethemiotaki 1,, Andrew Rethemiotakis 2
PMCID: PMC6704760  PMID: 31448344

Abstract

Introduction

The main purpose of this work is to study the malignant neoplasms of the breast and the incidence of strokes in the United States and to find not only statistically significant predictors for cancer, but also a possible association between breast cancer and stroke.

Material and methods

The statistical methods used to derive the results of this work are χ2 and one-way analysis of variance (ANOVA) tests, in order to check the statistical significance of breast cancer in relation to socio-economic factors of patients. In addition, a multivariate logistic regression analysis was used with the odds ratio (OR) to find statistically significant prognostic factors for breast cancer. The Pearson correlation coefficient was used to find the relationship between breast cancer and stroke.

Results

According to multiple logistic regression analysis, widowed women have 11 times higher risk developing breast cancer, while white women who are unemployed but have worked previously have two times higher risk for the occurrence of this type of cancer. In addition, a statistically significant relationship was found between the number of cases of breast cancer and stroke.

Conclusions

Our results describe for the first time the importance of deprivation (of work and partner) as a primary prognostic risk factor for cancer. Moreover, we found a link between breast cancer diagnosis and stroke.

Keywords: malignant neoplasms of the breast, prognostic factors, breast cancer, socio-economic factors, stroke

Introduction

Breast cancer is the most common malignancy worldwide, accounting for 14% of all new cancer cases in the world in 2016 [1]. The incidence of breast cancer is mainly observed in women over 40–49 years of age [2]. The main risk factors are age [3], positive family history of cancer [4], early menarche [5] and late childbearing [4, 5], woman’s age at menopause [6], and race [7], while in 75–80% of women no risk factor is found [8]. Regarding the socio-economic factors, increased incidence of breast cancer was found for women with higher education [912], highest income [10], and creative core occupation [10, 11]. A recent study suggests an association between socio-economic factors and breast cancer and, more specifically, proves that breast cancer tends to be higher across richer countries. Women from richer countries are prone to higher demand for treatments represented by oral contraceptives (OCs) and hormone therapy (HT), factors which increase the risk of breast cancer [13].

Prior studies have found increased risk of stroke in patients with breast cancer, who were given radiotherapy (RT). More specifically, it has been found that RT to the supraclavicular lymph nodes gives a significant dose of radiation to the proximal carotid artery, which increases the risk of carotid stenosis and ischaemic stroke [14]. Moreover, cancer is not a well-established independent risk factor for arterial thromboembolism, and cancer patients do not systematically receive treatments to prevent myocardial infarction and stroke, resulting in an increased risk for such cases in cancer patients [1517].

This work studies breast cancer and stroke in the United States in the years 2007–2017 in order to find statistically significant predictors for cancer and a possible link between breast cancer and stroke.

Material and methods

The data used in this work come from the National Health Interview Survey dataset [18] and cover the period 2007–2017. The number of breast cancer and stroke patients examined was 37,634 and 71,227, respectively.

Statistical analysis

The statistical methods used to extract the results of this work are the χ2 test for categorical and one-way analysis of variance (ANOVA) for continuous variables, to check the statistical significance of human breast cancer in relation to selected characteristics of patients such as gender, age, race, origin, education, family income, poverty status, health insurance coverage, place of residence, and region. Factors that determine the prevalence of cancer were assessed by using multiple logistic regression analysis. To better assess the predictors of cancer, we used data from patients with a new diagnosis of cancer compared to a matched cohort of patients without cancer. Predictors were represented using the OR and 95% confidence intervals, and p < 0.05 was considered as statistically significant. The Pearson correlation coefficient was used for the relationship between cancer and stroke for the years 2007–2017. The study was carried out using the IBMSPSS 25 software package for Windows.

Results

To check the zero hypotheses that the mean of the patients in the United States with malignant neoplasms of the breast did not differ according to their socio-economic characteristics, the χ2 test and one-way analysis of variance (ANOVA) were used. As shown in Table I, there is a statistically significant difference in the number of malignant neoplasms of the breast in relation to gender, and it occurs mainly in women (99.4%). Moreover, the age group with the most frequent occurrence of breast cancer is from 45 to 64 years old (69%), while the most common origin and race is white (88.9%), not Hispanic or Latino (48.6%). The education level that was found to be statistically significant was “less than a high school diploma” (13.2%). Employment status that was found to be statistically significant was “Not employed but has worked previously” (49.4%). The financial status that was found to be statistically significant was “not poor”, with a family income of $35,000 or more (38.6%). Health insurance coverage was found to be statistically significant in both age groups under 65 years (76.5%) and 65 years and over (59.5%) was “private”. In addition, the marital status that the most breast cancer patients had was “married” (52.2%). Finally, the region with the most frequent occurrence of breast cancer was the south (35%), with a population size of one million or more (51.3%).

Table I.

χ2 and one-way analysis of variance (ANOVA) test

Selected characteristics of breast cancer patients: United States 2007–2017 Number of patients Percentages P-value
Gender: 37.634 < 0.001
 Male 256 0.6
 Female 37.378 99.4
Age: < 0.001
 18–44 1.651 2.5
 45–64 14.569 69.0
 65–74 10.320 13.5
 75 and over 11.194 14.9
Race: < 0.001
 White 32.645 88.9
 Black or African American 3.107 8.1
 Asian 1.223 3.0
Origin: < 0.001
 Hispanic or Latino 2.485 3.3
 Mexican or Mexican American 1.479 1.9
 Not Hispanic or Latino 35.246 48.6
 White, single race 30.440 42.2
 Black or African American, single race 2.996 4.0
Education: < 0.001
 Less than a high school diploma 4.872 13.2
 High school diploma 5.526 29.5
 Some college 10.512 27.9
 Bachelor’s degree or higher 11.061 29.4
Employment:
 Employed 6.804 23.4 < 0.001
 Full-time 4.888 16.9
 Part-time 1.724 6.0
 Not employed but has worked previously 2.378 49.4
 Not employed and has never worked 1.193 4.3
Family income: < 0.001
 Less than $35,000 12.308 22.9
 $35,000 or more 20.877 38.6
 $35,000–$49,999 5.045 9.6
 $50,000–$74,999 5.424 10.1
 $75,000–$99,999 3.571 6.6
 $100,000 or more 6.838 12.3
Poverty status: < 0.001
 Poor 2.940 8.7
 Near poor 5.702 17.0
 Not poor 24.906 74.4
Health insurance coverage:
 Under 65: < 0.001
  Private 12.305 76.5
  Medicaid 2.070 12.8
  Other coverage 840 5.0
  Uninsured 917 5.7
 65 and over: 0.001
  Private 16.174 59.5
  Medicare and Medicaid 1.663 6.1
  Medicare only 7.474 28.3
  Other coverage 1.662 6.1
Marital status: < 0.001
 Married 19.851 52.2
 Widowed 9.055 24.5
 Divorced or separated 5.726 15.4
 Never married 1.966 5.1
 Living with a partner 1.042 2.7
Place of residence (metropolitan statistical area – MSA): < 0.001
 Large MSA (population size 1 million or more) 19.516 51.3
 Small MSA (less than 1 million) 11.388 30.3
 Not in MSA 6.830 18.4
Region: < 0.001
 Northeast 7.290 18.9
 Midwest 9.065 24.1
 South 13.164 35.0
 West 8.214 21.9

Table II shows the multiple logistic regression analysis and odds ratios in order to find the predictors for the occurrence of breast cancer.

Table II.

Statistically significant predictors of breast cancer in US using multivariate logistic regression

Socio-economic characteristics of breast cancer patients: 2007–2017 Patients Controls Odds ratio (95% CI) P-value
Gender: < 0.001
 Male 200 1.127.215 0.07 (0.05–0.07)
 Female 33.477 2.305.890 1.0 (ref.)
Age: < 0.001
 18–44 1.470 1112863 0.025 (0.024–0.027)
 45–64 13.099 794485 0.99 (0.96–1.0)
 65–74 9.130 224824 0.68 (0.6–0.7)
 75 and over 10.077 170.360 1.0 (ref.)
Race: < 0.001
 White 29.404 1.841.244 1.94
 Black or African American 2.688 278.992 1.17
 Asian 999 121.990 1.0 (ref.)
Origin: 0.000
 Hispanic or Latino 2.133 338.233 0.64 (0.6–0.68)
 Mexican or Mexican American 1.251 208.223 0.61 (0.57–0.65)
 Not Hispanic or Latino 31.640 1.964.300 1.64 (1.5–1.7)
 White, single race 27.449 1.533.489 1.82 (1.7–1.9)
 Black or African American, single race 2.624 267.881 1.0 (ref.)
Education: < 0.001
 Less than a high school diploma 4.416 276.082 1.01 (0.9–1.0)
 High school diploma 9.894 520.095 1.20 (1.17–1.24)
 Some college 9.370 571.173 1.04 (1.01–1.07)
 Bachelor’s degree or higher 9.871 626.702 1.0 (ref.)
Employment: < 0.001
 Employed 5.548 727.135 0.5 (0.4-0.53)
 Full-time 4.008 586.800 0.45 (0.42-0.48)
 Part-time 1.433 129.836 0.72 (0.67-0.79)
 Not employed but has worked previously 11.740 386.217 2.0 (1.8-2.1)
 Not employed and has never worked 1.017 67.103 1.0 (ref.)
Family income: < 0.001
 Less than $35,000 11.094 695.245 1.3 (1.2–1.34)
 $35,000 or more 18.716 1.419.425 1.07 (1.04–1.1)
 $35,000–$49,999 4.639 291.260 1.29 (1.2–1.34)
 $50,000–$74,999 4.923 380.211 1.05 (1.01–1.09)
 $75,000–$99,999 3.184 262.244 0.98 (0.94–1.0)
 $100,000 or more 5.971 485.707 1.0 (ref.)
Poverty status: < 0.001
 Poor 2.598 277.817 0.61 (0.59–0.64)
 Near poor 5.068 369.495 0.90 (0.88–0.93)
 Not poor 22.221 1.470.210 1.0 (ref.)
Health insurance coverage: < 0.001
 Under 65:
  Private 11.073 1.265.457 3.69 (3.4–3.9)
  Medicaid 1.856 198.207 3.95 (3.6–4.2)
  Other coverage 721 83.015 3.66 (3.3–4.0)
  Uninsured 831 351.007 1.0 (ref.)
 65 and over: < 0.001
  Private 15.032 195.568 1.27 (1.2–1.3)
  Medicare and Medicaid 1.538 26.007 0.98 (0.91–1.0)
  Medicare only 7.141 99.370 1.19 (1.12–1.26)
  Other coverage 1.535 25.478 1.0 (ref.)
Marital status: < 0.001
 Married 17.596 1.236.918 2.5 (2.4–2.7)
 Widowed 8.257 132.025 11.3 (10.6–12.1)
 Divorced or separated 5.202 258.718 3.6 (3.4–3.9)
 Never married 1.716 505.169 0.6 (0.57–0.67)
 Living with a partner 911 165.756 1.0 (ref.)
Place of residence (metropolitan statistical area – MSA): < 0.001
 Large MSA (population size 1 million or more) 17.321 1.223.889 0.81 (0.79–084)
 Small MSA (less than 1 million) 10.247 719.703 0.82 (0.79–0.85)
 Not in MSA 6.208 358.941 1.0 (ref.)
Region: < 0.001
 Northeast 6.400 405.297 1.12 (1.0–1.1)
 Midwest 8.142 532.672 1.09 (1.05–1.1)
 South 11.831 836.763 1.0 (0.9–1.03)
 West 7.402 527.800 1.0 (ref.)

As shown in Table II, all prognostic factors are statistically significant (p < 0.05). According to multiple logistic regression, the risk of breast cancer is significantly higher with female gender (odds ratio (OR) = 1.0), age over 75 years and 45–64 years old (OR 1.0 and 0.99, respectively), white race (OR = 1.94), and high school diploma education status (OR = 1.2). Moreover, those who were unemployed but had worked previously had twice the risk of developing breast cancer (OR = 2.0). In addition, the risk of cancer is significantly higher with family income “$35,000–$49,999” (OR = 1.29), poverty status “not poor” (OR = 1.0), and health insurance coverage “Medicaid” under 65 years old and “Private” over 65 years old (OR = 1.95 and OR = 1.27, respectively). Widowed women had 11 times the risk of developing breast cancer (OR = 11.3). Finally, the risk of breast cancer was significantly higher in the region “northeast” (OR = 1.2) and place of residence “not in a metropolitan statistical area” (OR = 1.0).

Figure 1 shows the trends in breast cancer and stroke during the years 2007–2017 in the United States. The incidence of breast cancer and stroke continued to increase from 2007 to 2017.

Figure 1.

Figure 1

Trends in breast cancer and stroke during the years 2007–2017 in the United States

Table III shows the Pearson correlation coefficient among the total number of breast cancer and stroke patients for the years 2007–2017. As can be seen from Table III, the incidence of cancer is statistically significant with stroke (p < 0.05). The Pearson correlation coefficient between the total number of cancer patients and stroke patients is 0.872, which indicates that there is a strong correlation between breast cancer and stroke.

Table III.

Pearson correlation coefficient

Variable Pearson correlation r P-value
Breast cancer 1
Stroke 0.872 < 0.01

Discussion

Increasing attention should be given to the increasing number of breast cancer patients in the United States during the years 2007–2017. It has been noted that the characteristic of patients with the highest risk is their marital status, and more specifically, it was found that widowed women have 11 times higher risk of developing breast cancer (OR = 11.3). Moreover, employment status plays a crucial role in developing this type of cancer. Women who were unemployed but had worked previously had twice the risk of developing breast cancer (OR = 2.0). Finally, white race is a prognostic risk for this type of cancer; it was found that white women in the U.S. have two times higher risk of developing breast cancer (OR = 1.94).

The importance of this study lies in the association of multiple socio-economic variables with cancer, which reflects the complexity and multidimensional nature of deprivation as well as the various roles of these dimensions throughout life, which in turn reflects the longest gestation period for cancer. More specifically, we found that partner and work deprivation were two determinants in an adult’s life, which rapidly increased the risk of cancer. We also found that not only deprivation but also the death of a partner plays a key role in the increased risk of developing cancer.

Moreover, we found a link between breast cancer diagnosis and stroke. One possible explanation is that cancer can cause a hypercoagulable state through circulating microparticles, secretion of proliferative factors, and alterations in platelet activity and endothelial function [19, 20]. Additionally, several cancer treatments, particularly platinum-based compounds, may increase thrombotic risk [19, 21].

In conclusion, this paper has highlighted that different socioeconomic variables are associated with different cancer risks, while deprivation (of work and husband) proved to be the primary prognostic risk factor for cancer. Moreover, incident cancer is associated with an increased risk of stroke.

Conflict of interest

The authors declare no conflict of interest.

References

  • 1.Kispert S, McHowat J. Recent insights into cigarette smoking as a lifestyle risk factor for breast cancer. Breast Cancer. 2017;9:127–32. doi: 10.2147/BCTT.S129746. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Shoemaker ML, White MC, Wu M, et al. Differences in breast cancer incidence among young women aged 20-49 years by stage and tumor characteristics, age, race, and ethnicity, 2004-2013. Breast Cancer Res Treat. 2018;169:595–606. doi: 10.1007/s10549-018-4699-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Chen HL, Zhou MQ, Tian W, Meng KX, He HF. Effect of age on breast cancer patient prognoses: a population-based study using the SEER 18 database. PLoS One. 2016;11:e0165409. doi: 10.1371/journal.pone.0165409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Petracci E, Decarli A, Schairer C, et al. Risk factor modification and projections of absolute breast cancer risk. J Natl Cancer Inst. 2011;103:1037–48. doi: 10.1093/jnci/djr172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Villeneuve S, Fevotte J, Anger A, et al. Breast cancer risk by occupation and industry: analysis of the CECILE study, a population-based case-control study in France. Am J Ind Med. 2011;54:499–509. doi: 10.1002/ajim.20952. [DOI] [PubMed] [Google Scholar]
  • 6.Collaborative Group on Hormonal Factors in Breast Cancer Menarche, menopause, and breast cancer risk: individual participant meta-analysis, including 118 964 women with breast cancer from 117 epidemiological studies. Lancet Oncol. 2012;13:1141–51. doi: 10.1016/S1470-2045(12)70425-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Maskarinec G, Sen C, Koga K, Conroy SM. Ethnic differences in breast cancer survival: status and determinants. Womens Health (Lond) 2011;7:677–87. doi: 10.2217/whe.11.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Bucholc M, Lepecka-Klusek C, Pilewska A, et al. Ryzyko zachorowania na raka piersi w opinii kobiet. Ginekol Pol. 2001;72:1460–56. [PubMed] [Google Scholar]
  • 9.Beiki O, Hall P, Ekbom A, Moradi T. Breast cancer incidence and case fatality among 4.7 million women in relation to social and ethnic background: a population-based cohort study. Breast Cancer Res. 2012;14:R5. doi: 10.1186/bcr3086. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Carlsen K, Hoybye MT, Dalton SO, Tjonneland A. Social inequality and incidence of and survival from breast cancer in a population-based study in Denmark, 1994-2003. Eur J Cancer. 2008;44:1996–2002. doi: 10.1016/j.ejca.2008.06.027. [DOI] [PubMed] [Google Scholar]
  • 11.Larsen SB, Olsen A, Lynch J, et al. Socioeconomic position and lifestyle in relation to breast cancer incidence among postmenopausal women: a prospective cohort study, Denmark, 1993-2006. Cancer Epidemiol. 2011;35:438–41. doi: 10.1016/j.canep.2010.12.005. [DOI] [PubMed] [Google Scholar]
  • 12.Vidarsdottir H, Gunnarsdottir HK, Olafsdottir EJ, et al. Cancer risk by education in Iceland; a census-based cohort study. Acta Oncol. 2008;47:385–90. doi: 10.1080/02841860801888773. [DOI] [PubMed] [Google Scholar]
  • 13.Chagpar A, Coccia M. Working Paper of Public Health, n. 7. Alessandria (Italy): Azienda Ospedaliera SS. Antonio e Biagio Arrigo; 2012. Breast cancer and socio-economic factors. [Google Scholar]
  • 14.Nilsson G, Holmberg L, Garmo H, Terent A, Blomqvist C. Increased incidence of stroke in women with breast cancer. Eur J Cancer. 2005;41:423–9. doi: 10.1016/j.ejca.2004.11.013. [DOI] [PubMed] [Google Scholar]
  • 15.Goff DC, Lloyd-Jones DM, Bennett G, et al. ACC/AHA guideline on the assessment of cardiovascular risk. J Am Coll Cardiol. 2014;63:2935–59. doi: 10.1016/j.jacc.2013.11.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Meschia JF, Bushnell C, Boden-Albala B, et al. American Heart Association Stroke Council; Council on Cardiovascular and Stroke Nursing; Council on Clinical Cardiology; Council on Functional Genomics and Translational Biology; Council on Hypertension. Guidelines for the primary prevention of stroke: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2014;45:3754–832. doi: 10.1161/STR.0000000000000046. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.McSweeney JC, Rosenfeld AG, Abel WM, et al. American Heart Association Council on Cardiovascular and Stroke Nursing, Council on Clinical Cardiology, Council on Epidemiology and Prevention, Council on Hypertension, Council on Lifestyle and Cardiometabolic Health, and Council on Quality of Care and Outcomes Research. Preventing and experiencing ischemic heart disease as a woman: state of the science: a scientific statement from the American Heart Association. Circulation. 2016;133:1302–31. doi: 10.1161/CIR.0000000000000381. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.National Center for Health Statistics Data file documentation, National Health Interview Survey. 2016. https://www.cdc.gov/nchs/nhis.htm.
  • 19.Gomes M, Khorana AA. Risk assessment for thrombosis in cancer. Semin Thromb Hemost. 2014;40:319–24. doi: 10.1055/s-0034-1370770. [DOI] [PubMed] [Google Scholar]
  • 20.Bick RL. Cancer-associated thrombosis. N Engl J Med. 2003;349:109–11. doi: 10.1056/NEJMp030086. [DOI] [PubMed] [Google Scholar]
  • 21.Li SH, Chen WH, Tang Y, et al. Incidence of ischemic stroke post-chemotherapy: a retrospective review of 10,963 patients. Clin Neurol Neurosurg. 2006;108:150–6. doi: 10.1016/j.clineuro.2005.03.008. [DOI] [PubMed] [Google Scholar]

Articles from Archives of Medical Sciences. Atherosclerotic Diseases are provided here courtesy of Termedia Publishing

RESOURCES