Abstract
Objective
Obesity and weight gain after breast cancer treatment are common among survivors, yet the relationship between weight and body image has received little attention. The purpose of the current study was to examine the relationship between current body mass index, weight gain since diagnosis, and largest weight fluctuation in adulthood with six dimensions of body image among overweight/obese breast cancer survivors.
Methods
The current study used data obtained from a weight control trial with 210 rural overweight/obese breast cancer survivors. Using data collected at baseline, multiple regression models were constructed to examine the relative association of the three weight variables with breast cancer-specific dimensions of body image, while controlling for demographic characteristics, and cancer treatment-related variables.
Results
Largest weight fluctuation in adulthood significantly predicted overall body image (p=.01) and was associated with the three socially-oriented dimensions of body image: social activity restriction, embarrassment about appearance, and sexuality (all ps = .01). Weight gain since diagnosis approached statistical significance in predicting overall body image (p = .05) and was associated with embarrassment about appearance (p = .03). Current body mass index was not significantly associated with overall body image when controlling for the other weight variables (p=.07) and was negatively associated with social activity restriction (p = .01) and sexuality (p = .01).
Conclusions
Obese breast cancer survivors with a history of a large weight fluctuation in adulthood may be prone to poorer breast-cancer specific body image several years after treatment.
Keywords: Breast cancer survivorship, body image, weight history, obesity, oncology
Background
Breast cancer and corresponding treatments can cause bodily changes that may put survivors at risk for poor body image [1,2]. Bodily changes can include appearance alterations (e.g., breast alterations, scarring), sensory changes (e.g., pain, numbness) and functional impairment (e.g., dysphagia, dysarthria) [1]. The degree and type of changes that occur depend on the characteristics of the disease, such as the tumor histology and stage, and the type of treatment(s) received [1]. Any type of surgery is associated with poorer body image compared to non-surgical treatments [3], and mastectomy and reconstruction surgeries generally result in poorer body image [4–6] than breast conserving surgeries [7]. Common side effects of treatment can also affect body appearance and functioning, including hair loss from chemotherapy [4], changes to sexuality and sexual functioning [8], change in body composition (decreased muscle mass and increased adiposity), and weight gain from treatment-induced menopause [9] or from changes in physical activity during and post-treatment [2,10]. Research indicates that over 70% of breast cancer survivors experience body dissatisfaction post-treatment [9,11]. Body image among breast cancer survivors generally decreases in the first 1–6 months after treatment [4,12,13] and remains lower but stable during the subsequent years [12,13].
Body image among breast cancer survivors is important to examine because it impacts survivors’ quality of life and physical rehabilitation following cancer treatment. Poor body image among survivors is associated with increased depression and emotional distress [14,15], poorer psychosocial functioning [15] and lower quality of life [16]. In addition, among women in physical therapy rehabilitation following breast cancer treatment, poor body image was associated with less improvement in functioning both during physical rehabilitation and after [17].
Obesity and weight gain during breast cancer treatment are common problems among survivors. As many as 68–71% of breast cancer patients are overweight/obese at diagnosis [18,19] and 50–80% of breast cancer patients gain weight during treatment [2,20]. Further, obese breast cancer patients have higher surgery complication rates when compared to their lean counterparts [21]. In addition to increasing the relative risk for breast cancer recurrence and long term survival [22], obesity and its complications during treatment may also make overweight/obese breast cancer survivors vulnerable to poor body image following treatment [5,23,24]. In addition to treatment-related weight gain, substantial weight gain during adulthood may exacerbate the body image consequences from breast cancer diagnosis and treatment to the extent that overweight/obese women have pre-existing body image distress [25,26]. However, the contribution of current body mass index (BMI), weight gain after diagnosis, and a prior history of weight gain to body image concerns among breast cancer survivors has received minimal attention. In a few studies, young breast cancer survivors and long-term survivors who gained weight after cancer diagnosis reported significantly poorer body image [5,8,24] when compared to those who did not gain weight post-diagnosis.
No studies have specifically examined body image among overweight and obese survivors; thus it is currently unknown whether and to what degree body image among overweight/obese survivors differs from body image in the general survivor population. Further, prior studies in breast cancer survivors have measured body image as a single construct, e.g. body dissatisfaction or distress [4–6,8,24]. While this is important to evaluate overall body image among survivors, it is also necessary to examine dimensions of body image. Body image is described as a multi-dimensional construct comprised of thoughts, feelings, and behaviors [1,27,28] and in breast cancer survivors, body image includes some unique dimensions such as loss of femininity and avoidance of activities due to embarrassment from treatment side effects [29]. The Body Image and Relationships Scale (BIRS) [29] was developed specifically for female breast cancer survivors and provides an overall body image score, as well as dimension scores, thus allowing for a nuanced examination of body image in this population and providing a venue through which body image scores among survivors with different characteristics, such as weight can be compared across samples.
The purpose of the current study was to evaluate the effects of weight gain since diagnosis, largest weight fluctuation in adulthood, and current BMI on breast cancer specific body image constructs among overweight/obese breast cancer survivors, as measured by the BIRS. Investigating the complex relationship between weight factors and multiple body image dimensions may facilitate the identification of women who may be at particular risk for poor body image following treatment and may inform the focus of potential prevention and intervention efforts. Because of a lack of prior research on this topic, no a priori hypotheses were specified.
Methods
Study Design
Data from the current study were obtained from a baseline assessment conducted during a randomized controlled trial designed to examine the effectiveness of an 18-month phone-delivered weight management intervention (NIH R01 CA155014) with 210 postmenopausal breast cancer survivors from large rural (n=98) or small rural/isolated (n=112) communities [30]. The study protocol has been described previously [31]. During the baseline study visit the following data were collected: anthropomorphic measurements, chart verified breast cancer history, and self-report questionnaires about medical history, physical activity, and body image. Eligible criteria consisted of: 1) female breast cancer survivor, 2) BMI between 27–45 kg/m2, 3) diagnosed with Stage 0-IIIc disease within the past 10 years, 4) completed treatment within three months of starting the study, and 5) had clearance from their oncologist/medical provider. Women were ineligible if they participated in a formal weight loss program or took medication for weight loss six months prior to enrollment, gained or lost 10 pounds or more within three months of enrollment, or if they screened positive for substance abuse, major depression, or binge eating disorder. The University of Kansas Medical Center Human Subjects Committee approved the study.
Measures
Body image
Breast cancer specific body image was measured with the Body Image and Relationships Scale [29]. The BIRS includes 32 items that assess self-perceptions of health and physical strength, appearance, sexuality, and social functioning. Items are phrased to assess the impact of breast cancer treatment on each of the domains, and are rated on a five-point Likert scale, from 1 “strongly disagree” to 5 “strongly agree” with higher scores indicating poorer body image. The BIRS has demonstrated internal consistency, test-retest reliability, and convergent validity with the Short-Form 36 and other quality of life measures [29,32]. Prior factor analysis using data from obese, rural breast cancer survivors revealed six dimensions: 1) social activity restriction due to concern about physical effects from breast cancer treatment (e.g., “I restricted my social activities because of my hot flashes”), 2) energy and strength (“My lack of energy prevented me from doing things I wanted to do”), 3) embarrassment about appearance (“I felt uncomfortable or embarrassed because I was out of shape”), 4) body integrity (“My body felt whole to me”), 5) sense of control over physical health (“The things that determined my health felt beyond my control”), and 6) sexuality (“I have felt sexually attractive”) [33].
Weight history
Weight history was measured with a Weight History Questionnaire modified from the National Health and Nutrition Examination Survey (NHANES) [34]. Items inquire about weight at the time of breast cancer diagnosis, heaviest weight in adulthood (since age 18, not including pregnancies) that was maintained within five pounds for at least one year, and lowest weight in adulthood that was maintained for at least one year. Retrospective recall of weight in early adulthood has been demonstrated to have adequate reliability and validity among older women [35–37] and correlates highly (r = .88) with weight reported up to 26 years earlier [37]. Weight change since diagnosis was calculated by subtracting self-reported weight at diagnosis from current weight, as has been done previously [24]. Largest weight fluctuation was calculated by subtracting heaviest weight in adulthood from lowest weight in adulthood. The retrospective self-report measure of largest weight fluctuation is an acceptable measure that has been used in previous studies [25,39,40].
Weight and BMI
Participants were weighed without shoes in light clothing (shorts and T-shirt) to the nearest 0.1 pound using a digital scale (Befour, Inc). Height was measured without shoes and rounded to the nearest 0.1 cm. Height and weight measurements were used to calculate body mass index (BMI; kg/m2).
Treatment information
Treatment-related information was reported by participants and verified by chart review including time since treatment completion, anti-hormone therapy status, surgery type, and history of radiation and chemotherapy.
Data Analysis
Analyses were conducted using SPSS Version 22 [41]. All data used in the current analyses were required for study entry and there were no missing data.
Multiple linear regression models were used to examine the relationship between three weight variables: weight gain since diagnosis, largest weight fluctuation in adulthood, and current BMI with breast cancer specific body image, while controlling for potential confounding variables: age, marital status, years since treatment completion, type of surgery (breast-conserving surgery or mastectomy), history of chemotherapy treatment, history of radiation therapy and current/past use of anti-hormone therapy [1,5,6,24,42]. Separate regression models were constructed for the BIRS total score and six body image subscales.
In addition to the main analyses, we explored whether a prior history of weight fluctuation and weight gain since diagnosis had compounded effects on body image by including an interaction term in the model predicting the BIRS total score.
Results
Participant demographic information is displayed in Table 1. Nineteen percent of participants were overweight (BMI of 27–29.9 kg/m2) and 81% were obese (BMI of 30–45 kg/m2).
Table 1.
Demographic Variable | M (SD) or n (%) |
---|---|
Age | 58.0 (8.2) |
Age at Diagnosis | 54.0 (8.3) |
BMI | 34.0 (4.4) |
Time since treatment (years) | 3.5 (2.4) |
Stage | |
0 | 18 (8.6%) |
I | 85 (40.5%) |
II | 76 (36.2%) |
III | 31 (14.8%) |
Race/Ethnicity (Caucasian) | 204 (97.1%) |
Marital Status | |
Married/Cohabitating | 182 (86.7%) |
Treatment Received | |
Breast-conserving surgery | 104 (49.5%) |
Mastectomy | 106 (50.5%) |
Radiation | 145 (69.0%) |
Chemotherapy | 145 (69.0%) |
Anti-hormone Therapy | 149 (71.0%) |
Table 2 presents descriptive statistics for predictor and outcome variables. Mean BMI for the sample was 34.0 (SD= 4.4). Mean weight change since diagnosis was 6.5 kg and the mean for largest weight fluctuation in adulthood was 32.1 kg. Mean total BIRS score was 81.7 (SD = 17.3). When accounting for the differences in the number of items in each subscale, scores on the energy and strength subscale were highest (M = 3.7 out of 5) and scores for social activity restriction subscale were the lowest (M = 1.9 out of 5). The Cronbach’s alpha for the six dimensions indicated high internal consistency among three dimensions (restriction of social activities: α= .88; energy and strength: α= .89; and body integrity: α= .82) and moderate internal consistency among three dimensions (embarrassment about appearance: α= .69; sense of control: α= .64; sexuality: α= .48).
Table 2.
Weight Predictor Variables | M ± SD (Range) | |
---|---|---|
BMI (kg/m2) | 34.0 ± 4.4 (27–45) | |
Weight change from diagnosis to current weight (kg) | 6.5 ± 9.7 (−20.8 – 36.2) | |
Largest weight fluctuation during adulthood (kg) | 32.1 ± 12.1 (4.5 – 67.1) | |
BIRS Outcome Variables |
Scores Standardized on a 5 Point Scale M± SD |
|
Total score | 81.7 ± 17.3 (33–129) | |
Dimension scores | ||
Restriction of social activities (9 items) | 16.9 ± 7.2 (6.0–38.7) | 1.9 ± 0.8 |
Energy and strength (7 items) | 22.2 ± 6.0 (7.0–28.7) | 3.7 ± 0.7 |
Discomfort or embarrassment due to appearance (5 items) | 17.9 ± 3.8 (6.0–25.0) | 3.6 ± 0.8 |
Body integrity (3 items) | 8.7 ± 2.7 (3.0–15.0) | 2.9 ± 0.9 |
Sense of control (3 items) | 6.5 ± 2.0 (3.0–12.0) | 2.2 ± 0.7 |
Sexuality (3 items) | 6.5 ± 2.0 (3.0–15.0) | 2.2 ± 0.7 |
Note: BIRS total score ranges from 23–160. BIRS dimension scores are presented as they were used in data analysis and also standardized on a 5 point scale to facilitate comparison of dimension score means in the table. Scores were standardized by dividing the each dimension score by the number of items in the dimension.
Multiple Regression Models
Results from our first multiple regression model indicated that largest weight fluctuation in adulthood was significantly associated with overall body image (b = 0.35, p = .006, CI = .12, .57) and weight change since diagnosis approached significance (b = 0.26, p = .05, CI = .002, .512) (Table 3). Every 1 kg increase in weight fluctuation in adulthood was associated with a 0.35 point increase in BIRS total score after controlling for age, marital status, years since treatment, type of surgery (breast-conserving surgery or mastectomy), history of chemotherapy, history of radiation, and current/past use of anti-hormone therapy. Every 1 kg increase in weight gain since diagnosis was associated with a 0.26 point increase in BIRS total score, when controlling for the aforementioned variables. Current BMI was not significantly associated with BIRS total score (b = −0.63, p = .07, CI = −1.31, .04; Table 3). In addition, age was significantly associated with BIRS total score, with older individuals having lower BIRS scores (indicating better body image) than younger individuals (b = −0.36, p = .02, CI = −0.66, −0.06; Table 3).
Table 3.
DV: BIRS total Score | ||||
---|---|---|---|---|
| ||||
b | SE | p | 95% CI (low, high) | |
Weight change since diagnosisa | 0.26 | 0.13 | .05 | (.002, .512) |
Largest weight fluctuationa | 0.35 | 0.12 | .006 | (0.12, 0.57) |
Current BMI | −0.63 | 0.34 | .07 | (−1.31, .04) |
Age | −0.36 | 0.15 | .02 | (−0.66, −0.06) |
Marital status (married/not married) | 4.85 | 3.50 | .17 | (−2.04, 11.75) |
Type of breast cancer surgeryb | 3.72 | 3.11 | .23 | (−2.41, 9.85) |
Years since treatment completion | 0.14 | 0.49 | .77 | (−0.83, 1.12) |
Chemotherapy treatment (yes/no) | 4.39 | 2.79 | .12 | (−1.11, 9.89) |
Radiation Therapy (yes/no) | 2.24 | 3.27 | .50 | (−4.21, 8.69) |
Anti-hormone therapy(yes/no) | 0.68 | 2.65 | .80 | (−4.54, 5.90) |
Note. DV: dependent variable; b: unstandardized regression coefficient; SE: standard error; p: p-value; CI: confidence interval; BMI: body mass index.
Weight change in kilograms.
Breast-conserving surgery/mastectomy. Breast-conserving surgery was the reference group.
Results from the model that included an interaction term between weight gain since diagnosis and weight fluctuation indicated there was no moderating relationship with total BIRS score when controlling for the aforementioned potential variables (b = −0.007, p= .52, CI = −.03, .01).
The remaining six multiple regression models examined the relationship between the three weight variables with each of six BIRS body image dimensions, again controlling for age, marital status, years since treatment, type of surgery (breast-conserving surgery or mastectomy), history of chemotherapy, history of radiation, and current/past use of anti-hormone therapy. Results are presented in Table 4. Larger weight fluctuation in adulthood was associated with greater social activity restriction (b = 0.15, p = .002, CI = .05, .24), more embarrassment about appearance (b = 0.06, p = .02, CI = .01, .11), and poorer sexuality (b = 0.04, p = .004, CI = .01, .07) as a result of breast cancer treatment. Weight change since diagnosis was significantly associated with greater embarrassment about appearance as a result of breast cancer treatment (b = 0.07, p = .03, CI = .01, .12). Higher current BMI was associated with less social activity restriction (b = −0.45, p = .002, CI = −.72, −.17) and better sexuality scores (b = −0.12, p = .01, CI = −.20, −.03). Weight gain since diagnosis, weight fluctuation, and current BMI were not significantly associated with energy and strength, body integrity, or sense of control dimensions (Table 4).
Table 4.
DV: BIRS Social Activity Restriction
|
||||
---|---|---|---|---|
b | SE | p | 95%CI (low, high) | |
Weight change since diagnosisa | 0.10 | .05 | .07 | (−.01, .20) |
Largest weight fluctuationa | 0.15 | .05 | .002 | (.05, .24) |
Current BMI | −0.45 | .14 | .002 | (−.72, −.17) |
Age | −0.11 | .06 | .07 | (−.23, .01) |
Marital status (married/not married)b | 0.86 | 1.43 | .55 | (−1.96, 3.68) |
Type of surgery (breast-conserving/mastectomy)c | 4.30 | 1.27 | .001 | (1.80, 6.81) |
Years since treatment completion | −0.45 | .20 | .03 | (−.85, −.05) |
Chemotherapy treatment (yes/no) | 0.30 | 1.14 | .80 | (−1.96, 2.55) |
Radiation Therapy (yes/no) | 2.24 | 1.34 | .10 | (−.40, 4.88) |
| ||||
DV: BIRS Energy and Strength
|
||||
b | SE | p | 95%CI (low, high) | |
| ||||
Weight change since diagnosisa | 0.04 | .05 | .40 | (−.05, .13) |
Largest weight fluctuationa | 0.06 | .04 | .12 | (−.02, .14) |
BMI | 0.02 | .12 | .87 | (−.22, .26) |
Age | −0.12 | .05 | .03 | (−.22, −.01) |
Marital status (married/not married) b | 2.37 | 1.23 | .06 | (−.05, 4.79) |
Type of surgery (lumpectomy/mastectomy)c | −0.65 | 1.09 | .55 | (−2.81, 1.50) |
Years since treatment completion | 0.24 | .17 | .17 | (−.10, .58) |
Chemotherapy treatment (yes/no) | 2.07 | .98 | .04 | (.14, 4.01) |
Radiation Therapy (yes/no) | 0.17 | 1.15 | .88 | (−2.09, 2.44) |
| ||||
DV: BIRS Embarrassment about Appearance
|
||||
b | SE | p | 95%CI (low, high) | |
| ||||
Weight change since diagnosisa | 0.07 | .03 | .03 | (.01, .12) |
Largest weight fluctuationa | 0.06 | .03 | .02 | (.01, .11) |
BMI | −0.08 | .08 | .33 | (−.23, .08) |
Age | −0.03 | .03 | .43 | (−.10, .04) |
Marital status (married/not married) b | 0.03 | .79 | .97 | (−1.52, 1.59) |
Type of surgery (lumpectomy/mastectomy)b | −0.21 | .70 | .77 | (−1.59, 1.18) |
Years since treatment completion | 0.16 | .11 | .15 | (−.06, .38) |
Chemotherapy treatment (yes/no) | 0.88 | .63 | .17 | (−.36, 2.12) |
Radiation Therapy (yes/no) | −0.02 | .74 | .98 | (−1.47, 1.43) |
| ||||
DV: BIRS Body Integrity
|
||||
b | SE | p | 95%CI (low, high) | |
| ||||
Weight change since diagnosisa | 0.03 | .02 | .14 | (−.01, .07) |
Largest weight fluctuationa | 0.01 | .02 | .50 | (−.02, .05) |
BMI | −0.02 | .06 | .73 | (−.13, .09) |
Age | −0.06 | .02 | .02 | (−.12, −.01) |
Marital status (married/not married) b | 0.75 | .56 | .19 | (−.36, 1.86) |
Type of surgery (lumpectomy/mastectomy)c | −0.56 | .50 | .26 | (−1.56, .43) |
Years since treatment completion | 0.03 | .08 | .68 | (−.12, .19) |
Chemotherapy treatment (yes/no) | 1.04 | .45 | .02 | (.15, 1.93) |
Radiation Therapy (yes/no) | −0.52 | .53 | .33 | (−1.56, .52) |
| ||||
DV: BIRS Sense of Control
|
||||
b | SE | p | 95%CI (low, high) | |
| ||||
Weight change since diagnosisa | 0.01 | .02 | .52 | (−.02, .04) |
Largest weight fluctuationa | 0.02 | .01 | .16 | (−.01, .05) |
BMI | 0.01 | .04 | .88 | (−.07, .09) |
Age | −0.02 | .02 | .35 | (−.05, .02) |
Marital status (married/not married) b | 0.80 | .42 | .06 | (−.02, 1.62) |
Type of surgery (lumpectomy/mastectomy)c | 0.43 | .37 | .25 | (−.30, 1.16) |
Years since treatment completion | 0.10 | .06 | .11 | (−.02, .21) |
Chemotherapy treatment (yes/no) | .0001 | .33 | 1.00 | (−.66, .66) |
Radiation Therapy (yes/no) | −0.07 | .39 | .86 | (−.84, .70) |
| ||||
DV: BIRS Sexuality
|
||||
b | SE | p | 95%CI (low, high) | |
| ||||
Weight change since diagnosisa | 0.02 | .02 | .29 | (−.02, .05) |
Largest weight fluctuationa | 0.04 | .02 | .004 | (.01, .07) |
BMI | −0.12 | .04 | .01 | (−.20, −.03) |
Age | −0.03 | .02 | .11 | (−.07, .01) |
Marital status (married/not married) b | 0 .04 | .45 | .94 | (−.84, .91) |
Type of surgery (lumpectomy/mastectomy)c | 0.41 | .40 | .30 | (−.37, 1.19) |
Years since treatment completion | 0.07 | .06 | .29 | (−.06, .19) |
Chemotherapy treatment (yes/no) | 0.11 | .36 | .76 | (−.59, .81) |
Radiation Therapy (yes/no) | 0.43 | .42 | .30 | (−.39, 1.26) |
Note. DV: dependent variable; b: unstandardized regression coefficient; SE: standard error; p: p-value; CI: confidence interval; BMI: body mass index.
Weight in kilograms.
Not married was the reference group.
Breast-conserving surgery was the reference group.
Conclusions
The purpose of the study was to examine the association between multiple dimensions of body image and weight-related variables that may be associated with breast-cancer specific body image. Our findings indicated that largest weight fluctuation in adulthood was associated with overall body image and the three socially-related body image dimensions (social activity restriction, embarrassment about appearance, and sexuality), indicating that the larger the weight fluctuation, he poorer the body image. These moderately-sized effects were present even when controlling for weight change since diagnosis, BMI, and treatment-related variables. It may be that pre-existing general body image concerns resulting from a history of weight gain predisposes women to breast-cancer specific body image concerns. We did investigate whether there were compound effects from both gaining weight previously in adulthood and after diagnosis with breast cancer, however a resultant non-significant interaction indicated that the two variables are independently associated with breast-cancer specific body image following treatment. There were small effect sizes that corresponded to the associations between weight history and three body image dimensions. In addition, there was a pattern to the associations with body image dimensions: significant associations were found with the socially-related dimensions, but not the internally-oriented dimensions (e.g., body integrity); thus our findings may suggest that largest weight fluctuation in adulthood may be relevant to the social aspects of body image.
Weight gain since diagnosis had weaker associations with overall body image and the six dimensions when we controlled for largest weight fluctuation in adulthood and current BMI. Thus, our findings indicate that among overweight/obese survivors who are several years (Mean = 3.5) beyond treatment, weight gained during treatment may not be as important to breast cancer specific body image as is weight fluctuation during adulthood.
Current BMI was not significantly associated with overall body image when controlling for the effects of largest weight fluctuation and weight gain since diagnosis. Our findings are in contrast to other studies with breast cancer survivors that reported significantly higher BMI was associated with worse body image [6,24,43,44]. Our results suggest that largest weight fluctuation in adulthood may actually be more strongly related to current body image than current BMI and speak to importance of examining weight fluctuation history. In addition, we found that current BMI was significantly associated with two body image dimensions related to social effects of breast cancer treatment, however the association was negative, indicating that women with higher current BMI had less social activity restriction and better body image related to their sexuality. Overweight/obese women often have a history of negative social interactions or negative feelings related to sexual attractiveness due to their weight [45], and this may make them more resilient when dealing with negative social or sexual breast cancer treatment effects. Alternatively, overweight/obese breast cancer survivors may already restrict social activities due to concerns about their bodies compared to normal weight peers [46], and thus the effects from the cancer treatment may not have further changed their concerns. More research in this area is warranted, particularly if it points to potential areas of resilience.
Finally, in line with previous research [1,9], we found small to moderate associations between age and breast cancer specific body image; older participants had better body image than younger participants. This relationship was maintained even after controlling for the weight and treatment-related variables. Thus, our results add to the body of literature indicating that younger breast cancer survivors may be at higher risk for poor body image following cancer treatment.
Our study was conducted in a sample of overweight/obese breast cancer survivors who were seeking treatment for weight management. Thus, it is possible that these participants may have had more body image concerns than overweight/obese survivors not seeking weight loss or the general survivor population. While there are no BIRS cut point scores that indicate clinically significant body image impairment, we can say that most scores were moderate when considered within each dimension’s subscale range and that our sample did have higher BIRS scores than those in a general breast cancer survivor sample [47]. Also, our sample had similar scores to survivors with lymphedema [48], a body and treatment-related issue. The degree to which these weight-related constructs are related to breast cancer-specific body image concerns in a general survivor population should be investigated. Further examination and comparison of these weight constructs in overweight/obese survivors versus normal weight survivors would provide information about the treatment needs of these individuals and would inform early supportive care and intervention efforts.
Several studies have evaluated change in body image among breast cancer survivors during lifestyle or physical activity-based interventions [43,47,48]; however, no studies have been conducted to directly treat body image dissatisfaction among obese breast cancer survivors. Findings from the current study indicate that for survivors with a large weight fluctuation in adulthood and weight gain following treatment, addressing these issues within the context of a weight loss or physical activity intervention may further enhance intervention effects on body image. For example, cognitive-behaviorally based interventions could add treatment modules on body image related to both cancer and weight, and directly address negative thought and behavior patterns that might be related to previous weight fluctuation and weight gain during treatment.
The study had several limitations. First, the study was cross-sectional and thus could not determine at what time in participants’ lives weight fluctuation influenced body image. Also, the study used retrospective recall of weight fluctuation and weight at diagnosis, however retrospective recall of weight during adulthood has been found to be valid, particularly in older women [35–37,49] and was assessed using a commonly used approach [34]. Finally, multiple analyses were run; thus the possibility of encountering a Type I error was increased. However, we chose not to adjust p values in these exploratory analyses to avoid increasing the probability of a Type II error [50–53], a method considered appropriate for exploratory investigations [54].
The study had several strengths. First, we assessed body image using a questionnaire designed specifically for female breast cancer survivors [29] and evaluated the influence of weight history variables on multiple dimensions of body image, providing a more nuanced approach to examining these relationships than has been conducted previously in the literature. In doing so, we identified that largest weight fluctuation during adulthood was more strongly associated with overall body image and socially-related body image dimensions than weight gain following diagnosis or BMI.
Implications
Our findings indicate that women with a history of a large weight fluctuation in adulthood and weight gain following cancer diagnosis may be particularly prone to poorer breast cancer specific body image after treatment. Largest weight fluctuation may be particularly relevant to social aspects of body image. Patients with a history of these weight issues should be identified at the time of diagnosis or early in cancer treatment in order to intervene early with body image issues that may arise. In this regard, basing risk for body image problems on current BMI alone may not be sufficient, and weight fluctuation in adulthood should be considered. Weight loss and physical activity interventions for obese breast cancer survivors that directly address these weight history factors may further improve survivors’ body image, a topic that warrants further investigation. Early intervention is ideal in order to help survivors optimize their quality of life post-treatment.
Footnotes
Registered Clinical Trial: NCT01441011
The authors declare no conflicts of interest.
References
- 1.Fingeret MC, Teo I, Epner DE. Managing body image difficulties of adult cancer patients: Lessons from available research. Cancer. 2014 Mar 1;120:633–641. doi: 10.1002/cncr.28469. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Helms RL, O’Hea EL, Corso M. Body image issues in women with breast cancer. Psychol Health Med. 2008 May 1;13:313–325. doi: 10.1080/13548500701405509. [DOI] [PubMed] [Google Scholar]
- 3.Montazeri A. Health-related quality of life in breast cancer patients: a bibliographic review of the literature from 1974 to 2007. J Exp Clin Cancer Res CR. 2008;27:32. doi: 10.1186/1756-9966-27-32. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Fobair P, Stewart SL, Chang S, D’Onofrio C, Banks PJ, Bloom JR. Body image and sexual problems in young women with breast cancer. Psychooncology. 2006 Jul 1;15:579–594. doi: 10.1002/pon.991. [DOI] [PubMed] [Google Scholar]
- 5.Falk Dahl CA, Reinertsen KV, Nesvold I-L, Fosså SD, Dahl AA. A study of body image in long-term breast cancer survivors. Cancer. 2010 Aug 1;116:3549–3557. doi: 10.1002/cncr.25251. [DOI] [PubMed] [Google Scholar]
- 6.Collins KK, Liu Y, Schootman M, Aft R, Yan Y, Dean G, et al. Effects of breast cancer surgery and surgical side effects on body image over time. Breast Cancer Res Treat. 2011 Feb;126:167–176. doi: 10.1007/s10549-010-1077-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Härtl K, Janni W, Kästner R, Sommer H, Strobl B, Rack B, et al. Impact of medical and demographic factors on long-term quality of life and body image of breast cancer patients. Ann Oncol. 2003 Jul 1;14:1064–1071. doi: 10.1093/annonc/mdg289. [DOI] [PubMed] [Google Scholar]
- 8.Raggio GA, Butryn ML, Arigo D, Mikorski R, Palmer SC. Prevalence and correlates of sexual morbidity in long-term breast cancer survivors. Psychol Health. 2014;29:632–650. doi: 10.1080/08870446.2013.879136. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Avis NE, Crawford S, Manuel J. Psychosocial problems among younger women with breast cancer. Psychooncology. 2004;13:295–308. doi: 10.1002/pon.744. [DOI] [PubMed] [Google Scholar]
- 10.DeGeorge D, Gray JJ, Fetting JH, Rolls BJ. Weight gain in patients with breast cancer receiving adjuvant treatment as a function of restraint, disinhibition, and hunger. Oncol Nurs Forum. 1990 Jun;17:23–28. discussion 28–30. [PubMed] [Google Scholar]
- 11.Avis NE, Crawford S, Manuel J. Quality of life among younger women with breast cancer. J Clin Oncol Off J Am Soc Clin Oncol. 2005 May 20;23:3322–3330. doi: 10.1200/JCO.2005.05.130. [DOI] [PubMed] [Google Scholar]
- 12.Parker PA, Youssef A, Walker S, Basen-Engquist K, Cohen L, Gritz ER, et al. Short-Term and Long-Term Psychosocial Adjustment and Quality of Life in Women Undergoing Different Surgical Procedures for Breast Cancer. Ann Surg Oncol. 2007 Nov 1;14:3078–3089. doi: 10.1245/s10434-007-9413-9. [DOI] [PubMed] [Google Scholar]
- 13.den Heijer M, Seynaeve C, Timman R, Duivenvoorden HJ, Vanheusden K, Tilanus-Linthorst M, et al. Body image and psychological distress after prophylactic mastectomy and breast reconstruction in genetically predisposed women: a prospective long-term follow-up study. Eur J Cancer Oxf Engl. 1990 Jun;48:1263–1268. doi: 10.1016/j.ejca.2011.10.020. 2012. [DOI] [PubMed] [Google Scholar]
- 14.Begovic-Juhant A, Chmielewski A, Iwuagwu S, Chapman LA. Impact of body image on depression and quality of life among women with breast cancer. J Psychosoc Oncol. 2012;30:446–460. doi: 10.1080/07347332.2012.684856. [DOI] [PubMed] [Google Scholar]
- 15.Moreira H, Canavarro MC. The association between self-consciousness about appearance and psychological adjustment among newly diagnosed breast cancer patients and survivors: the moderating role of appearance investment. Body Image. 2012 Mar;9:209–215. doi: 10.1016/j.bodyim.2011.11.003. [DOI] [PubMed] [Google Scholar]
- 16.Shimozuma K, Ganz PA, Petersen L, Hirji K. Quality of life in the first year after breast cancer surgery: rehabilitation needs and patterns of recovery. Breast Cancer Res Treat. 1999 Jul 1;56:45–57. doi: 10.1023/a:1006214830854. [DOI] [PubMed] [Google Scholar]
- 17.Morone G, Iosa M, Fusco A, Scappaticci A, Alcuri MR, Saraceni VM, et al. Effects of a Multidisciplinary Educational Rehabilitative Intervention in Breast Cancer Survivors: The Role of Body Image on Quality of Life Outcomes. Sci World J. 2014 Oct 28;2014:e451935. doi: 10.1155/2014/451935. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Cui Y, Whiteman MK, Flaws JA, Langenberg P, Tkaczuk KH, Bush TL. Body mass and stage of breast cancer at diagnosis. Int J Cancer. 2002 Mar 10;98:279–283. doi: 10.1002/ijc.10209. [DOI] [PubMed] [Google Scholar]
- 19.Porter GA, Inglis KM, Wood LA, Veugelers PJ. Effect of Obesity on Presentation of Breast Cancer. Ann Surg Oncol. 2006 Jan 30;13:327–332. doi: 10.1245/ASO.2006.03.049. [DOI] [PubMed] [Google Scholar]
- 20.Caan B, Sternfeld B, Gunderson E, Coates A, Quesenberry C, Slattery ML. Life After Cancer Epidemiology (LACE) Study: a cohort of early stage breast cancer survivors (United States) Cancer Causes Control CCC. 2005 Jun;16:545–556. doi: 10.1007/s10552-004-8340-3. [DOI] [PubMed] [Google Scholar]
- 21.Chen CL, Shore AD, Johns R, Clark JM, Manahan M, Makary MA. The impact of obesity on breast surgery complications. Plast Reconstr Surg. 2011 Nov;128:395e–402e. doi: 10.1097/PRS.0b013e3182284c05. [DOI] [PubMed] [Google Scholar]
- 22.Kroenke CH, Chen WY, Rosner B, Holmes MD. Weight, weight gain, and survival after breast cancer diagnosis. J Clin Oncol Off J Am Soc Clin Oncol. 2005 Mar 1;23:1370–1378. doi: 10.1200/JCO.2005.01.079. [DOI] [PubMed] [Google Scholar]
- 23.Befort CA, Klemp J. Sequelae of Breast Cancer and the Influence of Menopausal Status at Diagnosis Among Rural Breast Cancer Survivors. J Womens Health. 2011 Sep;20:1307–1313. doi: 10.1089/jwh.2010.2308. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Rosenberg SM, Tamimi RM, Gelber S, Ruddy KJ, Kereakoglow S, Borges VF, et al. Body image in recently diagnosed young women with early breast cancer. Psychooncology. 2013 Aug 1;22:1849–1855. doi: 10.1002/pon.3221. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Thomas CD. Stable vs unstable weight history, body-image, and weight concern in women of average body weight. Psychol Rep. 1991 Apr;68:491–499. doi: 10.2466/pr0.1991.68.2.491. [DOI] [PubMed] [Google Scholar]
- 26.McLaren L, Hardy R, Kuh D. Women’s body satisfaction at midlife and lifetime body size: A prospective study. Health Psychol. 2003 Jul;22:370–377. doi: 10.1037/0278-6133.22.4.370. [DOI] [PubMed] [Google Scholar]
- 27.Fingeret M. Body image and disfigurement. In: Duffy J, Valentine A, editors. Anderson Manual of Psychosocial Oncology. Columbus, OH: McGraw-Hill; 2010. pp. 271–288. [Google Scholar]
- 28.Cash T. Cognitive-behavioral perspectives on body image. In: Cash T, Smolak L, editors. Body Image: A Handbook of Science, Practice and Prevention. New York, NY: Guilford Press; 2011. pp. 39–47. [Google Scholar]
- 29.Hormes JM, Lytle LA, Gross CR, Ahmed RL, Troxel AB, Schmitz KH. The Body Image and Relationships Scale: Development and Validation of a Measure of Body Image in Female Breast Cancer Survivors. J Clin Oncol. 2008 Mar 10;26:1269–1274. doi: 10.1200/JCO.2007.14.2661. [DOI] [PubMed] [Google Scholar]
- 30.United States Census Bureau. 2010 Census Urban and Rural Classification and Urban Area Criteria [Internet] 2010 [cited 2014 Dec 10];Available from: http://www.census.gov/geo/reference/ua/urban-rural-2010.html.
- 31.Befort CA, Bennett L, Christifano D, Klemp JR, Krebill H. Effective recruitment of rural breast cancer survivors into a lifestyle intervention. Psychooncology. 2014 doi: 10.1002/pon.3614. n/a–n/a. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Hedin Larsson Y, Speck R, Schmitz KH, Johansson K, Gyllensten AL. The Body Image and Relationship Scale: A Swedish translation, cultural adaptation, and reliability and validity testing. Eur J Physiother. 2014 Jun 1;16:67–75. [Google Scholar]
- 33.Hunter R. Changes in Body Image and Sexuality in Rural Breast Cancer Survivors After a Weight Loss and Weight Maintenance Intervention. 2015 [Google Scholar]
- 34.National Center for Health Statistics. NHANES - National Health and Nutrition Examination Survey Homepage [Internet] [cited 2014 Dec 12];Available from: http://www.cdc.gov/nchs/nhanes.htm.
- 35.Stommel M, Schoenborn CA. Accuracy and usefulness of BMI measures based on self-reported weight and height: findings from the NHANES & NHIS 2001–2006. BMC Public Health. 2009 Nov 19;9:421. doi: 10.1186/1471-2458-9-421. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Casey VA, Dwyer JT, Coleman KA, Krall EA, Gardner J, Valadian I. Accuracy of recall by middle-aged participants in a longitudinal study of their body size and indices of maturation earlier in life. Ann Hum Biol. 1991 Apr;18:155–166. doi: 10.1080/03014469100001492. [DOI] [PubMed] [Google Scholar]
- 37.Kyulo NL, Knutsen SF, Tonstad S, Fraser GE, Singh PN. Validation of recall of body weight over a 26-year period in cohort members of the Adventist Health Study 2. Ann Epidemiol. 2012 Oct;22:744–746. doi: 10.1016/j.annepidem.2012.06.106. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Jeffery RW, Wing RR, French SA. Weight cycling and cardiovascular risk factors in obese men and women. Am J Clin Nutr. 1992 Mar;55:641–644. doi: 10.1093/ajcn/55.3.641. [DOI] [PubMed] [Google Scholar]
- 39.Melby CL, Sylliaasen S, Rhodes T. Diet-induced weight loss and metabolic changes in obese women with high versus low prior weight loss/regain [Internet] Nutr Res USA. 1991 [cited 2015 Aug 14];Available from: http://agris.fao.org/agris-search/search.do?recordID=US9170129.
- 40.Serdar KL, Mazzeo SE, Mitchell KS, Aggen SH, Kendler KS, Bulik CM. Correlates of weight instability across the lifespan in a population-based sample. Int J Eat Disord. 2011 Sep;44:506–514. doi: 10.1002/eat.20845. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.IBM. SPSS. 2013 [Google Scholar]
- 42.Ålgars M, Santtila P, Varjonen M, Witting K, Johansson A, Jern P, et al. The Adult Body: How Age, Gender, and Body Mass Index Are Related to Body Image. J Aging Health. 2009 Dec 1;21:1112–1132. doi: 10.1177/0898264309348023. [DOI] [PubMed] [Google Scholar]
- 43.Befort CA, Klemp JR, Austin HL, Perri MG, Schmitz KH, Sullivan DK, et al. Outcomes of a weight loss intervention among rural breast cancer survivors. Breast Cancer Res Treat. 2012 Apr 1;132:631–639. doi: 10.1007/s10549-011-1922-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 44.Herman DR, Ganz PA, Petersen L, Greendale GA. Obesity and cardiovascular risk factors in younger breast cancer survivors: The Cancer and Menopause Study (CAMS) Breast Cancer Res Treat. 2005 Sep;93:13–23. doi: 10.1007/s10549-005-2418-9. [DOI] [PubMed] [Google Scholar]
- 45.Puhl RM, Heuer CA. The Stigma of Obesity: A Review and Update. Obesity. 2009 May 1;17:941–964. doi: 10.1038/oby.2008.636. [DOI] [PubMed] [Google Scholar]
- 46.Kuskowska-Wolk A, Rössner S. Decreased social activity in obese adults. Diabetes Res Clin Pract. 1990;10(Suppl 1):S265–269. doi: 10.1016/0168-8227(90)90174-r. [DOI] [PubMed] [Google Scholar]
- 47.Benton MJ, Schlairet MC, Gibson DR. Change in quality of life among breast cancer survivors after resistance training: is there an effect of age? J Aging Phys Act. 2014 Apr;22:178–185. doi: 10.1123/japa.2012-0227. [DOI] [PubMed] [Google Scholar]
- 48.Speck RM, Gross CR, Hormes JM, Ahmed RL, Lytle LA, Hwang W-T, et al. Changes in the Body Image and Relationship Scale following a one-year strength training trial for breast cancer survivors with or at risk for lymphedema. Breast Cancer Res Treat. 2010 Jun;121:421–430. doi: 10.1007/s10549-009-0550-7. [DOI] [PubMed] [Google Scholar]
- 49.Perry GS, Byers TE, Mokdad AH, Serdula MK, Williamson DF. The validity of self-reports of past body weights by U.S. adults. Epidemiol Camb Mass. 1995 Jan;6:61–66. doi: 10.1097/00001648-199501000-00012. [DOI] [PubMed] [Google Scholar]
- 50.Cole P. The evolving case-control study. J Chronic Dis. 1979;32:15–27. doi: 10.1016/0021-9681(79)90006-7. [DOI] [PubMed] [Google Scholar]
- 51.Perneger TV. What’s wrong with Bonferroni adjustments. BMJ. 1998 Apr 18;316:1236–1238. doi: 10.1136/bmj.316.7139.1236. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Rothman KJ. No adjustments are needed for multiple comparisons. Epidemiol Camb Mass. 1990 Jan;1:43–46. [PubMed] [Google Scholar]
- 53.Thomas DC, Siemiatycki J, Dewar R, Robins J, Goldberg M, Armstrong BG. The problem of multiple inference in studies designed to generate hypotheses. Am J Epidemiol. 1985 Dec;122:1080–1095. doi: 10.1093/oxfordjournals.aje.a114189. [DOI] [PubMed] [Google Scholar]
- 54.Bender R, Lange S. Adjusting for multiple testing—when and how? J Clin Epidemiol. 2001 Apr;54:343–349. doi: 10.1016/s0895-4356(00)00314-0. [DOI] [PubMed] [Google Scholar]