Abstract
We examined the association of physical and non-physical IPV (intimate partner violence) with obesity. Women (n=1,179) were surveyed regarding demographics, obesity, and IPV exposure using HARK (humiliate-afraid-rape-kick), an IPV screening tool. A three-level lifetime IPV exposure variable measured physical, non-physical or no IPV. Healthcare provider-identified obesity was defined if participants were told by a medical provider within the past 5 years that they were obese. Bivariate analyses examined obesity by IPV and demographics. Multivariable logistic regression assessed odds of obesity by IPV type, adjusting for age, race/ethnicity, education and marital status. Among participants, 44% reported lifetime IPV (25% physical, 19% non-physical), and 24% reported healthcare provider-identified obesity. In unadjusted analyses, obesity was more prevalent among women exposed to physical IPV (30%) and non-physical IPV (27%), compared to women without IPV (20%, p=0.002). In multivariable models, women reporting physical IPV had 1.67 times greater odds of obesity (95% confidence interval [CI] 1.20, 2.33), and women reporting non-physical IPV had 1.46 times greater odds of obesity (95% CI 1.01, 2.10) compared to women reporting never exposure. This study extends prior data by showing not only an association between physical IPV and obesity, but also an association between obesity and non-physical IPV.
Keywords: domestic violence, spouse abuse, battered women, obesity, weight
BACKGROUND
The health of U.S. women is adversely affected by both intimate partner violence (IPV) and obesity. IPV is defined as emotional, physical, and/or sexual abuse which occurs between people in a close relationship and affects half of all women living in the U.S. (IOM 2010), with 36% of women reporting rape, physical violence or stalking and 48% reporting psychological aggression perpetrated by an intimate partner in their lifetimes (Black et al. 2010). IPV results in an estimated 4 million injuries among women yearly and is associated with numerous adverse physical and mental health consequences, such as post-traumatic stress disorder (PTSD), chronic pain, gastrointestinal disorders, depression, anxiety, and sleep disorders (Flegal et al. 2012). Women who experience both physical and non-physical IPV are at an increased risk for experiencing numerous health conditions and consequences (Black 2011; Bonomi et al. 2006). Non-physical forms of IPV include those in which the victim is controlled through humiliation, verbal abuse, threats of abuse to the victim or someone they love, and/or is made to feel afraid of her partner (Nelson, Bougatsos, Blazina 2012). Physical IPV includes rape, forced sexual activity, and other forms of physical violence including kicking, hitting, and slapping (Nelson, Bougatsos, Blazina 2012). Physical abuse occurs less frequently than non-physical IPV, and is often preceded by non-physical forms of IPV (Alpert 2010).
National data on obesity prevalence showed that one-third of U.S. adults were obese in 2009–2010, which translates to over 41 million women (Flegal et al. 2012). Illnesses with a higher prevalence among obese patients, include osteoarthritis, post-menopausal breast cancer, hypertension, coronary artery disease, and diabetes mellitus type 2 (IOM 2010) costing approximately 174 billion dollars each year (The Henry J. Kaiser Family Foundation 2002). Individuals with obesity and weight-related comorbidities identified by their healthcare provider tend to have more opportunities to participate in behavioral interventions (Waring et al. 2009; Sciamanna et al. 2000; Simkin et al. 2005). This allows the opportunity for discovery of other contributing factors to their obesity (Waring et al. 2009). Probing for conditions that may influence the patients’ obesity status is an important aspect when a healthcare provider performs a history and physical, and this can be done with an open respectful dialogue (Kushner 2012).
Prior research has suggested a plausible mechanism linking stressors such as IPV with obesity. Stress may lead to the development of obesity through multiple mechanisms including increased hormone release, such as cortisol or glucocorticoids, which increases desire for food (Lightman 2008). Moreover, reaction to stress may include the adoption of adverse health habits such as decreased exercise and poorer diet, allowing reinforcement of obesity-promoting habits (Dallman 2010). Increases in obesity have been observed among people facing even mild stressors, this may be secondary to their desire to eat foods high in sugar and fat (Torres and Nowson 2007). Additionally, IPV is associated with fewer visits to a primary care doctor (Bonomi et al. 2006; IOM 2010), potentially leading to decreased opportunities to intervene and prevent obesity and its related health complications.
Given that both IPV and obesity are prevalent, that IPV is likely to cause stress, and that stress and obesity are strongly linked, an association between IPV exposure and obesity appears plausible. Prior literature has shown an association between increased severe chronic stress, including physical forms of IPV, and obesity (Stene et al. 2013; Yount and Li 2011). However, these studies did not investigate or did not demonstrate an association between non-physical forms of IPV and obesity (Breiding, Black and Ryan 2008); thus, a definitive link has not been demonstrated between non-physical forms of IPV and obesity. We reasoned that obesity identified by a healthcare provider is most likely to be clinically relevant. Thus, we examined healthcare provider-identified obesity among a sample of women seeking care, and hypothesized that obesity rates would differ by history of lifetime IPV exposure (physical, non-physical or never exposed).
METHODS
Sample
The study sample was identified in two different ways. First, all women ages 18–64 years with at least one visit in the past year at an outpatient family practice network, were eligible to participate. The family practice network recruitment site included 10 unique primary care family practice locations serving a geographically diverse area of south and central Pennsylvania. Of the eligible sample of 24,338 women, potential participants were stratified by rurality (to oversample rural-residing women). Rurality was assessed using the zip-code based Rural-Urban Commuting Area codes, a classification taxonomy based on the sizes of cities and towns and daily commuting practices (Hall, Kauffman, Ricketts 2006). A three-level classification was used, allowing comparison of small rural, large rural and urban areas. To maximize participation of the most rural residents and balance participation between rural and urban residents for the parent study, we sampled 100% of the small rural residents (N=228), 42% of the large rural residents (N=1136), and 5% of the urban population (N=1136).
After stratification, a random sample of 2500 women was sent an invitation letter inviting them to participate, an informed consent document to review, and a brief survey with questions about demographics, health status, and factors that affect health, including health behaviors, IPV and other stressors. Also included was information with websites and telephone numbers to consult for questions about health, stress, adverse health behaviors and mental health.
The invitation letter clearly stated that participation was voluntary and that their medical care would not be affected in any way should they choose not to participate in the study. An upfront incentive of $2 was included with the letter and up to two reminder letters were also sent to encourage response. In addition to the introductory letter and survey, an informed consent document was included in the mailed packet. Informational materials clearly requested that all potential participants review the consent document, but did not require that the informed consent document be signed and returned by potential participants because we wanted participants to have the option to return the surveys to us anonymously. However, instructions on the paper survey clearly requested that the participant review the consent information prior to completing the survey.
This survey could be completed online, by telephone, or by mail, at the preference of the participant. If the survey was completed by telephone, the interviewer verified that the participant had fully reviewed the consent information, and again reviewed the consent information with the participant over the phone to ascertain verbal consent. If the survey was completed by the participant directly online, the consent document was embedded in the online survey, and the participant was asked to indicate that she had reviewed the consent document prior to entry into the online survey. Surveys that were returned by mail also had the consent document enclosed with the survey material, with clear instructions that the consent document be reviewed by potential participants prior to completing and returning the survey.
The sample of 2500 was pre-specified to meet the enrollment goals of the parent study. Briefly, the parent study is an ongoing, longitudinal examination of women’s strategic responses to recent and lifetime IPV, and the association of these responses with women’s mental health. The current study analyzed data collected as part of the screening process for the parent study. The sample of 2500 women was based on the anticipated participation rates in a followup survey to be administered in the parent study among women who: 1) screened positive for IPV on the survey described in this study, 2) provided their contact information and gave the investigators permission to recontact them for participation in a followup longitudinal survey, and 3) agreed to participate in the followup survey. Surveys were received from 1191 women from the clinical sample (a 48% response rate).
To augment the sample, posters were placed within a network of 26 domestic violence shelters serving Central Pennsylvania, inviting women to participate in the survey online, by phone or by mail. These shelters serve a wide variety of women in a variety of venues including housing, walk-in services, and group and individual services. The posters would also be visible to visitors to the centers who were not seeking services, as well as employees of these centers. Thus the, actual number of eligible women who viewed these posters is unknown and could not be tracked by the centers. An additional 73 women were recruited to participate in response to these posters, yielding the final sample size of 1264 women who completed the survey.
A comparison of the women recruited from the clinical sample and from the shelter population revealed no differences in age or educational level, but the shelter sample was less likely to be white, non-Hispanic (81% vs. 92%, p=0.002), more likely to be divorced or separated (30% vs. 8%, p<.001), and more likely to have experienced physical forms of violence (73% vs. 23%, p<.001) compared to the clinical sample. Obesity data were available for 1,179 participants, which comprised the analytic sample for this manuscript.
Our institution’s Institutional Review Board (IRB) reviewed and approved the study protocol and all study documents. As noted above, all women reviewed a written or verbal informed consent and consented to participate in this research. To protect participants further, and due to the sensitive nature of this study, a Certificate of Confidentiality (CC-MH-12-204) was obtained from the National Institutes of Health for this research.
Data Collection
Study data were entered and managed within REDCap (Research Electronic Data Capture), hosted by our institution. REDCap is a secure, web-based application designed to support data capture for research studies (Harris et al. 2009). Surveys were completed either directly online by the respondent or, if preferred, she could complete the survey by mail, and the data were entered by study personnel with a second study personnel performing audit verification of all data entry. Finally, if the participant requested, the survey could be completed over the phone with trained personnel reading the questions to the participant and recording her responses in the electronic data capture form.
Independent Variable
IPV exposure was determined using the humiliation-afraid-rape-kick (HARK) screening instrument, a validated 4-item screen to identify IPV in healthcare settings (Sohal, Eldridge and Feder 2007). This question was adapted to examine exposure to IPV over the respondent’s adult lifetime. A three-level IPV exposure variable was created based on a lifetime IPV exposure: physical IPV (rape-kick), non-physical IPV (humiliation-afraid) or never any IPV. Created response categories were mutually exclusive, such that if a participant reported both physical and non-physical IPV (which almost always coexist), that participant was placed into the “physical IPV” category. If a participant reported non-physical IPV only, but no physical IPV, she was placed in the “non-physical IPV” category. All other respondents were considered “never IPV.”
Dependent Variable
All respondents were asked to identify whether a doctor or health professional had told them they were obese within the last 5 years. This question was taken from the Kaiser Family Foundation Women’s Health Survey (KFFWHS) (The Henry J. Kaiser Family Foundation 2002) and stated, “In the past 5 years has a doctor or other health professional told you that you have any of the following health problems or conditions?” Answer choices were yes/no and included the line item “Obesity?” Although self-reported or measured height and weight was not asked in this survey, we felt that healthcare-provider identified obesity represented a clinically important construct for several reasons. First, physicians are more likely to provide counseling and discuss weight management with obese or overweight patients who have associated medical co-morbidities, thus more severe and clinically relevant disease (Waring et al. 2009; Tang et al. 2012; Eaton, Goodwin, and Stange 2002). Moreover, physicians are likely to promote healthy lifestyles and promote weight loss in patients who have co-morbidities associated with obesity (Waring et al. 2009 and Tang et al. 2012). Therefore, receiving a physician diagnosis of obesity likely indicated obesity that was clinically relevant and associated with other comorbidities (Waring et al. 2009; Ferguson et al. 2010). We did not perform chart abstraction as we allowed surveys to be submitted anonymously at the participant’s discretion, preventing possible links to chart abstraction for all participants.
Control Variables
Control variables, including age, education, relationship status, and race/ethnicity were selected based on strong literature linking these demographic factors to obesity (Mokdad et al. 1999; Sobal, Hanson and Frongillo 2009). Phrasing of all demographic questions were based on questions asked in population-based health surveys, including the KFFWHS, the Commonwealth Fund 1998 Survey of Women’s Health (CWF 1998), and the Central Pennsylvania Women’s Health Study (CePAWHS) (The Henry J. Kaiser Foundation 2002; Weisman et al. 2006). Educational attainment was determined based on the answer to the question, “What was the last grade or class completed in school?” and compiled into a 3-level variable (high school graduate or less, some college, college graduate or greater). We created a 4-level variable for current relationship status (married, partnered, divorced/separated, or widowed/single). Respondents were asked to describe their race/ethnicity by checking all which applied; options included white, African American/Black, Asian, Native American/American Indian, Native Hawaiian/Pacific Islander/Alaskan Native, or other (The Henry J. Kaiser Family Foundation 2002). Due to our sample being largely white, non-Hispanic, race/ethnicity was dichotomized into non-Hispanic white and other. Age was determined by asking the women “What is your age?”, identical to the phrasing in the CePAWHS survey (Weisman et al. 2006, 216–224).
Statistical Analysis
All variables were summarized with frequencies and percentages or means, medians, and standard deviations. Bivariate analyses using logistic regression examined the association between obesity and IPV type as well as the association between obesity and other demographic variables to be used as covariates for adjustment in a multivariable model. Odds ratios were used to quantify the magnitude and direction of any significant associations.
Multivariable logistic regression assessed the odds of obesity by IPV exposure, adjusting for age, race/ethnicity, education and relationship status. Our goal was not development of a parsimonious model. Rather, we retained all variables as covariates previously selected based on their association with obesity. We tested for multicollinearity using variance inflation factor (VIF) statistics from linear regression. In our study, all of the VIF statistics were less than 3; thus, no significant multicollinearity was found. To assess model fit, we used the Hosmer-Lemeshow Goodness of Fit test. In our final model, the p-value for the Hosmer-Lemeshow test was >0.05, indicating adequate fit. All analyses were performed using SAS version 9.3.
RESULTS
The mean age of respondents was 44 (SD ± 13) years, 91% of whom were non-Hispanic white; 62% were married, and 45% were college graduates. The lifetime rate of reported IPV exposure was 44% (25% physical, 19% non-physical). Twenty-four percent of the sample reported that a healthcare provider had told them they were obese within the last 5 years.
Obesity rates were higher among women exposed to physical IPV (30%), and non-physical IPV (27%) compared to women who reported no lifetime IPV exposure (20%, p=0.0021) (Table 1). Obesity was more frequent with increasing age and lower educational attainment. No significant association was observed between obesity and race/ethnicity or relationship status.
Table 1.
Characteristics | Total (N=1179) |
Obese (N=286) |
Non-Obese (N=893) |
p* |
---|---|---|---|---|
IPV type | 0.0021 | |||
No IPV exposure | 656 | 134 (20%) | 522 (80%) | |
Non-physical IPV | 223 | 61 (27%) | 162 (73%) | |
Physical IPV | 300 | 91 (30%) | 209 (70%) | |
| ||||
Age, years (mean +/− std dev.) | 43.5 ± 12.8 | 46.4 ±11.4 | 42.6 ±13.1 | <0.0001 |
| ||||
Relationship Status | 0.1630 | |||
Married | 721 | 178 (25%) | 543 (75%) | |
Partnered | 194 | 36 (19%) | 158 (81%) | |
Divorced/Separated | 109 | 32 (29%) | 77 (71%) | |
Widowed/Single | 141 | 36 (26%) | 105 (74%) | |
| ||||
Education | 0.0010 | |||
High school graduate or less | 271 | 77 (28%) | 194 (72%) | |
Some college | 366 | 105 (29%) | 261 (71%) | |
College graduate or more | 528 | 101 (19%) | 427 (81%) | |
| ||||
Race/Ethnicity | 0.7310 | |||
White, non-Hispanic | 1053 | 259 (25%) | 794 (75%) | |
Other | 104 | 24 (23%) | 80 (77%) |
P-values from logistic regression
In multivariable analyses, IPV exposure retained an independent association with obesity (p=0.0057) (Table 2). Women reporting physical IPV had 1.67 times greater odds of obesity (95% confidence interval [CI] 1.20, 2.33), and women reporting non-physical IPV had 1.46 times greater odds of obesity (95% CI 1.01, 2.10), compared to women reporting no exposure to IPV. Obesity was also associated with increasing age (adjusted odds ratio [aOR]=1.02 per one-year increase, 95% CI: 1.01,1.03) and retained an independent association with lower educational attainment with 1.42 times greater odds of obesity (95% CI: 0.99,2.04) (an association that approached significance) when comparing high school graduate or less to college graduate and 1.63 times greater odds of obesity (95% CI: 1.18, 2.25) when comparing some college education to college graduates.
Table 2.
Adjusted Odds Ratio* |
95% Confidence Interval |
||
---|---|---|---|
IPV Exposure | |||
Non-physical IPV vs. No IPV exposure | 1.46 | 1.01 | 2.10 |
Physical IPV vs. No IPV exposure | 1.67 | 1.20 | 2.33 |
| |||
Age (per one-year increase) | 1.02 | 1.01 | 1.03 |
| |||
Relationship Status | |||
Partnered vs. Married | 0.77 | 0.50 | 1.18 |
Divorced/separated vs. Married | 1.01 | 0.63 | 1.60 |
Widowed/single vs. Married | 1.14 | 0.73 | 1.78 |
| |||
Educational Status | |||
High school graduate or less vs. College graduate | 1.42 | 0.99 | 2.04 |
Some college vs. College graduate | 1.63 | 1.18 | 2.25 |
| |||
Race/Ethnicity | |||
White, non-Hispanic vs. Other | 1.05 | 0.64 | 1.71 |
Odds ratios from multivariable logistic regression
DISCUSSION
Our study reinforced prior evidence that women exposed to lifetime IPV had a greater likelihood of reporting obesity (Stene et al. 2013). Our findings extend this work by specifying healthcare provider-identified obesity, suggesting clinical relevance. Moreover, we broaden prior evidence to demonstrate an association between obesity and non-physical, in addition to physical forms, of IPV.
A possible mechanism for the association between IPV and obesity is the stress associated with IPV exposure in conjunction with underlying genetic and environmental predisposition. In response to an acute stressor, the hypothalamus-pituitary-adrenal axis releases stress hormones, such as cortisol. However, if chronic stress occurs, the stressed individual adapts such that cortisol levels remain elevated permanently (Lightman 2008). This heightened cortisol response may lead to an associated increase in obesity and other health-related problems, including cardiovascular risk factors, among those exposed to IPV (Foss and Dyrstad 2011).
In addition to increased likelihood of experiencing the hormonal stress response, IPV victims are less likely to pursue healthy diets and have good exercise habits (Foss and Dyrstad 2011; Mathew et al. 2012), contributing to increased odds of obesity. We suggest that these pathways are active both among women exposed to physical forms of IPV – as previously reported (Bonomi et al. 2006; Breiding, Black and Ryan, 2008) – and also active and affecting the health of women exposed to non-physical forms of IPV, as shown in our study.
We found a lifetime prevalence of IPV in our sample of 44%, which is similar to the prevalence reported in population-based studies (Black et al. 2010). The overall prevalence of IPV in our sample, as well as the frequency of physical IPV was slightly lower than was previously reported in a clinical sample by Coker et al. (2000). In that study, a total of 55.1% reported IPV, of whom 77.3% experienced physical IPV and 22.7% experienced non-physical IPV (Coker et al. 2000). This is likely due to the fact that Coker et al. used numerous assessment instruments to identify IPV exposure and type, whereas we used a single instrument, often used in clinical practice (Coker et al. 2000; Gerber et al. 2005; IOM. 2010; Nelson, Bougatsos, Blazina 2012; McCall-Hosenfeld, Chuang and Weisman 2013). Like the Coker study, we found a higher prevalence of physical IPV compared to non-physical IPV. This is likely because our sample was help-seeking (either engaged in primary care or recruited from domestic violence shelters). Thus, these individuals may be seeking care for the medical or psychosocial consequences of more severe forms of violence. In contrast to a help-seeking sample, a population-based sample, such as that represented by the CDC (Black et al. 2010), is likely to show a greater prevalence of nonphysical than physical IPV.
Our study findings also confirmed prior reports of greater obesity found among individuals with a lower educational level (Yu 2012), and among individuals with increasing age (Wang, Colditz and Kuntz 2007). Of note, we did not find a significant association between marital status and obesity in our study. This differs from a prior report which found increased obesity rates among married/cohabitating individuals compared to those who were single, divorced, or never married when controlled for age (Sobal, Rauschenbach and Frongillo 2003). The difference between our study and the prior report may be explained by the combined variable selection, as our study separated married individuals as the comparison group, whereas the Sobal study grouped both married and cohabitating women.
Of note, a comparison of the demographics of the women participating in this study to those available for rural Pennsylvania (The Center for Rural Pennsylvania, 2015) suggest that the women in our sample were slightly more likely to be married (61% compared to 54%), were slightly more likely to be of a race/ethnicity other than white, non-Hispanic (9% compared to 5%), and were more likely to have a bachelor’s degree or higher (45%compared to 18%).
STRENGTHS
This study had several strengths to consider, including a large sample size, allowing identification of large population exposed to both physical IPV and also non-physical IPV and providing good statistical power to detect associations with meaningful magnitude as statistically significant. Examination of non-physical IPV was also an important strength because it is a more frequent form of abuse and often is associated with other forms of abuse (Fisher, Zink and Regan 2011, 254–268). To our knowledge, this is the first study to identify the association between obesity and non-physical IPV.
LIMITATIONS
A possible limitation of our study was that the information was self-reported by participants and may have been affected by inaccurate recall. Nevertheless, self-report has been widely used, and the questions used in our survey were adapted from previous surveys of this type; thus, our use of these survey questions was concordant with research standards. Additionally, the overall prevalence of physician-identified obesity in our sample, at 25%, was slightly lower than obesity rates reported in population-based national samples, in which the prevalence of obesity among women was 35.8% (Torres and Nowson 2007). This is likely due to the fact that our obesity indicator specified identification by a healthcare provider. Physician counseling regarding obesity is inadequate (Kraschnewski et al. 2013); therefore, the slightly lower obesity prevalence in our sample likely reflects inadequate physician identification, or physician reluctance to use the potentially stigmatizing term “obesity,” rather than lower than average rates of obesity in this sample. However, as the cases of obesity in our sample were identified by a health care provider, these were likely to be clinically relevant cases of obesity (Dallman 2010; Kushner 2012).
Further limitations of our study included that the data were cross-sectional; thus, temporal relations and causality cannot be assessed. Further, the population assessed in this survey was largely white, non-Hispanic, reflective of the population of central Pennsylvania (U.S. Census Bureau Population Estimates Division 2010, Center for Rural Pennsylvania 2015). However, our findings may not be representative of more racially/ethnically diverse communities. In addition, the sample was care-seeking (either through healthcare or domestic violence shelters), and may not be representative of a population-based sample.
Moreover, our study did not capture other forms of abuse, such as Adverse Childhood Experiences – a composite measure of childhood abuse and household dysfunction (Felliti et al. 1998), which are associated with subsequent abuse and may directly predict adverse health consequences in adults, including obesity. Another potential limitation was the response rate of 48% from the mailed surveys. This modest rate compares reasonably well with other mailed and web-based surveys (Shih and Fan 2008), but nevertheless could have resulted in participation bias that could affect the accuracy and generalizability of the results.
Finally, as recommended in prior research (Zhang and Wang 2004), we used educational status as the most robust and stable marker for socioeconomic status (SES). Educational status is thought to be a better marker of SES than income, because a person’s income may be affected by body weight, and is a more stable indicator of SES over time compared to income or occupation (Zhang and Wang 2004). However, it is possible that had we chosen a different indicator of SES, our results might have been affected.
CONCLUSION
In light of the recent recommendations by the U.S. Preventive Services Task Force (USPSTF), clinicians should screen all women aged 18–44 years for IPV, allowing for earlier opportunities for intervention (Moyer 2013). Although IPV identification is important in all patient populations (Sweeney et al. 2013), it may be especially important among adult women determined by healthcare providers to be obese. We found that obesity was associated with both non-physical IPV and physical IPV. Although our study was not designed to establish a causal link between IPV and obesity or to establish firmly risk factors for obesity, its results remain clinically relevant.
Healthcare providers may leverage knowledge of risk factors, such as obesity, to improve screening rates for IPV among all women and help identify IPV-exposed women, including those women exposed to non-physical forms of IPV. The results of our study support screening for both primary and secondary prevention of IPV to reduce the adverse health consequences, such as obesity.
Acknowledgments
Supported by grant number 2012064 from the Doris Duke Charitable Foundation PI: Dr. McCall-Hosenfeld. Study data were collected and managed using REDCap electronic data capture tools hosted at Penn State. (Pennsylvania State University CTSI, NIH/NCATS grant number UL1 TR000127). Preliminary data from this work were previously presented, in part, as a poster at Women's Health 2014: The 22nd Annual Congress, Washington, DC, on 4/5/2014, and are available as an abstract in the conference proceedings.
Footnotes
Conflicts of interest: None.
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