Next Article in Journal
Medical Nature-Based Rehabilitation Program for Individuals with Exhaustion Syndrome: Changes in Quality of Life, Exhaustion Symptoms and Overall Health
Previous Article in Journal
Task-Shifting: Can Community Health Workers Be Part of the Solution to an Inactive Nation?
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Risk Factors of Health-Related Quality of Life among Gastrointestinal Cancer Survivors in the U.S.: With a Focus on Social and Behavioral Determinants of Health (SBDH)

1
Center for Healthy Aging, Self-Management and Complex Care, College of Nursing, Ohio State University, Columbus, OH 43210, USA
2
Cancer Treatment and Research Center, Ohio State University-James, Columbus, OH 43210, USA
3
Department of Biomedical Informatics, College of Medicine Ohio State University, Columbus, OH 43210, USA
4
Division of Colon and Rectal Surgery, Ohio State University-James, Columbus, OH 43210, USA
5
GI Medical Oncology Selection, Ohio State University-James, Columbus, OH 43210, USA
6
School of Nursing, University of North Carolina, Chapel Hill, NC 27514, USA
7
Division of Epidemiology, College of Public Health, Ohio State University, Columbus, OH 43210, USA
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2023, 20(17), 6676; https://doi.org/10.3390/ijerph20176676
Submission received: 5 July 2023 / Revised: 24 August 2023 / Accepted: 26 August 2023 / Published: 29 August 2023

Abstract

:
Background: Increasing numbers of long-term gastrointestinal (GI) cancer survivors highlight the importance of understanding the factors contributing to their health-related quality of life (HRQoL). We investigated the risk factors of HRQoL, including demographics, clinical characteristics, and social and behavioral determinants of health (SBDH). Methods: Data on adult GI cancer survivors (n = 3201) from the Behavioral Risk Factors Surveillance System (BRFSS) surveys from 2014–2021 (except for 2015) were analyzed. Unadjusted/adjusted logistic regression was used. Results: The majority were women (54%) and white (78%), with a median age of 67. Survivors who were 65 years or older, diagnosed with colorectal cancer, or who had fewer comorbidities were more likely to report significantly better HRQoL. Significant social factors of poor HRQoL included unmarried, racial and ethnic minorities, poor socioeconomic status, and poor healthcare access. Significant behavioral factors of poor HRQoL were lack of physical activity, heavy alcohol consumption, and current smoking, with lack of physical activity being the most significant factor. Conclusions: The SBDH has a critical role in HRQoL. Future studies are warranted to develop a tailored survivorship intervention, such as physical rehabilitation, and to explore machine learning/artificial intelligence-based predictive models to identify cancer survivors at a high risk of developing poor HRQoL.

1. Introduction

Gastrointestinal (GI) cancer is a group of cancers that can affect any part of the GI tract, such as esophageal, gastric, colorectal, anal, gall bladder, pancreatic, or liver [1]. This type of cancer is among the leading causes of death in the United States (U.S.) [2], estimated to account for 34% of cancer incidence [1]. The 5-year overall age-standardized relative GI cancer survival rate is rising due to improvements in early identification and treatment in the U.S. in all combined cancer stages and GI cancer types (from 42% in 1975–1990 to 94% in 2012–2018) [2]. It is predicted that by 2050, there will be 350,000 GI cancer survivors living in the U.S. [1,2,3].
As more GI cancer survivors live longer, their health-related quality of life (HRQoL) [3] becomes increasingly significant. Many GI cancer survivors experience poor HRQoL [4,5]. Indeed, a growing number of GI cancer survivors are not only living longer but are also burdened with the risk of cancer recurrence, financial distress, and the long-term consequences of cancer and its symptoms [5,6]. The multiple burdens for GI cancer survivors can significantly impact their HRQoL [2,4,5,7].
Notably, significant cancer survivorship disparities were observed across various social and behavioral determinants of health (SBDH), such as race, income status, education levels, and health risk behaviors [8,9]. Therefore, understanding the associations of SBDH factors with the HRQoL of GI cancer survivors can inform targeted interventions to improve their overall well-being. However, identifying GI cancer survivors at a high risk of developing poor HRQoL is under-investigated [10].
To our knowledge, while numerous studies have shown that SBDH has a significant impact on cancer survival and mortality rates [9,11,12], very few studies have examined these SBDH factors in relation to the HRQoL of cancer survivors in the U.S. [13]. For example, higher income was associated with better HRQoL, whereas lower educational status negatively impacted HRQoL among Hispanic/Latino-American cancer survivors in mixed cancer types [14] or in breast cancer survivors [15,16]. Burse et al. [13] also examined the association between SBDH and HRQoL in cancer survivors with mixed cancer types in the U.S. The study found that current smoking was positively and significantly associated with poor physical HRQoL, but healthy eating (i.e., fruit and vegetable consumption), heavy alcohol consumption, and health care coverage were not associated with HRQoL after covariate adjustment. However, these studies [13,14,15,16] were limited in identifying the most significant SBDH risk factors of poor HRQoL, specific to GI cancer survivors.
Understanding the roles of SBDH on HRQoL among GI cancer survivors is crucial to gaining insight into the specific social challenges and needs of this population. Lower socioeconomic status and poor lifestyle, including health risk behaviors, are associated with a higher risk of GI cancer, as well as higher mortality and recurrence rates in patients with GI cancers [15]. Poor diet (e.g., red meat, heavy alcohol, or fast food consumption), sedentary lifestyles, and smoking status contribute to GI cancer development as well as poor disease prognosis [17]. Overall, SBDH may play a role not only in the risk of GI cancer development but also in hastening the onset of symptoms and poor HRQoL. Researchers have identified that poor SBDH was associated with severe and frequent GI and psychological symptoms [4,5], which contribute to the risk of poor physical and mental HRQoL among GI cancer survivors. Marco et al. [18] reported that cancer survivors with prostate, melanoma, gynecological, or urological cancers had higher HRQoL scores than those with colorectal cancer. Thus, HRQoL can differ by cancer type, meaning it is important to identify SBDH risk factors of HRQoL specific to GI cancer survivors instead of examining these aspects in relation to all combined cancer types [18].
Therefore, the purpose of this study is to examine the associations of SBDH with HRQoL among GI cancer survivors in the U.S. Our aims are: (1) to identify the most influential or significant risk factors of poor general, physical, and mental HRQoL outcomes, including demographic and clinical characteristics, and SBDH (e.g., race, health risk behaviors, income, education, healthcare access, home ownership); and (2) to quantify the associations of SBDH with HRQoL following covariate adjustment among GI cancer survivors. This study focuses on SBDH as the primary risk factor for poor HRQoL. The significant demographic and clinical characteristics related to HRQoL that were initially identified (Aim 1) were subsequently adjusted as covariates in Aim 2.

2. Materials and Methods

2.1. Data Source and Study Population

A nationwide telephone survey known as the Behavioral Risk Factors Surveillance System (BRFSS) was launched by the Centers for Disease Control and Prevention (CDC) in 1984 [19]. In all 50 U.S. states, the District of Columbia, and three U.S. territories, BRFSS interviewers gather information on health-related behaviors, sociodemographic factors, the top preventable causes of death, and preventive health practices among non-institutionalized residents (i.e., residents 18 years of age or older). The BRFSS conducts surveys over landlines or cellular telephones using a random digit dialing sampling technique. The validity and reliability of BRFSS data have been demonstrated [19]. A secondary data analysis was conducted using publicly available BRFSS survey data. The Institutional Review Board (IRB) waived approval for this study.
A cross-sectional study was conducted by combining BRFSS data pertaining to GI cancer survivors from 2014 to 2021, with 2015 excluded due to a lack of availability of relevant data. Survey questions about diet were asked only in the survey for the years 2017, 2019, and 2021. Surveys from these specific years were merged to examine diet as a risk factor for HRQoL. Individuals ≥ 18 years of age who self-reported a personal history of esophageal, stomach, colon, rectal, liver, or pancreatic cancers were included as adult GI cancer survivors in this study. Individuals were excluded if they refused to respond to any of the survey questions or had missing responses or values for any of the included variables used in this study.

2.2. Measures

2.2.1. Primary Outcomes of Interest

The CDC HRQoL-4 measure was used in this study. This measure includes self-reported general, physical, and mental health status and usual activity limitations according to physical or mental health status [14]. The primary outcomes included all three items of the HRQoL-4 measure—general, physical, and mental health. The following survey questions were used to measure each health status [19]: For general health, “Would you say that in general, your health is excellent, very good, good, fair or poor?”; for physical health, “Now thinking about your physical health, which includes physical illness and injury, for how many days during the past 30 days was your physical health not good?”; and for mental health, “Now thinking about your mental health, which includes stress, depression, and problems with emotions, for how many days during the past 30 days was your mental health not good?” The cutoff for categorizing the primary outcomes was validated by the CDC [20]. General health was dichotomized as “better” if answered as “excellent”, “very good”, or “good” versus “poor” if answered as “fair” or “poor”. Physical and mental health status were also dichotomized as “better” versus “poor”. Better physical health was defined as having 0–13 physically unhealthy days, while poor physical health was defined as having 14 or more such days. Similarly, better mental health was defined as having 0–13 mentally unhealthy days, while poor mental health was defined as having 14 or more such days.

2.2.2. Demographic and Clinical Characteristics

In these BRFSS data, we included age, sex, GI cancer types, and comorbidities as demographic and clinical characteristics were included to examine associations with HRQoL as potential covariates.

2.2.3. Social and Behavioral Determinants of Health (SBDH)

In this study, SBDH was measured as a risk factor for poor HRQoL, including social determinants of health (SDOH) and health risk behaviors. The national health initiative, Healthy People 2030 [21], organizes SDOH into five key areas: economic status, education, social and community context, healthcare access and quality, and neighborhood and built environment. To correspond BRFSS data to the SDOH in accordance with Healthy People 2030, social community context (e.g., race, ethnicity, marital status), education, economic status (e.g., annual household income, employment status, homeownership—rent versus own home), and healthcare access (e.g., health care insurance coverage, time since the last health checkup, concerns of medical costs limited the number of doctor visits) were included. There were no available variables of BRFSS data that matched up with the neighborhood and built environment area of the Healthy People 2030. This study further included behavioral risk factors, including diet, physical activity, alcohol consumption, and smoking status (Figure 1). The diet variable (e.g., fruit and vegetable consumption per day) was grouped into two categories: “less than one time per day” and “one or more times per day”. The BRFSS physical activity questions, “Adults who reported doing overall routine physical activity or exercise during the past 30 days other than their regular jobs?” and “No physical activity or exercise during the past 30 days”, were used for the current study. The BRFSS defined heavy drinking as having more than seven drinks per week for women and more than 14 drinks per week for men. Current smoking was considered a binary variable (either “yes” or “no”) [22]. None of the variables related to social and community context, quality of care, or environmental factors (e.g., zip code, poverty index, environmental safety, transportation) were available in the BRFSS dataset of GI cancer survivors.

2.3. Statistical Analysis

The BRFSS was designed to obtain health-related information on the population of interest (i.e., the adult U.S. population residing in different states) [21]. Data weighting helped make these sample data more representative of the population from which these data were collected. The BRFSS data weights incorporated both population characteristics and BRFSS survey design, while the weighting methodology consisted of (1) weight or factors design and (2) a method for adjusting the population’s demographics, such as ranking or interactive proportional fitting [23]. Complex survey procedures with appropriate stratification and weighting of these data were applied to this study’s sample.
The statistical analysis for this study involved a combination of descriptive statistics, univariate analysis, and multivariate logistic regressions. All of our variables were normally distributed with skewness and kurtoses within the range of ±2, indicating the normal distribution; thus, we used parametric statistical methods. To examine the univariate correlations with HRQoL outcomes, the Chi-square test was used to analyze categorical independent variables, and the Analysis of Variance (ANOVA) was used for continuous independent variables. Logistic regression was then used to estimate the odds ratios (ORs) and 95% confidence intervals (CIs) for the association between SBDH and each HRQoL outcome. The SBDH factors were only included in the regression models if they were significantly associated with HRQoL outcomes. Most of the independent variables in our regression models were categorical variables. Given the assumption that categorical independent variables cannot be colinear in the regression model, stepwise eliminations were performed using multivariate regression models to select a parsimonious model while minimizing the collinearity among the variables [24]. The demographic and clinical characteristics significantly associated with HRQoL were adjusted as covariates for multivariate regression models. We also controlled surgery years for all regression models in this study. Univariate (i.e., unadjusted, other predictors) ORs and adjusted OR from multivariate regression models (AOR, i.e., adjusted other predictors) and 95% CIs were reported for the final models. Cox and Snell R squared and Nagelkerke R squared were used for the model fit test (goodness of fit) to see the variability of the independent variables in explaining the variability of the outcome variables (better versus worse HRQoL measures). All statistical analyses were performed using the R statistical software program. The level of significance for all analyses was set at p < 0.05 (two-sided).

3. Results

3.1. Demographic and Clinical Characteristics

The unweighted population consisted of 3201 GI cancer survivors. Following population weighting to the respective states, 229,428 adult GI cancer survivors were represented in the combined dataset from 2014 to 2021 (except for 2015). The demographic and clinical characteristics are presented in Table 1. In the main dataset, around half of the GI cancer survivors were 65 years or older (57%), with a median age of 67, and 54% were women (Table 1A). Among the GI cancer survivors, colorectal cancer was the most common cancer (72.5%), followed by liver cancer (10%) and stomach cancer (7.2%). In terms of comorbidities, diabetes (51.3%) was the most common chronic condition among the survivors, followed by chronic arthritis (48.9%). In the subset of the main dataset combining the 2017, 2019, and 2021 surveys with available diet variables (Table 1B), similar results were found: the majority of GI cancer survivors were 65 years or older (68%), women (52%), and had been diagnosed with colorectal cancer (77.1%). Diabetes (54.9%) and chronic arthritis (45.6%) remained the most common chronic conditions.

3.2. HRQoL Outcomes and SBDH

The HRQoL and SBDH factors are described in Table 2. In the main BRFSS dataset, over half of the GI cancer survivors reported better general (62%) and mental (56%) HRQoL, while 43% reported better physical HRQoL (Table 2A). In the main dataset, half of the GI cancer survivors were married or partnered (50%) and had at least a college education (50%), while 78% were non-Hispanic White. Approximately 57.3% of the cancer survivors had an annual household income of at least $35,000, and 93% had healthcare coverage. Most of the cancer survivors were on retirement benefits (55.3%), homeowners (79%), not heavy drinkers (91%), and not current smokers (83%). Approximately 65% of the GI cancer survivors reported partaking in routine physical activity or exercise over the last month. Similar results were found in the subset of BRFSS data combining the 2017, 2019, and 2021 surveys. In this subset (Table 2B), the majority of participants had consumed fruits (68%) and vegetables (80%) one or more times per day.

3.3. Univariate Associations of Demographic and Clinical Characteristics with HRQOL

This study examined specific demographic and clinical characteristics alongside HRQoL to identify potential covariates for primary analyses (i.e., SBDH and HRQoL) (Table 3). Being in an older age group, being married/partnered, and having no diagnosis of asthma were significantly associated with better general and mental HRQoL (all p < 0.001). Several chronic conditions were associated with poor HRQoL in all three HRQoL outcomes. Having ever been diagnosed with colorectal cancer—compared with other types of GI cancer such as liver or pancreatic cancers—and having no past medical history of coronary heart disease or chronic kidney disease were significantly associated with better general and physical HRQoL (all p < 0.05).

3.4. Univariate Associations of SBDH with HRQoL

The univariate associations of SBDH with HRQoL are described in Table 4. Many SBDH factors significantly increase the risk of poor general, mental, and physical HRQoL. However, daily fruit consumption, health insurance, and medical costs were not significantly associated with HRQoL measures.
Given the significant correlation of several SBDH with HRQoL (Table 4), the potential impact of SBDH on HRQoL was further quantified using multivariate regression models (Table 5). The unadjusted and adjusted ORs of each HRQoL outcome in relation to the SBDH are shown in Table 5. In multivariate analyses (AOR) (Table 5), R squared for each HRQoL outcome indicates a moderating fit of the regression model (e.g., the Nagelkerke R squared value of 0.42 in general HRQoL means that the independent variables can explain about 42% of the variation in the general HRQoL outcome, while the remaining 58% is due to other factors. In the adjusted, multivariate logistic models with adjusted covariates (e.g., survey years, age, GI cancer types, comorbidities) (Table 5), among the SDOH, being non-Hispanic Whites (AOR = 1.02, 95% CI: 1.01–1.12), being married/partnered status (AOR = 1.06, 95% CI = 1.01–1.23), having higher education levels (AOR = 1.33, 95% CI = 1.11–1.52), being employed (AOR = 1.12, 95% CI = 1.06–1.13), having higher income (AOR = 1.08, 95% CI = 1.05–1.32), and healthcare access within the past year with a primary care provider (AOR = 1.41, 95% CI = 1.13, 1.77), were associated with better general HRQoL. Similar results were found for mental and physical HRQoL. Regarding the behavioral determinants of health, alcohol consumption, current smoking status, and lack of physical activity were significantly associated with poor general HRQoL. Among all SBDH in this study, physical activity participation was the most significant risk factor for better HRQoL (AOR = 1.98 for general, AOR = 1.74 for mental, and AOR = 1.94 for physical HRQoL), followed by better healthcare access (i.e., frequent health checkup) (AOR = 1.41 for general, AOR = 1.46, for mental, and AOR = 1.49 for physical HRQoL).

4. Discussion

This study marks the initial exploration of SBDH risk factors on HRQoL among U.S. adults with various GI cancer types, encompassing an array of SBDH. The findings underscore the significant associations of poor HRQoL with many individual-level demographic and clinical characteristics as well as social-level (i.e., SBDH). Poor status SBDH—low economic stability, poor healthcare access, non-Hispanic Blacks, poor health risk behaviors—were significantly associated with poor general, mental, or physical HRQoL. Lack of physical activity and less healthcare access (i.e., less frequent health checkups) were the major SBDH factors of poor HRQoL in all three HRQoL outcomes.
This study is one of the few that examines HRQoL in relation to different GI cancer types. The analyses demonstrated significant evidence of GI cancer-type differences in general and physical HRQoL outcomes. Notably, GI cancer survivors diagnosed with esophageal, liver, pancreatic, or stomach cancers were more likely to report poor general and physical HRQoL compared with colorectal cancer survivors. One possible reason for this relates to how there is a higher cancer burden in certain GI cancer types compared with colorectal cancer. For example, liver and pancreatic cancers generally have a poor prognosis and are often diagnosed at advanced stages with high mortality rates [9]. Furthermore, this can be due to the better prognosis of colorectal cancer compared with liver or pancreatic cancer, as the early screening and diagnosis of colorectal cancer are well-established [25]. Future consideration of a weighted regression model is suggested to examine the contribution of each GI cancer type on HRQoL. Interestingly, the older adults (i.e., 65 years or older) reported better general and mental, but not physical, HRQoL in this study. This could be due to the fact that older adults have higher resilience and are more capable of managing or resolving conflicts, regardless of socioeconomic status and personal health conditions, or older adults in the retirement stage might have fewer responsibilities in terms of major life events, compared with younger adults (i.e., 18–64 years old) [26]. It is important to identify different risk factors that contribute to HRQoL between younger and older age groups in view of providing age-tailored cancer survivorship interventions.
In this study, non-Hispanic Black and other racial and ethnic groups had a higher prevalence of reporting poor general HRQoL at 22.7%, compared to 17% who reported better general HRQoL (p < 0.001). Similarly, in a Surveillance, Epidemiology, and End Results (SEER) study, non-Hispanic White cancer survivors had better HRQoL scores than Black and Hispanic cancer survivors in the U.S. [27]. This might be due to the structural racism that exists in the U.S., including in the healthcare system, which could result in poor healthcare access, low health literacy, disparities in cancer survivorship care and treatment options, comorbidity burdens, socioeconomic status, insurance coverage, and lack of community resources and policy support [27]. Marital status, which is often used as a proxy of social support, was significantly related to better general and mental HRQoL [27]. Consistent with previous research [13,27], being married/partnered, having high-income status, high educational levels, owning a home, frequent healthcare access, and optimal health behaviors were associated with better HRQoL outcomes. Marital status, which is often used as a proxy of social support, was significantly related to better general and mental HRQoL [28]. Future studies should explore the influence of structural racism and social support on HRQoL outcomes [29].
In analyzing the impact of SBDH on HRQoL after covariate adjustment, this study showed that current engagement in physical activity was the most impactful factor related to better HRQoL outcomes. Numerous studies have demonstrated significant associations between physical activity and better mental and physical HRQoL among cancer survivors [30,31,32,33]. The mechanisms through which physical activity improves the HRQoL are unknown. One explanation could be symptoms such as fatigue and psychological distress acting as a mediator between physical activity and HRQoL in cancer survivors [34,35,36]. Other potential mechanisms that could explain the link between physical activity and HRQoL include systemic inflammation, the release of endorphins, or the blocking or diminishing of external or internal forces that cause stress in cancer survivors [36,37,38]. A significant association between daily fruit and vegetable consumption and HRQoL in the adjusted models was not found. It is possible that daily fruit and vegetable consumption may not be a sufficient measure for diet or do not fully reflect the nutritional status, such as diet quality and food groups, which is significantly associated with the risk of GI cancers and cancer survivorship [37]. Other health risk behaviors, including smoking status and alcohol habits, were also associated with HRQoL. These health risk behaviors can increase the risk of cancer recurrence and poor disease progress in cancer survivors in the long term [38].
These findings have important implications for clinical practice and public health interventions. They suggest that lifestyle interventions—specifically targeting physical activity—and the screening and prevention of health risk behaviors, as well as the promotion of healthy behaviors, must be an integral part of cancer survivorship care. For example, healthcare providers should emphasize the importance of physical activity and smoking cessation for GI cancer survivors and consider referral to functional or mental health rehabilitation for those with poor mental or physical HRQoL. Policymakers should consider supporting a community-based cancer survivorship program to improve healthcare access. The findings of the study could be leveraged to develop a machine learning and artificial intelligence-based predictive model of HRQoL. These models could incorporate data on demographics, clinical characteristics, and SBDH risk factors to identify patients at risk of poor HRQoL and create personalized interventions to improve their HRQoL. Furthermore, these models could help identify factors most strongly associated with HRQoL, which could inform the development of more effective interventions.
The strengths of this study include the utilization of BRFSS data as a reliable data source, with national representation to increase the generalizability of the research findings [23]. This study adds to the body of literature by identifying possible risk factors of poor HRQoL with a primary focus on the roles of SBDH, specific to GI cancer survivors. However, this study also involves a number of limitations. First, the study is limited by the cross-sectional nature of these data, which hindered the ability to establish causality. For example, whether poor SDOH status mediates the relationships between racial and ethnic minorities and poor HRQoL could not be determined. Second, self-reported HRQoL data may be subject to reporting bias. Specific symptoms—particularly fatigue, psychological distress, and GI symptoms—as well as dietary factors (e.g., red meat, fruit, and vegetable consumption) have been found to be associated with the HRQoL among GI cancer survivors. However, these variables were not examined in the current study. Additionally, other SBDH factors such as poverty level, neighborhood and environmental factors, and social support level data were not available for this study. Finally, the study could not adjust for cancer stages or types of cancer treatments (e.g., radiation, chemotherapy, surgery) in association with HRQoL in GI cancer survivors [18].

5. Conclusions

Our findings provide valuable insights into the SBDH and demographic and clinical characteristics that may influence the HRQoL among GI cancer survivors in the U.S. The results of this study highlight the important impact of age, comorbidities, and type of GI cancer (i.e., non-colorectal cancer) on HRQoL. In addition, among multiple SBDH factors, specifically low economic stability, unemployment, poor health care access, smoking/alcohol health risk behaviors, and lack of physical activity, significantly contribute to poor HRQoL among GI cancer survivors. Thus, future studies should consider the comprehensive assessment of HRQoL in view of developing and testing tailored cancer survivorship interventions for GI cancer survivors, particularly those in underserved and racial and ethnic minority populations with social or economic disadvantages.

Author Contributions

All authors contributed to the study’s conception and design. Material preparation was performed by C.J.H. and reviewed by all authors. C.J.H. (first author) and F.T. conducted primary data analyses. C.J.H. wrote the first draft of the manuscript, and all authors commented on previous versions. All authors have reviewed, discussed, and agreed to their individual contributions ahead of this time. Conceptualization: C.J.H., F.T.; Data curation and analysis: C.J.H., F.T.; Methodology, Study Design, Writing Original Draft: C.J.H., D.V.A., N.R.B., F.T.; Supervision: C.J.H., D.V.A.; Writing: review and editing: C.J.H., D.V.A., N.R.B., E.D.P., M.K., A.M.N. All authors have read and agreed to the published version of the manuscript.

Funding

The work was original research that had not been published previously. Claire Han: Cancer Research Seed Grant from the Ohio State University College of Nursing and the Ohio State University Comprehensive Cancer Center. Natasha Burse was funded by the National Cancer Institute of the National Institutes of Health under Award Number K00CA253762. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

Institutional Review Board Statement

For this current study, we used a secondary analysis of the BRFSS survey data that is publicly available. Thus, the Institutional Review Board (IRB) waived approval for this study.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study from the original BRFSS surveys. In the BRFSS original study, written informed consent was obtained from the patient(s) to publish this paper.

Data Availability Statement

Behavioral Risk Factor Surveillance System (BRFSS) survey data and the questionnaires are publicly available to researchers.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the study’s design, in the collection, analyses, or interpretation of data, in the writing of the manuscript, or in the decision to publish the results.

References

  1. Arnold, M.; Abnet, C.C.; Neale, R.E.; Vignat, J.; Giovannucci, E.L.; McGlynn, K.A.; Bray, F. Global Burden of 5 Major Types of Gastrointestinal Cancer. Gastroenterology 2020, 159, 335–349.e15. [Google Scholar] [CrossRef] [PubMed]
  2. National Cancer Institute, DCCPS, Surveillance Research Program. Surveillance, Epidemiology, and End Results (SEER) Program Populations (1969–2020). 2022. Available online: www.seer.cancer.gov/popdata (accessed on 1 June 2023).
  3. Centers for Disease Control and Prevention. Centers for Disease Control and Prevention Health-Related Quality of Life (HRQOL). 2018. Available online: https://www.cdc.gov/hrqol/index.html (accessed on 23 May 2023).
  4. Tantoy, I.Y.; Cataldo, J.K.; Aouizerat, B.E.; Dhruva, A.; Miaskowski, C. A Review of the Literature on Multiple Co-occurring Symptoms in Patients with Colorectal Cancer Who Received Chemotherapy Alone or Chemotherapy with Targeted Therapies. Cancer Nurs. 2016, 39, 437–445. [Google Scholar] [CrossRef] [PubMed]
  5. Han, C.J.; Reding, K.; Cooper, B.A.; Paul, S.M.; Conley, Y.P.; Hammer, M.; Wright, F.; Cartwright, F.; Levine, J.D.; Miaskowski, C. Symptom Clusters in Patients with Gastrointestinal Cancers Using Different Dimensions of the Symptom Experience. J. Pain Symptom Manag. 2019, 58, 224–234. [Google Scholar] [CrossRef]
  6. Firkins, J.; Hansen, L.; Driessnack, M.; Dieckmann, N. Quality of life in “chronic” cancer survivors: A meta-analysis. J. Cancer Surviv. 2020, 14, 504–517. [Google Scholar] [CrossRef] [PubMed]
  7. Sipaviciute, A.; Sileika, E.; Burneckis, A.; Dulskas, A. Late gastrointestinal toxicity after radiotherapy for rectal cancer: A systematic review. Int. J. Color. Dis. 2020, 35, 977–983. [Google Scholar] [CrossRef]
  8. Ashktorab, H.; Kupfer, S.S.; Brim, H.; Carethers, J.M. Racial Disparity in Gastrointestinal Cancer risk. Gastroenterology 2017, 153, 910–923. [Google Scholar] [CrossRef]
  9. Bui, A.; Yang, L.; Soroudi, C.; May, F.P. Racial and ethnic disparities in incidence and mortality for the five most common gastrointestinal cancers in the United States. J. Natl. Med. Assoc. 2022, 114, 426–429. [Google Scholar] [CrossRef]
  10. LeMasters, T.; Madhavan, S.; Sambamoorthi, U.; Kurian, S. A population-based study comparing HRQoL among breast, prostate, and colorectal cancer survivors to propensity score matched controls, by cancer type, and gender. Psycho-Oncology 2013, 22, 2270–2282. [Google Scholar] [CrossRef]
  11. Singh, G.K.; Jemal, A. Socioeconomic and Racial/Ethnic Disparities in Cancer Mortality, Incidence, and Survival in the United States, 1950–2014: Over Six Decades of Changing Patterns and Widening Inequalities. J. Environ. Public Health 2017, 2017, 2819372. [Google Scholar] [CrossRef]
  12. Pinheiro, L.C.; Reshetnyak, E.; Akinyemiju, T.; Phillips, E.; Safford, M.M. Social determinants of health and cancer mortality in the Reasons for Geographic and Racial Differences in Stroke (REGARDS) cohort study. Cancer 2022, 128, 122–130. [Google Scholar] [CrossRef]
  13. Burse, N.R.; Weng, X.; Wang, L.; Cuffee, Y.L.; Veldheer, S. Influence of social and behavioral determinants on health-related quality of life among cancer survivors in the USA. Support. Care Cancer 2022, 31, 67. [Google Scholar] [CrossRef]
  14. Santee, E.J.; King, K.A.; Vidourek, R.A.; Merianos, A.L. Health Care Access and Health Behavior Quality of Life among Hispanic/Latino-American Cancer Survivors. Appl. Res. Qual. Life 2020, 15, 637–650. [Google Scholar] [CrossRef]
  15. Coughlin, S.S. Social determinants of breast cancer risk, stage, and survival. Breast Cancer Res. Treat. 2019, 177, 537–548. [Google Scholar] [CrossRef] [PubMed]
  16. Oberguggenberger, A.; Meraner, V.; Sztankay, M.; Hilbert, A.; Hubalek, M.; Holzner, B.; Gamper, E.; Kemmler, G.; Baumgartner, T.; Lackinger, I.; et al. Health Behavior and Quality of Life Outcome in Breast Cancer Survivors: Prevalence Rates and Predictors. Clin. Breast Cancer 2018, 18, 38–44. [Google Scholar] [CrossRef] [PubMed]
  17. Choi, J.W.; Hua, T.N.M. Impact of Lifestyle Behaviors on Cancer Risk and Prevention. J. Lifestyle Med. 2021, 11, 1–7. [Google Scholar] [CrossRef]
  18. Marco, D.J.T.; White, V.M. The impact of cancer type, treatment, and distress on health-related quality of life: Cross-sectional findings from a study of Australian cancer patients. Support. Care Cancer 2019, 27, 3421–3429. [Google Scholar] [CrossRef]
  19. Pierannunzi, C.; Hu, S.S.; Balluz, L. A systematic review of publications assessing reliability and validity of the Behavioral Risk Factor Surveillance System (BRFSS), 2004–2011. BMC Med. Res. Methodol. 2013, 13, 49. [Google Scholar] [CrossRef] [PubMed]
  20. Casebeer, A.W.; Antol, D.D.; Hopson, S.; Khoury, R.; Renda, A.; Parikh, A.; Stein, A.; Michael, T.; Stemkowski, S.; Bunce, M. Using the Healthy Days Measure to Assess Factors Associated with Poor Health-Related Quality of Life for Patients with Metastatic Breast, Lung, or Colorectal Cancer Enrolled in a Medicare Advantage Health Plan. Popul. Health Manag. 2019, 22, 440–448. [Google Scholar] [CrossRef]
  21. U.S. Department of Health and Human Services. Social Determinants of Health. Healthy People. 2020. Available online: https://health.gov/healthypeople/objectives-and-data/social-determinants-health (accessed on 5 April 2023).
  22. Centers for Disease Control and Prevention (CDC). Alcohol and Public Health. 2021. Available online: https://www.cdc.gov/alcohol/index.htm (accessed on 3 June 2023).
  23. Iachan, R.; Pierannunzi, C.; Healey, K.; Greenlund, K.J.; Town, M. National weighting of data from the behavioral risk factor surveillance system (BRFSS). BMC Med. Res. Methodol. 2016, 16, 155. [Google Scholar] [CrossRef]
  24. Chowdhury, M.Z.I.; Turin, T.C. Variable selection strategies and its importance in clinical prediction modelling. Fam. Med. Community Health 2020, 8, e000262. [Google Scholar] [CrossRef]
  25. Hoskins, B.; Wasuwanich, P.; Scheimann, A.O.; Karnsakul, W. Screening strategy for gastrointestinal and hepatopancreatobiliary cancers in cystic fibrosis. World J. Gastrointest. Oncol. 2021, 13, 1121–1131. [Google Scholar] [CrossRef] [PubMed]
  26. MacLeod, S.; Musich, S.; Hawkins, K.; Alsgaard, K.; Wicker, E.R. The impact of resilience among older adults. Geriatr. Nurs. 2016, 37, 266–272. [Google Scholar] [CrossRef] [PubMed]
  27. Pinheiro, L.C.; Wheeler, S.B.; Chen, R.C.; Mayer, D.K.; Lyons, J.C.; Reeve, B.B. The effects of cancer and racial disparities in health-related quality of life among older Americans: A case-control, population-based study. Cancer 2015, 121, 1312–1320. [Google Scholar] [CrossRef] [PubMed]
  28. Gonzalez-Saenz de Tejada, M.; Bilbao, A.; Baré, M.; Briones, E.; Sarasqueta, C.; Quintana, J.M.; Escobar, A.; CARESS-CCR Group. Association between social support, functional status, and change in health-related quality of life and changes in anxiety and depression in colorectal cancer patients. Psycho-Oncology 2017, 26, 1263–1269. [Google Scholar] [CrossRef] [PubMed]
  29. Zavala, V.A.; Bracci, P.M.; Carethers, J.M.; Carvajal-Carmona, L.; Coggins, N.B.; Cruz-Correa, M.R.; Davis, M.; de Smith, A.J.; Dutil, J.; Figueiredo, J.C.; et al. Cancer health disparities in racial/ethnic minorities in the United States. Br. J. Cancer 2021, 124, 315–332. [Google Scholar] [CrossRef] [PubMed]
  30. Ng, S.M.; Fung, M.H.; Chan, J.S.; Chan, C.H.; Chan, C.L. Physical activity, confidence and quality of life among cancer patient-carer dyads. Sports Med. Open 2021, 7, 46. [Google Scholar] [CrossRef]
  31. Campbell, K.L.; Winters-Stone, K.; Wiskemann, J.; May, A.M.; Schwartz, A.L.; Courneya, K.S.; Zucker, D.; Matthews, C.; Ligibel, J.; Morris, S.; et al. Exercise Guidelines for Cancer Survivors: Consensus Statement from International Multidisciplinary Roundtable. Med. Sci. Sports Exerc. 2019, 51, 2375–2390. [Google Scholar] [CrossRef]
  32. Bouillet, T.; Bigard, X.; Brami, C.; Chouahnia, K.; Copel, L.; Dauchy, S.; Delcambre, C.; Descotes, J.M.; Joly, F.; Lepeu, G.; et al. Role of physical activity and sport in oncology: Scientific commission of the National Federation Sport and Cancer CAMI. Crit. Rev. Oncol. Hematol. 2015, 94, 74–86. [Google Scholar] [CrossRef]
  33. Serra, M.C.; Ryan, A.S.; Ortmeyer, H.K.; Addison, O.; Goldberg, A.P. Resistance training reduces inflammation and fatigue and improves physical function in older breast cancer survivors. Menopause 2018, 25, 211–216. [Google Scholar] [CrossRef]
  34. LaVoy, E.C.; Fagundes, C.P.; Dantzer, R. Exercise, inflammation, and fatigue in cancer survivors. Exerc. Immunol. Rev. 2016, 22, 82–93. [Google Scholar]
  35. Diggins, A.D.; Hearn, L.E.; Lechner, S.C.; Annane, D.; Antoni, M.H.; Whitehead, N.E. Physical activity in Black breast cancer survivors: Implications for quality of life and mood at baseline and 6-month follow-up. Psycho-Oncology 2017, 26, 822–828. [Google Scholar] [CrossRef] [PubMed]
  36. Himbert, C.; Warby, C.A.; Gigic, B.; Ose, J.; Lin, T.; Viskochil, R.; Peoples, A.R.; Ashworth, A.; Schrotz-King, P.; Scaife, C.L.; et al. Associations of Individual and Combined Physical Activity and Body Mass Index Groups with Proinflammatory Biomarkers among Colorectal Cancer Patients. Cancer Epidemiol. Biomark. Prev. 2022, 31, 2148–2156. [Google Scholar] [CrossRef] [PubMed]
  37. Moazzen, S.; Cortes-Ibañez, F.O.; van der Vegt, B.; Alizadeh, B.Z.; de Bock, G.H. Diet quality indices and gastrointestinal cancer risk: Results from the Lifelines study. Eur. J. Nutr. 2022, 61, 317–327. [Google Scholar] [CrossRef] [PubMed]
  38. Lopez, V.; Klainin-Yobas, P. Health Promotion among Cancer Patients: Innovative Interventions. In Health Promotion in Health Care–Vital Theories and Research; Haugan, G., Eriksson, M., Eds.; Springer: Cham, Switzerland, 2021; Chapter 17. [Google Scholar] [CrossRef]
Figure 1. Healthy People 2030 framework’s five domains of social determinants of health and behavioral risk factors are relevant to the social and behavioral determinants of health (SBDH) in the current study.
Figure 1. Healthy People 2030 framework’s five domains of social determinants of health and behavioral risk factors are relevant to the social and behavioral determinants of health (SBDH) in the current study.
Ijerph 20 06676 g001
Table 1. Demographic and Clinical Characteristics among GI Cancer Survivors.
Table 1. Demographic and Clinical Characteristics among GI Cancer Survivors.
A. Main Dataset (2014 to 2021, Except for 2015)
Total Weighted Study N = 229,428
Unweighted n = 3201
B. Subset of Main Dataset (2017, 2019, and 2021 with Diet Variables)
Total Weighted Study N = 123,261
Unweighted n = 835
Year, n (%) 229,428Years, n (%)123,261
201412,576 (5.5)2014not included
201620,718 (9.0)2016not included
201716,870 (7.3)201757,933 (47)
201814,128 (6.1)2018not included
2019196 (<0.1)20193,697 (3.0)
2020141,212 (62)2020not included
202123,729 (10)202161,631 (50)
Demographics (% otherwise specified)
Age, median (Interquartile range, IQR) 67 (58, 76)67 (58, 77)
Age group18–6443%32%
65 or older57%68%
SexMale46%48%
Female54%52%
Clinical Characteristics, n (%)
Types of GI CancerColorectal (intestine)72.5%77.1%
Esophageal5.2%6%
Liver10%7.4%
Pancreatic5.1%4.6%
Stomach7.2%4.9%
Comorbidities, n (%)
The participants self-reported if they had ever been told by a health professional that they had(“yes”/no”)
Heart Attack (Yes)12%9.2%
Coronary Heart Disease (Yes)12%11%
Asthma (Yes)17%14%
Stroke (Yes)8.3%8.3%
Chronic Obstructive Pulmonary Disease (Yes)14.5%13.2%
Diabetes (Yes)51.3%54.9%
Chronic Arthritis (Yes)48.9%45.6%
Chronic Kidney Disease (Yes)8.4%11%
Overweight or obese per Body Mass Index (Yes)29.5%14%
Note. Interquartile range, IQR.
Table 2. HRQoL Outcomes and SBDH among GI Cancer Survivors (%).
Table 2. HRQoL Outcomes and SBDH among GI Cancer Survivors (%).
A. Main Dataset (2014 to 2021, Except for 2015)
Total Weighted Study N = 229,428
Unweighted n = 3201
B. Subset of Main Dataset
(2017, 2019, and 2021 with Diet Variables).
Total Weighted Study N = 123,261
Unweighted n = 835
HRQOL OUTCOMES
General HealthPoor (38%), Better (62%)Poor (37%), Better (63%)
Mental HealthPoor (44%), Better (56%)Poor (13%), Better (87%)
Physical HealthPoor (57%), Better (43%)Poor (24%), Better (76%)
SOCIAL AND COMMUNITY CONTEXT
Race/EthnicityNon-Hispanic White78%82%
Non-Hispanic Black12%6%
Non-Hispanic Other5.5%7.8%
Hispanic4.5%4.2%
Marital statusMarried/Partnered50%51%
Divorced/Widowed/Single50%49%
EDUCATION
High school or less50%35%
Attended College or technical school31%32%
Graduated from College or technical school19%33%
ECONOMIC STABILITY
Employment StatusEmployed28%25.5%
Unemployed11.7%10.5%
Retirement Benefits55.3%58.5%
Homemaker5%5.5%
Household Income (annual)
Less than $15,0009.4%9.2%
$15,000 to < $25,00018%15.4%
$25,000 to < $35,00015.3%15.4%
$35,000 to < $50,00022.7%22.9%
$50,000 to < $100,00033.1%32.2%
$100,000 or more1.5%4.9%
HomeownershipOwn79%79%
Rent18%18%
Other arrangement3%3%
HEALTHCARE ACCESS
Health InsuranceYes93%96.2%
No6.2%3.1%
Don’t know/Not sure0.8%0.7%
Medical Costs: In the past year, could not see doctor due to medical costs?
(Yes or No)Yes (8%)Yes (6.9%)
Health Care Access: Time since last checkup with primary care providers
Within past years87%86%
1 but <2 years ago7.8%8%
2 but <5 years ago3.3%3%
5 or more years ago1.6%2%
Never0.1%1%
BEHAVIORAL RISK FACTORS
At least one alcohol in the past 30 daysYes/No40%/60%39%/61%
Heavy drinking per weekYes/No9%/91%7%/93%
Smoking StatusCurrent17%11.5%
Former40%37.5%
Never43%51%
Physical ActivityYes/No65%/35%65%/35%
Diet (Fruits)Less than one time per dayno data available29%
One or more times per day71%
Diet (Vegetables)Less than one time per dayno data available17%
One or more times per day83%
Table 3. Univariate Associations of Demographic and Clinical Characteristics with HRQOL. (To identify potential covariates between SBDH and HRQOL).
Table 3. Univariate Associations of Demographic and Clinical Characteristics with HRQOL. (To identify potential covariates between SBDH and HRQOL).
Main Dataset (2014 to 2021, Except for 2015), Total Weighted Study N = 229,428, Unweighted n = 3201
VariablesGeneral HRQoL aMental HRQoL aPhysical HRQoL a
PoorBetterChi2/p bPoorBetterChi2/p bPoorBetterChi2/p b
DEMOGRAPHICS (% OTHERWISE SPECIFIED)
Age, Median (IQR)64 (13)65 (14)3.41
0.367 c
57 (15)60 (15)2.93
0.314 c
63 (13)61 (16)3.01
0.840 c
Age group18–6437.529.015.4256.542.616.5140.537.33.62
65 or older61.570.0<0.00142.557.0<0.00158.861.9440
SexMale46.746.02.4138.839.53.2145.542.32.31
Female53.354.00.67461.260.50.82254.557.70.237
CLINICAL CHARACTERISTICS(%)
Types of GI cancer 9.21
<0.001
1.21
0.710
12.31
<0.001
Colorectal 71.083.871.973.168.078.3
Esophageal6.04.26.55.57.34.4
Liver10.24.510.08.410.65.8
Pancreatic6.33.94.56.67.35.3
Stomach6.64.67.27.56.86.2
Comorbidities
Heart AttackYes18.77.513.4116.410.415.8618.812.22.50
No80.291.9<0.00182.388.20.02380.486.70.003
Coronary Heart Disease 15.42
<0.001
1.31
0.380
16.99
<0.001
Yes18.88.015.712.220.311.5
No79.390.482.886.078.486.5
AsthmaYes20.211.310.5125.615.59.4820.518.81.21
No79.588.4<0.00174.484.3<0.00179.380.70.576
StrokeYes13.35.223.2214.28.024.4811.38.426.51
No85.994.6<0.00184.191.60.00187.991.20.002
COPDYes23.59.012.2226.416.413.5624.915.711.24
No75.490.6<0.00171.961.00.00174.183.5<0.001
DiabetesYes33.321.436.2131.325.234.5931.626.938.83
No63.476.8<0.00165.471.80.04365.470.50.023
Chronic ArthritisYes59.242.926.0866.451.425.5762.254.328.21
No40.556.5<0.00133.748.1<0.00137.445.20.011
Chronic Kidney Disease
Yes13.05.615.6411.710.11.4513.88.416.77
No86.094.0<0.00187.188.90.55685.290.90.012
Overweight/Obese 1.22
0.886
1.09
0.123
1.29
0.323
Yes31.531.830.636.431.932.9
No64.364.366.459.964.562.1
Note. Interquartile range, IQR; Significant findings (p < 0.05) were highlighted in bold. a Levene’s test statistics for the age median variable showed the homogeneity of variance in the ANOVA models: For general HRQoL (0.121, significance = 0.728), for mental HRQoL (0.721, significance = 0.428), and for physical HRQOL (0.851, significance = 0.356). b Chi-square statistics and p values except for the age median variable. c For the age median variable, F/p statistics from ANOVA were used.
Table 4. Univariate Associations of SBDH with HRQoL.
Table 4. Univariate Associations of SBDH with HRQoL.
Main Dataset (2014 to 2021, Except for 2015). Total Weighted Study N = 229,428, Unweighted n = 3201
SBDH Risk FactorsGeneral HRQoLMental HRQoLPhysical HRQoL
PoorBetterChi2/p aPoorBetterChi2/p aPoorBetterChi2/p a
SOCIAL AND COMMUNITY CONTEXT (%)
Race/Ethnicity: 34.94
<0.001
2.26
0.230
80.678.32.35
0.398
Non-Hispanic White77.383.077.479.66.88.9
Non-Hispanic Black8.96.26.27.13.54.1
Non-Hispanic Other 6.74.66.28.43.94.0
Hispanic4.42.44.03.33.42.9
Marital Status: 9.42
<0.001
10.32
0.002
3.12
0.096
Married/Partnered44.052.241.049.749.346.3
Divorced/Widowed/Single56.047.859.050.350.753.7
EDUCATION (%)
High school or less47.235.821.41
<0.001
41.338.422.52
0.014
12.59.925.62
<0.001
Attended College or technical school30.929.433.432.433.128.7
Bachelor’s degree or graduate or more21.634.524.967.554.560.9
ECONOMIC STABILITY (%)
Employment Status: 30.42
<0.001
22.31
<0.001
29.62
<0.001
Employed17.029.017.427.316.025.3
Unemployed20.117.145.333.032.518.5
Retirement Benefits58.948.931.147.045.751.7
Homemaker4.05.06.22.75.84.5
Household Income/year: 36.52
<0.001
33.52
<0.001
36.31
0.002
Less than $25,00036.420.742.827.138.729.3
$25,000 to <$35,00012.010.98.710.410.68.9
$35,000 to <$50,00012.612.811.715.112.412.6
$50,000 to <$100,00021.935.222.629.123.130.8
$100,000 or more0.82.20.22.80.71.8
HomeownershipOwn72.781.825.166.975.229.371.275.92.31
Rent22.915.1<0.00126.121.90.01224.019.90.234
HEALTHCARE ACCESS (%)
Health InsuranceYes94.294.71.1191.093.31.4393.994.22.12
No5.14.30.5807.56.30.2895.35.30.786
Medical Costs: 1.03
0.101
1.33
0.108
5.21
0.050
In the past year, could not see a doctor due to medical costs. (Yes/No)Yes (10.3)Yes (6.6)Yes (15.1)Yes (8.9)Yes (11.9)Yes (8.1)
Time since last checkup with PCP: 14.24
0.021
10.582
0.049
11.52
0.032
Within the past year84.687.585.480.884.388.3
More than 1 year ago or never15.412.514.619.215.711.7
BEHAVIORAL RISK FACTORS (%)
At least one alcoholic drink in last monthYes28.142.314.3132.639.95.6228.538.115.41
No71.357.0<0.00167.459.60.05070.861.40.001
Heavy drinking per weekYes94.792.315.41
0.022
92.892.91.09
0.184
94.293.72.31
0.731
No4.46.77.05.84.95.7
Smoking StatusCurrent17.98.817.63
<0.001
28.013.319.31
<0.001
18.813.623.41
0.004
Former41.938.837.336.641.038.1
Never39.451.933.849.439.448.0
Physical ActivityYes50.573.124.3149.365.426.5146.565.325.61
No52.826.7<0.00150.234.6<0.00153.034.7<0.001
Subset of the main dataset (2017, 2019, and 2021 with diet variables)
Weighted Study N = 123,261, unweighted n = 835
Diet (Fruits): 1.41
0.290
1.65
0.574
1.39
0.119
Less than one time/day69.764.965.659.572.064.8
One or more times/day27.031.731.837.926.931.5
Diet (Vegetables): 19.51
0.004
20.41
0.025
18.51
0.046
Less than one time/day80.574.484.471.682.872.7
One or more times/ day15.223.312.325.015.623.6
Note. Significant findings (p < 0.05) were highlighted in bold. PCP, Primary Care Provider. a Chi-square statistics and p values.
Table 5. Potential Impact of SBDH on HRQoL among GI Cancer Survivors.
Table 5. Potential Impact of SBDH on HRQoL among GI Cancer Survivors.
Exp (B) is an Odds Ratio (OR)/OR as a Univariate Association. AOR as an Adjusted OR
That Controls for Other
Predictor Variables
in Multivariate Regression.
Main Dataset (2014 to 2021, Except for 2015). Total Weighted Study N = 229,428, Unweighted n = 3201
Better General HRQoL
(62%, Weighted n = 137,905)
Better Mental HRQoL
(56%, Weighted n = 124,559)
Better Physical HRQoL
(43%, Weighted n = 98,654)
UnivariateMultivariate Model b
Cox and Snell R2 (0.37)
Nagelkerke R2 (0.42)
UnivariateMultivariate Model b
Cox and Snell R2 (0.28)
Nagelkerke R2 (0.35)
UnivariateMultivariate Model b
Cox and Snell R2 (0.29)
Nagelkerke R2 (0.35)
OR (95% CI)AOR (95% CI)WaldOR (95% CI)AOR (95% CI)WaldOR (95% CI)AOR (95% CI)Wald
SOCIAL AND COMMUNITY CONTEXT
Race: 6.123not applicablenot applicable
Non-Hispanic Whites1.05 ** 1.02 *
Racial/ethnic minorities (ref) a(1.01, 1.10)(1.01, 1.12)
Marital status: 6.323 0.523not applicable
Married/Partnered1.10 **1.06 *1.13 *1.01
Divorced/Widowed/Single (ref)(1.05, 1.16)(1.01, 1.23)(1.03, 1.24)(0.98, 1.20)
EDUCATION
Bachelor’s/graduate or more
High school or less/College(ref)
1.27 *
(1.22, 1.32)
1.33 *
(1.11, 1.52)
7.6231.18 **
(1.07, 1.28)
1.06(0.98,1.19)0.4231.18 **
(1.11, 1.26)
1.11 *
(1.01, 1.21)
4.651
ECONOMIC STABILITY
Employment Status:
Employed
Unemployed/Homemakers/
Retired benefits (ref)
1.14 **
(1.12, 1.7)
1.12 **
(1.06, 1.13)
4.3251.13 **
(1.07, 1.19)
1.13 **
(1.06, 1.19)
5.6731.11 **
(1.06, 1.15)
1.09 **
(1.03, 1.14)
4.965
Household Income/year: 5.621 4.652 0.014
Equal to more than $35,0001.11 **1.08 **1.10 **1.07 *1.07 **0.96
Less than $35,000 (ref)(1.08, 1.14)(1.05, 1.32)(1.05, 1.16)(1.01, 1.12)(1.03, 1.10)(0.92, 1.01)
Homeownership: 0.162 0.123not applicable.
Own 1.25 **1.111.37 **1.11
Rent (ref)(1.12, 1.40)(0.91, 1.25)(1.11, 1.69)(0.90, 1.36)
HEALTHCARE ACCESS
Time since the last checkup with PCP:
Within the past year.
More than one year ago/never (ref)
1.27 *
(1.03, 1.56)
1.41 **
(1.13, 1.77)
8.7531.38 *
(1.02, 1.42)
1.46 *
(1.01, 2.11)
6.4511.41 *
(1.02, 1.92)
1.49 *
(1.07, 2.08)
8.912
HEALTH RISK BEHAVIORS
At least one alcoholic drink in the past 30 days:
No
Yes (ref)
1.21 **
(1.21, 1.43)
1.39 **
(1.22, 1.56)
8.4120.98
(0.6, 1.10)
1.21
(0.93, 1.56)
0.1231.32 **
(1.09, 1.59)
1.21
(0.99, 1.48)
0.199
Heavy drinking/week: 4.641not applicablenot applicable
No1.051.16 **
Yes (ref)(0.99, 1.13)(1.02,1.26)
Smoking Status: 7.312 7.521 0.312
Former/Never1.25 **1.21 **1.28 **1.21 **1.12 *1.02
Current (ref)(1.29, 1.30)(1.14, 1.27)(1.19, 1.36)(1.01, 1.31)(1.02, 1.20)(0.91, 1.12)
Physical Activity: 11.754 9.856 10.523
Yes2.34 **1.98 **1.93 **1.74 **2.15 **1.94 **
No (ref)(2.01, 2.73)(1.71, 2.32)(1.45, 2.51)(1.33, 2.28)(1.73, 2.71)(1.55, 2.43)
Subset of the main dataset (2017, 2019, and 2021 with diet variables). Weighted Study N = 123,261, unweighted n = 835
Better General HRQoL
(63%, Weighted n = 75,717)
Better Mental HRQoL
(87%, Weighted n = 104,880)
Better Physical HRQoL
(76%, Weighted n = 90,251)
Diet (Vegetables): 0.589 0.121 0.161
One or more times per day.1.110.911.111.320.960.99
Less than one time per day (ref)(0.90, 1.23)(0.78, 1.06)(0.90, 1.26)(0.91, 1.53)(0.87, 1.06)(0.85, 1.11)
Note. * p < 0.05, ** p < 0.01. a Racial/ethnic minorities include Hispanic, Non-Hispanic Blacks, and Others; other GI Cancers include liver, esophageal, pancreatic, and stomach cancers. b R-squared Goodness of fit. We adjusted for survey years, age, types of GI cancers, and comorbidities in unadjusted and adjusted models as covariates. PCP, Primary Care Provider.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Han, C.J.; Tounkara, F.; Kalady, M.; Noonan, A.M.; Burse, N.R.; Paskett, E.D.; Von Ah, D. Risk Factors of Health-Related Quality of Life among Gastrointestinal Cancer Survivors in the U.S.: With a Focus on Social and Behavioral Determinants of Health (SBDH). Int. J. Environ. Res. Public Health 2023, 20, 6676. https://doi.org/10.3390/ijerph20176676

AMA Style

Han CJ, Tounkara F, Kalady M, Noonan AM, Burse NR, Paskett ED, Von Ah D. Risk Factors of Health-Related Quality of Life among Gastrointestinal Cancer Survivors in the U.S.: With a Focus on Social and Behavioral Determinants of Health (SBDH). International Journal of Environmental Research and Public Health. 2023; 20(17):6676. https://doi.org/10.3390/ijerph20176676

Chicago/Turabian Style

Han, Claire J., Fode Tounkara, Matthew Kalady, Anne M. Noonan, Natasha R. Burse, Electra D. Paskett, and Diane Von Ah. 2023. "Risk Factors of Health-Related Quality of Life among Gastrointestinal Cancer Survivors in the U.S.: With a Focus on Social and Behavioral Determinants of Health (SBDH)" International Journal of Environmental Research and Public Health 20, no. 17: 6676. https://doi.org/10.3390/ijerph20176676

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop