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Article

Comparison of Quality of Life in Breast Cancer Survivors with and without Persistent Depressive Symptoms: A 12-Month Follow-Up Study

by
Fernanda Elisa Ribeiro
1,
William Rodrigues Tebar
2,
Gerson Ferrari
3,
Mariana Romanholi Palma
1,
Cristina Elena Fregonesi
1,
Daniela Tanajura Caldeira
1,
Gabriela Caroline Rodrigues Silva
1,
Luiz Carlos Marques Vanderlei
1,
Victor Spiandor Beretta
1 and
Diego Giulliano Destro Christofaro
1,*
1
Physical Education Department, Graduate Program in Movement Sciences, School of Technology and Sciences, São Paulo State University (Unesp), São Paulo 19060-900, Brazil
2
Center of Clinical and Epidemiological Research, University Hospital, University of Sao Paulo, São Paulo 05403-000, Brazil
3
Faculty of Health Sciences, Universidad Autónoma de Chile, Providencia 7500912, Chile
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2023, 20(4), 3663; https://doi.org/10.3390/ijerph20043663
Submission received: 25 January 2023 / Revised: 14 February 2023 / Accepted: 15 February 2023 / Published: 18 February 2023
(This article belongs to the Section Sport and Health)

Abstract

:
Although breast cancer treatments reduce mortality, their adverse effects can increase depression which impacts one’s quality of life (QoL). Physical activity (PA) seems to improve the QoL of breast cancer survivors (BCS). However, an unanswered question is the influence of PA on the QoL in BCS with depressive symptoms. Thus, we analyzed the influence of PA on the QoL in BCS with persistent depressive symptoms during 12 months of follow-up. The sample included 70 female BCS. Depression and QoL domains (i.e., functional capacity, physical limitations, body pain, general health status, vitality, social and emotional aspects, and mental health) were assessed at baseline and follow-up periods by the Hospital Anxiety and Depression Scale and SF-36, respectively. Habitual PA was assessed by Baecke’s questionnaire. Our results indicate a prevalence of 17.1% of depressive symptoms. Non-depressives BCS improved their physical limitations and general health status domains over time, but there were no observed differences in depressive BCS. BCS with persistent depressive symptoms (baseline and follow-up) showed worse QoL scores than non-depressives in all domains, regardless of confounding factors. When adjusted for PA, the difference between BCS depressives and non-depressives lost its significance in the functional capacity domain. In conclusion, habitual PA practice positively influenced the functional capacity domain of the QoL in BCS.

1. Introduction

Cancer is the most common cause of premature death, increasing the number of deaths before 70 years old [1]. Thus, it is considered an important barrier to extending life expectancy worldwide [2]. The global prevalence of cancer has risen over the past years and in 2020, approximately 19 million new cases of cancer were estimated around the world [3]. The prevalence of cancer globally is expected to increase by 47% in 2040 in relation to 2020 [3].
In men from the USA, the most prevalent types of cancer are prostate, melanoma of the skin, and colon and rectum, while the most prevalent types of cancer in women are breast, uterine, and thyroid [4]. In 2020, approximately two million new cases of female breast cancer were diagnosed worldwide [3]. Breast cancer is considered one of the main causes of death worldwide, mainly in transitioning countries [3,5], and the second most common type of cancer in the Brazilian female population [6,7]. However, post-breast cancer survival has increased substantially in recent years, mainly due to early diagnosis and treatment efficacy [8]. Although the treatments for breast cancer contribute substantially to reducing mortality, their adverse effects have negatively impacted quality of life (QoL) [8,9,10,11,12,13]. Thus, the QoL of breast cancer survivors has been widely studied, since this population experiences several physical and psychological confrontations from diagnosis to the post-treatment period [13,14,15,16].
As a result of the increase in the survival rate and prolonged life expectancy due to diagnosis and treatment efficacy, the relevance of QoL and mental health in breast cancer survivors is growing [17]. Fatigue and pain are the most frequently reported physical complaints after cancer treatment, and they have been associated with psychological disorders such as anxiety and depression [15,18,19]. Approximately 22% to 38% of patients diagnosed with breast cancer have depression symptoms, with 22% of them demonstrating moderate to severe depression levels [19,20]. Substantial evidence has shown that psychological disorders, mainly depression, have been associated with worse QoL in breast cancer survivors [13,15,16,18,21]. In this sense, depression symptoms may affect several factors related to the QoL of breast cancer survivors, such as their body image, functional capacity, mental well-being, and involvement in regular physical activity [13,15].
Increasing the practice of physical activity seems to improve functional capacity and decrease the chance of developing several side effects during cancer treatment by 26% [22]. Breast cancer patients who are more physically active present a better QoL, mainly in the functional capacity domain, than sedentary patients [23]. Physical activity is also considered indispensable for maintaining the health of breast cancer survivors due to the physical and metabolic benefits it provides. In addition, physical activity is considered an important strategy for improving QoL and positively affecting physical functioning, fatigue, pain, and sexual function [17], besides serving as a protective measure against disease recurrence [15,24,25].
Although the relationship between depression and QoL in breast cancer survivors is well-established [13,15,16,18,21], little is known about the influence of persistent depressive symptoms on the QoL of this population over time [26]. This influence should be highlighted since the physical and emotional consequences of breast cancer treatment can persist throughout the years, even after the disease has been treated [27]. Furthermore, physical activity is able to reduce the risk of disease recurrence, improve mental well-being, and prevent other comorbidities [28,29,30,31]. In addition, while the benefits of physical activity in the QoL of breast cancer survivors are known, it is not clear whether physical activity can influence the QoL domains of breast cancer survivors with symptoms of depression, especially when considering the repercussions of postoperative time. Most studies that have assessed QoL and mental health in breast cancer survivors are cross-sectional or short-term, which highlights the need for a prolonged follow-up investigation on this topic.
Therefore, the aim of this study was to compare the QoL domains of breast cancer survivors according to persistent depressive symptoms (over 12 months) and to analyze the influence of physical activity on the QoL domains in this population. We hypothesize that breast cancer survivors with depression symptoms would present lower QoL domains than non-depressive individuals. We also expect that higher levels of physical activity would be able to attenuate these effects.

2. Materials and Methods

2.1. Study Design and Participants

This is a longitudinal study developed in the city of Presidente Prudente, located in the southeastern region of Brazil, with a Human Development Index of 0.806, where 1 is the best and 0 is the worst. The study was conducted according to the guidelines of the Declaration of Helsinki and all procedures used in the study were approved by the Ethics and Research Committee of São Paulo State University (Protocol 019093/2016). All participants signed an informed consent form accepting to voluntarily participate in the study, being duly informed of the research procedures and objectives.
The study sample was composed of female breast cancer survivors. The inclusion criteria were: (1) not having neurodegenerative diseases such as Parkinson’s and Alzheimer’s disease; (2) not presenting other dementias. The exclusion criterion was: (1) not answering all the items in the questionnaire. Participants were recruited from institutions that support breast cancer and by the indication of mastologist doctors from Presidente Prudente. The required sample size was calculated by the formula of Snedecor and Cochran [30]: n = 2 + C(s/d)2, where “C” was a constant of 7.85 derived from an alpha error of 0.05 and statistical power 1-β of 0.8, “d” was the mean difference between the averages of the eight QoL domains at baseline and follow-up (3.36), and “s” was the standard deviation of mean difference (9.81), which resulted in a minimum required sample of 69 participants. At the end, a total of 70 women participated in both phases of the study (i.e., baseline and 12-month follow-up).

2.2. Data Collection

At first, personal data (name, age, and marital status) and clinical information about the presence of comorbidities, time of diagnosis, whether they had surgery for breast cancer, and what type of surgical procedure, as well as adjuvant treatments, were collected. Body mass and height were assessed by a digital scale with a coupled stadiometer (Welmy®, W110H, Brazil). These measurements were used to calculate body mass index (BMI), through body mass (in kilograms) divided by height (in meters) squared.
Thereafter, a face-to-face interview was performed by previously trained researchers. The interview was composed of self-reported instruments to assess depression symptoms, the QoL, habitual physical activity, and socioeconomic status. The participants were assessed at baseline and after 12 months. In both periods, the same assessments were performed. Data collection for all periods of the study ranged from 2016 to 2018.

2.3. Depression Symptoms

The Hospital Anxiety and Depression Scale (HADS) was used to assess the presence of depression symptoms. The HADS questionnaire contains 14 multiple-choice questions, which separately assess the symptoms of anxiety (seven questions) and depression (seven questions). Each item scored from 0 to 3, with a higher score representing a greater occurrence of anxiety and depression symptoms. The range for each outcome (i.e., anxiety and depression) is 0 to 21 [32,33,34]. In this study, only the questions related to depressive symptoms were considered, with a score ≥9 corresponding to the presence of depression symptoms [32,33,34]. This cutoff was adopted to classify the sample into “Breast cancer survivors with depressive symptoms (depressive)” and “Breast cancer survivors without depressive symptoms (non-depressive)”. Participants who were classified as breast cancer survivors with depressive symptoms in both evaluations (baseline and 12 months of follow-up) were considered “persistent depressive symptoms”.

2.4. Quality of Life (HRQoL)

The Short Form Health Survey (SF-36) questionnaire was used to assess the QoL of the sample. SF-36 was previously translated to Portuguese and validated for the Brazilian population [35,36]. This instrument is composed of 36 items that assess QoL in eight different domains: functional capacity, physical limitations, body pain, general health status, vitality, social aspects, emotional aspects, and mental health. Each domain has a score ranging from 0 to 100, where 0 represents the worst and 100 points represents the best QoL [35,36].

2.5. Physical Activity Level

The physical activity level was assessed by Baecke’s questionnaire [37]. This instrument assesses physical activity level (habitual practice) considering the last 12 months in three different domains (i.e., occupational activities, sports practice at leisure, and leisure time and commuting activities) through 16 questions. The occupational activities domain is assessed by eight questions about the physical intensity of the work routine, the frequency of carrying out activities in the work environment (e.g., carrying loads, the need to walk, staying sitting and standing), and if there is fatigue in performing these tasks. The sports practice at leisure domain is evaluated by four questions about the intensity, frequency, and number of hours in sportive and training activities practiced per week, and for how long the activity is practiced. The leisure time and commuting activities domain is determined by four questions about the frequency of walking and cycling for leisure and commuting, as well as the frequency of watching television in leisure time. The Baecke questionnaire provides a dimensionless score for each assessed domain, which ranges from 1 to 5. The overall physical activity score was calculated by the sum of the three domain scores. It should be noted that the Baecke questionnaire is considered to be a valid measure of physical activity level as observed by its good performance when evaluated by gold-standard assessment methods [38].

2.6. Socioeconomic Level

The Brazilian Criteria for Economic Classification [39] were used to assess the socioeconomic status of the sample. This instrument considers the educational level and the presence and quantity of specific rooms and consumer goods at home. The questionnaire provides a specific score that classified economic classes from highest to lowest (A1, A2, B1, B2, C1, C2, and D), with “high class” being A1 and A2, “medium class” being B1, B2, and C1, and “low class” being C2 and D [39].

2.7. Statistical Analysis

The characteristics of the sample were presented in frequencies, mean values, and standard deviation. Mean differences between QoL scores at baseline and follow-up periods were analyzed by paired t-test. The comparison of domain scores of QoL between persistent depressive and non-depressive groups (not considering the period of assessment) was performed by ANCOVA considering two models. For that, the mean of the value in each domain of QoL at baseline and follow-up was included in the analysis. The first model (Model 1) was adjusted for age, type of surgery, marital status, and socioeconomic status. The second model (Model 2) was composed of Model 1 and physical activity was inserted into this model in order to verify its influence on mean differences. The level of significance was set at p < 0.05 and the confidence interval at 95%. All statistical analyses were performed at SPSS Statistical Package, version 15.0.

3. Results

Table 1 shows the characteristics of the sample. Most of our participants were married and were classified as having medium socioeconomic status. Regarding the presence of depressive symptoms, 17.1% of the participants from our study (n = 12) were classified as having the persistent presence of depressive symptoms. The most frequent types of surgery and adjuvant treatment were mastectomy and chemotherapy, respectively. Approximately 35% of breast cancer survivors underwent all three types of adjuvant treatment (i.e., chemotherapy, radiotherapy, and hormonal therapy).
The domain scores of QoL at baseline and follow-up are presented in Table 2. Statistical analysis indicated that breast cancer survivors without depressive symptoms improved the scores of QoL in the physical limitations and general health status domains after 12 months (Table 2). No statistical difference was observed between baseline and follow-up (i.e., 12 months) for the QoL domains when considering the breast cancer survivors with persistent depressive symptoms (Table 2).
Table 3 shows the comparison of QoL domains between depressive and non-depressive breast cancer survivors. Regarding Model 1, the statistical analysis demonstrated that breast cancer survivors with persistent depressive symptoms (i.e., participants classified as depressed at baseline and at a 12-month follow-up) present lower QoL values in all domains of the QoL when compared with participants without persistent depressive symptoms (i.e., non-depressive). However, in Model 2 (when including the physical activity level as an adjustment in addition to the confounding factors of Model 1), no significant difference was observed between groups for the functional capacity domain of QoL. The difference between breast cancer survivors with depressive symptoms and participants without depressive symptoms in the other domains of QoL remains significant (Table 3). These results may reflect the possible influence of physical activity level on the functional capacity domain of QoL.

4. Discussion

The present study aimed to compare the QoL domains of breast cancer survivors according to persistent depressive symptoms (over 12 months) and analyze the influence of physical activity in the QoL domains in this population. Our results indicated that breast cancer survivors without depressive symptoms improved the QoL (i.e., increased scores) regarding the domains of physical limitations and general health status after 12 months. On the other hand, breast cancer survivors with depressive symptoms did not show significant differences over time. As expected, breast cancer survivors with depressive symptoms showed the worst scores of QoL in all domains when compared with non-depressives, even after adjustment for potential confounding factors (i.e., age, type of surgery, marital status, and socioeconomic status). In addition, after adjusting for physical activity practice, the difference in the scores of the functional capacity domain lost its significance. This result suggests a possible positive effect of physical activity in this QoL domain among breast cancer survivors with depressive symptoms.
Breast cancer survivors with depressive symptoms showed the worst scores in all domains of QoL when compared with women without depressive symptoms. Depression is associated with the individual’s inability to adapt to the stressors of the environment in which they live. Thus, this disorder is characterized by a loss of interest in daily activities, fatigue, pessimism, intense sadness, and guilt [40]. Depression is one of the most prevalent psychological conditions in individuals affected by breast cancer [18]. Despite the well-documented higher prevalence of depression in breast cancer patients, some factors may contribute to the incidence of depression in this population with an impact directly on the QoL. The age (i.e., younger patients), socioeconomic level (i.e., lower income), and level of disease (i.e., severe disease) increase the depression level in breast cancer patients [41]. The time of diagnosis, the type of adjuvant treatment (i.e., chemotherapy), and the number of chemotherapies were related to the presence of depressive symptoms in breast cancer patients [42]. It should be highlighted that depressive symptoms can occur during treatment and also persist after the cure of the disease [18]. In breast cancer survivors, negative thoughts about the future are common and the intensity of such expectations can define the degree of pessimism, which is related to the variability of psychological suffering in this population [18]. Thus, higher degrees of pessimism were associated with a worse QoL in breast cancer survivors [43]. Although the consequences of the disease imply psychological distress, the presence of a previous emotional disorder or concomitant with a physical illness can be considered an aggravating factor for health. Goldney et al. [44] demonstrated that the QoL of individuals with depression was lower than in individuals with the same disease but without depressive symptoms. This result was also evidenced in breast cancer patients [42], mainly in those individuals with several sessions of chemotherapy and more severe disorders [42]. Thus, due to the possibility of depression symptoms persisting after the cure of the disease, which would directly impact the QoL in this population, depression should be considered an important condition to be prevented and treated, especially in breast cancer survivors.
Breast cancer survivors without depressive symptoms improved their QoL regarding the physical limitations and general health domains after 12 months, while participants with depressive symptoms did not show significant differences over time. Breast cancer survivors have had several psychological challenges since the diagnosis of the disease, such as the fear of imminent death, isolation [40], and doubts about the cure [15]. In addition, the physical consequences of treatments to combat breast cancer, such as breast amputation, lymphedema, fatigue, skin changes, pain, and loss of function of the limb homolateral to the surgery, compromise the body image and self-esteem of this population [15,45]. The sum of these factors can contribute to the emergence of mental health issues such as depression [15]. In addition, cancer symptoms associated with depression may be more intense when there is persistent depression, which has a negative impact on physical, emotional, and social health [21]. Moreover, as mentioned previously, depressive symptoms associated with some characteristics of the disease (e.g., number of chemotherapy sessions and disease severity) exacerbate the impairment in the QoL of this population [42]. Such a circumstance may justify the results of this study, since breast cancer survivors who remained depressed over the course of a year presented worse QoL when compared to those without depression.
Although the most of QoL domains remain impaired in breast cancer survivors with depressive symptoms, the “functional capacity” domain seems to be influenced by the level of physical activity in this population. Evidence suggests that changes in lifestyle such as physical activity practice can promote physical [8] and mental [46] benefits, especially in the QoL [8] and depressive symptoms [46] of breast cancer survivors [47]. Likewise, regular practice of physical activity seems to minimize the deleterious effects of breast cancer treatment [46]. Our previous study indicated that the improvement of depression was evidenced mainly in breast cancer survivors with a higher level of physical activity in the leisure/time commuting domain [48]. Breast cancer survivors who participated in a regular program of strength training for six months demonstrated lower depression symptoms and physical fatigue when compared to participants who did not practice strength training [49]. In addition, a recent meta-analysis indicated that mind-body exercise (i.e., activities that combine body movement with mental concentration) may benefit physical fitness, sleep quality, depression, and anxiety [50]. Physical activity programs adapted for the participant’s condition are safe, contribute to the maintenance of a physically active lifestyle, and improve the QoL in breast cancer survivors [47]. The regular practice of physical activity promotes stimulation in several neuroplastic processes involved in cancer disease. For this reason, physical activity helps to reduce the symptoms of depression [28,51] and can contribute to self-esteem and social support [51], which are important aspects of QoL in breast cancer survivors. In addition, physical exercise is associated with reduced inflammation and resistance to oxidative stress [51], factors associated with breast cancer and its recurrence.
Regardless of the attenuation of the functional capacity domains of QoL and depression symptoms in breast cancer survivors, the positive effects of physical activity were not evidenced in other domains of QoL. A possible explanation is that this population has a lower general level of physical activity, since the physical and mental sequelae associated with cancer treatment may result in a reduced engagement in physical activity, which may affect mental health [8,24]. Other factors such as physical and psychological limitations, family responsibilities, lack of transportation, and socioeconomic status have also been reported as important barriers to physical activity [24]. In this sense, evidence about the biological and psychosocial benefits of physical activity may encourage a higher engagement in the practice of physical activity in breast cancer survivors. The lack of knowledge about the benefits of exercise in the sequelae of the breast is one of the barriers to this population’s adherence to physical activity [24]. Thus, we believe that in addition to the adaptation of physical activity considering the participant characteristics, information about the health and benefits of exercise is a key point for maintaining a physically active lifestyle. This is important since physical activity is associated with a better QoL and reduced levels of mental disorders, such as anxiety and depression, among breast cancer survivors [52].
The main limitation of this study is the subjective assessment of physical activity by Baecke’s questionnaire, which did not provide information in minutes per week or account for the intensity of the activities that were performed, precluding more inferences. However, despite this limitation, the Baecke questionnaire is a reliable and valid measurement of habitual physical activity in adults [38]. In addition, the longitudinal design with 12 months of follow-up of the present study, as well as the control of confounding variables in the statistical models, may reduce the chance of possible biases. It is evident that our results indicated that physical activity attenuates the deleterious effect of depressive symptoms on the QoL in breast cancer survivors. Thus, considering that depression is a common mental health issue in general cancer survivors, and that the treatment is specific for each condition, future studies are needed to investigate the influence of physical activity practice in different types of cancer [53].

5. Conclusions

Depressive breast cancer survivors have worse QoL than non-depressive women. However, after adjustment for the practice of physical activity, the difference in the functional capacity domain was attenuated, which suggests that physical activity can improve the QoL of breast cancer survivors with depression. This finding reinforces the need for public policies that promote the physical and mental health of breast cancer survivors, including the increase of physical activity as a habitual practice.

Author Contributions

Conceptualization was performed by F.E.R., M.R.P. and D.G.D.C. Methodology was performed by F.E.R., M.R.P., L.C.M.V. and D.G.D.C. Data curation was performed by F.E.R., M.R.P., C.E.F. and D.T.C. Formal analysis was performed by G.F., G.C.R.S., W.R.T., V.S.B. and D.G.D.C. Investigation was performed by W.R.T., L.C.M.V., V.S.B. and D.G.D.C. The first draft of the manuscript was written by F.E.R. All authors reviewed the manuscript critically for important intellectual content. All authors have read and agreed to the published version of the manuscript.

Funding

This research was financed by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (Capes) [Finance code 001].

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and was approved by the Ethics Committee of School of Technology and Sciences from São Paulo State University (Protocol 019093/2016).

Informed Consent Statement

All participants signed an informed consent form accepting to voluntarily participate in the study, being duly informed of the research procedures and objectives.

Data Availability Statement

All data are available from the corresponding author upon reasonable request.

Conflicts of Interest

The authors have no relevant financial or non-financial conflicts of interest to disclose.

References

  1. World Health Organization (WHO) Global Health Estimates 2020: Deaths by Cause, Age, Sex, by Country and by Region, 2000–2019. Available online: who.int/data/gho/data/themes/mortality-and-global-health-estimates/ghe-leading-causes-of-death (accessed on 10 February 2023).
  2. Bray, F.; Laversanne, M.; Weiderpass, E.; Soerjomataram, I. The Ever-increasing Importance of Cancer as a Leading Cause of Premature Death Worldwide. Cancer 2021, 127, 3029–3030. [Google Scholar] [CrossRef] [PubMed]
  3. Sung, H.; Ferlay, J.; Siegel, R.L.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J. Clin. 2021, 71, 209–249. [Google Scholar] [CrossRef] [PubMed]
  4. Miller, K.D.; Nogueira, L.; Devasia, T.; Mariotto, A.B.; Yabroff, K.R.; Jemal, A.; Kramer, J.; Siegel, R.L. Cancer Treatment and Survivorship Statistics, 2022. CA Cancer J. Clin. 2022, 72, 409–436. [Google Scholar] [CrossRef] [PubMed]
  5. International Agency for Research on Cancer (IARC). Latest Global Cancer Data: Cancer Burden Rises to 18.1 Million New Cases and 9.6 Million Cancer Deaths in 2018. Available online: https://www.iarc.fr/wpcontent/uploads/2018/09/-pr263_E.pdf (accessed on 23 October 2022).
  6. Reinert, T.; Pellegrini, R.; Rol, R.; Werutsky, G.; Barrios, C.H. Estimation of the Number of Brazilian Women Living With Metastatic Breast Cancer. JCO Glob. Oncol. 2020, 6, 307–312. [Google Scholar] [CrossRef]
  7. Bonadio, R.C.; Moreira, O.A.; Testa, L. Breast Cancer Trends in Women Younger than 40 Years in Brazil. Cancer Epidemiol. 2022, 78, 102139. [Google Scholar] [CrossRef]
  8. Fontes, K.P.; Veiga, D.F.; Naldoni, A.C.; Sabino-Neto, M.; Ferreira, L.M. Physical Activity, Functional Ability, and Quality of Life after Breast Cancer Surgery. J. Plast. Reconstr. Aesthetic Surg. 2019, 72, 394–400. [Google Scholar] [CrossRef] [PubMed]
  9. Taghian, N.R.; Miller, C.L.; Jammallo, L.S.; O’Toole, J.; Skolny, M.N. Lymphedema Following Breast Cancer Treatment and Impact on Quality of Life: A Review. Crit. Rev. Oncol. Hematol. 2014, 92, 227–234. [Google Scholar] [CrossRef]
  10. Ho, S.S.M.; So, W.K.W.; Leung, D.Y.P.; Lai, E.T.L.; Chan, C.W.H. Anxiety, Depression and Quality of Life in Chinese Women with Breast Cancer during and after Treatment: A Comparative Evaluation. Eur. J. Oncol. Nurs. 2013, 17, 877–882. [Google Scholar] [CrossRef]
  11. Hormozi, M.; Hashemi, S.-M.; Shahraki, S. Investigating Relationship between Pre- and Post- Chemotherapy Cognitive Performance with Levels of Depression and Anxiety in Breast Cancer Patients: A Cross-Sectional Study. Asian Pac. J. Cancer Prev. 2019, 20, 3831–3837. [Google Scholar] [CrossRef] [Green Version]
  12. Ribeiro, F.E.; Vanderlei, L.C.M.; Palma, M.R.; Tebar, W.R.; Caldeira, D.T.; Teles Fregonesi, C.E.P.; Christofaro, D.G.D. Body Dissatisfaction and Its Relationship with Overweight, Sedentary Behavior and Physical Activity in Survivors of Breast Cancer. Eur. J. Obstet. Gynecol. Reprod. Biol. 2018, 229, 153–158. [Google Scholar] [CrossRef]
  13. Hsiao, F.-H.; Kuo, W.-H.; Jow, G.-M.; Wang, M.-Y.; Chang, K.-J.; Lai, Y.-M.; Chen, Y.-T.; Huang, C.-S. The Changes of Quality of Life and Their Correlations with Psychosocial Factors Following Surgery among Women with Breast Cancer from the Post-Surgery to Post-Treatment Survivorship. Breast 2019, 44, 59–65. [Google Scholar] [CrossRef] [PubMed]
  14. Lopes-Conceição, L.; Brandão, M.; Araújo, N.; Severo, M.; Dias, T.; Peleteiro, B.; Fontes, F.; Pereira, S.; Lunet, N. Quality of Life Trajectories during the First Three Years after Diagnosis of Breast Cancer: The NEON-BC Study. J. Public Health 2021, 43, 521–531. [Google Scholar] [CrossRef] [PubMed]
  15. Galiano-Castillo, N.; Ariza-García, A.; Cantarero-Villanueva, I.; Fernández-Lao, C.; Díaz-Rodríguez, L.; Arroyo-Morales, M. Depressed Mood in Breast Cancer Survivors: Associations with Physical Activity, Cancer-Related Fatigue, Quality of Life, and Fitness Level. Eur. J. Oncol. Nurs. 2014, 18, 206–210. [Google Scholar] [CrossRef] [PubMed]
  16. Abrahams, H.J.G.; Gielissen, M.F.M.; Verhagen, C.A.H.H.V.M.; Knoop, H. The Relationship of Fatigue in Breast Cancer Survivors with Quality of Life and Factors to Address in Psychological Interventions: A Systematic Review. Clin. Psychol. Rev. 2018, 63, 1–11. [Google Scholar] [CrossRef] [PubMed]
  17. Shin, W.; Song, S.; Jung, S.-Y.; Lee, E.; Kim, Z.; Moon, H.-G.; Noh, D.-Y.; Lee, J.E. The Association between Physical Activity and Health-Related Quality of Life among Breast Cancer Survivors. Health Qual. Life Outcomes 2017, 15, 132. [Google Scholar] [CrossRef] [Green Version]
  18. Calderon, C.; Carmona-Bayonas, A.; Hernández, R.; Ghanem, I.; Castelo, B.; Martinez de Castro, E.; Ferreira, E.; Ciria, L.; Muñiz, M.; Jimenez-Fonseca, P. Effects of Pessimism, Depression, Fatigue, and Pain on Functional Health-Related Quality of Life in Patients with Resected Non-Advanced Breast Cancer. Breast 2019, 44, 108–112. [Google Scholar] [CrossRef]
  19. Tsaras, K.; Papathanasiou, I.V.; Mitsi, D.; Veneti, A.; Kelesi, M.; Zyga, S.; Fradelos, E.C. Assessment of Depression and Anxiety in Breast Cancer Patients: Prevalence and Associated Factors. Asian Pac. J. Cancer Prev. 2018, 19, 1661–1669. [Google Scholar] [CrossRef]
  20. Purkayastha, D.; Venkateswaran, C.; Nayar, K.; Unnikrishnan, U. Prevalence of Depression in Breast Cancer Patients and Its Association with Their Quality of Life: A Cross-Sectional Observational Study. Indian J. Palliat. Care 2017, 23, 268. [Google Scholar] [CrossRef]
  21. Kim, S.-Y.; Kim, S.-W.; Shin, I.-S.; Park, M.-H.; Yoon, J.-H.; Yoon, J.-S.; Kim, J.-M. Changes in Depression Status during the Year after Breast Cancer Surgery and Impact on Quality of Life and Functioning. Gen. Hosp. Psychiatry 2018, 50, 33–37. [Google Scholar] [CrossRef]
  22. Boing, L.; Pereira, G.S.; Vieira, M.D.C.S.; Seemann, T.; Cardoso, A.A.; Sperandio, F.F.; Borgatto, A.F.; Baptista, F.; Guimarães, A.C.D.A. Physical activity and quality of life in women with breast cancer—A cross-sectional study. Rev. Bras. Med. Esporte 2018, 24, 377–381. [Google Scholar] [CrossRef]
  23. Canário, A.C.G.; Cabral, P.U.L.; Paiva, L.C.D.; Florencio, G.L.D.; Spyrides, M.H.; Gonçalves, A.K.D.S. Physical Activity, Fatigue and Quality of Life in Breast Cancer Patients. Rev. Assoc. Med. Bras. 2016, 62, 38–44. [Google Scholar] [CrossRef] [Green Version]
  24. Pudkasam, S.; Polman, R.; Pitcher, M.; Fisher, M.; Chinlumprasert, N.; Stojanovska, L.; Apostolopoulos, V. Physical Activity and Breast Cancer Survivors: Importance of Adherence, Motivational Interviewing and Psychological Health. Maturitas 2018, 116, 66–72. [Google Scholar] [CrossRef] [Green Version]
  25. Spei, M.-E.; Samoli, E.; Bravi, F.; La Vecchia, C.; Bamia, C.; Benetou, V. Physical Activity in Breast Cancer Survivors: A Systematic Review and Meta-Analysis on Overall and Breast Cancer Survival. Breast 2019, 44, 144–152. [Google Scholar] [CrossRef]
  26. Aydin, M.; Kose, E.; Odabas, I.; Meric Bingul, B.; Demirci, D.; Aydin, Z. The Effect of Exercise on Life Quality and Depression Levels of Breast Cancer Patients. Asian Pac. J. Cancer Prev. 2021, 22, 725–732. [Google Scholar] [CrossRef] [PubMed]
  27. Bai, L.; Arver, B.; Johansson, H.; Sandelin, K.; Wickman, M.; Brandberg, Y. Body Image Problems in Women with and without Breast Cancer 6-20 Years after Bilateral Risk-Reducing Surgery-A Prospective Follow-up Study. Breast 2019, 44, 120–127. [Google Scholar] [CrossRef] [Green Version]
  28. Fisher, H.M.; Jacobs, J.M.; Taub, C.J.; Lechner, S.C.; Lewis, J.E.; Carver, C.S.; Blomberg, B.B.; Antoni, M.H. How Changes in Physical Activity Relate to Fatigue Interference, Mood, and Quality of Life during Treatment for Non-Metastatic Breast Cancer. Gen. Hosp. Psychiatry 2017, 49, 37–43. [Google Scholar] [CrossRef]
  29. Lugo, D.; Pulido, A.L.; Mihos, C.G.; Issa, O.; Cusnir, M.; Horvath, S.A.; Lin, J.; Santana, O. The Effects of Physical Activity on Cancer Prevention, Treatment and Prognosis: A Review of the Literature. Complement. Ther. Med. 2019, 44, 9–13. [Google Scholar] [CrossRef] [PubMed]
  30. Snedecor, G.W.; Cochran, W.G. Statistical Methods, 8th ed.; Iowa State Press: Ames, IA, USA, 1989. [Google Scholar]
  31. Chen, X.; Wang, Q.; Zhang, Y.; Xie, Q.; Tan, X. Physical Activity and Risk of Breast Cancer: A Meta-Analysis of 38 Cohort Studies in 45 Study Reports. Value Health J. Int. Soc. Pharm. Outcomes Res. 2019, 22, 104–128. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Botega, N.J.; Bio, M.R.; Zomignani, M.A.; Garcia, C., Jr.; Pereira, W.A.B. Transtornos Do Humor Em Enfermaria de Clínica Médica e Validação de Escala de Medida (HAD) de Ansiedade e Depressão. Rev. Saude Publica 1995, 29, 359–363. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Zigmond, A.S.; Snaith, R.P. The Hospital Anxiety and Depression Scale. Acta Psychiatr. Scand. 1983, 67, 361–370. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Ghrouz, A.K.; Noohu, M.M.; Dilshad Manzar, M.; Warren Spence, D.; BaHammam, A.S.; Pandi-Perumal, S.R. Physical Activity and Sleep Quality in Relation to Mental Health among College Students. Sleep Breath. 2019, 23, 627–634. [Google Scholar] [CrossRef]
  35. Laguardia, J.; Campos, M.R.; Travassos, C.; Najar, A.L.; Anjos, L.A.D.; Vasconcellos, M.M. Brazilian Normative Data for the Short Form 36 Questionnaire, Version 2. Rev. Bras. Epidemiol. 2013, 16, 889–897. [Google Scholar] [CrossRef]
  36. Ware, J.E.J.; Sherbourne, C.D. The MOS 36-Item Short-Form Health Survey (SF-36). I. Conceptual Framework and Item Selection. Med. Care 1992, 30, 473–483. [Google Scholar] [CrossRef]
  37. Baecke, J.A.; Burema, J.; Frijters, J.E. A Short Questionnaire for the Measurement of Habitual Physical Activity in Epidemiological Studies. Am. J. Clin. Nutr. 1982, 36, 936–942. [Google Scholar] [CrossRef]
  38. Tebar, W.R.; Ritti-Dias, R.M.; Fernandes, R.A.; Damato, T.M.; Barros, M.V.D.; Mota, J.; Andersen, L.B.; Christofaro, D.G.D. Validity and Reliability of the Baecke Questionnaire against Accelerometer-Measured Physical Activity in Community Dwelling Adults According to Educational Level. PLoS ONE 2022, 17, e0270265. [Google Scholar] [CrossRef] [PubMed]
  39. ABEP-Associação Brasileira de Empresas de Pesquisa Critérios de Classificação Econômica Brasileira. Available online: https://www.abep.org/criterio-brasil (accessed on 30 October 2022).
  40. Cvetković, J.; Nenadović, M. Depression in Breast Cancer Patients. Psychiatry Res. 2016, 240, 343–347. [Google Scholar] [CrossRef]
  41. Sun, F.-K.; Lu, C.-Y.; Yao, Y.; Chiang, C.-Y. Social Functioning, Depression, and Quality of Life among Breast Cancer Patients: A Path Analysis. Eur. J. Oncol. Nurs. 2023, 62, 102237. [Google Scholar] [CrossRef] [PubMed]
  42. Cáceres, M.C.; Nadal-Delgado, M.; López-Jurado, C.; Pérez-Civantos, D.; Guerrero-Martín, J.; Durán-Gómez, N. Factors Related to Anxiety, Depressive Symptoms and Quality of Life in Breast Cancer. Int. J. Environ. Res. Public Health 2022, 19, 3547. [Google Scholar] [CrossRef] [PubMed]
  43. Petersen, L.R.; Clark, M.M.; Novotny, P.; Kung, S.; Sloan, J.A.; Patten, C.A.; Vickers, K.S.; Rummans, T.A.; Frost, M.H.; Colligan, R.C. Relationship of Optimism–Pessimism and Health-Related Quality of Life in Breast Cancer Survivors. J. Psychosoc. Oncol. 2008, 26, 15–32. [Google Scholar] [CrossRef]
  44. Goldney, R.D.; Phillips, P.J.; Fisher, L.J.; Wilson, D.H. Diabetes, Depression, and Quality of Life. Diabetes Care 2004, 27, 1066–1070. [Google Scholar] [CrossRef] [Green Version]
  45. Temur, K.; Kapucu, S. The Effectiveness of Lymphedema Self-Management in the Prevention of Breast Cancer-Related Lymphedema and Quality of Life: A Randomized Controlled Trial. Eur. J. Oncol. Nurs. 2019, 40, 22–35. [Google Scholar] [CrossRef] [PubMed]
  46. Bedillion, M.F.; Ansell, E.B.; Thomas, G.A. Cancer Treatment Effects on Cognition and Depression: The Moderating Role of Physical Activity. Breast 2019, 44, 73–80. [Google Scholar] [CrossRef]
  47. Garcia, D.O.; Thomson, C.A. Physical Activity and Cancer Survivorship. Nutr. Clin. Pract. 2014, 29, 768–779. [Google Scholar] [CrossRef] [PubMed]
  48. Ribeiro, F.E.; Palma, M.R.; Silva, D.T.C.; Tebar, W.R.; Vanderlei, L.C.M.; Fregonesi, C.E.P.T.; Christofaro, D.G.D. Relationship of Anxiety and Depression Symptoms with the Different Domains of Physical Activity in Breast Cancer Survivors. J. Affect. Disord. 2020, 273, 210–214. [Google Scholar] [CrossRef]
  49. Chaves, S.N.; Lima, F.D.D.; Perondi, B.B.; Vieira, J.; Elias, J.D.M.; Ribeiro, L.A.; Silva, A.K.S.; Clael, S.; de Oliveira, R.J. Fatigue and Depression Improvements on Breast Cancer Survivors Practitioners of Strength Training. Rev. Bras. Cineantropometria Desempenho Hum. 2021, 23, e73039. [Google Scholar] [CrossRef]
  50. Duan, L.; Xu, Y.; Li, M. Effects of Mind-Body Exercise in Cancer Survivors: A Systematic Review and Meta-Analysis. Evidence-Based Complement. Altern. Med. 2020, 2020, 1–13. [Google Scholar] [CrossRef]
  51. Kandola, A.; Ashdown-Franks, G.; Hendrikse, J.; Sabiston, C.M.; Stubbs, B. Physical Activity and Depression: Towards Understanding the Antidepressant Mechanisms of Physical Activity. Neurosci. Biobehav. Rev. 2019, 107, 525–539. [Google Scholar] [CrossRef]
  52. Kugbey, N.; Meyer-Weitz, A.; Oppong Asante, K. Access to Health Information, Health Literacy and Health-Related Quality of Life among Women Living with Breast Cancer: Depression and Anxiety as Mediators. Patient Educ. Couns. 2019, 102, 1357–1363. [Google Scholar] [CrossRef]
  53. Yi, J.C.; Syrjala, K.L. Anxiety and Depression in Cancer Survivors. Med. Clin. N. Am. 2017, 101, 1099–1113. [Google Scholar] [CrossRef]
Table 1. Characteristics of the sample (n = 70).
Table 1. Characteristics of the sample (n = 70).
Variablesn (%) or
Mean ± Standard Deviation
Demographic characteristics
Age, years50.8 ± 9.7
Body Mass Index, kg/m228.8 ± 4.7
Physical Activity Level, score7.8 ± 1.7
Marital status
Single7 (10.0)
Married45 (64.3)
Divorced7 (10.0)
Widow11 (15.7)
Socioeconomic status
High class11 (15.7)
Medium class55 (78.6)
Low class4 (5.7)
Type of surgery
Quadrantectomy30 (42.9)
Mastectomy40 (57.1)
Adjuvant treatment
Chemotherapy52 (74.3)
Radiotherapy44 (62.9)
Hormonal Therapy41 (58.6)
None6 (4.2)
Table 2. Domain scores of quality of life at baseline and after a 12-month follow-up according to persistent depressive symptoms in breast cancer survivors (n = 70).
Table 2. Domain scores of quality of life at baseline and after a 12-month follow-up according to persistent depressive symptoms in breast cancer survivors (n = 70).
Non-Depressive (n = 58)Depressive (n = 12)
BaselineFollow-Up BaselineFollow-Up
Mean (SE)Mean (SE)p-Value *Mean (SE)Mean (SE)p-Value *
Functional capacity73.6 (3.0)72.8 (3.2)0.76352.7 (6.1)55.0 (7.1)0.797
Physical limitations63.4 (5.8)81.1 (4.8)0.00215.9 (9.7)25.0 (11.2)0.519
Body pain60.5 (3.0)59.9 (2.8)0.83733.8 (5.9)40.4 (5.1)0.367
General health status80.1 (2.4)84.9 (1.9)0.03756.6 (7.0)54.6 (7.7)0.713
Vitality65.4 (2.5)62.7 (2.8)0.32538.6 (6.5)44.4 (8.7)0.439
Social aspects86.7 (2.9)89.6 (2.5)0.33144.3 (7.2)43.2 (9.9)0.867
Emotional limitations75.3 (5.3)78.9 (4.9)0.48415.1 (9.4)30.3 (13.8)0.211
Mental health75.4 (2.3)76.0 (2.5)0.77548.7 (8.5)46.9 (8.5)0.758
* p-value of paired t-test. SE = Standard error; Bold value indicates significant difference.
Table 3. Multiple comparison models of quality-of-life domain scores after a 12-month follow-up between depressive and non-depressive breast cancer survivors (n = 70).
Table 3. Multiple comparison models of quality-of-life domain scores after a 12-month follow-up between depressive and non-depressive breast cancer survivors (n = 70).
Non-Depressive (n = 58)Persistent-Depressive (n = 12)Model 1Model 2
Mean (SE)Mean (SE)p-Value *Effect Sizep-Value *Effect Size
Functional capacity73.01 (3.36)53.81 (8.15)0.0370.0670.0540.060
Physical limitations81.50 (4.66)23.06 (11.30)0.0000.2580.0000.277
Body pain60.20 (2.71)38.86 (6.58)0.0050.1200.0030.132
General health status84.70 (2.15)55.84 (5.20)0.0000.2860.0000.285
Vitality62.80 (2.98)43.64 (7.22)0.0190.0840.0340.072
Social aspects89.63 (2.81)43.27 (6.82)0.0000.3750.0000.361
Emotional limitations78.43 (5.04)32.53 (12.23)0.0010.1550.0020.150
Mental health75.62 (2.75)48.99 (6.66)0.0010.1720.0010.172
* p-value of analysis of covariance (ANCOVA). Model 1 = Adjusted for age, type of surgery, marital status, and socioeconomic status; Model 2 = Model 1+ physical activity; SE = Standard error; Bold values indicate significant difference.
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MDPI and ACS Style

Ribeiro, F.E.; Tebar, W.R.; Ferrari, G.; Palma, M.R.; Fregonesi, C.E.; Caldeira, D.T.; Silva, G.C.R.; Vanderlei, L.C.M.; Beretta, V.S.; Christofaro, D.G.D. Comparison of Quality of Life in Breast Cancer Survivors with and without Persistent Depressive Symptoms: A 12-Month Follow-Up Study. Int. J. Environ. Res. Public Health 2023, 20, 3663. https://doi.org/10.3390/ijerph20043663

AMA Style

Ribeiro FE, Tebar WR, Ferrari G, Palma MR, Fregonesi CE, Caldeira DT, Silva GCR, Vanderlei LCM, Beretta VS, Christofaro DGD. Comparison of Quality of Life in Breast Cancer Survivors with and without Persistent Depressive Symptoms: A 12-Month Follow-Up Study. International Journal of Environmental Research and Public Health. 2023; 20(4):3663. https://doi.org/10.3390/ijerph20043663

Chicago/Turabian Style

Ribeiro, Fernanda Elisa, William Rodrigues Tebar, Gerson Ferrari, Mariana Romanholi Palma, Cristina Elena Fregonesi, Daniela Tanajura Caldeira, Gabriela Caroline Rodrigues Silva, Luiz Carlos Marques Vanderlei, Victor Spiandor Beretta, and Diego Giulliano Destro Christofaro. 2023. "Comparison of Quality of Life in Breast Cancer Survivors with and without Persistent Depressive Symptoms: A 12-Month Follow-Up Study" International Journal of Environmental Research and Public Health 20, no. 4: 3663. https://doi.org/10.3390/ijerph20043663

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