Association of Physical Activity and Sedentary Behavior With the Risk of Colorectal Cancer

Sanghyun An; Sungjin Park

doi:10.3346/jkms.2022.37.e158

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An and Park: Association of Physical Activity and Sedentary Behavior With the Risk of Colorectal Cancer

Original Article

Preventive & Social Medicine

Journal of Korean Medical Science 2022; 37(19): e158.

Published online: 10 May 2022

DOI: https://doi.org/10.3346/jkms.2022.37.e158

Association of Physical Activity and Sedentary Behavior With the Risk of Colorectal Cancer

Sanghyun An¹

, Sungjin Park²

¹Department of Surgery, Yonsei University Wonju College of Medicine, Wonju, Korea.

²Department of Occupational and Environmental Medicine, Incheon Nasaret International Hospital, Incheon, Korea.

Address for Correspondence: Sungjin Park, MD, PhD. Department of Occupational and Environmental Medicine, Incheon Nasaret International Hospital, 98 Meonugeum-ro, Yeonsu-gu, Incheon 21972, Republic of Korea. psjin9318@yonsei.ac.kr

Received 6 February 2022 Accepted 18 April 2022

The Korean Academy of Medical Sciences

https://creativecommons.org/licenses/by-nc/4.0/

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Although recent evidence supports that prolonged sedentary behavior and reduced physical activity are associated with colorectal cancer risk, there are few studies analyzing the colorectal cancer risk according to different types of physical activity and combined effects of sedentary behavior and physical activity on colorectal cancer. This study aimed to investigate the association of sedentary behavior and physical activity with colorectal cancer.

Methods

A cross-sectional study included a total of 33,403 participants from the Korea National Health and Nutrition Examination Survey from 2014 to 2019. Sedentary behavior was dichotomized into < 10 hr/day and ≥ 10 hr/day, and three types of physical activity were investigated, including leisure-time, occupational, and transportation physical activity. Multiple logistic regression analyses were performed to assess the risk of colorectal cancer in relation to sedentary behavior and physical activity.

Results

Sedentary behavior was associated with an increased risk of colorectal cancer (odds ratio [OR] 1.64; 95% confidence interval [CI], 1.22–2.21), while the different domains of physical activity were not significantly associated with colorectal cancer risk. In a combined analysis, those with sedentary behavior and without physical activity showed an increased risk of colorectal cancer compared to that of the reference category without sedentary behavior and with physical activity (OR, 1.49; 95% CI, 1.02–2.16).

Conclusion

This study found that sedentary behavior was significantly associated with the increased risk of colorectal cancer. Moreover, sedentary behavior without physical activity increased the risk of colorectal cancer. Reducing sedentary behavior and recommending any type of physical activity may reduce the risk of colorectal cancer.

Graphical Abstract

Keywords: Colorectal Neoplasm, Risk Factors, Sedentary Behavior, Physical Activity, Exercise

INTRODUCTION

Colorectal cancer (CRC) is the third most commonly diagnosed cancer and the second leading cause of cancer-related deaths worldwide.1 The incidence of CRC is known to be high in developed countries, and its incidence is increasing in Asia as socioeconomic development progresses. South Korea has the second highest incidence of CRC worldwide with 44.5 cases per 100,000 persons per year.2 With well-recognized risk factors such as aging, alcohol consumption, smoking, obesity, and family history, lifestyle changes in diets or in work patterns are emerging as risk factors for CRC.3 4

Recent evidence suggests that sedentary behavior (SB) can increase the risk of chronic diseases including CRC.5 SB is a concept separate from physical inactivity and refers to all activities with an energy expenditure of ≤ 1.5 metabolic equivalents of task, such as sitting, reclining, or lying postures.6 Modern individuals spend their time sitting while watching TV, reading, driving, and using computers in an office or at home. A review article estimated that adults in Korea spend 8.3 hours per day in SB, which was much higher than the standard recommended sedentary time in Korea and other countries.7 Previous studies have reported that the risk of chronic disease increases with increased SB.8 In addition to SB, physical activity (PA) is well-known for health-related lifestyle benefits, and may also influence the development of CRC.9 10 PA refers to any kind of body movement that requires energy expenditure, and can be classified into four domains: leisure-time PA (LTPA), occupational PA (OPA), domestic PA, and transportation PA (TPA).11 Both SB and PA are modifiable lifestyle-related factors, so interventions to correct them have significant potential in reducing the burden of cancer worldwide.

The relationship between PA, SB, and CRC requires a deeper understanding. First, the types of PA can have different effects on health. For example, LTPA has been consistently shown to have a favorable health effect, whereas OPA was often reported to have adverse effects on health.12 13 It is necessary to study whether this phenomenon, termed the “PA health paradox,” also applies to CRC. Second, it is essential to include both SB and PA when estimating their association with CRC. This is because some office workers who spend much time in SB at work can meet PA standards after work. Conversely, manual workers who have less SB but enough OPA at work due to strenuous physical labor may spend much time in SB after work. To our knowledge, no study has analyzed how the association of SB with CRC varies with different types of PA. Therefore, this study aimed to investigate the association of SB and different types of PA with the risk of CRC.

METHODS

Data and participants

This cross-sectional study was conducted in November 2021, based on the Korea National Health and Nutrition Examination Survey (KNHANES) data VI–VIII collected by the Korea Centers for Disease Control Prevention (KCDC) from 2014 to 2019. KNHANES is conducted annually to assess the health and nutritional status of the Korean population.

A total of 47,309 participants were identified from the data from 2014 to 2019. A final sample of 33,403 participants was selected which included all adults aged ≥ 20 years old with complete information on PA, SB, and CRC. Participants with missing values for PA (n = 2,028) and CRC (n = 2,060) were excluded.

Measurements

For CRC, participants were asked if they had ever been diagnosed with CRC by a physician. Those who had not been diagnosed with CRC were included in the non-CRC group. SB and PA were evaluated using the Global Physical Activity Questionnaire (GPAQ) as a part of the KNHANES. The GPAQ was devised by the WHO and consisted of a self-reported questionnaire on OPA, LTPA, TPA, and SB.14 The validity and reliability of the Korean version has been verified.15 SB was evaluated by asking the question, “Except for sleeping time, how many hours a day do you usually spend sitting or reclining?” In this study, SB was dichotomized into < 10 hours and ≥ 10 hours modifying the criteria of a previous study in Korea.16

PA was defined based on the questions on OPA, LTPA, and TPA of the GPAQ. In these questions, “vigorous-intensity activity” referred to PA that required strenuous physical efforts and significantly increased breathing or heart rate, whereas “moderate-intensity activity” referred to PA that required moderate physical effort and slightly increased breathing or heart rate. The WHO recommended standard for PA in adults is ≥ 150 minutes of moderate-intensity activity per week or ≥ 75 minutes of vigorous-intensity activity per week.17 Therefore, those who engaged in ≥150 minutes of moderate-intensity activity per week or ≥ 75 minutes of vigorous-intensity activity per week were defined as participants of PA in both OPA and LTPA.18 TPA was defined as physical activity such as walking or cycling for ≥ 150 minutes per week when moving from place to place, except for work-related movement. If any one of the above three types of PA was performed, it was defined as any PA (+), and if no PA was performed, it was classified as any PA (−). Also, four groups were created using any PA and SB as combined variables: 1) SB (−) and PA (+) as the reference group, 2) SB (−) and PA (−), 3) SB (+) and PA (+), and 4) SB (+) and PA (−).

This study included the following demographic and health-related factors: age group (20–29, 30–39, 40–49, 50–59, ≥ 60 years), sex (male or female), marital status (married or other [divorced, single, widowed]), obesity (body mass index ≥ 25 or < 25 kg/m²), income level (high, mid-high, mid-low, and low), educational level (middle school or lower, high school, college or higher), smoking status (current smoker, ex/non-smoker), binge drinking, presence of cancer (any cancer except for CRC), and chronic disease (hypertension, diabetes, dyslipidemia, and cardiovascular disease). Binge drinking was defined as intake of ≥ 7 drinks for men or ≥ 5 drinks for women at least twice a week during the past year.

Statistical analysis

The χ² tests were performed to analyze the relationship between CRC and the demographic and health-related variables. Multiple logistic regression analysis was used to determine the odds ratios (ORs) and 95% confidence intervals (CIs) of SB and different types of PA for CRC risk, after adjusting covariates included age, sex, marital status, obesity, smoking status, educational level, chronic diseases, and cancer diagnosis. Finally, to investigate the combined effect of SB and PA on the risk of CRC, ORs and 95% CIs for CRC risk were calculated according to the four groups of combined SB and PA. All analyses were performed using IBM SPSS Statistics for Windows ver. 25.0 (IBM Corp., Armonk, NY, USA), and statistical significance was set at P < 0.05.

Ethics statement

The KNHANES was approved by the Institutional Review Board of the KCDC, and written informed consent was obtained from all participants.

RESULTS

Table 1 shows the association of CRC prevalence and participant demographics and health-related factors. The prevalence of CRC was significantly associated with male sex, older age, being married, obesity, being a non- or ex-smoker, lower educational level, the presence of chronic disease or cancer, and sitting time of ≥ 10 hr/day. However, binge drinking, income level, and all types of PA were not significantly associated with CRC.

Table 1

Association between general characteristics and CRC prevalence

Characteristics		Total (N = 33,403)	CRC diagnosed		P value^a
Characteristics		Total (N = 33,403)	No	Yes	P value^a
Sex					< 0.001
	Male	14,425 (43.18)	14,303 (99.15)	122 (0.85)
	Female	18,978 (56.82)	18,907 (99.63)	71 (0.37)
Age, yr					< 0.001
	20–29	3,706 (11.09)	3,706 (100.00)	0 (0.00)
	30–39	5,222 (15.63)	5,221 (99.98)	1 (0.02)
	40–49	6,060 (18.14)	6,054 (99.90)	6 (0.10)
	50–59	6,508 (19.48)	6,475 (99.49)	33 (0.51)
	60 and above	11,907 (35.65)	11,754 (98.72)	153 (1.28)
Marital status					< 0.001
	Married	28,182 (84.37)	27,992 (99.33)	190 (0.67)
	Other status	5,220 (15.63)	5,217 (99.94)	3 (0.06)
Body mass index, kg/m²					0.050
	< 25	31,666 (94.8)	31,477 (99.40)	189 (0.60)
	≥ 25	1,737 (5.2)	1,733 (99.77)	4 (0.23)
Smoking status					0.022
	Non- or ex-smoker	27,241 (82.14)	27,072 (99.38)	169 (0.62)
	Current smoker	5,922 (17.86)	5,900 (99.63)	22 (0.37)
Binge drinking					0.615
	No	29,499 (88.91)	29,327 (99.42)	172 (0.58)
	Yes	3,678 (11.09)	3,659 (99.48)	19 (0.52)
Income level					0.678
	Low	8,374 (25.15)	8,319 (99.34)	55 (0.66)
	Middle low	8,378 (25.17)	8,331 (99.44)	47 (0.56)
	Middle high	8,377 (25.16)	8,328 (99.42)	49 (0.58)
	High	8,161 (24.51)	8,119 (99.49)	42 (0.51)
Education level					< 0.001
	Middle school or lower	10,580 (31.86)	10,474 (99.00)	106 (1.00)
	High school	10,588 (31.89)	10,542 (99.57)	46 (0.43)
	College or higher	12,035 (36.25)	11,998 (99.69)	37 (0.31)
Chronic disease					< 0.001
	No	22,491 (67.33)	22,405 (99.62)	86 (0.38)
	Yes^b	10,912 (32.67)	10,805 (99.02)	107 (0.98)
Cancer					0.007
	No	32,196 (96.39)	32,017 (99.44)	179 (0.56)
	Yes^c	1,207 (3.61)	1,193 (98.84)	14 (1.16)
Sedentary behavior					0.018
	No	20,399 (62.27)	20,300 (99.51)	99 (0.49)
	Yes^d	12,358 (37.73)	12,273 (99.31)	85 (0.69)
OPA					0.122
	No	31,506 (94.32)	31,319 (99.41)	187 (0.59)
	Yes^e	1,897 (5.68)	1,891 (99.68)	6 (0.32)
LTPA					0.985
	No	28,194 (84.41)	28,031 (99.42)	163 (0.58)
	Yes^f	5,209 (15.59)	5,179 (99.42)	30 (0.58)
TPA					0.197
	No	23,691 (70.92)	23,546 (99.39)	145 (0.61)
	Yes^g	9,712 (29.08)	9,664 (99.51)	48 (0.49)

CRC = colorectal cancer, OPA = occupational physical activity, LTPA = leisure-time physical activity, TPA = transportation physical activity, PA = physical activity.

^a P value from χ² test.

^bHaving any chronic diseases including hypertension, diabetes, dyslipidemia, and cardiovascular disease diagnosed by a physician.

^cHaving any cancers including stomach, liver, uterine cervical, breast, lung, and thyroid cancer diagnosed by physician.

^dSitting time ≥ 10 hr/day.

^eDoing ≥ 150 minutes of moderate PA or ≥ 75 minutes of vigorous PA in a week at work.

^fDoing ≥ 150 minutes of moderate PA or ≥ 75 minutes of vigorous PA in a week during leisure time.

^gDoing ≥ 150 minutes of PA in a week during transportation.

Table 2 shows the Ors for the association between SB, different types of PA, and CRC. In a fully adjusted model, SB was significantly associated with an increased risk of CRC (OR, 1.62; 95% CI, 1.20–2.17). However, different types of PA such as OPA, LTPA, and TPA were not significantly associated with CRC risk. Any PA of at least one of the above three activity types was also not associated with CRC risk.

Table 2

Association of colorectal cancer risk with sedentary behavior and PA

Variables		Crude	Adjusted^a
Sedentary behavior
	No	1.00 (reference)	1.00 (reference)
	Yes^b	1.42 (1.06–1.90)	1.64 (1.22–2.21)
OPA
	No	1.00 (reference)	1.00 (reference)
	Yes^c	0.53 (0.24–1.20)	0.92 (0.41–2.10)
LTPA
	No	1.00 (reference)	1.00 (reference)
	Yes^d	1.00 (0.67–1.47)	1.25 (0.83–1.88)
TPA
	No	1.00 (reference)	1.00 (reference)
	Yes^e	0.81 (0.58–1.12)	0.92 (0.66–1.29)
Any PA
	No	1.00 (reference)	1.00 (reference)
	Yes^f	0.82 (0.61–1.10)	1.01 (0.75–1.36)

PA = physical activity, OPA = occupational physical activity, LTPA = leisure-time physical activity, TPA = transportation physical activity.

^aAdjusted covariates included sex, age, marital status, obesity, smoking status, educational level, having chronic diseases and cancer.

^bSitting time ≥ 10 hr/day.

^cDoing ≥ 150 minutes of moderate PA or ≥ 75 minutes of vigorous PA in a week at work.

^dDoing ≥ 150 minutes of moderate PA or ≥ 75 minutes of vigorous PA in a week during leisure time.

^eDoing ≥ 150 minutes of PA in a week during transportation.

^fPerforming at least one of three types of PA, including OPA, LTPA, or TPA.

Table 3 describes the risk of CRC according to four categories using SB and PA as combined variables. Compared to the reference group without SB and with PA, those with SB and without PA were significantly associated with an increased risk of CRC (OR, 1.49; 95% CI, 1.02–2.16). The other two groups did not show a significant association with CRC risk (Fig. 1).

Table 3

Combined effect of SB and PA on colorectal cancer risk

SB^a	PA^b	Crude	Adjusted^c
No	Yes	1.00 (reference)	1.00 (reference)
No	No	1.31 (0.90–1.91)	0.80 (0.55–1.18)
Yes	Yes	1.30 (0.80–2.10)	1.38 (0.85–2.26)
Yes	No	1.91 (1.33–2.75)	1.49 (1.02–2.16)

SB = sedentary behavior, PA = physical activity.

^aSitting time ≥ 10 hr/day.

^bPerforming at least one of three types of PA, including occupational PA, leisure-time PA, or transportation PA.

^cAdjusted covariates included sex, age, marital status, obesity, smoking status, educational level, having chronic diseases and cancer.

Fig. 1

Fully adjusted odds ratios and 95% confidence intervals for colorectal cancer associated with SB and PA, performing at least one of three types of PA, including occupational PA, leisure-time PA, or transportation PA.

SB = sedentary behavior, PA = physical activity.

DISCUSSION

This study has several important findings. First, SB was associated with an increased risk of CRC, while each type of PA was not associated with an increased risk of CRC. Second, those with SB and without any PA showed an increased risk of CRC as compared to those without SB and with PA. This relationship was seen in those with sitting time ≥ 10 hr/day and engagement in at least one kind of PA, regardless of whether it was LTPA, OPA, or TPA. The findings of this study suggest that with reduced sitting time, higher PA levels can reduce the risk of CRC regardless of the type of PA.

Although few previous studies on the association between SB and CRC varied by PA could be found, high PA levels was reported to alter the relationship between SB and overall cancer risk.19 More importantly, a Japanese study investigated the effect of modification of LTPA levels on the relationship between SB and CRC mortality.20 The authors found that time spent watching television was significantly associated with the risk of CRC only among those with high levels of LTPA, and thus assumed that low levels of LTPA had a greater effect on CRC mortality than SB.

SB has mainly been reported to be associated with an increased risk of CRC,21 but several studies have also reported no association.22 23 However, this study found a strong association between SB and the increased risk of CRC that had a dose-response relationship wherein each 1-hour increment in sitting time per day was related to a 6% increased risk of CRC (OR, 1.06; 95% CI, 1.02–1.10) (data not shown).

Although each type of PA did not show a significant association with CRC risk in this study, there is strong evidence that PA has a protective effect against the development of CRC.24 Furthermore, diverse subdomains, such as LTPA, OPA, and TPA, have been established to lower the risk of CRC.25 Therefore, it can be inferred that a wide range of PAs can reduce the risk of CRC.

Several possible mechanisms have been suggested to explain the association between SB, PA, and CRC. First, prolonged SB and reduced PA can induce metabolic dysfunction, such as insulin resistance, which may lead to hyperinsulinemia and hyperglycemia.26 Hyperinsulinemia plays a role in tumorigenesis by activating insulin-like growth factor 1, and the hyperglycemic environment contributes to tumor cell proliferation by upregulation of the glucose transporter, epidermal growth factor, and epidermal growth factor receptor.27 28 Second, excessive SB is known to induce chronic systemic inflammation with an increase in circulating inflammatory markers.29 It is well known that chronic inflammation promotes genetic mutations and tumor development through continuous tissue damage and regeneration. Moreover, numerous chemokines and cytokines from activated inflammatory cells may lead to tumor growth, migration, and differentiation by releasing growth factors, stimulating DNA damage.30 In this context, PA may lower systemic inflammation and cancer risk by releasing anti-inflammatory cytokines, such as interleukin (IL)-6 and IL-10, by reducing the circulating number of pro-inflammatory monocytes.31 In addition, energy expenditure from PA affects the metabolism of tumor cells, thereby hindering their growth and progression.32

Unlike the recently proposed hypothesis “PA health paradox,” this study suggests that a higher level of any type of PA, including even OPA, can be helpful in reducing the risk of CRC with reduced SB. OPA has shown inconsistent effects on health. It has been linked to an increased mortality,33 and poor subjective health34 but high OPA levels have also been associated with general health benefits.35 Meanwhile, LTPA has been shown to have a consistent protective effect on health and is inversely related to all-cause mortality.36 Although there are few studies on CRC risk and types of PA, a recent study found that both OPA and LTPA were associated with a lower risk of CRC.37

This study has several limitations. First, the cross-sectional design could not be used to determine the causal relationships. Therefore, the findings remain purely hypothesis generating. Further studies are required to verify the hypothesis on the joint effects of SB and different types of PA on CRC risk. Second, the main variables in this study were investigated using self-reported questionnaires in the KNHANES, which may have resulted in reporting bias. Third, although some research has indicated that the relationship between CRC and SB can differ depending on the anatomical sites of CRC,38 the KNHANES did not provide such information and therefore this factor could not be analyzed. Similarly, information on dietary habits, such as vegetable or fruit intake and frequency of eating out, was not consistently collected, and could not be included in the analysis. Future research should include these potential risk factors for CRC.

Despite these limitations, this study found a significant association between SB and CRC risk and the combined effect of SB and different types of PA on CRC risk. The strengths of this study are that it is based on validated and widely employed questionnaires on PA and SB, and the large sample size and its random homogenous characteristics permit reliable generalization.

In conclusion, this study shows that SB is significantly associated with an increased risk of CRC. The results also suggest that those who engaged in SB without PA were at higher risk of CRC. Reducing sitting time as well as increasing PA in any environment can be recommended to help reduce the risk of CRC.

Notes

Disclosure: The authors have no potential conflicts of interest to disclose.

Author Contributions:

Conceptualization: An S, Park S.
Data curation: Park S.
Formal analysis: Park S.
Funding acquisition: An S.
Investigation: An S, Park S.
Methodology: An S, Park S.
Software: An S.
Supervision: Park S.
Validation: An S, Park S.
Visualization: An S, Park S.
Writing - original draft: An S, Park S.
Writing - review & editing: An S, Park S.

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