Fasting Blood Glucose Variability and Unfavorable Trajectory Patterns Are Associated with the Risk of Colorectal Cancer.

Background/Aims: The relationship between fasting blood glucose (FBG) variability and colorectal cancer (CRC) remains ill-defined. This study aimed to evaluate the association of FBG variability with CRC risk in the healthy population without overt diabetes.
Methods: In the data from the Korean National Health Insurance Service-Health Screening Cohort, we included individuals examined by FBG testing at least 3 times between 2002 and 2007. FBG variability was calculated using standard deviation (SD) and coefficient of variation (CV).
Results: Regarding FBG variability, an increase in the quintile of SD or CV was independently associated with CRC risk (all p for trend <0.01). When the change in FBG was classified into six trajectory patterns, unfavorable trajectory patterns (high stable and upward) were significantly associated with increased CRC risk (hazard ratio [HR] 2.30, p=0.003; HR 1.19, p=0.007, respectively). In subgroup analyses according to the sex, a significant association between FBG variability (SD or CV) and CRC risk was observed in men but not in women. The high stable and upward pattern were also associated with CRC risk in men (HR 2.47, p=0.002; HR 1.21, p=0.012) but not in women. Conclusions: This study identified that FBG variability and unfavorable trajectory patterns were significantly associated with increased CRC risk in the healthy population without overt diabetes. Our findings suggest that FBG variability as well as FBG itself may be a predictive factor for the development of CRC.

INTRODUCTION

Colorectal cancer (CRC) is one of the most frequent malignancies worldwide. According to the reports of the Global Burden of Disease Study, CRC-related mortalities are steadily increasing annually worldwide.1 There have been many studies that suggest that the development of CRC is associated with abnormal metabolic conditions, such as obesity, diabetes mellitus (DM), and metabolic syndrome.2-4 However, the exact underlying mechanisms still remain unclear.

Meanwhile, DM incidence has been greatly increasing in most countries, including Korea.5,6 The mortality rate from DM and its complications are also increasing in Korea.6 To date, several studies have investigated the association between DM and CRC. Some studies have shown that DM is associated with increased risk of CRC or that DM is related to higher CRC-related mortality.7-11 Common identified risk factors for both DM and CRC are Westernized diet, obesity, smoking, and lack of physical activity.12 Recently, fasting blood glucose (FBG) variability has emerged as a considerable risk factor for long-term diabetic complications.13 The Verona Diabetes Study has shown that long-term variability of FBG was significantly predictive of cardiovascular events and mortality in type 2 DM patients who were followed for 10 years.14 However, few studies have investigated the relationship between FBG variability and cancer risk.14

Therefore, we aimed to investigate the association of FBG variability with CRC risk in Korean men and women without overt DM using the nationwide health screening cohort.

MATERIALS AND METHODS

1. Data source

This study was performed using the data from the Korean National Health Insurance Service-Health Screening Cohort (NHIS-Health Screening Cohort), which includes 514,866 Koreans (aged 40 to 79 in 2002) who were randomly selected 10% among the national health screening participants during 2002 to 2003. It is a national database established in 2015 by the NHIS. All Koreans have an obligation to join the NHIS, a single health insurance system, and all data related to insurance eligibility and medical claims are stored in the NHIS database. We used data from the general health screening program, which can be applied at least once every 2 years for the aged Korean population (40 years or older). It includes data on demographic variables, bioclinical laboratory results, and questionnaires about risk factors, such as smoking status. NHIS-Health Screening Cohort contains data for all participants followed up until December 31, 2015. Detailed information of the cohort can be found in the cohort profile paper.15

2. Study population

After excluding subjects with inconsistent date of examination, this study included 514,795 subjects who had taken general health screening at least once between 2002 and 2003. For this study, we excluded subjects who belong to the following criteria: those with missing data for FBG level at baseline (n=658), those who participated in health screening less than 3 times between 2002 and 2007 (n=230,778), and/or those with a history of inflammatory bowel disease (ICD-10: K50 and K51) (n=3,281) during the entire study period (between 2002 and 2015). Subjects diagnosed with any type of cancer (ICD-10: C00-96) (n=8,458) and DM (ICD-10: E10-14 and ≥1 claim for antidiabetic medication) (n=24,684) between 2002 and 2007 were excluded. Additionally, subjects who died between 2002 and 2007 (n=507) or those with glucose measurements less than 3 times between 2002 and 2007 (n=188) were excluded. Finally, 246,241 subjects were included in this study (Fig. 1).

Fig. 1

Flow diagram of the study subjects.

NHIS-HEALS, National Health Insurance Service-Health Screening Cohort; FBG, fasting blood glucose.

Between 2002 and 2003, the date of health screening was considered as the index date. Regarding the incident case, the first hospital admission with CRC diagnostic code (ICD-10: C18-20) was defined as the date of CRC occurrence between 2008 and 2015. Thus, the follow-up period was defined from date of the health screening to either the date of CRC diagnosis or the date of the last follow-up (12/31/2015) if CRC did not develop. This study was approved by the Institutional Review Board of the Ewha Womans University Mokdong Hospital (IRB number: EUMC 2018-12-007). Informed consent was waived due to the retrospective design of this study.

3. Variability definition

We defined FBG variability using repeatedly measured FBG data for each individual between 2002 and 2007. FBG variability was calculated using standard deviation (SD) and coefficient of variation (CV). The variability was divided into quintiles and analyzed: quintiles of SD (Q1, <4.97; Q2, 4.97–7.49; Q3, 7.50–10.11; Q4, 10.12–14.19; and Q5, ≥14.20) and quintiles of CV (Q1, <5.45; Q2, 5.45–8.18; Q3, 8.19–11.08; Q4, 11.09–15.26; and Q5, ≥15.27). Additionally, we defined the trajectory patterns using the measured values in the years 2002–2003 (T1), 2004–2005 (T2), and 2006–2007 (T3). FBG concentrations at each time point were divided into three levels using cutoff values of 100 mg/dL and 126 mg/dL, and then, six trajectory patterns were formed using the change of fasting glucose status (Supplementary Table 1, Supplementary Fig. 1). The NHIS-Health Screening Cohort provides income level data as medical aid beneficiaries, deciles for insured employees, and deciles for insured self-employed based on income-based insurance contributions. Thus, we classified medical aid beneficiaries and the first and second deciles into one group. Sequentially, the two deciles were grouped and applied to the analysis.

4. Statistical analyses

Descriptive results were summarized as means with SD for numerical data and as number of subjects with percentage for categorical data. The incidence rate of CRC was estimated as 100,000 person-years. The risk of developing CRC according to FBG variability was estimated using the Cox proportional hazard model analyses, and the results were presented as hazard ratio (HR) with 95% confidence interval (CI). Its assumption was tested by the Schoenfeld residuals, and the assumption was satisfied. We considered age, income level, body mass index status (<20 kg/m2, 20–24.9 kg/m2, and ≥25 kg/m2), smoking (never, former, and current smoker), alcohol intake (never, 2–3 times/month, 1–2 times/week, and ≥3 times/week), physical activity (none, 1–2 times/week, and ≥3 times/week), and Charlson comorbidity index (CCI) as confounding variables. Sensitivity analysis was performed by excluding subjects who had developed CRC within 2 years by adjusting various covariates. In addition, to visually assess the shape of association between FBG variability and incident CRC, restricted cubic spline was used. Thus, based on the low Akaike information criterion values, Cox models with restricted cubic spline were conducted using 3 knots at the 10th, 50th, and 90th percentiles. All statistical analyses were conducted using SAS version 9.4 (SAS Institute, Cary, NC, USA), and p<0.05 was considered significant under two-sided test.

RESULTS

1. Baseline characteristics of the study population

The study was analyzed on a total of 246,241 subjects, 143,623 men and 102,618 women. The mean age of the study population was 51.20±8.81 years (50.44±8.64 years in men, 52.26±8.95 in women) (Table 1). With regard to body mass index, more women were underweight (<20 kg/m2) than men (8.45% in women, 7.34% in men). Conversely, more men were overweight (≥25 kg/m2) than women (34.07% in men, 31.36% in women). Current smokers among men were 40.14%, being approximately 40 times as many as women. The proportion of individuals consuming alcohol more than 3 times a week was much higher in men (17.41%) than in women (1.58%). However, more women did not exercise any physical activity during the week (65.68%) than men (46.30%). The average of FBG level at baseline was higher in men (93.88±23.16 mg/dL) than in women (91.05±24.87 mg/dL), and the indicators of variability, SD and CV, were also higher in men.

Table 1

Baseline Characteristics of the Study Subjects

Characteristics		Total(n=246,241)	Men(n=143,623)	Women(n=102,618)
Age, mean±SD, yr		51.20±8.81	50.44±8.64	52.26±8.95
Income level, No. (%)*	Medical aid beneficiaries + ≤20th	37,455 (15.21)	15,407 (10.73)	22,048 (21.49)
	21–40th	31,994 (12.99)	15,193 (10.58)	16,801 (16.37)
	41–60th	37,004 (15.03)	21,916 (15.26)	15,088 (14.70)
	61–80th	50,683 (20.58)	32,455 (22.60)	18,228 (17.76)
	≥81th	89,105 (36.19)	58,652 (40.84)	30,453 (29.68)
Body mass index, No. (%)	<20 kg/m2	19,194 (7.80)	10,531 (7.34)	8,663 (8.45)
	20–24.9 kg/m2	145,825 (59.26)	84,103 (58.59)	61,722 (60.19)
	≥25 kg/m2	81,053 (32.94)	48,899 (34.07)	32,154 (31.36)
Smoking, No. (%)	Never	160,867 (66.45)	61,071 (43.69)	99,796 (97.54)
	Previous	23,397 (9.66)	22,610 (16.17)	787 (0.77)
	Current	57,840 (23.89)	56,105 (40.14)	1,735 (1.70)
Alcohol intake, No. (%)	Never	128,654 (53.19)	46,447 (32.78)	82,207 (82.03)
	2–3 times/mo	41,834 (17.29)	30,609 (21.61)	11,225 (11.20)
	1–2 times/wk	45,160 (18.67)	39,958 (28.20)	5,202 (5.19)
	≥3 times/wk	26,244 (10.85)	24,659 (17.41)	1,585 (1.58)
Physical activity, No. (%)	None	130,023 (54.39)	64,469 (46.30)	65,554 (65.68)
	1–2 times/wk	63,578 (26.60)	45,763 (32.86)	17,815 (17.85)
	≥3 times/wk	45,453 (19.01)	29,020 (20.84)	16,433 (16.47)
CCI score, mean±SD		0.41±0.75	0.35±0.70	0.51±0.81
FBG, mean±SD, mg/dL		92.70±23.93	93.88±23.16	91.06±24.87
SD of FBG, mean±SD		10.78±13.53	11.44±13.12	9.85±14.02
CV of FBG, mean±SD		11.04±7.78	11.56±7.98	10.31±7.42

CCI, Charlson comorbidity index; FBG, fasting blood glucose; SD, standard deviation; CV, coefficient of variation.

*Income level: The National Health Insurance Service-Health Screening Cohort provides income level data as medical aid beneficiaries, deciles for insured employees, and deciles for insured self-employed individuals.

2. Association of FBG variability with CRC risk

The incidence of CRC during the follow-up period was 116.7 per 100,000 person-years (n=3,669). We evaluated the effect of FBG variability on CRC risk using the Cox proportional hazard regression analysis (Table 2). To analyze the association of FBG variability, SD or CV, with CRC incidence, model 1 was adjusted for the age and sex in the crude model, and model 2 was adjusted for various confounding factors (economic income, body mass index, smoking habits, alcohol intake, physical activity, and CCI) in model 1. The highest quintile of SD showed a significantly higher risk of incident CRC (HR, 1.41; 95% CI, 1.27 to 1.56) compared with the lowest quintile of SD. The significance remained after adjusting for various covariates (HR, 1.19; 95% CI, 1.07 to 1.32). When SD of FBG was divided into five quintiles, an increase in the quintile of SD was significantly associated with increased risk of CRC in the crude model (p for trend <0.001), model 1 (p for trend <0.001), and model 2 (p for trend=0.001). An increase in the quintile of CV was also associated with CRC risk in the crude model (p for trend <0.001), model 1 (p for trend=0.001), and model 2 (p for trend=0.009). In the sensitivity analysis excluding subjects who developed CRC within 2 years, the influence of the SD or CV FBG variability on CRC incidence remained as shown in Table 2 and Supplementary Table 2. Among the confounding variables, male, age, current smoking status, high intake of alcohol, high body mass index and CCI were independently associated with CRC (Supplementary Table 3). For CRC, there was no interactive effect between FBG variability and confounding variables (Supplementary Table 4). Even when separately evaluated for rectal cancer, the effect of the variability evaluated by SD and CV was similar to the above results (Supplementary Table 5). After the median value of FBG variability assessed by SD or CV, the risk of CRC gradually increased as the variability increased, but the CV-derived results showed a wider CI (Fig. 2A and B).

Table 2

Cox Proportional Hazards Regression Analysis of Colorectal Cancer Incidence by FBG Variability

FBG variability		No.	Incidence rate(per 100,000 person-years)	Crude model			Model 1†			Model 2‡
				HR (95% CI)	p-value		HR (95% CI)	p-value		HR (95% CI)	p-value
SD*	Q1	49,137	101.7	1			1			1
	Q2	49,309	102.9	1.02 (0.91–1.13)	0.787		1.03 (0.93–1.15)	0.575		1.04 (0.93–1.16)	0.545
	Q3	49,286	120.5	1.19 (1.07–1.32)	0.001		1.18 (1.06–1.31)	0.002		1.17 (1.05–1.30)	0.005
	Q4	49,224	116.3	1.15 (1.04–1.28)	0.009		1.10 (0.99–1.23)	0.075		1.08 (0.96–1.20)	0.190
	Q5	49,285	141.9	1.41 (1.27–1.56)	<0.001		1.23 (1.11–1.37)	<0.001		1.19 (1.07–1.32)	0.001
	Trend			1.09 (1.06–1.11)	<0.001		1.05 (1.03–1.07)	<0.001		1.04 (1.02–1.06)	0.001
CV*	Q1	49,111	105.7	1			1			1
	Q2	49,284	103.5	0.98 (0.88–1.10)	0.753		1.01 (0.90–1.12)	0.932		1.02 (0.91–1.13)	0.791
	Q3	49,285	121.4	1.16 (1.04–1.28)	0.007		1.16 (1.05–1.29)	0.004		1.15 (1.04–1.28)	0.009
	Q4	49,276	115.0	1.10 (0.99–1.22)	0.092		1.07 (0.97–1.19)	0.190		1.06 (0.95–1.18)	0.298
	Q5	49,285	137.7	1.32 (1.19–1.46)	<0.001		1.18 (1.07–1.31)	0.001		1.15 (1.03–1.27)	0.011
	Trend			1.07 (1.05–1.09)	<0.001		1.04 (1.02–1.07)	0.001		1.03 (1.01–1.06)	0.009
Trajectory patterns	Low stable	60,365	99.0	1			1			1
	Middle stable	6,214	122.6	1.24 (1.01–1.54)	0.044		1.06 (0.86–1.31)	0.599		1.06 (0.85–1.31)	0.614
	High stable	398	259.4	2.67 (1.55–4.62)	<0.001		2.35 (1.36–4.07)	0.002		2.30 (1.33–3.99)	0.003
	Upward	23,843	135.9	1.38 (1.23–1.56)	<0.001		1.24 (1.10–1.40)	0.001		1.19 (1.05–1.34)	0.007
	Downward	17,208	126.4	1.28 (1.12–1.47)	<0.001		1.14 (0.99–1.30)	0.074		1.09 (0.94–1.25)	0.251
	Fluctuant	19,553	129.5	1.32 (1.15–1.50)	<0.001		1.15 (1.01–1.31)	0.042		1.13 (0.99–1.29)	0.070

FBG, fasting blood glucose; SD, standard deviation; CV, coefficient of variation; HR, hazard ratio; CI, confidence interval.

*Quintiles of SD; Q1: <4.97, Q2: 4.97–7.49, Q3: 7.50–10.11, Q4: 10.12–14.19, Q5: ≥14.20. Quintiles of CV; Q1: <5.45, Q2: 5.45–8.18, Q3: 8.19–11.08, Q4: 11.09–15.26, Q5: ≥15.27; †Model 1: adjusted for sex and age; ‡Model 2: Model 1+ economic income, body mass index status, smoking, alcohol intake, physical activity, and Charlson comorbidity index.

Fig. 2

Association of FBG variability assessed by SD (A) or CV (B) with incident CRC risk and association of FBG variability assessed by SD with incident CRC risk in men (C) and women (D). The solid line indicates the HR, and dashed lines indicate the 95% CI. The model was fitted by a restricted cubic spline with three knots located at the 10th, 50th, and 90th percentiles of the FBG variability (vertical lines). HRs with 95% CIs were obtained after adjusting for sex, age, income, body mass index status, smoking habits, alcohol intake, physical activity, and the Charlson comorbidity index.

FBG, fasting blood glucose; SD, standard deviation; CV, coefficient of variation; CRC, colorectal cancer; HR, hazard ratio; CI, confidence interval.

When the change of FBG level was classified into six trajectory patterns, unfavorable patterns, namely high stable, upward, and fluctuant patterns showed a significantly increased risk of CRC in model 1 (HR 2.35, p=0.002; HR 1.24, p=0.001; HR 1.15, p=0.042, respectively). In model 2, high stable and upward trajectory patterns were significantly associated with increased CRC risk (HR 2.30, p=0.003; HR 1.19, p=0.007, respectively) (Table 2). However, the association of the fluctuant pattern with CRC risk did not reach statistical significance in model 2 (HR 1.13, p=0.070). In the sensitivity analysis, a high stable trajectory pattern was still significantly associated with an increased risk of CRC, and an upward trajectory pattern was associated with a borderline significance level (Supplementary Table 2).

3. Association of FBG variability with CRC risk among men and women

During the 8-year follow-up (between 2008 and 2015), the incidence of CRC was 135.2 per 100,000 person-years (n=2,487) in men and 90.5 per 100,000 person-years (n=1,182) in women. To evaluate whether the association between FBG variability and CRC incidence differed according to the sex of the subjects, univariate (crude model) and multivariate analyses (model 1 and model 2) were carried out for male and female subjects. In men, an increase in the quintile of SD was significantly associated with increased risk of CRC in the crude model (p for trend <0.001), model 1 (p for trend <0.001), and model 2 (p for trend=0.007). An increase in the quintile of CV was also associated with increased CRC risk in the crude model (p for trend <0.001), model 1 (p for trend=0.001), and model 2 (p for trend=0.027). With regard to trajectory patterns, unfavorable patterns (high stable, upward, and fluctuant patterns) were significantly associated with increased CRC risk in the crude model. Compared with the low stable trajectory pattern, high stable and upward patterns were shown to significantly increase the risk of CRC in model 1 (HR 2.54, p=0.001; HR 1.27, p=0.001, respectively). Even after adding various covariates (model 2), the high stable and upward pattern was significantly associated with increased CRC risk (HR 2.47, p=0.002; HR 1.21, p=0.012, respectively) (Table 3). Among the confounding variables, age, income level, current smoking, and high intake of alcohol were independently associated with CRC (Supplementary Table 6). In the sensitivity analysis, high stability and upward patterns still showed a significant association for CRC risk (Supplementary Table 2). In addition, a positive association between rectal cancer with SD or CV of FBG was significant, and the risk of rectal cancer was significantly higher in the high-stable group compared to the low-stable group (HR 2.59, p=0.037) (Supplementary Table 5).

Table 3

Cox Proportional Hazards Regression Analysis of Colorectal Cancer Incidence by FBG Variability among Men

FBG variability		No.	Incidence rate(per 100,000 person-years)	Crude model			Model 1†			Model 2‡
				HR (95% CI)	p-value		HR (95% CI)	p-value		HR (95% CI)	p-value
SD*	Q1	24,929	124.5	1			1			1
	Q2	27,440	115.1	0.93 (0.81–1.06)	0.277		0.97 (0.85–1.12)	0.713		0.98 (0.85–1.13)	0.798
	Q3	28,430	138.1	1.11 (0.98–1.27)	0.110		1.16 (1.01–1.32)	0.030		1.14 (1.00–1.31)	0.057
	Q4	30,068	134.9	1.09 (0.95–1.24)	0.210		1.11 (0.98–1.27)	0.111		1.07 (0.93–1.22)	0.359
	Q5	32,756	158.1	1.28 (1.13–1.45)	<0.001		1.24 (1.09–1.40)	0.001		1.17 (1.03–1.33)	0.018
	Trend			1.07 (1.04–1.10)	<0.001		1.06 (1.03–1.09)	<0.001		1.04 (1.01–1.07)	0.007
CV*	Q1	25,660	126.2	1			1			1
	Q2	27,668	118.2	0.94 (0.82–1.07)	0.355		0.99 (0.86–1.13)	0.843		0.99 (0.86–1.14)	0.919
	Q3	28,558	139.1	1.11 (0.97–1.26)	0.128		1.16 (1.02–1.32)	0.026		1.14 (0.99–1.30)	0.064
	Q4	29,703	133.0	1.06 (0.93–1.20)	0.399		1.09 (0.96–1.24)	0.193		1.05 (0.92–1.20)	0.454
	Q5	32,034	155.9	1.24 (1.10–1.41)	0.001		1.21 (1.07–1.37)	0.002		1.14 (1.01–1.30)	0.042
	Trend			1.06 (1.03–1.09)	<0.001		1.05 (1.02–1.08)	0.001		1.03 (1.00–1.06)	0.027
Trajectory patterns	Low stable	31,477	115.3	1			1			1
	Middle stable	4,490	133.3	1.15 (0.91–1.47)	0.248		1.10 (0.87–1.41)	0.427		1.12 (0.87–1.43)	0.378
	High stable	337	281.8	2.46 (1.39–4.37)	0.002		2.54 (1.43–4.50)	0.001		2.47 (1.39–4.38)	0.002
	Upward	15,940	147.9	1.29 (1.11–1.49)	0.001		1.27 (1.10–1.47)	0.001		1.21 (1.04–1.41)	0.012
	Downward	10,862	135.7	1.18 (0.99–1.40)	0.060		1.12 (0.94–1.33)	0.193		1.06 (0.89–1.26)	0.516
	Fluctuant	12,810	141.5	1.23 (1.05–1.44)	0.011		1.16 (0.99–1.36)	0.069		1.13 (0.97–1.33)	0.127

FBG, fasting blood glucose; SD, standard deviation; CV, coefficient of variation; HR, hazard ratio; CI, confidence interval.

*Quintiles of SD; Q1: <4.97, Q2: 4.97–7.49, Q3: 7.50–10.11, Q4: 10.12–14.19, Q5: ≥14.20. Quintiles of CV; Q1: <5.45, Q2: 5.45–8.18, Q3: 8.19–11.08, Q4: 11.09–15.26, Q5: ≥15.27; †Model 1: adjusted for age; ‡Model 2: Model 1+ income, body mass index status, smoking, alcohol intake, physical activity, and Charlson comorbidity index.

In women, a significant association was observed between the quintile of SD and CV and CRC incidence in the crude model (p for trend=0.001 and p for trend=0.014, respectively); however, this association did not reach statistical significance in model 1 (p for trend=0.099 and p for trend=0.264, respectively) and model 2 (p for trend=0.067 and p for trend=0.162, respectively). In addition, there was also no significant difference in the sensitivity analysis (Supplementary Table 2). Similarly, regarding trajectory patterns, there was no significant difference in CRC risk among the trajectory patterns in models 1 and 2 among women (Table 4). Among the confounding variables, age, physical activity level, and CCI score were independently associated with CRC (Supplementary Table 7). The risk of rectal cancer according to FBG variability was also insignificant (Supplementary Table 5). In both sexes, the risk of CRC gradually increased after the median value of FBG variability assessed by SD. However, a statistical significance was observed in men, but not in women (Fig. 2C and D).

Table 4

Cox Proportional Hazards Regression Analysis of Colorectal Cancer Incidence by FBG Variability among Women

FBG variability		No.	Incidence rate(per 100,000 person-years)	Crude model			Model 1†			Model 2‡
				HR (95% CI)	p-value		HR (95% CI)	p-value		HR (95% CI)	p-value
SD*	Q1	24,208	78.0	1			1			1
	Q2	21,869	87.5	1.13 (0.94–1.34)	0.196		1.14 (0.96–1.37)	0.141		1.14 (0.95–1.37)	0.167
	Q3	20,856	96.4	1.24 (1.04–1.48)	0.017		1.23 (1.03–1.46)	0.023		1.22 (1.02–1.46)	0.032
	Q4	19,156	87.0	1.12 (0.93–1.35)	0.227		1.08 (0.89–1.29)	0.443		1.09 (0.90–1.32)	0.363
	Q5	16,529	109.6	1.42 (1.18–1.70)	<0.001		1.22 (1.01–1.46)	0.035		1.24 (1.03–1.49)	0.026
	Trend			1.07 (1.03–1.12)	0.001		1.03 (0.99–1.08)	0.099		1.04 (1.00–1.08)	0.067
CV*	Q1	23,451	82.9	1			1			1
	Q2	21,616	84.6	1.02 (0.86–1.22)	0.805		1.04 (0.87–1.25)	0.650		1.06 (0.88–1.27)	0.544
	Q3	20,727	97.0	1.17 (0.99–1.40)	0.072		1.18 (0.99–1.41)	0.062		1.19 (0.99–1.42)	0.060
	Q4	19,573	87.5	1.06 (0.88–1.27)	0.527		1.04 (0.87–1.25)	0.664		1.07 (0.89–1.29)	0.475
	Q5	17,251	104.0	1.27 (1.06–1.51)	0.011		1.12 (0.93–1.34)	0.226		1.15 (0.96–1.38)	0.141
	Trend			1.05 (1.01–1.10)	0.014		1.02 (0.98–1.07)	0.264		1.03 (0.99–1.07)	0.162
Trajectory patterns	Low stable	28,888	80.9	1			1			1
	Middle stable	1,724	93.9	1.16 (0.74–1.82)	0.524		0.96 (0.61–1.51)	0.849		0.92 (0.58–1.47)	0.726
	High stable	61	132.9	1.64 (0.23–11.67)	0.620		1.37 (0.19–9.76)	0.754		1.42 (0.20–10.10)	0.729
	Upward	7,903	111.1	1.38 (1.10–1.71)	0.005		1.21 (0.97–1.51)	0.095		1.16 (0.92–1.46)	0.204
	Downward	6,346	110.2	1.37 (1.08–1.74)	0.011		1.20 (0.94–1.52)	0.145		1.18 (0.92–1.50)	0.199
	Fluctuant	6,743	106.2	1.31 (1.04–1.67)	0.024		1.14 (0.90–1.45)	0.275		1.15 (0.90–1.46)	0.256

FBG, fasting blood glucose; SD, standard deviation; CV, coefficient of variation; HR, hazard ratio; CI, confidence interval.

*Quintiles of SD; Q1: <4.97, Q2: 4.97–7.49, Q3: 7.50–10.11, Q4: 10.12–14.19, Q5; ≥14.20. Quintiles of CV; Q1: <5.45, Q2: 5.45–8.18, Q3: 8.19–11.08, Q4: 11.09–15.26, Q5: ≥15.27; †Model 1: adjusted for age; ‡Model 2: Model 1+ income, body mass index status, smoking, alcohol intake, physical activity, and Charlson comorbidity index.

DISCUSSION

In the comprehensive health screening cohort in Korean men and women excluding patients with overt DM, we investigated the association of FBG variability with CRC risk. Multivariate analyses adjusted for several covariates found that FBG variability, represented by SD or CV, was significantly associated with increased CRC risk. Regarding FBG trajectory patterns, unfavorable patterns (high stable and upward) were positively associated with increased CRC risk.

Various previous studies have reported that increased FBG level is related with CRC incidence. It is well-known that DM is significantly associated with the increased risk of CRC.4,12,16 Type 2 DM, in particular, increases the risk of CRC by 1.3 times17 and is an independent risk factor for mortality of several solid cancers, including colon cancer.18 In the Korean Cancer Prevention Study-II, a large-scale prospective cohort study, CRC incidence was positively associated with increased FBG levels.19 The Framingham Offspring Cohort study has also shown that the presence of impaired fasting glucose >10 years before the event was correlated with increased risk of obesity-related cancers, particularly CRC.20 The association between increased FBG and CRC has been explained by several hypotheses. Hyperinsulinemia,21,22 hyperglycemia,22 or associated cofactors are associated with increased risk of CRC. Hyperinsulinemia through insulin-like growth factor system23-25 can influence the differentiation of epithelial cells in the intestine and can contribute to colorectal neoplasia.26 Other factors, such as chronic inflammation,27,28 imbalanced intestinal microbiota,29 or delayed bowel transit,30 have also been proposed.

Meanwhile, the clinical significance of FBG variability was found to be associated with diabetic complications or mortality. In the Verona Diabetes Study, long-term variability of FBG was significantly predictive of cardiovascular events and mortality in type 2 DM patients followed up for 10 years.14 Recently, a meta-analysis investigated the association of FBG variability with complications and mortality in five studies including patients with type 2 DM.31 This analysis reported that high FBG variability was significantly associated with the risk of retinopathy (odds ratio, 3.68; 95% CI, 1.01 to 13.4) and all-cause mortality (HR, 1.28; 95% CI, 1.12 to 1.46). In Korea, one prospective cohort study (Ansung-Ansan cohort) has investigated the relationship between glucose variability and vascular adverse events in middle-aged individuals without DM at baseline.32 This study reported that higher FBG variability and post 2-hour blood glucose were predictive factors for macrovascular events, including coronary artery disease, myocardial infarction, and congestive heart failure and stroke but not for microvascular events.32 With regard to the underlying mechanisms, FBG variability may be associated with oxidative stress, inflammatory cytokine production, and some epigenetic changes such as cellular memory.33-37

Thus far, few studies have evaluated the association between FBG variability and cancer risk. The Verona Diabetes Study identified that high FBG variability (represented by the CV value) was the risk factor of mortality from malignancies as well as all-cause or cardiovascular-related mortalities.14 Although this association may be explained by the deterioration of FBG over time in individuals with high CV of FBG, it has not been supported by any clinical or experimental studies. Similar to the Verona Diabetes Study, our study reports a significant association between high CV (or SD) of FBG and CRC risk. In addition, high stable and upward FBG trajectory patterns were independent predictors of CRC incidence. Among six FBG trajectory patterns in our study, high stable, upward, and fluctuant groups could be classified as unfavorable patterns considering the long-term outcomes related to DM. Although the fluctuant FBG trajectory pattern tended to be associated with the risk of CRC, it did not reach statistical significance. To verify and confirm our results, further large-scale studies across different ethnic populations are warranted.

In this study, we also evaluated the association between FBG variability and CRC risk according to the sex. Consequently, SD or CV of FBG was significantly associated with the risk of CRC in men but not in women. Some unfavorable trajectory patterns were also significantly associated with CRC risk in men (high stable and upward patterns) but not in women. These results are similar to the CRC risk in DM patients according to the sex. In the Cancer Prevention Study II Nutrition Cohort, a significant association between type 2 DM and CRC incidence was found among men but not women.38 In addition, the Korean Cancer Prevention Study-II, a prospective cohort study of a large Korean population, showed that high FBG (≥100 mg/dL) including impaired fasting glucose correlated with the risk of CRC only in men.19 When analyzed according to the sex, the risk associated with developing CRC in study subjects with high FBG was statistically significant in men (HR, 1.51; 95% CI, 1.11 to 2.05), whereas no such association was noted in women (HR, 1.23; 95% CI, 0.67 to 2.26).19 Another Korean cohort study has also reported that the association of impaired fasting glucose with CRC risk was observed only in men.39 Taken together, our results suggest that men are more susceptible to CRC than women if they have FBG variability or some unfavorable trajectory patterns.

The present study has some limitations. First, as this was a retrospective study, our results may have been influenced by the accuracy and availability of the medical records. In particular, a considerable number of subjects (n=230,778) were excluded if they participated in health screening less than 3 times between 2002 and 2007. This may have led to selection bias and caused the insufficient sample size in the specific groups to evaluate the association between FBG variability and CRC risk. Second, since the major outcome in our study was CRC, there may be a length time bias when considering the limited period of this study. Third, we did not reflect all the changes in various factors (drugs, health behaviors, etc.) during the FBG variability assessment period. However, when the CCI calculated using the claims data for 2002 to 2007 was applied, the results did not change (data not shown). Fourth, regarding FBG trajectory patterns, the high stable group had much fewer cases than other groups. We excluded subjects diagnosed with DM between 2002 and 2007. DM was defined as prescribing one or more antidiabetic medications along with E10-14 in the ICD-10 code in our study. Accordingly, if any individual with FBG levels ≥126 mg/dL 3 times was diagnosed with DM and was prescribed antidiabetic medications, they were excluded from our study. However, despite the small sample size, the high stable trajectory pattern was independently associated with the CRC risk in the overall and male subjects. Fifth, there was lack of information or separate diagnostic code for family history of CRC or hereditary CRC syndrome in our cohort data from the Korean NHIS database. Thus, we could not exclude those with hereditary CRC syndrome or with a family history of CRC. In addition, we could not include the colonoscopy performance and polypectomy history in our study. Thus, further studies to conduct with more organized algorithm were needed to verify our result. Despite these limitations, it is meaningful that this study is the first to evaluate the association between the various indicators of FBG variability and CRC risk and to find its sex differences.

In conclusion, in this study, we found that FBG variability and the unfavorable trajectory patterns—high stable and upward—were significantly associated with increased CRC risk in the healthy population without overt DM. The association of FBG variability and the unfavorable patterns with CRC risk persisted in men, but not in women. Thus, our findings suggest that FBG variability as well as FBG itself may be a predictive factor for the development of CRC. Further researches on FBG variability in a healthy population may be used to individually tailor a CRC screening strategy.

SUPPLEMENTARY MATERIALS

Supplementary materials can be accessed at https://doi.org/10.5009/gnl210048.