Abstract
Background: As the world has become a 24 h society, people’s demands have generated various work schedules, leading to an increase in workers’ health problems. The study aimed to investigate the association between nighttime work and HbA1c levels among South Korean adults over the age of 30. Methods: Participants were selected from the 2016–2019 Korea National Health and Nutrition Survey; those diagnosed with diabetes were excluded. The dependent variable was the HbA1c level reported in the KNHANES health examination report. The main independent variable was the participant’s work schedule. Work schedules were classified into three categories based on the participant’s report: (1) day; (2) night and overnight, and (3) other. Generalized multiple linear regression was used, and the significance level was defined as p < 0.05. Results: The participants comprised 4773 men and 4818 women. Those engaged in the “day” schedule served as the reference group. Among the male participants, the “night and overnight” group had significantly larger HbA1c (%) levels than the “day” group (β = 0.061, p = 0.0085). Among these nighttime male workers, HbA1c (%) levels were particularly higher in the people who were physically inactive (β = 0.094, p = 0.0031), slept less than 7 h (β = 0.108, p = 0.0009), and skipped meals (β = 0.064, p = 0.0401). Conclusion: Our results revealed an association of nighttime work with increased HbA1c levels in male participants. High-risk groups for HbA1c levels require careful observation of physical activity, sleeping time, and eating habits.
Keywords: shift work, work schedule, nighttime, HbA1c
1. Introduction
Shift work has become an essential part of the modern society with the emergence of occupational conditions requiring 24 h labor in the fields of healthcare, manufacturing, wholesale and retail businesses [1]. The term “shift work” often refers to the employment practice designed to provide service across the entire day including nighttime and early morning. Recently, there has been a growing number of publications suggesting the association between shift work and negative health outcomes. In particular, work hours outside of the conventional daytime is likely to cause disruption of circadian rhythms, which could potentially lead to the development of chronic diseases, including metabolic disorders, cardiovascular disease, and cancer [2,3,4,5].
Diabetes is one of the most prevalent metabolic disorders worldwide. According to the International Diabetes Federation (IDF), 463 million people (9.3%) were suffering from it in 2019 [6,7]. Given the increased life expectancy due to the advances in medicine, population aged 65 years and older will account for 20% of the global population within the next few years [6]. Hence, this implies that the growing population of elderly people corresponds to the epidemiologic concept of increased prevalence of diabetes. The current trend estimates that a sharp increase in the prevalence of diabetes will result in as many as 700 million patients by 2045 [7]. In South Korea, diabetes is a substantial contributor to public health concerns, affecting nearly 10% of the national population, and has been reported as one of the leading causes of death among both sexes [6,7,8,9]. Thus, it is anticipated that diabetes will increase its burden on the healthcare system in the future.
Potential health-related risk factors associated with shift work, such as irregular living habits, work stress, and sleep complaints, can act as part of a diabetes outbreak [10,11,12]. It has been suggested that shift workers are more likely to experience the destruction of their biorhythms around the clock [13,14,15,16]. Of the various work schedules, those who conduct labor during the nighttime have reported lower scores in perceived health. Hemoglobin A1c (HbA1c) is a central biomarker for the presence and severity of hyperglycemia that is used as a predictive biomarker for diabetes [17]. Thus, this study aimed to investigate the potential effect of nighttime (i.e., night and overnight) work on HbA1c in comparison to the conventional daytime work.
2. Methods
2.1. Study Participants
We collected data from the 2016–2019 Korea National Health and Nutrition Examination Survey (KNHANES). The KNHANES is a self-reported nationally representative survey of South Koreans of all ages designed to gather annual national data on sociodemographic, economic, and health-related conditions and behaviors. Since 2007, the collected data have been subjected to an annual review and approval by the KCDCP Research Ethics Review Committee. The KNHANES comprises secondary data and is publicly available to researchers [18].
There were 32,379 participants in the 2016–2019 KNHANES. A total of 2435 people who had already been diagnosed with diabetes at the time of the survey were excluded to ensure the reliability of the results. Additionally, 9541 participants under the age of 30 were excluded because the majority of them did not undergo blood testing as part of the survey. We also excluded 10,812 participants with no response/other missing values from each variable’s survey items. Finally, a total of 9591 participants (4773 men and 4818 women) were selected for analysis.
2.2. Variables
HbA1c level, the dependent variable in this study, was measured in the blood samples collected after 8 h of fasting. HbA1c was considered as a continuous variable. Blood samples are among the key components of health examination reported in the KNHANES which was conducted at mobile examination centers that travel to the survey location [18].
The main independent variable was the work schedule. Work schedules were classified into three categories based on the survey report as follows: (1) day; (2) night and overnight; and (3) other (rotational, flexible, split, or irregular working hours/schedules).
Demographic, socioeconomic, health, and disease-related factors were also assessed to account for the confounding. The demographic factors included age (30~39, 40~49, 50~59, 60~69, and ≥70 years). The socioeconomic factors included educational level (≤elementary, middle, high, ≥college), occupational status (white, pink, blue), household income (low, middle, high), and household composition (one person, one-generation household, ≥two-generation household). The health-related factors included physical activity (active, inactive), smoking status (current smoker, former smoker, non-smoker), drinking status (2~4 times/week, 2~4 times/month, never or occasionally), sleeping hours (<7 h, ≥7 h), eating habits (eating three meals regularly, skipping meals), total energy intake (proteins, fats, carbohydrates; quintile 1, quintile 2, quintile 3, quintile 4, quintile 5), and body mass index (BMI)-defined obesity status (obese (≥ 25), normal (18.5~24.9), underweight (<18.5)). The disease-related factors included hypertension (hypertension (SBP ≥ 140 mm Hg), prehypertension (120 ≤ SBP ≤ 139 mm Hg), normal (SBP < 120 mm Hg)) and fasting glucose level (impaired fasting glucose (100~125 mg/dL), normal (<100 mg/dL)).
2.3. Statistical Analysis
The mean HbA1c level was calculated for each of the categorized variables included in the study. Analysis of variance (ANOVA) was performed to compare the mean HbA1c levels within each categorized variable to assess for significant differences. A generalized linear regression model (GLM) adjusted for confounding variables was used to assess the HbA1c level according to the reported work schedule. Those who reported the “day” schedule served as the reference group. The stratified, clustering, and weight variables developed by the KNHANES were applied to all the analyses to improve the representativeness of the sample and account for the limited proportion of participants retained in the final analysis. All the statistical analyses were performed using SAS version 9.4 (SAS Inc., Cary, NC, USA).
3. Results
Table 1 summarizes the general characteristics of the study population (male: 4773; female: 4818). Among the male participants, 4103 (86.0%) reported “day”, 302 (6.3%) reported “night and overnight”, and 368 (7.7%) reported “other” as their ordinary work schedule. Of the male workers, those who reported “night and overnight” had the highest mean HbA1c level (5.64) with the lowest standard deviation. The p-value for ANOVA within the work schedule was 0.0071.
Table 1.
General characteristics of the study subjects and analysis of variance for the HbA1c levels.
| Variables | HbA1c (%) | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total | Male | Female | ||||||||||||
| n | % | n | % | Mean ± SD | p-Value | n | % | Mean ± SD | p-Value | |||||
| Total | 9591 | 100.0 | 4773 | 49.8 | 5.60 | ± | 0.39 | 4818 | 50.2 | 5.55 | ± | 0.34 | ||
| Work schedule | 0.0071 | 0.2566 | ||||||||||||
| Day | 8180 | 85.3 | 4103 | 86.0 | 5.59 | ± | 0.43 | 4077 | 84.6 | 5.55 | ± | 0.42 | ||
| Night and overnight | 883 | 9.2 | 302 | 6.3 | 5.64 | ± | 0.46 | 581 | 12.1 | 5.56 | ± | 0.42 | ||
| Other | 528 | 5.5 | 368 | 7.7 | 5.64 | ± | 0.49 | 160 | 3.3 | 5.60 | ± | 0.44 | ||
| Age | <0.0001 | <0.0001 | ||||||||||||
| 30–39 | 2107 | 22.0 | 1135 | 23.8 | 5.43 | ± | 0.31 | 972 | 20.2 | 5.31 | ± | 0.30 | ||
| 40–49 | 2623 | 27.3 | 1253 | 26.3 | 5.53 | ± | 0.42 | 1370 | 28.4 | 5.42 | ± | 0.34 | ||
| 50–59 | 2441 | 25.5 | 1138 | 23.8 | 5.65 | ± | 0.41 | 1303 | 27.0 | 5.64 | ± | 0.37 | ||
| 60–69 | 1615 | 16.8 | 821 | 17.2 | 5.73 | ± | 0.47 | 794 | 16.5 | 5.78 | ± | 0.45 | ||
| ≥70 | 805 | 8.4 | 426 | 8.9 | 5.83 | ± | 0.58 | 379 | 7.9 | 5.90 | ± | 0.51 | ||
| Educational level | 0.8381 | 0.8638 | ||||||||||||
| ≤Elementary | 1404 | 14.6 | 515 | 10.8 | 5.74 | ± | 0.49 | 889 | 18.5 | 5.79 | ± | 0.50 | ||
| Middle | 919 | 9.6 | 446 | 9.3 | 5.72 | ± | 0.48 | 473 | 9.8 | 5.68 | ± | 0.41 | ||
| High | 2982 | 31.1 | 1418 | 29.7 | 5.62 | ± | 0.46 | 1564 | 32.5 | 5.54 | ± | 0.40 | ||
| ≥College | 4286 | 44.7 | 2394 | 50.2 | 5.53 | ± | 0.39 | 1892 | 39.3 | 5.43 | ± | 0.34 | ||
| Occupational status | 0.0719 | 0.0607 | ||||||||||||
| White | 3936 | 41.0 | 1952 | 40.9 | 5.52 | ± | 0.39 | 1984 | 41.2 | 5.43 | ± | 0.35 | ||
| Pink | 1886 | 19.7 | 565 | 11.8 | 5.61 | ± | 0.44 | 1321 | 27.4 | 5.60 | ± | 0.45 | ||
| Blue | 3769 | 39.3 | 2256 | 47.3 | 5.66 | ± | 0.47 | 1513 | 31.4 | 5.68 | ± | 0.44 | ||
| Household income | 0.451 | 0.3665 | ||||||||||||
| Low | 1022 | 10.7 | 386 | 8.1 | 5.72 | ± | 0.58 | 636 | 13.2 | 5.74 | ± | 0.50 | ||
| Middle | 5143 | 53.6 | 2,621 | 54.9 | 5.60 | ± | 0.42 | 2522 | 52.3 | 5.56 | ± | 0.42 | ||
| High | 3426 | 35.7 | 1,766 | 37.0 | 5.56 | ± | 0.43 | 1660 | 34.5 | 5.48 | ± | 0.37 | ||
| Household composition | 0.5193 | 0.3746 | ||||||||||||
| One-person household | 936 | 9.8 | 412 | 8.6 | 5.56 | ± | 0.47 | 524 | 10.9 | 5.70 | ± | 0.53 | ||
| One-generation household | 2280 | 23.8 | 1238 | 25.9 | 5.68 | ± | 0.49 | 1042 | 21.6 | 5.66 | ± | 0.44 | ||
| ≥Two-generation household | 6375 | 66.5 | 3123 | 65.4 | 5.57 | ± | 0.41 | 3252 | 67.5 | 5.50 | ± | 0.38 | ||
| Physical activity | 0.7231 | 0.9600 | ||||||||||||
| Active | 4086 | 42.6 | 2161 | 45.3 | 5.57 | ± | 0.43 | 1,925 | 40.0 | 5.54 | ± | 0.41 | ||
| Inactive | 5505 | 57.4 | 2612 | 54.7 | 5.62 | ± | 0.45 | 2,893 | 60.0 | 5.56 | ± | 0.43 | ||
| Smoking status | <0.0001 | 0.4196 | ||||||||||||
| Current smoker | 1864 | 19.4 | 1648 | 34.5 | 5.61 | ± | 0.45 | 216 | 4.5 | 5.47 | ± | 0.37 | ||
| Former smoker | 2381 | 24.8 | 2100 | 44.0 | 5.62 | ± | 0.45 | 281 | 5.8 | 5.43 | ± | 0.45 | ||
| Non-smoker | 5346 | 55.7 | 1025 | 21.5 | 5.54 | ± | 0.40 | 4,321 | 89.7 | 5.57 | ± | 0.42 | ||
| Drinking status | <0.0001 | <0.0001 | ||||||||||||
| 2–4 times/week | 2471 | 25.8 | 1824 | 38.2 | 5.57 | ± | 0.42 | 647 | 13.4 | 5.41 | ± | 0.38 | ||
| 2–4 times/month | 2289 | 23.9 | 1264 | 26.5 | 5.58 | ± | 0.45 | 1025 | 21.3 | 5.47 | ± | 0.40 | ||
| Never or occasionally | 4831 | 50.4 | 1685 | 35.3 | 5.64 | ± | 0.44 | 3146 | 65.3 | 5.61 | ± | 0.43 | ||
| Hours of sleep | 0.0426 | 0.2398 | ||||||||||||
| <7 h | 3779 | 39.4 | 1932 | 40.5 | 5.62 | ± | 0.46 | 1847 | 38.3 | 5.59 | ± | 0.41 | ||
| ≥7 h | 5812 | 60.6 | 2841 | 59.5 | 5.58 | ± | 0.42 | 2971 | 61.7 | 5.53 | ± | 0.43 | ||
| Eating habits | 0.0975 | <0.0001 | ||||||||||||
| Eating three meals regularly | 5438 | 56.7 | 2773 | 58.1 | 5.64 | ± | 0.46 | 2665 | 55.3 | 5.63 | ± | 0.43 | ||
| Skip meal (s) | 4153 | 43.3 | 2000 | 41.9 | 5.54 | ± | 0.41 | 2153 | 44.7 | 5.46 | ± | 0.39 | ||
| Total energy intake (kcal) a | 0.4732 | 0.8141 | ||||||||||||
| Quintile 1 | 1919 | 20.0 | 956 | 20.0 | 5.64 | ± | 0.48 | 963 | 20.0 | 5.56 | ± | 0.46 | ||
| Quintile 2 | 1918 | 20.0 | 954 | 20.0 | 5.62 | ± | 0.49 | 964 | 20.0 | 5.57 | ± | 0.40 | ||
| Quintile 3 | 1919 | 20.0 | 955 | 20.0 | 5.58 | ± | 0.41 | 964 | 20.0 | 5.56 | ± | 0.43 | ||
| Quintile 4 | 1918 | 20.0 | 954 | 20.0 | 5.60 | ± | 0.44 | 964 | 20.0 | 5.55 | ± | 0.43 | ||
| Quintile 5 | 1917 | 20.0 | 954 | 20.0 | 5.54 | ± | 0.35 | 963 | 20.0 | 5.53 | ± | 0.39 | ||
| BMI (kg/m2) b | <0.0001 | <0.0001 | ||||||||||||
| Obese (≥25) | 3340 | 34.8 | 2015 | 42.2 | 5.66 | ± | 0.44 | 1325 | 27.5 | 5.71 | ± | 0.46 | ||
| Normal (18.5~24.9) | 5964 | 62.2 | 2669 | 55.9 | 5.55 | ± | 0.43 | 3295 | 68.4 | 5.51 | ± | 0.39 | ||
| Underweight (<18.5) | 287 | 3.0 | 89 | 1.9 | 5.51 | ± | 0.35 | 198 | 4.1 | 5.33 | ± | 0.34 | ||
| Hypertension (mm Hg) | 0.0017 | <0.0001 | ||||||||||||
| Hypertension (≥140) | 2758 | 28.8 | 1582 | 33.1 | 5.71 | ± | 0.47 | 1176 | 24.4 | 5.78 | ± | 0.48 | ||
| Prehypertension (120~139) | 2605 | 27.2 | 1520 | 31.8 | 5.58 | ± | 0.43 | 1085 | 22.5 | 5.59 | ± | 0.39 | ||
| Normal (<120) | 4228 | 44.1 | 1671 | 35.0 | 5.51 | ± | 0.39 | 2557 | 53.1 | 5.44 | ± | 0.36 | ||
| Fasting glucose level (mg/dL) | <0.0001 | <0.0001 | ||||||||||||
| Impaired fasting glucose (100~125) | 3206 | 33.4 | 1930 | 40.4 | 5.79 | ± | 0.49 | 1276 | 26.5 | 5.85 | ± | 0.48 | ||
| Normal (<100) | 6385 | 66.6 | 2843 | 59.6 | 5.47 | ± | 0.35 | 3542 | 73.5 | 5.45 | ± | 0.34 | ||
| Year | <0.0001 | <0.0001 | ||||||||||||
| 2016 | 2258 | 23.5 | 1144 | 24.0 | 5.57 | ± | 0.45 | 1114 | 23.1 | 5.50 | ± | 0.40 | ||
| 2017 | 2382 | 24.8 | 1181 | 24.7 | 5.55 | ± | 0.40 | 1201 | 24.9 | 5.53 | ± | 0.41 | ||
| 2018 | 2492 | 26.0 | 1220 | 25.6 | 5.58 | ± | 0.41 | 1272 | 26.4 | 5.55 | ± | 0.43 | ||
| 2019 | 2459 | 25.6 | 1228 | 25.7 | 5.68 | ± | 0.49 | 1231 | 25.6 | 5.64 | ± | 0.43 | ||
a Total energy intake = (carbohydrates (g) × 4 kcal/g) + (proteins (g) × 4 kcal/g) + (fats (g) × 9 kcal/g). b Obesity status defined by body mass index (BMI) based on the 2014 Clinical Practice Guidelines for Overweight and Obesity in Korea.
Among the 4818 female participants, 4077 (84.6%) reported “day”, 581 (12.1%) reported “night and overnight”, and 160 (3.3%) reported “other” as their ordinary work schedule. Of the male workers, those who reported “night and overnight” had the highest mean HbA1c level (5.64) with the lowest standard deviation. The p-value for ANOVA was not statistically significant.
Table 2 summarizes the results of the generalized multiple regression analysis for HbA1c levels according to the types of work schedule. The HbA1c levels are represented as adjusted beta (β) coefficient in relation to “day” work schedules. Among the male workers, the “night and overnight” workers had the highest HbA1c levels (β = 0.061), and that was statistically significant (p = 0.0085). On the other hand, there was no significant difference among the female workers according to their reported work schedules.
Table 2.
Generalized multiple linear regression for HbA1c levels according to work schedule.
| Variable | HbA1c (%) | |||||
|---|---|---|---|---|---|---|
| Male | Female | |||||
| β | SE | p-Value | β | SE | p-Value | |
| Work schedule | ||||||
| Day | Ref. | Ref. | ||||
| Night and overnight | 0.061 | 0.023 | 0.0085 | 0.019 | 0.017 | 0.2687 |
| Other | 0.008 | 0.025 | 0.7557 | 0.049 | 0.032 | 0.1273 |
| Age | ||||||
| 30–39 | Ref. | Ref. | ||||
| 40–49 | 0.056 | 0.015 | 0.0002 | 0.062 | 0.013 | <0.0001 |
| 50–59 | 0.135 | 0.017 | <0.0001 | 0.200 | 0.017 | <0.0001 |
| 60–69 | 0.207 | 0.022 | <0.0001 | 0.272 | 0.024 | <0.0001 |
| ≥70 | 0.296 | 0.039 | <0.0001 | 0.326 | 0.038 | <0.0001 |
| Educational level | ||||||
| ≤Elementary | −0.017 | 0.028 | 0.5471 | 0.009 | 0.026 | 0.7357 |
| Middle | −0.020 | 0.026 | 0.4381 | 0.014 | 0.024 | 0.5605 |
| High | −0.012 | 0.015 | 0.4321 | −0.003 | 0.013 | 0.8335 |
| ≥College | Ref. | Ref. | ||||
| Occupational status | ||||||
| White | Ref. | Ref. | ||||
| Pink | 0.040 | 0.020 | 0.0460 | 0.014 | 0.014 | 0.3233 |
| Blue | 0.036 | 0.015 | 0.0166 | −0.010 | 0.017 | 0.5349 |
| Household income | ||||||
| Low | 0.005 | 0.031 | 0.8590 | −0.001 | 0.022 | 0.9491 |
| Middle | 0.013 | 0.013 | 0.3162 | 0.013 | 0.011 | 0.2480 |
| High | Ref. | Ref. | ||||
| Household composition | ||||||
| One-person household | −0.040 | 0.021 | 0.0522 | 0.032 | 0.021 | 0.1370 |
| One-generation household | −0.002 | 0.016 | 0.9219 | 0.010 | 0.015 | 0.4869 |
| ≥Two-generation household | Ref. | Ref. | ||||
| Physical activity | ||||||
| Active | Ref. | Ref. | ||||
| Inactive | 0.006 | 0.012 | 0.5834 | −0.002 | 0.011 | 0.8164 |
| Smoking status | ||||||
| Current smoker | 0.080 | 0.016 | < 0.0001 | −0.010 | 0.023 | 0.6642 |
| Former smoker | 0.015 | 0.015 | 0.3137 | −0.027 | 0.023 | 0.2503 |
| Non-smoker | Ref. | Ref. | ||||
| Drinking status | ||||||
| 2–4 times/week | −0.113 | 0.014 | < 0.0001 | −0.118 | 0.016 | <0.0001 |
| 2–4 times/month | −0.046 | 0.015 | 0.0020 | −0.035 | 0.013 | 0.0077 |
| Never or occasionally | Ref. | Ref. | ||||
| Hours of sleep | ||||||
| <7 h | 0.021 | 0.012 | 0.0727 | 0.023 | 0.011 | 0.0393 |
| ≥7 h | Ref. | Ref. | ||||
| Eating habits | ||||||
| Eating three meals regularly | Ref. | Ref. | ||||
| Skipping meals | −0.020 | 0.013 | 0.1198 | −0.045 | 0.011 | <0.0001 |
| Total energy intake (kcal) a | ||||||
| Quintile 1 | 0.004 | 0.018 | 0.8165 | −0.014 | 0.018 | 0.4402 |
| Quintile 2 | 0.022 | 0.019 | 0.2519 | 0.000 | 0.016 | 0.9795 |
| Quintile 3 | Ref. | Ref. | ||||
| Quintile 4 | 0.018 | 0.018 | 0.3109 | −0.007 | 0.016 | 0.6509 |
| Quintile 5 | 0.000 | 0.017 | 0.9834 | 0.007 | 0.016 | 0.6596 |
| BMI (kg/m2) b | ||||||
| Obese (≥25) | 0.071 | 0.012 | <0.0001 | 0.080 | 0.013 | <0.0001 |
| Normal (18.5~24.9) | Ref. | Ref. | ||||
| Underweight (<18.5) | −0.031 | 0.031 | 0.3094 | −0.067 | 0.025 | 0.0079 |
| Hypertension (mm Hg) | ||||||
| Hypertension (≥140) | 0.064 | 0.016 | <0.0001 | 0.079 | 0.018 | <0.0001 |
| Prehypertension (120~139) | 0.022 | 0.014 | 0.1189 | 0.030 | 0.014 | 0.0272 |
| Normal (<120) | Ref. | Ref. | ||||
| Fasting glucose level (mg/dL) | ||||||
| Impaired fasting glucose (100~125) | 0.267 | 0.013 | <0.0001 | 0.297 | 0.015 | <0.0001 |
| Normal (<100) | Ref. | Ref. | ||||
| Year | ||||||
| 2016 | Ref. | Ref. | ||||
| 2017 | −0.021 | 0.016 | 0.1844 | 0.033 | 0.015 | 0.0321 |
| 2018 | −0.003 | 0.017 | 0.8475 | 0.048 | 0.015 | 0.0018 |
| 2019 | 0.095 | 0.018 | <0.0001 | 0.120 | 0.015 | <0.0001 |
BMI—body mass index. a Total energy intake = (carbohydrates (g) × 4 kcal/g) + (proteins (g) × 4 kcal/g) + (fats (g) × 9 kcal/g). b Obesity status defined by BMI based on the 2014 Clinical Practice Guidelines for Overweight and Obesity in Korea.
Table 3 summarizes the subgroup results of generalized multiple linear regression for HbA1c levels stratified by physical activity, hours of sleep, and daily eating. Among the 302 male “night and overnight” workers, the average HbA1c level significantly increased to 0.108 (p = 0.009) for those who reported having less than 7 h of sleep daily, to 0.064 (p = 0.0401) for those who reported skipping meals, and to 0.108 (p = 0.0579) for those who intook the least amount of energy. Those who reported being physically inactive also showed an increased level of HbA1c (β = 0.094; p = 0.0031).
Table 3.
Generalized multiple linear regression for HbA1c levels stratified by physical activity, hours of sleep, and daily eating.
| Variable | HbA1c (%) | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Day | Male (n = 4773) | Female (n = 4818) | |||||||||||
| Night and Overnight (n = 302) | Other (n = 368) | Night and Overnight (n = 581) | Other (n = 160) | ||||||||||
| Β | β | SE | p-Value | β | SE | p-Value | β | SE | p-Value | β | SE | p-Value | |
| Physical activity | |||||||||||||
| Active | Ref. | 0.023 | 0.034 | 0.4995 | 0.014 | 0.035 | 0.6842 | −0.011 | 0.027 | 0.6791 | −0.015 | 0.038 | 0.7016 |
| Inactive | Ref. | 0.094 | 0.032 | 0.0031 | −0.002 | 0.037 | 0.9605 | 0.037 | 0.022 | 0.0899 | 0.092 | 0.048 | 0.0561 |
| Hours of sleep | |||||||||||||
| <7 h | Ref. | 0.108 | 0.033 | 0.0009 | −0.049 | 0.038 | 0.2011 | 0.024 | 0.026 | 0.3685 | 0.053 | 0.048 | 0.2747 |
| ≥7 h | Ref. | 0.034 | 0.032 | 0.2894 | 0.065 | 0.032 | 0.0434 | 0.014 | 0.022 | 0.5105 | 0.042 | 0.041 | 0.3095 |
| Eating habits | |||||||||||||
| Eating three meals regularly | Ref. | 0.053 | 0.033 | 0.1095 | −0.008 | 0.035 | 0.8227 | −0.006 | 0.025 | 0.8017 | 0.056 | 0.050 | 0.2661 |
| Skipping meals | Ref. | 0.064 | 0.031 | 0.0401 | 0.028 | 0.036 | 0.4494 | 0.035 | 0.022 | 0.1206 | 0.055 | 0.041 | 0.1852 |
| Total energy intake (kcal) a | |||||||||||||
| Quintile 1 | Ref. | 0.108 | 0.057 | 0.0579 | 0.067 | 0.077 | 0.3870 | 0.025 | 0.038 | 0.5129 | 0.132 | 0.110 | 0.2336 |
| Quintile 2 | Ref. | 0.059 | 0.056 | 0.2922 | −0.042 | 0.045 | 0.3539 | 0.008 | 0.038 | 0.8297 | 0.079 | 0.074 | 0.2863 |
| Quintile 3 | Ref. | 0.057 | 0.041 | 0.1679 | −0.075 | 0.052 | 0.1555 | 0.010 | 0.044 | 0.8155 | 0.036 | 0.052 | 0.4823 |
| Quintile 4 | Ref. | −0.021 | 0.050 | 0.6658 | 0.021 | 0.057 | 0.7097 | 0.021 | 0.036 | 0.5720 | −0.011 | 0.057 | 0.8546 |
| Quintile 5 | Ref. | 0.045 | 0.046 | 0.3293 | 0.070 | 0.053 | 0.1913 | 0.066 | 0.030 | 0.0298 | 0.070 | 0.047 | 0.1352 |
a Total energy intake = (carbohydrates (g) × 4 kcal/g) + (proteins (g) × 4 kcal/g) + (fats (g) × 9 kcal/g).
Figure 1 demonstrates the results of generalized multiple linear regression for HbA1c levels according to the specific work schedules. In the male participants, HbA1c levels increased the greatest among those who worked overnight (β = 0.092; p = 0.0247), followed by those who worked during the night (β = 0.500; p = 0.0441).
Figure 1.
Generalized multiple linear regression for HbA1c levels according to the specific types of work schedules; * p-value < 0.05.
4. Discussion
After controlling for confounding variables such as demographic, socioeconomic, health, and disease-related factors, the male participants who worked during the night and overnight showed increased levels of HbA1c in comparison to those who worked during the conventional daytime. On the other hand, there was no significant difference in HbA1c levels among the female participants according to their ordinary work schedules. Sex differences in glycated hemoglobin levels have not been widely discussed [19]. Although no consensus has been reached regarding sex effects on HbA1c, hormonal changes during the menstrual cycle may account for the differences in HbA1c levels in male and female participants [19,20,21]. Previous literature suggested that women have a shorter red blood cell survival in comparison to men, and this may lower HbA1c levels. Other empirical evidence showed that estrogen plays a role in suppressing erythropoiesis in vitro and in vivo, which is implicated in lowering HbA1c levels in women [21].
Metabolism operates on circadian rhythms around the clock. Work schedules outside the standard daytime period may impair physiological activities and are likely to result in aberrant glucose homeostasis [22,23]. The findings of our study add empirical evidence to support the existing phenomenon that workers who work during the nighttime have increased HbA1c levels [23,24,25,26,27,28]. In particular, the study showed that HbA1c levels increased in the nighttime workers who were physically inactive, those who slept less than 7 h, and those who had the least amount of energy intake.
Exercise promotes glucose metabolism, which leads to elevated insulin sensitivity and lower blood sugar. Furthermore, lack of exercise can increase the risk of diabetes. Prior research publications showed that people with impaired fasting glucose disorder showed a statistically significant difference in the relative risk for non-exercising groups (1.375 for men and 1.124 for women), confirming the benefits of exercise [29]. Studies of diabetic and prediabetic men also showed that one to two physical activities a week were more effective in controlling blood sugar than inactivity [29,30].
HbA1c levels of people working during the nighttime with less than seven hours of sleep were significantly higher. Adequate sleeping time can help the body recover from fatigue and maintain biorhythms. According to the recommended sleeping time for each age group provided in the National Sleep Foundation (NSF) guidelines for 2015, the optimal sleeping time for adults is more than seven hours [31]. Structural changes in modern society are affecting the amount and quality of sleep as shifts increase and various types of working hours arise [32]. In addition, the amount and quality of this poor sleep are consistent with previous studies that linked them with the risk of type 2 diabetes [33,34].
Regarding eating habits, higher HbA1c levels are found in people who skip more than one meal a day compared to those who regularly eat three meals a day while working evenings and nights. Dining patterns have changed to Westernized eating habits since industrialization, which has also affected the development of diabetes, closely related to insulin secretion [30,31,32,33,34]. Carlson et al. assessed the effect of glucose metabolism on healthy men and women of normal weight without decreasing energy consumption [35,36]. They found that the morning fasting blood sugar level of the meal skipping group was higher than that of the group who regularly ate three meals a day. A prior study that investigated the relationship between the regularity of meals and impaired blood glucose disorder in adult non-diabetes groups also showed aligned results, with a 1.27 times higher incidence of impaired fasting glucose disorder in the groups that skipped meals [36,37].
In this study, HbA1c levels did not reach the prediabetes level. However, previous studies reported higher rates of the incidence of diabetes for five years according to glycated hemoglobin levels. Notably, HbA1c levels increased to less than 9% if they previously were 5.0–5.5%, to 9–25% if they previously were 6.0–6.5%, and to 25–50% if they previously were 6.0–6.5% [2]. Another previous study tracked HbA1c levels for six years, excluding those with a history of diabetes. It showed the highest sensitivity (59%) and specificity (77%) when the HbA1c level was initially 5.6%, with a 2.4 times increase in men and 3.1 times increase in women [38].
This study has several limitations. First, the cross-sectional design rendered us unable to determine a causal relationship between nighttime work and HbA1c levels. Second, the key covariates considered in this study, including physical activity, sleeping time, and eating habits were self-reported, possibly subject to recall bias. Third, the duration in working years of the current shift work was not considered. Lastly, the types of shift work were not specified in the survey data, and the workers were only specified by “collar colors”. Despite these limitations, this study also has certain strengths. First, it was the first study to analyze the association between shift work and HbA1c for non-diabetes groups in South Korea. Second, the data used in this study came from a national health statistics survey that calculated more than 500 health indicators such as eating habits and chronic diseases. The National Health and Nutrition Survey comprised a representative sample of the South Korean population, representing the actual health status of Koreans, and an updated questionnaire every year can identify changes in health status. Therefore, it can contribute to improving the health of the people by reflecting on health policies.
5. Conclusions
This study investigated the association between nighttime work and HbA1c levels among Korean adults aged 30 or older. We found a significant association between working night shifts and HbA1c levels in the men. Lack of exercise, sleeping less than 7 h, and skipping more than one meal a day were especially highly associated with increased HbA1c levels. High-risk groups with increased HbA1c levels require careful monitoring of physical activity, sleeping time, eating habits, and BMI. However, our study could not determine a causal relationship between HbA1c and night work, and further studies are needed for validation.
Acknowledgments
We thank the Korea Centers for Disease Control (KCDC) which produced and provided the national-level survey data. We also thank those colleagues from the Institute of Health Services Research at Yonsei University who gave advice regarding important intellectual content.
Author Contributions
Y.-S.L. and E.-C.P. designed the study, collected the data, performed the statistical analysis, and wrote the manuscript. J.H.J. contributed to the discussion and reviewed and edited the manuscript. E.-C.P. is the guarantor of this work and as such had full access to all of the data. J.H.J. and E.-C.P. assume responsibility for the integrity of the data and the accuracy of the data analysis, and they are the corresponding authors of the manuscript. All authors have read and agreed to the published version of the manuscript.
Institutional Review Board Statement
This study was an analysis of the existing data; thus, it did not require approval by an ethics review board. The data used in this study came from the KNHANES, and it has been annually reviewed and approved by the Korea Centers for Disease Control (KCDC) Research Ethics Review Committee since 2007.
Informed Consent Statement
Informed consent was obtained from all subjects involved in the study. The data used in the study is a secondary data with encrypted personal information.
Data Availability Statement
The data is publicly accessible on the website of KNHANES administered by the Korea Disease Control and Prevention Agency (https://knhanes.cdc.go.kr/knhanes/index.do, accessed on 4 October 2022).
Conflicts of Interest
The authors declare that they have no competing interest.
Funding Statement
This research received no external funding.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Lee Y.K. Analysis of the Relationship between Working Hour Mismatch and Worker’s Health. Health Soc. Welf. Rev. 2015;35:135–165. [Google Scholar]
- 2.Sparks K., Cooper C., Fried Y., Shirom A. Managerial, Occupational and Organizational Stress Research. Routledge; Oxfordshire, UK: 2018. The effects of hours of work on health: A meta-analytic review; pp. 451–468. [Google Scholar]
- 3.Caruso C.C., Hitchcock E.M., Dick R.B., Russo J.M., Schmitt J.M. Overtime and Extended Work Shifts; Recent Findings on Illnesses, Injuries, and Health Behaviors. U.S. Department of Health and Human Services, NIOSH Publication; Washington, DC, USA: 2004. p. 143. [Google Scholar]
- 4.Spurgeon A., Harrington J.M., Cooper C.L. Health and safety problems associated with long working hours: A review of the current position. Occup. Environ. Med. 1997;54:367–375. doi: 10.1136/oem.54.6.367. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Tucker P., Folkard S. Working Time, Health and Safety: A Research Synthesis Paper. ILO; Geneva, Switzerland: 2012. (Conditions of Work and Employment Series 31). [Google Scholar]
- 6.Won J.C., Lee J.H., Kim J.H., Kang E.S., Won K.C., Kim D.J., Lee M.K. Diabetes Fact Sheet in Korea, 2016: An Appraisal of Current Status. Diabetes Metab. J. 2018;42:415–424. doi: 10.4093/dmj.2018.0017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7.Seuring T., Archangelidi O., Suhrcke M. The Economic Costs of Type 2 Diabetes: A Global Systematic Review. Pharmacoeconomics. 2015;33:811–831. doi: 10.1007/s40273-015-0268-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Tabák A.G., Herder C., Rathmann W., Brunner E.J., Kivimäki M. Diabetes 1: Prediabetes: A high-risk state for diabetes development. Lancet. 2012;379:2279–2290. doi: 10.1016/S0140-6736(12)60283-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Forouhi N.G., Luan J., Hennings S., Wareham N.J. Incidence of type 2 diabetes in England and its association with baseline impaired fasting glucose: The Ely study 1990–2000. Diabet. Med. 2007;24:200–207. doi: 10.1111/j.1464-5491.2007.02068.x. [DOI] [PubMed] [Google Scholar]
- 10.Nathan D.M., Davidson M.B., DeFronzo R.A., Heine R.J., Henry R.R., Pratley R., Zinman B. Impaired fasting glucose and impaired glucose tolerance: Implications for care. Diabetes Care. 2007;30:753–759. doi: 10.2337/dc07-9920. [DOI] [PubMed] [Google Scholar]
- 11.Diabetes Prevention Program Research Group 10-year follow-up of diabetes incidence and weight loss in the Diabetes Prevention Program Outcomes Study. Lancet. 2009;374:1677–1686. doi: 10.1016/S0140-6736(09)61457-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.The DREAM (Diabetes Reduction Assessment with ramipril and rosiglitazone Medication) Trial Investigators Effect of rosiglitazone on the frequency of diabetes in patients with impaired glucose tolerance or impaired fasting glucose: A randomised controlled trial. Lancet. 2006;368:1096–1105. doi: 10.1016/S0140-6736(06)69420-8. [DOI] [PubMed] [Google Scholar]
- 13.Diabetes Prevention Program Research Group Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. N. Engl. J. Med. 2002;346:393–403. doi: 10.1056/NEJMoa012512. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Ramachandran A., Snehalatha C., Mary S., Mukesh B., Bhaskar A.D., Vijay V. The Indian Diabetes Prevention Programme shows that lifestyle modification and metformin prevent type 2 diabetes in Asian Indian subjects with impaired glucose tolerance (IDPP-1) Diabetologia. 2006;49:289–297. doi: 10.1007/s00125-005-0097-z. [DOI] [PubMed] [Google Scholar]
- 15.Torgerson J.S., Hauptman J., Boldrin M.N., Sjöström L. XENical in the prevention of diabetes in obese subjects (XENDOS) study: A randomized study of orlistat as an adjunct to lifestyle changes for the prevention of type 2 diabetes in obese patients. Diabetes Care. 2004;27:155–161. doi: 10.2337/diacare.27.1.155. [DOI] [PubMed] [Google Scholar]
- 16.Tuomilehto J., Lindström J., Eriksson J.G., Valle T.T., Hämäläinen H., Ilanne-Parikka P., Uusitupa M. Prevention of type 2 diabetes mellitus by changes in lifestyle among subjects with impaired glucose tolerance. N. Engl. J. Med. 2001;344:1343–1350. doi: 10.1056/NEJM200105033441801. [DOI] [PubMed] [Google Scholar]
- 17.Cho N.H. Diabetes epidemiology in Korean. Diabetes. 2001;25:1–10. [Google Scholar]
- 18.Kweon S., Kim Y., Jang M., Kim Y., Kim K., Choi S., Chun C., Khang Y.H., Oh K. Data resource profile: The Korea National Health and Nutrition Examination Survey (KNHANES) Int. J. Epidemiol. 2014;43:69–77. doi: 10.1093/ije/dyt228. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Simon D., Senan C., Gamier P., Saint-Paul M. Papoz L: Epidemiological features of glycated haemoglobin Ale-distribution in a healthy population. Diabetologa. 1989;32:864–869. doi: 10.1007/BF00297451. [DOI] [PubMed] [Google Scholar]
- 20.Dukes P.P., Goldwasser E. Inhibition of erythropoiesis by estrogens. Endocrinology. 1961;69:21–25. doi: 10.1210/endo-69-1-21. [DOI] [PubMed] [Google Scholar]
- 21.Peschle C., Magli M.C., Cillo C., Lettieri F., Cacciapuoti A., Pizzella E., Marone G. Erythroid colony formation and erythropoietin activity I mice treated with estradiol benzoate. Life Sci. 1977;21:1303–1310. doi: 10.1016/0024-3205(77)90011-X. [DOI] [PubMed] [Google Scholar]
- 22.Roenneberg T., Merrow M. The circadian clock and human health. Curr. Biol. 2016;26:R432–R443. doi: 10.1016/j.cub.2016.04.011. [DOI] [PubMed] [Google Scholar]
- 23.Kecklund G., Axelsson J. Health consequences of shift work and insufficient sleep. BMJ. 2016;355:i5210. doi: 10.1136/bmj.i5210. [DOI] [PubMed] [Google Scholar]
- 24.Wang X.S., Armstrong M.E.G., Cairns B.J., Key T.J., Travis R.C. Shift work and chronic disease: The epidemiological evidence. Occup. Med. 2011;61:78–89. doi: 10.1093/occmed/kqr001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Gan Y., Yang C., Tong X., Sun H., Cong Y., Yin X., Li L., Cao S., Dong X., Gong Y., et al. Shift work and diabetes mellitus: A meta-analysis of observational studies. Occup. Environ. Med. 2015;72:72–78. doi: 10.1136/oemed-2014-102150. [DOI] [PubMed] [Google Scholar]
- 26.Claus M., Schuster M., Oberlinner C., Webendörfer S. Rotating shift work and prevalence of diabetes mellitus and prediabetes in male employees of a large german chemical company: Results of a cross-sectional study. Occup. Environ. Med. 2017;74:A73. [Google Scholar]
- 27.Pan A., Schernhammer E.S., Sun Q., Hu F.B. Rotating night shift work and risk of type 2 diabetes: Two prospective cohort studies in women. PLoS Med. 2011;8:e1001141. doi: 10.1371/journal.pmed.1001141. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Seo E.K., Lee M.Y., Jeong E.S., Sung D.J. Difference of Selected Metabolic Syndrome Makers in Nurses on Rotating Shift and Daytime Fixed Work Schedules. Korean Soc. Wellness. 2018;13:61–72. doi: 10.21097/ksw.2018.11.13.4.61. [DOI] [Google Scholar]
- 29.Hong D.U., Lee D.C., Lee S.Y., Kim Y.S. A Prospective Cohort Study of Exercise and the Incidence of Type 2 Diabetes in Impaired Fasting Glucose Group. J. Prev. Med. Public Health. 2008;41:45–50. doi: 10.3961/jpmph.2008.41.1.45. [DOI] [PubMed] [Google Scholar]
- 30.Park S.Y., Lee S.W., Lee H.S., Byun A.R., Kwon Y.E. Effects of Intermittent Leisure Time Physical Activity on Glycemic Control in Korean Adult Men with Diabetes and Prediabetes. Korean Acad. Fam. Med. 2019;9:29–35. doi: 10.21215/kjfp.2019.9.1.29. [DOI] [Google Scholar]
- 31.Hirshkowitz M., Whiton K., Albert S.M., Alessi C., Bruni O., DonCarlos L., Hillard P.J.A. National Sleep Foundation’s sleep time duration recommendations: Methodology and results summary. Sleep Health. 2015;1:40–43. doi: 10.1016/j.sleh.2014.12.010. [DOI] [PubMed] [Google Scholar]
- 32.Jun K.Y. Master’s Thesis. Hanyang University Graduate School; Seoul, Korea: 2015. Association between Occupational Environments including Working Hours and Sleep Duration among Korean Adults. [Google Scholar]
- 33.Ha Y.M. Master’s Thesis. Chung-Ang University Graduate School of Health and Nursing; Anseong, Korea: 2015. The Effect of Sleep Quality and Quantity on Type II Diabetes Mellitus. [Google Scholar]
- 34.Knutson K.L., Ryden A.M., Mander B.A., Cauter E.V. Role of sleep duration and quality in the risk and severity of type 2 diabetes mellitus. Arch. Intern. Med. 2006;166:1768–1774. doi: 10.1001/archinte.166.16.1768. [DOI] [PubMed] [Google Scholar]
- 35.Carlson O., Martin B., Stote K.S., Golden E., Maudsley S., Najjar S.S., Ferrucci L., Ingram D.K., Longo D.L., Rumpler W.V., et al. Impact of reduced meal frequency without caloric restriction on glucose regulation in healthy, normal-weight middle-aged men and women. Metabolism. 2007;56:1729–1734. doi: 10.1016/j.metabol.2007.07.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.You H.S., Lee J.H., Choi W.J., Lee J.W. Relationship between Skipping Meals and Impaired Fasting Glucose in Non-Diabetic Korean Adults. Korean J. Fam. Pract. 2017;7:824–829. doi: 10.21215/kjfp.2017.7.6.824. [DOI] [Google Scholar]
- 37.Zhang X., Gregg E.W., Williamson D.F., Barker L.E., Thomas W., Bullard K.M., Imperatore G., Williams D.E., Albright A.L. A1C level and future risk of diabetes: A systematic review. Diabetes Care. 2010;33:1665–1673. doi: 10.2337/dc09-1939. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Choi S.H., Kim T.H., Lim S., Park K.S., Jang H.C., Cho N.H. Hemoglobin A1c as a diagnostic tool for diabetes screening and new-onset diabetes prediction: A 6-year community-based prospective study. Diabetes Care. 2011;34:944–949. doi: 10.2337/dc10-0644. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data is publicly accessible on the website of KNHANES administered by the Korea Disease Control and Prevention Agency (https://knhanes.cdc.go.kr/knhanes/index.do, accessed on 4 October 2022).

