Literature DB >> 35954622

The Combination of Sleep Disorders and Depression Significantly Increases Cancer Risk: A Nationwide Large-Scale Population-Based Study.

Fang-Chin Hsu1, Chih-Hsiung Hsu2,3, Chi-Hsiang Chung4,5,6, Ta-Wei Pu7, Pi-Kai Chang8, Tzu-Chiao Lin8, Shu-Wen Jao8, Chao-Yang Chen8, Wu-Chien Chien4,5,9, Je-Ming Hu2,7,10.   

Abstract

Introduction: Sleep disorders, depression, and cancer have become increasingly prevalent worldwide. However, it is unknown whether coexistence of sleep disorders and depression influences the risk of cancer development. Therefore, we conducted a nationwide population-based study to examine this association among patients in Taiwan. Materials and
Methods: A total of 105,071 individuals diagnosed with cancer and 420,284 age- and sex-matched patients without a diagnosis of cancer between 2000 and 2015 were identified from Taiwan's National Health Insurance Research Database. The underlying chronic diseases of patients that may developed cancer were gathered and studied as the predictor. A multivariate Cox proportional odds model was used to estimate the crude and adjusted odds ratios (aORs) with 95% confidence intervals (CIs) to estimate the interaction effect between sleep disorders and depression on the risk of cancer.
Results: After adjusting for age, sex, comorbidities, and other covariates, the cancer group was associated with increased exposure to sleep disorders than the non-cancer group (aOR = 1.440, 95% CI = 1.392-1.489, p < 0.001). In addition, patients with both sleep disorders and depression were at an even higher risk for cancer than the general population (aOR = 6.857, p < 0.001). Conclusions: This retrospective cohort study shows that patients with both sleep disorders and depression are at a higher risk of cancer. Clinically, a meticulous cancer risk evaluation is recommended for patients with both sleep disorders and depression.

Entities:  

Keywords:  cancer; depression; sleep disorder

Mesh:

Year:  2022        PMID: 35954622      PMCID: PMC9368707          DOI: 10.3390/ijerph19159266

Source DB:  PubMed          Journal:  Int J Environ Res Public Health        ISSN: 1660-4601            Impact factor:   4.614


1. Introduction

Sleep is a naturally recurring state of the mind and body that accounts for approximately one-third of a person’s life. Sleep enables the human body to recover after waking activities, ensuring optimal subsequent functioning [1]. However, the prevalence of sleep disorders has increased worldwide, ranging from approximately 10% to 30% in Western countries [2,3] and approximately 20% to 30% in Asian populations [4,5]. According to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V), people with sleep disorders are dissatisfied with their quality, timing, and amount of sleep, resulting in daytime distress and impairment. Numerous detrimental effects have been reported, including the risk of cardiovascular disease, diabetes mellitus, obesity, and mortality [6,7,8]. In patients with cancer, sleep disorders often occur because of the physical or psychological impact of the cancer or its treatment. However, several studies have shown that sleep disorders may be associated with the development of cancers, such as breast cancer [9], colorectal cancer [10], lung cancer [11,12], and liver cancer [12]. Furthermore, sleep disorders are a serious health challenge and often coexist with mental disorders, such as major depression disorder (MDD) [13]. Since the 1980s, research has shown that the immune system, the endocrine system, cancer metastasis, treatment tolerance, and other processes are all impacted by depression [14]. It has been suggested that depression and anxiety, the two most prevalent mental disorders with past-year prevalence rates of 5% and 7%, respectively, in the general population, may potentially play an etiologic role and have a prognostic impact on cardiovascular diseases, such as stroke and coronary heart disease [15,16]. Furthermore, depression is much more prevalent among cancer patients, affecting up to 20% of cancer patients [17]. However, when investigating the relationship between depression and cancer, most researchers have focused on cancer-induced depression, and only few have explored depression as a risk factor for subsequent cancer. Although some meta-analysis studies have investigated the relationship between depression and overall cancer risk over the past decade [14,18], the results of these studies are inconsistent or require larger sample sizes for confirmation. To the best of our knowledge, no study has examined if and how the coexistence of sleep disorders and depression impacts cancer risk in the human population. Thus, we conducted a population-based cohort study to assess the interaction effect between sleep disorders and depression on cancer risk in a large general population in Taiwan using a longitudinal health insurance dataset selected from the National Health Insurance Research Database (NHIRD).

2. Materials and Methods

2.1. Data Source

The current study was a population-based retrospective cohort study conducted using the medical claims dataset from Taiwan’s NHIRD. The National Health Insurance (NHI) program is a single-payer mandatory enrollment program implemented by the government of Taiwan in 1995, enrolling up to 99% of Taiwan’s population (approximately 23 million people) [19]. The NHIRD contains comprehensive, high-quality information on epidemiological research and data on diagnoses, prescription use, and health-care information, including inpatient/ambulatory claims, prescription claims, demographic data, and hospitalization; these data have been widely used in academic studies [20,21]. Diseases in the database were defined using International Classification of Disease, Ninth Revision (ICD-9) codes.

2.2. Study Subjects

Patients with cancer between January 2000 and December 2015 were selected from the longitudinal health insurance dataset and categorized according to ICD codes (140–149, 150, 151, 153–154, 155, 160–161, 162, 174, 179–184, 185, 88–189, 193, 200–208); this group comprised the study cohort (Figure 1). To identify patients with sufficient accuracy, we ascertained patients with cancer according to the Registry for Catastrophic Illness Patient Database (RCIPD), a subset of the NHIRD. In Taiwan, a patient must provide an official hospital diagnosis certificate with confirmation based on laboratory results, pathology, and/or diagnostic imaging in order to obtain a certificate of catastrophic disease. Therefore, the diagnosis of cancer in our study was reliable. We also enrolled a 1:4 age-, sex-, and index year-matched group of patients from the NHIRD. These patients were enrolled as the unexposed group or control cohort since they were not diagnosed with cancer throughout the study period. The diagnoses of all sleep disorders were made by certified psychiatrists and in accordance with the DSM-V criteria, which required at least two outpatient visits or one admission record for ICD-9-CM codes: 307.4 and 780.5. Patients under the age of 18, those of unknown sex, those who used drugs, and those who had the last sleep disorders (SD) diagnosis before the first cancers diseases diagnosis, but less than 2 years in retrospective duration, were all excluded.
Figure 1

Flowchart of participant selection (nested case-control study) from the National Health Insurance Research Database in Taiwan.

2.3. Variables of Interest

The covariates included age, sex, monthly insured premiums, comorbidities, locations, urbanization levels of residence, and the level of healthcare provided at the facility of diagnosis. Covariates that were potential confounders in the association between sleep disorders and cancer included age, sex, and underlying chronic diseases. The chronic diseases of patients that may developed cancer were gathered and studied as the predictor, and they included hypertension (HTN, ICD-9-CM codes: 401, 404, and 405), diabetes mellitus (DM) (ICD-9-CM code: 250), stroke (ICD-9-CM code: 430–438), dementia (ICD-9-CM codes: 290, 294.1, and 331.0), chronic kidney disease (CKD, ICD-9-CM code: 585), and depression. All depression diagnoses were made by certified psychiatrists and in accordance with the DSM-V criteria, which required at least two outpatient visits or one admission record for ICD-9-CM codes: 296.2–296.3, 296.82, 300.4, 311.

2.4. Statistical Analysis

The distribution of comorbidities and sociodemographic data was compared between the case group (with cancer) and the control group (without cancer) using the chi-squared test to examine categorical variables and Student’s t-test to examine continuous variables. We computed the odds ratios (ORs) and 95% confidence intervals (CIs) using logistic proportional odds models after adjusting for the potential confounders mentioned above (including age, sex, monthly insured premiums, comorbidities, locations, urbanization levels of residence, and the level of healthcare provided at the facility of diagnosis). All confounders, such as covariates and comorbidities, were calculated separately. Further analysis was done to assess the interaction effect between sleep disorders and depression on the risk of cancer, and adjusted ORs were also estimated for 12 specific cancer types using conditional logistic regression. All statistical analyses were performed using the SPSS software (version 22.0; SPSS Inc., Chicago, IL, USA). For two-sided testing, the significance level was set at p < 0.05.

3. Results

In total, 525,355 patients were enrolled in this study, including 105,071 adult patients with cancer and 420,284 patients without cancer. The percentage of pre-existing sleep disorders was 4.92% in the case group and 3.86% in the control group. The participants’ age and sex, monthly insured premium, comorbidities, location and urbanization level of residence, and level of hospitals for medical help are summarized in Table 1. There were no significant differences in age, sex, or insurance premiums (NT$). Most patients were aged ≥65 years. The cancer group tended to have a higher prevalence of HTN, depression, stroke, and CKD. Furthermore, cancer patients tended to live in Taiwan’s north and south, in areas with a high level of urbanization, and sought medical treatment from tertiary hospital centers.
Table 1

Characteristics of the study population.

CancersTotalWithWithout p
Variablesn%n%n%
Total 525,355 105,07120.00420,28480.00
Gender 0.999
Male300,05057.1160,01057.11240,04057.11
Female225,30542.89 45,06142.89180,24442.89
Age (years) 63.42 ± 16.6363.49 ± 15.1363.40 ± 16.990.117
Age group (years) 0.999
18–4468,10512.9613,62112.9654,48412.96
45–64192,77536.6938,55536.69154,22036.69
≥65264,47550.3452,89550.34211,58050.34
Married 0.004
Without67,42312.8313,44512.8053,97812.84
With276,91352.7155,69753.01221,21652.63
Divorce61,46811.7012,45611.8549,01211.66
Spouse death119,46722.7423,45422.3296,01322.84
Unknown840.02190.02650.02
Education <0.001
Elementary/junior high school50,7609.6610,1549.6640,6069.66
(Vocational) high school296,35256.4159,90157.01236,45156.26
Univeristy/college/graduate178,21133.9235,01033.32143,20134.07
Others320.0160.01260.01
Insured premium (NT$) 0.951
<18,000469,29389.3393,83189.30375,46289.34
18,000–34,99939,8277.5879827.6031,8457.58
≥35,00016,2353.0932583.1012,9773.09
DM 0.359
Without417,40779.4583,37479.35334,03379.48
With107,94820.5521,69720.6586,25120.52
HT <0.001
Without410,044 78.0581,34377.42328,70178.21
With115,311 21.9523,72822.5891,58321.79
Depression <0.001
Without517,915 98.58 102,600 97.65 415,315 98.82
With7440 1.42 2471 2.35 4969 1.18
Stroke <0.001
Without474,272 90.28 94,073 89.53 380,199 90.46
With51,083 9.72 10,998 10.47 40,085 9.54
Dementia <0.001
Without519,570 98.90 104,173 99.15 415,397 98.84
With5785 1.10 898 0.85 4887 1.16
CKD 0.025
Without466,555 88.81 93,106 88.61 373,449 88.86
With58,800 11.19 11,965 11.39 46,835 11.14
Season <0.001
Spring (March–May)120,264 22.89 24,086 22.92 96,178 22.88
Summer (June–August)131,700 25.07 25,691 24.45 106,009 25.22
Autumn (September–November)151,076 28.76 28,862 27.47 122,214 29.08
Winter (December–February)122,315 23.28 26,432 25.16 95,883 22.81
Location <0.001
Northern Taiwan213,017 40.55 45,624 43.42 167,393 39.83
Middle Taiwan149,055 28.37 26,980 25.68 122,075 29.05
Southern Taiwan131,872 25.10 27,744 26.41 104,128 24.78
Eastern Taiwan29,294 5.58 4402 4.19 24,892 5.92
Outlets islands2117 0.40 321 0.31 1796 0.43
Urbanization level <0.001
1 (The highest)164,309 31.28 39,844 37.92 124,465 29.61
2236,316 44.98 48,746 46.39 187,570 44.63
338,416 7.31 4060 3.86 34,356 8.17
4 (The lowest)86,314 16.43 12,421 11.82 73,893 17.58
Level of care <0.001
Hospital center189,094 35.99 57,044 54.29 132,050 31.42
Regional hospital234,975 44.73 37,663 35.85 197,312 46.95
Local hospital101,286 19.28 10,364 9.86 90,922 21.63
Sleep disorders <0.001
Without503,952 95.93 99,898 95.08 404,054 96.14
With21,403 4.07 5173 4.92 16,230 3.86
Apnea 0.508
Without523,931 99.73 104,776 99.72 419,155 99.73
With1424 0.27 295 0.28 1129 0.27
Insomnia <0.001
Without512,702 97.59 101,590 96.69 411,112 97.82
With12,653 2.41 3481 3.31 9172 2.18
Non-apnea non-insomnia sleep disorders 0.035
Without517,051 98.42 103,356 98.37 413,695 98.43
With8304 1.58 1715 1.63 6589 1.57

p-value (category variable: Chi-square/Fisher exact test; continue variable: t-test).

Table 2 shows the results of the logistic regression analysis of the risk factors for cancer. A significantly higher risk of cancer development was observed in patients with sleep disorders. The crude OR was 1.789 (95% CI = 1.648–1.991, p < 0.001). After adjusting for age, sex, comorbidities, geographical area of residence, urbanization level of residence, and monthly income, the adjusted OR was 1.440 (95% CI = 1.392–1.489; p < 0.001). In addition, male sex, age ≥ 45 years, and presence of DM, HTN, depression, stroke, dementia, and/or CKD were associated with an increased risk of cancer development.
Table 2

Factors of cancers by using conditional logistic regression.

VariablesCrude OR95% CI95% CI p Adjusted OR95% CI95% CI p
Sleep disorders
WithoutReference Reference
With1.7891.6481.991<0.0011.4401.392 1.489<0.001
Gender
Male1.289 1.248 1.331 <0.0011.153 1.120 1.186 <0.001
FemaleReference Reference
Age group
18–44Reference Reference
45–641.441 1.367 1.518 <0.0011.442 1.367 1.520 <0.001
≥651.793 1.706 1.885 <0.0011.715 1.828 1.807 <0.001
Married
Without0.816 0.345 1.672 0.492 0.842 0.452 1.726 0.374
WithReference Reference
Divorce1.208 0.897 1.397 0.124 1.113 0.571 1.453 0.288
Spouse death1.552 0.701 2.163 0.106 1.298 0.642 1.772 0.115
Unknown0.000 --0.931 0.000 --0.989
Education
Elementary/junior high schoolReference Reference
(Vocational) high school1.154 0.495 1.798 0.462 1.018 0.312 1.843 0.509
Univeristy/college/graduate1.298 0.501 1.881 0.337 1.174 0.477 2.092 0.426
Others0.000 --0.872 0.000 --0.911
Insured premium (NT$)
<18,000Reference Reference
18,000–34,9990.935 0.832 1.052 0.264 0.952 0.847 1.071 0.415
≥35,0000.617 0.468 0.981 0.041 0.761 0.577 1.014 0.073
DM
WithoutReference Reference
With1.095 1.058 1.133 <0.0011.071 1.034 1.110 <0.001
HT
WithoutReference Reference
With1.948 1.818 2.177 0.001 1.914 1.884 1.945 <0.001
Depression
WithoutReference Reference
With3.072 2.822 3.344 <0.0013.408 3.128 3.714 <0.001
Stroke
WithoutReference Reference
With1.188 1.133 1.244 <0.0011.126 1.073 1.181 <0.001
Dementia
WithoutReference Reference
With1.882 1.693 2.091 <0.0011.612 1.449 1.794 <0.001
CKD
WithoutReference Reference
With1.889 1.741 2.049 <0.0011.708 1.574 1.855 <0.001
Season
SpringReference Reference
Summer 1.113 1.068 1.160 <0.0011.108 1.063 1.155 <0.001
Autumn 1.325 1.274 1.377 <0.0011.305 1.255 1.356 <0.001
Winter 1.121 1.075 1.169 <0.0011.111 1.062 1.157 <0.001
Location Had multicollinearity with urbanization level
Northern TaiwanReference Had multicollinearity with urbanization level
Middle Taiwan1.340 1.296 1.386 <0.001 Had multicollinearity with urbanization level
Southern Taiwan1.189 1.147 1.233 <0.001 Had multicollinearity with urbanization level
Eastern Taiwan1.922 1.824 2.026 <0.001 Had multicollinearity with urbanization level
Outlets islands1.738 1.477 2.088 <0.001 Had multicollinearity with urbanization level
Urbanization level
1 (The highest)0.673 0.647 0.700 <0.0010.814 0.779 0.851 <0.001
20.725 0.699 0.752 <0.0010.827 0.796 0.860 <0.001
30.833 0.786 0.881 <0.0010.872 0.823 0.923 <0.001
4 (The lowest)Reference Reference
Level of care
Hospital center0.626 0.603 0.650 <0.0010.636 0.609 0.664 <0.001
Regional hospital0.778 0.752 0.805 <0.0010.774 0.747 0.801 <0.001
Local hospitalReference Reference

OR: odds ratio; CI: confidence interval; Adjusted OR: adjusted variables listed in the table.

The overall incidence of cancer was 17.94 per 1000 person-years in the study cohort and 6.83 per 1000 person-years in the control cohort in the subgroup analysis comparing patients with and without sleep disturbances (Table 3). Sleep disturbances were linked to an elevated risk of cancer in both female and male patients (1.399 in the corresponding age group of women, p < 0.001; 1.469 in the corresponding age group of males, p < 0.001). On age group analysis, the presence of sleep disorders in all age groups was independently associated with an increased risk of cancer diagnosis relative to the absence of sleep disorders (aOR = 1.280, p < 0.001 in 18–44, aOR = 1.280, p < 0.001 in 45–64, aOR = 1.280, p < 0.001 in ≥65 years). In the preexisting condition group analysis, patients with sleep disorders showed an increased risk of developing cancer, regardless of whether they had DM, HTN, depression, stroke, dementia, or CKD (aOR = 1.338–2.854, all p < 0.001). Interestingly, patients with sleep disorders showed an increased risk of developing cancer, regardless of the season (aHR = 1.302–1.633, p < 0.001), urbanization level (aHR = 1.389–1.506, p < 0.001), or level of care group analysis (aHR = 1.420–1.820, p < 0.001).
Table 3

Factors of cancers stratified by variables listed in the table by using conditional logistic regression.

Sleep Disorders (With vs. Without)WithWithoutRatioAdjusted OR95%CI95%CI p
StratifiedExposurePYsRate (per 103 PYs)ExposurePYsRate (per 103 PYs)
Total 5173 288,330.74 17.94 16,230 2,377,934.41 6.83 2.629 1.440 1.392 1.489 <0.001
Gender
Male3206 166,695.38 19.23 9977 1,390,636.46 7.17 2.681 1.469 1.410 1.598 <0.001
Female1967 121,635.36 16.17 6253 987,297.95 6.33 2.553 1.399 1.252 1.444 <0.001
Age group
18–44555 39,942.92 13.89 1318 221,566.17 5.95 2.336 1.280 1.137 1.304 <0.001
45–641773 97,440.27 18.20 5307 749,270.05 7.08 2.569 1.407 1.345 1.469 <0.001
≥652845 150,947.55 18.85 9605 1,407,098.19 6.83 2.761 1.513 1.460 1.678 <0.001
Married
Without810 38,801.75 20.88 2916 306,989.47 9.50 2.198 1.204 1.102 1.385 0.001
With2098 144,232.45 14.55 5925 1,066,714.45 5.55 2.619 1.435 1.374 1.571 <0.001
Divorce1144 62,067.42 18.43 4433 642,980.13 6.89 2.673 1.529 1.411 1.601 <0.001
Spouse death1121 43,121.08 26.00 2956 360,245.12 8.21 3.168 1.671 1.520 1.798 <0.001
Unknown0 108.04 0.00 0 1005.24 0.00 -----
Education
Elementary/junior high school907 73,201.45 12.39 3373 506,601.45 6.66 1.861 1.019 0.984 1.127 0.298
(Vocational) high school2021 119,454.24 16.92 6345 1,000,845.06 6.34 2.669 1.462 1.349 1.602 0.011
Univeristy/college/graduate2245 94,248.57 23.82 6512 797,715.11 8.16 2.918 1.598 1.445 1.798 0.006
Others0 1426.48 0.00 0 72,772.79 0.00 -----
Insured premium (NT$)
<18,0005101 284,012.19 17.96 15,901 2,332,537.19 6.82 2.635 1.495 1.407 1.572 0.005
18,000–34,99955 3594.56 15.30 240 37,892.06 6.33 2.416 1.302 1.215 1.480 0.010
≥35,00017 723.99 23.48 89 7505.16 11.86 1.980 1.082 1.009 1.133 0.042
DM
Without4506 248,115.42 18.16 12,674 1,797,644.23 7.05 2.576 1.411 1.364 1.459 <0.001
With667 40,215.32 16.59 3556 580,290.18 6.13 2.707 1.483 1.433 1.533 <0.001
HT
Without4230 241,960.51 17.48 11,192 1,570,819.26 7.12 2.454 1.344 1.299 1.390 <0.001
With943 46,370.23 20.34 5038 807,115.15 6.24 3.258 1.785 1.725 1.845 <0.001
Depression
Without5070 286,741.71 17.68 15,819 2,348,030.54 6.74 2.624 1.338 1.290 1.402 <0.001
With103 1589.03 64.82 411 29,903.87 13.74 4.716 2.854 2.497 2.671 <0.001
Stroke
Without4964 277,924.03 17.86 14,340 2,071,846.60 6.92 2.581 1.414 1.367 1.463 <0.001
With209 10,406.71 20.08 1890 306,087.81 6.17 3.252 1.782 1.722 1.897 <0.001
Dementia
Without5146 287,148.59 17.92 15,871 2,333,477.43 6.80 2.635 1.443 1.382 1.487 <0.001
With27 1182.15 22.84 359 44,456.98 8.08 2.828 1.519 1.498 1.601 <0.001
CKD
Without4986 281,046.24 17.74 15,758 2,322,854.16 6.78 2.615 1.433 1.372 1.479 <0.001
With187 7284.50 25.67 472 55,080.25 8.57 2.996 1.641 1.586 1.708 <0.001
Season
Spring 997 62,060.76 16.06 3489 516,204.92 6.76 2.377 1.302 1.259 1.346 <0.001
Summer1242 70,358.21 17.65 3961 568,305.95 6.97 2.533 1.387 1.341 1.435 <0.001
Autumn1699 84,211.27 20.18 4930 728,515.28 6.77 2.981 1.633 1.579 1.689 <0.001
Winter1235 71,700.50 17.22 3850 564,908.26 6.82 2.527 1.384 1.338 1.432 <0.001
Urbanization level
1 (The highest)1720 101,539.67 16.94 4420 661,751.90 6.68 2.536 1.389 1.343 1.469 <0.001
22370 135,786.88 17.45 6921 1,069,017.83 6.47 2.696 1.477 1.428 1.571 <0.001
3190 12,557.40 15.13 1100 198,584.58 5.54 2.732 1.496 1.411 1.598 <0.001
4 (The lowest)893 38,446.79 23.23 3789 448,580.10 8.45 2.750 1.506 1.402 1.672 <0.001
Level of care
Hospital center2153 147,056.04 14.64 3898 709,805.57 5.49 2.666 1.420 1.305 1.477 <0.001
Regional hospital2161 112,013.98 19.29 7564 1,128,912.29 6.70 2.879 1.557 1.425 1.701 <0.001
Local hospital859 29,260.72 29.36 4768 539,216.55 8.84 3.320 1.820 1.558 1.978 <0.001

PYs = person-years; Adjusted OR = adjusted odds ratio: adjusted for the variables listed in Table 2; CI = confidence interval.

Notably, patients with sleep disorders were associated with a higher risk of cancer than those without sleep disorders, and patients with both sleep disorders and depression were associated with an even higher risk of cancer (aOR = 6.857, p < 0.001) (Figure 2). In the subgroup analysis of specific cancer types, our data suggest an increased risk of 12 types of cancer, especially esophageal and hematologic cancers, in patients with both sleep disorders and depression (Figure 3).
Figure 2

Incidence of cancers stratified by sleep disorders and depression using conditional logistic regression. OR, odds ratio.

Figure 3

Subgroup analysis of specific cancer types in patients with both sleeping disorders and depression.

4. Discussion

To the best of our knowledge, this is the first large-scale, population-based study of Asian individuals that investigated the interaction effect between sleep disorders and depression, particularly MDD, on the risk of developing cancer. There is growing evidence that sleep disorders are associated with an increased incidence of cancer [12,22,23]. However, previous studies investigating the relationship between depression and cancer showed inconsistent results [14,24,25]. The most valuable finding of our study is that patients with coexisting sleep disorders and depression were 6.85 times more likely to develop cancer than the general population. Previous studies in animal models have demonstrated that circadian disruption may increase the risk of cancer development [26,27]. Additionally, intermittent hypoxia and sleep fragmentation mimicking obstructive sleep apnea (OSA) are known to accelerate tumor growth and invasiveness [28,29]. However, evidence of the association between sleep disorders and cancer in humans is more limited than in animal models, and most studies have focused on the association between shift work and cancer [30,31]. Our study showed that patients with sleep disorders had a higher cancer risk than those without sleep disorders. This result is compatible with previous studies in which the researchers also applied data from the NHIRD using different study designs [12,23]. Several mechanisms could explain the link between sleep disorders and cancer incidence. For example, melatonin production is suppressed in sleep disorders. Melatonin can neutralize and remove free radicals and has a protective effect against the DNA-damaging effects of hydrogen peroxide [32]. Decreased melatonin inactivates melatonin receptor MT1 and increases expression of the tumor suppressor gene p53 [33], leading to cancer. Another possible mechanism could be immunosuppression. Sleep and the circadian system are strong regulators of immunological processes. Suppression of the immune system may lead to the establishment and growth of malignant clones [34]. In patients with obstructive sleep apnea, intermittent hypoxia and sleep fragmentation may lead to increased oxidative stress and systemic inflammation, resulting in an increased risk of tumors [22]. Depression and cancer commonly co-occur. Most studies on depression and cancer have focused on diagnosing psychological illnesses in cancer patients to increase the treatment effects on both cancer and depression. Recent epidemiological studies suggested that new-onset depression may be associated with a modestly increased risk of certain cancers [35,36]. Our findings align with these results and contribute to the evidence by showing that patients with both sleep disorders and depression had a high risk of cancer, and this risk was approximately six times higher than that in the general population. Several mechanisms may explain the association between depression and cancer incidence. The first possible mechanism involves dysregulation of the hypothalamic–pituitary–adrenal (HPA) axis, especially diurnal variations in cortisol and melatonin [37]. Burke et al. reported that depression is associated with blunted cortisol stress reactivity and impaired stress recovery in patients with MDD [38]. Alteration in cytokine regulation is another possible explanation for the increase in incident cancer [39]. Howren et al. found a positive association between C-reactive protein (CRP), interleukin-1 (IL-1), interleukin-6 (IL-6), and depression [40]. Elevated brain IL-1 levels are sufficient to produce a high incidence of depression [39], and IL-1 is known to exert a critical function in malignancies, influencing the tumor microenvironment and promoting cancer initiation and progression [41]. Moreover, Nunes et al. conducted a study including 40 non-medicated, depressed adults and 34 healthy non-depressed adults, and found that their immune and hormonal measurements differed significantly [42]. Depression may predispose individuals to an unhealthy lifestyle or behavior that puts them at a higher cancer risk [24]. This study recorded a significantly higher risk of hematologic and esophageal cancer in patients with coexisting sleep disorders and depression, but no significant increase was found in the incidence of aggressive breast cancer. By contrast, several studies have suggested that women who are short sleepers may develop more aggressive breast cancers than those who sleep longer hours [9,43,44]. A possible reason for this inconsistency may be related to the Taiwanese free cancer screening program. Cervical, oral, breast, and colorectal cancers were the main targets of the screening program. Early screening can detect carcinoma in situ at an early stage; thus, patients could receive cancer treatment before the disease progresses or becomes invasive. Moreover, epidemiologic studies have shown that patients with sleep disorders frequently practice unhealthy lifestyles, including smoking and drinking alcohol [45,46]. Chronic smoking and alcohol consumption are the primary etiologies of esophageal cancer, especially squamous cell carcinoma, which is the most common type of esophageal cancer in Taiwan. These mechanisms combined with the suppressed immune system due to insufficient sleep may explain the results of the present study. The case-control study design and detailed information regarding various potential confounders constitute the critical strengths of our study. However, this study had several limitations that must be considered. First, despite controlling for various potential confounding factors, certain demographic variables, such as socioeconomic status and family history of cancer, could not be considered because the corresponding data were not available. Second, we did not obtain information on sleep duration and lifestyle (e.g., smoking and drinking), which can be important additional factors when assessing the severity of sleep disorders. Finally, future studies with more extended follow-up periods are necessary to detect certain cancers.

5. Conclusions

This retrospective cohort study showed that patients with coexisting sleep disorders and MDD were 6.85 times more likely to develop cancer than the general population, indicating that the interaction between sleep disorders and depression may synergistically increase cancer occurrence. The results of this study could serve as a reminder for clinicians who provide long-term care for patients with consistent sleep disorders and MDD. Further biological mechanistic research and prospective studies are needed to confirm our findings. Clinically, a meticulous cancer risk evaluation is recommended for patients with both sleep disorders and depression.
  44 in total

1.  Validation of the National Health Insurance Research Database with ischemic stroke cases in Taiwan.

Authors:  Ching-Lan Cheng; Yea-Huei Yang Kao; Swu-Jane Lin; Cheng-Han Lee; Ming Liang Lai
Journal:  Pharmacoepidemiol Drug Saf       Date:  2010-12-29       Impact factor: 2.890

Review 2.  Cognitive behavior therapy for chronic insomnia occurring within the context of medical and psychiatric disorders.

Authors:  Michael T Smith; Mary I Huang; Rachel Manber
Journal:  Clin Psychol Rev       Date:  2005-07

3.  Immune and hormonal activity in adults suffering from depression.

Authors:  S O V Nunes; E M V Reiche; H K Morimoto; T Matsuo; E N Itano; E C D Xavier; C M Yamashita; V R Vieira; A V Menoli; S S Silva; F B Costa; F V Reiche; F L V Silva; M S Kaminami
Journal:  Braz J Med Biol Res       Date:  2002-05       Impact factor: 2.590

4.  Depression as an aetiologic and prognostic factor in coronary heart disease: a meta-analysis of 6362 events among 146 538 participants in 54 observational studies.

Authors:  Amanda Nicholson; Hannah Kuper; Harry Hemingway
Journal:  Eur Heart J       Date:  2006-11-02       Impact factor: 29.983

5.  Association of sleep duration and breast cancer OncotypeDX recurrence score.

Authors:  Cheryl L Thompson; Li Li
Journal:  Breast Cancer Res Treat       Date:  2012-07-03       Impact factor: 4.872

6.  Epidemiology of insomnia in korean adults: prevalence and associated factors.

Authors:  Yong Won Cho; Won Chul Shin; Chang Ho Yun; Seung Bong Hong; Juhan Kim; Christopher J Earley
Journal:  J Clin Neurol       Date:  2009-03-31       Impact factor: 3.077

Review 7.  Associations of depression with C-reactive protein, IL-1, and IL-6: a meta-analysis.

Authors:  M Bryant Howren; Donald M Lamkin; Jerry Suls
Journal:  Psychosom Med       Date:  2009-02-02       Impact factor: 4.312

8.  Brain interleukin-1 mediates chronic stress-induced depression in mice via adrenocortical activation and hippocampal neurogenesis suppression.

Authors:  I Goshen; T Kreisel; O Ben-Menachem-Zidon; T Licht; J Weidenfeld; T Ben-Hur; R Yirmiya
Journal:  Mol Psychiatry       Date:  2007-08-14       Impact factor: 15.992

9.  Intermittent hypoxia promotes melanoma lung metastasis via oxidative stress and inflammation responses in a mouse model of obstructive sleep apnea.

Authors:  Lian Li; Fangyuan Ren; Chao Qi; Leiqian Xu; Yinshan Fang; Maoli Liang; Jing Feng; Baoyuan Chen; Wen Ning; Jie Cao
Journal:  Respir Res       Date:  2018-02-12

Review 10.  Data resource profile: the National Health Insurance Research Database (NHIRD).

Authors:  Liang-Yu Lin; Charlotte Warren-Gash; Liam Smeeth; Pau-Chung Chen
Journal:  Epidemiol Health       Date:  2018-12-27
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