Abstract
Objectives
Sleep deprivation is a common issue for modern people and leads to many morbidities and mortality. Some papers also suspected the relationship between Immunoglobulin E (IgE) level and sleep deprivation. The purpose of this article is to make the vicious circle between serum IgE level and sleep deprivation clear.
Materials and methods
In this study, we included 4,460 population aged around 48 years old respective 2,145 males and 2,315 females enrolled in the National Health and Nutrition Examination Survey (NHANES). Sleep durations were recorded, in hours, in whole numbers by the participants. The levels of total IgE were measured by anti-IgE. All procedures were analyzed using SPSS version 18 (SPSS, Inc., Chicago, IL, USA).
Result
The statistical significance between higher IgE level and ≤5 h sleep duration was noted (Beta coefficients: 64.04, 95% confidence interval (CI): 2.35, 125.72, P = 0.042). In sex difference, the correlation between short sleep duration and high serum IgE levels was noted in male [Beta coefficients: 120.225 (P = 0.008)] but not in female. There were no positive findings in the ethnicity-based correlation between serum IgE levels and sleep duration.
Conclusion
This study indicated that short sleep duration (≤5 h) is associated with higher serum IgE levels, especially in men. Further longitudinal investigations concerning the effect of sleep deprivation on serum IgE might provide a better explanation for the pathophysiology underlying autoimmune disease and sleep deprivation.
Keywords: sleep, sleep disorders, sleep deprivation, serum immunoglobulin E level, sleep duration
Introduction
Sleep has an important role to play in the human immune system and is critical for the restoration and maintenance of homeostasis (1). Sleep deprivation is a common issue in modern life, leading to the impaired quality of life for patients and their families (2). Several different scales are used to measure sleep quality. The Epworth sleepiness scale is a short easy way to measure sleepiness in ordinary life situations. Users rate their chances of sleeping in eight situations on a 4-point scale (3). The Pittsburgh sleep quality index (PSQI) is composed of 19 items classified into seven components: subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of sleeping medication, and daytime dysfunction during the past month (4). To date, many different reasons of sleep deprivation have been reported in the literature. Stimuli such as stress or anxiety may be the cause of sleep deprivation (5). Hormone, such as melatonin, is involved in the regulation of the human sleep–wake cycle and circadian rhythm (6). Melatonin and melatonin receptor agonists have been shown to be therapeutic agents for the treatment of circadian rhythm sleep disorders and some type of insomnia (7). Metabolic disease has also been linked to sleep deprivation in several studies (8). An inadequately short sleep duration may lead to mortality and morbidity (9). A previous study confirmed that rheumatoid arthritis (RA) patients have severe sleep fragmentation compared to the control group (10). Seventy-five percent of primary Sjögren’s syndrome patients had moderate or severe sleep disturbances in a cross-sectional study (11). In 1995, one study showed that the systemic lupus erythematosus (SLE) group had greater overall fatigue and longer sleep latency and total sleep time than the control groups (12).
Immunoglobulin E (IgE) is a type of antibody, which is monomeric and consists of four constant regions, in contrast to other immunoglobulins that contain only three constant regions (13). Typically, IgE is the least abundant Ig isotype, with a concentration of ∼150 ng/mL in the sera of healthy individuals (14). There are two types of IgE molecules: free IgE produced by plasma cells and membrane-bound IgE maintained on the surface of B cells (15). IgE plays an essential role in the immunity against parasites and in type 1 hypersensitivity, which manifests in allergic diseases, including allergic asthma, allergic rhinitis, food allergies, and some types of atopic dermatitis (16, 17). More recently, IgE autoantibodies have been found to participate in the damaging immune responses that characterize autoimmunity (18). It is now recognized that SLE, RA, bullous pemphigoid (BP), and chronic urticaria are most likely mediated by IgE autoantibodies (19).
To date, it is unclear whether a vicious circle links sleep deprivation and serum IgE level. Our purpose is to identify the association between levels of serum IgE and sleep deprivation by analyzing information from the National Health and Nutrition Examination Survey (NHANES).
Materials and methods
Study design and participants
The NHANES data consisted of a comprehensive interview and a health examination conducted by the National Center for Health Statistics (NCHS). We conducted a cross-sectional study using the NHANES database in 2001–2004 period. The exclusion criteria included individuals without complete information about laboratory results or clinical examinations. In this study, we included 4,460 individuals–2,145 males and 2,315 females, approximately 48 years of age.
Measurement of sleep duration
Sleep duration was evaluated with the measure item, “On average, for how long do you usually sleep at night on weekdays or workdays?” Answers were categorized as whole numbers into five groups (≤5, 6, 7, 8, and ≥9 h) for analysis by the participants.
Assessment of covariates
We collected participant information on age, sex and race-ethnicity (including Mexican American, non-Hispanic white, and non-Hispanic black). Smoking status was categorized as “non-smoker” for subjects who never smoked and “smoker” for subjects who were ex-smokers or current smokers by asking the question, “Do you now smoke cigarettes?” Alcohol drinking was determined through the participants’ self-reports. Co-morbidities, including asthma, congestive heart failure, coronary heart disease, angina, and stroke, were ascertained by self-reports. The total IgE level was measured using anti-IgE, which was covalently coupled to the ImmunoCap™ reaction vessel. CRP levels were measured by latex-enhanced nephelometry using the Behring Nephelometer System. Total bilirubin levels were evaluated by biochemical profiling. The levels of total cholesterol, triglycerides, and HDL-C were assessed using the Hitachi-704 analyzer. Creatine was assessed using the Beckman UniCel® DxC800 Synchron. Fasting glucose was assessed using the Hexokinase-mediated reaction Roche/Hitachi Cobas C Chemistry Analyzer. Insulin was assessed with human insulin immunoassay by using the Molecular Devices, SpectraMax 250. Vitamin B12 are measured by using the Bio-Rad Laboratories.
Statistical analysis
All procedures were analyzed using SPSS version 18 (SPSS, Inc., Chicago, IL, USA). Descriptive information related to continuous and categorical covariates was presented as mean ± standard deviation and number (%). The comparison of characteristics and covariates across subgroups was performed using ANOVA for continuous variables and the chi-squared test for categoric variables. We analyzed the association between sleep duration and serum IgE levels using a multivariate linear regression model. Three models were executed for covariate calibration. Model 1 was adjusted for age, gender, and race. Model 2 was model 1 along with adjustment for body mass index (BMI), CRP, total bilirubin, total cholesterol, triglycerides, HDL, creatine, fasting glucose, insulin, vitamin B12. Model 3 was Model 2 along with adjustment for sleep disorders, snorting/stop breathing, mental health service use, asthma, congestive heart failure, coronary heart disease, angina, stroke, cancer, smoking, and alcohol drinking.
Results
Sample characteristics
A total of 4,480 participants, for whom serum IgE level data were available and who reported their sleep duration from 2001 to 2004, were enrolled from the NHANES database. Table 1 presents the clinical characteristics and demographic data of the participants classified by sleep duration.
TABLE 1.
Characteristics of study participants.
| Sleep duration at night | |||||||
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| Characteristic | ≤5 h N = 673 | 6 h N = 1,001 | 7 h N = 1,190 | 8 h N = 1,232 | ≥9 h N = 364 | Total N = 4460 | P-value |
| Continuous variables* | |||||||
| Age (years) | 47.84 (17.87) | 48.16 (17.92) | 46.97 (17.75) | 49.49 (19.98) | 50.72 (22.42) | 48.36 (18.88) | 0.002 |
| BMI (kg m–2) | 30.22 (7.60) | 29.17 (6.77) | 28.23 (5.79) | 28.35 (6.41) | 28.59 (8.67) | 28.80 (6.77) | <0.001 |
| Serum total IgE Ab (kU/L) | 196.63 (440.10) | 182.30 (676.33) | 151.36 (396.09) | 144.03 (403.55) | 160.46 (377.84) | 163.85 (480.19) | 0.11 |
| CRP (mg/dL) | 0.51 (0.70) | 0.48 (0.84) | 0.42 (0.86) | 0.51 (0.88) | 0.59 (0.89) | 0.49 (0.84) | 0.008 |
| Total bilirubin (mg/dL) | 0.70 (0.28) | 0.70 (0.29) | 0.73 (0.48) | 0.69 (0.28) | 0.67 (0.28) | 0.70 (0.35) | 0.042 |
| Total cholesterol (mg/dL) | 198.39 (46.06) | 199.04 (40.74) | 201.70 (45.22) | 202.58 (43.87) | 200.66 (44.69) | 200.77 (43.98) | 0.193 |
| Triglyceride (mg/dL) | 154.86 (130.60) | 145.78 (101.16) | 157.79 (141.20) | 160.06 (120.54) | 155.14 (94.24) | 155.07 (122.22) | 0.079 |
| HDL cholesterol (mg/dL) | 53.96 (16.91) | 54.69 (15.92) | 55.36 (17.04) | 55.63 (17.18) | 56.29 (16.81) | 55.15 (16.80) | 0.139 |
| Creatinine (mg/dL) | 0.95 (0.45) | 0.97 (0.42) | 0.92 (0.30) | 0.94 (0.58) | 0.92 (0.33) | 0.94 (0.44) | 0.133 |
| Fasting Glucose (mg/dL) | 106.20 (34.92) | 105.16 (35.18) | 101.67 (22.52) | 106.06 (36.74) | 107.44 (40.93) | 104.89 (33.46) | 0.116 |
| Insulin (μU/mL) | 12.86 (11.98) | 12.47 (11.35) | 12.47 (18.46) | 11.87 (12.27) | 10.91 (9.35) | 12.24 (13.69) | 0.529 |
| Vitamin B12 (pg/mL) | 637.40 (2742.34) | 602.50 (1494.84) | 598.25 (1465.21) | 577.04 (806.48) | 530.57 (407.01) | 593.79 (1549.13) | 0.864 |
| Categorical variables† | |||||||
| Male | 344 (51.1) | 495 (49.5) | 581 (48.8) | 583 (47.3) | 142 (39.0) | 2145 (48.1) | 0.003 |
| Race-ethnicity | <0.001 | ||||||
| Mexican American | 124 (18.4) | 196 (19.6) | 238 (20.0) | 280 (22.7) | 69 (19.0) | 907 (20.3) | |
| Other Hispanic | 21 (3.1) | 31 (3.1) | 46 (3.9) | 33 (2.7) | 6 (1.6) | 137 (3.1) | |
| Non-Hispanic White | 256 (38.0) | 446 (44.6) | 666 (56.0) | 678 (55.0) | 202 (55.5) | 2248 (50.4) | |
| Non-Hispanic Black | 245 (36.4) | 284 (28.4) | 193 (16.2) | 202 (16.4) | 71 (19.5) | 995 (22.3) | |
| Sleep disorders | 100 (14.9) | 67 (6.7) | 59 (5.0) | 59 (4.8) | 21 (5.8) | 306 (6.9) | <0.001 |
| Snorting/Stop breathing | 160 (26.7) | 223 (24.4) | 189 (17.1) | 192 (17.2) | 56 (17.0) | 820 (20.2) | <0.001 |
| Mental health service use | 68 (10.1) | 59 (5.9) | 75 (6.3) | 81 (6.6) | 38 (10.4) | 321 (7.2) | 0.001 |
| Asthma | 121 (18.0) | 135 (13.5) | 132 (11.1) | 142 (11.5) | 44 (12.1) | 574 (12.9) | <0.001 |
| Congestive heart failure | 38 (5.6) | 31 (3.1) | 20 (1.7) | 44 (3.6) | 15 (4.1) | 148 (3.3) | <0.001 |
| Coronary heart disease | 33 (4.9) | 43 (4.3) | 28 (2.4) | 58 (4.7) | 13 (3.6) | 175 (3.9) | 0.052 |
| Angina/Angina pectoris | 32 (4.8) | 31 (3.1) | 29 (2.4) | 34 (2.8) | 11 (3.0) | 137 (3.1) | 0.116 |
| Stroke | 36 (5.3) | 41 (4.1) | 34 (2.9) | 34 (2.8) | 27 (7.4) | 172 (3.9) | <0.001 |
| Cancer/Malignancy | 47 (7.0) | 68 (6.8) | 99 (8.3) | 110 (8.9) | 46 (12.6) | 370 (8.3) | 0.001 |
| Smoking | 339 (50.4) | 486 (48.6) | 542 (45.5) | 575 (46.7) | 171 (47.0) | 2113 (47.4) | 0.453 |
| Alcohol drinking | 394 (62.9) | 646 (70.1) | 801 (71.7) | 789 (69.1) | 220 (64.9) | 2850 (68.7) | 0.003 |
*Continuous variables are presented as mean (standard deviation).
†Categorical variables are presented as number (percentage).
BMI, body mass index; IgE, Immunoglobulin E; Ab, Antibody; CRP, C-reactive protein; HDL, high-density lipoprotein.
The mean age was 48.36 ± 18.88 years, and 48% of the participants were male. The race/ethnicity also presented a distinctive distribution.
Association between immunoglobulin E level and sleep duration
The relationship between the IgE level and sleep deprivation is shown in Table 2. We used 7 h sleep duration as the reference group. After we adjusted covariates in model 2 and model 3, the β coefficients of ≤5 h of sleep duration were 64.84 [95% confidence interval (CI): 3.93, 125.75, P = 0.037] and 64.04 (95% CI: 2.35, 125.72, P = 0.042). Compared to other groups, higher levels of serum IgE were significantly associated with a sleep duration ≤5 h; the P < 0.05 for sleep duration ≤5 h after adjusting the covariates. However, the P-values were >0.05 in individuals whose sleep duration was 6, 8, and ≥9 h.
TABLE 2.
Association between different sleep duration and immunoglobulin E (IgE) level.
| Models* | Sleep duration† | β‡ (95% CI) | P |
| Model 1 | ≦5 h 6 h 7 h 8 h ≧9 h |
71.74 (11.20, 132.29) 41.13 (−14.16, 96.41) reference −6.02 (−57.80, 45.77) 3.78 (−70.97, 78.54) |
0.020 0.145 − 0.820 0.921 |
| Model 2 | ≦5 h 6 h 7 h 8 h ≧9 h |
64.84 (3.93, 125.75) 37.48 (−17.98, 92.94) reference −6.23 (−58.35, 45.88) 2.91 (−72.18, 77.99) |
0.037 0.185 − 0.815 0.939 |
| Model 3 | ≦5 h 6 h 7 h 8 h ≧9 h |
64.04 (2.35, 125.72) 36.91 (−18.77, 92.59) reference −8.67 (−60.93, 43.58) 4.34 (−71.05, 79.73) |
0.042 0.194 − 0.745 0.910 |
*Adjusted covariates:
Model 1 = age, gender, race/ethnicity.
Model 2 = Model 1 + (BMI, CRP, total bilirubin, total cholesterol, triglycerides, HDL, creatine, fasting glucose, insulin, vitamin B12).
Model 3 = Model 2 + (sleep disorders, snorting/stop breathing, mental health service use, asthma, congestive heart failure, coronary heart disease, angina, stroke, cancer) + (smoking, alcohol drinking).
†Subjects with 7-h sleep length were the reference group.
‡β coefficient can be interpreted as differences in the mean homocysteine comparing subjects in the other 4 groups of sleep duration to those in the 7-h sleep length.
IgE, Immunoglobulin E; BMI, Body Mass index; CRP, C-reactive protein; HDL, high-density lipoprotein.
Correlation of sex and ethnicity with sleep duration and serum immunoglobulin E levels
Figure 1 shows the results of our analysis of the correlation of sex with serum IgE levels and sleep duration. Interestingly, compared with the reference group (7-h sleep duration), the shortest sleep duration (≤5 h) in model 1 had regression coefficients of 120.225 (P = 0.008) for men and 15.332 (P = 0.718) for women. In different models, the trend with the shortest sleep duration and elevated serum IgE levels remained unchanged in men (P < 0.05) but not in women, even after adjusting all the covariates. Table 3 shows the ethnicity-based correlation between sleep duration and serum IgE levels. There were no positive findings in the Mexican American, Other Hispanic, non-Hispanic White, and non-Hispanic black groups even after we adjusted for several covariates in models 2 and 3.
FIGURE 1.
(A) Association between sleep duration and serum IgE level in male participants. (B) Association between sleep duration and serum IgE level in female participants.
TABLE 3.
Race specific association between sleep duration and serum immunoglobulin E (IgE) level.
| Mexican American | Other Hispanic | Non-Hispanic white | |||||
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|
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| Models* | Sleep duration† | β‡ (95% CI) | P | β‡ (95% CI) | P | β‡ (95% CI) | P |
| Model 1 | ≦5 h 6 h 7 h 8 h ≧9 h |
−17.439 (−155.482, 120.604) −1.173 (−123.575, 121.229) reference 11.495 (−99.108, 122.097) −93.054 (−258.782, 72.675) |
0.804 0.985 − 0.838 0.270 |
−130.681 (−342.533, 81.172) −139.397 (−331.660, 52.866) reference −99.996 (−312.198, 112.205) −280.693 (−64.547, 625.932) |
0.221 0.151 − 0.348 0.109 |
53.993 (−11.237, 119.223) 13.254 (−44.178, 70.685) reference −4.199 (−54.091, 45.694) 48.928 (−23.118, 120.974) |
0.105 0.651 − 0.869 0.183 |
| Model 2 | ≦5 h 6 h 7 h 8 h ≧9 h |
−1.385 (−138.373, 135.602) −5.310 (−129.620, 118.999) reference −6.153 (−119.944, 107.638) −86.109 (−252.198, 79.981) |
0.984 0.933 − 0.915 0.309 |
−112.991 (−335.184, 109.202) −182.513 (−392.017, 26.991) reference −104.089 (−362.034, 153.855) 342.078 (−26.371, 710.526) |
0.310 0.086 − 0.419 0.068 |
49.467 (−16.332, 115.265) 11.077 (−46.605, 68.758) reference −7.777 (−57.954, 42.400) 41.956 (−30.656, 114.569) |
0.140 0.706 − 0.761 0.257 |
| Model 3 | ≦5 h 6 h 7 h 8 h ≧9 h |
6.160 (−136.460, 148.781) −18.058 (−146.095, 109.979) reference −1.054 (−117.759, 115.652) −84.688 (−253.309, 83.932) |
0.932 0.782 − 0.986 0.324 |
−273.604 (−548.544, 1.336) −281.914 (−528.446, −35.381) reference −138.006 (−422.746, 146,733) 425.882 (−9.677, 861.440) |
0.051 0.026 − 0.330 0.055 |
34.725 (−31.574, 101.023) 4.147 (−53.459, 61.754) reference −8.687 (−58.521, 41.146) 44.137 (−28.562, 116.836) |
0.304 0.888 − 0.732 0.234 |
|
| |||||||
| Non-Hispanic black | Others | ||||||
|
|
|
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| Models* | Sleep duration † | β‡ (95% CI) | P | β‡ (95% CI) | P | ||
|
| |||||||
| Model 1 | ≤5 h 6 h 7 h 8 h ≥9 h |
88.241 (−89.656, 266.139) 108.650 (−68.053, 285.352) reference −36.265 (−226.652, 154.122) −47.163 (−323.467, 229.141) |
0.330 0.227 − 0.708 0.737 |
520.806 (63.728, 977.884) 13.358 (−311.690, 338.407) reference −8.973 (−355.247, 337.301) −78.890 (−485.328, 327.549) |
0.026 0.935 − 0.959 0.700 |
||
| Model 2 | ≤5 h 6 h 7 h 8 h ≥9 h |
70.723 (−111.160, 252.606) 106.895 (−72.673, 286.463) reference −39.714 (−233.874, 154.446) −51.406 (−331.712, 228.899) |
0.445 0.242 − 0.688 0.719 |
621.197 (121.578, 1120.816) 17.856 (−337.593, 373.306) reference 65.887 (−310.837, 442.611) −97.807 (−537.231, 341.616) |
0.016 0.920 − 0.728 0.658 |
||
| Model 3 | ≤5 h 6 h 7 h 8 h ≥9 h |
55.327 (−131.194, 241.847) 100.367 (−79.665, 280.399) reference −68.470 (−263.526, 126.586) −80.437 (−363.387, 202.513) |
0.560 0.274 − 0.490 0.576 |
713.323 (90.219, 1336.426) 68.785 (−357.429, 494.999) reference 60.213 (−360.114, 480.539) −148.380 (−656.653, 359.894) |
0.026 0.747 − 0.775 0.560 |
||
*Adjusted covariates:
Model 1 = age, race/Ethnicity.
Model 2 = Model 1 + (BMI, CRP, total bilirubin, total cholesterol, triglycerides, HDL, creatine, fasting glucose, insulin, vitamin B6 and B12, folate).
Model 3 = Model 2 + (sleep disorders, snorting/stop breathing, mental health service use, asthma, congestive heart failure, coronary heart disease, angina, stroke, cancer) + (smoking, alcohol drinking).
†Subjects with 7-h sleep length were the reference group.
‡β coefficient can be interpreted as differences in the mean homocysteine comparing subjects in the other 4 groups of sleep duration to those in the 7-h sleep length.
IgE, Immunoglobulin E; BMI, Body Mass index; CRP, C-reactive protein; HDL, high-density lipoprotein.
Discussion
After analyzing the data, which represented a sample of the US adult population, we found that short sleep duration (≤5 h) was associated with high IgE levels. The association remained significant even after we adjusted different covariates (P < 0.05). Conversely, there was no association between longer sleep duration and IgE levels. Further, the association between the shortest sleep duration (≤5 h) and elevated serum IgE levels was observed in men but not women. Our study is the first observational study with a large sample size, stratified by sex and race/ethnicity, to analyze the relationship between sleep duration and serum IgE levels.
Direct evidence of the relationship between sleep duration and serum IgE levels was limited. One review article published in 2015 indicated that sleep deprivation may induce the onset of autoimmune disease (20). A large cohort study by Hsiao et al. indicated that the overall risk for incident autoimmune diseases was significantly higher in patients with non-apnea sleep disorders (NSD) [hazard ratio (HR) = 1.47, 95% CI = 1.41–1.53] (21). Another cohort study found that the hazard ratio (95% CI = 1.32–2.77, p < 0.001) for the development of autoimmune disease during a five-year follow-up period was 1.91 times greater for patients with obstructive sleep apnea (OSA) than others (22).
Our study had some noteworthy findings. First, we found out that only men showed a significant association between high serum IgE levels and short sleep duration (≤5 h). Sex hormones are known to affect the immune system and contribute to sex-based differences in immune-mediated disease responses. Testosterone inhibits immune responses, whereas estrogen and progesterone tend to enhance immune responses (23). The immune-enhancing effects of sex hormones tend to increase the predisposition of women to several autoimmune diseases, such as multiple sclerosis, SLE, and RA (24). Further, several studies suggested that, both as children and adults, men have higher IgE levels than women [odds ratio (OR) 95% CI: 1.6 (1.4–1.8, p-value < 0.001)] (25). Thus, the levels of IgE and the prevalence of sensitization was higher in men than women (26). As a result, although the prevalence of auto-immune disease was higher in women, the serum IgE levels in men played a more important role than in women, contributing to the results of our study.
Second, our analysis revealed that there was no difference in the association between serum IgE levels and sleep duration in different racial groups. The evidence for an association between sleep duration and serum IgE levels by race/ethnicity is limited. One study reported that serum IgE levels vary by age, occupation, environment, and race/ethnicity (27). As the association between ethnicity and sleep duration is reported to be unclear, more studies were needed to better understand the role of ethnicity in sleep duration and serum IgE levels (28).
Our study has a few limitations. First, this was a cross-sectional observational study. Further cohort studies are needed to confirm our findings. Second, because sleep duration was evaluated by self-reported questionnaires, recall bias cannot be ignored. Third, there were several important unmeasured confounding factors that may influence these results. For example, recent psychosocial stress and individual lifestyles might influence sleep duration but were not considered in our analyses. Finally, the baseline serum IgE level might vary by ethnicity, nutritional support, environment, and genetics. Thus, the results of these correlations between serum IgE levels and various factors must be interpreted carefully.
Conclusion
Our study indicated that sleep deprivation (sleep duration ≤5 h) is associated with higher serum IgE levels, especially in men. High serum IgE levels may increase the risk of autoimmune disease. Further longitudinal investigations concerning the effect of sleep deprivation on serum IgE might provide a better explanation for the pathophysiology underlying autoimmune disease and sleep deprivation.
Data availability statement
The original contributions presented in this study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.
Ethics statement
The studies involving human participants were reviewed and approved by Protocol #98-12. The patients/participants provided their written informed consent to participate in this study.
Author contributions
S-WY and W-LC designed the initial study and responsible for the decisions of data analysis. S-WY also managed and retrieved the data, contributed to primary data analysis and explanation, and drafted the initial script. S-WY, H-FY, Y-YC, and W-LC decided on the methods of data collection. W-LC conceptualized the study, inspected all sides of the study, critically reviewed and revised the initial script, and approved the final manuscript as submitted. All authors meet the ICMJE criteria for authorship.
Abbreviations
- IgE
immunoglobulin E
- RA
rheumatoid arthritis
- SLE
systemic lupus erythematosus
- BP
bullous pemphigoid
- NHANES
National Health and Nutrition Examination Survey
- NCHS
National Center for Health Statistics
- CI
confidence interval
- NSD
non-apnea sleep disorders
- HR
hazard ratio
- OSA
obstructive sleep apnea
- OR
odds ratio
- IRB
Institutional Review Board.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The original contributions presented in this study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

