DOI: https://doi.org/10.21203/rs.2.23848/v2
Background: As a complex phenomenon, sleep quality is difficult to objectively define and measure, and multiple factors related to sleep quality, such as age, lifestyle, physical activity, and physical fitness, feature prominently in older adult populations. The aim of the present study was to evaluate subjective sleep quality using the Pittsburgh Sleep Quality Index (PSQI) and to associate sleep quality with health-related physical fitness factors, depressive symptoms, and the number of chronic diseases in the middle-aged and elderly.
Methods: We enrolled a total of 283 middle-aged and elderly participants from a rehabilitation clinic or health examination department. The PSQI was used to evaluate sleep quality. The health-related fitness assessment included anthropometric and physical fitness parameters. Depressive symptoms were measured with the Center for Epidemiologic Studies Depression Scale (CES-D) short form. Data were analyzed with SPSS 18.0, and descriptive statistics and logistic regression analysis were used for the analyses.
Results: Overall, 27.9% of participants in this study demonstrated poor sleep quality (with a PSQI score of >5), 10.2% of study participants frequently used sleep medication to help them fall asleep, and 6.0% reported having significant depressive symptoms (with a CES-D score of ≥10). There are two major findings: (1) depression symptoms, the number of chronic diseases, self-rated health, and arthritis were significantly associated with a poor sleep quality, and (2) the 2-min step test was associated with longer sleep latency. These results confirmed that the 2-min step was associated with a longer sleep latency among the health-related physical fitness items.
Conclusions: Our study found that depressive syndrome, chronic disease numbers, a poor self-rated health status, and arthritis were the main risk factors that influenced subjective sleep quality.
As a complex phenomenon, sleep quality is difficult to define and measure objectively (1), and it is not directly associated with sleep quantity. The best assessment of sleep quality includes both subjective and objective measures (2). Polysomnography (PSG) is the gold standard objective measure of sleep (3), and the Pittsburgh Sleep Quality Index (PSQI) is a widely used self-administered sleep questionnaire (1). Self-reported sleep does not correlate well with PSG-defined sleep (4). Multiple factors are related to sleep quality in old age, including lifestyle, physical activity, and physical fitness; moreover, alcohol consumption patterns (5), depressive symptoms (6), and rheumatoid arthritis (RA) (7) may also affect sleep quality. Among multiple factors related to sleep quality, recent studies began to focus on physical activity and physical fitness (8, 9).
Sleep is important to physical, cognitive, and psychological health. Sleep quality changes as a function of normal aging, there is no association between subjective sleep quality and cognitive performance in healthy young adults (10), and only half of middle-aged and elderly Chinese reported good sleep quality (11). Age-related sleep changes may lead to poor sleep quality in older adults with physical or psychiatric disorders (12). Many middle-aged and older adults do not sleep well, and they are more likely to take pharmacological sleep aids (13). Studies revealed that 49% of community-dwelling older adults reported poor sleep quality (6), and 41.9% of adults aged 60 years or older suffer from sleep disturbances in Taiwan (14). Sleep disturbances are also associated with lower physical fitness levels, a reduced health-related quality of life (15), nocturia, poor self-reported functional status, and one's mental status (14). Moreover, symptoms of depression were identified as factors most significantly associated with poor sleep quality among older adults (6, 14).
Young female adults with poor sleep quality are more likely to have lower levels of physical activity (muscle endurance, flexibility, and cardiovascular fitness) (16). Studies revealed the benefits of physical activity and regular exercise in improving sleep quality and reducing the occurrence of sleep disturbances (8, 9, 17) in middle-aged and elderly adults. Physical activity in middle-aged and elderly adults differs from that of younger populations. Health-related fitness is the ability to become and remain physically healthy. Health-related physical fitness includes muscle strength, muscle endurance, cardiovascular endurance, joint flexibility, and body composition (American Alliance for Health, Physical Education, Recreation and Dance, 1980). Few studies have investigated relationships of depression with the quality of sleep and health-related physical fitness level. Therefore, the aim of the present study was to evaluate the subjective sleep quality using the PSQI, depression, and chronic diseases and their associations with the influence of health-related physical fitness factors in community-dwelling middle-aged and elderly.
Design and Sample
A cross-sectional survey was conducted in our study. We recruited older adults in northern Taiwan from August 2010 to July 2013. The inclusion criteria of the sample were as follows: (a) aged 40 years or older; (b) with no ambulatory problems or using any assistance for walking; and (c) able to communicate verbally. Those who had severe cardiovascular disease, neurological disease, or musculoskeletal impairment were excluded. In total, the sample size was 283 individuals. The study was approved (no. 098101-3) by the Ethics Committee of Far Eastern Memorial Hospital, and all subjects provided written informed consent before they were allowed to participate in the study.
Measures
The evaluated characteristics of respondents included sex, age, marital status, educational level, religious beliefs, number of current diseases (hypertension, heart disease, diabetes mellitus, pulmonary disease, peptic ulcers, liver disease, arthritis, osteoporosis, and cancer), smoking and alcohol consumption habits, tea and coffee consumption, and regular exercise (more than 30 min at least 3 days per week)(6). Self-ratings of the health status, which reflected an individual’s personal perception of their overall health condition, were indicated on a 5-point Likert scale (scored 1 = very poor to 5 = excellent).
The PSQI was used to evaluate sleep quality (1), and the Chinese version (CPSQI) was used in this study (18). The CPSQI had an overall reliability coefficient of 0.82~0.83 for community-dwelling adults with primary insomnia and control subjects, and also acceptable test-retest reliability over a 14~21-day interval with a coefficient of 0.85 for all subjects and 0.77 for primary insomniacs (18). Participants self-rate their sleep situation with respect to seven components: sleep duration, sleep disturbance, sleep latency, daytime dysfunction, sleep efficiency, subjective sleep quality, and use of sleep medication in the past month. The score of each component ranges 0~3, and the sum of these component scores, ranging 0~21, is the total score that serves as a measure of sleep quality. A global score higher than five was defined as an indicator of poor sleep. In our study, we also used the original scores of the seven components and individually recoded them as dichotomous variables to examine the association of the correlates with these seven components.
The health-related fitness assessment included the following anthropometric and physical fitness measurements: (1) body weight and height were measured with a calibrated scale (within ±0.1cm), and participants were asked to wear light clothes and no shoes. body-mass index (BMI) calculated according to the body weight (kg) divided by the height (in m2); (2) mid-arm circumference, waist circumference, and buttock circumference measured according to standard methods; (3) body composition assessed using a bioelectrical impedance analysis (TANITA’s body composition analyzer, TBF 300, Tokyo, Japan) to derive the percentage of body fat, fat mass, and fat-free mass; and (4) physical activity measured using the International Physical Activity Questionnaire (IPAQ) short version, which comprises four generic items. The questionnaire was developed in Geneva in 1998 and has undergone extensive reliability and validity testing across many countries and has been translated into several different languages. We adopted the Taiwanese version (19). Participants were asked to report their physical activity during the previous 7 days as an estimate of their habitual level of physical activity. IPAQ scores were categorized into three levels of physical activity: low, moderate, and high.
Physical fitness assessment: We used a set of senior fitness test tools developed by Accuratus International Health Company of Taiwan. The test contained the following seven items: (1) sit-and-reach test, which is commonly used to measure the flexibility of the lower back; (2) one-leg stance test, which is used to assess static balance; (3) 2-min step test, which assesses cardiovascular endurance; (4) back muscle strength, which measures the maximal isometric strength of the trunk muscles in a standing posture with 30° lumbar flexion using a back muscle strength meter; (5) 30-s chair-stand test, which is used to assess lower-body strength; (6) grip strength, which measures the muscle strength of the upper arms; and (7) up-and-go test, which measures the speed, agility, and balance when the body is moving. For grip strength (no. 6), participants were asked to stand and grasp a grip strength-measuring device (Jamar® Plus+ Digital Hand Dynamometer; Sammons Preston, Rolyon, Bolingbrook, IL, USA). They performed this action three times, and the best score was recorded. All physical fitness measurements were performed by well-trained personnel, and the results were recorded on a computer.
Depressive symptoms were measured using the Center for Epidemiologic Studies Depression Scale (CES-D) short form (20). The Chinese version of 10 self-reported items was used to measure depressive symptoms that occurred in the previous week. The score of each question ranges 0~3, with the total score ranging 0~30; we considered that a score of ≥10 indicated depression (20).
Statistical analysis
Descriptive statistics were recorded for each variable of the characteristics of subjects and health-related fitness, with quantitative data shown as the mean and standard deviation (SD). Differences in comparisons of two group were analyzed with an independent t-test, Chi-squared test, Fisher’s exact test, and Mann-Whitney U-test. Spearman's correlation was used for the PSQI and health-related fitness. A logistic regression analysis was performed to assess the characteristics and physical fitness associated with PQSI variables. The level of significance was set to α=0.05. Data were analyzed with SPSS for Windows vers. 19 software (IBM, SPSS, Chicago, IL, USA).
In total, 283 individuals completed the entire physical fitness evaluation, and the PSQI questionnaire. Table 1 lists participants’ characteristics. The mean age was 59±7.3 years, and approximately third-fourths of the study population were female and had religious beliefs. Only 5.3% of participants had a smoking history, 18% used alcohol at least once a week, about 60% used tea and coffee at least once a week, 49.5% engaged in regular exercise, only 5.7% did not achieve a moderate to high level of physical activity, 57.2% (162 subjects) had chronic disease, and 6% had depressive symptoms. Older adults, those with less alcohol use, and those with fewer depression symptom had significantly better sleep. A greater number of chronic diseases, especially heart disease and arthritis, were associated with poor sleep quality.
Overall, table 2 shows the distribution of the quality of sleep according to the PSQI questionnaire. Global scores indicated that 27.9% of participants had poor sleep quality. The majority of participants (69.6%) reported that they usually had more than 7 h of sleep at night, most (86.9%) reported only a slight problem with sleep disturbances, and 26.9% of participants reported needing more than 30 min to fall asleep. Results of sleep efficiency revealed that three-quarters of participants had sleep efficiency exceeding 87.6%; however, approximately one-third of participants self-rated their sleep quality as poor, and most (83.7%) had not used sleep medication during the previous month.
Results of the distribution of health-related fitness between good and poor sleep quality using the Mann-Whitney U-test are presented in Table3. Participants with poor sleep quality reported significantly higher depression symptoms, chronic disease numbers, and up-and-go times than participants with a good quality of sleep. In terms of self-rated health, participants with a poor quality of sleep reported lower health conditions. Other anthropometric indices and physical fitness parameters did not significantly differ between participants with good and those with poor quality of sleep.
Table 4 shows results of Spearman's correlations between the PSQI and health-related fitness. In a basic condition, depression symptoms (r=0.491, p=0.000), and chronic disease numbers (r=0.200, p=0.001) were significantly positively correlated with the PSQI, and self-rated health (r=-0.391, p=0.000) was significantly negatively correlated with the PSQI. As to health-related fitness, sit-and-reach (r=-0.131, p=0.028), 2-min steps (r=-0.133, p=0.026), and up-and-go (r=-0.169, p=0.004) were significantly negatively correlated with the PSQI. Other health-related fitness factors were not significantly correlated with the PSQI (all p>0.05).
Results of the logistic regression analysis are presented in Table 5A and B with each of the seven components of the PSQI and the global score as dependent variables. Covariates of age, sex, alcohol use, depression, number of chronic diseases, self-rated health, arthritis, and the four physical fitness items were used as independent variables. Results were as follows. Only depression was associated with a short sleep duration (OR=1.172, p<0.05); depression (OR=1.225, p<0.001) and arthritis (OR=5.515, p<0.05) were associated with sleep disturbances. Depression symptoms (OR=1.096, p<0.05), chronic disease numbers (OR=0.604, p<0.0), self-rated health (OR=0.885, p<0.01), and 2-min steps (OR=0.985, p<0.05) were associated with a longer sleep latency, and only depression (OR=1.143, p<0.01) was associated with daytime dysfunction. No other physical fitness items were associated with poor sleep efficiency; depression (OR=1.260, p<0.001) and self-rated health (OR=0.856 and p<0.001) were associated with poor subjective sleep quality; depression (OR=1.148, p<0.01) and self-rated health (OR=0.869, p<0.01) were associated with use of sleep medication; and depressive symptoms (OR=1.220, p<0.001), chronic disease numbers (OR=0.524, p<0.05), self-rated health (OR=0.865, p<0.001), and arthritis (OR=4.562, p<0.01) were associated with poor sleep quality. Among the controlling variables, sex, alcohol use, heart disease, chair stand in 30 s, up-and-go, and [constant/what is this??] were not associated with any component of the PQSI.
Our study have two major findings: (1) depression symptoms, the number of chronic diseases, self-rated health, and arthritis were significantly associated with poor sleep quality; and (2) the 2-min step test was associated with longer sleep latency.
These results confirmed the correlation of health-related physical fitness with sleep quality in the middle-aged and elderly, and among the health-related physical fitness items measured, only the 2-min step test was associated with longer sleep latency. Our study revealed that 27.9% of participants reported poor sleep quality. We discovered that 10.2% of study participants frequently used sleep medication to help them fall asleep, and 6.0% reported having significant depressive symptoms (CES-D ³10). The components of sleep quality evaluated in this study were diverse, and sit-and reach, 2-min step test, and up-and-go physical fitness items were significantly correlated with components of sleep quality; but only the 2-min step test was associated with longer sleep latency after controlling for confounding factors. However, depressive symptoms, the number of chronic diseases, self-rated health status, and arthritis were main risk factors influencing poor sleep quality among the middle-aged and elderly.
We found that depressive symptom caused a short sleep duration. Gerber et al. (21) reported that low fitness levels and a perceived lack of physical activity were associated with longer sleep onset latency. We similarly found better 2-min step endurance was associated with a lower risk of longer sleep latency. In our questionnaire, daytime functions, including driving, eating meals, and engaging in social activities, were less affected by depression. Lee and Lin (16) reported greater sit-and-reach distances in young women with favorable sleep quality, and we found that fewer depressive symptoms and chronic disease numbers, and better self-rated health were associated with subjective good sleep quality. Furthermore, the self-rated health status also had major influences on sleep latency, subjective sleep quality, and global sleep quality.
In this study, the logistic regression analysis disclosed associations of sleep disturbances and poor sleep quality with arthritis. Patients with RA suffer from a variety of symptoms such as joint pain, fatigue, stiffness, sleep disturbances, and functional disability (7). High prevalences of abnormal sleep quality were observed in both RA and osteoarthritis patient populations. The most common abnormality was sleep fragmentation, with an increased sleep disturbance score (22). Only 18.5% of RA patients reported good sleep quality, with depression and risk of sleep apnea being independently associated with sleep impairment (23).
Older adults with a long sleep duration had weaker hand grip strength irrespective of muscle mass (24). More muscle power corresponded to a lower probability of using sleep medication. Upper-arm muscle strength was a factor related to sleep medication use (24). We found that sleep medication use was associated with self-rated health and depressive symptoms. Approximately 90% of patients with depression reported poor sleep quality (25), for which depressive symptoms may have a greater influence than physical fitness.
This study has several limitations, including a small sample size, an unbalanced number of men and women recruited, sleep measurement based on subjective descriptions, and the lack of a control group. Furthermore, many factors, such as those pertaining to genetics and the environment, were not considered in our study and may have influential effects on sleep quality (26).
This study revealed that depressive symptoms, the number of chronic diseases, self-rated health status, and arthritis were the main risk factors that influenced global sleep quality among the middle-aged and elderly who participated in this study.
All authors declare that they have no financial motivations or conflicts of interest in relation to the current manuscript.
Ethics approval and consent to participate
The study was approved by the Ethics Committee of the Far Eastern Memorial Hospital (no. 098101-3), and all patients provided informed written consent before they were allowed to participate in the study.
Acknowledgments
The authors thank the patients and personnel at the hospital for their cooperation during the course of this study.
Funding
This study was supported by grants from the Ministry of Science and Technology (MOST 99-2410-H-418-001-MY3 and MOST 108-2314-B-038-113-MY3) and Taipei Medical University (106TMU-SHH-17 and 107TMU-SHH-04).
Authors' contributions
All authors were involved in the conception, design, data interpretation, manuscript preparation, and conduct of the study and have read and approved the final version of the manuscript.
BMI, body-mass index; CES-D, Center for Epidemiologic Studies Depression Scale; FFMI, free fat mass index; IPAQ, International Physical Activity Questionnaire; PSQI, Pittsburgh Sleep Quality Index.
Table1. Characteristics of the study subjects (N=283)
Quality of sleep
Variable n (%) Good n (%) Poor n (%) p value
Age (years) (59±7.3) 0.020#
<65 227 (80.2) 161 (70.9) 66 (29.1)
65~74 45 (15.9) 38 (54.4) 7 (15.6)
³75 11 (3.9) 5 (45.5) 6 (54.5)
Sex 0.317
Male 60 (21.2) 47 (78.3) 13 (21.7)
Female 223 (78.8) 157 (71.2) 66 (22.6)
Religious beliefs 0.513
No 61 (21.6) 46 (75.4) 15 (24.6)
Yes 222 (78.4) 158 (71.2) 64 (28.8)
Smoking history 0.284
No 268 (94.7) 195 (72.8) 73 (27.2)
Yes 15 (5.3) 9 (60.0) 6 (40.0)
Alcohol consumption 0.048
No 232 (82.0) 162 (69.8) 70 (30.2)
At least once a week 51 (18.0) 42 (82.4) 9 (17.6)
Tea consumption 0.407
No 116 (41.0) 85 (73.3) 31 (26.7)
At least once a week 167 (59.0) 119 (72.3) 48 (28.7)
Coffee consumption 0.521
No 110 (38.9) 79 (71.8) 31 (28.2)
At least once a week 173 (61.1) 125 (72.3) 48 (27.7)
Regular exercise 0.526
No 143 (50.5) 101 (70.6) 42 (29.4)
Yes 140 (49.5) 103 (73.6) 37 (26.4)
Chronic disease a 0.025
No 121 (42.8) 95 (78.5) 26 (21.5)
Yes 162 (57.2) 109 (67.3) 53 (32.7)
Heart disease 0.017
No 250 (88.3) 186 (74.4) 64 (25.6)
Yes 33 (11.7) 18 (54.5) 15 (45.5)
Arthritis 0.002
No 258 (91.2) 193 (74.8) 65 (25.2)
Yes 25 ( 8.8) 11 (44.0) 14 (56.0)
Physical activity b (Mets) 0.949#
Low 15 (5.7) 11 (73.3) 4 (26.7)
Moderate 135 (51.1) 95 (70.4) 40 (29.6)
High 114 (43.2) 83 (72.8) 31 (27.2)
Depressive symptoms c 0.004
No 264 (94.0) 195 (73.9) 69 (26.1)
Yes 17 (6.0) 7 (41.2) 10 (58.8)
a Chronic diseases included heart disease, arthritis, hypertension, diabetes mellitus, lung disease, peptic ulcers, liver disease, osteoporosis, gout, and cataracts. Heart disease and arthritis were significant, while the others were not. b mean±standard deviation: 4129.72±4811.94; c CES-D score:2.74±4.02. # Fisher’s exact test. Mets, metabolic equivalents.
Table 2 Distribution of quality of sleep
Variable items n %
Sleep duration (h)
0: ³7 197 69.6
1: 6~6.9 66 23.3
2: 5~5.9 15 5.3
3: £4.9 5 1.8
Sleep disturbance (scores)
0: 0 19 6.7
1: 1~9 246 86.9
2: 10~18 17 6.0
3: 19~27 1 0.4
Sleep latency (min)
0: £15 142 50.2
1: 16~30 65 23.0
2: 31~60 46 16.3
3: ³60 30 10.6
Daytime dysfunction
0: Very good 213 75.3
1: Fairly good 49 17.3
2: Fairly bad 19 6.7
3: Very bad 2 0.7
Sleep efficiency (%)
0: ³85 248 87.6
1: 75~84 23 8.1
2: 65~74 7 2.5
3: £64 5 1.8
Subjective sleep quality
0: Very good 32 11.3
1: Fairly good 162 57.2
2: Fairly bad 63 22.3
3: Very bad 26 9.2
Use of sleep medication
0: Not during past month 237 83.7
1: Less than once a week 10 3.5
2: Once or twice a week 7 2.5
3: Three or more times a week 29 10.2
Global sleep quality
Good quality (£5) 204 72.1
Poor quality (>5) 79 27.9
Table 3 Distribution of health-related fitness between good and poor sleep quality using the Mann-Whitney U-test (N=283)
Variables With good sleep quality (n=204) With poor sleep quality (n=79) z/p
Mean rank Sum of ranks Mean rank Sum of ranks
Basic condition
Age 143.77 29329.00 137.43 10857.00 -0.585/0.558
Depression 120.49 24338.00 193.46 15283.00 -7.190/0.000
Chronic disease numbers 135.97 27737.50 157.58 12448.50 -2.125/0.034
Self-rated health 157.17 31906.00 98.91 7715.00 -5.399/0.000
Anthropometric index
BMI (kg/m2) 145.34 29648.50 131.47 10254.50 -1.278/0.201
FFMI 144.65 28896.50 141.11 11006.50 -0.050/0.960
Mid-arm circumference (cm) 145.22 29625.00 131.77 10278.00 -1.239/0.215
Waist/hip ratio 142.12 28992.00 139.88 10911.00 -0.206/0.837
Physical fitness
Sit-and-reach (cm) 145.06 29447.00 130.44 10174.00 -1.351/0.177
One leg stance (s) 141.44 28711.00 139.87 10909.80 -1.860/0.853
Two-min step (no. of times) 146.35 29710.00 127.06 9911.00 -1.782/0.075
Chair stand in 30 s (no. of times) 145.77 29592.00 128.58 10029.00 -1.593/0.111
Grip muscle strength (kg) 145.51 29539.00 127.29 9801.00 -1.682/0.093
Up-and-go (s) 134.13 27229.00 158.87 12392.00 -2.324/0.020
Back muscle strength (kg) 143.68 28736.00 128.87 10045.00 1.388/0.165
BMI, body-mass index; FFMI, free fat mass index.
Table 4 Spearman correlation between the Pittsburgh Sleep Quality Index (PSQI) and health-related fitness
PSQI
r p
Basic condition
Age .004 0.952
Depression .491 0.000
Self-rate health -.391 0.000
Chronic disease (Numbers) 0.200 0.001
Anthropometric index
BMI -.076 0.204
FFMI .001 0.987
Waist / hip ratio .011 0.857
Physical Fitness
Sit-and reach -.131 0.028
One-leg stand -.080 0.179
Two-min steps -.133 0.026
Chair stand in 30s -.158 0.080
Grip muscle strength -.105 0.195
Up-and-go -.169 0.004
Back muscle strength -.100 0.096
Table 5A. Logistic regression analysis of poor sleep quality with the global score and with seven components of the Pittsburgh Sleep Quality Index (PSQI) (N=283)
Variable |
Odds ratio |
|||||||
Poor sleep quality |
Short sleep duration |
Sleep disturbance |
Longer sleep latency |
Daytime dysfunction |
Poor sleep efficiency |
Poor subjective sleep quality |
Use of sleep medication |
|
Age |
1.005 |
1.010 |
0.925* |
0.974 |
1.010 |
1.008 |
0.986 |
1.036 |
Sex |
1.529 |
4.753 |
3.910 |
0.836 |
1.027 |
2.465 |
1.238 |
0.737 |
Alcohol consumption |
0.573 |
0.876 |
1.015 |
0.790 |
0.826 |
1.747 |
0.648 |
0.405 |
CES-D score |
1.220*** |
1.172* |
1.225*** |
1.096* |
1.143* |
1.003 |
1.260*** |
1.148** |
Chronic disease numbers |
0.524* |
0.404 |
0.8722 |
0.604* |
0.629 |
0.830 |
0.650* |
0.962 |
Self-rated health |
0.865*** |
0.948 |
0.972 |
0.885** |
0.960 |
0.926 |
0.856*** |
0.869** |
Arthritis |
4.562** |
4.180 |
5.815** |
2.38 |
2.126 |
2.922 |
2.959 |
1.622 |
Heart disease |
2.296 |
0.000 |
0.869 |
1.430 |
1.665 |
0.000 |
1.046 |
2.298 |
Sit-and-reach |
0.991 |
0.956 |
0.962 |
0.994 |
0.980 |
0.985 |
1.004 |
0.994 |
Two-min step |
1.000 |
0.984 |
0.981 |
0.985* |
1.003 |
0.998 |
0.993 |
0.993 |
Up-and-go |
1.109 |
1.130 |
1.384 |
1.044 |
1.109 |
1.063 |
1.098 |
0.994 |
Constant |
0.548 |
0.071 |
0.950 |
40.344 |
0.024 |
0.060 |
5.251 |
0.246 |
Note: * p<0.05, ** p<0.01, *** p<0.001.
CES-D, Center for Epidemiological Studies Depression Scale.
Table 5B. Logistic regression analysis of poor sleep quality with the global score and with seven components of Pittsburgh Sleep Quality Index (PQSI) (N=283)
Variable |
95% Confidence interval |
|||||||
Poor sleep quality |
Short sleep duration |
Sleep disturbance |
Longer sleep latency |
Daytime dysfunction |
Poor sleep efficiency |
Poor subjective sleep quality |
Use of sleep medication |
|
Age |
(0.960, 1.052) |
(0.936, 1.090) |
(0.846, 1.011) |
(0.931, 1.018) |
(0.941, 1.083) |
(0.937, 1.084) |
(0.943, 1.032) |
(0.979, 1.095) |
Sex |
(0.625, 3.742) |
(0.494, 45.703) |
(0.512, 29.751) |
(0.383, 1.825) |
(0.283, 3.725) |
(0.487, 12.475) |
(0.528, 2.902) |
(0.283, 1.923) |
Alcohol consumption |
(0.234, 1.404) |
(0.173, 4.427) |
(0.193, 5.338) |
(0.356, 1.751) |
(0.212, 3.222) |
(0.503, 6.072) |
(0.281, 1.497) |
(0.114, 1.435) |
CES-D score |
(1.116, 1.333) |
(1.043, 1.318) |
(1.091, 1.376) |
(1.015, 1.183) |
(1.034, 1.262) |
(0.884, 1.137) |
(1.145, 1.387) |
(1.051, 1.235) |
Chronic disease numbers |
(0.789, 6.684) |
(0.165, 0.986) |
(0.389, 1.951) |
(0.382, 0.954) |
(0.306, 1.294) |
(0.401, 1.719) |
(0.403, 1.049) |
(0.568, 1.630) |
Self-rated health |
(0.792, 0.944) |
(0.822, 1.093) |
(0.833, 1.135) |
(0.815, 0.961) |
(0.838, 1.100) |
(0.808, 1.063) |
(0.785, 0.934) |
(0.784, 0.963) |
Arthritis |
(1.513, 13.753) |
(0.503, 34.773) |
(1.115, 30.324) |
(0.701, 5.926) |
(0.410, 11.408) |
(0.556, 15.351) |
(0.995, 8.798) |
(0.994, 5.329) |
Heart disease |
(0.315, 0.873) |
(0.000 ) |
(0.148, 5.087) |
(0.511, 3.999) |
(0.339, 8.183) |
(0.000) |
(0.358, 3.053) |
(0.776, 6.808) |
Sit-and-reach |
(0.963, 1.020) |
(0.914, 0.999) |
(0.916, 1.011) |
(0.967, 1.023) |
(0.938, 1.024) |
0.941, 1.031) |
(0.975, 1.033) |
(0.961, 1.028) |
Two-min step |
(0.986, 1.015) |
(0.960, 1.009) |
(0.954, 1.010) |
(0.972, 0.999) |
(0.980, 1.028) |
(0.975, 1.021) |
(0.979, 1.007) |
(0.975, 1.011) |
Up-and-go |
(0.890,1.415) |
(0.767, 1.666) |
(0.902, 2.123) |
(0.826, 1.319) |
(0.761, 1.616) |
(0.726, 1.554) |
(0.865, 1.393) |
(0.752, 1.315) |