Healthcare innovation

Prevalence of Sleep Disorders Among Patients With…

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Prevalence of Sleep Disorders Among Patients With…

Background: Due to rising rates of morbidity and mortality associated with type 2 diabetes mellitus (T2DM), Saudi Arabia is ranked second in the Middle East and seventh overall among nations with the greatest incidence of diabetes mellitus (DM). Significant sleep abnormalities have been linked to difficulties in managing blood sugar levels, suggesting a link between sleep disorders and diabetes. This study aimed to find out how common sleep disturbances were among patients with T2DM in Makkah, Saudi Arabia.

Methods: This descriptive cross-sectional study was conducted between June and August 2022 in Makkah City, Saudi Arabia. Patients with T2DM who visited primary healthcare facilities in Makkah during the study’s duration were included in the study. To evaluate sleep quality, the Pittsburgh Sleep Quality Index in Arabic was employed. Patients who met the inclusion criteria were given an interview questionnaire to fill out.

Results: In total, 355 patients with T2DM were enrolled in this study. The patients’ median age was 49.24 years. Other than DM, a majority of them (58.9%) had chronic illnesses, with hypertension (64.5%) and cardiovascular disease (65.5%) as the most prevalent comorbidities. Only 22% of the patients had controlled diabetes. Of the individuals who had sleep disorders, 63.7% stated having poor sleep quality.

Conclusion: Sleep problems are a common occurrence in patients with T2DM. Additionally, compared to people with other chronic disorders, people with endocrine diseases had poorer sleep quality. Hence, the duration of diabetes has an impact on sleep quality.

Introduction

Patients with type 2 diabetes mellitus (T2DM) frequently experience sleep issues. Additionally, patients with endocrine dysfunction experience lower quality of sleep compared to those with other chronic disorders. Sleep quality is impacted by prolonged diabetes duration [1-3].

Sleep disturbances have been known to cause inflammatory processes, predisposing a person to develop diabetes [4]. Uncontrolled diabetes has been linked to a reduction in sleep quality [4]. According to prior studies, more than 50% of patients with T2DM have trouble sleeping [5]. Additionally, ineffective glucose management is hampered by poor sleep, which is linked to diabetes-related complications [5].

Patients with sleep-disordered breathing may have impaired glucose metabolism due to obstructive sleep apnea (OSA). The American Academy of Sleep Medicine defines OSA as “repeated episodes of total or partial upper airway obstruction while sleeping” [1]. These complete or incomplete obstructions cause brief awakenings and a decline in blood oxygen saturation [6]. Respiratory disturbances may cause frequent arousals, which could lead to sleep loss and predispose to metabolic disorders [7]. Untreated OSA is also linked to a number of harmful health outcomes, such as chronic fatigue syndrome, decrease in quality of life, increase in the risk of death, systemic hypertension (HTN), diabetes, coronary artery disease, stroke, atrial fibrillation, and congestive heart failure [8].

In a prior study at King Abdulaziz Medical City in the Kingdom of Saudi Arabia, it was discovered that obesity with a body mass index of more than 30 kg/m2 (39.1%), HTN (33.9%), diabetes mellitus (DM) (20.8%), depression (4.3%), asthma (17.3%), chronic obstructive pulmonary disease (6.6%), and hyperlipidemia (2.7%) were the conditions most often related to a less than seven hours of sleep per night [9]. Another study conducted in Jazan found that the occurrence of poor sleep quality is 55.4% (95% CI: 49.7-60.8) and that it is related to sociodemographic and factors like being elderly, female, uneducated, smoker, with diabetes or other comorbidities, or having psychiatric symptoms [10]. According to a study done in Taif, 26.9% of patients had a moderate risk for OSA, while 15.2% of patients had a severe risk.

When combining both oral medications and insulin, more patients had a serious risk of sleep abnormality than when taking either oral medications alone or insulin alone [11]. Research on the prevalence of sleep problems in people with T2DM is scarce in Saudi Arabia. Consequently, the purpose of this study was to evaluate the prevalence of sleep difficulties among people with T2DM and its contributing factors in the Makkah region of Saudi Arabia.

Materials & Methods

Study design, duration, and setting

This was a descriptive, cross-sectional study carried out in Makkah City, Saudi Arabia from June to August 2022.

Participants

The study included patients with T2DM who visited primary healthcare facilities in the Makkah region during the study period. Patients with T2DM who were ≥18 years old and of either sex were required to meet the inclusion criteria. Patients with type 1 DM, those with known psychiatric conditions, people who take sleeping medicines, women who are pregnant, and people who work night shifts were all excluded from the study.

Sampling methodology

Patients were randomly chosen from the lists of patients in the primary healthcare facilities in the Makkah region. Recruitment was carried out at each healthcare facility until the appropriate number of participants was reached.

Determination of sample size

Using OpenEpi (version 3.0), the minimum sample size required for this investigation was calculated [12]. The number of T2DM patients [13], 95% confidence interval (CI), an anticipated frequency of 50%, and a design effect of 1 were taken into account while calculating the sample size. The calculated minimum sample size was 334 patients.

Data collection

Patients who met the inclusion criteria were given a questionnaire, which was then used to gather data. After receiving the participants’ informed consent, face-to-face interviews were conducted and the questionnaires were given. The following information was gathered: demographics, the number of children, type of dwelling, employment status, smoking, income level, BMI, duration of diabetes, chronic conditions, and glycosylated hemoglobin (HbA1c) levels.

To evaluate the quality of sleep, the validated Pittsburgh Sleep Quality Index (PSQI) was utilized [14]. This scale was used to evaluate the quality of sleep over the previous month and comprises seven components on the following items: daytime dysfunction, daytime dysfunction quality, daytime dysfunction duration, and daytime dysfunction efficiency. Each element is given a score between 0 and 3, and the PSQI values range from 0 to 21. Poor sleep quality is indicated by high scores, with PSQI scores of more than 5 having a sensitivity of 89.6% and a specificity of 86.5% [14].

Data analysis

Data were statistically analyzed using SPSS version 26 software (IBM Corp., Armonk, NY). The chi-squared test (χ2) was used for analyzing qualitative data, which were expressed as percentages and numbers, and for examining the variables. Quantitative data were presented as mean and standard deviation (mean ± D). Correlation analysis was performed using Spearman’s test. A p-value < 0.05 was considered statistically significant.

Results

After non-respondents were excluded from the trial, 355 patients remained. The patients’ average BMI was 28.35 kg/m2, with an average age of 49.24 years (Table 1). Each patient had an average of four children (± 1.17). The patients’ mean HbA1c level was 7.22 ± 1.25, and they had had diabetes for an average of 8.83 ± 7.99 years. Males made up 58.9% of the patients, Saudi nationals made up 92.1% of the patients, and 49.9% of the patients had a university or diploma-level education. Of the patients, 36.9% lived in rented homes, and 72.1% of the patients were married. Of them, 41.4% earned between 10,000 and 20,000 Saudi riyals (SR) per month, while 24.2% of them were unemployed. Of them, 36.3% were smokers and the most common comorbidities were cardiovascular disease (CVD) (65%) and HTN (64.5%).

Variable No. (%)
Age (years) 49.24 ± 16.14
BMI (kg/m2) 28.35 ± 3.12
Number of children 4.09 ± 1.17
DM duration (years) 8.83 ± 7.99
HbA1C level 7.22 ± 1.25
Sex  
Female 146 (41.1)
Male 209 (58.9)
Nationality  
Saudi 327 (92.1)
Non-Saudi 28 (7.9)
Educational level  
Less than secondary school 118 (33.2)
University/diploma 177 (49.9)
PhD 33 (9.3)
Master’s degree 27 (7.6)
Marital status  
Widow 28 (7.9)
Single 71 (20)
Married 256 (72.1)
Employment status  
Unemployed 86 (24.2)
Retired 93 (26.2)
Employee in the private sector 69 (19.4)
Employee in the governmental sector 107 (30.1)
House  
Rented 131 (36.9)
Owned 224 (63.1)
Monthly income  
<10,000 SR 149 (42)
10,000-20,000 SR 147 (41.4)
>20,000 SR 59 (16.6)
Smoking status  
Non-smoker 226 (63.7)
Smoker 129 (36.3)
Other chronic diseases  
Yes 209 (58.9)
No 146 (41.4)
If yes, what disease? (N = 209)  
Endocrine 39 (18.4)
CVS 136 (65)
HTN 135 (64.5)
Respiratory disease 51 (24.4)
Kidney disease 20 (9.5)
Liver disease 4 (1.9)
Neuropathy and retinopathy 13 (6.2)
DM control  
Controlled 78 (22)
Uncontrolled 277 (78)
Table 1: Distribution of studied diabetic patients according to their demographics, BMI, DM duration, HbA1C level, and comorbidities (N = 355)

DM: diabetes mellitus; HbA1C: glycosylated hemoglobin; SR: Saudi riyals; CVS: cardiovascular system; HTN: hypertension.

The average PSQI score for patients was 7.25. After categorizing the patients’ PSQI scores, it was discovered that 63.7% of them experienced poor sleep (Figure 1).

-Distribution-of-the-participants-according-to-sleep-quality-based-on-their-Pittsburgh-Sleep-Quality-Index-scores-(N-=-355)

Figure 1: Distribution of the participants according to sleep quality based on their Pittsburgh Sleep Quality Index scores (N = 355)

When compared to patients without endocrine disorders, patients with endocrine disorders other than DM had a substantially greater percentage of people who reported having bad sleep (p < 0.05; Table 2). Patient demographics, BMI, DM duration, HbA1c level, and other comorbidities were all connected with sleep quality (p > 0.05; Table 2).

Variable Sleep quality χ2 P-value
Good, No. (%) Poor, No. (%)
Age 49.35 ± 15.12 49.18 ± 16.71 0.009* 0.93
BMI 28.3 ± 83.1 28.33 ± 3.14 0.71* 0.475
Number of children 4.05 ± 2.89 4.11 ± 3.33 0.13* 0.894
DM duration 7.59 ± 6.66 9.54 ± 8.59 1.54* 0.122
HbA1C level 7.18 ± 1.09 7.25 ± 1.33 0.007* 0.994
Sex        
Female 47 (32.2) 99 (67.8) 1.84 0.175
Male 82 (39.2) 127 (60.8)    
Nationality        
Saudi 121 (37) 206 (63) 0.79 0.373
Non-Saudi 8 (28.6) 20 (71.4)    
Educational level        
Less than secondary school 45 (38.1) 73 (61.9) 4.72 0.193
University/diploma 56 (31.6) 121 (68.4)    
PhD 16 (48.5) 17 (51.5)    
Master’s degree 12 (44.4 15 (55.6)    
Marital status        
Widow 7 (25) 21 (75) 3.25 0.196
Single 22 (31) 49 (69)    
Married 100 (39.1) 156 (60.9)    
Employment status        
Unemployed 26 (30.2) 60 (69.8) 2.33 0.506
Retired 33 (35.5) 60 (64.5)    
Employee in the private sector 27 (39.1) 42 (60.9)    
Employee in the governmental sector 43 (40.2) 64 (59.8)    
Smoking status        
Non-smoker 80 (35.4) 146 (64.6) 0.23 0.626
Smoker 49 (38) 80 (62)    
Other chronic diseases        
Yes 71 (34) 138 (66) 1.23 0.267
No 58 (39.7) 88 (60.3)    
Type of chronic disease        
Endocrine 7 (5.4) 32 (14.2) 6.4 0.011
CVS 47 (36.4) 89 (39.4) 0.3 0.583
HTN 46 (35.7) 89 (65.9) 0.48 0.487
Respiratory disease 22 (17.1) 29 (12.8) 1.19 0.275
Kidney disease 7 (5.4) 13 (5.8) 0.01 0.898
Liver disease 2 (1.6) 2 (0.9) 0.32 0.568
Neuropathy and retinopathy 7 (5.4) 6 (2.7) 1.78 0.181
DM control        
Controlled 27 (34.6) 51 (65.4) 0.12 0.72
Uncontrolled 102 (36.8) 175 (63.2)    
Table 2: Relationship between sleep quality and patients’ demographics, BMI, DM duration, HbA1C level, and comorbidities (N = 355)

* Mann-Whitney test.

DM: diabetes mellitus; HbA1C: glycosylated hemoglobin; CVS: cardiovascular system; HTN: hypertension.

A non-significant positive association was found between the PSQI score and age, the number of children, and the HbA1c level (p > 0.05; Table 3). Furthermore, a negative correlation between PSQI score and BMI (p > 0.05) was found. The outcome, nevertheless, was not noteworthy.

Variable Pittsburgh Sleep Quality Index (PSQI) score
r P-value
Age 0.002 0.968
BMI -0.02 0.588
Number of children 0.008 0.879
HbA1C level 0.03 0.574
Table 3: Spearman’s correlation analysis between Pittsburgh Sleep Quality Index (PSQI) scores and participants’ age, BMI, number of children, and HbA1C level

HbA1C: glycosylated hemoglobin.

Additionally, DM duration and PSQI score had a strong positive correlation (r = 0.12, p = 0.022; Figure 2). The outcome, nevertheless, was not substantial.

Spearman's-correlation-analysis-of-the-correlation-between-the-Pittsburgh-Sleep-Quality-Index-(PSQI)-and-the-duration-of-diabetes-mellitus-(DM)

Figure 2: Spearman’s correlation analysis of the correlation between the Pittsburgh Sleep Quality Index (PSQI) and the duration of diabetes mellitus (DM)

Patients who lived in rented homes or had low monthly incomes (10,000 SR) had a noticeably greater percentage of those who reported having bad sleep than patients who owned their homes or had higher monthly incomes (p < 0.05; Figures 3, 4).

Relationship-between-sleep-quality-and-type-of-residence

Figure 3: Relationship between sleep quality and type of residence

Relationship-between-sleep-quality-and-monthly-income

Figure 4: Relationship between sleep quality and monthly income

Discussion

The goal of this cross-sectional study was to determine the prevalence of sleep disorders among patients with T2DM in Makkah, Saudi Arabia. In the present study, more than half (63.75) of the patients were classified as having poor sleep quality based on their PSQI scores. Studies conducted in Jazan (55.4%) and Abha (72%) yielded similar results [15,16]. The present study revealed that the socioeconomic status and comorbidities of the patients strongly influenced the prevalence of poor sleep quality.

More than half of the patients in the current study were men with high BMI. This result is in line with a study done in Japan, where 342 participants (82.5% of whom were men) had T2DM and poor sleep quality [17]. The two comorbid conditions that affected patients with T2DM the most in the current study were CVD and HTN. This result is in line with a previous Ethiopian study, which discovered that patients with T2DM and HTN were more likely than those with T2DM alone to have poor sleep quality [18]. Moreover, the current study found that those with low earnings had worse sleep quality (42%) than people with high incomes in terms of socioeconomic characteristics. Similar results were found in a study done in Turkey using the PSQI, where 54% of the female participants and 50% of the male participants reported having poor sleep quality [7]. Poor sleep quality and type of dwelling were shown to be substantially associated in the current study. Compared to patients who lived in their own homes, those who leased homes had poorer sleep quality. However, there is not enough evidence to support this conclusion in the present.

DM is one of the most widespread diseases in the world. DM has been linked to a number of chronic illnesses, including OSA, in addition to diabetic complications such as neuropathy and neuropathic pain, which were found to disrupt sleep [1]. Additional sleep-related diabetes symptoms include polyuria, nocturia, snoring, and prolonged daytime tiredness. Diabetes and snoring are related conditions. Furthermore, chronic daytime sleepiness might cause insulin resistance [19]. Depression, cerebrovascular accidents, CVD problems, and HTN can all have a poor impact on sleep and general quality of life. Insufficient or disturbed sleep can have a detrimental influence on a patient’s recovery, ability to control their diabetes, and quality of life. Healthcare professionals must address these problems to provide DM patients with the best care possible. Additionally, sleep education is a vital method for improving the sleep quality of these patients [20].

Of the participants of the current study, 63.7% were classified as having poor sleep quality based on their PSQI ratings. Additionally, the findings showed a positive correlation between PSQI score and age, HbA1c level, and the number of children (p = 0.05). Additionally, the results showed a negative correlation between BMI and PSQI score (p = 0.05). Additionally, there was a strong significant correlation between PSQI score and DM duration (r = 0.12, p = 0.022). The association between PSQI subscales and diabetes control was also supported by a different study that reached a similar conclusion [14]. The Simultaneous Risk Factor Control Using Telehealth project participants in that study completed surveys, and the findings showed that patients with HbA1c levels below 7% had significantly lower global and PSQI subscale ratings than those in the control group (p = 0.01) [14].

The findings of the current investigation are supported by the results of a separate cross-sectional study done in Turkey by Ayaz and Dincer in 2021. The study found a strong relationship between low sleep quality and high HbA1c levels in patients with T2DM [20].

Limitations

The limitations of this study are numerous. Firstly, clinical data were gathered based on patients’ answers, for example, HbA1c levels. This poses a significant bias. Also, the background section outlines how anti-hyperglycemic medication and sleep quality are associated. Secondly, the projected sample size was initially not attained by the actual sample size, but statistical analysis nevertheless produced meaningful results. Thirdly, because this was a cross-sectional study, it was unable to determine how sleep disturbances and diabetes relate to one another. Moreover, the patients verbally provided their data. Hence, data on BMI and Hb1Ac levels may not have been accurate.

Conclusions

This study demonstrated that people with T2DM frequently experience sleep difficulties. Additionally, the findings showed that patients with endocrine disorders have poorer sleep quality than individuals with other chronic diseases. The findings also indicated that prolonged hyperglycemia has an impact on sleep quality.

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