Background
Cardiovascular disease (CVD) is the leading cause of mortality in patients with end-stage renal disease on hemodialysis(HD), and the relative risk of death from CVD in HD patients is 20 times higher than in individuals with normal renal function [
1]. The American Heart Association (AHA) has defined 7 ideal cardiovascular health (CVH) metrics, which include healthy lifestyle behaviors and ideal metabolic measures, to promote optimal cardiovascular health in the population [
2,
3]. Indeed, a higher number of ideal CVH metrics has been linked to a lower incidence of cardiovascular outcomes, such as heart failure and stroke, as well as other non-cardiovascular outcomes [
4].
Although the concept of primary prevention of CVD to promote CVH has been widely recognized, preventive measures have still been insufficiently implemented. HD Patients suffer greater cardiovascular risks due to Sleep complaints, such as obstructive sleep apnea (OSA) and abnormal sleep duration, which are prevalent among HD patients [
5,
6]. OSA may exacerbate oxidative stress, and endothelial dysfunction, and stimulate the sympathetic system through recurrent drops in oxygen saturation and sleep disturbances. On the other hand, abnormal sleep duration is usually closely related to circadian rhythm misalignment, adverse emotions, and underlying health issues, all of which increase the risk of CVD events in HD patients [
7‐
9]. Several population-based studies have reported that both high risk of OSA and abnormal sleep duration are associated with poor CVH [
2,
3,
9]. However, these associations have not been explored in HD patients. The individual and combined effects of OSA and sleep duration on ideal CVH metrics in HD patients remain to be established.
Therefore, this study aimed to explore the separate and combined associations of OSA risk and sleep duration with ideal CVH metrics in HD patients. This study may provide a reference for the role of good sleep habits in better CVH and may accelerate the process of clinical and public health promotion of CVH, particularly in HD patients.
Results
The basic characteristics of the 470 HD patients (281 men and 189 women; average age: 59.48 ± 12.89 years) included in this study are presented based on the number of Ideal Cardiovascular Health Metrics in Table
1. They were divided into three groups according to the number of ideal CVH metrics: 0–2 (poor CVH,
n = 88), 3–4 (intermediate CVH,
n = 273), and 5–7 (ideal CVH,
n = 109, reference group). Compared with patients with ideal CVH, poor and intermediate CVH individuals had worse CVH indicators, including BMI, smoking, physical activity, salty diet, glucose, blood lipids and blood pressure. HD patients with poor and moderate CVH who had higher age, spkt/v and potassium, they were also more likely to be male, drinker, fluid overload, shorter sleepers and at a higher OSA risk.
Table 1
Characteristics of participants by number of Ideal Cardiovascular Health Metrics
Age, y | 59.48 ± 12.89 | 60.39 ± 12.58 | 60.33 ± 12.89* | 56.61 ± 12.84 | 0.029 |
BMI, kg/m2 | 23.14 ± 3.53 | 25.31 ± 3.66* | 22.96 ± 3.48* | 21.85 ± 2.70 | <0.001 |
Male, n(%) | 281(59.8) | 75(85.2)* | 169(61.9)* | 37(33.9) | <0.001 |
Educational level, n(%) | | | | | 0.493 |
0 year | 18(3.8) | 1(1.1) | 13(4.8) | 4(3.7) | |
1–6 years | 81(17.3) | 11(12.5) | 49(18.0) | 21(19.3) | |
7–9 years | 165(35.2) | 37(42.0) | 90(33.1) | 38(34.9) | |
>9 years | 206(43.7) | 39(44.3) | 121(44.1) | 46(42.2) | |
Widowed, n(%) | 34(7.2) | 2(2.3) | 23(4.9) | 9(8.3) | 0.132 |
Living alone, n(%) | 28(6.0) | 6(6.8) | 14(5.1) | 8(7.4) | 0.652 |
Job category, n(%) | | | | | 0.030 |
Manual work | 137(29.1) | 29(33.0) | 77(28.2) | 31(28.7) | |
Non-manual work | 192(40.9) | 26(29.5) | 110(40.3) | 56(51.8) | |
Mixed work | 141(30.0) | 33(37.5) | 86(31.5) | 22(20.4) | |
Drinker, n(%) | 56(11.9) | 16(18.2)* | 33(12.1)* | 7(6.4) | 0.040 |
Smoker, n(%) | 97(20.6) | 31(35.2)* | 62(22.7)* | 4(3.7) | <0.001 |
Fluid overload, n(%) | 247(52.6) | 50(56.8)* | 128(27.2)* | 68(62.4) | 0.019 |
MIS,score | 3.80 ± 2.40 | 3.62 ± 2.39 | 3.83 ± 2.43 | 3.86 ± 2.37 | 0.755 |
CCI, score | 3.23 ± 1.34 | 3.42 ± 1.36 | 3.23 ± 1.41 | 3.08 ± 1.11 | 0.214 |
IPAQ, Met/wk | 1386(693,3465) | 693(396,1386)* | 1386(693,3251)* | 3238(1569, 5656) | <0.001 |
Sp Kt/v | 1.40 ± 0.32 | 1.32 ± 0.38* | 1.39 ± 0.31 | 1.47 ± 0.27 | 0.006 |
Blood biochemical indexes | | | | |
SBP,mmHg | 152.74 ± 25.46 | 156.61 ± 21.77* | 153.58 ± 25.58 | 147.58 ± 27.30 | 0.033 |
DBP, mmHg | 84.23 ± 16.09 | 82.05 ± 16.94 | 85.09 ± 15.64 | 83.82 ± 16.44 | 0.292 |
TCH, mmol/L | 3.97 ± 1.30 | 3.82 ± 1.05 | 4.05 ± 1.47 | 3.91 ± 0.98 | 0.305 |
TG, mmol/L | 1.81 ± 1.49 | 2.93 ± 2.91 | 2.54 ± 8.08 | 1.81 ± 1.49 | 0.434 |
LDL, mmol/L | 2.34 ± 0.80 | 2.23 ± 0.61 | 2.37 ± 0.86 | 2.34 ± 0.77 | 0.345 |
HDL, mmol/L | 0.97 ± 0.28 | 0.85 ± 0.30* | 0.98 ± 0.28 | 1.03 ± 0.26 | <0.001 |
GLU, mmol/L | 7.50 ± 3.55 | 9.54 ± 4.26* | 7.52 ± 3.42* | 5.78 ± 2.03 | <0.001 |
Hemoglobin, g/L | 111.70 ± 15.97 | 109.68 ± 15.89 | 112.63 ± 16.31 | 111.01 ± 15.10 | 0.282 |
Albumin, g/L | 40.44 ± 14.03 | 39.39 ± 3.04 | 39.88 ± 3.23 | 42.72 ± 28.53 | 0.149 |
CRP, mg/L | 6.18 ± 14.06 | 6.92 ± 12.57 | 5.82 ± 12.31 | 6.49 ± 18.87 | 0.816 |
BUN, mmol/L | 25.87 ± 6.49 | 25.93 ± 7.57 | 25.72 ± 6.45 | 26.20 ± 5.65 | 0.805 |
Scr, µmoI/L | 1012 ± 274 | 1069 ± 332 | 1004 ± 266 | 984 ± 233 | 0.074 |
UA, µmoI/L | 450.25 ± 96.91 | 458.69 ± 106.02 | 449.51 ± 97.24 | 444.92 ± 88.15 | 0.648 |
Phosphate, mmol/L | 1.97 ± 0.82 | 2.24 ± 0.22 | 2.58 ± 5.34 | 2.29 ± 0.24 | 0.415 |
Potassium, mmol/L | 4.88 ± 0.83 | 4.62 ± 0.76 | 4.88 ± 0.84 | 5.07 ± 0.80 | 0.003 |
Total calcium, mmol/L | 2.45 ± 4.07 | 2.24 ± 0.22 | 2.58 ± 5.34 | 2.29 ± 0.24 | 0.712 |
Sleep characteristic |
Sleep duration | | | | | 0.004 |
<7 h | 215(45.7) | 56(63.6)* | 115(42.1) | 44(40.4) | |
7-9 h | 207(44.0) | 25(28.4)* | 126(46.2) | 56(51.4) | |
>9 h | 48(10.2) | 7(8.0) | 32(11.7) | 9(8.3) | |
NOA | 1.64 ± 1.36 | 1.65 ± 1.46 | 1.73 ± 1.37 | 1.40 ± 1.25 | 0.107 |
Sleep mediation, n(%) | 111(23.6) | 23(26.1) | 66(24.2) | 22(20.2) | 0.586 |
Sleep quality, n(%) | | | | | 0.056 |
Very well | 142(30.2) | 18(20.5) | 90(33.0) | 34(31.2) | |
Good | 188(40.0) | 35(39.8) | 105(38.5) | 48(44.0) | |
Not enough | 64(13.6) | 20(22.7)* | 35(12.8)* | 9(8.3) | |
Very poor | 76(16.2) | 15(17.0) | 43(15.8) | 18(16.5) | |
OSA risk, n(%) | 234(49.8) | 64(72.7) | 135(49.5) | 35(32.1) | <0.001 |
The ORs of ideal CVH metrics across different levels of sleep duration and OSA risk are shown in Table
2. In ordinal logistic regression models, for HD patients who slept < 7 h, the proportional odds of having better CVH (ideal vs. intermediate; intermediate vs. poor) were 47% lower (odds ratio 0.53 [95% CI 0.30, 0.92];
P = 0.025, Model 3), compared with 7-9 h sleep duration. Furthermore, for HD patients at risk for OSA, the proportional odds of having better CVH (ideal vs. intermediate; intermediate vs. poor) were 42% lower (odds ratio 0.58 [95% CI 0.32, 0.83];
P = 0.007, Model 3).
Table 2
Ordinal logistic regression analyses for the associations between number of Ideal Cardiovascular Health Metrics and Sleep characteristic
OSA | | | | | | |
OSA risk (+) | 0.38(0.25,0.57) | <0.001 | 0.62(0.39,0.97) | 0.035 | 0.58(0.32,0.83) | 0.007 |
OSA risk (-) | Reference | | Reference | | Reference | |
Sleep duration | | | | | | |
<7 h | 0.55(0.36,0.85) | 0.007 | 0.55(0.35,0.85) | 0.007 | 0.53(0.30,0.92) | 0.025 |
7-9 h | Reference | | Reference | | Reference | |
>9 h | 0.61(0.32,1.19) | 0.145 | 0.54(0.33,1.26) | 0.194 | 0.77(0.37,1.58) | 0.474 |
The association of the combination of sleep duration and OSA risk with ideal CVH metrics was included in Table
3. The sleep duration ‘7–9 h’ and OSA risk(-) were both viewed as reference categories. In general, short sleeper (< 7 h) combined OSA risk (+) was associated with lower ORs of better CVH among HD patients (odds ratio 0.28 [95% CI 0.13, 0.60];
P = 0.001).
Table 3
Ordinal logistic regression analyses for the associations between number of Ideal Cardiovascular Health Metrics and sleep duration stratified according to OSA risk
OSA risk(+) | 0.28(0.13,0.60) | 0.001 | 0.58(0.29,1.16) | 0.123 | 0.36(0.11,1.15) | 0.084 |
OSA risk (-) | 0.57(0.27,1.20) | 0.141 | Reference | | 0.89(0.35,2.25) | 0.804 |
Discussion
This study evaluated the relationship between sleep characteristics and ideal cardiovascular health (CVH) metrics in HD patients. After adjusting for age, sex, job category, drinker, IPAQ, fluid overload, spkt/v, HDL, and potassium, this study showed that short sleep duration(< 7 h) and OSA risk were independently associated with poor cardiovascular health metrics (0–2 components), in comparison to ideal cardiovascular health metrics (5–7 components). Furthermore, the assessment of the combined effects of sleep duration and OSA risk on ideal CVH metrics in our study indicated the presence of OSA risk discrepancies in the correlation between sleep duration and ideal CVH metrics in HD patients. To our knowledge, this is the first study to explore the separate and combined associations of sleep duration and OSA risk with ideal cardiovascular health metrics in HD patients.
Consistent with previous studies [
4,
18], our study found that only 23.19% of HD patients met 5–7 ideal CVH metrics, less than half of the general Chinese population. In fact, traditional risk factors for cardiovascular disease, such as hypertension, diabetes, obesity, and lack of exercise, are more common in HD patients. Dialysis-related factors, such as anemia, inflammation, oxidative stress, and fluid overload, also contribute to an increased incidence of CVD events [
1]. However, the results of our study showed that despite regular visits to hospitals, HD patients have a higher risk of cardiovascular disease than the general population, and their condition is not well-controlled. Cardiovascular disease is the most common complication and the leading cause of death in HD patients. Therefore, more attention should be focused on the prevention and control of CVD in HD patients.
Sleep complaints, such as OSA risk and short sleep duration, have been linked to an increased risk of CVD events in several epidemiological studies [
3,
7‐
9]. Notably, the prevalence of OSA and short sleep duration increases with the deterioration of chronic kidney disease. The risk of OSA in HD patients may be 10 times higher than in the general population, and the proportion of short sleep duration in HD patients is also substantially higher than in the general population [
6,
8,
10,
19]. The characteristic airflow limitation and repetitive arousal in OSA were related to periodic hypoxemia and re-oxygenation, as well as enhanced sympathetic activation. These factors may lead to oxidative stress, endothelial dysfunction, and an inflammatory response that ultimately damage cardiovascular health [
7]. Similar to the findings of this study, the American Heart Association Go Red for Women Strategically Focused Research Network (AHA GRFW SFRN) population study study showed that short sleep duration (< 7 h) and OSA risk were associated with 60–289% higher odds of having poor CVH [
9]. The mechanisms of short sleep duration associated with CVD events include the mutual changes in leptin and ghrelin circulation levels. These changes can increase appetite and reduce energy consumption, potentially promoting the occurrence of obesity [
20]. Moreover, short sleep duration was associated with dialysis-related fluid overload, circadian rhythm disorders, inflammatory response activation, etc., thereby increasing the risk of CVD [
8,
9].
In HD patients, the management of cardiovascular risk factors is crucial, particularly modifiable ones. The ideal cardiovascular health metrics defined by the American Heart Association (AHA) do not include sleep but encompass several traditional cardiovascular risk factors (blood pressure, TCH, total cholesterol, fasting plasma glucose and BMI) and non-traditional cardiovascular risk factors (smoking status, dietary habits, and physical activity). Beyond their potential influence on clinical cardiovascular risk factors, sleep complaints may also be associated with other modifiable lifestyle behaviors, including diet, physical activity and smoking. Previous studies have reported that short sleepers and OSA patients are more likely to have irregular eating habits, such as fewer main meals, frequent intake of energy-dense snacks, or consuming more animal viscera, fried foods, and salted foods [
21,
22]. The influence of OSA and sleep duration on physical activity (PA) is not well-established. Only one study reported that OSA was linked to lower physical activity levels, while the quality of evidence for the impact of exercise on sleep intervention in patients with chronic kidney disease was low, indicting a potential behavioral mechanism for the cardiovascular impairments associated with sleep complaints [
23,
24].
Data from the Henan Rural Cohort and NHANES also showed that people who slept less were more likely to smoke [
2,
8]. Among OSA patients, the proportion of frequent and occasional smokers was significantly higher compared to non-OSA patients [
22]. There is weak evidence that insomnia exacerbates smoking and discourages quitting. Genetic correlations and bidirectional causal effects between sleep complaints and smoking indicate that sleep could be a potential target for smoking treatment and prevention [
25].
Considering the interactive and confounding effects, we further explored the associations between the combination of OSA risk and sleep duration in relation to ideal CVH metrics in HD patients. The results of this study showed that for HD patients with short sleep duration and OSA risk, the proportional odds of ideal CVH were reduced by 72%.The combination of OSA risk and short sleep duration appears to be more detrimental to cardiovascular health. Although recent studies have shown that OSA patients with short sleep duration are closely related to hypertension, central obesity, and insulin resistance, the relationship between OSA combined with short sleep and cardiovascular disease remains unclear [
26,
27]. Tetyana et al. found that among 21% of subjects without OSA (Apnea Hypopnea Index < 5) but at risk for OSA, subjects with an objective sleep duration of 4.9 h had a lower risk of CVD events than those with an objective sleep duration of 6.4 h [
28]. Nevertheless, the results of Xiaoman et al. were quite different. OSA showed a strong correlation with moderate-to-high 10-year CVD risk, however, there was no significant association between sleep duration and CVD risk in the population with OSA [
29]. Since most previously published studies on OSA risk, sleep duration, and cardiovascular health were cross-sectional, we were unable to determine the role of OSA risk and sleep duration. In this study, we explored the basic characteristics of HD patients in different sleep duration groups according to OSA risk stratification. We observed that poor sleep characteristics tended to be concentrated, and HD patients with OSA risk combined with short sleep duration had the worst sleep (including the use of sleep medications and sleep quality)(see Supplementary Table
1). Poor CVH metrics may be related to the cumulative impact of multiple sleep problems. HD patients with multiple sleep problems should embrace a healthy lifestyle and consistently monitor cardiovascular indicators to effectively engage in primary prevention of CVD.
Strength and limitations
This study is the first to demonstrate that in HD patients with OSA risk and short sleep duration are significantly associated with poor CVH, respectively. Moreover, the co-existence of OSA risk and short sleep has a greater impact on poor CVH. Our assessment of clinical and lifestyle risk factors for CVD is very rigorous. The validity and reliability of the questionnaire are verified by standardized and widely used questionnaires [
11,
16]. Standardized anthropometric and blood pressure measurements are carried out by trained research staff and blood indicators are assessed using standardized protocols [
10]. Furthermore, we thoroughly examined the relationship between OSA risk, sleep duration and ideal CVH metrics. The results of this study could imply the significant role of sleep in the primary prevention of CVD in HD patients, and offer guidance for clinical intervention.
This study also has some limitations. Firstly, information about OSA risk and sleep duration was obtained from self-reported questionnaires rather than objectively assessed sources. Polysomnography (PSG) is the gold standard for diagnosing obstructive sleep apnea (OSA), and can also accurately measure sleep duration. However, the detection process of standard PSG is complex and needs to be carried out in a professional sleep laboratory, which is difficult to promote in a large sample population [
30]. The STOP-BANG questionnaire and self-reported sleep duration are the most commonly used methods for subjectively assessing sleep. The STOP-BANG questionnaire has been proven to be an effective tool for screening OSA risk in different medical populations. It also shows a certain degree of consistency with PSG measurement assessment and self-reported sleep duration [
31,
32]. Secondly, the sample size of this study is moderate, which limits the ability to analyze ideal CVH metrics stratified by different sleep problems. Therefore, the investigation into the combined effects of different sleep problems was exploratory. Finally, our study is a cross-sectional study, indicating a significant correlation between OSA risk and sleep duration are significantly correlated with ideal CVH metrics. However, the lack of temporality limits the ability to infer causality, highlighting the need for more prospective studies with larger sample sizes.
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