Literature DB >> 32457400

Interactive effect of sleep duration and sleep quality on risk of stroke: An 8-year follow-up study in China.

Ailing Ji1, Heqing Lou2, Peian Lou3, Chunrong Xu1, Pan Zhang2, Cheng Qiao2, Qing Yang1.   

Abstract

Inappropriate sleep duration and poor sleep quality are associated with risk of stroke, but their interactive effect on stroke is unknown. We explored the interactive effect of sleep quality and duration on stroke risk. A prospective cohort study was conducted with 41,786 adults. Sleep quality was assessed using the Pittsburgh Sleep Quality Index. Sleep duration was measured by average hours of sleep per night. Cox regression models were used to calculate the association of sleep duration and quality with stroke. The delta method and a non-conditional logistic regression model were used and the relative excess risk due to interaction (RERI), the attributable proportion (AP), and the synergy index (S) were calculated. Compared with sleep duration 6-8 h/day, the risk ratio of stroke was 1.63 (1.23-2.11) times for sleep duration <6 h/day and 1.40 (1.08-1.75) times for >8 h/day. The stroke risk ratio was 2.37 (1.52-3.41) times in subjects with poor sleep quality compared with those with good sleep quality. Women who slept <6 h/day had higher stroke risk than men who slept <6 h/day. Men who slept >8 h/day had higher stroke risk than women who slept >8 h/day. Men with poor sleep quality had higher stroke risk than women with poor sleep quality. Stroke was associated with short/long sleep duration and poor sleep quality in subjects aged >46 years, compared with those aged 18-45 years. Stroke occurred more frequently in subjects with poor sleep quality combined with short sleep duration (odds ratio: 6.75; 95% confidence interval (CI): 2.45-14.12). RERI, AP, and S values (and their 95% CIs) were 5.54 (3.75-8.12), 0.72 (0.56-0.80), and 5.69 (4.23-9.90) for the poor sleep quality interact with short sleep duration. In persons with poor sleep quality accompanied by long sleep duration, RERI, AP, and S (95% CI) were 1.12 (1.01-1.27), 0.35 (0.26-0.51), and 2.05 (1.57-2.96), respectively. Subjective sleep disturbances are related with risk of stroke in Chinese adults. There are additive interactions between short/long sleep duration and poor sleep quality that affect risk of stroke.

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Year:  2020        PMID: 32457400      PMCID: PMC7250859          DOI: 10.1038/s41598-020-65611-y

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


Introduction

As the top cause of death and disability and the second leading cause of years of potential life lost, stroke killed over 6 million deaths in 2015 worldwide, and the number will be doubled by 2030, with over 200 million disability-adjusted life years each year[1,2]. The burden is the biggest in China: 1,114.8/100,000 of the age-standardized prevalence rate in 2013[3] and annual increase of 11.9% for the first-ever stroke morbidity during 1992-2015[4]. With respect to the traditional risk factors of stroke in China, hypertension, smoking, alcohol use, diabetes, and hypercholesterolemia are prevalent and could also be modified[3,5]. Some studies have shown that stroke is associated with poor sleep quality and sleep duration[6-8], while others have insistent results[9,10], which might partly due to different races[11]. Therefore, sleep quality in relation with stroke should be further investigated to determine whether stroke prevention programs should incorporate efforts to reduce sleep disturbances in different races. Sleep disturbances and insufficient sleep quantity are very common in Chinese adults[12,13]. However, few studies report the relationship between sleep quality and stroke[14,15]. Therefore, identifying and describing the relationship, and implementing early intervention measures to are extremely important in modifying the risk factor and in further slowing the progression of the disease in China. To this end, the current study aims to examine the effects and the interactive effect of sleep quality and sleep duration on stroke, respectively, in Chinese adults.

Methods

Study protocol and population

The baseline survey with a sample selected from all of the eleven regions of Xuzhou city, Jiangsu province, China, was conducted in, during May to November 2009. A two-stage sampling probability proportional to size (PPS) was used, and each region was considered a stratum, yielding a total of 11 strata. Five subdistricts/townships in urban/rural areas were firstly selected randomly from each stratum using PPS based on the population data. Then five communities/villages were randomly selected from each subdistrict/township using PPS and a total of 275 villages or communities, as clusters, were selected. In each selected village or community, a list of households containing adults aged ≥18 years and living their current residence for at least 5 years was generated. Finally, a Kish selection table was used to select one person from each household. The exclusion criteria included: (1) previous diagnosis of neuropathy, psychosis, or difficulty in communication, or (2) the floating population or temporary residents, or (3) obstructive sleep apnea. At least 13,500 people should be recruited assuming an estimation incidence of stroke of 2.0%[15] with 90% power, α level of 0.05, and allowing for a dropout rate of 15%. Overall 41,786 permanent residents aged ≥18 years participated in the survey, with a response rate of 91.6% (41,786/45,618). All participants were rechecked from May to November 2017. A total of 672 participants had stroke, and 1,585 participants were excluded owing to missing information about sleep duration or sleep quality; diagnosis of neuropathy or psychosis; use of any kind of psychotropic medication; severe heart, liver, or kidney disease, and/or cancer, producing a total of 39,533 participants in this prospective observational study. The interval of follow-up duration was the time between the baseline assessment and the diagnosis of stroke, death, or the date on which the 2017 questionnaire was finished. Those who developed strokes or died from strokes in the follow-up, and those who fulfilled the final research, were included in the present study. The main reasons for participant loss were death, migration, or other personal reasons at follow-up. All participants were of Han nationality.

Key measures

Sleep quality and disturbance over a 1-month length was estimated by a Chinese version of the Pittsburgh Sleep Quality Index (PSQI)[16]. This version has seven components and a total score from 0 to 21 points with reliability coefficient of 0.82–0.83 and acceptable test–retest reliability of 0.77–0.85[17]. PSQI score of ≤5 and >5 was correspondingly differentiated as good and poor sleep quality, respectively. The diagnostic sensitivity and specificity in differentiating poor from good sleepers were 89.6% and 86.5%, respectively. Sleep quantity was calculated on self-reported average total hours of per night sleep in the previous year, and was categorized as <6, 6–8, and >8 h per night, following previous studies[6,7,12]. In the follow-up, data on strokes were collected using self-reports and medical record questionnaires. Self-reported stroke should meet the criteria of an acute disorder of focal areas in the brain continuing for ≥24 h caused by intracranial hemorrhage or ischemia[18] with a diagnosis of computed tomography and magnetic resonance imaging scans. By definition, asymptomatic stroke and transient ischemic attack were excluded.

Variables

Participants were interviewed face-to-face and privately by trained interviewers using a standard questionnaire that assessed age, gender, marriage, occupation, educational level, cigarette use, alcohol use, physical activity, history of disease (type 2 diabetes mellitus (T2DM), obstructive sleep apnea, dyslipidemia, hypertension, heart disease, and cancer), and family history of disease (T2DM, hypertension, and stroke). Occupation was defined as manual, non-manual, unemployed, and retired. Educational level was classified as below high school, high school, and above high school level. Marriage was categorized as single, divorced, widowed, or separated; living conditions were sorted out as living alone or with someone else. Those who have smoked at least 100 cigarettes over the lifetime were defined as smokers. A drinker was defined as the consumption of no less than 30 g alcohol per week lasting 1 year or more. Physical activity was defined as joining moderate or vigorous activity for at least 30 min per day no less than 3 days a week. Weight in kilograms divided by height in meters squared was defined as body mass index (BMI) with categorized as underweight (≤18.5 kg/m2), normal weight (18.5–24.0 kg/m2), and overweight/obese (≥24.0 kg/m2); Women with waist circumference of >85 cm and men with that of >90 cm were defined as abdominal obesity[19]. T2DM was defined as fasting blood glucose of ≥7.0 mmol/L, or the use of any antidiabetic drugs, or self-reported history of T2DM[20]. Hypertension was characterized as systolic blood pressure ≥140 mmHg and/or diastolic blood pressure ≥90 mmHg, or the use of any antihypertensive drugs, or self-reported history of hypertension[21]. Dyslipidemia was defined as any lipid-lowering medication use or self-reported history of dyslipidemia. History of cardiovascular disease was defined as previous diagnosed ischemic heart disease and/or cerebrovascular events. A score of ≥3 on the STOP-Bang questionnaire indicated the presence of obstructive sleep apnea[22].

Statistical analysis

Epidata 3.1 was used to build a database. Data were input separately by two people and a conformance test was performed. All statistical analyses were conducted by SPSS 16.0 (SPSS Inc., Chicago, USA). Categorical variables were presented as frequencies and proportions or means (±standard deviation) and medians (interquartile range). Baseline characteristics of participants and non-participants in the follow-up examination were compared using the chi-square test, Student’s t-test, and the Mann–Whitney U test, as appropriate. The Mann–Whitney U test and Fisher’s exact test were used to compare the characteristics and sleep duration/qualities of participants who developed stroke with those who did not develop stroke. Risk ratios (RRs) and corresponding 95% confidence intervals (CI) were calculated using Cox regression models with reference to the risk of 7–8 h/day of sleep duration or good sleep quality, adjusting for age, gender, marital status, current employment status, educational level, BMI, cigarette use, alcohol intake, physical activity, DM2, fasting plasma sugar, lipids, dyslipidemia, hypertension, heart disease, family history of DM2, family history of hypertension, and family history of stroke. The observed prevalence of stroke was plotted and stratified by sleep quality and sleep duration. RRs and 95% CIs were also calculated for sleep duration and sleep quality in relation with age, adjusted by potential confounding factors, (gender, marital status, current employment status, educational level, BMI, cigarette use, alcohol intake, physical activity, DM2, fasting plasma sugar, lipids, dyslipidemia, hypertension, heart disease, family history of DM2, family history of hypertension, family history of stroke, and sleep quality and duration). The Excel table compiled by Anderss et al.[23] was introduced into the database using the delta method and relevant indicators of interaction were computed. The value obtained from the logistic regression model was taken as the estimated additive interaction between sleep quality and sleep duration. The following measures of interaction were examined to estimate biological interactions: the relative excess risk due to interaction (RERI), the attributable proportion due to interaction (AP), and the synergy index (S)[24,25]. The RERI is the excess risk attributed to the interaction relative to the risk without exposure. AP refers to the attributable proportion of disease caused by the interaction in subjects with both exposures. S is the excess risk from both exposures when there is a biological interaction relative to the risk from both exposures without interaction. In the absence of additive interactions, RERI and AP are equal to 0[25]. Indicative biological interactions would be considered when RERI > 0, AP > 0, or S > 1. A P value <0.05 (two-tailed) was considered statistically significant.

Results

General characteristics of participants

A total of 39,533 participants (males, 48.1%) who did not have stroke at baseline and 27,712 out of them completed the follow-up in 2017, of whom 617 developed stroke The median follow-up duration was 7 years. At baseline, the mean age and the average sleep duration per night were 45.7 ± 15.1 years and 7.16 ± 1.07 h in 2009, respectively. The non-responder group was older (50.7 ± 16.8 vs 44.6 ± 15.1 years, P < 0.001), with more short- sleepers [(2,098/11,821) vs. (5,368/27,712), P < 0.01], more long-sleepers [(2,021/11,821) vs (5,232/27,712), P < 0.01], and more individuals with poor sleep quality [(1,053/11,821) vs (1,989/27,712), P < 0.01]. There were no significant between-group differences in other risk factors. With respective of the 27,712 participants, those with stroke tended to be older, smokers and drinkers and have a higher BMI. There were no significant gender differences in the other risk factors (Table 1).
Table 1

Patients’ baseline characteristics in 2009 by presence of stroke (N = 27,712).

TotalStrokeP value
Yes (n = 617)No (n = 27095)
Sex
Male13247334 (54.1)12913 (47.7)
Female14465283 (45.9)14182 (52.3)0.002
Age (years)45.7 ± 15.161.0 ± 15.544.6 ± 15.2<0.001
Occupational
Manual21789432 (70.0)21357 (78.8)
Non-manual170337 (6.0)1666 (6.1)
Unemployed176133 (5.3)1728 (6.4)<0.001
Retired2459115 (18.1)2344 (8.7)
Education level
Below high school11457280 (45.4)11177 (41.3)0.043
high school14339306 (49.6)14033 (51.8)
Above high school191631 (5.0)1885 (7.0)
Not married249023 (3.7)2467 (9.1)<0.001
Living alone7141103 (16.7)7038 (26.0)<0.001
Smoker5621204 (33.1)5417 (20.0)<0.001
alcohol use4402133 (21.6)4269 (15.8)<0.001
Regular exercise6699141 (22.9)6558 (24.2)0.467
Family history of DM273513 (2.1)722 (2.7)0.468
Family history of stroke57821 (3.4)557 (2.1)0.030
Family history of hypertension209753 (8.6)2044 (7.5)0.371
BMI (≥24 kg/m2)12374397 (64.3)11977 (44.2)<0.001
Hypertension6524403 (65.3)6121 (22.6)<0.001
DM21943103 (16.7)1840 (6.8)<0.001
FPG (mmol/L)5.6 ± 1.25.6 ± 1.26.4 ± 1.5<0.001
Dyslipidemia3714111 (18.0)3603 (13.3)<0.001
TC (mmol/L)4.67 ± 1.124.67 ± 1.124.72 ± 1.130.277
HDL-Cl (mmol/L)1.40 ± 0.321.40 ± 0.321.37 ± 0.330.025
LDL-C (mmol/L)2.59 ± 0.902.60 ± 0.902.56 ± 0.920.285
TG (mmol/L)1.58 (1.11, 2.07)1.57 (1.11, 2.07)1.61 (1.12, 2.15)0.245
<65386172 (27.9)5196 (19.2)<0.001
>85232143 (23.2)5089 (18.8)0.007
Sleep quality
Good8050145 (23.5)7905 (29.2)0.002
Poor189887 (14.1)1811 (6.7)<0.001

Unless indicated otherwise, data are means ± standard deviations, medians (interquartile ranges) or frequencies (%). P values are from the Mann–Whitney U test (continuous variables) or Fisher’s exact test (categorical variables). Dyslipidemia: LDL-C ≥ 2.6 mmol/L, HDL-C < 1.0 mmol/L, TG ≥ 2.3 mmol/L, and/or concurrent use of lipid-regulating drugs.

BMI: body mass index; DM2: type 2 diabetes mellitus; FPG: fasting plasma sugar; TC: total cholesterol; HDL-C: high-density lipoprotein cholesterol; LDL-C: low-density lipoprotein cholesterol; TG: triglycerides.

Patients’ baseline characteristics in 2009 by presence of stroke (N = 27,712). Unless indicated otherwise, data are means ± standard deviations, medians (interquartile ranges) or frequencies (%). P values are from the Mann–Whitney U test (continuous variables) or Fisher’s exact test (categorical variables). Dyslipidemia: LDL-C ≥ 2.6 mmol/L, HDL-C < 1.0 mmol/L, TG ≥ 2.3 mmol/L, and/or concurrent use of lipid-regulating drugs. BMI: body mass index; DM2: type 2 diabetes mellitus; FPG: fasting plasma sugar; TC: total cholesterol; HDL-C: high-density lipoprotein cholesterol; LDL-C: low-density lipoprotein cholesterol; TG: triglycerides.

Sleep quality and sleep duration in relation with stroke

The cumulative incidence of stroke was 2.22% in participants who completed the study. Individuals with short sleep duration (<6 h/day) significantly increased risk of stroke compared with those with sleep duration 6–8 h/day (for all, RR: 1.63, 95% CI: 1.23–2.11, P < 0.001; for men, RR: 1.45, 95% CI: 1.19–1.73, P < 0.001; for women, RR: 1.77, (95% CI: 1.41–2.37, P < 0.00), after adjusting for confounding factors. Women had a slightly stronger relationship than men. Individuals with long sleep duration also increased risk of stroke compared with those with sleep duration 6–8 h (for all, RR: 1.40, 95% CI: 1.08–1.75, P < 0.01; for men, RR: 1.48, 95% CI: 1.02–1.57, P < 0.01; for women, RR; 1.23, 95% CI: 1.12–1.79, P < 0.01), after adjusting for confounding factors (Table 2). males had a slightly stronger relationship than females. The population-attributable risk of short and long sleep duration on risk of stroke was 0.35 and 0.23, respectively. Subjects with poor sleep quality greatly raised risk of stroke compared with those with good sleep quality (RR: 2.37, 95% CI: 1.52–3.41, P < 0.001). The subgroup analysis classified by gender found a similar association between men and women. The RRs were 2.65 (95% CI: 1.72–4.57, P < 0.01) for men and 2.13 (95% CI: 1.45–2.77, P < 0.01) for women after adjustment, the association was stronger in males than that in females. The population-attributable risk of poor sleep quality on risk of stroke was 0.39. There was no significant association between good sleep quality and stroke with normal sleep quality as reference (RR: 1.10, 95% CI: 0.95–1.40, P = 0.336) (see Table 2). Subgroup analysis classified by age showed only a significant association between sleep duration, sleep quality and stroke for participants aged >46 years (Tables 3 and 4).
Table 2

Risk ratios for the association between sleep quality, sleep duration, and stroke (N = 27,712).

VariablesStrokeNo strokeRR (95%CI)P
Sleep qualityGood145 (1.8%)78951
Common385 (2.2%)173911.10 (0.95–1.40)0.336
Poor87 (4.6%)18092.37 (1.52–3.41)<0.001
Sleep duration6–8 h302 (1.8%)168231
<6 h172 (3.2%)51901.63 (1.23–2.11)<0.001
>8 h143 (2.7%)50821.40 (1.08–1.75)<0.01

Adjusted for age, gender, marital status, current employment status, educational level, body mass index, cigarette use, alcohol intake, physical activity, type 2 diabetes mellitus, dyslipidemia, hypertension, heart disease, family history of type 2 diabetes mellitus, family history of hypertension, family history of stroke, fasting plasma sugar, and lipids. RR: risk ratio; CI: confidence interval.

Table 3

Risk ratios (95% confidence intervals) for stroke according to sleep quality by age.

agessleep qualityStrokeRR (95%CI)P
YesNo
18–35Good1015491
Common815440.72 (0.03–1.65)0.36
35–45Good3018501
Common3518051.05 (0.53–2.55)0.62
Poor167751.15 (0.38–6.84)0.4
46–55Good2214381
Common9243191.27 (0.81–2.29)0.24
Poor245272.58 (1.52–7.87)0.007
55–65Good4219311
Common16456281.24 (0.96–2.42)0.07
Poor345122.64 (1.15–4.75)<0.001
65–80Good3916291
Common8334310.96 (0.80–2.85)0.74
Poor181275.39 (2.15–8.42)<0.001

Adjusted for gender, marital status, current employment status, educational level, body mass index, cigarette use, alcohol intake, physical activity, type 2 diabetes mellitus, dyslipidemia, hypertension, heart disease, family history of type 2 diabetes mellitus, family history of hypertension, family history of stroke, fasting plasma sugar, and lipids.

RR: risk ratio; CI: confidence interval.

Table 4

Risk ratios (95% confidence intervals) for stroke according to sleep duration by age.

agessleep durationStrokeRR (95%CI)P
YesNo
18–356–8 h1120091
<6 h45651.15 (0.94–1.82)0.46
>8 h35191.01 (0.21–2.02)0.45
35–456–8 h5128671
<6 h187411.24 (1.01–3.05)0.002
>8 h128220.69 (0.45–1.54)0.57
46–556–8 h794050
<6 h2910991.25 (1.01–3.04)<0.001
>8 h3011651.24 (1.01–2.85)<0.001
55–656–8 h9946311
<6 h7315911.91 (1.12–3.63)<0.001
>8 h6818491.49 (1.16–2.67)<0.001
65–806–8 h6232661
<6 h4711941.81 (1.22–3.76)<0.001
>8 h317271.92 (1.23–5.00)<0.001

Adjusted for, gender, marital status, current employment status, educational level, body mass index, cigarette use, alcohol intake, physical activity, type 2 diabetes mellitus, dyslipidemia, hypertension, heart disease, family history of type 2 diabetes mellitus, family history of hypertension, family history of stroke, fasting plasma sugar, and lipids.

RR: risk ratio; CI: confidence interval.

Risk ratios for the association between sleep quality, sleep duration, and stroke (N = 27,712). Adjusted for age, gender, marital status, current employment status, educational level, body mass index, cigarette use, alcohol intake, physical activity, type 2 diabetes mellitus, dyslipidemia, hypertension, heart disease, family history of type 2 diabetes mellitus, family history of hypertension, family history of stroke, fasting plasma sugar, and lipids. RR: risk ratio; CI: confidence interval. Risk ratios (95% confidence intervals) for stroke according to sleep quality by age. Adjusted for gender, marital status, current employment status, educational level, body mass index, cigarette use, alcohol intake, physical activity, type 2 diabetes mellitus, dyslipidemia, hypertension, heart disease, family history of type 2 diabetes mellitus, family history of hypertension, family history of stroke, fasting plasma sugar, and lipids. RR: risk ratio; CI: confidence interval. Risk ratios (95% confidence intervals) for stroke according to sleep duration by age. Adjusted for, gender, marital status, current employment status, educational level, body mass index, cigarette use, alcohol intake, physical activity, type 2 diabetes mellitus, dyslipidemia, hypertension, heart disease, family history of type 2 diabetes mellitus, family history of hypertension, family history of stroke, fasting plasma sugar, and lipids. RR: risk ratio; CI: confidence interval.

Sleep quality interacted with sleep duration on risk of stroke

The results from the multiple logistic regression models were showed in Table 5. Individuals with poor sleep quality combined short sleep duration significantly increased risk of stroke compared with those with good sleep quality combined sleep duration 6–8 h (RR: 1.39, 95% CI: 1.13–1.70 and RR: 1.35, 95% CI: 1.09–1.67, respectively, P < 0.001).
Table 5

Risk ratios for the association between sleep quality and stroke by sleep duration.

Sleep durationSleep qualitystrokeNo strokeRR (95%CI)P
6–8 hGood10563071
Common16894091.00 (0.92–1.30)0.210
Poor2910711.39 (1.13–1.70)<0.001
<6 hGood2610061.35 (1.09–1.67)<0.001
Common11339351.55 (1.24–1.83)<0.001
Poor322496.75 (2.45–14.12)<0.001
>8 hGood145821.23 (0. 95–1.34)0.257
Common10440111.37 (1.10–1.73)<0.001
Poor264892.77 (1.41–7.99)<0.001

Adjusted for age, gender, marital status, current employment status, educational level, body mass index, cigarette use, alcohol intake, physical activity, type 2 diabetes mellitus, dyslipidemia, hypertension, heart disease, family history of type 2 diabetes mellitus, family history of hypertension, family history of stroke, fasting plasma sugar, and lipids. RR: risk ratio; CI: confidence interval.

Risk ratios for the association between sleep quality and stroke by sleep duration. Adjusted for age, gender, marital status, current employment status, educational level, body mass index, cigarette use, alcohol intake, physical activity, type 2 diabetes mellitus, dyslipidemia, hypertension, heart disease, family history of type 2 diabetes mellitus, family history of hypertension, family history of stroke, fasting plasma sugar, and lipids. RR: risk ratio; CI: confidence interval. The risk of stroke was greatest in those with poor sleep quality combined short sleep duration (RR: 6.75, 95% CI: 2.45–14.12, P < 0.001). In addition, subjects with long sleep duration and good sleep quality had no increased risk of stroke compared with those who had good sleep quality and sleep duration of 6–8 h (RR: 1.23, 95% CI: 0.95–1.34, P = 0. 257). Those with both poor sleep quality and long sleep duration had higher risk of being stroke (RR: 2.77, 95% CI: 1.41–7.99, P < 0.001) compared with those with sleep duration of 6–8 h.

Sensitivity analysis

There was a strong additive interaction between sleep quality and sleep duration on stroke, with 72% of stroke events attributed to the interaction between poor sleep quality and short sleep duration and 35% attributed to the interaction between poor sleep quality and long sleep duration(Table 6).
Table 6

Estimates of the biological interaction between sleep quality and sleep duration for stroke.

Measures of biological interactionEstimate (95% CI)
Poor sleep quality versus sleep duration <6 h
RERI5.54 (3.75–8.12)
AP0.72 (0.56–0.80)
S5.69 (4.23–9.90)
Poor sleep quality versus sleep duration >8 h
RERI1.12 (1.01–1.27)
AP0.35 (0.26–0.51)
S2.05 (1.57–2.96)

Reference group is good sleep quality and 6–8 h sleep duration. RERI: relative excess risk due to interaction; AP: attributable proportion due to interaction; S: synergy index; CI: confidence interval.

Estimates of the biological interaction between sleep quality and sleep duration for stroke. Reference group is good sleep quality and 6–8 h sleep duration. RERI: relative excess risk due to interaction; AP: attributable proportion due to interaction; S: synergy index; CI: confidence interval.

Discussion

Our study showed that poor sleep quality and sleep duration (<6 h/d or >8 h/d) increased the risk of being stroke independent of the potential confounders in a Chinese population. This association was only found in participants aged >45 years, not in those aged 18–45 years. Sex differences showed that women had a slightly stronger relationship between sleep duration of <6 h/d and stroke than men, while men had a slightly stronger relationship between. In addition, there was also an interactive effect of long sleep duration and poor sleep quality on stroke. The findings suggest that sleep quality and quantity should be included in the evaluation of stroke risks and development of prevention methods and interventions. Many studies indicated that both short and long sleep duration increased risk of stroke[7,26-29], consistent with our study. Eguchi et al. conducted a multivariable Cox regression analysis with 1,268 hypertensive patients and found that sleep duration less than 7.5 h/d was independently associated with stroke risk (hazard ratio = 2.21; P = 0.003)[26]. One systematic review analyzed with 474,684 participants from 15 studies (24 cohort samples) and suggested that short sleep duration was positively related with risk of developing stroke (relative risk: 1.15, 95% CI: 1.00–1.31, P = 0.047)[27]. A 8-year cohort study including 23,620 participants found that risk of stroke increased 2.06 times (95% CI: 1.18–3.59) in those with sleep duration <6 h/d compared with those with duration 7-8 h/d[28]. A meta-analysis by Ge and Guo with 12 cohort studies reported a hazard ratio for stroke risk of 1.13 (95% CI: 1.02–1.25) in individuals having short sleep duration[7]. Results from a meta-analysis included six cross-sectional studies showed an pooled odds ratio of 1.71 (95% CI: 1.39–2.02) for individuals with short sleep duration developing stroke[7]. Li et al. reported a pooled relative risks by 7% per hour of sleep reduction for stroke events were among individuals having sleep duration <7 h/d[29]. Furthermore, our findings showed a U- shaped association between sleep duration and risk of stroke, consistent with previous report[30]. However, there was difference by sex and age. The risk of being stroke seemed slightly higher in female with short sleep duration, and in male with long sleep duration. Both short and long sleep duration were associated with stroke in participants aged 46-80 years, while this association was not found younger ones, consistent with a 10-year cohort study report[31]. The results suggest that flexibility to insufficient sleep or vulnerability to prolonged sleep as risk factors for stroke may differ by age. Our study also found risk of stroke in relation with poor sleep quality, and men had a slightly stronger relationship than women. Zhang et al. Reported[14] an odds ratio of 1.811 (95% CI: 1.116–2.939) for being stroke among poor-quality sleepers aged 18–45 years compared with good-quality sleepers. Conversely we found the association only occurring in the age over 46 years, which may be partly due to higher risk of carotid intima-media thickness in relation with poor sleep quality in stroke-free individuals aged ≥40 years[32]. Short sleep duration may increase cortisol levels via activation of sympathetic activity and hypothalamic–pituitary–adrenal axis[33,34], which can further result in hypertension and harm brain tissue, and accelerate the development of stroke. Short sleep duration also results in insulin resistance, which alters vascular endothelial function, causes abnormal fibrinolysis and systemic inflammation, and elevates high-sensitivity C-reactive protein levelsand hypercoagulability[35-38], which tends to promote atherosclerosis and subsequent stroke[35,39,40]. Poor sleep quality is related to impaired glucose tolerance and insulin sensitivity, and increased interleukin 6 level, and plasma concentration[41-43], which increases the risk of stroke. Consistent with previous reports, the current study showed an association between stroke and long sleep duration. Cappuccio and colleagues systematically analyzed 15 studies including 474,684 participants and had a result of positive relationship between long sleep durationand risk of stroke with odds ratio of 1.65 (95% CI: 1.45–1.87, P < 0.0001)[26]. A 10-year cohort study including 7,844 adults showed a greater risk of stroke in persons with sleep duration >8 h per night than those with duration of 6–8 h per night (relative risk: 1.5, 95% CI: 1.1–2.0)[31] A 7.5-year prospective study found a positive association between long sleep duration and ischemic stroke in 93,175 women aged 50–79 years[44]. Similar results were also reported by a prospective study including 9,692 stroke-free participants aged 42–81 years long sleep duration was significantly associated with an increased risk of stroke with a hazard ratio of 1.46(95% CI: 1.08–1.98) for being stroke in long-time sleepers[45]. Meta-analyzed results from the 12 cohort and 6 cross-sectional studies showed t a hazard ratio of 1·40(95% CI: 1.16–1.64) and odds ratio of 2.12 (95% CI: 1.51–2.73), respectively, for risk of stroke in individuals with long sleep duration[7]. Another meta-analysis of 11 studies showed a pooled relative risk of increased 17% per hour of sleep increment in those having sleep duration >7 h/d compared with those with 7 h/d[29]. Sleep duration more than 8 hour is reported association with elevated blood C-reactive protein, interleukin 6, fibrinogen, and total leukocyte numbers, and decreased albumin levels, compared with sleep duration of 6–8 h[46-49]. Increases in inflammatory markers can damage blood sugar stability and β-cell function, leading to insulin resistance and the development of stroke. Taken together, the evidence shows that long sleep duration increases inflammatory cytokines and insulin resistance, and poor sleep quality also increases inflammatory cytokines and decreases insulin sensitivity; these factors all increase stroke risk. Some main traditional modifiable risk factors are prevalent in China. For example, the incidence of hypertension is as high as 32.5%[50], the incidence of diabetes is 11.6%[51], and the prevalence of smoking is 28.3%[52]. As a relatively new modifiable risk factor, the prevalence of sleep disorders is 41.5%[33]. Therefore, the government and general practitioners should seriously consider both traditional and new modifiable risk factors in the development of stroke prevention methods and interventions. Given the difficulties of screening and treating stroke patients, recommendations to improve sleep quality and sleep duration are inexpensive and practical means of decreasing risk of stroke. Our study has some limitations. Firstly, information on sleep quality and duration was self-reported, information bias may be inevitable. Secondly, we did not include clinical diagnoses for sleep disorders. Thirdly, other confounders associated with sleep disorders, such as depression and general health[53], were not measured. Fourthly, our findings were derived from Chinese subjects which may not be generalized to other ethnic populations. Fifthly, lost-to-follow-up participants were older, and had poor sleep quality and short or long sleep duration, which may reduce the strength of the associations. Sixth, recreational drug use was not collected, which might be small affect on the relationship of sleep quality and stroke. In summary, poor sleep quality and short/long sleep duration increase the risk of being stroke. Moreover, there is an interactive effect of poor sleep quality and short sleep duration on increased risk of stroke. As inappropriate sleep duration and poor sleep quality are common in Chinese adults, appropriate identification and treatment of sleep disturbances is very important to prevent the development of stroke. In the further, We would analyze the association between the specific sleep disorders, sleep patterns, environmental, behavioral and medical comorbid risk factors and stroke, and added the evidence of the relationship between sleep and stroke.

Ethics approval and consent to participate

The study protocol was approved by the Xuzhou Center for Disease Control and Prevention, and conducted in accordance with the principles of the Declaration of Helsinki (1975, revised 2000). All participants provided written informed consent.
  46 in total

Review 1.  Short and long sleep durations are both associated with increased risk of stroke: a meta-analysis of observational studies.

Authors:  Beihai Ge; Xiaomei Guo
Journal:  Int J Stroke       Date:  2014-11-03       Impact factor: 5.266

Review 2.  Correlation between Sleep Duration and Risk of Stroke.

Authors:  Sazal Patyar; Rakesh Raman Patyar
Journal:  J Stroke Cerebrovasc Dis       Date:  2015-03-25       Impact factor: 2.136

3.  Increased Stroke Burdens Among the Low-Income Young and Middle Aged in Rural China.

Authors:  Xianjia Ning; Jian Sun; Rongcai Jiang; Hongyan Lu; Lingling Bai; Min Shi; Jun Tu; Yanan Wu; Jinghua Wang; Jianning Zhang
Journal:  Stroke       Date:  2016-12-06       Impact factor: 7.914

4.  Self-reported sleep duration in relation to incident stroke symptoms: nuances by body mass and race from the REGARDS study.

Authors:  Megan E Ruiter Petrov; Abraham J Letter; Virginia J Howard; Dawn Kleindorfer
Journal:  J Stroke Cerebrovasc Dis       Date:  2013-10-08       Impact factor: 2.136

5.  Prevalence, Incidence, and Mortality of Stroke in China: Results from a Nationwide Population-Based Survey of 480 687 Adults.

Authors:  Wenzhi Wang; Bin Jiang; Haixin Sun; Xiaojuan Ru; Dongling Sun; Linhong Wang; Limin Wang; Yong Jiang; Yichong Li; Yilong Wang; Zhenghong Chen; Shengping Wu; Yazhuo Zhang; David Wang; Yongjun Wang; Valery L Feigin
Journal:  Circulation       Date:  2017-01-04       Impact factor: 29.690

Review 6.  Sleep and Stroke.

Authors:  Kimberly Nicole Mims; Douglas Kirsch
Journal:  Sleep Med Clin       Date:  2016-01-09

7.  Sleep characteristics and cardiovascular events in a large Swedish cohort.

Authors:  Anna Westerlund; Rino Bellocco; Johan Sundström; Hans-Olov Adami; Torbjörn Åkerstedt; Ylva Trolle Lagerros
Journal:  Eur J Epidemiol       Date:  2013-04-04       Impact factor: 8.082

Review 8.  Traditional Risk Factors for Stroke in East Asia.

Authors:  Young Dae Kim; Yo Han Jung; Gustavo Saposnik
Journal:  J Stroke       Date:  2016-09-30       Impact factor: 6.967

Review 9.  Global and regional burden of stroke during 1990-2010: findings from the Global Burden of Disease Study 2010.

Authors:  Valery L Feigin; Mohammad H Forouzanfar; Rita Krishnamurthi; George A Mensah; Myles Connor; Derrick A Bennett; Andrew E Moran; Ralph L Sacco; Laurie Anderson; Thomas Truelsen; Martin O'Donnell; Narayanaswamy Venketasubramanian; Suzanne Barker-Collo; Carlene M M Lawes; Wenzhi Wang; Yukito Shinohara; Emma Witt; Majid Ezzati; Mohsen Naghavi; Christopher Murray
Journal:  Lancet       Date:  2014-01-18       Impact factor: 79.321

10.  Sleep duration and risk of incident stroke by age, sex, and race: The REGARDS study.

Authors:  Megan E Petrov; George Howard; Michael A Grandner; Dawn Kleindorfer; Jennifer R Molano; Virginia J Howard
Journal:  Neurology       Date:  2018-10-03       Impact factor: 11.800

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  11 in total

1.  The independent and combined association of napping and night sleep duration with stroke in Chinese rural adults.

Authors:  Jing Yang; Xiaotian Liu; Zhihan Zhai; Wei Liao; Yaling He; Xueyan Wu; Chongjian Wang; Chunyang Sun; Yuqian Li
Journal:  Sleep Breath       Date:  2022-04-25       Impact factor: 2.816

2.  Relationship Between Sleep Duration and Stroke History in Middle-Aged and Elderly in Guiyang: A Cross-Sectional Survey.

Authors:  Li Liu; Jingyuan Yang; Junhua Wang; Meng Nie; Ziyun Wang; Han Guan; Jin Hu; Feng Hong
Journal:  Neuropsychiatr Dis Treat       Date:  2022-02-11       Impact factor: 2.570

Review 3.  Sleep and Stroke: Opening Our Eyes to Current Knowledge of a Key Relationship.

Authors:  Valerio Brunetti; Eleonora Rollo; Aldobrando Broccolini; Giovanni Frisullo; Irene Scala; Giacomo Della Marca
Journal:  Curr Neurol Neurosci Rep       Date:  2022-10-03       Impact factor: 6.030

4.  Self-Reported Sleep Characteristics Associated with Cardiovascular Disease Among Older Adults Living in Rural Eastern China: A Population-Based Study.

Authors:  Yu Qin; Rui Liu; Yongxiang Wang; Jiyou Tang; Lin Cong; Juan Ren; Shi Tang; Yifeng Du
Journal:  Clin Interv Aging       Date:  2022-05-18       Impact factor: 3.829

5.  The Relationship between Sleep Duration and Stroke Risk: The Mediating Role of Physical Activity.

Authors:  Xingyue Liu; Juhua Zhang; Yanmei Wang; Changlian Lu; Xuefeng Gu; Guoqing Wan; Peng Zhang
Journal:  Brain Sci       Date:  2022-05-05

6.  Factors associated with stroke among patients with type 2 diabetes mellitus in China: a propensity score matched study.

Authors:  Chenlu He; Wei Wang; Qian Chen; Ziyuan Shen; Enchun Pan; Zhongming Sun; Peian Lou; Xunbao Zhang
Journal:  Acta Diabetol       Date:  2021-06-14       Impact factor: 4.280

7.  Pooled incidence and case-fatality of acute stroke in Mainland China, Hong Kong, and Macao: A systematic review and meta-analysis.

Authors:  Fan He; Irene Blackberry; Liqing Yao; Haiyan Xie; Tshepo Rasekaba; George Mnatzaganian
Journal:  PLoS One       Date:  2022-06-27       Impact factor: 3.752

8.  Sleep duration, daytime napping, and risk of incident stroke: Nuances by metabolic syndrome from the China health and retirement longitudinal study.

Authors:  Yuanyuan Fang; Yuqin He; Yanzhu Huang; Lusen Ran; Wenhui Song; Jiahuan Hao; Di Yao; Rong Li; Dengji Pan; Tingting Qin; Minghuan Wang
Journal:  Front Cardiovasc Med       Date:  2022-09-02

9.  Sleep duration and risk of cardio-cerebrovascular disease: A dose-response meta-analysis of cohort studies comprising 3.8 million participants.

Authors:  Yi-Ming Huang; Wei Xia; Yi-Jun Ge; Jia-Hui Hou; Lan Tan; Wei Xu; Chen-Chen Tan
Journal:  Front Cardiovasc Med       Date:  2022-09-27

10.  Sleep disorders and acute stroke: profile and research opportunities.

Authors:  Xiang Fu; Shou-Jiang You; Jie Li; Chun-Feng Liu
Journal:  Chin Med J (Engl)       Date:  2021-02-23       Impact factor: 2.628

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