CC BY-NC-ND 4.0 · Sleep Sci 2018; 11(04): 217-230
DOI: 10.5935/1984-0063.20180036
ORIGINAL ARTICLE

Sleep duration, lifestyles and chronic diseases: a cross-sectional population-based study

Cátia Reis
1   Faculdade de Medicina, Universidade de Lisboa, Lisboa, Portugal, Instituto de Saúde Ambiental (ISAMB) - Lisboa - Lisboa - Portugal.
2   CENC - Sleep Medicine Center, Sleep and circadian rhythms - Lisboa - Lisboa - Portugal.
,
Sara Dias
3   EpiDoC Unit, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Centro de Estudos de Doenças Crónicas (CEDOC) - Lisboa - Lisboa - Portugal.
6   EpiSaúde, Associação Científica -Évora - Évora - Portugal.
7   Escola Superior de Saúde do Instituto Politécnico de Leiria, CiTechCare, Center for innovative care and health technology - Leiria - Leiria - Portugal.
,
Ana Maria Rodrigues
3   EpiDoC Unit, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Centro de Estudos de Doenças Crónicas (CEDOC) - Lisboa - Lisboa - Portugal.
4   Sociedade Portuguesa de Reumatologia, Sociedade Portuguesa de Reumatologia - Lisboa - Lisboa - Portugal.
5   Instituto de Medicina Molecular, Rheumatology Research Unit - Lisboa - Lisboa - Portugal.
6   EpiSaúde, Associação Científica -Évora - Évora - Portugal.
,
Rute Dinis Sousa
3   EpiDoC Unit, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Centro de Estudos de Doenças Crónicas (CEDOC) - Lisboa - Lisboa - Portugal.
6   EpiSaúde, Associação Científica -Évora - Évora - Portugal.
,
Maria João Gregório
3   EpiDoC Unit, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Centro de Estudos de Doenças Crónicas (CEDOC) - Lisboa - Lisboa - Portugal.
8   Direção-Geral da Saúde, Programa Nacional para a Promoção da Alimentação Saudável - Lisboa - Lisboa - Portugal.
9   Universidade do Porto, Faculdade de Ciências da Nutrição e Alimentação - Porto - Porto - Portugal.
,
Jaime Branco
3   EpiDoC Unit, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Centro de Estudos de Doenças Crónicas (CEDOC) - Lisboa - Lisboa - Portugal.
4   Sociedade Portuguesa de Reumatologia, Sociedade Portuguesa de Reumatologia - Lisboa - Lisboa - Portugal.
10   Centro Hospitalar Lisboa Ocidental (CHLO- E.P.E.), Serviço de Reumatologia do Hospital Egas Moniz - Lisboa - Lisboa - Portugal.
,
Helena Canhão
3   EpiDoC Unit, NOVA Medical School, Universidade Nova de Lisboa (NMS/UNL), Centro de Estudos de Doenças Crónicas (CEDOC) - Lisboa - Lisboa - Portugal.
4   Sociedade Portuguesa de Reumatologia, Sociedade Portuguesa de Reumatologia - Lisboa - Lisboa - Portugal.
6   EpiSaúde, Associação Científica -Évora - Évora - Portugal.
,
Teresa Paiva
2   CENC - Sleep Medicine Center, Sleep and circadian rhythms - Lisboa - Lisboa - Portugal.
› Author Affiliations
 

BACKGROUND Adequate sleep is essential for health. Both, short and long sleep durations are associated to worse quality of life and poor health outcomes. Portugal represents a specific population model, since according to European statistics it has high rates of chronic diseases like depression, hypertension, diabetes and stroke; and low quality of life as well as low index of physical activity, while in parallel it has some other good health indicators such as: low age-standardized mortality for both genders, nutrition in terms of energy and fruit consumption, smoking and alcohol, obesity and overweight prevalence. The aim of this study was to characterize health and chronic diseases, lifestyles and quality of life in subjects with short and long sleep duration.

Methods A population-based cross-sectional evaluation of the third wave of follow-up of the EpiDoC Cohort was carried between 2015-2016. A sample of 5,436 adults ≥18 years, representative of the national population, self-reported their daily total sleep time. Associations between short sleep duration (SSD ≤5h), long sleep duration (LSD≥9h) and independent variables were determined.

Results The prevalence for SSD was high (20.7%) and the LSD (5.9%) was low. Being older, with lower education, retired and unemployed were associated to SSD and LSD (p<0.01). Being obese was associated to SSD as well as hypertension, gastrointestinal disease and hypercholesterolemia (p<0.01). SSD and LSD, were associated with diabetes (p<0.01 and p=0.03) and depression (p<0.01 and p=0.02) respectively. Cardiovascular disease (p<0.01) was associated to LSD. Multimorbidity (p<0.01) was associated to SSD. Worse quality of life and bad physical function were associated to SSD and LSD, as well as being hospitalized in the previous 12 months (p<0.01).

Conclusions Socio-demographic, physical activity and chronic diseases were associated to reduction and extension of sleep duration. There was no association between rheumatic diseases and cancer with sleep duration, as found in other studies. This study emphasizes the burden of self-reported SSD for Portugal, its consequences to health and the need to increase sleep awareness campaigns enhancing the importance of sleep in health. Furthermore, it emphasizes that chronic diseases risks are dependent on multiple parameters which varying in different countries or regions, imply the need of regional studies and interventions.


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INTRODUCTION

Sleep is an active process providing daily restoration due to production of the fundamental anabolic hormones, involved in cellular growth and regeneration such as: growth hormone, testosterone, prolactin, etc.[1]. Sleep represents an essential element for health and well-being, including cognitive performance, physiological processes, emotion regulation, physical development, and quality of life[2].

Optimal sleep duration is a question often posed to sleep specialists, although it varies significantly between individuals, age, gender[2], and world region[3]. The value established for short sleep duration in adults has been sometimes controversial, but a National study in the United States of America (USA)[4] and other one in Brazil[5] point out to ≤6 hours, or by the recent values established by the National Sleep Foundation ≤5 hours[2]. The value established for long sleep is much more consensual, ≥9 hours[2] , [6]. Insufficient sleep is well recognized and declared as a “public health problem” by the Center of Disease and Control in the United States, and has high economic impact on a country's economy[7]. It has been demonstrated unequivocally that duration, timing, and quality of sleep critically affect physical and mental health, performance and safety[8].

Short and long sleep duration are positively associated with chronic diseases like obesity, type 2 diabetes, hypertension, and cardiovascular disease among adults[6] , [9] Several studies suggest that short sleep duration is associated with poor general health[10] , [11]. This association is less evident for the relationship between longer sleep duration and adverse health status: only a few studies associate poorer general health or increased risk/presence of disease with ≥9 hours of sleep[12]. Evidence between association to long sleep and poor health was only clear for mortality risk, showing a U-shaped relationship[12]. In a recent longitudinal study from a Swedish cohort this U-shaped relationship was also observed with mortality and age: among younger individuals (≤65 years) there was an increased mortality rate and a subsequent decrease in life expectancy. In older individuals (≥65 years) this association was not detected[13].

Culture, socioeconomic status and environment have an important influence on sleep duration. In a large twin study, authors determined the relative importance of environmental contributions associated to sleep duration and body mass index (BMI), accounting for genetics and shared environment. They support the environmental hypothesis that voluntary changes to usual sleep duration influence BMI independently of familial factors[14]

Eurostat data indicate that Portugal (PT) is the EU-28 country with higher rates of chronic depression and diabetes, 2nd rank in reported prescribed medicines, and in 7th rank for hypertension[15]; but the relationship to these high prevalent chronic conditions, consumptions and sleep, were not yet evaluated.

There are two possible conditions for having short sleep duration: insomnia or sleep deprivation. Since the prevalence for insomnia in PT is approximately the same as in other countries[16] , [17] the other option might be sleep deprivation.

The aim of this population-based study was to characterize health and chronic diseases, lifestyles and quality of life in subjects with disturbances in short and long sleep duration.


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METHODS

Study population

This study is a cross-sectional evaluation of the third wave of follow-up of the EpiDoC Cohort (i.e., the EpiDoC3 study). EpiDoc3 participants who answer the “hours of sleep per day” question, were included in the current analysis. EpiDoC cohort was designed to study health determinants and outcomes, chronic non-communicable diseases and their impact in health resources consumption. The EpiDoC cohort enrolled 10,661 adults living in PT (mainland and the archipelagos of Azores and Madeira). EpiDoC sample size calculation was performed to capture health related conditions whose prevalence were of 0.5% as described elsewhere[18] , [19]. The study included non-institutionalized adults (≥18 years old) living in private homes in the Portuguese mainland and archipelagos (Madeira and Azores). The study sample was stratified by administrative territorial units [(NUTSII) (Norte, Centro, Lisboa & Vale do Tejo, Alentejo, Algarve, Açores archipelago (Azores) and Madeira archipelago (Madeira)], and the size of the population within each locality (<2,000; 2,000-9,999; 10,000-19,999; 20,000-99,999; and ≥100,000 inhabitants, respectively). Detailed methodology has been published[18]. EpiDoC3 study included 5,653 adult participants ([Figure 1]), of whom 5,436 reported their daily total sleep time. Data collection was performed from September 2015 to July 2016 by a trained research assistant team who randomly called all individuals by telephone.

Zoom Image
Figure 1 Flowchart of the study.

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EpiDoC cohort measurements

Sociodemographic and socioeconomic characteristics

Information regarding sociodemographic factors (sex, age, ethnicity, years of education, marital status, household composition, Nomenclature of Territorial Units for Statistics [NUTS]II region), as well as socioeconomic variables (employment status), were collected in the EpiDoC1 study. During the EpiDoC3 interview, subjects were asked whether any of these characteristics had changed. The variable age was also categorized as <65 years and ≥65 years of age, since there are important changes in sleep duration and architecture during the life span and after retirement[2] , [13].


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Lifestyle characteristics

The daily total sleep time was assessed by the question “On average, how many hours do you sleep per day?” and the sleep categories were established as short sleep duration (SSD) (≤5h), normal sleep duration (NSD) (>5h and <9h) and long sleep duration (LSD) (≥9h), according to the National Sleep Foundation[2].

Self-reported height and weight were collected. Based on these data, body mass index (BMI; weight/height[2] in kg/m2) was calculated and categorized according to the World Health Organization (WHO) classification system[20] EpiDoC3 study included several questions concerning lifestyle habits, such as frequency of alcohol intake (never, daily, occasionally), smoking habits (current smoker, past smoker and never smoked), physical activity and dietary habits. Physical activity level was classified according to self-reported weekly frequency of physical activity and categorized by active or inactive. For the time watching TV a categorical variable was used (<5 hours/day or ≥5 hours/day). For the dietary intake, a proxy of healthy diet was assessed by calculating the adherence to the Mediterranean diet through the PREDIMED score[21].


#

Health characteristics and healthcare consumption and costs

In EpiDoC3 study, individuals were asked whether they had been previously diagnosed with the following chronic diseases: hypercholesterolemia, hypertension, rheumatic disease, allergy, gastrointestinal disease, cardiac disease, diabetes, pulmonary disease, cancer, or neurologic disease, depression and anxiety. Multimorbidity was defined as the coexistence of two or more of these self-reported chronic diseases[22]. Health-related quality of life was assessed using the European Quality of Life questionnaire with five dimensions and three levels (EQ-5D-3L)[23] , [24], for which a higher score corresponds to a higher quality of life. Physical function was evaluated using the Health Assessment Questionnaire (HAQ; ranging from 0 to 3, with higher scores representing worse functional ability)[25].

We used Portuguese validated versions of the assessment scales. Number of hospitalizations were also assessed.


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Statistical analysis

To verify the representativeness of the sample according to the Portuguese population (mainland and islands), we first compared the participants and non-participants of EpiDoC3 study with respect to their sociodemographic, socioeconomic, and health status characteristics. Based on this comparison, we adjusted the weights according to stratification by NUTSII region, sex, and age group. Extrapolation weights were computed and used in the subsequent statistical analysis. These were obtained by calibrating the extrapolation weights originally designed for the EpiDoC1 study sample.

Baseline characteristics of the study cohort were described according to the three categories of reported sleep duration: SSD (≤5h), NSD (>5h and <9h) and LSD (≥9h).

Absolute frequencies and weighted proportions were used to summarize categorical variables. Continuous variables were described by weighted mean values and standard deviations. Differences in baseline variables across categories of reported sleep duration were statistically assessed using the Student t-test for continuous variables and the Chi-square test for categorical variables. For the post-hoc comparisons between groups the Sheffé's method was used. Logistic regression was used to computed odds ratio (OR) and respective 95% confidence intervals (95% CI) to quantify the association between explanatory variable and sleep duration SSD and LSD. Crude and gender, age (<65 years vs ≥65 years), NUTSII and educational level adjusted OR were estimated. All analyses were weighted and performed using STATA IC v.12 (StataCorp. 2011. Stata Statistical Software: Release 12. College Station, TX: StataCorp LP).


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Ethical issues and personal protection

Details of ethical issues of the EpiDoC1 (EpiReumaPt) study were described elsewhere[18] , [19] , [26]. The study was reviewed and approved by the National Committee for Data Protection (Comissão Nacional de Proteção de Dados) and by NOVA Medical School Ethics Committee. Informed consent was obtained from all individual participants included in all phases of the study.

EpiDoC3 was also approved by the National Committee for Data Protection (in accordance with the Portuguese law number 67/98, October 26th, regarding protection of personal data) and by the same Ethics Committee as EpiDoC1. The study was conducted in accordance with the applicable laws and regulations including, but not limited to, the Guidelines for Good Clinical Practice and the ethical principles stated in the Declaration of Helsinki[27]. Participants' confidentiality was safeguarded by the absence of identifiers in the database (only a unique identification code was used for each participant). The name and contact information for each subject were stored separately from the study data transmitted to the coordinating center (based at the headquarters of the Portuguese Society of Rheumatology). All data were kept anonymously and secured by authorized EpiDoC staff.


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RESULTS

In total, 5,436 participants reported their daily total sleep time. Participants' mean age was 56.7±16.4 years old and 3,473 (52.7%) were females. For the adult Portuguese population, self-reported SSD prevalence was 20.7%, and LSD prevalence was 5.9%. For the Portuguese country distribution, the region with a higher prevalence value of reported SSD was the Algarve (south of PT) (26.5%), while the Atlantic Islands of Azores have the lowest value (16.4%), and the higher prevalence of LSD (10.2%). Lisbon was the region with a higher prevalence value of normal sleep duration (75.8%). Participants with reported SSD (≤5h) were older (≥65), most frequently women, with lower education level, widowed and retired, unemployed or in a temporary work. The same pattern was found for reported LSD (≥9) ([Table 1]).

Table 1

Baseline characteristics by categories of short (≤5 h/day) and long (≥9h/day) sleep duration, having as reference group the normal sleep duration (6-8 h/day) for the Portuguese population.

 

 

 

 

 

Post-hoc comparisons (Sheffé's method)

 

 

 

 

 

Short*Normal

Short*Long

Normal*Long

Characteristic

Short sleep duration (≤ 5 h/day)

Normal sleep duration (6-8 h/day)

Long sleep duration (≥9h/day)

p-value a

p-value

p-value

p-value

N (%)

1337 (20.7)

3693 (73.4)

406 (5.9)

 

 

 

 

Sex, N (%)

 

 

 

 

 

 

 

Male

411 (19.4)

1401 (75.0)

151 (5.7)

0.2514

___

___

___

Female

926 (22.0)

2292 (71.9)

255 (6.1)

 

___

___

___

Age, mean ± (SD)

58.5 (17.2)

46.1 (16.5)

56.3 (22.9)

<0.0001

<0.0001

___

<0.0001

Age groups, N (%)

 

 

 

 

 

 

 

< 65 years

717 (15.8)

2704 (79.7)

199 (4.5)

<0.0001

<0.0001

<0.0001

<0.001

≥ 65 years

620 (36.4)

989 (53.2)

207 (10.4)

 

<0.0001

<0.0001

<0.0001

NUTS II region, N (%)

 

 

 

 

 

 

 

North

404 (20.3)

1080 (73.7)

120 (6.0)

0.1802

___

___

___

Centre

260 (20.9)

688 (72.1)

91 (7.0)

 

___

___

___

Lisbon

244 (20.3)

798 (75.8)

53 (3.9)

 

___

___

___

Alentejo

75 (21.8)

208 (70.7)

28 (7.5)

 

___

___

___

Algarve

57 (26.5)

109 (66.0)

8 (7.5)

 

___

___

___

Azores

130 (16.4)

430 (73.4)

76 (10.2)

 

___

___

___

Madeira

167 (21.5)

380 (74.2)

30 (4.3)

 

___

___

___

BMI, mean ± (SD)

27.0 (4.7)

25.5 (4.2)

26.2 (5.5)

<0.0001

<0.0001

___

<0.0001

Education level, N (%)

 

 

 

 

 

 

 

> 12 years

142 (11.0)

870 (86.7)

30 (2.4)

<0.0001

<0.0001

<0.0001

<0.0001

10-12 years

164 (13.9)

801 (80.7)

66 (5.4)

 

<0.0001

<0.001

___

5-9 years

263 (20.1)

767 (75.1)

64 (4.8)

 

___

___

<0.05

0-4 years

756 (34.7)

1244 (55.7)

239 (9.7)

 

<0.0001

<0.0001

<0.0001

Marital status, N (%)

 

 

 

 

 

 

 

Single

134 (9.6)

713 (85.1)

57 (5.3)

<0.0001

<0.0001

<0.001

___

Married

833 (23.9)

2267 (70.3)

235 (5.7)

 

___

___

___

Divorced

86 (26.9)

266 (66.7)

28 (6.4)

 

___

___

___

Widowed

250 (39.5)

319 (51.0)

72 (9.5)

 

<0.0001

<0.0001

<0.001

Consensual union

34 (15.2)

126 (80.5)

12 (4.3)

 

___

___

___

Employment status, N (%)

 

 

 

 

 

 

 

Employed full-time/part-time/ domestic

 

 

 

 

 

 

 

1023 (21.0)

 

 

 

 

 

 

 

2978 (73.5)

 

 

 

 

 

 

 

311 (5.6)

0.3085

___

___

___

 

 

 

Retired/unemployed/ temporary work

 

 

 

 

 

 

 

311 (19.4)

 

 

 

 

 

 

 

710 (73.2)

 

 

 

 

 

 

 

95 (7.3)

 

___

___

___

 

 

 

Alcohol intake, N (%)

 

 

 

 

 

 

 

Daily

371 (23.9)

1058 (70.8)

113 (5.3)

<0.0001

<0.0001

<0.001

<0.01

Occasionally

389 (16.0)

1487 (79.0)

115 (5.0)

 

___

___

___

Never

573 (23.7)

1142 (68.6)

176 (7.7)

 

<0.0001

<0.001

<0.01

Smoking habits, N (%)

 

 

 

 

 

 

 

Current smoker

157 (14.0)

654 (81.0)

58 (5.0)

0.0003

<0.05

___

___

Past smoker

276 (21.5)

764 (72.1)

93 (6.4)

 

___

___

___

Never

901 (23.0)

2272 (70.9)

255 (6.1)

 

<0.001

<0.01

___

Physical activity, N (%)

 

 

 

 

 

 

 

Inactive

803 (21.3)

2035 (72.4)

261 (6.4)

0.3879

___

___

___

Active

534 (20.1)

1658 (74.6)

145 (5.3)

 

___

___

___

Time watching TV, N (%) 

 

 

 

 

 

 

 

< 5 hours/per day

1170 (20.4)

3366 (74.0)

333 (5.5)

0.0961

___

___

___

≥ 5 hours/per day

163 (23.6)

318 (66.8)

71 (9.6)

 

___

___

___

Adherence to Mediterranean diet, N (%)

 

 

 

 

 

 

 

High adherence to MD (PREDIMED ≥ 10)

122 (16.4)

439 (78.2)

40 (5.3)

0.0672

___

___

___

Low adherence to MD (PREDIMED ≤ 10)

1215 (21.3)

3254 (72.7)

366 (6.0)

 

___

___

___

Non-communicable chronic diseases (self-reported), N (%))

 

 

 

 

 

 

 

Hypertension

585 (34.6)

1053 (58.5)

151 (6.9)

<0.0001

<0.0001

<0.0001

<0.05

Diabetes

224 (39.4)

354 (51.2)

66 (9.4)

<0.0001

<0.0001

<0.001

<0.01

Hypercholesterolemia

565 (32.7)

1054 (60.2)

141 (7.2)

<0.0001

<0.0001

<0.001

___

Pulmonary disease

65 (31.0)

113 (59.7)

20 (9.3)

0.0010

<0.05

<0.05

___

Cardiac disease

218 (33.9)

359 (54.4)

90 (11.8)

<0.0001

<0.001

<0.0001

<0.0001

Gastrointestinal disease

190 (33.7)

287 (58.8)

47 (7.5)

<0.0001

<0.0001

<0.001

___

Neurologic disease

54 (18.3)

129 (74.9)

19 (6.8)

0.7257

___

___

___

Allergy

135 (18.5)

371 (76.7)

28 (4.8)

0.4468

___

___

___

Neoplasm disease

93 (31.2)

181 (59.8)

31 (9.0)

0.0045

<0.05

___

___

Rheumatic disease

154 (25.9)

296 (65.8)

43 (8.4)

0.0497

<0.01

<0.05

___

Depression

141 (31.4)

265 (59.1)

37 (5.8)

<0.0001

<0.01

<0.05

___

Anxiety

79 (26.1)

159 (65.7)

23 (5.8)

0.1338

___

___

___

Multimorbidity, N (%)

 

 

 

 

 

 

 

Yes

532 (36.3)

899 (56.1)

142 (7.6)

<0.0001

<0.0001

<0.0001

<0.01

No

698 (16.0)

2585 (79.2)

207 (4.8)

 

<0.0001

<0.001

<0.05

Hospitalized in previous 12 months, N (%)

 

 

 

 

 

 

 

212 (28.1)

 

 

 

 

 

 

 

425 (61.9)

 

 

 

 

 

 

 

70 (10.0)

<0.0001

<0.01

<0.05

<0.05

 

 

 

Physical function, mean + (SD)

 

 

 

 

 

 

 

HAQ score (0-3)

0.6 (0.7)

0.3 (0.5)

0.5 (0.7)

<0.0001

<0.0001

<0.01

<0.0001

Quality of life, mean + (SD)

 

 

 

 

 

 

 

EQ-5D-3L score

0.7 (0.3)

0.8 (0.2)

0.7 (0.3)

<0.0001

<0.0001

___

<0.0001

Drugs for sleep (self- reported) , N (%)

 

 

 

 

 

 

 

Yes

93 (40.3)

122 (53.1)

19 (6.6)

<0.0001

<0.0001

<0.01

___

No

1244 (20.2)

3571 (74.0)

387 (5.9)

 

___

___

___

aAnova and Pearson Qui2 tests.

There is a higher percentage of overweight subjects in the SSD group, as well as people that drink alcohol on a daily basis and the ones that never smoke. The percentage of inactive and active individuals was similar for both sleep duration groups, except for the LSD with a higher prevalence in the inactive group. Subjects that adhere to a Mediterranean diet were the ones with higher percentage of reported normal sleep (78.2%), although a very high percentage of individuals did not have a high adherence to the Mediterranean diet (88.1%) according to the PREDIMED score.

The self-reported non-communicable chronic diseases with a prevalence value above 30% for the reported SSD group were: hypertension (34.6%), diabetes (39.4%), hypercholesterolemia (32.7%), pulmonary disease (31.0%), cardiac disease (33.9%), gastrointestinal disease (33.7%) and neoplasm disease (31.2%). For the reported LSD group, the self-reported non-communicable chronic diseases with higher prevalence's were: diabetes (9.4%), pulmonary disease (9.3%), cardiac disease (11.8%) and neoplasm disease (9.0%). The pathology with lower prevalence for reported normal sleep duration was diabetes with 51.2%. The percentage of individuals with anxiety was higher in the SSD group (26.1%) and the percentage of individuals with depression and anxiety was the same in the reported LSD group, 5.8%. For the SSD the percentage of individuals with depression was 31.4%.

The percentage of multimorbidity was high in the groups of SSD and LSD with 36.3% and 7.6% respectively although it was only statistically significant associated to SSD, when adjusted to age, gender, educational level and regions. For physical function, the group with SSD presented the lowest physical function (0.61±0.74), comparing to the LSD group. LSD group presented a low physical function when compared to the normal group. The number of hospitalizations in the previous 12 months was higher in the SSD group (28.1%). Asked about medication, 234 (2.8%) individuals reported specifically taking medication for sleep, and 40.3% of those belong to the SSD group.

SSD was weakly associated “to drinking alcohol occasionally”, never smoke and to have a high adherence to Mediterranean diet ([Table 2]).

Table 2

Lifestyles factors associated with short and long sleep durations for the Portuguese population.

 

Crude

Multivariable adjusteda

 

Sleep duration (≤ 5 h/day vs 6-8h/day)

Sleep duration (≥ 9h/day vs 6-8 h/day)

Sleep duration (≤ 5 h/day vs 6-8h/day)

Sleep duration (≥ 9h/day vs 6-8 h/day)

 

OR 95 % CI

OR 95 % CI

OR 95 % CI

OR 95 % CI

Alcohol intake

 

 

 

 

Daily

0.98 0.73-1.31

0.67 0.48-0.93

0.99 0.75-1.32

0.62 0.42-0.90

Occasionally

0.59 0.45-0.77

0.56 0.39-0.81

0.87 0.67-1.13

0.80 0.56-1.15

Smoking habits

 

 

 

 

Past smoker

0.92 0.70-1.21

1.03 0.75-1.42

0.99 0.74-1.33

1.20 0.81-1.77

Never

0.53 0.39-0.72

0.72 0.46-1.11

0.75 0.53-1.07

1.05 0.65-1.68

Physical activity

 

 

 

 

Active

0.91 0.73-1.15

0.82 0.61-1.10

1.11 0.89-1.39

1.02 0.76-1.37

Time watching TV 

 

 

 

 

≥ 5 hours/per day

1.28 0.77-2.13

1.92 1.15-3.21

0.78 0.52-1.17

1.25 0.80-1.96

Mediterranean diet

 

 

 

 

High adherence to MD (PREDIMED ≥ 10)

0.71 0.53-0.97

0.83 0.53-1.30

0.79 0.56-1.10

0.85 0.54-1.33

aOdds ratios from logistic regression model adjusted for age, sex, NUTS II regions and educational level.

Lifestyle variables weakly associated to reported LSD (≥9 hours/day) were “to drink alcohol daily and occasionally” (OR=0.56; 95%CI:0.39-0.81); and to watch TV ≥5 hours/day (OR=1.92; 95%CI:1.15-3.21). In the adjusted model, the only lifestyle variable associated to LSD (≥9 hours/day) was daily alcohol consumption (OR=0.62; 95%CI:0.42-0.90) ([Table 2]). For the remaining lifestyles studied no association was obtained for sleep duration.

[Table 3] displays data on health conditions and health resources consumptions crude and adjusted for age, gender, NUTSII regions and educational level. To be overweight or obese (OR=1.57; 95%CI:1.24-1.99) was statistically significant associated to reported short sleep duration. Diabetes and depression presented higher prevalence values for SSD and LSD presenting an increased risk for both conditions. Hypercholesterolemia had an increased risk for SSD (OR=1.47; 95%CI:1.16-1.86). Gastrointestinal disease presented also an increased risk for the same group (OR=1.68; 95%CI:1.19-2.37). Cardiac disease was associated to LSD (OR=2.01; 95%CI:1.45-2.78).

Table 3

Health and health resources consumption factors associated with short and long sleep durations for the Portuguese population.

 

Crude

Multivariable adjusteda

 

Sleep duration (≤ 5 h/day vs. 6-8h/day)

Sleep duration (≥ 9h/day vs. 6-8 h/day)

Sleep duration (≤ 5 h/day vs. 6-8h/day)

Sleep duration (≥ 9h/day vs. 6-8 h/day)

 

OR 95 % CI

OR 95 % CI

OR 95 % CI

OR   95 % CI

Drugs for sleep (self- reported)

 

 

 

 

Yes

0.36 0.25-0.52

0.64 0.36-1.16

0.62 0.42-0.91

1.12 0.62-2.03

BMI

 

 

 

 

Overweight and obese 

 

 

 

 

(≥ 25 kg/m2)

2.01 1.59-2.54

1.29 0.95-1.74

1.57 1.24-1.99

1.00 0.72-1.38

Non-communicable chronic diseases (self-reported)

 

 

 

 

Hypertension

2.86 2.27-3.60

1.75 1.32-2.33

1.43 1.11-1.83

0.98 0.74-1.31

Diabetes

3.10 2.20-4.36

2.58 1.82-3.66

1.60 1.15-2.24

1.48 1.04-2.10

Hypercholesterolemia

2.53 2.01-3.18

1.77 1.33-2.36

1.47 1.16-1.86

1.11 0.82-1.49

Pulmonary disease

1.88 1.26-2.80

2.00 1.14-3.52

1.13 0.77-1.67

1.22 0.68-2.18

Cardiac disease

2.45 1.74-3.46

3.15 2.27-4.37

1.42 0.99-2.03

2.01 1.45-2.78

Gastrointestinal disease

2.22 1.57-3.15

1.69 1.04-2.74

1.68 1.19-2.37

1.40 0.88-2.24

Neurologic disease

0.86 0.56-1.33

1.14 0.55-2.36

0.75 0.45-1.25

1.04 0.49-2.19

Allergy

0.84 0.59-1.20

0.77 0.43-1.38

1.16 0.84-1.62

0.99 0.53-1.83

Neoplastic disease

1.91 1.17-3.12

1.95 1.22-3.12

1.15 0.71-1.87

1.29 0.80-2.09

Rheumatic disease

1.43 0.95-2.14

1.65 1.07-2.54

1.08 0.75-1.55

1.36 0.88-2.09

Depression

1.98 1.47-2.67

2.16 1.36-3.42

1.56 1.16-2.11

1.77 1.08-2.88

Anxiety

1.43 1.00-2.06

1.60 0.75-3.39

1.29 0.86-1.94

1.39 0.60-3.23

Multimorbidity

 

 

 

 

Yes

3.20 2.51-4.08

2.24 1.67-3.01

1.56 1.20-2.02

1.28 0.94-1.76

Physical function

 

 

 

 

HAQ score

2.84 2.37-3.41

2.32 1.87-2.88

1.75 1.42-2.15

1.58 1.22-2.05

Quality of life

 

 

 

 

EQ-5D-3L score

0.20 0.14-0.28

0.53 0.35-0.79

0.15 0.10-0.23

0.31 0.20-0.50

Hospitalised in previous 12 months

1.71 1.33-2.20

2.23 1.56-3.19

1.36 1.05-1.76

1.83 1.25-2.70

aOdds ratios from logistic regression model adjusted for age, sex, NUTS II regions and educational level.

For the remaining chronic diseases studied like rheumatic, neoplastic and pulmonary diseases there was an association to sleep duration only in the univariate analysis, this association was not found for the adjusted analysis. Allergic and neurologic diseases had no association to SSD and LSD in this population ([Table 3]).

Multimorbidity presented only an increased risk for SSD in the adjusted model (OR=1.56; 95%CI:1.20-2.02). The relationship between sleep duration and mean number of comorbidities for the Portuguese population is showed in [Figure 2].

Zoom Image
Figure 2 Relationship between sleep duration and chronic diseases.

Physical function and quality of life were reduced for both groups (SSD: OR=1.75; 95%CI:1.42-2.15; LSD: OR=1.58; 95%CI:1.22-2.05) and (SSD: OR=0.15; 95%CI:0.10-0.23; LSD: OR=0.31; 95%CI: 0.20-0.50) respectively, indicating that poor sleep is related to poor quality of life and poor physical functioning. As a proxy for the costs for the National Health Care System we used the number of hospitalizations in the previous twelve months; both groups presented an increased risk of being hospitalized in the previous twelve months to the inquire (SSD: OR=1.36; 95%CI:1.05-1.76; LSD: OR=1.83; 95%CI:1.25-2.70) ([Table 3]).

Splitting the sample in two groups, bellow and above 65 years, some differences were found. Marital status was (p<0.0001) only associated to sleep duration in the age group bellow 65 years, with a high percentage of divorced people in the SSD group. Also, a higher percentage of retired/unemployed or with a temporary work was associated to SSD in this age group (p=0.0198); and the alcohol intake (p=0.0157) was also higher for SSD. More statistically significant associations in this age group were found in non-communicable chronic diseases: diabetes (p<0.0001), hypercholesterolemia (p<0.0001), gastrointestinal disease (p=0.0001), rheumatic diseases (p=0.0191), depression (p<0.0001) and anxiety (p=0.0477). A higher number of hospitalizations (p=0.0007) and a higher use of drugs for sleep was associated to SSD for the age group < 65 years. The only variable associated to sleep duration for the age group ≥65 was the adherence to Mediterranean diet, where participants with a lower adherence were more present in the SSD group ([Table 4]).

Table 4

Baseline characteristics by categories of short (≤5 h/day) and long (≥9h/day) sleep duration, having as reference group the normal sleep duration (6-8 h/day) for age groups (< 65years and ≥65 years).

 

Age group < 65 years

Age group ≥65 years

Characteristic

Short sleep duration (≤5 h/day)

Normal sleep duration (6-8 h/day)

Long sleep duration (≥ 9h/day)

p-value a

Short sleep duration (≤ 5 h/day)

Normal sleep duration (6-8 h/day)

Long sleep duration (≥ 9h/day)

p-value a

N (%)

717 (19.8)

2704 (74.7)

199 (5.5)

 

620 (34.1)

989 (54.5)

207 (11.4)

 

Sex, N (%)

 

 

 

 

 

 

 

 

Male

501 (17.1)

1653 (78.4)

129 (4.6)

0.2605

425 (36.5)

639 (52.8)

126 (10.7)

0.9130

Female

216 (14.4)

1051 (81.2)

70 (4.4)

 

195 (36.2)

350 (53.8)

81 (10.0)

 

Age, mean ± (SD)

47.6 (12.2)

40.2 (11.7)

41.8 (14.8)

<0.0001

73.6 (6.0)

74.2 (6.8)

76.1 (7.9)

0.0014

NUTS II region N(%)

 

 

 

 

 

 

 

 

North

225 (15.7)

831 (79.4)

65 (4.9)

0.1755

179 (37.4)

249 (52.7)

55 (9.9)

0.0840

Centre

131 (16.0)

476 (79.4)

35 (4.6)

 

129 (33.4)

212 (53.2)

56 (13.4)

 

Lisbon

127 (14.1)

583 (83.0)

28 (3.0)

 

117 (42.0)

215 (50.9)

25 (7.1)

 

Alentejo

40 (20.1)

125 (74.4)

12 (4.7)

 

35 (23.7)

83 (63.0)

16 (13.3)

 

Algarve

22 (18.7)

68 (72.3)

6 (9.0)

 

35 (46.9)

41 (49.4)

2 (3.6)

 

Azores

81 (13.6)

338 (78.6)

40 (7.8)

 

49 (28.0)

92 (52.1)

36 (19.9)

 

Madeira

91 (16.9)

283 (79.9)

13 (3.2)

 

76 (40.3)

97 (8.5)

17 (8.5)

 

BMI, mean ± (SD)

26.9 (5.1)

25.2 (4.1)

25.5 (5.3)

<0.0001

27.1 (3.8)

26.8 (4.3)

27.2 (5.2)

0.0097

Education level, N (%)

 

 

 

 

 

 

 

 

> 12 years

115 (10.4)

782 (87.5)

23 (2.1)

<0.0001

27 (18.8)

88 (75.9)

7 (5.3)

<0.0001

10-12 years

136 (13.3)

730 (81.7)

52 (5.1)

 

28 (24.9)

71 (64.6)

14 (10.5)

 

5-9 years

197 (19.4)

629 (76.2)

42 (4.4)

 

66 (24.5)

138 (68.2)

22 (7.4)

 

0-4 years

266 (25.9)

558 (66.7)

80 (7.4)

 

490 (40.7)

686 (48.2)

159 (11.2)

 

Marital status, N (%)

 

 

 

 

 

 

 

 

Single

108 (9.2)

665 (85.7)

46 (5.1)

<0.0001

26 (21.2)

48 (66.6)

11 (12.2)

0.5327

Married

460 (19.3)

1643 (76.7)

114 (4.0)

 

373 (35.3)

624 (54.5)

121 (10.2)

 

Divorced

63 (20.5)

211 (73.7)

20 (5.8)

 

23 (47.0)

55 (44.7)

8 (8.4)

 

Widowed

55 (41.3)

61 (54.7)

8 (4.0)

 

195 (39.1)

258 (50.1)

64 (10.8)

 

Consensual union

31 (14.7)

122 (81.3)

11 (4.5)

 

3 (34.3)

4 (48.6)

1 (17.2)

 

Employment status, N (%)

 

 

 

 

 

 

 

 

Employed full-time/part-time/ domestic

483 (15.1)

2095 (81.1)

128 (3.9)

0.0198

540 (36.9)

883 (52.9)

183 (10.2)

0.5384

Retired/unemployed/ temporary work

233 (17.9)

607 (75.5)

71 (6.7)

 

78 (31.2)

103 (56.3)

24 (12.5)

 

Alcohol intake, N (%)

 

 

 

 

 

 

 

 

Daily

283 (18.1)

755 (75.9)

81 (6.0)

0.0157

290 (37.1)

387 (51.2)

95 (11.7)

0.7278

Occasionally

179 (17.0)

704 (80.0)

40 (3.0)

 

192 (36.7)

354 (53.7)

73 (9.6)

 

Never

253 (13.7)

1240 (81.9)

78 (4.4)

 

136  (33.9)

247 (9.6)

37 (9.4)

 

Smoking habits, N (%)

 

 

 

 

 

 

 

 

Current smoker

443 (16.9)

1565 (78.9)

104 (4.2)

0.3933

458 (38.0)

707 (51.2)

151 (10.9)

0.2133

Past smoker

141 (15.9)

532 (78.9)

49 (5.2)

 

135 (35.4)

232 (55.2)

44 (9.5)

 

Never

132 (13.4)

605 (82.0)

46 (4.5)

 

25 (22.0)

49 (9.5)

12 (9.3)

 

Physical activity, N(%)

 

 

 

 

 

 

 

 

Inactive

413 (16.3)

1442 (79.6)

113 (4.2)

0.6342

390 (35.0)

593 (52.6)

148 (12.4)

0.1156

Active

304 (15.3)

1262 (79.9)

86 (4.9)

 

230 (38.5)

396 (54.3)

59 (10.4)

 

Time watching TV, N (%)

 

 

 

 

 

 

 

 

< 5 hours/per day

655 (15.8)

2562 (80.0)

171(4.3)

0.3449

515 (37.4)

804 (52.5)

162 (10.1)

0.5578

≥ 5 hours/per day

60 (16.0)

139 (76.3)

28 (7.7)

 

103 (32.5)

179 (55.7)

43 (11.8)

 

Adherence to Mediterranean diet, N (%)

 

 

 

 

 

 

 

 

High adherence to MD (PREDIMED ≥ 10)

68 (14.0)

327 (82.3)

20 (3.4)

0.4111

54 (25.2)

112 (62.6)

20 (10.4)

0.0372

Low adherence to MD (PREDIMED ≤ 10)

649 (16.1)

2377 (79.3)

179 (4.6)

 

566 (37.7)

877 (52.1)

187 (10.2)

 

Non-communicable chronic diseases (self-reported), N (%)

 

 

 

 

 

 

 

 

Hypertension

218 (26.7)

530 (69.1)

50 (4.2)

<0.0001

367 (41.7)

523 (48.9)

101 (9.4)

0.0238

Diabetes

75 (32.3)

144 (61.3)

19 (6.4)

<0.0001

149 (44.1)

210 (44.6)

47 (11.3)

0.0689

Hypercholesterolemia

245 (26.2)

597 (68.2)

55 (5.6)

<0.0001

320 (40.9)

457 (50.0)

86 (9.8)

0.1583

Pulmonary disease

26 (25.0)

65 (70.7)

4 (4.3)

0.0803

39 (38.4)

48 (46.3)

16 (15.3)

0.3096

Cardiac disease

62 (24.0)

155 (69.8)

21 (6.3)

0.0147

156 (40.7)

204 (43.8)

69 (15.6)

0.0097

Gastrointestinal disease

98 (28.7)

164 (66.2)

20 (5.1)

0.0001

92 (42.4)

123 (46.1)

27 (11.5)

0.2634

Neurologic disease

27 (14.5)

98 (79.6)

10 (4.5)

0.7730

27 (30.2)

31 (60.3)

9 (9.6)

0.6007

Allergy

90 (15.9)

310 (80.9)

12 (4.5)

0.6601

45 (35.9)

61 (48.7)

16 (15.3)

0.2834

Neoplasm disease

34 (20.0)

98 (76.4)

7 (3.7)

0.4149

59 (41.9)

83 (44.0)

24 (14.1)

0.2785

Rheumatic disease

89 (18.8)

204 (73.3)

24 (8.0)

0.0191

65 (41.2)

92 (49.6)

19 (9.2)

0.6672

Depression

89 (30.0)

181 (61.6)

20 (4.5)

<0.0001

52 (34.6)

84 (53.3)

17 (12.1)

0.7781

Anxiety

51 (25.0)

113 (68.7)

9 (6.4)

0.0477

28 (30.5)

46 (55.0)

14 (14.5)

0.4362

Multimorbidity,  N (%)

 

 

 

 

 

 

 

 

Yes

281 (26.9)

696 (67.9)

65 (5.2)

<0.0001

369 (43.3)

534 (47.4)

107 (9.3)

0.0003

No

367 (12.4)

1878 (83.6)

115 (4.1)

 

175 (28.2)

314 (63.2)

51 (8.6)

 

Hospitalized in previous 12 months N(%)

89 (20.9)

266 (70.1)

26 (8.4)

0.0007

123 (40.1)

159 (47.4)

44 (10.4)

0.1925

Physical function, mean ± (SD)

 

 

 

 

 

 

 

 

HAQ score (0-3)

0.4 (0.7)

0.2 (0.4)

0.3 (0.6)

<0.0001

0.8 (0.7)

0.6 (0.7)

0.8 (0.7)

<0.0001

Quality of life, mean ± (SD)

 

 

 

 

 

 

 

 

EQ-5D-3L score

0.6 (0.3)

0.9 (0.2)

0.8 (0.3)

<0.0001

0.6 (0.3)

0.7 (0.3)

0.5 (0.3)

<0.0001

Drugs for sleep (self- reported), N(%)

 

 

 

 

 

 

 

 

Yes

35 (36.2)

48 (59.4)

4 (4.4)

0.0002

58 (43.8)

74 (47.7)

15 (8.5)

0.2720

No

682 (15.4)

2656 (80.1)

195 (4.5)

 

562 (35.9)

915 (53.6)

192 (10.5)

 

aAnova and Pearson Qui2 tests

For the < 65 years group the lifestyle factors with a predictive value for SSD were being married (OR=1.95; 95%CI:1.33-2.86), divorced (OR=1.26; 95%CI:1.26-3.56) and widowed (OR=4.59; 95%CI:2.51-8.37); and for LSD only to consume alcohol daily (OR=0.41; 95%CI:0.24-0.70). For the ≥65 years group they were, for SSD, never smoked (OR=0.39; 95%CI:0.16-0.96) and the high adherence to the Mediterranean diet (OR=0.56; 95%CI:0.36-0.86). For the LSD it was being active (OR=0.60; 95%CI:0.39-0.92) ([Table 5]).

Table 5

Lifestyles factors associated with short and long sleep durations for age groups (< 65 and ≥ 65 years).

 

<65 years

≥65 years

 

Crude

Multivariable adjusted a

Crude

Multivariable adjusted a

 

Sleep duration (≤5 h/day vs. 6-8h/day)

Sleep duration (≥9h/day vs. 6-8 h/day)

Sleep duration (≤5 h/day vs. 6-8h/day)

Sleep duration (≥9h/day vs. 6-8 h/day)

Sleep duration (≤5 h/day vs. 6-8h/day)

Sleep duration (≥9h/day vs. 6-8 h/day)

Sleep duration (≤5 h/day vs. 6-8h/day)

Sleep duration (≥9h/day vs. 6-8 h/day)

 

OR 95% CI

OR 95% CI

OR 95% CI

OR 95% CI

 

 

 

 

Alcohol intake

 

 

 

 

 

 

 

 

Daily

0.89 0.65-1.23

0.47 0.29-0.77

0.97 0.69-1.38

0.41 0.24-0.70

0.94 0.60-1.49

0.78 0.50-1.21

0.99 0.61-1.60

0.89 0.53-1.49

Occasionally

0.70 0.51-0.97

0.68 0.43-1.08

0.83 0.61-1.13

0.74 0.48-1.45

0.82 0.56-1.21

0.72 0.42-1.22

1.06 0.70-1.58

0.77 0.44-1.34

Smoking habits

 

 

 

 

 

 

 

 

Past smoker

0.94 0.69-1.28

1.24 0.79-1.95

0.91 0.69-1.37

1.36 0.81-2.27

0.86 0.54-1.38

0.81 0.52-1.25

0.92 0.54-1.55

0.91 0.52-1.59

Never

0.76 0.55-1.06

1.08 0.65-1.81

0.83 0.57-1.20

1.19 0.70-2.04

0.41 0.20-0.91

0.64 0.25-1.61

0.39 0.16-0.96

0.56 0.19-1.64

Physical activity

 

 

 

 

 

 

 

 

Active

0.93 0.72-1.21

1.17 0.78-1.72

1.07 0.82-1.39

1.33 0.90-1.96

1.07 0.71-1.61

0.57 0.38-0.85

1.17 0.78-1.73

0.60 0.39-0.92

Time watching TV

 

 

 

 

 

 

 

 

≥5 hours/per day

1.06 0.52-2.20

1.89 0.84-4.26

0.87 0.47-1.62

1.63 0.78-3.42

0.82 0.48-1.40

1.10 0.68-1.79

0.74 0.46-1.21

1.06 0.63-1.78

Marital status

 

 

 

 

 

 

 

 

Married

2.36 1.60-3.51

0.87 0.55-1.35

1.95 1.33-2.86

0.66 0.41-1.05

2.04 0.89-4.67

1.02 0.39-2.69

2.01 0.78-5.22

1.02 0.37-2.85

Divorced

2.60 1.54-4.41

1.32 0.67-2.58

2.12 1.26-3.56

0.91 0.46-1.80

3.31 0.85-12.96

1.02 0.30-3.51

3.52 0.97-12.77

1.21 0.32-4.52

Widowed

7.06 3.89-12.82

1.24 0.42-3.62

4.59 2.51-8.37

0.62 0.21-1.84

2.46 1.06-5.67

1.17 0.43-3.23

2.13 0.80-5.62

1.08 0.37-3.13

Consensual union

1.70 0.91-3.15

0.82 0.38-1.78

1.53 0.82-2.84

0.73 0.34-1.60

2.22 0.31-16.12

1.93 0.16-23.83

3.14 0.54-18.37

2.52 0.22-28.41

Mediterranean diet

 

 

 

 

 

 

 

 

High adherence to MD (PREDIMED ≥ 10)

0.84 0.56-1.24

0.71 0.39-1.31

0.88 0.57-1.34

0.69 0.36-1.31

0.56 0.36-0.86

1.00 0.51-1.93

0.65 0.43-0.99

1.07 0.56-2.05

aOdds ratios from logistic regression model adjusted for sex, NUTS II regions and educational level.

For the < 65 years group the health and health resources consumption factors with a predictive value to SSD were the consumption of drugs for sleep (OR=0.44; 95%CI:0.24-0.80), to be obese (OR=1.74; 95%CI:1.30-2.32), to be hypertense (OR=1.80; 95%CI:1.36-2.39), to have diabetes (OR=2.14; 95%CI:1.41-3.23), to have hypercholesteremia (OR=1.98; 95%CI:1.52-2.58), to have a cardiac disease (OR=1.75; 95%CI:1.06-2.88), to suffer from a gastrointestinal disease (OR=2.20; 95%CI:1.42-3.41), depression (OR=2.14; 95%CI:1.48-3.08), multimorbidity (OR=2.28; 95%CI:1.75-2.97), worse physical function (OR=2.46; 95%CI:1.98-3.05), worse quality of life (OR=0.30; 95%CI:0.14-0.38) and the number of hospitalizations in the previous 12 months (OR=1.48; 95%CI:1.04-2.10); for the LSD they were to suffer from a rheumatic disease (OR=1.88; 95%CI:1.06-3.33), depression (OR=2.55; 95%CI:1.16-4.35), worse physical function (OR=1.74; 95%CI:1.21-2.50), worse quality of life (OR=0.30; 95%CI:0.15-0.60) and to be hospitalized in the previous 12 months (OR=2.19; 95%CI:1.26-3.80).

For the ≥65 years group the health and health resources consumption factors with a predictive value to SSD were to be hypertense (OR=1.57; 95%CI:1.07-2.31), to suffer from cardiac disease (OR=1.54; 95%CI:1.00-2.37), multimorbidity (OR=2.06; 95%CI:1.41-3.02) and worse physical function (OR=1.56; 95%CI:1.14-2.12. For the LSD they were to suffer from a cardiac disease, worse physical function (OR=1.50; 95%CI:1.06-2.11) and quality of life (OR=0.30; 95%CI:0.17-0.52) ([Table 6]).

Table 6

Health and health resources consumption factors associated with short and long sleep durations for age groups (<65 and ≥65 years).

 

<65 years

≥65 years

 

Crude

Multivariable adjusted a

Crude

Multivariable adjusted a

 

Sleep duration (≤5 h/day vs. 6-8h/day)

Sleep duration (≥9h/day vs. 6-8 h/day)

Sleep duration (≤5 h/day vs. 6-8h/day)

Sleep duration (≥9h/day vs. 6-8 h/day)

Sleep duration (≤5 h/day vs. 6-8h/day)

Sleep duration ≥9h/day vs. 6-8 h/day)

Sleep duration (≤5 h/day vs. 6-8h/day)

Sleep duration (≥9h/day vs 6-8 h/day)

 

OR 95 % CI

OR 95 % CI

OR 95 % CI

OR 95 % CI

 

 

 

 

Drugs for sleep (self- reported)

 

 

 

 

 

 

 

 

Yes

0.32 0.17-0.60

0.76 0.26-2.23

0.44 0.24-0.80

0.92 0.32-2.65

0.73 0.46-1.14

1.10 0.55-2.22

0.78 0.50-1.23

1.21 0.60-2.44

BMI

 

 

 

 

 

 

 

 

Overweight and obese

 

 

 

 

 

 

 

 

(≥25 kg/m2)

1.96 1.49-2.59

1.36 0.76-1.69

1.74 1.30-2.32

0.99 0.66-1.49

1.33 0.86-2.07

1.02 0.63-1.64

1.26 0.83-1.90

0.99 0.60-1.64

Non-communicable chronic diseases (self-reported)

 

 

 

 

 

 

 

 

Hypertension

2.27 1.73-3.00

1.11 0.72-1.69

1.80 1.36-2.39

0.90 0.59-1.37

1.63 1.08-2.44

1.07 0.71-1.61

1.57 1.07-2.31

1.10 0.72-1.69

Diabetes

2.83 2.91-4.20

1.96 1.07-3.58

2.14 1.41-3.23

1.54 0.85-2.78

1.63 0.99-2.66

1.47 0.94-2.28

1.52 0.99-2.32

1.44 0.92-2.24

Hypercholesterolemia

2.34 1.80-3.04

1.61 1.07-2.44

1.98 1.52-2.58

1.41 0.95-2.10

1.38 0.92-2.06

0.98 0.65-1.47

1.37 0.95-1.99

0.92 0.60-1.40

Pulmonary disease

1.81 1.05-3.13

1.11 0.38-3.25

1.36 0.80-2.29

0.86 0.29-2.54

1.22 0.69-2.17

1.76 0.89-3.50

1.26 0.70-2.27

1.56 0.73-3.31

Cardiac disease

1.81 1.11-2.94

1.66 0.92-1.99

1.75 1.06-2.88

1.63 0.94-2.83

1.49 0.95-2.35

2.32 1.56-3.46

1.54 1.00-2.37

2.18 1.43-3.30

Gastrointestinal disease

2.38 1.52-3.70

1.44 0.73-2.83

2.20 1.42-3.41

1.55 0.80-3.02

1.43 0.89-2.29

1.35 0.73-2.50

1.59 0.99-2.55

1.43 0.75-2.72

Neurologic disease

0.91 0.51-1.65

1.35 0.50-3.63

0.86 0.47-1.56

1.30 0.52-3.27

0.73 0.37-1.43

0.82 0.32-2.12

0.65 0.31-1.40

0.74 0.28-1.98

Allergy

1.00 0.66-1.50

0.68 0.29-1.60

1.10 0.73-1.67

0.77 0.30-1.96

1.08 0.66-1.79

1.71 0.87-3.35

1.11 0.67-1.84

1.60 0.78-3.25

Neoplastic disease

1.34 0.82-2.19

0.85 0.34-2.14

1.13 0.68-1.89

0.76 0.30-1.91

1.44 0.72-2.90

1.77 0.99-3.14

1.49 0.75-2.97

1.69 0.90-3.17

Rheumatic disease

1.31 0.91-1.90

2.05 1.17-3.61

1.15 0.80-1.65

1.88 1.06-3.33

1.25 0.61-2.50

0.95 0.51-1.77

1.18 0.65-2.14

0.88 0.47-1.64

Depression

2.67 1.85-3.86

2.62 1.40-4.90

2.14 1.48-3.08

2.25 1.16-4.35

0.94 0.58-1.54

1.22 0.63-2.36

1.03 0.64-1.66

1.34 0.68-2.64

Anxiety

1.91 1.24-2.94

1.71 0.57-5.14

1.70 1.09-2.66

1.58 0.49-5.10

0.80 0.44-1.45

1.42 0.61-3.27

0.75 0.41-1.37

1.31 0.54-3.19

Multimorbidity

 

 

 

 

 

 

 

 

Yes

2.68 2.06-4.47

1.58 1.02-2.45

2.28 1.75-2.97

1.42 0.88-2.29

2.05 1.40-3.00

1.44 0.88-2.35

2.06 1.41-3.02

1.39 0.83-2.34

Physical function

 

 

 

 

 

 

 

 

HAQ score

2.97 2.43-3.64

2.12 1.50-3.00

2.46 1.98-3.05

1.74 1.21-2.50

1.63 1.21-2.21

1.56 1.16-2.10

1.56 1.14-2.12

1.50 1.06-2.11

Quality of life

 

 

 

 

 

 

 

 

EQ-5D-3L score

0.17 0.11-0.26

0.24 0.12-0.47

0.23 0.14-0.38

0.30 0.15-0.60

0.70 0.40-1.23

0.26 0.16-0.43

0.77 0.44-1.33

0.30 0.17-0.52

Hospitalised in previous 12 months

1.56 1.11-2.20

2.34 1.36-4.04

1.48 1.04-2.10

2.19 1.26-3.80

1.29 0.89-1.89

1.45 0.93-2.27

1.41 0.98-2.03

1.49 0.94-2.35

aOdds ratios from logistic regression model adjusted for sex, NUTS II regions and educational level.

#

DISCUSSION

The associations to chronic diseases and abnormal total sleep time namely SSD were found for PT. The prevalence for SSD in PT is very high, contrary to LSD. In the USA, data from the National Health Interview Survey, for the same cut-off value (≤5h/day) the prevalence was much lower, 7.8%[28], and in a sample of the Brazilian population, the prevalence value for reported SSD with a cut-off value of ≤6h/day, was 15.8%[5]. The prevalence value for LSD (≥9h/day) in PT is low (5.9%) if compared with the USA (8.5%) and even lower than the Brazilian cohort (21.9%)[5]. The metropolitan area of Lisbon, the most populated urban region of the all country, with a high 24h/7days rhythm, was the region with a higher prevalence value of NSD (75.8%). No explanation for this result was found, as so, future studies evaluating sleep duration comparing urban and rural areas should be performed in PT.

Diabetes and depression presented a significant association with SSD and LSD with an increased risk for both conditions. This was also found in the USA [9]diabetes, and cardiovascular disease; and although 7-8 h of sleep seems to confer the least health risk, these findings are often based on non-representative data. We hypothesize that short sleep (<7 h in Brazil[5], and in a recent revision study[6]. This is in line with the very high prevalence of both in the country[29]. PT has the highest prevalence of diabetes when compared with European countries[29]; in our data the crude odds ratio is 3.10 for SSD and 2.58 for LSD; these values are lower, but still significant for the multivariable adjusted model. In clinical terms these associations reflect a share of sleep duration in the risk of diabetes, although other factors such as low physical activity also shown in our study, must have significant contributions.

The prevalence of depression in PT is among the highest values in the WHO European Region (5.7%), since only Ukraine and Estonia present higher values[30] The odds ratio between depression and SSD is 1.98 and LSD is 2.16 for the crude analysis, with values a bit lower but significant for the multivariable adjusted model; in our sample the influence of age, gender, region and education in the association between sleep duration and depression is minor when compared with diabetes. However in the sub-sample of older adults from the EpiDoc cohort, the prevalence of depression is higher in the elder (11.8%)[31] when compared to WHO data[30].

Obesity was a predictor for SSD. These results were in accordance with previous studies[6] , [9] , [32] in a twin study[14] and also in adolescents[33]. The mean BMI for Portuguese males and females was 26.7kg/m2 and 25.7kg/m2 respectively; the prevalence of obesity was in 2014 19.8% for males and 20.3% for females. In fact these data are a bit lower when compared with the mean EU data[29], and therefore this low obesity prevalence may explain the low odds ratio values found. For LSD, in the adjusted model, this association was not found, contrary as observed in other studies; LSD was associated with an increased sedentary behavior, inactivity, and obesity[6] , [32]. Abdominal fat, besides being a health risk by itself for cardiometabolic diseases[34], the waist circumference was not measured, although the association to BMI is well established[35].

The adherence to Mediterranean diet was analyzed as a proxy of healthy diet. Although being a protective variable to SSD, in the adjusted analysis this association was not found. A previous study resulting from an analysis of the adherence to the Mediterranean diet between 1961 and 2003 had already showed that the adherence to Mediterranean diet has gradually declined in the last years in the Portuguese population[36].

In the USA's, the U-shaped risk was observed for hypertension and cardiovascular disease[9]. In our study hypertension had an increased risk only for SSD and cardiovascular disease only for LSD. The prevalence of high blood pressure in PT is high (28.1%) in 2014, and it is the 9thhighest prevalence in Europe[29], the highest values include Russian Federation, other countries from the Eastern Europe and Luxembourg. The odds ratio for SSD is high (2.86) but decreases, although remaining significant in the multivariable adjusted model (1.43); these results suggest that sleep reduction is included in a set of other risk factors for hypertension. The age standardized prevalence for 100,000 inhabitants of cardiovascular disease in PT in 2015 is 4,765 for females and 5,764 for males, which, within the European framework, are among the lowest values[29]. This might be a partial explanation for the absent association with SSD, which has been found by other authors in the USA[37] and Netherlands[38]. In fact this result deserves further studies since the prevalence of cardiovascular disease is similar in Netherlands and PT. For the association only to LSD to cardiovascular disease no explanation can be found since like stated by Covassin & Singh[39], experimental evidence corroborating harmful cardiovascular effects of excessive sleep duration is lacking, which contributes to making any causal association between long sleep and cardiovascular disease more elusive. Hypercholesterolemia had an increased risk for SSD in accordance to literature which indicates SSD as a risk factor for metabolic function[40] , [41] PT has a reasonable prevalence of raised blood cholesterol (16.7), which is much lower than in most Northern and Eastern EU countries[29] and USA[42]. The Mediterranean diet might be an explanation in spite of the reduced adherence. Contrary to a previous study[5] rheumatic diseases were not associated with sleep duration. Most of the rheumatic diseases are inflammatory diseases so, an association namely to SSD was expected[43]. The same happened to cancer, in this population an association with sleep duration was not found. The association to sleep duration and cancer, namely for LSD, was described in studies for cancer related mortality[44] , [45]. In this study, there was an increased risk for neoplasm disorders in SSD and LSD, although, adjusting for age, gender, regions and educational level this association was not found; the low prevalence of LSD may be a possible explanation, as well as the low rates of cancer for PT comparing to other countries[15]. The reduced immunological defenses in individuals with short or increased sleep durations was demonstrated by Patel et al.[46] in a study where pneumonia risk was higher for these individuals; in our study pulmonary disease, had an association in the univariate analysis, which was missed in the adjusted data. An association with SSD was however expected since the chronic obstructive pulmonary disease is usually one of the most prevalent pulmonary diseases and is associated to SSD[47] , [48]. Even separating by age groups below and above 65 years this association was still not found.

Anxiety is usually associated to insomnia; nevertheless in this population the association to SSD was not found, only in the group <65 years this association was present[49].

An increased risk of multimorbidity for people reporting SSD was also found in our study like in a Brazilian cohort, where it was stated that people suffering from chronic diseases have a greater chance of exhibiting a SSD pattern, and that such individuals may have a tendency towards an accumulation of sleep problems, generating a deficiency in the normal sleep pattern[5]. In [Figure 2] it was possible to observe the U shape for the relationship between sleep duration and number of comorbidities. Like in other study where 7h of sleep presented a lower mortality risk[13] also in our study 7h of sleep presented the lower number of comorbidities, increasing with higher or lower sleep time.

Poor quality of life and poor physical functioning presented an increased risk for both conditions SSD and LSD. This was also well demonstrated in a representative sample from the USA population[50]. Worse quality of life and health complaints were also reported for sleep deprivation in Portuguese adolescents[33].

The number of hospitalizations represents costs to the National Health Care System and in this study almost 30% of the total sample, had abnormal sleep (SSD or LSD) and reported to be hospitalized in the previous 12 months.

A recent study in the UK presented the economics costs of insufficient sleep across five different OECD countries: up to $680 billion are lost each year across these countries due to insufficient sleep. Insufficient sleep increases mortality risk, and the amounts of working time lost due to absenteeism or presenteeism[7]. All the countries evaluated in this study presented lower prevalence values for SSD than PT, demonstrating that this might be a very important issue for the Portuguese economy.

One of the major strengths of our study is its large sample size and representativeness with mainland and islands. The other is the fact that in the EpiDoc1 participants had a complete clinical examination performed by a physician and besides EpiDoc3 being a telephonic interview, the registries to confirm chronic diseases were consulted. Our study had also some limitations: since this is a cross-sectional study it was not possible to establish the temporal nature of the association between the tested variables and self-reported sleep duration; daily sleep duration was measured subjectively by self-report, an objective measure like actigraphy would be of great value, giving the possibility of register workdays and off-days; asking for workdays and off-days separately would be something very important since a recent study[51] showed that when asking about total sleep time duration, the answer reflects only workdays times. Sleep timing and sleep quality were also variables not considered in this study and are important factors when studying sleep. The influence of menopause was not evaluated in this study and there are clear evidences that menopause by itself influences objective sleep patterns[52].

Like in the majority of questionnaires there were some questions that the volunteers did not know or refused to answer, resulting in some missing values. However, it was not possible to eliminate those participants because the representativeness for the Portugal could be compromised.

This study screens the self-reported daily sleep duration for the Portuguese population and shows the very high prevalence of self-reported SSD in the population. Also, the increased risk for chronic diseases and the high costs for the Portuguese National Health Care System were well demonstrated, with the association between SSD and LSD with chronic diseases and with a higher number of hospitalizations. Although some of the chronic diseases that are commonly associated to SSD and LSD like rheumatic diseases and cancer were not significantly associated in this population. Looking closer to the population bellow 65 years of age some significant differences were found. Being unemployed before retirement is associated to SSD as well as being divorced and widowed, these are stress factors that can steal sleep. For some chronic diseases the association to SSD or LSD is only present in individuals bellow 65 years of age. The significant association to sleep duration and increased mortality risk only for this age group and not in older individuals was shown in a Swedish cohort[13], the same relationship might be present in our sample. In a future follow up of this cohort, this relationship should be tested for Portugal.

Future studies are needed evaluating not only reported daily total sleep time, but also the time of the day that people sleep, preferably with objective quantitative measures. Studies on interventions aimed at sleep duration should be conducted to investigate whether adverse health risks decrease in different community settings.

This study emphasizes the burden of self-reported SSD for PT, its consequences to health and the need to increase sleep awareness campaigns enhancing the importance of sleep in health.

Furthermore, it emphasizes that chronic diseases risks are dependent on multiple parameters which varying in different countries or regions, imply the need of regional studies taking into account the local specificities.


#
#

Conflict of Interests

The authors have no conflict of interests to declare.

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  • 43 Mullington JM, Haack M, Toth M, Serrador JM, Meier-Ewert HK. Cardiovascular, inflammatory, and metabolic consequences of sleep deprivation. Prog Cardiovasc Dis. 2009;51(4):294-302. DOI: 10.1016/j. pcad.2008.10.003.
  • 44 Ma QQ, Yao Q, Lin L, Chen GC, Yu JB. Sleep duration and total cancer mortality: a meta-analysis of prospective studies. Sleep Med. 2016;28:39-44. DOI: 10.1016/j.sleep.2016.06.036
  • 45 Zhao H, Yin JY, Yang WS, Qin Q, Li TT, Shi Y, et al. Sleep duration and cancer risk: a systematic review and meta-analysis of prospective studies. Asian Pacific J Cancer Prev. 2013;14(12):7509-15. DOI: 10.7314/ APJCP.2013.14.12.7509
  • 46 Patel SR, Malhotra A, Gao X, Hu FB, Neuman MI, Fawzi WW. A Prospective study of sleep duration and pneumonia risk in women. Sleep. 2012;35(1):97-101. DOI: 10.5665/sleep.1594
  • 47 Budhiraja R, Siddiqi TA, Quan SF. Sleep disorders in chronic obstructive pulmonary disease: etiology, impact, and management. J Clin Sleep Med. 2015;11(3):259-70. DOI: 10.5664/jcsm.4540
  • 48 Kutty K. Sleep and chronic obstructive pulmonary disease. Curr Opin Pulm Med. 2004;10(2):104-12.
  • 49 Neckelmann D, Mykletun A, Dahl AA. Chronic insomnia as a risk factor for developing anxiety and depression. Sleep. 2007;30(7):873-80.
  • 50 Pandey A, Demede M, McKoy F, Zizi F, Girardin JL. Race/ethnicity, sleep duration and quality of life: Analysis of the behavioral risk factor surveillance system. Sleep Med. 2011;12(Suppl 1):S92.
  • 51 Pilz LK, Keller LK, Lenssen D, Roenneberg T. Time to rethink sleep quality: PSQI scores reflect sleep quality on workdays. Sleep. 2018;41(5). DOI: 10.1093/sleep/zsy029
  • 52 Hachul H, Frange C, Bezerra AG, Hirotsu C, Pires GN, Andersen ML, et al. The effect of menopause on objective sleep parameters: data from anepidemiologic study in São Paulo, Brazil. Maturitas. 2015;80(2):170-8. DOI: 10.1016/j.maturitas.2014.11.002

Corresponding author:

Cátia Reis

Publication History

Received: 23 July 2018

Accepted: 27 September 2018

Article published online:
16 October 2023

© 2023. Brazilian Sleep Association. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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  • 44 Ma QQ, Yao Q, Lin L, Chen GC, Yu JB. Sleep duration and total cancer mortality: a meta-analysis of prospective studies. Sleep Med. 2016;28:39-44. DOI: 10.1016/j.sleep.2016.06.036
  • 45 Zhao H, Yin JY, Yang WS, Qin Q, Li TT, Shi Y, et al. Sleep duration and cancer risk: a systematic review and meta-analysis of prospective studies. Asian Pacific J Cancer Prev. 2013;14(12):7509-15. DOI: 10.7314/ APJCP.2013.14.12.7509
  • 46 Patel SR, Malhotra A, Gao X, Hu FB, Neuman MI, Fawzi WW. A Prospective study of sleep duration and pneumonia risk in women. Sleep. 2012;35(1):97-101. DOI: 10.5665/sleep.1594
  • 47 Budhiraja R, Siddiqi TA, Quan SF. Sleep disorders in chronic obstructive pulmonary disease: etiology, impact, and management. J Clin Sleep Med. 2015;11(3):259-70. DOI: 10.5664/jcsm.4540
  • 48 Kutty K. Sleep and chronic obstructive pulmonary disease. Curr Opin Pulm Med. 2004;10(2):104-12.
  • 49 Neckelmann D, Mykletun A, Dahl AA. Chronic insomnia as a risk factor for developing anxiety and depression. Sleep. 2007;30(7):873-80.
  • 50 Pandey A, Demede M, McKoy F, Zizi F, Girardin JL. Race/ethnicity, sleep duration and quality of life: Analysis of the behavioral risk factor surveillance system. Sleep Med. 2011;12(Suppl 1):S92.
  • 51 Pilz LK, Keller LK, Lenssen D, Roenneberg T. Time to rethink sleep quality: PSQI scores reflect sleep quality on workdays. Sleep. 2018;41(5). DOI: 10.1093/sleep/zsy029
  • 52 Hachul H, Frange C, Bezerra AG, Hirotsu C, Pires GN, Andersen ML, et al. The effect of menopause on objective sleep parameters: data from anepidemiologic study in São Paulo, Brazil. Maturitas. 2015;80(2):170-8. DOI: 10.1016/j.maturitas.2014.11.002

Zoom Image
Figure 1 Flowchart of the study.
Zoom Image
Figure 2 Relationship between sleep duration and chronic diseases.