Insomnia and Sleep Duration in a Large Cohort of Patients With Major Depressive Disorder and Anxiety Disorders
Objective: Disturbed sleep has a high impact on daily functioning and has been correlated with psychopathology. We investigated the extent to which insomnia and sleep duration were associated with both current and remitted depressive and anxiety disorders in a large-scale epidemiologic study, taking sociodemographics, health factors, and medication use into account.
Method: Data of 2,619 individuals from the Netherlands Study of Depression and Anxiety (NESDA) were analyzed. Psychopathology was classified as no, current, or remitted DSM-IV–based diagnosis of major depressive or anxiety disorder. Outcome measures were insomnia (Women’s Health Initiative Insomnia Rating Scale score ≥ 9) and sleep duration (≤ 6 hours, 7–9 hours, ≥ 10 hours). Baseline measurement was conducted between September 2004 and February 2007.
Results: Both current and remitted depressive disorder and current anxiety disorder were associated with insomnia and short sleep duration with odds ratios (ORs) for insomnia ranging from 1.42 to 3.23 and for short sleep duration ranging from 1.41 to 2.53. Associations were stronger for current than for remitted diagnoses and stronger for depressive than for anxiety disorders. Also long sleep duration was associated with current depressive disorder and anxiety disorders (OR range, 1.53–2.66). Sociodemographic factors, health indicators, and psychotropic medication use did contribute to sleep outcomes but could not explain much of the psychopathology and sleep associations.
Conclusion: Depressive disorder—but also anxiety disorder—is strongly associated with sleep disturbances. Insomnia and short sleep duration persist after remittance of these disorders, suggesting that these are residual symptoms or possibly trait markers. Also, long sleep duration is associated with current depressive or anxiety disorders.
J Clin Psychiatry 2010;71(3):239–246
© Copyright 2010 Physicians Postgraduate Press, Inc.
Submitted: March 16, 2009; accepted September 28, 2009 (doi:10.4088/JCP.09m05218gry).
Corresponding author: B. W. J. H. Penninx, PhD, Department of Psychiatry, VU University Medical Center, AJ Ernststraat 887, 1081 HL Amsterdam, The Netherlands (email@example.com).
Humans spend approximately one-third of their lives sleeping. Although at first glance sleeping may seem a passive process, the brain is in a highly active state and various important processes take place during the night, such as the secretion of neuroendocrine hormones1 and the facilitation of memory consolidation.2,3 The restorative function of sleep is essential for maintaining both physical and mental health, and over the past years, there has been a vested interest in sleep-related research. Sleeping well is crucial for optimal functioning not only of an individual but also of society as a whole—sleep disturbances increase risks of accidents, rates of absenteeism at work, and health care costs.4
Psychopathology has been found to be strongly associated with sleep disturbances.5 This seems to be especially true for major depressive disorders5 but has been shown for anxiety disorders as well.6,7 In individuals referred to an insomnia clinic, 40% are diagnosed with a primary psychiatric disorder.8 Moreover, persistent insomnia is associated with the development of a new episode of a major depressive disorder (MDD).9,10
Depressive and anxiety disorders share a high degree of comorbidity,11 complicating the investigation of the link between psychopathology and sleep disturbances and leaving some questions as to whether anxiety disorders really show sleep disturbances independent of comorbid depressive disorder. In addition, some studies also found past psychiatric disorders to be associated with sleep complaints,12 possibly reflecting either a “scar” effect of the disease or a trait of the formerly depressed or anxious persons.13 This illustrates that not only current but also remitted psychiatric diagnoses are important in investigating the link between psychopathology and sleep disturbances. Finally, sleep disturbances cover a broad spectrum of complaints and can range from problems with falling asleep, frequent nocturnal awakenings, early morning awakenings, or a disturbed sleep duration (either too short or too long). Recent research has pointed out that subjective sleep assessment and sleep duration are not equally associated with psychopathology and should be analyzed separately.14 It is important not only to explore the relationship between psychopathology and short sleep duration but to also focus on long sleep duration, since hypersomnia is a common complaint in depression, and subjects with anxiety disorders have been shown also to report an extended sleep duration.15
Epidemiologic studies have investigated sleep in psychopathology, but most large-scale studies do not rely on standardized psychiatric interviews in diagnosing both current and remitted psychopathology, do not study depression and anxiety in concert, or do not have data on a large set of possible confounders. The latter is important since—besides psychopathology—sleep is also influenced by factors such as sociodemographics (age, gender, marital status, life events), somatic health (chronic diseases, pain conditions), and use of medication (antidepressants, benzodiazepines).5,10,16–18 Therefore, the aim of this study is to describe the association between both insomnia and sleep duration with current and remitted depressive and anxiety disorders in a large cohort study, taking sociodemographics, somatic health, and medication use into account.
For this study, data were analyzed from the baseline measurement of the Netherlands Study of Depression and Anxiety (NESDA). The NESDA study is an ongoing 8-year longitudinal cohort study designed to investigate the long-term course of depressive and anxiety disorders in individuals ranging from 18 to 65 years of age. The research protocol was approved by the ethical committees of participating universities, and all respondents provided written informed consent. The NESDA respondents were recruited from 3 different settings: the general population, primary health care, and secondary mental health care. Individuals from the general population had previously participated in the Netherlands Mental Health Survey and Incidence Study (NEMESIS)19 or the Adolescents at Risk for Anxiety and Depression (ARIADNE) study.20 Individuals from primary care were recruited through a 3-stage screening procedure, including the Kessler-1021 and a short-form Composite International Diagnostic Interview phone interview (CIDI).22 Individuals from secondary care were recruited after they were newly enrolled for anxiety or depressive disorders at one of the participating mental health clinics.
Exclusion criteria for the NESDA study were not speaking the Dutch language and a known primary clinical diagnosis of bipolar disorder, obsessive-compulsive disorder, severe addiction disorder, psychotic disorder, or organic psychiatric disorder. A more detailed description about the study’s sampling procedures is described elsewhere.23
The final sample size of the NESDA study consisted of 2,981 subjects (18.9% from the community, 54.0% from primary care, and 27.0% from secondary mental health care). Of these participants, 362 (12.2%) had missing data on the questionnaire concerning sleep and were excluded from the current study, resulting in a sample size of 2,619 persons. Excluded individuals were significantly younger (37.9 versus 42.4 years of age, P < .001), more often female (67.1% versus 61.0%, P = .02), and suffered more frequently from a current major depressive disorder (53.3% versus 35.3%, P ≤ .001) or anxiety disorder (57.7% versus 41.8%, P < .001) than included individuals.
Between September 2004 and February 2007, participating individuals visited 1 of the 7 interview locations for the baseline measurement. This measurement consisted among others of a standardized diagnostic psychiatric interview, drawing of a blood sample, a medical assessment, computer tasks, and 2 self-assessment questionnaires (1 before and 1 after the interview).
Insomnia and Sleep Duration
Sleep was assessed by insomnia and sleep duration. Both insomnia and sleep duration were part of a questionnaire that subjects filled out after the interview or at home (median time log for returning the questionnaire was 4 days). Insomnia was assessed with the Women’s Health Initiative Insomnia Rating Scale (IRS).24 This scale was developed by Levine et al24 and consists of 5 questions addressing trouble falling asleep, waking up during the night, early morning awakenings, trouble getting back to sleep after waking up, and sleep quality in the past month. The total summary score ranged from 0 (no insomnia) to 20 (severe insomnia). Validity of the IRS has been reported: test-retest reliability was 0.96 (same day) and 0.66 (1 year later),25 and the IRS has shown to be strongly correlated with other actigraphy derived sleep measures. 25 In our study, Cronbach α was 0.83. Scores on the IRS were dichotomized at a cut-off point of 9, which has shown to indicate clinically significant insomnia.25 Sleep duration was assessed by asking subjects to estimate the average number of hours of sleep per night during the past month, ranging from less than 5 hours to more than 10 hours. Answers were categorized in sleep duration of ≤ 6 hours (short sleep duration), 7–9 hours, or ≥ 10 hours (long sleep duration). Sleep duration and IRS score were only mildly correlated (r = −0.45, P = <.001), confirming that sleep duration and sleep complaints are separate concepts.
Psychopathology. The presence of psychiatric disorders was determined using the CIDI.22 The CIDI is a standardized diagnostic psychiatric interview that uses Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria to establish diagnoses.22 Major depressive disorder status was categorized as follows: current diagnosis (ie, in the past 6 months), remitted diagnosis (ie, lifetime diagnosis but not in the past 6 months), or controls (no lifetime diagnosis). Assessed anxiety disorders included panic disorder, agoraphobia, generalized anxiety disorder (GAD), and social phobia and were categorized similarly as current diagnosis, remitted diagnosis, or controls.
Sociodemographics. Sociodemographic characteristics that could possibly affect sleep included age (in years), gender, current partner status, education (in years), and working status. A total count of negative life events in the past year was made through Brugha and colleague’s List of Threatening Experiences.26
Health indicators. A number of health factors that have been associated with both sleep and psychopathology were assessed. Smoking was categorized as “current smoker,” “former smoker,” or “nonsmoker.” Alcohol intake was calculated by categorizing the number of alcoholic drinks per week in none (less than 1 per week), moderate (for males, 1–21 per week; for females, 1–14 per week), and heavy (for males, > 21 per week; for females, > 14 per week). Hypertension was defined as a mean systolic blood pressure ≥ 140 mmHg, a mean diastolic blood pressure ≥ 90 mmHg, or the reported use of antihypertensive drugs (based on drug container inspection and categorized according to Anatomic Therapeutic Chemical Classification (ATC)27 (codes CO2, CO3, CO7–CO9).
Body mass index (BMI) was computed by weight in kilograms divided by height in meters squared. Diabetes was defined as either a fasting blood glucose level > 7 mmol/L (126 mg/dL) or use of antidiabetic drugs (ATC code A10). Cardiovascular disease (including myocardial infarction, angina pectoris, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, or cerebrovascular accidents) was adjudicated using standardized algorithms considering self-report and medication use. A total count of the following other (chronic) diseases was made, based on self-report: lung disease, cancer, osteoarthritis, intestinal disorders, liver disease, epilepsy, chronic fatigue syndrome, thyroid gland disease, and intestinal ulcers. The intensity of chronic pain was measured with the Chronic Pain Grade scale.28
Psychotropic medication. Sleep can be influenced by psychotropic medication, which can therefore confound the association between psychopathology and sleep outcomes. Based on drug container inspection of all drugs used in the past month, medication use was classified according to the World Health Organization’s ATC classification.27 Psychotropic medication included antidepressants and benzodiazepines and was considered present if subjects reported use of medication > 50% of the time. Antidepressants were categorized as selective serotonin reuptake inhibitors (SSRIs) (ATC code NO6AB), tricyclic antidepressants (TCAs) (ATC code NO6AA), and other antidepressants (ATC codes N05BA, N05CF, N05CD, and N03AE). Benzodiazepines included ATC codes NO5BA, NO5CF, NO5CD, and NO3AE.
Statistical analyses. Data were analyzed using SPSS 15.0 (SPSS Inc, Chicago, Illinois). Mean (unadjusted) IRS scores and sleep duration were calculated according to psychopathology status. To compare characteristics across insomnia and sleep duration categories, analyses of variance (ANOVAs), t tests, χ2 statistics, or Fisher exact tests were used. Subsequently, logistic regression analyses were performed with insomnia (yes versus no, IRS score ≥ 9) as the outcome, first unadjusted, followed by adjustment for sociodemographic and health factors, and finally adjusted for all covariates. Similarly, multinomial logistic regression analyses were performed for sleep duration categories in which short- and long-duration outcomes were compared to normal duration as the reference group. We directly compared current MDD and current anxiety disorder in a subsample analysis, adjusting for sociodemographic and somatic health factors. Interaction effects between current MDD and current anxiety disorder were tested to explore whether comorbidity of these conditions had multiplicative effects on sleep outcomes. Finally, within currently anxious individuals, we tested whether associations with sleep outcomes were consistent across anxiety subtypes by testing specific indicators for anxiety subtypes in logistic and multinomial regression analyses.
The mean age of the study sample (n = 2,619) was 42.4 years (SD = 13.1), 67.1% of the sample was female, and 61.9% of the sample was currently working. Mean sleep duration was 7.2 hours (SD = 1.3), and mean IRS score was 8.1 (SD = 5.1). Almost half of the individuals (43.7%) had an IRS score ≥ 9, indicating clinically significant insomnia. Of all subjects, 23.5% never had a diagnosis of major depression or anxiety disorders, 22.3% had a remitted major depressive or anxiety disorder but no current disorder, 12.6% had a current major depressive but no current anxiety disorder, 19.3% had a current anxiety disorder but no current MDD, and 22.6% suffered from both current disorders. Of individuals with remitted major depressive or anxiety disorder but no current disorder, 27.1% slept ≤ 6 hours, and 1.7% slept ≥ 10 hours. Of individuals suffering from current MDD only, 31.1% slept ≤ 6 hours, and 6.0% slept ≥ 10 hours per night. In the case of a current anxiety disorder, 25.3% slept ≤ 6 hours, and 3.0% slept ≥ 10 hours per night. When both disorders were present, 41.8% slept ≤ 6 hours, and 8.8% slept ≥ 10 hours per night.
Table 1 shows that more insomnia was found for subjects with current depressive and anxiety disorders and for those with a higher age, less education, both “no alcohol intake” or “heavy alcohol intake,” a higher BMI, more hypertension, more cardiovascular disease or other diseases, a higher pain intensity, and more psychotropic medication and benzodiazepine use. For sleep duration, additional differences were found for female gender, more recent life events, and current smoking.
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Figure 1 shows mean IRS scores according to psychopathology status and illustrates that insomnia scores differed according to psychopathology: individuals with no lifetime diagnosis had the lowest scores, followed by individuals with remitted disorders, whereas the highest scores were found in subjects suffering from both disorders. Table 2 shows that both current and remitted MDD as well as current and remitted anxiety disorder were associated with insomnia. Except for remitted anxiety disorder, this association could not be explained by sociodemographic or somatic health factors, since ORs remained significant when adding these factors to the model. In multivariable analyses, independent of psychopathology, higher age, current smoking status, heavy alcohol intake, more chronic diseases, and a higher pain intensity were also independently associated with insomnia. Even after adding psychotropic medication to the model, associations with psychopathology remained. Use of SSRIs was associated with less insomnia, and use of benzodiazepines was associated with more insomnia.
When we directly compared currently depressed individuals with currently anxious individuals (n = 1,427), associations for MDD appeared to be stronger than for anxiety disorder (OR for MDD = 1.98, 95% CI, 1.56 to 2.51, P < .001). To determine if comorbid depressive and anxiety disorders were more associated with insomnia complaints than the sum of the single diagnoses, interaction effects were tested, revealing that there was no significant multiplicative interaction effect (P > .10).
In a subset of currently anxious individuals (n = 1,097), we explored whether associations with insomnia were consistent for the specific anxiety subtypes using a logistic regression analysis adjusted for age and gender. Within the anxiety group, it appeared that especially those with GAD had a higher odds of insomnia compared to subjects with social phobia (OR for GAD = 1.74, 95% CI, 1.34 to 2.26).
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Sleep Duration Analyses
Figure 2 shows differences in sleep duration categories (short, normal, long) according to psychopathology status. Table 3 shows that short sleep duration (≤ 6 hours) was associated with current MDD and anxiety disorder as well as with remitted MDD but not with remitted anxiety disorder. Even after adding covariates to the model, associations remained. Also, higher age, less education, male gender, more recent life events, higher BMI, no hypertension, and higher pain intensity were independently associated with short sleep duration. The use of SSRIs and other antidepressants was independently associated with a significantly lower risk of reporting short sleep duration, but benzodiazepine use was not significantly associated with short sleep duration. Additional adjustment for psychotropic medication did not largely change the short sleep duration risks for depressive and anxiety disorders.
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Long sleep duration was also associated with current MDD and anxiety disorder, and these associations remained significant after adding covariates, but a lower age, female gender, not currently working, and more chronic diseases also contributed to long sleep duration. No associations were found for remitted disorders. In line with a lower risk for short sleep duration, the use of antidepressants (TCAs and SSRIs) did significantly increase the risk for long sleep duration. After adding psychotropic medication to the model, associations remained for current MDD but not for current anxiety disorder. When we directly compared currently depressed individuals with currently anxious individuals (n = 1,427), associations for MDD appeared to be stronger than for anxiety disorder both for short sleep duration (OR = 2.03, 95% CI, 1.55 to 2.65) and long sleep duration (OR = 2.72, 95% CI, 1.50 to 4.93). To determine if comorbid depressive and anxiety disorders were more strongly associated with short or long sleep duration than the sum of single diagnoses, interaction effects were tested but not found to be present (both P > .10).
In the subset of currently anxious individuals (n = 1,097), we found no significant differences across anxiety subtypes in their association with short sleep duration (all P > .10 for contrasts between subtypes). For long sleep duration, we found that GAD was associated with significantly higher odds compared to the other anxiety disorders (OR = 1.70, 95% CI, 1.02 to 2.84).
Our findings indicate that both current and remitted MDD as well as current anxiety disorders are associated with insomnia and short sleep duration. Long sleep duration is associated with current major depressive and anxiety disorders. Associations were stronger for depressive than for anxiety disorders and were independent of sociodemographic factors, health factors, or psychotropic medication use. Associations were also stronger for current than for remitted depressive diagnoses, although the latter still had a significant impact on sleep, suggesting sleep disturbances are possibly a trait marker or a residual symptom of major depression. After adjusting for confounding variables, anxiety disorders were only associated with insomnia and short and long sleep duration in the case of current disorders, suggesting that these sleep disturbances resolve after recovery from the disorder.
As expected, the strongest associations for both insomnia and sleep duration were found for MDD, which is in line with other studies,5 but we also found an independent association with anxiety disorders. Interestingly, not only current MDD but also remitted disorders are associated with insomnia and short sleep duration. In previous studies, sleep complaints were found to be one of the most common residual symptoms after achieving remission from a major depressive episode, next to fatigue and loss of interest. This finding was irrespective of the subjects’ baseline severity depression, length of the episode, age, gender, or marital status.29 Residual depressive symptoms are also associated with a significantly earlier relapse rate than asymptomatic recovery.30 Some studies suggest a more vigorous approach of treating MDD resulting in as few residual symptoms as possible,31 although this enhances the risk of side effects and noncompliance. The literature is inconsistent on sleep disturbances being a trait marker for depression: some studies find persistent electroencephalographic (EEG) changes in remitted depressed individuals,32 whereas other studies do not find these differences.33 This may be due to methodological differences, but possibly, certain subgroups of depressed individuals are more prone to relapse of the disorder and display such trait markers, whereas others recover from these abnormalities.33
The association between psychopathology and insomnia and sleep duration was not altered significantly by adding covariates to the model. However, in addition to psychopathology, some of these factors, such as higher pain intensity, do independently contribute to sleep disturbances. Other factors contributing to the association, such as chronic diseases, are a known risk factor for sleep disturbances not only because of the disease itself but also because of side effects of related medications.17
The use of benzodiazepines was associated with more insomnia, which is likely due to indication bias, since benzodiazepines are most likely to be used by subjects who experience the most severe insomnia. Strikingly, although benzodiazepine use was associated with more insomnia, the use of certain antidepressants was associated with less insomnia and longer sleep duration. This opposite effect of antidepressants could potentially reflect efficacious effects of antidepressants: randomized controlled trials testing TCAs have shown sleep complaints to diminish and sleep duration to increase among antidepressants users.34
Interestingly, current depressive and anxiety disorders were associated with not only shorter sleep duration but also longer sleep duration. For depressive disorders, this may have to do with the fact that depressive disorders can present with both melancholic and atypical symptoms, resulting in both short sleep duration and long sleep duration. As for subtypes of current anxiety disorders, in our study, GAD was most prominently associated with insomnia and long sleep duration. Generalized anxiety disorder has, in previous studies, been associated with a sleep maintenance insomnia,35 but an association with long sleep duration has not been reported before.
Although this study had the advantage of a large psychiatric sample and could adjust for a large set of possible confounders in investigating the relationship between psychopathology and sleep disturbances, there are a few limitations to be mentioned. First, because the data in this study are cross-sectional, it is impossible to draw conclusions on causality regarding sleep disturbances and psychopathology. Therefore, future longitudinal research is needed. Second, sleep outcomes (both insomnia complaints and sleep duration) were based on self-reported measures. Overestimation as well as underestimation of sleep complaints and sleep duration could have been influenced by psychopathological status, as has been shown before.36 Third, the IRS has been validated for women only. Fourth, insomnia was treated as categorical outcome, which may have influenced precision, but using categorical outcome measures facilitates comparison between these clinically relevant outcome groups. Fifth, we had no information available on premorbid sleep quality or sleep duration or on specific medical conditions that have been associated with altered sleep duration, such as sleep apnea. In spite of these limitations, our study stresses the importance of addressing sleep disturbances in psychopathology, not only in current diagnoses but also in remitted disorders.
To conclude, subjects with depressive and anxiety disorders disorder may experience insomnia and altered sleep duration even after remittance of the disorder. Inquiring about short sleep duration only may not be sufficient, as our study clearly shows that both extremes of the sleep duration spectrum are associated with both depressive and anxiety disorders. Clinicians should actively ask about insomnia and sleep duration not only in depressive disorders but also in anxiety disorders.
Author affiliations: NeuroCampus Amsterdam, VU University Medical Center, Amsterdam (Drs van Mill, Hoogendijk, and Penninx); Department of Psychiatry and the EMGO Institute for Health and Care Research (Drs Vogelzangs, van Dyck, and Penninx); and Department of Psychiatry, Leiden University Medical Center, and Department of Psychiatry, University Medical Center Groningen (Dr Penninx), The Netherlands.
Potential conflicts of interest: Dr Hoogendijk has received grant/research support from Servier Inc. Drs van Mill, Vogelzangs, van Dyck, and Penninx report no conflicts of interest.
Funding/support: The infrastructure for the NESDA study (www.nesda.nl) is funded through the Geestkracht program of the Netherlands Organisation for Health Research and Development (Zon-Mw, grant number 10-000-1002) and is supported by participating universities and mental health care organizations (VU University Medical Center, GGZ inGeest, Arkin, Leiden University Medical Center, GGZ Rivierduinen, University Medical Center Groningen, Lentis, GGZ Friesland, GGZ Drenthe, IQ Healthcare, the Netherlands Institute for Health Services Research (NIVEL), and the Netherlands Institute of Mental Health and Addiction (Trimbos). Data analyses were supported by an unrestricted grant from Servier, Leiden, The Netherlands. J. van Mill, N. Vogelzangs, W. Hoogendijk, and B. Penninx carried out the analyses. Servier was not involved in the interpretation of the data nor the preparation or review of the manuscript prior to submission.
1. Kaufman DM. Sleep disorders. In: Kaufman DM, ed. Clinical Neurology for Psychiatrists. 6th ed. Philadelphia, PA: Saunders Elsevier; 2007:371–391.
2. Zisapel N. Sleep and sleep disturbances: biological basis and clinical implications. Cell Mol Life Sci. 2007;64(10):1174–1186. PubMed doi:10.1007/s00018-007-6529-9
3. Andrews G, Peters L. The psychometric properties of the Composite International Diagnostic Interview. Soc Psychiatry Psychiatr Epidemiol. 1998;33(2):80–88. PubMed doi:10.1007/s001270050026
4. Daley M, Morin CM, LeBlanc M, et al. Insomnia and its relationship to health-care utilization, work absenteeism, productivity and accidents. Sleep Med. 2009;7(2):123–130.
5. Hartz AJ, Daly JM, Kohatsu ND, et al. Risk factors for insomnia in a rural population. Ann Epidemiol. 2007;17(12):940–947. PubMed doi:10.1016/j.annepidem.2007.07.097
6. Tsuno N, Besset A, Ritchie K. Sleep and depression. J Clin Psychiatry. 2005;66(10):1254–1269. PubMed
7. Mellman TA. Sleep and anxiety disorders. Psychiatr Clin North Am. 2006;29(4):1047–1058, abstract x. PubMed doi:10.1016/j.psc.2006.08.005
8. Mahendran R, Subramaniam M, Chan YH. Psychiatric morbidity in patients referred to an insomnia clinic. Singapore Med J. 2007;48(2):
9. Ford DE, Kamerow DB. Epidemiologic study of sleep disturbances and psychiatric disorders: an opportunity for prevention? JAMA. 1989;262(11):1479–1484. PubMed doi:10.1001/jama.262.11.1479
10. Ohayon MM. Epidemiology of insomnia: what we know and what we still need to learn. Sleep Med Rev. 2002;6(2):97–111. PubMed doi:10.1053/smrv.2002.0186
11. Fava M, Rankin MA, Wright EC, et al. Anxiety disorders in major depression. Compr Psychiatry. 2000;41(2):97–102. PubMed doi:10.1016/S0010-440X(00)90140-8
12. Carney CE, Segal ZV, Edinger JD, et al. A comparison of rates of residual insomnia symptoms following pharmacotherapy or cognitive-behavioral therapy for major depressive disorder. J Clin Psychiatry. 2007;68(2):
254–260. PubMed doi:10.4088/JCP.v68n0211
13. Hatzinger M, Hemmeter UM, Brand S, et al. Electroencephalographic sleep profiles in treatment course and long-term outcome of major depression: association with DEX/CRH-test response. J Psychiatr Res. 2004;38(5):
453–465. PubMed doi:10.1016/j.jpsychires.2004.01.010
14. Kaneita Y, Ohida T, Osaki Y, et al. Association between mental health status and sleep status among adolescents in Japan: a nationwide cross-sectional survey. J Clin Psychiatry. 2007;68(9):1426–1435. PubMed doi:10.4088/JCP.v68n0916
15. Ohayon MM. From wakefulness to excessive sleepiness: what we know and still need to know. Sleep Med Rev. 2008;12(2):129–141. PubMed doi:10.1016/j.smrv.2008.01.001
16. Bastien CH, Vallières A, Morin CM. Precipitating factors of insomnia. Behav Sleep Med. 2004;2(1):50–62. PubMed doi:10.1207/s15402010bsm0201_5
17. Thase ME. Correlates and consequences of chronic insomnia.
Gen Hosp Psychiatry. 2005;27(2):100–112. PubMed doi:10.1016/j.genhosppsych.2004.09.006
18. Gursky JT, Krahn LE. The effects of antidepressants on sleep: a review. Harv Rev Psychiatry. 2000;8(6):298–306. PubMed doi:10.1093/hrp/8.6.298
19. Bijl RV, van Zessen G, Ravelli A, et al. The Netherlands Mental Health Survey and Incidence Study (NEMESIS): objectives and design.
Soc Psychiatry Psychiatr Epidemiol. 1998;33(12):581–586. PubMed doi:10.1007/s001270050097
20. Landman-Peeters KMC, Hartman CA, van der Pompe G, et al. Gender differences in the relation between social support, problems in parent-offspring communication, and depression and anxiety. Soc Sci Med. 2005;60(11):2549–2559. PubMed doi:10.1016/j.socscimed.2004.10.024
21. Kessler RC, Andrews G, Colpe LJ, et al. Short screening scales to monitor population prevalences and trends in non-specific psychological distress. Psychol Med. 2002;32(6):959–976. PubMed doi:10.1017/S0033291702006074
22. World Health Organization. Composite International Diagnostic Interview (CIDI): version 2.1. Geneva, Switzerland: 1997.
23. Penninx BW, Beekman AT, Smit JH, et al. NESDA Research Consortium. The Netherlands Study of Depression and Anxiety (NESDA): rationale, objectives and methods. Int J Methods Psychiatr Res. 2008;17(3):121–140. PubMed doi:10.1002/mpr.256
24. Levine DW, Kaplan RM, Kripke DF, et al. Factor structure and measurement invariance of the Women’s Health Initiative Insomnia Rating Scale. Psychol Assess. 2003;15(2):123–136. PubMed doi:10.1037/1040-35220.127.116.11
25. Levine DW, Kripke DF, Kaplan RM, et al. Reliability and validity of the Women’s Health Initiative Insomnia Rating Scale. Psychol Assess. 2003;15(2):137–148. PubMed doi:10.1037/1040-3518.104.22.168
26. Brugha T, Bebbington P, Tennant C, et al. The List of Threatening Experiences: a subset of 12 life event categories with considerable long-term contextual threat. Psychol Med. 1985;15(1):189–194. PubMed doi:10.1017/S003329170002105X
27. World Health Organization, Collaborating Centre for Drug Statistics Methodology. Anatomical Therapeutic Chemical (ATC) classification. 2007
28. Von Korff M, Ormel J, Keefe FJ, et al. Grading the severity of chronic pain. Pain. 1992;50(2):133–149. PubMed doi:10.1016/0304-3959(92)90154-4
29. Nierenberg AA, Keefe BR, Leslie VC, et al. Residual symptoms in
depressed patients who respond acutely to fluoxetine. J Clin Psychiatry. 1999;60(4):221–225. PubMed
30. Judd LL, Akiskal HS, Maser JD, et al. Major depressive disorder: a prospective study of residual subthreshold depressive symptoms as predictor of rapid relapse. J Affect Disord. 1998;50(2–3):97–108. PubMed doi:10.1016/S0165-0327(98)00138-4
31. Nierenberg AA, Wright EC. Evolution of remission as the new standard in the treatment of depression. J Clin Psychiatry. 1999;60(suppl 22):7–11. PubMed
32. Modell S, Ising M, Holsboer F, et al. The Munich Vulnerability Study on Affective Disorders: stability of polysomnographic findings over time.
Biol Psychiatry. 2002;52(5):430–437. PubMed doi:10.1016/S0006-3223(02)01398-7
33. Leistedt S, Dumont M, Coumans N, et al. The modifications of the long-range temporal correlations of the sleep EEG due to major depressive episode disappear with the status of remission. Neuroscience. 2007;148(3):782–793. PubMed doi:10.1016/j.neuroscience.2007.06.032
34. Mayers AG, Baldwin DS. Antidepressants and their effect on sleep. Hum Psychopharmacol. 2005;20(8):533–559. PubMed doi:10.1002/hup.726
35. Monti JM, Monti D. Sleep disturbance in generalized anxiety disorder and its treatment. Sleep Med Rev. 2000;4(3):263–276. PubMed doi:10.1053/smrv.1999.0096
36. Bliwise DL, Friedman L, Yesavage JA. Depression as a confounding variable in the estimation of habitual sleep time. J Clin Psychol. 1993;49(4):471–477. PubMed doi:10.1002/1097-4679(199307)49:4<471::AID-JCLP2270490403>3.0.CO;2-7