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Nature and Science of Sleep logoLink to Nature and Science of Sleep
. 2012 May 29;4:63–71. doi: 10.2147/NSS.S23490

Sleep patterns and the risk for unipolar depression: a review

Sabrina T Wiebe 1, Jamie Cassoff 1, Reut Gruber 1,
PMCID: PMC3630972  PMID: 23620679

Abstract

Psychological disorders, particularly mood disorders, such as unipolar depression, are often accompanied by comorbid sleep disturbances, such as insomnia, restless sleep, and restricted sleep duration. The nature of the relationship between unipolar depression and these sleep disturbances remains unclear, as sleep disturbance may be a risk factor for development, an initial manifestation of the disorder, or a comorbid condition affected by similar mechanisms. Various studies have examined the impact of sleep deprivation on the presence of (or exacerbation of) depressive symptoms, and have examined longitudinal and concurrent associations between different sleep disturbances and unipolar depression. This review examines the evidence for sleep disturbances as a risk factor for the development and presence of depression, as well as examining common underlying mechanisms. Clinical implications pertaining to the comorbid nature of various sleep patterns and depression are considered.

Keywords: sleep, depression, insomnia, sleep deprivation, development

Introduction

Sleep difficulties are often comorbid with psychological conditions, particularly mood disorders, such as unipolar depression.1 To what extent sleep problems are a risk for development of unipolar depression or are an outcome of depression is, however, unclear. Evidence suggests that, for depression, there is a bi-directional relationship, such that sleep problems contribute to increased manifestation of depressive symptoms (eg, mood dysregulation), and depressive psychopathology contributes to worsened sleep.2 Therefore, this review will examine (1) evidence for various sleep aspects being risk factors for both development and exacerbation of unipolar depression; (2) common underlying mechanisms between sleep disturbance and depression; and (3) clinical implications of the interplay between sleep and depression.

Methods

A search using PubMed, Google Scholar, and PsycInfo® databases was carried out. Combinations of the following keywords were used: “sleep”, “psychopathology”, “depression”, “risk factor”, “predictor”, “development”, “sleep restriction”, “sleep deprivation”, “sleep patterns”, “insomnia,” and “sleep problems”. Other relevant articles were obtained by examining the reference sections of appropriate articles. Articles were kept that directly assessed variables of interest (sleep patterns and unipolar depression). Precedence was given to studies that showed a directional relationship between sleep and psychopathology. Studies with the elderly were excluded, due to the presence of additional complications, such as increased risk of illness and injury, which may contribute to the development of sleep problems and/or depression. Two articles pertaining to experimental sleep deprivation and depression were found and reviewed, along with twelve articles examining the longitudinal relationship between sleep disturbance and depression, and 14 articles which examined sleep phenotype and risk for depression. Although definitions of sleep terminology varied between different studies, for the purposes of this review, insomnia refers to the clinical condition of non-restorative sleep, usually due to difficulties initiating and/or maintaining sleep, which interferes with daily functioning and lasts for a period of at least 1 month;3 sleep deprivation refers to the purposeful elimination of sleep, during at least one 24-hour period;4 and sleep disturbance refers to dysfunctions of sleep, including diagnosable sleep disorders, such as insomnia, parasomnias, and other sleep disorders, as well as dysfunctions of sleep architecture and continuity.5

Sleep and unipolar depression

Unipolar depression is a common psychological condition, consisting of feelings of low self-worth, sadness, lack of interest or pleasure in normally enjoyable activities, with an adverse effect on relationships and everyday functioning.3 It has a prevalence of approximately 4%–11% in children and adolescents,6,7 and 3%–3.5% in adults.8 Given that almost 90% of individuals who experience depression have comorbid sleep disorders,9 the following section will examine the influence of sleep deprivation, insomnia, and sleep phenotypes on the development and/or exacerbation of depressive symptoms. It is followed by consideration of common pathophysiological mechanisms. Finally, clinical implications regarding the interplay between sleep and depression are discussed.

Sleep deprivation as a risk factor for depressive symptoms

Studies that examined the impact of sleep deprivation on depressive symptomology show an interesting phenomenon: sleep deprivation can be beneficial in reducing symptoms,10 or it can aggravate or precipitate a negative mood state.11 Such phenomena make it more difficult to understand the nature of the relationship between sleep and depression.

Studies that experimentally manipulate the amount of sleep healthy participants receive have found a relationship between sleep deprivation and increased depressive symptoms.11 In a study by Kahn-Greene and colleagues,11 healthy military participants were asked to complete a baseline assessment of the Personality Assessment Inventory,12 which examines symptoms of various psychological disorders, and were required to stay awake for 56 hours before again completing the Personality Assessment Inventory. The researchers found that, following sleep deprivation, scores on the affective psychological disorder components of the inventory were significantly increased. Of note is that physical aspects of depressive symptoms did not change from baseline to post-deprivation, but the cognitive and affective aspects did. Although values fell within a normal range, the researchers noted that the increases for depressive scores would be considered clinically significant.11,12

In another study, by Bernier and colleagues,13 healthy women and women experiencing unipolar depression were restricted to 2.5 hours in bed for 1 night. Participants completed the Profile of Mood States assessment14 at baseline and following sleep restriction. Although negative mood states were not exacerbated for the women experiencing depression, healthy women experienced a significant increase in anhedonia ratings, from baseline to post-restriction. This finding is important, as it suggests that, while healthy women may not develop unipolar depression following sleep restriction, they are prone to developing depressive-like symptoms following acute sleep restriction.

These experimental studies provide insight into the effect that acute sleep deprivation or restriction can have on depressive symptoms. However, it is unclear from these studies how chronic sleep problems may contribute to developing depressive symptoms, or depression itself. Therefore, it is important to examine longitudinal studies that investigate the effects of chronic sleep disturbance, such as encountered with insomnia, and how they relate to the risk of developing depression.

Insomnia as a risk factor for developing depression

Accumulating evidence suggests that sleep problems, such as insomnia, are risk factors for the development of depression.15 Longitudinal associations have been examined over different time periods, from 1 to 45 years, and age groups (Table 1). Although some studies have failed to find an association between sleep problems and the development of depression,16,17 more generally, the presence of insomnia has been associated with 2.118 to 39.815 greater odds of developing depression at follow-up, compared to those not suffering from insomnia.

Table 1.

Studies examining the risk of developing depression based on sleep disturbances

Author Sample size Age at T1 Sleep measures Diagnostic measures Time-frame Main findings
Ford and Kamerow15 10,534 at T1; 7954 at T2 18+ years Diagnostic interview schedule63 Diagnostic interview schedule63 1 year If insomnia was present at both interviews, there were 39.8 greater odds of developing depression; These odds were reduced to 1.6 if insomnia resolved by the follow-up
Vollrath et al17 457 21 years Psychiatric interview DSM-III64 criteria 7 years Depression levels were elevated for insomniacs at follow-up, but not significantly so
Breslau et al65 1007 at T1; 979 at T2 21–30 years DIS-III-R66 DIS-III-R66 3.5 years Insomnia predicted 2.1 greater odds of developing depression
Chang et al18 1053 men ~26 years Habit survey questionnaire67 Questionnaires and medical reports 1–45 years (median, 34 years) Presence of insomnia in medical school was related to 2.1 greater odds of developing depression
Johnson et al24 823 at T1; 7l7 at T2 6 years Child behavior checklist68 Child behavior checklist68 and teacher report form68 5 years Trouble sleeping was related to 6.9 greater odds of increased Anxious/Depressed scores; Relationships were stronger at 11 years than at 6 years
Gregory and O’Connor22 490 at T1; 360 final 4 years Child behavior checklist68 Child behavior checklist68 11 years Sleep problems at age 4 predicted mid-adolescent Anxious/Depressed scores; Early Anxious/Depressed scores did not predict later sleep problems
Gregory et al16 943 children Five time points: 5, 7, 9, 21, and 26 years Self-developed measure of persistent sleep problems Rutter child behaviour scale65; diagnostic interview schedule63 21 years Sleep problems did not predict development of depression, although 46% of children with persistent sleep problems developed anxiety problems
Johnson et al20 1014 adolescents 13–15 years Computerized diagnostic interview schedule for children-IV70 Computerized diagnostic interview schedule for children-IV70 Based on self-reported age of onset Insomnia occurred before depression in 69% of cases; Prior depression was not related to future insomnia
Ong et al21 220 at T1; 164 final 6–23 years Restrospective report for the dimensions of temperament survey7 SADS-L72 and K-SADS-E73 20 years Irregular sleep schedules related to 1.3 greater odds of adolescent onset of major depressive disorder
Gregory et al23 2076 at T1; 1615 at T6 4–16 years Child behavior checklist68 Child behavior checklist68 and young adult self-report74 14 years Sleeping less than others, overtiredness, and trouble sleeping were related to increased odds for higher Anxious/Depressed scores at follow-up (1.43, 1.37, and 1.39 greater odds, respectively)
Roane and Taylor35 4494 at T1; 3582 at T2 12–18 years Nonvalidated questionnaire Nonvalidated questionnaire 6–7 years If insomnia was present in adolescence, there were 2.3 greater odds of developing depression
Gregory et al19 300 twin pairs at T1;250 at T2 8 years Children’s sleep habits questionnaire73 Children’s depression inventory76 ~2 years Sleep problems at age 8 predicted development of depression by age 11, while the opposite was not true

Abbreviations: T1, time 1 (first assessment); T2, time 2; T6, time 6; DIS-III-R, Diagnostic Interview Schedule Version 3, Revised; DSM, Diagnostic and Statistical Manual of Mental Disorders; SADS-L, Schedule for Affective Disorders and Schizophrenia-Lifetime version; K-SADS-E, Schedule for Affective Disorders and Schizophrenia in School-age children.

An initial study to examine the ability of sleep problems to predict future development of major depression was conducted by Ford and Kamerow.15 In this study, adults aged 18 years and older were interviewed at baseline and 1 year later, using clinical diagnostics for sleep problems and major depression. It was found that adults who experienced insomnia both at baseline and follow-up were 39.8 times more likely to develop depression than those who never experienced insomnia. These odds were reduced to 1.6 times greater risk if insomnia symptoms resolved during the intervening period. At the time of this study, these findings were ground-breaking; they have led the way to many more studies that examine the relationship between sleep problems and future development of depression.

One area that has received particular attention is the association between childhood sleep problems, defined in various ways (Table 1), and the subsequent development of depression or anxiety/depression in adolescence or adulthood. It has been found generally that the presence of insomnia, or sleep problems, predicts later development of unipolar depression1921 or anxious/depressive symptoms,2224 while the converse is not true.19,20,22 This suggests that sleep problems are either an initial symptom of depression or that they increase vulnerability to developing depression later in life, which emphasizes the importance of examining insomnia and trouble sleeping from an early age.

Sleep phenotypes as risk factors for development and recurrence of depression

In a meta-analysis of 177 adult studies, which examined the association between various psychiatric disorders and sleep phenotypes, Benca et al25 found that REM sleep pressure, which refers to shorter rapid eye movement (REM) sleep latency, as well as to an overall increased duration and density of REM during the night, was related to increased risk for the development and presence of affective disorders such as depression.2629 Other common sleep phenotype characteristics that indicated increased risk for developing depression included increased sleep onset latency, and reduced slow-wave activity.2629

Developmental considerations

Although findings regarding sleep architecture and its relation to depression are fairly consistent in adults, associations between sleep architecture and depression are not as consistent in children and adolescents.30 While some researchers find that at-risk children and adolescents present with increased sleep onset latency, decreased sleep efficiency, and increased REM sleep pressure,3133 others have shown no relationship with REM sleep characteristics,30 or limited relations with other sleep aspects common to depressed adults.34,35 This suggests there may be a developmental aspect in the way that sleep and depression are related, which is consistent with findings that sleep physiology undergoes significant changes from pre-pubescence, through puberty, and into adulthood.36,37

Further examination of sleep architecture with children and adolescents, either experiencing depression or at risk for developing major depression, has found that such individuals display reduced sleep spindle activity during Stage 2 sleep, compared to healthy controls.38 Additionally, this relationship was stronger in girls than in boys,38 suggesting that girls who display reduced sleep spindle activity may be particularly vulnerable for developing unipolar depression – or that those girls most likely to develop depression show more pronounced differences in sleep characteristics.

Given the evidence supporting the increased risk of developing depression, or having recurrence of depression, when certain sleep characteristics are present, understanding the common pathophysiology of sleep disturbance and depression is important for recognizing how we can treat both these disorders.

Methodological considerations

Although a number of studies have examined the relationship between various sleep patterns and risks for depression and depressive symptomology, several methodological considerations need to be addressed. First, depression and sleep problems, such as insomnia, have been defined in different ways among the studies. Especially in pediatric literature, depression is often combined with anxiety,2224 and diagnosis is based on a questionnaire, rather than through the use of strict diagnostic criteria. Furthermore, sleep measurements are obtained from parent-report or self-report,16,18,19,2124,39 rather than being objective measures, such as polysomnography or actigraphy. Research shows that parents may not be as aware of sleep difficulties experienced by their children,4042 and that what is considered a problem to one person may not be viewed as the same by another. In addition, estimates of sleep quality have been found to have low correlation with objective measures, particularly in individuals that experience unipolar depression,43 which suggests that studies’ findings may differ, depending on the type of measure used.

Another problem arising from the use of subjective measures is the lack of standardization in their use. Sleep problems are often defined by a small number of questions, with different studies using different questionnaires (Table 1). As such, it is unclear how various sleep problems may relate to the risk of developing depression, and how sleep problems found in one study compare with those defined in another study.

Finally, although some longitudinal studies have provided very interesting and relevant information, the majority of studies are both subjective and correlational by nature. Although the use of objective measurements can be relatively costly, longitudinal work would benefit from the use of objective measures, on a sub-sample of participants, over the period of examination. The use of objective measures, in conjunction with a longitudinal design, would both strengthen findings and help us to better understand the nature of the relationship between various disordered sleep patterns and the development of depression.

Common underlying pathophysiology of sleep disturbance and depression

Several hypotheses have been put forth to explain a mechanism that might underlie the interplay between the sleep/wake system and depression, including regulation by the prefrontal cortex (PFC) and the serotonergic system. These hypotheses are not mutually exclusive, and may provide a better explanation of the reasons that sleep disturbance and depression co-occur.

Prefrontal cortex

The PFC is involved in both arousal control and mood regulation; therefore, it has been proposed as a brain area underlying the relationship between sleep disturbance and depression.44 In particular, it is thought that the PFC plays a significant role in the coordination of sleep and wakefulness, such that higher activity in the PFC promotes wakefulness, while reduced activity or metabolic levels in the PFC may promote sleep.45 Evidence for this comes from studies that examined metabolic activity in the PFC; with the greatest change in activity being from wakefulness (when PFC function is highest) to sleep (when the PFC displays the lowest levels of activity).46 Moreover, sleep deprivation leads to both an increased need to sleep and an associated decrease in the level of activity in the PFC,11 further suggesting that the PFC is involved in regulation of the sleep/wake system.

The PFC is not only linked to regulation of sleep and arousal, but also to other higher-order processes, including the regulation of affect. The orbital and medial PFC are connected, either directly or indirectly, with the amygdala and hypothalamus structures in the limbic system, which are important for affect regulation.47 Sleep deprivation has been shown to lead to weaker functional connectivity between these areas,48 suggesting that impairment due to sleep problems affects mood regulation. In evidence of this, studies indicate that impairment of the PFC, such as reduced volume and metabolic activity,49,50 can lead to affective disorders, such as depression.45 Given the evidence for the PFC’s role in regulating arousal and affect, as well as the links found between sleep deprivation and connectivity with areas important for mood regulation, the PFC appears to be an area likely to be responsible for the co-occurrence of sleep disturbance and depression.

Serotonergic system

Serotonin is a neurotransmitter that decreases in level during sleep, and is implicated in the pathophysiology of unipolar depression.51 Despite serotonin’s implication in both sleep and affective disorders, research has only recently begun to examine links between serotonin, sleep impairment, and depression. In two recent studies, the effect of sleep restriction on serotonin receptor sensitivity was experimentally tested.52,53 It was hypothesized that the sensitivity of serotonin receptor 1A, a receptor with decreased sensitivity in depressed individuals, would decrease following chronic sleep restriction. Rats were restricted to 4 hours of sleep per day for either 2 or 8 days, and were subjected to a serotonin challenge. It was found that there was no change in the sensitivity of serotonin receptor 1A following 2 days of sleep restriction.53 However, following 8 days of sleep restriction, both studies reported significant desensitization of the serotonin receptor, with responses similar to those found in depressed individuals.25,26 These findings suggest that sleep restriction leads to a decreased response to the presence of serotonin, thereby limiting the brain’s ability to optimally use the serotonin available to it, and creating a situation that has also been found to be present for individuals suffering from unipolar depression.

In the study by Roman et al,53 a follow-up experiment was conducted which examined how long desensitization lasted once recovery sleep was allowed. They found that even after 7 days of recovery sleep, receptor sensitivity was still not back to baseline levels. The authors suggested that chronic sleep restriction, such as occurs commonly within Western society, and is experienced by insomniacs, may make individuals more vulnerable to the development of depression.

Further evidence for serotonin’s role in the association between sleep disturbance and depression comes from animal54,55 and human56,57 studies, which show that expression of the short allele of the serotonin transporter gene is related both to the presence of insomnia56 and to a greater vulnerability for developing depression.54,55,57,58 This is important, as the short allele variant is related to decreased efficiency of serotonin transcription and expression,59 leading to reduced levels of serotonin available for transmission. As the presence of the short allele variant affects sleep disturbance and increases vulnerability to depression, there is strong support for the role of serotonin as a common underlying mechanism.

Clinical implications

The presence of sleep disturbances prior to depressive episodes, especially insomnia and increased REM pressure, provide a warning sign of the impending onset of depression, or the possible recurrence of a depressive episode. As such, clinicians and health care providers should pay special attention to the sleep patterns of individuals who are at particular risk for developing depression. Moreover, the occurrence of sleep difficulties prior to the onset of depression may provide a possible timeframe within which depression can be prevented. It is possible that by treating the sleep problem, the risk of having a future depressive episode may be reduced. Evidence from a study by Ford and Kamerow15 supports this idea; individuals whose sleep problems resolved over the course of the study also had a decreased risk of developing depression. Following diagnosis of depression, it is important to ensure treatment of depression and any sleep problem that may be present, as alleviating sleep problems can accelerate the rate of recovery from depressive symptoms.60 Additionally, if the resolution of sleep problems can reduce the risk of developing depression,15 it suggests that treating a sleep problem during depression can reduce the likelihood of relapse following successful treatment of the depressive episode.

As sleep deprivation has been found to have beneficial effects in patients who experience major depression,10,13 it has been thought that this may be a means of intervention in treating depression. However, it remains a controversial method, and has been shown to be a very temporary solution for depression management. Although patients improve following a night of total or REM sleep deprivation, the beneficial effects disappear following 1 night of recovery sleep.13 Also, since sleep deprivation can exacerbate a negative mood state, it is also possible that, in some individuals, using sleep deprivation may actually worsen depressive symptoms. Furthermore, although sleep deprivation may prove feasible in a clinical setting, where much help is available for keeping the patient from sleeping, such a treatment method becomes much harder for the outpatient, who must rely on his or her own means for staying awake when the drive to sleep is at its highest.

Despite the limitations of using sleep deprivation as a treatment method, it can be beneficial when used in conjunction with other treatment options, such as antidepressant medications, sleep phase advancement (advancing the time of day when one normally goes to sleep and wakes up), and light therapy (using bright light early in the morning to reset one’s circadian rhythm earlier).61 In particular, while most antidepressant treatments take weeks for effects to be seen,62 sleep deprivation can be used to accelerate relief from depressive symptoms, usually within 1 day. Medication, sleep phase advancement, and light therapy have been found to sustain the positive treatment effects of sleep deprivation.61

Finally, when pharmacological interventions are required, it is important to consider the effect on comorbid sleep problems. Medications that may increase insomnia symptoms, such as certain selective serotonin reuptake inhibitors,60 are likely to impair response to treatment. Therefore, it is important to monitor sleep following pharmacological intervention.

Summary and future directions

Current evidence clearly shows that sleep and depression are strongly interrelated. Sleep deprivation studies show that sleep can increase depressive symptoms, while longitudinal studies suggest that insomnia and trouble sleeping can be among initial manifestations of unipolar depression. In addition, certain sleep phenotypes, such as prolonged sleep onset latencies, reduced latency to REM sleep, and reduced sleep spindle activity may represent an increased vulnerability to developing depressive episodes. The relationships between sleep phenotypes and depression seem to change according to developmental stage, providing different markers for increased vulnerability in pre-pubertal and postpubertal individuals. Sleep phenotype has also been related to increased risk of recurrence of depressive episodes, and to decreased responsiveness to intervention. As such, it is important to take sleep into consideration when identifying individuals at risk for developing depression, when choosing appropriate interventions, and while monitoring the effects of treatment for depression over time.

In order to provide the best possible treatments for comorbid sleep problems and unipolar depression, it is important to better understand the mechanisms underlying these disorders. Evidence suggests that the PFC may be involved in the manifestation of both sleep disturbance and depression, and that serotonin plays an important role in this relationship.

Future research would benefit from closer examination of the relationship between sleep in prepubescent individuals and depression, to better understand the changes that occur during development. Additionally, understanding the impact of puberty on sleep’s relationship with depression is important for determining whether interventions that are suitable for adults may be suitable for youth. Given the findings of Ford and Kamerow,15 future studies are needed that examine to what extent treating sleep problems may reduce the risk of developing unipolar depression.

Further elucidation of the ways in which the PFC and serotonergic systems relate both to sleep and to the presence of psychological disorders during development can help improve interventions, by appropriately targeting both the disorder and the sleep disturbances involved at particular developmental stages. By examining and monitoring sleep disturbances that may be present in depression, more efficacious intervention treatments can be created, with the aim of improving both sleep quality and psychological condition.

Footnotes

Disclosure

The authors report no conflicts on interest in this work.

References

  • 1.Krahn LE. Psychiatric disorders associated with disturbed sleep. Semin Neurol. 2005;25(1):90–96. doi: 10.1055/s-2005-867077. [DOI] [PubMed] [Google Scholar]
  • 2.Alfano CA, Gamble AL. The role of sleep in childhood psychiatric disorders. Child Youth Care Forum. 2009;38(6):327–340. doi: 10.1007/s10566-009-9081-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.American Psychiatric Association . Diagnostic and statistical manual of mental disorders. 4th ed. Washington, DC: American Psychiatric Association; 2000. [Google Scholar]
  • 4.Reynolds AC, Banks S. Total sleep deprivation, chronic sleep restriction and sleep disruption. Prog Brain Res. 2010;185:91–103. doi: 10.1016/B978-0-444-53702-7.00006-3. [DOI] [PubMed] [Google Scholar]
  • 5.Cormier RE. Sleep Disturbances. In: Walker HK, Hall WD, Hurst JW, editors. Clinical Methods: The History, Physical, and Laboratory Examinations. 3rd ed. Boston, MA: Butterworths; 1990. [PubMed] [Google Scholar]
  • 6.Zisook S, Rush AJ, Albala A, et al. Factors that differentiate early vs later onset of major depression disorder. Psychiatry Res. 2004;129(2):127–140. doi: 10.1016/j.psychres.2004.07.004. [DOI] [PubMed] [Google Scholar]
  • 7.Shaffer D, Fisher P, Dulcan MK, et al. The NIMH Diagnostic Interview Schedule for Children Version 2.3 (DISC-2.3): description, acceptability, prevalence rates, and performance in the MECA study. Methods for the Epidemiology of Child and Adolescent Mental Disorders Study. J Am Acad Child Adolesc Psychiatry. 1996;35:865–877. doi: 10.1097/00004583-199607000-00012. [DOI] [PubMed] [Google Scholar]
  • 8.Moussavi S, Chatterji S, Verdes E, Tandon A, Patel V, Ustun B. Depression, chronic diseases, and decrements in health: results from the World Health Surveys. Lancet. 2007;370(9590):851–858. doi: 10.1016/S0140-6736(07)61415-9. [DOI] [PubMed] [Google Scholar]
  • 9.Mendelson WB, Gillin JC, Wyatt RD. Human Sleep and Its Disorders. New York, NY: Plenum Press; 1977. [Google Scholar]
  • 10.Wirz-Justice A, Van den Hoofdakker RH. Sleep deprivation in depression: what do we know, where do we go? Biol Psychiatry. 1999;46(4):445–453. doi: 10.1016/s0006-3223(99)00125-0. [DOI] [PubMed] [Google Scholar]
  • 11.Kahn-Greene ET, Killgore DB, Kamimori GH, Balkin TJ, Killgore WD. The effects of sleep deprivation on symptoms of psychopathology in healthy adults. Sleep Med. 2007;8(3):215–221. doi: 10.1016/j.sleep.2006.08.007. [DOI] [PubMed] [Google Scholar]
  • 12.Morey LC. Personality Assessment Inventory. Lutz, FL: Psychological Assessment Resources; 1991. [Google Scholar]
  • 13.Bernier D, Bartha R, Devarajan S, Macmaster FP, Schmidt MH, Rusak B. Effects of overnight sleep restriction on brain chemistry and mood in women with unipolar depression and healthy controls. J Psychiatry Neurosci. 2009;34(5):352–360. [PMC free article] [PubMed] [Google Scholar]
  • 14.McNair ML, Lorr M, Droppleman LF. Manual for the Profile of Mood States Revised. San Diego, CA: Edits/Educational and Industrial Testing Service; 1992. [Google Scholar]
  • 15.Ford DE, Kamerow DB. Epidemiologic study of sleep disturbances and psychiatric disorders. An opportunity for prevention? JAMA. 1989;262(11):1479–1484. doi: 10.1001/jama.262.11.1479. [DOI] [PubMed] [Google Scholar]
  • 16.Gregory AM, Caspi A, Eley TC, Moffitt TE, Oconnor TG, Poulton R. Prospective longitudinal associations between persistent sleep problems in childhood and anxiety and depression disorders in adulthood. J Abnorm Child Psychol. 2005;33(2):157–163. doi: 10.1007/s10802-005-1824-0. [DOI] [PubMed] [Google Scholar]
  • 17.Vollrath M, Wicki W, Angst J. The Zurich study. VIII. Insomnia: association with depression, anxiety, somatic syndromes, and course of insomnia. Eur Arch Psychiatry Neurol Sci. 1989;239(2):113–124. doi: 10.1007/BF01759584. [DOI] [PubMed] [Google Scholar]
  • 18.Chang PP, Ford DE, Mead LA, Cooper-Patrick L, Klag MJ. Insomnia in young men and subsequent depression. The Johns Hopkins Precursors Study. Am J Epidemiol. 1997;146(2):105–114. doi: 10.1093/oxfordjournals.aje.a009241. [DOI] [PubMed] [Google Scholar]
  • 19.Gregory AM, Rijsdijk FV, Lau JY, Dahl RE, Eley TC. The direction of longitudinal associations between sleep problems and depression symptoms: a study of twins aged 8 and 10 years. Sleep. 2009;32(2):189–199. doi: 10.1093/sleep/32.2.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Johnson EO, Roth T, Breslau N. The association of insomnia with anxiety disorders and depression: exploration of the direction of risk. J Psychiatr Res. 2006;40(8):700–708. doi: 10.1016/j.jpsychires.2006.07.008. [DOI] [PubMed] [Google Scholar]
  • 21.Ong SH, Wickramaratne P, Tang M, Weissman MM. Early childhood sleep and eating problems as predictors of adolescent and adult mood and anxiety disorders. J Affect Disord. 2006 Nov;96(1–2):1–8. doi: 10.1016/j.jad.2006.05.025. [DOI] [PubMed] [Google Scholar]
  • 22.Gregory AM, O’Connor TG. Sleep problems in childhood: a longitudinal study of developmental change and association with behavioral problems. Journal of the American Academy of Child and Adolescent Psychiatry. 2002;41(8):964–971. doi: 10.1097/00004583-200208000-00015. [DOI] [PubMed] [Google Scholar]
  • 23.Gregory AM, Van der Ende J, Willis TA, Verhulst FC. Parent-reported sleep problems during development and self-reported anxiety/depression, attention problems, and aggressive behavior later in life. Arch Pediatr Adolesc Med. 2008;162(4):330–335. doi: 10.1001/archpedi.162.4.330. [DOI] [PubMed] [Google Scholar]
  • 24.Johnson EO, Chilcoat HD, Breslau N. Trouble sleeping and anxiety/depression in childhood. Psychiatry Res. 2000;94(2):93–102. doi: 10.1016/s0165-1781(00)00145-1. [DOI] [PubMed] [Google Scholar]
  • 25.Benca RM, Obermeyer WH, Thisted RA, Gillin JC. Sleep and psychiatric disorders. A meta-analysis. Arch Gen Psychiatry. 1992;49(8):651–668. 669–670. doi: 10.1001/archpsyc.1992.01820080059010. discussion. [DOI] [PubMed] [Google Scholar]
  • 26.Kupfer DJ, Foster FG. Interval between onset of sleep and rapid-eye-movement sleep as an indicator of depression. Lancet. 1972;2(7779):684–686. doi: 10.1016/s0140-6736(72)92090-9. [DOI] [PubMed] [Google Scholar]
  • 27.Kupfer DJ, Ulrich RF, Coble PA, et al. Electroencephalographic sleep of younger depressives. Comparison with normals. Arch Gen Psychiatry. 1985;42(8):806–810. doi: 10.1001/archpsyc.1985.01790310068009. [DOI] [PubMed] [Google Scholar]
  • 28.Rush AJ, Erman MK, Giles DE, et al. Polysomnographic findings in recently drug-free and clinically remitted depressed patients. Arch Gen Psychiatry. 1986;43(9):878–884. doi: 10.1001/archpsyc.1986.01800090068009. [DOI] [PubMed] [Google Scholar]
  • 29.Rush AJ, Giles DE, Roffwarg HP, Parker CR. Sleep EEG and dexamethasone suppression test findings in outpatients with unipolar major depressive disorders. Biol Psychiatry. 1982;17(3):327–341. [PubMed] [Google Scholar]
  • 30.Emslie GJ, Armitage R, Weinberg WA, Rush AJ, Mayes TL, Hoffmann RF. Sleep polysomnography as a predictor of recurrence in children and adolescents with major depressive disorder. Int J Neuropsychopharmacol. 2001;4(2):159–168. doi: 10.1017/S1461145701002383. [DOI] [PubMed] [Google Scholar]
  • 31.Dahl RE, Puig-Antich J, Ryan ND, et al. EEG sleep in adolescents with major depression: the role of suicidality and inpatient status. J Affect Disord. 1990;19(1):63–75. doi: 10.1016/0165-0327(90)90010-6. [DOI] [PubMed] [Google Scholar]
  • 32.Emslie GJ, Rush AJ, Weinberg WA, Rintelmann JW, Roffwarg HP. Children with major depression show reduced rapid eye movement latencies. Arch Gen Psychiatry. 1990;47(2):119–124. doi: 10.1001/archpsyc.1990.01810140019003. [DOI] [PubMed] [Google Scholar]
  • 33.Emslie GJ, Rush AJ, Weinberg WA, Rintelmann JW, Roffwarg HP. Sleep EEG features of adolescents with major depression. Biol Psychiatry. 1994;36(9):573–581. doi: 10.1016/0006-3223(94)90067-1. [DOI] [PubMed] [Google Scholar]
  • 34.Dahl RE, Ryan ND, Birmaher B, et al. Electroencephalographic sleep measures in prepubertal depression. Psychiatry Res. 1991;38(2):201–214. doi: 10.1016/0165-1781(91)90045-q. [DOI] [PubMed] [Google Scholar]
  • 35.Ivanenko A, Crabtree VM, Gozal D. Sleep and depression in children and adolescents. Sleep Med Rev. 2005;9(2):115–129. doi: 10.1016/j.smrv.2004.09.006. [DOI] [PubMed] [Google Scholar]
  • 36.Carskadon MA, Vieira C, Acebo C. Association between puberty and delayed phase preference. Sleep. 1993;16:258–262. doi: 10.1093/sleep/16.3.258. [DOI] [PubMed] [Google Scholar]
  • 37.Gruber R, Sheshko D. Circadian sleep disorders and comorbid psychiatric and behavioral disorders in children and adolescents. In: Ivanenko A, editor. Sleep and Psychiatric Disorders in Children and Adolescents. London, UK: Taylor and Francis; 2008. [Google Scholar]
  • 38.Lopez J, Hoffmann R, Armitage R. Reduced sleep spindle activity in early-onset and elevated risk for depression. J Am Acad Child Adolesc Psychiatry. 2010;49(9):934–943. doi: 10.1016/j.jaac.2010.05.014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Roane BM, Taylor DJ. Adolescent insomnia as a risk factor for early adult depression and substance abuse. Sleep. 2008;31(10):1351–1356. [PMC free article] [PubMed] [Google Scholar]
  • 40.Sadeh A. Evaluating night wakings in sleep-disturbed infants: a methodological study of parental reports and actigraphy. Sleep. 1996;19(10):757–762. doi: 10.1093/sleep/19.10.757. [DOI] [PubMed] [Google Scholar]
  • 41.Paavonen EJ, Aronen ET, Moilanen I, et al. Sleep problems of school-aged children: a complementary view. Acta Paediatrica. 2000;89(2):223–228. doi: 10.1080/080352500750028870. [DOI] [PubMed] [Google Scholar]
  • 42.Owens JA, Spirito A, McGuinn M, Nobile C. Sleep habits and sleep disturbance in elementary school-aged children. Journal of Developmental and Behavioral Pediatrics. 2000;21(1):27–36. doi: 10.1097/00004703-200002000-00005. [DOI] [PubMed] [Google Scholar]
  • 43.Armitage R, Trivedi M, Hoffmann R, Rush AJ. Relationship between objective and subjective sleep measures in depressed patients and healthy controls. Depress Anxiety. 1997;5(2):97–102. doi: 10.1002/(sici)1520-6394(1997)5:2<97::aid-da6>3.0.co;2-2. [DOI] [PubMed] [Google Scholar]
  • 44.Dahl RE. The regulation of sleep and arousal: development and psychopathology. Development and Psychopathology. 1996;8:3–27. [Google Scholar]
  • 45.Horne JA. Human sleep, sleep loss and behaviour. Implications for the prefrontal cortex and psychiatric disorder. Br J Psychiatry. 1993;162:413–419. doi: 10.1192/bjp.162.3.413. [DOI] [PubMed] [Google Scholar]
  • 46.Muzur A, Pace-Schott EF, Hobson JA. The prefrontal cortex in sleep. Trends Cogn Sci. 2002;6(11):475–481. doi: 10.1016/s1364-6613(02)01992-7. [DOI] [PubMed] [Google Scholar]
  • 47.Miller EK, Cohen JD. An integrative theory of prefrontal cortex function. Annu Rev Neurosci. 2001;24:167–202. doi: 10.1146/annurev.neuro.24.1.167. [DOI] [PubMed] [Google Scholar]
  • 48.Gregory AM, Sadeh A. Sleep, emotional and behavioral difficulties in children and adolescents. Sleep Med Rev. 2012;16(2):129–136. doi: 10.1016/j.smrv.2011.03.007. [DOI] [PubMed] [Google Scholar]
  • 49.Kimbrell TA, Ketter TA, George MS, et al. Regional cerebral glucose utilization in patients with a range of severities of unipolar depression. Biol Psychiatry. 2002;51(3):237–252. doi: 10.1016/s0006-3223(01)01216-1. [DOI] [PubMed] [Google Scholar]
  • 50.Soares JC, Mann JJ. The anatomy of mood disorders – review of structural neuroimaging studies. Biol Psychiatry. 1997;41(1):86–106. doi: 10.1016/s0006-3223(96)00006-6. [DOI] [PubMed] [Google Scholar]
  • 51.Adrien J. Neurobiological bases for the relation between sleep and depression. Sleep Med Rev. 2002;6(5):341–351. [PubMed] [Google Scholar]
  • 52.Novati A, Roman V, Cetin T, et al. Chronically restricted sleep leads to depression-like changes in neurotransmitter receptor sensitivity and neuroendocrine stress reactivity in rats. Sleep. 2008;31(11):1579–1585. doi: 10.1093/sleep/31.11.1579. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Roman V, Walstra I, Luiten PG, Meerlo P. Too little sleep gradually desensitizes the serotonin 1A receptor system. Sleep. 2005;28(12):1505–1510. [PubMed] [Google Scholar]
  • 54.Barr CS, Newman TK, Shannon C, et al. Rearing condition and rh5-HTTLPR interact to influence limbic-hypothalamic-pituitary-adrenal axis response to stress in infant macaques. Biol Psychiatry. 2004;55(7):733–738. doi: 10.1016/j.biopsych.2003.12.008. [DOI] [PubMed] [Google Scholar]
  • 55.Champoux M, Bennett A, Shannon C, Higley JD, Lesch KP, Suomi SJ. Serotonin transporter gene polymorphism, differential early rearing, and behavior in rhesus monkey neonates. Mol Psychiatry. 2002;7(10):1058–1063. doi: 10.1038/sj.mp.4001157. [DOI] [PubMed] [Google Scholar]
  • 56.Deuschle M, Schredl M, Schilling C, et al. Association between a serotonin transporter length polymorphism and primary insomnia. Sleep. 2010;33(3):343–347. doi: 10.1093/sleep/33.3.343. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Caspi A, Sugden K, Moffitt TE, et al. Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene. Science. 2003;301(5631):386–389. doi: 10.1126/science.1083968. [DOI] [PubMed] [Google Scholar]
  • 58.Uher R, McGuffin P. The moderation by the serotonin transporter gene of environmental adversity in the aetiology of mental illness: review and methodological analysis. Mol Psychiatry. 2008;13(2):131–146. doi: 10.1038/sj.mp.4002067. [DOI] [PubMed] [Google Scholar]
  • 59.Lesch KP, Bengel D, Heils A, et al. Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region. Science. 1996;274(5292):1527–1531. doi: 10.1126/science.274.5292.1527. [DOI] [PubMed] [Google Scholar]
  • 60.National Sleep Foundation Depression and Sleep. [Internet] 2011Available from: http://www.sleepfoundation.org/article/sleep-topics/depression-and-sleepAccessed December 21, 2011
  • 61.Benedetti F, Barbini B, Colombo C, Smeraldi E. Chronotherapeutics in a psychiatric ward. Sleep Med Rev. 2007;11(6):509–522. doi: 10.1016/j.smrv.2007.06.004. [DOI] [PubMed] [Google Scholar]
  • 62.Wu JC, Kelsoe JR, Schachat C, et al. Rapid and sustained antidepressant response with sleep deprivation and chronotherapy in bipolar disorder. Biol Psychiatry. 2009;66(3):298–301. doi: 10.1016/j.biopsych.2009.02.018. [DOI] [PubMed] [Google Scholar]
  • 63.Robins LN, Helzer JE, Croughan J, Ratcliff KS. National Institute of Mental Health Diagnostic Interview Schedule. Its history, characteristics, and validity. Arch Gen Psychiatry. 1981;38(4):381–389. doi: 10.1001/archpsyc.1981.01780290015001. [DOI] [PubMed] [Google Scholar]
  • 64.American Psychiatric Association . Diagnostic and Statistical Manual of Mental Disorder. 3rd ed. Washington, DC: American Psychiatric Association; 1980. [Google Scholar]
  • 65.Breslau N, Roth T, Rosenthal L, Andreski P. Sleep disturbance and psychiatric disorders: a longitudinal epidemiological study of young adults. Biol Psychiatry. 1996;39(6):411–418. doi: 10.1016/0006-3223(95)00188-3. [DOI] [PubMed] [Google Scholar]
  • 66.Robins LN, Helzer JE, Cottler L, Golding E. NIMH Diagnostic Interview Schedule, Version III, Revised. St Louis, MO: Washington University; 1989. [Google Scholar]
  • 67.Thomas CB, Pederson LA. Psychobiological Studies. Ii. Sleep Habits of Healthy Young Adults with Observations on Levels of Cholesterol and Circulating Eosinophils. J Chronic Dis. 1963;16:1099–1114. doi: 10.1016/0021-9681(63)90044-4. [DOI] [PubMed] [Google Scholar]
  • 68.Achenbach TM. Integrative Guide for the 1991 CBCL/4–18, YSR, and TRF Profiles. Dept of Psychiatry, University of Vermont; 1991. [Google Scholar]
  • 69.Rutter M, Tizard J, Whitmore K. Education, Health and Behaviour. London: Longman; 1970. [Google Scholar]
  • 70.Shaffer D, Fisher P, Lucas CP, Dulcan MK, Schwab-Stone ME. NIMH Diagnostic Interview Schedule for Children Version IV (NIMH DISC-IV): description, differences from previous versions, and reliability of some common diagnoses. J Am Acad Child Adolesc Psychiatry. 2000;39(1):28–38. doi: 10.1097/00004583-200001000-00014. [DOI] [PubMed] [Google Scholar]
  • 71.Lerner RM, Palermo M, Spiro A, Nessleroade J. Assessing the dimensions of temperament individuality across the life span: the Dimensions of Temperament Survey (DOTS) Child Development. 1982;53:149–159. [Google Scholar]
  • 72.Mannuzza S, Fyer AJ, Klein DF, Endicott J. Schedule for Affective Disorders and Schizophrenia – Lifetime Version modified for the study of anxiety disorders (SADS-LA): rationale and conceptual development. J Psychiatr Res. 1986;20(4):317–325. doi: 10.1016/0022-3956(86)90034-8. [DOI] [PubMed] [Google Scholar]
  • 73.Orvaschel H, Puig-Antich J, Chambers W, Tabrizi MA, Johnson R. Retrospective assessment of prepubertal major depression with the Kiddie-SADS-e. J Am Acad Child Psychiatry. 1982;21(4):392–397. doi: 10.1016/s0002-7138(09)60944-4. [DOI] [PubMed] [Google Scholar]
  • 74.Achenbach TM. Manual for the Young Adult Self-Report and Young Adult Behavior Checklist. Burlington: Department of Psychiatry, University of Vermont; 1997. [Google Scholar]
  • 75.Owens JA, Spirito A, McGuinn M. The Children’s Sleep Habits Questionnaire (CSHQ): Psychometric properties of a survey instrument for school-aged children. Sleep. 2000;23(8):1043. [PubMed] [Google Scholar]
  • 76.Kovacs M. The Children’s Depression Inventory (CDI) Psychopharmacology Bulletin. 1985;21(4):995–998. [PubMed] [Google Scholar]

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