Large-scale brain networks and psychopathology: a unifying triple network model

http://nwkpsych.rutgers.edu/~jose/courses/578_mem_learn/2012/readings/Broyd_2009.pdf

Default-mode brain dysfunction in mental disorders: A systematic review

Neurocircuitry of Mood Disorders

The recently discovered default mode network (DMN) is a group of areas in the human brain characterized, collectively, by functions of a self-referential nature. In normal individuals, activity in the DMN is reduced during nonself-referential goal-directed tasks, in keeping with the folk-psychological notion of losing one's self in one's work. Imaging and anatomical studies in major depression have found alterations in both the structure and function in some regions that belong to the DMN, thus, suggesting a basis for the disordered self-referential thought of depression. Here, we sought to examine DMN functionality as a network in patients with major depression, asking whether the ability to regulate its activity and, hence, its role in self-referential processing, was impaired. To do so, we asked patients and controls to examine negative pictures passively and also to reappraise them actively. In widely distributed elements of the DMN [ventromedial prefrontal cortex prefrontal cortex (BA 10), anterior cingulate (BA 24/32), lateral parietal cortex (BA 39), and lateral temporal cortex (BA 21)], depressed, but not control subjects, exhibited a failure to reduce activity while both looking at negative pictures and reappraising them. Furthermore, looking at negative pictures elicited a significantly greater increase in activity in other DMN regions (amygdala, parahippocampus, and hippocampus) in depressed than in control subjects. These data suggest depression is characterized by both stimulus-induced heightened activity and a failure to normally down-regulate activity broadly within the DMN. These findings provide a brain network framework within which to consider the pathophysiology of depression.

/pdf/the-default-mode-network-and-self-referential-processes-in-26p9fy0pa9.pdf

The default mode network and self-referential processes in depression

In the 40 years since Aaron Beck first proposed his cognitive model of depression, the elements of this model — biased attention, biased processing, biased thoughts and rumination, biased memory, and dysfunctional attitudes and schemas — have been consistently linked with the onset and maintenance of depression. Although numerous studies have examined the neural mechanisms that underlie the cognitive aspects of depression, their findings have not been integrated with Beck's cognitive model. In this Review, we identify the functional and structural neurobiological architecture of Beck's cognitive model of depression. Although the mechanisms underlying each element of the model differ, in general the negative cognitive biases in depression are facilitated by increased influence from subcortical emotion processing regions combined with attenuated top-down cognitive control.

Neural mechanisms of the cognitive model of depression

Localised two-dimensional J-resolved spectroscopy (JPRESS) is optimised for the in vivo detection of J-coupled metabolites using magnetic resonance spectroscopy at 3 T. The acquisition of echo signals starts as early as possible (i.e. maximum-echo sampling). This sampling scheme increases sensitivity and decreases overlap of peak tails, hence alleviating baseline problems. Reconstruction issues are discussed and the sensitivity is compared analytically with that of 1D PRESS. The qualitative behaviour of eddy currents in JPRESS is outlined and a 2D eddy current correction procedure based on the 1D phase deconvolution method is proposed.

/pdf/improved-two-dimensional-j-resolved-spectroscopy-3hybp1j7cw.pdf

Improved two-dimensional J-resolved spectroscopy.

Objectives. Burnout is a state of work-related emotional and physical exhaustion. Burnout is related to sleep complaints. By contrast, people with optimistic attitude seem to be less vulnerable to ...

Associations between satisfaction with life, burnout-related emotional and physical exhaustion, and sleep complaints

In the last decade, brain-derived neurotrophic factor (BDNF) has become increasingly accepted as a central mediator of the effects of stress on neuronal plasticity and its implication for psychopathology. Neurotrophic functions of BDNF are implicated with neuronal survival, learning, memory, appetite and sleep.1, 2 The neurotrophin hypothesis is based on these features and proposes that stress-related mental disorders result from stress-induced decreases in BDNF expression.3 Sleep problems are common features in many stress-related mental disorders, problems that may lead to impairment of physical and mental health because sleep loss is often followed by higher stress vulnerability.4 Thus, insomnia is very common among depressed patients.5 Of note, in accordance with the ‘neurotrophin hypothesis of depression', BDNF seems to be involved in major depression and antidepressant action.6, 7 Although a majority of studies have concentrated on specifying the role of BDNF in depression, the relation between BDNF and insomnia has not been a focus of recent research.

Here we investigated serum BDNF levels of adults with current symptoms of insomnia and non-sleep disturbed controls. The study was approved by the local ethics committee of the University of Basel. The sample pool consisted of 50 adults (mean±s.d. age=54.66±11.63 years), including patients with a previous diagnosis of restless legs syndrome (RLS) or periodic limb movement (PLM) but without other neurological symptoms, and age-matched controls. The eligibility criterion for sleep-disturbed participants was to suffer from at least sub-threshold insomnia (n=26, including 19 patients previously diagnosed with RLS/PLM and 7 controls); participants qualified as sleep-healthy subjects (n=24, including 7 patients with previous RLS diagnosis and 17 controls) by scoring below the cut-off (sum score of 8) for sub-threshold insomnia according to the insomnia severity index, which is based on the DSM-IV diagnostic criteria for insomnia.

Consistent with previous work,8 there was a significant difference in serum BDNF levels between smokers and non-smokers (t(47)=3.066; P=0.004, ns: age, BMI and sex). Therefore, smoking was included as a covariate in subsequent analyses. Of note, participants suffering from current symptoms of insomnia (n=26) exhibited significantly decreased serum BDNF levels compared with sleep-healthy controls (n=24; F(1)=5.017; P=0.03; Figure 1a). In addition, serum BDNF levels were significantly correlated with severity of insomnia in all paricipants (n=50; rp=−0.409; P=0.004; Figure 1). There were no differences in serum BDNF levels between participants on medication (RLS medications included pramipexol and ropinirol, hypnotics, antidepressants, antipsychotics and others) and those without such drugs. Furthermore, serum BDNF levels did not differ between those with previous RLS/PLM diagnosis (n=26, including 19 patients with and 7 patients without insomnia symptoms) and those without such diagnoses (n=24, including 17 controls without and 7 with insomnia symptoms), which supports the view that serum BDNF levels are associated with sleep independently of diagnosis. We found subjective sleep impairment to be associated with lower serum BDNF levels, whereas reported good sleep was related to higher serum BDNF levels, as shown for those suffering from current insomnia compared with sleep-healthy subjects. To confirm the relevance of our preliminary findings, we investigated an additional independent control sample of adults (n=12, male non-smokers) that had recovered from occupational burnout and after 12 weeks of aerobic exercise training. To assess insomnia, we used the sleep-related items of the Beck Depression Inventory. Again, serum BDNF levels were significantly lower in those reporting symptoms of fatigue (n=6) compared with sleep-healthy subjects (n=6; t=2.2625; P=0.025; Figure 1b) and were significantly correlated (n=12, rp=−0.639; P=0.025) with the symptoms of tiredness and fatigue known to reflect malfunction of sleep as the prime cause of impairments in daily life. The results from these two different samples are not strictly comparable, given the different methods of assessing disturbed sleep wake regulation as insomnia and day time fatigue, but despite or perhaps because of this, we believe that these findings support the hypothesis of an increased stress vulnerability due to sleep loss, which may lead to decreased BDNF secretion. Such a decrease might be associated with a decrease in BDNF mRNA expression in peripheral blood mononuclear cells and/or may correspond to a decline of BDNF concentration in the brain. To what extent peripheral BDNF levels correspond to brain BDNF levels remains unknown. However, the use of serum BDNF concentration as potential indicator of brain alteration is justified by extensive evidence.9 Although we report a reduction of BDNF levels linked to sleep disturbance, others have consistently shown that prolonged wakefulness as a result of sleep deprivation, which can be considered as a stressor for the brain, leads to an increase in BDNF.10 Using a bidirectional stress model as an explanatory approach, we hypothesise that chronic stress induces a deregulation of the HPA system, leading in the long term to sleep disturbance and decreased BDNF levels, whereas acute sleep deprivation, for example, one night of sleep deprivation, can be used as therapeutic intervention in some insomniac or depressed patients as a compensatory process to normalise BDNF levels.



Figure 1

Correlation between serum brain-derived neurotrophic factor (BDNF) levels and insomnia severity index ratings. Analysis showed a significant correlation of BDNF levels with severity of insomnia across the sample as a whole (rp=−0.409; P=0.004). ...



BDNF has also been considered as a predictor of therapeutic response in major depression. However, very recent data indicate that the increase in serum levels of BDNF during antidepressant treatment appears to be confined to some but not all antidepressants and does not coincide with amelioration of clinical symptoms.6 On the basis of our results, this discrepancy might stem from changes in central BDNF concentrations, following reduced insomnia rather than depressive symptoms and antidepressants differentially influencing sleep. Thus, our preliminary findings suggest that serum BDNF levels are not associated with a specific (categorical) diagnosis, but may be associated with insomnia symptoms independent of diagnosis (dimensional). In line with this, we suggest that, when analysing serum BDNF levels in depressed patients, insomnia symptoms should be carefully controlled, as well as improvements in sleep during therapy. Further studies with a larger number of patients and a design including objective measurements of sleep, such as sleep polysomnography, should be conducted to verify the results of our exploratory investigation and to elucidate the underlying mechanisms more closely, especially the role of the stress hormone system.

/pdf/bdnf-an-indicator-of-insomnia-3mq5xs18q1.pdf

BDNF: an indicator of insomnia?

Evidence for similarities between adolescents and parents in sleep patterns

It is commonly assumed that physical activity exerts a favorable impact on sleep, although scientific evidence is lacking. This study investigated the impact of football sports on the sleep patterns of 36 male chronic and intense football players and 34 controls. Participants completed a sleep log for seven consecutive days. Compared to controls, football players reported shorter sleep onset latency, fewer awakenings, higher scores of sleep quality and a lower variability of sleep from weekdays to weekends. The findings suggest that football sports activity is positively associated with both quantitative and qualitative dimensions of sleep.

'Football is good for your sleep': favorable sleep patterns and psychological functioning of adolescent male intense football players compared to controls.

Johannes Beck

Papers

Improved two-dimensional J-resolved spectroscopy.

Associations between satisfaction with life, burnout-related emotional and physical exhaustion, and sleep complaints

BDNF: an indicator of insomnia?

Evidence for similarities between adolescents and parents in sleep patterns

'Football is good for your sleep': favorable sleep patterns and psychological functioning of adolescent male intense football players compared to controls.