Aerobic Exercise Clinical Trial
Official title:
Neural and Stress Correlates of Resilience in an Exercise-behavioural Programme
Stress-related disorders have a profound impact on public health. The World Health Organisation (WHO) found major depressive disorder (MDD) to be one of the most important human health problems with a prevalence of about 10%. In the current proposal the aim is to investigate mechanisms of resilience against stress-related disorders and to examine changes in quality of life, health, brain structure and brain function in individuals performing a "resilience" programme. Therefore, the investigators will recruit forty healthy subjects from the hospital staff exposed to "normal" day-to-day stress and not participating already in a fitness programme. Half of the subjects will be randomised to a cognitive behavioural self-experience and exercise programme for 20 weeks carried out by experienced supervisors, coaches and trainers. Clinical psychological and psychiatric examinations will be carried out weekly and a range of sophisticated neuroimaging techniques - high angular resolution diffusion imaging (HARDI) and functional MRI (fMRI) - will be conducted before and after the "resilience" program in order to investigate its effectiveness on brain structure and function. The stress system will also be tested by examining cortisol awaking response (CAR) and daily rhythms of cortisol secretion. These techniques are all well established in our laboratories. The proposed research will likely stimulate the development of new prevention strategies for this common and important disorder, and in the future could be applied to other illnesses. Moreover, when successful it could be patented and offered for implementation in the daily routine of median to large companies.
Mental disorders are a major cause of long-term disability and are a direct cause of
mortality, with approximately 800,000 individuals dying from suicide every year worldwide -
a high proportion of them arise from major depressive disorder (MDD). Knowledge of MDD has
expanded in recent years by detecting that neuroplasticity may play a core role in the
pathophysiology of the disease. Neuroplasticity in this context refers to the brain's
ability to change and thus might be the presupposition for building up strategies against
mental disorders.
The best-characterized and most studied examples of neuroplasticity are the molecular and
cellular adaptations underlying learning and exercise. Exercise improves cognition, has
antidepressant effects and was also found to have positive effects on the brain structure as
measured with magnetic resonance imaging (MRI). Further, research in older adults indicates
that increased aerobic fitness can be neuroprotective and can enhance brain structure and
function. Increase of gray matter volume in parietal and frontal brain regions and
corresponding increases of diffusivity in white matter fibres were seen as early as after 2
weeks of training a balancing task.
On the other hand experimental studies found that stress and chronic exposure to high levels
of glucocorticoids leads to depressive-like states. These states were accompanied by atrophy
and loss of neurons in the adult hippocampus which is a temporal lobe brain region involved
in learning, memory and mood regulation. Hippocampal damage, resulting from excessive
exposure of the brain to glucocorticoids, leads to impaired feedback inhibition of
hypothalamic-pituitary-adrenal (HPA) axis by glucocorticoids, causing unrestrained release
of the axis - the "Glucocorticoid Cascade Hypothesis". Prolonged stress, or an excess
allostatic load, is thus harmful and is probably important in the processes mediating
dementias. Efficient stress responses are necessary to cope with changes in the environment
and an ability to terminate the stress response is of central importance in the return to
homeostasis. Individuals with depression have relatively high cortisol secretory tone with
blunted diurnal secretory patterns of cortisol secretion, reflecting poor regulatory
feedback in the hippocampus. Higher cortisol stress responses to awakening (CAR),
conversely, are found in those who are chronically stressed, depressed or remitted from
depression or bipolar disorder, and in adolescents who will later develop depression.
Interestingly, the investigators found that structural changes of the hippocampus, a brain
region involved in memory and emotion regulation, become more pronounced when a patient with
depression develops a chronic disease course. Recently, they detected that hippocampal
volumes from patients with MDD, who carry also a genetic risk-allele (SLC6A4, 5-HTTLPR),
were smaller when they had a history of emotional neglect compared to patients who had only
the genetic or the emotional neglect risk factor separately. In the context of neuroimaging,
diffusion tensor imaging (DTI), which is a significant step forward for characterizing
microstructural changes or differences, is highly interesting. Using high angular resolution
diffusion imaging, the investigators found that unaffected healthy first degree relatives of
patients with MDD with stronger fiber connections between prefrontal and temporo-parietal
brain regions managed incidences of early life adversity without later developing depression
suggesting that resilience may be associated with stronger connections. This line of
research suggests that structural and functional brain changes are already there before the
manifestation of the disease and that these changes seem to be related to the individuals'
vulnerability.
Thus, preventing these brain changes, normalizing the stress functions and increasing the
resilience of individuals is a major challenge for the future in order to prevent major
stress-related mental disorders. The ability of the brain to adapt suggests that it might be
possible to increase resilience in order to protect an individual from becoming depressed.
In addition to exercise and learning, cognitive behavioral therapy (CBT) and remediation
programs have been shown to have effects on brain structure and function in patients with
manifest disorders like depression or schizophrenia and especially the combination of CBT
with exercise and learning might result in most prominent outcomes. Neuroplastic brain
changes have been reported with CBT. For example, behavioral activation therapy for
depression, a psychotherapy modality designed to increase engagement with positive stimuli
and reduce avoidance behaviors, resulted in decreased activations in prefrontal structures,
including the paracingulate gyrus, the right orbitofrontal cortex, and the right frontal
pole, while symptoms of depression improved. Elevated amygdala-hippocampal activity
decreased and reduced ACC activity increased during 16 weeks of CBT in 16 patients with MDD.
A recent review highlights the effects of brief working memory training across different
studies on brain activation in multiple regions including the dorsolateral prefrontal
cortex, parietal cortex, and occipital cortex. Interestingly, cycling has been shown to
increase the volume of the hippocampus in both patients with schizophrenia and healthy
comparison subjects, with no change in the non-exercise group of patients. This suggests
that CBT and exercise can have an impact on the recovery of the brain system from conditions
like schizophrenia and MDD.
Effects of a resilience program have never been investigated with neuroimaging, although it
would be possible to achieve information about the structure of the white matter fiber
bundles that connect certain brain regions. Psychological constructs that promote resilience
- the ability to cope with stressful situations - include commitment, patience, optimism and
self-esteem, in addition to the capacity to modulate emotions and to develop adaptive social
behavior. These traits implicate the brain's cognitive-emotional interplay, which seems to
be a critical determinant of the emergence of pathological rather than resilient phenotypes.
The cognitive-emotional interplay and its functional brain connectivity can be studied using
functional MRI. Interestingly, using functional MRI it has been shown that a bias between
emotional and cognitive processing exists in patients with MDD.
Aims:
The aim of the current proposal is to carry out a 20 weeks lasting extensive resilience
program in order to stimulate resilience in a healthy unaffected population that is exposed
to normal day-to-day work stress in the hospital. The investigators will measure the
effectiveness of this program by examining behavioral, diurnal cortisol secretion rhythms
and stress responses, microstructural as well as functional neural changes.
Hypotheses:
The "Resilience" program stimulates resilience indicated by
1. improved mood stability, better sleep quality and higher life quality
2. increase of hippocampal and anterior cingulate cortex volumes
3. increase of functional connectivity between frontal and limbic brain regions.
4. increase of fractional anisotropy (FA), which is a measure for the functioning of white
matter fibers, between limbic and frontal brain regions.
5. increased gradient of the diurnal secretion in cortisol; and decrease in stress
responses as measured by the cortisol awakening response
Methods and Materials Participants Forty healthy volunteers, e.g. from Adelaide and Meath
Hospital, Dublin (AMiNCH) staff, will be recruited. They will have no history of
neurological, mental (axis I and axis II) or chronic internal diseases. Further exclusion
criteria for all participants will be a previous head injury with loss of consciousness.
Moreover, they will not be members of fitness clubs or engage in intensive day to day
activity. The 40 healthy volunteers will be randomized to a 20 week "resilience" program, 45
minutes exercise two times per week under the supervision of a physiotherapist as well as 2
home session; or to a control group without this program, and a further two sessions of
45-minute exercise/jogging will be completed each week Clinical assessments will be done
weekly. Neuroimaging and salivary cortisol awaking tests will be carried out at baseline and
after 20 weeks for both the resilience program group (N=20) and the control group (N=20).
Clinical assessments The NEO-FFI personality questionnaire and structured clinical interview
for DSM disorders (SCID)-I and II will be carried out initially to exclude and history of,
or current, psychiatric disorder. Mood will be assessed using the Hamilton Depression Rating
Scale (HDRS), the Hamilton Anxiety Rating Scale (HAM-A), and the Beck Depression Inventory
(BDI) at baseline and then bi-weekly. Moreover, current life stressors will be evaluated in
an interview conducted according to Keller et al. on a weekly basis; Life quality
(Study-Short Form 36-Item Health Survey (SF-36, QoL-Bref) and the Pittsburgh sleep quality
index (PSQI), will also be carried out bi-weekly. Early life stress will be assessed using
the childhood trauma questionnaire (CTQ). The NEO-FFI personality questionnaire and SCID-I
and II will also be carried out at inclusion once. Handedness will be determined by the
Edinburgh inventory.
Neuroimaging techniques MRI images will be obtained with a 3.0 Tesla MRI (Phillips Achieva),
located in the Trinity College Institute of Neuroscience (TCIN). MRI will be carried out
using a 60 minutes imaging protocol.
Diffusion Tensor Imaging (DTI): In vivo DTI will be acquired using a single-shot echo-planar
imaging (EPI) sequence with SENSE parallel imaging scheme (SENSivitiy Encoding). The
diffusion weighting will be encoded in 61 independent directions. After pre-processing in
the program ExploreDTI, tractography with ExploreDTI and tract-based spatial statistics
using TBSS (www.fmrib.ox.ac.uk/fsl/tbss/index.html, FSL) will be carried out. We have
experience in using these technique and performing the analyses (25).
Functional MRI: In order to identify functional changes in the emotion regulation system, we
will apply an fMRI paradigm. We will use an Echo Planar Imaging (EPI), T2*-weighted
gradient-echo imaging to visualise BOLD contrast (TR 2000 ms, TE 30 ms, flip angle of 90°,
matrix 80 x 80, FOV 224 x 224 x 150 mm, resolution: 3.5 x 3.5 mm, slice thickness: 3.5 mm).
A cognitive-emotional inhibition task, which is well established in our laboratory, will be
used. Participants will be asked to process visual emotional stimuli either in emotional or
cognitive way. This task is chosen specifically, because it is known to elicit activity in
prefrontal cortex, amygdala, gyrus cinguli, orbitofrontal cortex, regions implicated in the
pathophysiology of MDD. SPM8-based standard analysis, functional connectivity analysis (33)
and Psycho-Physiological Interaction (PPI) analysis will be done.
Structural techniques: Additionally, the aim is to track any structural changes and to
confirm as well as extend recent findings in this area. Therefore, all subjects will be
scanned with a T1-weighted 3D-MPRAGE sequence (repetition time, 8.5 ms; echo time, 3.5 ms;
total acquisition time, 7 min 30 sec; number of acquisitions, 1; field of view, 250 x 256 x
160 mm; resolution: 0.86x0.86x0.86 mm). Region of interest (ROI) analysis of the hippocampus
and amygdala as well as optimised voxel-based morphometry (VBM) will be used for data
analysis as previously done in our lab.
Saliva cortisol samples These will be collected by participating subjects on two successive
week-days, or working days. Subjects spit into a small plastic tube at wakening, and 30, 45,
60 and 90 min later; and in the evening (12h after waking) and just prior to going to bed.
The samples can be stored by participants in a domestic fridge and posted in batch in a
prepared envelope to the research centre.
Calculation of sample size The investigators have previously conducted a number of
longitudinal imaging studies. Based on these experiences, 20 subjects in each group should
be more than sufficient to obtain significant effects, where signal changes in the order of
0.2% to 0.3% are typically found in cognitive-emotional tasks or at least 5 %
microstructural changes should be found in structural MRI or DTI. Thus, with 20 subjects the
effects should be detectable.
;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Basic Science
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