Depression Clinical Trial
Official title:
Aging: Sleep and Inflammatory Mechanism in Depression Prevention
The objective of this study is to evaluate the ability of a behavioral intervention, cognitive behavioral therapy for sleep quality (CBT-SQ) to reduce sleep complaints, depression recurrence, and cellular and genomic markers of inflammation in older adults with sleep complaints who have a prior history of depression. The investigators aim to: 1) evaluate the effects of CBT-SQ vs. Sleep Seminar (SS) on objective (actigraphy) and subjective (sleep diary; questionnaire) measures of sleep symptoms over a two-year follow-up; 2) determine the effects of CBT-SQ vs. SS on recurrence of depressive symptoms and depression episode(s) over a two-year follow-up. The investigators will also secondarily examine the effects of CBT-SQ vs. SS on cellular and genomic markers of inflammation over a two-year follow-up, and explore whether markers of inflammation and cytokine genes can explain variability in the risk of depression recurrence in those older adults receiving CBT-SQ vs. SS. The present study is highly significant by being the first study, to the investigators knowledge, to focus on the prevention of depression in community dwelling older adults who have a history of depression, and by targeting sleep disturbance, a modifiable risk factor to prevent depression recurrence.
Depression, one of the most common diseases in older adults, carries significant risk for
morbidity, and mortality. However, many older adults with depression are not identified and
even when identified, they face protracted courses of treatment, with over 60% of elderly
patients failing to achieve symptomatic remission. Given the burgeoning population of older
adults, as well as the enormous burden of depression, efforts to maximize depression
prevention are needed.
Despite advances in understanding the behavioral pathways that contribute to depression,
there has been little attention aimed at targeting behavioral risk factors such as sleep
disturbance, even though such strategies have the potential to optimize efficiency (i.e.,
decrease number needed to treat (NNT) among vulnerable older adults with a history of
depression. In this study, we hypothesize that recognition and treatment of sleep
disturbance, a modifiable behavioral risk factor, will prevent depression incidence in older
adults. Whereas sleep disturbance in depressed patients often lingers and its persistence can
represent a residual phase of a major mood disorder, emergence of disturbed sleep in
non-depressed older adults serves as an independent risk factor depression that occurs later
in life. In a 2-year prospective cohort study of community-dwelling older adults aged 60
years or older (N=351), we have found that sleep disturbance is prospectively associated with
depression incidence independent of other current depressive symptoms, as well as
antidepressant and hypnotic medication use, and medical status. To evaluate sleep disturbance
at the community level, sleep disturbance was defined by a self-report measure (i.e. scores >
5 on the Pittsburgh Sleep Quality Index (PSQI), which highly correlates with insomnia
diagnosis. We have found similar prospective results between reported sleep disturbance and
depression in adults (N=1716).
Increasing evidence also implicates inflammation as a biological mechanism that contributes
to depression, and we further hypothesize that increases in inflammation are associated with
the link between sleep disturbance and depression incidence. Whereas multiple other factors
including but not limited to, psychosocial stress, medical illness, obesity, sedentary
lifestyle, social isolation, low socio-economic status, female sex, and smoking can drive
inflammation and are associated with depression, our preliminary data have found that sleep
disturbance induces activation of inflammatory signaling,and additional naturalistic and
epidemiologic preliminary findings show that sleep disturbance is associated with increases
in markers of inflammation especially among those with a history of depression. In turn, we
and others have found that inflammation prospectively predicts depression recurrence in
community dwelling adults who have a history of depression (N=1716)16 Although there is also
evidence that this association can be reciprocal,33 our experimental preliminary data show
that inflammatory activation induces depressed mood. In contrast, cognitive behavioral
therapy for insomnia (CBT-I)) reduces cellular markers of inflammation in older adults who
show a remission of clinical sleep complaints.
The over-arching objectives of this study are to evaluate the ability of CBT-I vs. an active
comparator control, Sleep Education Therapy (SET) to reduce sleep complaints, depression
incidence, and cellular and genomic markers of inflammation in older adults with
self-reported sleep disturbance with follow-up up to three years.
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