Ignite Creation Date:
2024-05-06 @ 9:20 AM
Last Modification Date:
2024-10-26 @ 12:13 PM
Study NCT ID:
NCT02957591
Status:
COMPLETED
Last Update Posted:
2021-04-23
First Post:
2016-11-01
Brief Title:
Probiotic Supplementation in Severe Depression
Sponsor:
Psychiatric Hospital of the University of Basel
Organization:
Psychiatric Hospital of the University of Basel
Study Overview
Official Title:
The Effect of Probiotic Supplementation on the Efficacy of Antidepressant Treatment in Depression
Status:
COMPLETED
Status Verified Date:
2021-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Recent research demonstrates that the composition of the gut microbiome is a master regulator of key neurophysiological processes that are affected in depression Indeed contemporary studies showed that faecal microbiota is altered in patients with major depressive disorder MDD Furthermore it has also been shown that supplementation of probiotics ameliorated depressive symptoms in unmedicated patients with mild to moderate depression However no study has yet explored the efficacy of a probiotic-based therapy in patients with severe MDD in addition to a standard antidepressant treatment As dietary and lifestyle interventions may be a desirable effective pragmatical and non-stigmatizing prevention and adjuvant therapy in addition to antidepressant treatment in depression this project is aimed at investigating for the first time if probiotic supplementation compared to a placebo treatment improves the effect of standard antidepressant medication on depressive symptoms ie better and faster remission in patients with severe MDD Furthermore this study will further test if probiotic supplementation modulates immune signalling and inflammatory processes macrophage migration inhibitory factor and interleukin 1 beta hypothalamic-pituitaryadrenal HPA axis responses saliva cortisol neurogenesis brain-derived neurotrophic factor BDNF expression the release of appetite-regulating hormones leptin and ghrelin the composition of gut microbiota in particular levels of Enterobacteriaceae Alistipes and Faecalibacterium and brain perfusion structure and activation and if these changes are associated with the probiotic-induced effect on depressive symptoms
Detailed Description:
Major depression is a recurrent and debilitating mental disorder with a lifetime prevalence of up to 20 in the general population among the highest for psychiatric disorders Its diagnosis is based upon the presence of persisting affective cognitive and behavioural symptoms with a depressive episode requiring at least five of these symptoms during a period of at least two weeks When considering the biological mechanisms that underpin depression the most conclusive findings include deficits in the serotonergic 5-HT neurotransmission alterations in the expression of BDNF deficient immune activation and neuroinflammation and dysregulation of the hypothalamic-pituitary-adrenal HPA axis Thus understanding the pathophysiological mechanisms of MDD has widespread implications for the development of novel treatment and prevention strategies However despite advancements in the development of novel therapeutics current treatment options have not reached optimal efficacy Treatment resistant depression occurs in up to 40 of patients and standard antidepressant medication has a variety of undesirable side effects such as sedation decrease of blood pressure increase of weight indigestion or sexual dysfunction This often results in patients poor compliance resulting in a break-up of medication with recurrence of depressive symptoms and increased suicidal risk As there is an unmet need to develop safer and more effective treatments in depression a major topic of future psychiatric care is to focus on different possible physiologically relevant mechanisms in order to establish alternative causative and easy available treatment strategies
In the past few years it has become increasingly evident that resident gut bacteria are an important contributor to healthy metabolism and there is significant evidence linking altered composition of the gut microbiota and metabolic disorders such as obesity and depression Preclinical work in animals have reported associations between alterations of the gut microbiome the community of microorganism that live in the human gut and anxiety-like behaviour depressive-like symptoms and stress responsiveness In line with these preclinical findings a recent study found an altered composition of faecal microbiota in patients with MDD Most notably the MDD group had increased levels of Enterobacteriaceae and Alistipes but reduced levels of Faecalibacterium which was negatively correlated with the severity of depressive symptoms
Accumulating evidence suggest that there exits a bi-directional communication system between the gastrointestinal tract and the brain Changes in gut microbiota can influence cognitive and emotional stress processes through interactions with the brain and altered emotional states and dysfunction of the gut microbiome-brain axis has been implicated in stress-related disorders such as depression Brain-gut interactions could occur in various ways 1 microbial compounds communicate via the vagus nerve which connects the brain and the digestive tract and 2 microbially derived metabolites interact with the immune system which maintains its own communication with the brain Although the pathways linking gut bacteria with the brain are incompletely understood one of the principal mechanisms proposed to underlie stress-induced alterations is the leaky gut phenomenon Specifically increased translocation of bacterial products due to a compromised gut barrier has been linked to activation of the immune system and HPA axis In line with these findings human studies have demonstrated a stress-induced increase in bacterial translocation in depression The stress-induced interactions between the gut microbiome and the brain are further mediated via central processes such as neurotransmission and neurogenesis For instance there is substantial evidence to demonstrate a role for the gut commensals in the regulation and development of the 5-HT system and the expression of BDNF Virtually all corticolimbic brain structures that are involved in mood regulation and stress response express 5-HT receptors These include the prefrontal cortex amygdala hippocampus and nucleus accumbens A recent meta-analyses of fMRI studies support hyperactivation of several of these regions in response to fearful faces in MDD which extent correlated positively with the severity of depressive symptoms Furthermore during resting state fMRI MDD patients showed lower connectivity between the amydgala hippocampus parahippocampus and brainstem while the connectivity strength was inversely correlated with general depression The hippocampus and its connection to other limbic striatal and PFC regions seems to play a key role in stress regulation given that hippocampal neurogenesis mediates antidepressant effects via the ventral hippocampus influence on the HPA axis and mechanisms by which antidepressants may reverse chronic stress-induced 5-HT and neurogenic changes Notably BDNF may contribute to the modulation of neurogenesis in response to both stress and antidepressants as hippocampal BDNF levels decrease in response to chronic stress and increase in response to antidepressant treatments
Besides being a fundamental player in eating processes and in hypothalamic regulation of energy balance the appetite-regulating hormones leptin and ghrelin had been implicated in the etiology of mood disorders Importantly particular species of bacteria in the gut are know to affect the levels of leptin and ghrelin In humans the onset of depression was associated with a combination of high leptin levels coupled with high visceral fat and the link between leptin levels and severity of depressive symptoms was mediated by adiposity It was suggested that leptin might influence depression by acting on leptin receptors present on 5-HT neurons within the raphe nuclei and dopamine neurons in the midbrain and thus might influence reward processes Consistent with this supposition when leptin receptors in the rat hippocampus were genetically deleted a stressor-induced depressive profile was apparent and deletion of leptin receptors on midbrain dopamine neurons in mice elicited elevated anxiety Thus identifying the key brain regions that mediate leptins antidepressant activity and dissecting its intracellular signal transduction pathways may provide new insights into the pathogenesis of depression and facilitate the development of novel therapeutic strategies for the treatment of this illness
The gut peptide ghrelin also plays a fundamental role in eating and energy regulation and there have been indications that ghrelin functioning might contribute to depressive illness Like leptin ghrelin receptors have been reported in the midbrain and the dorsal raphe nucleus and have been associated with reward processes as well as stressor-induced depressive-like symptoms such as anhedonia In line with a role for ghrelin in stressor-elicited depression negative events promote an increase of circulating ghrelin levels and in emotionally reactive individuals the normalization of ghrelin levels after stress may be attenuated Moreover ghrelin was elevated among depressed patients and declined following pharmacotherapy and among patients who did not respond to treatment ghrelin levels were higher than among patients who responded positively
Compelling preclinical data demonstrated the beneficial effect of probiotics in normalizing HPA axis functioning BDNF levels and 5-HT neurotransmission In particular certain probiotics such as lactobacilli and bifidobacteria can reverse psychological stress-induced HPA axis activation and possess antidepressant or anxiolytic activity in rats A seminal work in experimental animals showed that altered stress responsiveness has been partially reversed by colonization of the gut Importantly a recent and innovative study showed that short-term consumption of mostly animal or mostly plant diet rapidly and reproducibly altered the human gut microbiome suggesting that the development of dietary interventions may provide a novel promising adjuvant therapy in addition to pharmacological antidepressant treatments in MDD Indeed recent reports of trials administrating a combination of probiotics to healthy subjects demonstrated improvements in depression or anxiety outcome measures Moreover urinary free cortisol levels were significantly reduced by the probiotics providing a potential mechanism for the improvement in psychological symptoms observed Consistent with this finding other studies in healthy subjects found that the consumption of a probiotic-containing yogurt improved mood and that a multispecies probiotic different strains of lactobacilli and bifidobacteria reduced rumination and aggressive thoughts Moreover a pioneer study in healthy subjects revealed by using fMRI that consumption of probiotic bacteria including strains of lactobacilli and bifidobacteria in fermented milk for 4 weeks modulated brain activation in corticolimbic regions while viewing frightened and angry facial expressions Most important a very recent study demonstrated that administration of probiotics a mixture of lactobacilli and bifidobacteria ameliorated depressive symptoms in unmedicated patients with mild to moderate depression These studies together suggest that restoring disturbed gut microbiome-brain interactions via probiotic bacteria might be a desirable treatment strategy for depression especially as most of the clinically depressed patients additionally suffer from obesity weight loss or gain appetite disturbances and constipation
This project is aimed at investigating for the first time if probiotic supplementation improves the effect of antidepressants on depressive symptoms ie better and faster remission in patients with severe MDD Furthermore this study will also test if probiotic supplementation modulates immune signalling and inflammatory processes HPA axis responses neurogenesis the release of appetite-regulating hormones the composition of gut microbiota and brain perfusion structure and activation and if these changes are associated with the probiotic-induced effect on depressive symptoms
In the past few years it has become increasingly evident that resident gut bacteria are an important contributor to healthy metabolism and there is significant evidence linking altered composition of the gut microbiota and metabolic disorders such as obesity and depression Preclinical work in animals have reported associations between alterations of the gut microbiome the community of microorganism that live in the human gut and anxiety-like behaviour depressive-like symptoms and stress responsiveness In line with these preclinical findings a recent study found an altered composition of faecal microbiota in patients with MDD Most notably the MDD group had increased levels of Enterobacteriaceae and Alistipes but reduced levels of Faecalibacterium which was negatively correlated with the severity of depressive symptoms
Accumulating evidence suggest that there exits a bi-directional communication system between the gastrointestinal tract and the brain Changes in gut microbiota can influence cognitive and emotional stress processes through interactions with the brain and altered emotional states and dysfunction of the gut microbiome-brain axis has been implicated in stress-related disorders such as depression Brain-gut interactions could occur in various ways 1 microbial compounds communicate via the vagus nerve which connects the brain and the digestive tract and 2 microbially derived metabolites interact with the immune system which maintains its own communication with the brain Although the pathways linking gut bacteria with the brain are incompletely understood one of the principal mechanisms proposed to underlie stress-induced alterations is the leaky gut phenomenon Specifically increased translocation of bacterial products due to a compromised gut barrier has been linked to activation of the immune system and HPA axis In line with these findings human studies have demonstrated a stress-induced increase in bacterial translocation in depression The stress-induced interactions between the gut microbiome and the brain are further mediated via central processes such as neurotransmission and neurogenesis For instance there is substantial evidence to demonstrate a role for the gut commensals in the regulation and development of the 5-HT system and the expression of BDNF Virtually all corticolimbic brain structures that are involved in mood regulation and stress response express 5-HT receptors These include the prefrontal cortex amygdala hippocampus and nucleus accumbens A recent meta-analyses of fMRI studies support hyperactivation of several of these regions in response to fearful faces in MDD which extent correlated positively with the severity of depressive symptoms Furthermore during resting state fMRI MDD patients showed lower connectivity between the amydgala hippocampus parahippocampus and brainstem while the connectivity strength was inversely correlated with general depression The hippocampus and its connection to other limbic striatal and PFC regions seems to play a key role in stress regulation given that hippocampal neurogenesis mediates antidepressant effects via the ventral hippocampus influence on the HPA axis and mechanisms by which antidepressants may reverse chronic stress-induced 5-HT and neurogenic changes Notably BDNF may contribute to the modulation of neurogenesis in response to both stress and antidepressants as hippocampal BDNF levels decrease in response to chronic stress and increase in response to antidepressant treatments
Besides being a fundamental player in eating processes and in hypothalamic regulation of energy balance the appetite-regulating hormones leptin and ghrelin had been implicated in the etiology of mood disorders Importantly particular species of bacteria in the gut are know to affect the levels of leptin and ghrelin In humans the onset of depression was associated with a combination of high leptin levels coupled with high visceral fat and the link between leptin levels and severity of depressive symptoms was mediated by adiposity It was suggested that leptin might influence depression by acting on leptin receptors present on 5-HT neurons within the raphe nuclei and dopamine neurons in the midbrain and thus might influence reward processes Consistent with this supposition when leptin receptors in the rat hippocampus were genetically deleted a stressor-induced depressive profile was apparent and deletion of leptin receptors on midbrain dopamine neurons in mice elicited elevated anxiety Thus identifying the key brain regions that mediate leptins antidepressant activity and dissecting its intracellular signal transduction pathways may provide new insights into the pathogenesis of depression and facilitate the development of novel therapeutic strategies for the treatment of this illness
The gut peptide ghrelin also plays a fundamental role in eating and energy regulation and there have been indications that ghrelin functioning might contribute to depressive illness Like leptin ghrelin receptors have been reported in the midbrain and the dorsal raphe nucleus and have been associated with reward processes as well as stressor-induced depressive-like symptoms such as anhedonia In line with a role for ghrelin in stressor-elicited depression negative events promote an increase of circulating ghrelin levels and in emotionally reactive individuals the normalization of ghrelin levels after stress may be attenuated Moreover ghrelin was elevated among depressed patients and declined following pharmacotherapy and among patients who did not respond to treatment ghrelin levels were higher than among patients who responded positively
Compelling preclinical data demonstrated the beneficial effect of probiotics in normalizing HPA axis functioning BDNF levels and 5-HT neurotransmission In particular certain probiotics such as lactobacilli and bifidobacteria can reverse psychological stress-induced HPA axis activation and possess antidepressant or anxiolytic activity in rats A seminal work in experimental animals showed that altered stress responsiveness has been partially reversed by colonization of the gut Importantly a recent and innovative study showed that short-term consumption of mostly animal or mostly plant diet rapidly and reproducibly altered the human gut microbiome suggesting that the development of dietary interventions may provide a novel promising adjuvant therapy in addition to pharmacological antidepressant treatments in MDD Indeed recent reports of trials administrating a combination of probiotics to healthy subjects demonstrated improvements in depression or anxiety outcome measures Moreover urinary free cortisol levels were significantly reduced by the probiotics providing a potential mechanism for the improvement in psychological symptoms observed Consistent with this finding other studies in healthy subjects found that the consumption of a probiotic-containing yogurt improved mood and that a multispecies probiotic different strains of lactobacilli and bifidobacteria reduced rumination and aggressive thoughts Moreover a pioneer study in healthy subjects revealed by using fMRI that consumption of probiotic bacteria including strains of lactobacilli and bifidobacteria in fermented milk for 4 weeks modulated brain activation in corticolimbic regions while viewing frightened and angry facial expressions Most important a very recent study demonstrated that administration of probiotics a mixture of lactobacilli and bifidobacteria ameliorated depressive symptoms in unmedicated patients with mild to moderate depression These studies together suggest that restoring disturbed gut microbiome-brain interactions via probiotic bacteria might be a desirable treatment strategy for depression especially as most of the clinically depressed patients additionally suffer from obesity weight loss or gain appetite disturbances and constipation
This project is aimed at investigating for the first time if probiotic supplementation improves the effect of antidepressants on depressive symptoms ie better and faster remission in patients with severe MDD Furthermore this study will also test if probiotic supplementation modulates immune signalling and inflammatory processes HPA axis responses neurogenesis the release of appetite-regulating hormones the composition of gut microbiota and brain perfusion structure and activation and if these changes are associated with the probiotic-induced effect on depressive symptoms
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None