Managing Depression as an Inflammatory Condition

Lylen Ferris, ND | March 17, 2021

Patients with major depression have been found to exhibit increased peripheral blood inflammatory biomarkers, including inflammatory cytokines. Cytokines have been shown to access the brain and interact with virtually every pathophysiologic domain known to be involved in depression, including neurotransmitter synthesis and metabolism, neuroendocrine function, and neural plasticity.  

A 2014 study examined 50 non medicated patients with major depressive disorder (MDD). Before treatment, the inflammatory markers IL-1β, IL-5, IL-6, IL-7, IL-8, IL-10, and IFNγ were significantly elevated in depressed patients at baseline compared to healthy controls. After 12 weeks of treatment, the plasma levels of these seven cytokines had decreased significantly compared to baseline and did not differ from those in the healthy controls. Researchers concluded, “Recovery from depression was associated with reduction to normal levels of the majority of the measured cytokines. These results strongly support the notion that a complex network of cytokines is involved in the pathophysiology of MDD.” 

Once cytokine signals reach the brain, they have the capacity to influence the synthesis, release, and reuptake of neurotransmitters like serotonin, dopamine, glutamate, and norepinephrine. Testing the neurotransmitter imbalance driven by these inflammatory cytokines provides information on how to approach patient support. Once imbalances are identified via spot or 24-hour urinary neurotransmitter testing, therapies such as amino acids, nervine and adaptogenic herbs, and essential nutrients can be implemented as appropriate. However, the underlying inflammation must not be overlooked.  

Identifying the source of inflammation is essential, but it can be daunting to know where to begin. Common drivers of inflammation are lifestyle related: Does the patient smoke? Are they physically active? Obese? What does their diet look like and are food sensitivities a possibility? Dental health is an often-overlooked etiology of inflammation, as many patients do not have dental insurance and are neglectful of this area of health. Periodontal disease and dental cares can be sources of inflammation.  

Hormone imbalance is often a reflection of inflammation, and perhaps a driver of it, as insomnia promotes inflammation, but can also be the result of inflammatory conditions and pain. Stress drives inflammation. Stress and insomnia are typically reflected in the disordered release of cortisol. Additionally, inflammatory metabolic syndrome drives androgen imbalance and estrogen dominance in males and females alike.  

Another common etiology of inflammation is gastrointestinal dysbiosis and digestive issues. The intestinal epithelial lining, together with factors secreted from it, forms a barrier that separates the host from the environment. In pathologic conditions, the permeability of the epithelial lining may be compromised allowing the passage of food particles, toxins, antigens, and bacteria in the lumen to enter the blood stream and drive inflammation. Assessing the heath of the microbiome as well as digestive and inflammatory markers can provide essential information on gastrointestinal health.  

When it comes to sources of inflammation, the good news is that most of these factors are plastic, and potentially amenable to therapeutic and preventative interventions. Taking a thorough history and employing appropriate laboratory testing will provide the practitioner with insight as to where to focus anti-inflammatory efforts in the management of depression and other neuroendocrine imbalances.

References

Berk M, et al. So depression is an inflammatory disease, but where does the inflammation come from? BMC Med. 2013 Sep 12;11:200. 

Dahl J et al. The plasma levels of various cytokines are increased during ongoing depression and are reduced to normal levels after recovery. Psychoneuroendocrinology. 2014 Jul;45:77-86.  

Miller AH, et al. Inflammation and its Discontents: The Role of Cytokines in the Pathophysiology of Major Depression. Biol Psychiatry. 2009 <May 1;65(9): 732-741.  

Qinghui Mu, Jay Kirby, Christopher M. Reilly, Xin M. Luo. Leaky Gut As a Danger Signal for Autoimmune Diseases. Front Immunol. 2017;8:598.  

Wellness Wednesday Webinar

Neurotransmitter Primer

Fiona Campbell, ND

April 7, 2021 at 9 AM and 12 PM Pacific

Each session is approximately 60 minutes in length with Q&A

Review the anatomy and physiology of neurotransmitter (NT) secretion and function

Exam the role of individual NTs and how imbalances present clinically

Learn to incorporate NT evaluation and treatment in your hormone balancing practice

Obtain treatment considerations for addressing neurotransmitter imbalances, without prescription medications

Beyond Adrenal Fatigue: Reframing our Understanding of Stress and the HPA Axis

Tom Guilliams PhD

April 21, 2021 | 12-1 PM Pacific

For too long, complex stress-related changes to HPA axis function have been labeled as "adrenal fatigue." This outdated and incorrect nomenclature has often prevented clinicians from properly understanding how the HPA axis adapts to stressors and why simplistic solutions (i.e., adrenal support) are inadequate for most patients. Our knowledge of the stress response system, HPA axis maladaptation, and the factors that influence glucocorticoid signaling have greatly advanced in just the past decade, though much of this knowledge is not well leveraged in most clinical practices. This webinar will reframe our orientation of stress in a way that focuses on the brain (rather than the adrenal gland), and shows that the stress response is not as linear as it is often perceived. While navigating through one of the premier resources to help clinicians understand the functional medicine approach to stress and the HPA axis, this lecture will also help re-frame the stress response within the larger (non-stress) functions performed by the HPA axis

 
 
 

Disclaimer: All information given about health conditions, treatment, products, and dosages are for educational purposes only and do not constitute medical advice.

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