
- Vol 43, Issue 1
A Network-Based Approach to Depression, Neuropathic Pain, and Substance Use Disorder Using Coadministered TMS and Ketamine
Key Takeaways
- Combining TMS and ketamine enhances treatment outcomes for depression, neuropathic pain, and substance use disorders by targeting interconnected brain networks.
- The salience, default mode, and central executive networks are key neurocircuitry involved in these conditions, influencing emotional and cognitive processes.
Innovative combinations of transcranial magnetic stimulation and ketamine therapy offer new hope for treatment-resistant depression, pain, and substance use disorders.
Recent advances in transcranial magnetic stimulation (TMS) and ketamine therapy are offering new hope to patients burdened by complex, treatment-resistant illness conditions, including depression, neuropathic pain, and substance use disorders.1,2 While the practice was initially developed to make TMS more tolerable and practical, more than 15 years of clinical and imaging evidence now indicate that coadministering TMS and ketamine produces more robust and durable improvement than either therapy alone, even for the most refractory presentations.3,4
Moving From Circuits to Clinical Care
Clinical neuroscience increasingly recognizes that many psychiatric and neuropsychiatric syndromes reflect disruptions in interconnected brain networks, rather than isolated regions. Network-focused neuroimaging has revealed shared patterns of dysfunction across affective, pain, and substance use disorders.5 The brain’s functional architecture—including the salience, default mode, and central executive networks—can help reframe and target these complex conditions.
Key Neurocircuitry Involved
Salience network (anterior cingulate cortex [ACC], anterior insula): coordinates the brain’s response to salient emotional and somatic stimuli. Hyperactivity is linked to pain amplification and emotional reactivity.
Default mode network (DMN) (medial prefrontal cortex, posterior cingulate cortex, precuneus): central to rumination and self-referential thinking; its overactivity sustains depressive thinking and craving.
Active (central executive) attention network (dorsolateral prefrontal cortex, parietal cortex): enables cognitive control over emotion, behavior, and pain; hypoactivity here is seen in depression and impulsivity.
Why Combine TMS and Ketamine?
Mounting evidence demonstrates that multimodal interventions deliver superior clinical results across the psychiatric spectrum: psychotherapy plus medication for anxiety disorders, electroconvulsive therapy plus pharmacotherapy for catatonia, and, for depression, the innovative pairing of noninvasive brain stimulation (eg, TMS) with ketamine. This combination is uniquely office-based, practical, and effective.
Neuroanatomic Targets and Network Modulation
TMS, especially directed to the ACC, recalibrates the salience network, mitigating pain hypersensitivity and emotional dysregulation. Ketamine, by rapidly dampening DMN overactivity and enhancing neuroplasticity, interrupts cycles of ruminative thought and addictive craving. Their combined administration has been shown to restore more normalized global network activity and connectivity and is reflected in improved clinical and imaging outcomes as well as patient-reported functioning.6
Case series and real-world clinical reports support the efficacy of this strategy, with many patients experiencing major recovery after failure of conventional, algorithm-driven approaches. Dramatic recoveries are regularly observed in patients with severe depression, intractable pain, and histories of suicidality or relapse.7
Looking Ahead: Integrative Neuropsychiatry
Mastery of trimorbidity conditions—chronic depression, neuropathic pain, and substance use disorder—demands collaboration across psychiatry, neurology, psychiatry, addiction medicine, and pain management. Brain network–informed diagnostics and therapeutics, such as TMS plus ketamine, promise a new standard for those previously deemed treatment-resistant. Future studies may lead to even more optimized protocols, patient stratification, and long-term outcomes—paving the way toward precision network therapeutics.
Dr Best is the director of the Neuroscience Center in Deerfield, Illinois.
References
1. Doan L, Manders T, Wang J.
2. Onwumere J, Stubbs B, Stirling M, et al.
3. Best SRD, Haustrup N, Pavel DG.
4. Arubuolawe OO, Folorunsho IL, Busari AK, et al.
5. De Ridder D, Vanneste S, Smith M, et al.
6. Jiang W, Isenhart R, Sutherland R, et al.
7. Best SRD, Pavel DG, Haustrup N.
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