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Berk, Michael

https://orcid.org/0000-0002-5554-6946

Mayo Clinic

Barwon Health

Citations 23

Hyperthermia for Major Depressive Disorder?
Berk, Michael , Tye, Susannah J. , McGee, Sean L. , Tye, Susannah, Walder, Ken R. , Berk, Michael , Tye, Susannah J

JAMA Psychiatry | September 14, 2016 | Volume: 73 | Issue: 10 | Pages: 1095

10.1001/jamapsychiatry.2016.1532 Get It

Evolution of optogenetic microdevices
Kale, Rajas P. , Berk, Michael , Tye, Susannah J. , Kouzani, Abbas Z. , Walder, Ken R. , Berk, Michael , Tye, Susannah J

Neurophotonics | June 26, 2015 | Volume: 2 | Issue: 3 | Pages: 031206

10.1117/1.nph.2.3.031206 Get It

Biomarkers in bipolar disorder: A positional paper from the International Society for Bipolar Disorders Biomarkers Task Force
Frey, Benício N. , Andreazza, Ana C. , Houenou, Josselin , Jamain, Stéphane , Goldstein, Benjamin I. , Frye, Mark A. , Leboyer, Marion , Berk, Michael , Malhi, Gin S. , López‐Jaramillo, Carlos , Taylor, Valerie H. , Frangou, Sophia , Hall, Geoffrey B. , Fernandes, Brisa S. , Kauer‐Sant’Anna, Marcia , Yatham, Lakshmi N. , Kapczinski, Flávio , Young, L. Trevor , Dodd, Seetal , Andreazza, Ana C , Frangou, Sophia , López-Jaramillo, Carlos , Yatham, Lakshmi N , Jamain, Stéphane , Leboyer, Marion , Berk, Michael , Malhi, Gin S , Goldstein, Benjamin I

Australian & New Zealand Journal of Psychiatry | February 15, 2013 | Volume: 47 | Issue: 4 | Pages: 321-332

10.1177/0004867413478217 Get It

Although the etiology of bipolar disorder remains uncertain, multiple studies examining neuroimaging, peripheral markers and genetics have provided important insights into the pathophysiologic processes underlying bipolar disorder. Neuroimaging studies have consistently demonstrated loss of gray matter, as well as altered activation of subcortical, anterior temporal and ventral prefrontal regions in response to emotional stimuli in bipolar disorder. Genetics studies have identified several potential candidate genes associated with increased risk for developing bipolar disorder that involve circadian rhythm, neuronal development and calcium metabolism. Notably, several groups have found decreased levels of neurotrophic factors and increased pro-inflammatory cytokines and oxidative stress markers. Together these findings provide the background for the identification of potential biomarkers for vulnerability, disease expression and to help understand the course of illness and treatment response. In other areas of medicine, validated biomarkers now inform clinical decision-making. Although the findings reviewed herein hold promise, further research involving large collaborative studies is needed to validate these potential biomarkers prior to employing them for clinical purposes. Therefore, in this positional paper from the ISBD-BIONET (biomarkers network from the International Society for Bipolar Disorders), we will discuss our view of biomarkers for these three areas: neuroimaging, peripheral measurements and genetics; and conclude the paper with our position for the next steps in the search for biomarkers for bipolar disorder.