Michael Berk

Michael Berk


Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 March 2018 in Bipolar Disorders
Verified
Journal Article
Open access
PDF file
LYLakshmi N Yatham
Lakshmi N Yatham
SKSidney H Kennedy
Sidney H Kennedy
SPSagar V Parikh
Sagar V Parikh
ASAyal Schaffer
Ayal Schaffer
DBDavid J Bond
David J Bond
MBMichael Berk
Michael Berk
The Canadian Network for Mood and Anxiety Treatments (CANMAT) previously published treatment guidelines for bipolar disorder in 2005, along with international commentaries and subsequent updates in 2007, 2009, and 2013. The last two updates were published in collaboration with the International Society for Bipolar Disorders (ISBD). These 2018 CANMAT and ISBD Bipolar Treatment Guidelines represent the significant advances in the field since the last full edition was published in 2005, including updates to diagnosis and management as well as new research into pharmacological and psychological treatments. These advances have been translated into clear and easy to use recommendations for first, second, and third‐ line treatments, with consideration given to levels of evidence for efficacy, clinical support based on experience, and consensus ratings of safety, tolerability, and treatment‐emergent switch risk. New to these guidelines, hierarchical rankings were created for first and second‐ line treatments recommended for acute mania, acute depression, and maintenance treatment in bipolar I disorder. Created by considering the impact of each treatment across all phases of illness, this hierarchy will further assist clinicians in making evidence‐based treatment decisions. Lithium, quetiapine, divalproex, asenapine, aripiprazole, paliperidone, risperidone, and cariprazine alone or in combination are recommended as first‐line treatments for acute mania. First‐line options for bipolar I depression include quetiapine, lurasidone plus lithium or divalproex, lithium, lamotrigine, lurasidone, or adjunctive lamotrigine. While medications that have been shown to be effective for the acute phase should generally be continued for the maintenance phase in bipolar I disorder, there are some exceptions (such as with antidepressants); and available data suggest that lithium, quetiapine, divalproex, lamotrigine, asenapine, and aripiprazole monotherapy or combination treatments should be considered first‐line for those initiating or switching treatment during the maintenance phase. In addition to addressing issues in bipolar I disorder, these guidelines also provide an overview of, and recommendations for, clinical management of bipolar II disorder, as well as advice on specific populations, such as women at various stages of the reproductive cycle, children and adolescents, and older adults. There are also discussions on the impact of specific psychiatric and medical comorbidities such as substance use, anxiety, and metabolic disorders. Finally, an overview of issues related to safety and monitoring is provided. The CANMAT and ISBD groups hope that these guidelines become a valuable tool for practitioners across the globe.

1 April 2016 in The Lancet
Verified
Journal Article
Closed access
IGIria Grande
Iria Grande
MBMichael Berk
Michael Berk
BBBoris Birmaher
Boris Birmaher
Eduard VietaEduard Vieta
Eduard Vieta

12 September 2013 in BMC Medicine
Verified
Journal Article
Open access
PDF file
MBMichael Berk
Michael Berk
LWLana J Williams
Lana J Williams
FJFelice N Jacka
Felice N Jacka
AOAdrienne O’nEil
Adrienne O’nEil
JPJulie Pasco
Julie Pasco
MMMichael Maes
Michael Maes
We now know that depression is associated with a chronic, low-grade inflammatory response and activation of cell-mediated immunity, as well as activation of the compensatory anti-inflammatory reflex system. It is similarly accompanied by increased oxidative and nitrosative stress (O&NS), which contribute to neuroprogression in the disorder. The obvious question this poses is ‘what is the source of this chronic low-grade inflammation?’ This review explores the role of inflammation and oxidative and nitrosative stress as possible mediators of known environmental risk factors in depression, and discusses potential implications of these findings. A range of factors appear to increase the risk for the development of depression, and seem to be associated with systemic inflammation; these include psychosocial stressors, poor diet, physical inactivity, obesity, smoking, altered gut permeability, atopy, dental cares, sleep and vitamin D deficiency. The identification of known sources of inflammation provides support for inflammation as a mediating pathway to both risk and neuroprogression in depression. Critically, most of these factors are plastic, and potentially amenable to therapeutic and preventative interventions. Most, but not all, of the above mentioned sources of inflammation may play a role in other psychiatric disorders, such as bipolar disorder, schizophrenia, autism and post-traumatic stress disorder.

1 April 2011 in Progress in Neuro-Psychopharmacology and Biological Psychiatry
Verified
Journal Article
Closed access
MMMichael Maes
Michael Maes
PGPiotr Galecki
Piotr Galecki
YCYong Seun Chang
Yong Seun Chang
MBMichael Berk
Michael Berk

1 January 2011 in Neuroscience & Biobehavioral Reviews
Verified
Journal Article
Closed access
MBMichael Berk
Michael Berk
FKF. Kapczinski
F. Kapczinski
AAA.C. Andreazza
A.C. Andreazza
ODO.M. Dean
O.M. Dean
FGF. Giorlando
F. Giorlando
GMG.S. Malhi
G.S. Malhi

16 December 2016 in Journal of Medical Internet Research
Verified
Journal Article
Open access
WLWei Luo
Wei Luo
DPDinh Phung
Dinh Phung
TTTruyen Tran
Truyen Tran
SGSunil Gupta
Sunil Gupta
SRSantu Rana
Santu Rana
MBMichael Berk
Michael Berk
Journal of Medical Internet Research - International Scientific Journal for Medical Research, Information and Communication on the Internet