Philip  McGuire

Philip McGuire

Professor of Psychiatry and Cognitive Neuroscienc



Biography:


Overview


The IOPPN hosts one of the world’s largest groups conducting research on psychosis. Our work is focused on understanding the neurobiological mechanisms underlying psychosis, particularly those related to the onset of psychotic disorders. We have particular strengths in neuroimaging, -omic, cognitive, and psychopharmacological studies in the early phases of psychosis. These often involve people who are at ‘ultra high risk’ for psychosis (but have not yet developed a psychotic disorder), and patients with first episode psychosis (who have just become psychotic for the first time). Research in this field is facilitated by an international network of early detection and intervention centres that provides a unique platform for recruiting and following up these subjects. We also have excellent partnerships with the pharmaceutical industry and with SMEs with expertise in developing clinical tools. Our findings in clinical subjects are broadly consistent with data from animal models of psychosis, and we are very keen on work that integrates human and basic science research in this field.

The long term ambition is to use our research findings to provide a scientific rationale for the development of: a) tools that use biomarkers to predict key clinical outcomes, such as the onset of psychosis, or the response to treatment in psychosis; and b) new forms of treatment that can be used to prevent the onset of psychosis and to improve outcomes in patients who have a psychotic disorder.

Links:

KCL PURE: https://kclpure.kcl.ac.uk/portal/philip.mcguire.html

Selected publications:

Colizzi M, Weltens N, McGuire P, Lythgoe D, Williams S, Van Oudenhove L, Bhattacharyya S (2019) Delta-9-tetrahydrocannabinol increases striatal glutamate levels in healthy individuals: implications for psychosis. Mol Psychiatry

Minichino A, Rutigliano G, Merlino S, Davies C, Oliver D, De Micheli A, Patel R, McGuire P, Fusar-Poli P (2019) Unmet needs in patients with brief psychotic disorders: Too ill for clinical high risk services and not ill enough for first episode services. Eur Psychiatry 57: 26-32

Modinos G, ?im?ek F, Azis M, Bossong M, Bonoldi I, Samson C, Quinn B, Perez J, Broome MR, Zelaya F, Lythgoe DJ, Howes OD, Stone JM, Grace AA, Allen P, McGuire P (2018) Correction: Prefrontal GABA levels, hippocampal resting perfusion and the risk of psychosis. Neuropsychopharmacology 43: 2660