2008
DOI: 10.1016/j.schres.2008.07.012
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Validation of “prodromal” criteria to detect individuals at ultra high risk of psychosis: 2 year follow-up

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Cited by 324 publications
(306 citation statements)
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“…The underlying substrate for such a 'swelling' prior to the actual conversion to psychosis could be an increased apoptotic activity involving a transient controlled inflammatory response while removing apoptotic cells, or cell parts (axons and dendrites) (Berger et al, 2003;Lieberman et al, 2007). If true, this may imply that new benign neuroprotective treatment strategies may be especially effective in this late phase of prodrome and be able to modulate underlying neurobiological processes and potentially delay or even prevent the onset of psychosis Our study may not be fully comparable to other structural MRI studies because different research groups have used slightly different ways of defining their high risk (Fusar-Poli P et al, 2008;Yung et al, 2008) and first episode psychosis (McGorry et al, 2004;Schimmelmann et al 2005) cohorts, used different ascertainment strategies, different anatomic boundaries of the hippocampus (with or without amygdala) as well as applied different techniques to measure HV (i.e. manual vs. automated methods).…”
Section: Arms-nt)mentioning
confidence: 89%
“…The underlying substrate for such a 'swelling' prior to the actual conversion to psychosis could be an increased apoptotic activity involving a transient controlled inflammatory response while removing apoptotic cells, or cell parts (axons and dendrites) (Berger et al, 2003;Lieberman et al, 2007). If true, this may imply that new benign neuroprotective treatment strategies may be especially effective in this late phase of prodrome and be able to modulate underlying neurobiological processes and potentially delay or even prevent the onset of psychosis Our study may not be fully comparable to other structural MRI studies because different research groups have used slightly different ways of defining their high risk (Fusar-Poli P et al, 2008;Yung et al, 2008) and first episode psychosis (McGorry et al, 2004;Schimmelmann et al 2005) cohorts, used different ascertainment strategies, different anatomic boundaries of the hippocampus (with or without amygdala) as well as applied different techniques to measure HV (i.e. manual vs. automated methods).…”
Section: Arms-nt)mentioning
confidence: 89%
“…Additionally, around 10% of ARMS individuals have attempted suicide shortly before presentation [32]. In terms of transition rates to psychosis a recent meta-analysis (mean age 19.9 years) estimated around 18% of such individuals develop psychosis by six months, reaching 36% after three years [33] with existing data suggesting transition is most likely within the first six months after identification [34].…”
Section: Introductionmentioning
confidence: 99%
“…Individuals with an "at-risk mental state" (ARMS) present with prodromal symptoms of psychosis and have a very high risk for the disease developing within the next 2 years. 10 The ARMS is characterized by poor psycho social functioning 11 and neurocognitive impairments. 12 Interestingly, 3 recent independent studies of individuals at enhanced risk for psychosis have confirmed that P300 ab normalities are already evident in the prepsychotic phases.…”
Section: Introductionmentioning
confidence: 99%