The main clinical aims of diagnosis include the optimisation of treatments and allowing useful prognostic statements to be made. The history of medicine suggests that therapeutic and prognostic decision-making are usually facilitated, often greatly, as classifications move closer to the underlying biological mechanisms. For this reason, it is desirable to move towards a classification that maps the expression of illness onto the underlying biological systems. It is not yet clear whether this will be most usefully achieved by using multiple overlapping ‘categorical’ domains of psychopathology or multiple dimensions. [link] [link] [link] Clinicians benefit from the simplest, most user-friendly model that is clinically useful. Of course, the traditional dichotomy is simple and this perhaps explains its persistence despite increasingly questioned clinical usefulness. [link] In our 2005 editorial we suggested that recent evidence made it necessary to consider a mood-psychosis clinical dimension with at least three possible overlapping broad domains of psychopathology (’prototype schizophrenia’, ‘schizoaffective’ and ‘prototype bipolar’). More recent genetic data are broadly consistent with such a model. However, these newer data also point to the need to consider a broader clinical spectrum that includes also autism and mental [ret*rdation]/cognitive impairment at one end and non-psychotic mood disorder at the other.
- Nick Craddock and Michael J. Owen, “The Kraepelinian dichotomy - going, going... but still not gone” in The British Journal of Psychiatry 196(2): February 2010 (link)














