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Descriptive Psychopathology: The Signs and Symptoms of ...

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374 Section 4: Evidence-based classificationsuppression test), <strong>and</strong> note that the specificity <strong>and</strong> sensitivity <strong>of</strong> such measures aresimilar to those for scalp-recorded EEG in the recognition <strong>of</strong> seizure disorder. <strong>The</strong>yalso recommend the use <strong>of</strong> a lorazepam challenge test to confirm the diagnosis <strong>of</strong>catatonia. 2 First <strong>and</strong> Zimmerman (2006) also recommend all-night sleep EEG as anindicator for depressive illness, <strong>and</strong> report that such a study correctly classified 82%<strong>of</strong> a mixed sample <strong>of</strong> normal persons, persons with primary insomnia, <strong>and</strong> patientswith depression.Some writers place their hopes on classification by gene identification,i.e. genetic nosology. 3 But attempts to delineate specific diseases by specific genotypeare premature as the syndromes <strong>of</strong> interest are phenotypically ill-defined <strong>and</strong>likely multifactorial in etiology. 4Mood disorders 5Since 1980, depressive illness has been defined as the single construct, majordepression, with variations based on illness duration <strong>and</strong> severity (e.g. dysthymia<strong>and</strong> psychotic depression). Abnormal bereavement <strong>and</strong> perinatal depression are givenseparate status. Modest depressions associated with personal stress are designatedadjustment disorder. Persons with only recurrent depressive episodes are classified asunipolar. Those who also experience hypomania or mania are said to be bipolar <strong>and</strong>to be suffering from a different illness requiring different treatments. 6Clinical presentations <strong>and</strong> pathophysiology <strong>of</strong> the unipolar form are consideredto be so alike that similar treatments are <strong>of</strong>fered, varying mainly in dosage,numbers <strong>of</strong> agents, or augmentations. <strong>The</strong> recommended treatment algorithmsare the same for all patients with non-psychotic major depression, <strong>and</strong> slightlymodified for patients with psychotic depression <strong>and</strong> bipolar depression.Research <strong>and</strong> clinical samples <strong>of</strong> depressed patients selected by list criteria,however, are heterogeneous <strong>and</strong> account in part for poor treatment outcomes. 7Predictors <strong>of</strong> good outcomes with newer antidepressants have not been identified.Similar critiques are <strong>of</strong>fered for the poor outcomes in the STEP-BD study <strong>of</strong> antimanicagents 8 <strong>and</strong> the CATIE study <strong>of</strong> atypical antipsychotics. 9Dividing the major depression category into melancholia <strong>and</strong> non-melancholiadepressive disorders is an alternative paradigm to the present classification <strong>of</strong>mood disorders that fits the evidence better. This approach minimizes intra-sampleheterogeneity <strong>and</strong> encourages more specific treatments <strong>and</strong> precise research. <strong>The</strong>division also alters the category’s unipolar–bipolar formulation (see below).While several present categories can be combined in the melancholia construct,non-melancholic depression remains heterogeneous. Dysthymia is not a validentity <strong>and</strong> likely represents patients with poorly treated depressive illness, depressivedisorders that are exaggerations <strong>of</strong> temperament traits (depressive personality),

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