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Evaluating differential developmental trajectories to adolescent-onset mood and psychotic disorders
被引:47
|作者:
Hickie, Ian B.
[1
]
Hermens, Daniel F.
[1
]
Naismith, Sharon L.
[1
]
Guastella, Adam J.
[1
]
Glozier, Nick
[1
]
Scott, Jan
[2
,3
,4
]
Scott, Elizabeth M.
[1
,5
]
机构:
[1] Univ Sydney, Brain & Mind Res Inst, Clin Res Unit, Camperdown, NSW 2050, Australia
[2] Newcastle Univ, Inst Neurosci, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[3] Inst Psychiat, Ctr Affect Disorders, London, England
[4] Ctr Ageing & Vital, Wolfson Unit, Newcastle Upon Tyne, Tyne & Wear, England
[5] Univ Notre Dame, Sch Med, Sydney, NSW, Australia
来源:
基金:
英国医学研究理事会;
澳大利亚国家健康与医学研究理事会;
关键词:
Youth;
Neuropsychology;
Clinical staging;
Sub-syndromal;
Phenotype;
Illness trajectory;
MENTAL-DISORDERS;
BIPOLAR DEPRESSION;
PROLONGED FATIGUE;
META-STRUCTURE;
RATING-SCALE;
CO-MORBIDITY;
DSM-IV;
SCHIZOPHRENIA;
PSYCHIATRY;
DIAGNOSIS;
D O I:
10.1186/1471-244X-13-303
中图分类号:
R749 [精神病学];
学科分类号:
100205 ;
摘要:
Background: It is an open question as to whether differential developmental trajectories, potentially representing underlying pathophysiological processes, can form the basis of a more useful typology in young persons who present for mental health care. Methods: A cohort of 605 young people was recruited from youth mental health services that target the early phases of anxiety, mood or psychotic disorders. Participants were assigned to one of three clinical sub-types (anxious-depression; mania-fatigue; developmental-psychotic) according to putative developmental trajectories. Results: The distribution of subtypes was: 51% anxiety-depression, 25% mania-fatigue and 24% developmental-psychotic, with key differences in demographic, clinical, family history and neuropsychological characteristics. When analyses were limited to 286 cases with 'attenuated' or sub-threshold syndromes, the pattern of differences was similar. Multinomial logistic regression demonstrated that compared to the developmental-psychotic subtype, both the mania-fatigue and anxiety-depression subtypes were younger and more depressed at presentation, but less functionally impaired. Other discriminating variables between the developmental-psychotic and mania-fatigue sub-types were that the latter were significantly more likely to have a family history of bipolar disorder but have less likelihood of impaired verbal learning; whilst the anxious-depression group were more anxious, more likely to have a family history of depression, and had a higher premorbid IQ level. Conclusions: This cross-sectional evaluation provides preliminary support for differing developmental trajectories in young persons presenting for mental health care. Prospective follow-up is needed to examine the predictive validity of this approach and its relationships to underlying pathophysiological mechanisms.
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