Areas of controversy in neuroprogression in bipolar disorder

被引:142
作者
Passos, I. C. [1 ,2 ]
Mwangi, B. [3 ]
Vieta, E. [4 ]
Berk, M. [5 ,6 ,7 ,8 ]
Kapczinski, F. [1 ,2 ]
机构
[1] Hosp Clin Porto Alegre HCPA, Lab Mol Psychiat, Bipolar Disorder Program, Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande Sul UFRGS, Dept Psychiat, Porto Alegre, RS, Brazil
[3] Univ Texas Sci Ctr Houston, Dept Psychiat & Behav Sci, Ctr Excellence Mood Disorder, Houston, TX USA
[4] Univ Barcelona, Hosp Clin, Bipolar Disorders Program, Inst Invest Biomed Agusti Pi Sunyer,CIBERSAM, Barcelona, Catalonia, Spain
[5] Deakin Univ, Fac Hlth, Sch Med, IMPACT Strateg Res Ctr, Geelong, Vic, Australia
[6] Univ Melbourne, Natl Ctr Excellence Youth Mental Hlth, Orygen, Parkville, Vic, Australia
[7] Univ Melbourne, Ctr Youth Mental Hlth, Dept Psychiat, Parkville, Vic, Australia
[8] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
bipolar disorder; neuroprogression; treatment refractoriness; functional impairment; inflammation; machine learning; MAGNETIC-RESONANCE SPECTROSCOPY; DORSOLATERAL PREFRONTAL CORTEX; TREATMENT ENHANCEMENT PROGRAM; VS; LATE-STAGE; COGNITIVE IMPAIRMENT; I DISORDER; NEUROTROPHIC FACTOR; PREVIOUS EPISODES; OLDER-ADULTS; 1ST EPISODE;
D O I
10.1111/acps.12581
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: We aimed to review clinical features and biological underpinnings related to neuroprogression in bipolar disorder (BD). Also, we discussed areas of controversy and future research in the field. Method: We systematically reviewed the extant literature pertaining to neuroprogression and BD by searching PubMed and EMBASE for articles published up to March 2016. Results: A total of 114 studies were included. Neuroimaging and clinical evidence from cross-sectional and longitudinal studies show that a subset of patients with BD presents a neuroprogressive course with brain changes and unfavorable outcomes. Risk factors associated with these unfavorable outcomes are number of mood episodes, early trauma, and psychiatric and clinical comorbidity. Conclusion: Illness trajectories are largely variable, and illness progression is not a general rule in BD. The number of manic episodes seems to be the clinical marker more robustly associated with neuroprogression in BD. However, the majority of the evidence came from cross-sectional studies that are prone to bias. Longitudinal studies may help to identify signatures of neuroprogression and integrate findings from the field of neuroimaging, neurocognition, and biomarkers.
引用
收藏
页码:91 / 103
页数:13
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