Microstructural white-matter abnormalities associated with treatment resistance, severity and duration of illness in major depression

被引:112
|
作者
de Diego-Adelino, J. [1 ]
Pires, P. [2 ]
Gomez-Anson, B. [2 ]
Serra-Blasco, M. [1 ,3 ]
Vives-Gilabert, Y. [3 ]
Puigdemont, D. [1 ]
Martin-Blanco, A. [1 ]
Alvarez, E. [1 ]
Perez, V. [1 ]
Portella, M. J. [1 ]
机构
[1] Univ Autonoma Barcelona, Dept Psychiat, Hosp Santa Creu & St Pau, CIBERSAM,IIB St Pau, Barcelona 08025, Spain
[2] Univ Autonoma Barcelona, Dept Neuroradiol, Hosp Santa Creu & St Pau, IIB St Pau, Barcelona 08025, Spain
[3] Univ Autonoma Barcelona, Barcelona 08025, Spain
关键词
Diffusion tensor imaging; fractional anisotropy; major depression; DIFFUSION TENSOR; BIPOLAR DISORDER; SPATIAL STATISTICS; FRACTIONAL ANISOTROPY; PREFRONTAL CORTEX; SCHIZOPHRENIA; INTEGRITY; ADULTS; METAANALYSIS; MORPHOLOGY;
D O I
10.1017/S003329171300158X
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background. Although white-matter abnormalities have been reported in middle-aged patients with major depressive disorder (MDD), few data are available on treatment-resistant MDD and the influence of relevant variables related to clinical burden of illness is far from being well established. Method. The present study examined white-matter microstructure in a sample of 52 patients with MDD in different stages (treatment-resistant/chronic MDD, n=18; remitted-recurrent MDD, n=15; first-episode MDD, n=19) and 17 healthy controls, using diffusion tensor imaging with a tract-based spatial statistics approach. Groups were comparable in age and gender distribution, and results were corrected for familywise error (FWE) rate. Results. Widespread significant reductions of fractional anisotropy (FA) - including the cingulum, corpus callosum, superior and inferior longitudinal fascicule - were evident in treatment-resistant/chronic MDD compared with first-episode MDD and controls (p<0.05, FWE-corrected). Decreased FA was observed within the ventromedial prefrontal region in treatment-resistant/chronic MDD even when compared with the remitted-recurrent MDD group (p<0.05, FWE-corrected). Longer duration of illness (beta=-0.49, p=0.04) and higher depression severity (at a trend level: beta=-0.26, p=0.06) predicted lower FA in linear multiple regression analysis at the whole-brain level. The number of previous episodes and severity of symptoms were significant predictors when focused on the ventromedial prefrontal area (beta=-0.28, p=0.04; and beta=-0.29, p=0.03, respectively). Medication effects were controlled for in the analyses and results remained unaltered. Conclusions. Our findings support the notion that disruptions of white-matter microstructure, particularly in fronto-limbic networks, are associated with resistance to treatment and higher current and past burden of depression.
引用
收藏
页码:1171 / 1182
页数:12
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