4.6 Article

White Matter Abnormalities in Major Depression Biotypes Identified by Diffusion Tensor Imaging

期刊

NEUROSCIENCE BULLETIN
卷 35, 期 5, 页码 867-876

出版社

SPRINGER
DOI: 10.1007/s12264-019-00381-w

关键词

Major depressive disorder; Hierarchal clustering; Diffusion tensor imaging; Biotype; Heterogeneity

资金

  1. National Natural Science Foundation of China [81630030, 81130024, 81801326, 81571320]
  2. National Natural Science Foundation of China/Research Grants Council of Hong Kong Joint Research Scheme [81461168029]
  3. National Basic Research Development Program of China [2016YFC0904300]
  4. 1.3.5 Project for Disciplines of Excellence, West China Hospital of Sichuan University
  5. National High-Technology Research and Development Project (863 Project) of China [2015AA020513]
  6. Scientific Project of Sichuan Science and Technology Department, China [2015JY0173]

向作者/读者索取更多资源

Identifying data-driven biotypes of major depressive disorder (MDD) has promise for the clarification of diagnostic heterogeneity. However, few studies have focused on white-matter abnormalities for MDD subtyping. This study included 116 patients with MDD and 118 demographically-matched healthy controls assessed by diffusion tensor imaging and neurocognitive evaluation. Hierarchical clustering was applied to the major fiber tracts, in conjunction with tract-based spatial statistics, to reveal white-matter alterations associated with MDD. Clinical and neurocognitive differences were compared between identified subgroups and healthy controls. With fractional anisotropy extracted from 20 fiber tracts, cluster analysis revealed 3 subgroups based on the patterns of abnormalities. Patients in each subgroup versus healthy controls showed a stepwise pattern of white-matter alterations as follows: subgroup 1 (25.9% of patient sample), widespread white-matter disruption; subgroup 2 (43.1% of patient sample), intermediate and more localized abnormalities in aspects of the corpus callosum and left cingulate; and subgroup 3 (31.0% of patient sample), possible mild alterations, but no statistically significant tract disruption after controlling for family-wise error. The neurocognitive impairment in each subgroup accompanied the white-matter alterations: subgroup 1, deficits in sustained attention and delayed memory; subgroup 2, dysfunction in delayed memory; and subgroup 3, no significant deficits. Three subtypes of white-matter abnormality exist in individuals with major depression, those having widespread abnormalities suffering more neurocognitive impairments, which may provide evidence for parsing the heterogeneity of the disorder and help optimize type-specific treatment approaches.

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