Myelin deficits in patients with recurrent major depressive disorder: An inhomogeneous magnetization transfer study
•qihMT can be used to investigate the alterations of myelin content in rMDD.•Convergent and divergent WM alterations could be found from qihMT and qMT.•Disruption of myelin integrity in fornix could be gradually cumulative. The recently developed myelin imaging method, inhomogeneous magnetization tr...
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Veröffentlicht in: | Neuroscience letters 2021-04, Vol.750, p.135768-135768, Article 135768 |
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Zusammenfassung: | •qihMT can be used to investigate the alterations of myelin content in rMDD.•Convergent and divergent WM alterations could be found from qihMT and qMT.•Disruption of myelin integrity in fornix could be gradually cumulative.
The recently developed myelin imaging method, inhomogeneous magnetization transfer (ihMT), is a surrogate measure of myelin content. The goal of the current study was to investigate alterations in myelin integrity in patients with recurrent major depressive disorder (rMDD).
Fifty-two patients with rMDD (36 female and 16 male) and 42 healthy controls (HC, 29 female and 13 male) were included. Two ihMT indices, quantitative ihMT (qihMT) and quantitative MT (qMT), were estimated from the ihMT data. A 50 white matter atlas was used to extract the regional quantitative values for each subject. The differences in qihMT and qMT values between the rMDD and HC groups were compared by a general linear model. Pearson correlation analyses were conducted to investigate associations between the significantly altered ihMT indices and clinical measures (Hamilton Depression Rating Scale scores and disease duration) in rMDD group.
The rMDD group showed significantly lower qihMT values in the fornix, left anterior limb of internal capsule, and left sagittal stratum, and lower qMT values in the fornix and left anterior limb of internal capsule than those of the HC group (p < 0.05, false discovery rate corrected). Both the qihMT and qMT values in the fornix of patients with rMDD were negatively correlated with disease duration (qihMT: r = -0.478, p < 0.001, Bonferroni corrected; qMT: r = -0.433, p = 0.001, Bonferroni corrected).
Our findings suggested that rMDD is associated with myelin impairment in the fornix, left anterior limb of internal capsule, and left sagittal stratum. In addition, this disruption of myelin integrity in the fornix could be cumulative as the disease progresses. |
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ISSN: | 0304-3940 1872-7972 |
DOI: | 10.1016/j.neulet.2021.135768 |