4.7 Article

Altered structural covariance network of nucleus accumbens is modulated by illness duration and severity of symptom in depression

期刊

JOURNAL OF AFFECTIVE DISORDERS
卷 324, 期 -, 页码 334-340

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ELSEVIER
DOI: 10.1016/j.jad.2022.12.159

关键词

Depression; Structural covariance; Nucleus accumbens

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This study aimed to investigate the altered structural covariance of nucleus accumbens (NAcc) in never-treated first-episode patients with depression and how it was modulated by illness duration and severity of symptom. The results revealed that patients with depression exhibited abnormal structural covariance of NAcc connected to key brain regions in the reward system, and this abnormality was distinctly modulated by illness duration and the severity of symptom.
The differential structural covariance of nucleus accumbens (NAcc), playing a vital role in etiology and treat-ment, remains unclear in depression. We aimed to investigate whether structural covariance of NAcc was altered and how it was modulated by illness duration and severity of symptom measured with Hamilton Depression scale (HAMD). T1-weighted anatomical images of never-treated first-episode patients with depression (n = 195) and matched healthy controls (HCs, n = 78) were acquired. Gray matter volumes were calculated using voxel-based morphometry analysis for each subject. Then, we explored abnormal structural covariance of NAcc and how the abnormality was modulated by illness duration and severity of symptom. Patients with depression exhibited altered structural covariance of NAcc connected to key brain regions in reward system including the medial orbitofrontal cortex, amygdala, insula, parahippocampa gyrus, precuneus, thalamus, hippocampus and cere-bellum. In addition, the structural covariance of the NAcc was distinctly modulated by illness duration and the severity of symptom in patients with depression. What is more, the structural covariance of the NAcc connected to hippocampus was modulated by these two factors at the same time. These results elucidate altered structural covariance of the NAcc and its distinct modulation of illness duration and severity of symptom.

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