Jean-Marie Batail, Isabelle Corouge, Tristan Blanchard, Jean-Charles Roy, Gabriel Robert, Dominique Drapier
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引用次数: 0
Abstract
Systemic inflammation has been linked with major depressive episode (MDE) severity and treatment-resistant depression (TRD), but not for all patients. Brain mechanisms underlying these processes are still under investigation. Objectives: based on an integrative approach, we aimed at identifying clinical, inflammatory and perfusion markers predictive of depression outcome at 6 months. We conducted a longitudinal study including 60 patients diagnosed with MDE, focusing on anxiety and anhedonia as main clinical candidates, inflammation (C-Reactive Protein - CRP) and cerebral blood flow (CBF) using pseudo-continuous arterial spin labeling (pcASL) MRI. A bootstrapped elastic net regression analysis was conducted including clinical, CBF and inflammation as predictors with depressive severity at 6 months as the dependent variable. Our findings exhibited positive association of depression outcome with baseline depression intensity, duration of current episode, CRP, right accumbens, as well as left and right orbito-frontal CBF. Negative predictors were age, disease duration, right and left caudate nuclei, left amygdala, left mid frontal gyrus, and right ventromedial prefrontal cortex CBF. Neither anxiety nor anhedonia were significant predictors. Combining clinical, inflammation and brain imaging outperformed other models in diagnosing depression severity change over time, highlighting the interest of integrative approaches. These results suggested that systemic inflammation and cerebral perfusion abnormalities in key regions involved in emotion, reward processing and decision making, may serve as biomarkers for identifying patients at risk for persistence of depression.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.