2016
DOI: 10.1016/j.biopsych.2014.11.024
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Elevated Monoamine Oxidase-A Distribution Volume in Borderline Personality Disorder Is Associated With Severity Across Mood Symptoms, Suicidality, and Cognition

Abstract: These results suggest that elevated MAO-A VT is associated with multiple indicators of BPD severity, including BPD symptomatology, mood symptoms, suicidality, and neurocognitive impairment.

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Cited by 35 publications
(23 citation statements)
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“…Although sources of oxidative stress outside the brain cannot be ruled out, brain metabolism accounts for 20% of the body's oxygen (O 2 ) budget, out of proportion to its mass. This is because the principal sources of oxidative species are neural activity itself (Halliwell, 1992), intracellular energy cycling (Cobley, Fiorello, & Bailey, 2018), nitrosamine signaling between neurons (Finnell & Wood, 2018), and catabolism of monoamine neuromodulators such as serotonin and norepinephrine by the mitochondrial enzyme monoamine oxidase A (MAO-A; Kolla et al, 2016). Increased neural signaling during periods of psychological stress would thus be expected to increase the oxidation burden.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Although sources of oxidative stress outside the brain cannot be ruled out, brain metabolism accounts for 20% of the body's oxygen (O 2 ) budget, out of proportion to its mass. This is because the principal sources of oxidative species are neural activity itself (Halliwell, 1992), intracellular energy cycling (Cobley, Fiorello, & Bailey, 2018), nitrosamine signaling between neurons (Finnell & Wood, 2018), and catabolism of monoamine neuromodulators such as serotonin and norepinephrine by the mitochondrial enzyme monoamine oxidase A (MAO-A; Kolla et al, 2016). Increased neural signaling during periods of psychological stress would thus be expected to increase the oxidation burden.…”
Section: Discussionmentioning
confidence: 99%
“…Increased neural signaling during periods of psychological stress would thus be expected to increase the oxidation burden. Interestingly, elevated MAO-A activity is increased in the prefrontal cortex of individuals with BPD (Kolla et al, 2016). Upregulation of MAO-A activity would be expected to generate oxidative species through the oxidation of monoamine neurotransmitters and could increase circulating 8-OH-DG levels.…”
Section: Discussionmentioning
confidence: 99%
“…To address this issue and increase the robustness of the analyses, BPD and ASPD subjects were combined into a single group. Although ASPD and BPD have been conceptualized as different aspects of the same disorder manifested in a gender‐specific manner , it is now widely accepted that the two conditions are separate disorders , with growing research to suggest that ASPD and BPD have distinct neurobiological underpinnings . While externalized aggression is a DSM‐5 diagnostic criterion for both disorders and several laboratories investigating aggression include mixed samples of ASPD and BPD subjects , it is likely that there are subtle differences in the personality characteristics of ASPD and BPD underlying high trait physical aggression.…”
Section: Discussionmentioning
confidence: 99%
“…A few studies that investigated neurotransmitter systems other than 5-HT implicated the ACC in relation to SI. For example, a positive association was shown between SI and ACC monoamine oxidase-A density in adults with BPD [88]. A relation between SI and increased ACC neuroinflammation (as assessed by translocator protein (TSPO) availability) was reported in adults with MDD [89].…”
Section: Anterior Cingulate Cortexmentioning
confidence: 98%