Publications by authors named "L Coulbault"

Background: Subclinical depressive symptoms increase the risk of developing Alzheimer's disease (AD). The neurobiological mechanisms underlying this link may involve stress system dysfunction, notably related to the hippocampus which is particularly sensitive to AD. We aimed to investigate the links between blood stress markers and changes in brain regions involved in the stress response in older adults with or without subclinical depressive symptoms.

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Alcohol use is a leading cause of mortality, brain morbidity, neurological complications and minor to major neurocognitive disorders. Alcohol-related neurocognitive disorders are consecutive to the direct effect of chronic and excessive alcohol use, but not only. Indeed, patients with severe alcohol use disorders (AUD) associated with pharmacological dependence suffer from repetitive events of alcohol withdrawal (AW).

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  • TMAO and indoxyl sulfate (IS) are linked to brain aging and cognitive issues, and this study investigates their levels in patients with alcohol-use disorder (AUD) versus healthy controls.
  • In a comparison of 30 AUD patients to 15 healthy individuals, TMAO levels were similar, but significant differences in nutritional and liver function biomarkers were found among AUD patients with lower TMAO.
  • IS levels were notably lower in AUD patients and positively correlated with serum prealbumin changes, indicating potential benefits from personalized nutrition during alcohol withdrawal, despite no links to AUD severity or cognitive impairments.
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Brain abnormalities observed in alcohol use disorder are highly heterogeneous in nature and severity, possibly because chronic alcohol consumption also affects peripheral organs leading to comorbidities that can result in exacerbated brain alterations. Despite numerous studies focussing on the effects of alcohol on the brain or liver, few studies have simultaneously examined liver function and brain damage in alcohol use disorder, and even fewer investigated the relationship between them except in hepatic encephalopathy. And yet, liver dysfunction may be a risk factor for the development of alcohol-related neuropsychological deficits and brain damage well before the development of liver cirrhosis, and potentially through inflammatory responses.

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  • Left ventricular remodelling after a heart attack increases the risk of heart failure and death, and while various risk factors exist, no clinical markers can currently predict it.
  • This study aimed to see if the level of coenzyme Q10 in plasma at the time of a ST-elevation myocardial infarction (STEMI) could help predict left ventricular remodelling after six months.
  • Results showed no significant relationship between coenzyme Q10 levels and left ventricular remodelling, indicating it may not be a useful early prediction marker for this condition.
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