Platelet monoamine oxidase activity in underweight and weight-recovered females with anorexia nervosa

Pharmacopsychiatry. 2008 Nov;41(6):226-31. doi: 10.1055/s-2008-1078749. Epub 2008 Dec 9.

Abstract

Introduction: Central serotonergic pathways may play an important role in the etiology of anorexia nervosa (AN). Although platelet monoamine oxidase activity (MAO-B) has been proposed as an index of cerebral serotonin activity, studies in patients with AN are scarce.

Methods: Platelet MAO-B activity was determined in 59 acutely underweight AN patients (acAN, aged 14-29 years, BMI=15.2+/-1.4), 35 weight-recovered AN patients (recAN, aged 15-29, BMI=20.8+/-2.2) and 59 healthy control women (HCW, aged 14-26, BMI=21.6+/-2.1). Plasma leptin served as an indicator of malnutrition. Results were compared by ANCOVA controlling for confounding variables.

Results: Platelet MAO-B activity in acAN patients (5.2+/-1.4 nmol/10 (9)pltx15 min) was similar to HCW (5.5+/-1.9) but significantly lower in recAN patients (4.4+/-1.5). BMI and leptin showed a significant negative correlation with MAO-B activity in AN patients, but not in HCW.

Discussion: Our results highlight the importance of malnutrition for the interpretation of abnormalities in neurotransmitter systems in AN. Whether low MAO-B activity in weight-recovered AN patients indicates a premorbid trait or a secondary change due to recovery remains to be elucidated.

MeSH terms

  • Adipocytes / drug effects
  • Adipocytes / metabolism
  • Adolescent
  • Adult
  • Anorexia Nervosa / enzymology*
  • Blood Platelets / enzymology*
  • Body Weight / physiology
  • Eating / physiology
  • Energy Metabolism / physiology
  • Female
  • Gonads / physiology
  • Humans
  • Hypothalamo-Hypophyseal System / physiology
  • Leptin / blood
  • Monoamine Oxidase / blood*
  • Nutritional Physiological Phenomena
  • Psychiatric Status Rating Scales
  • Serotonin / metabolism
  • Thinness / enzymology*
  • Thinness / etiology
  • Young Adult

Substances

  • Leptin
  • Serotonin
  • Monoamine Oxidase