Department of Psychiatry, University of Naples SUN, Naples, Italy.
Psychol Med. 2011 Apr;41(4):839-48. doi: 10.1017/S0033291710001303. Epub 2010 Jul 1.
Studies investigating neurocognitive impairment in subjects with eating disorders (EDs) have reported heterogeneous patterns of impairment and, in some instances, no dysfunction. The present study aimed to define the pattern of neurocognitive impairment in a large sample of bulimia nervosa (BN) patients and to demonstrate that neuroendocrine, personality and clinical characteristics influence neurocognitive performance in BN.
Attention/immediate memory, set shifting, perseveration, conditional and implicit learning were evaluated in 83 untreated female patients with BN and 77 healthy controls (HC). Cortisol and 17β-estradiol plasma levels were assessed. Cloninger's Temperament and Character Inventory - Revised (TCI-R), the Bulimic Investigation Test Edinburgh (BITE) and the Montgomery-Asberg Depression Rating Scale (MADRS) were administered.
No impairment of cognitive performance was found in subjects with BN compared with HC. Cortisol and 'Self-directedness' were associated with better performance on conditional learning whereas 17β-estradiol had a negative influence on this domain; 'Reward dependence' was associated with worse performance on implicit learning; and depressive symptomatology influenced performance on the Wisconsin Card Sorting Test (WCST) negatively.
No cognitive impairment was found in untreated patients with BN. Neuroendocrine, personality and clinical variables do influence neurocognitive functioning and might explain discrepancies in literature findings.
研究表明,患有饮食失调症(EDs)的个体存在神经认知功能障碍,且在某些情况下无功能障碍。本研究旨在确定大量神经性贪食症(BN)患者的神经认知障碍模式,并证明神经内分泌、人格和临床特征会影响 BN 的神经认知表现。
对 83 名未经治疗的女性 BN 患者和 77 名健康对照者(HC)进行注意力/即时记忆、转换能力、持续注意、条件和内隐学习评估。检测皮质醇和 17β-雌二醇的血浆水平。采用 Cloninger 的气质与性格量表修订版(TCI-R)、爱丁堡 BN 调查测试(BITE)和蒙哥马利-阿斯伯格抑郁评定量表(MADRS)进行评估。
与 HC 相比,BN 患者的认知表现未受损。皮质醇和“自我导向”与条件学习的表现呈正相关,而 17β-雌二醇对这一领域有负面影响;“奖励依赖”与内隐学习的表现较差相关;抑郁症状与威斯康星卡片分类测试(WCST)的表现呈负相关。
未经治疗的 BN 患者未发现认知障碍。神经内分泌、人格和临床变量会影响神经认知功能,并可能解释文献结果的差异。