Section of Eating Disorders, Institute of Psychiatry, King's College London, UK.
Ann Gen Psychiatry. 2010 Jun 25;9:29. doi: 10.1186/1744-859X-9-29.
Set-shifting is impaired in people with anorexia nervosa (AN), but the underlying physiological and biochemical processes are unclear. Animal studies have established that glutamatergic pathways in the prefrontal cortex play an important role in set-shifting ability. However, it is not yet understood whether levels of serum glutamatergic amino acids are associated with set-shifting performance in humans. The aim of this study was to determine whether serum concentrations of amino acids related to glutamatergic neurotransmission (glutamine, glutamate, glycine, l-serine, d-serine) are associated with set-shifting ability in people with acute AN and those after recovery.
Serum concentrations of glutamatergic amino acids were measured in 27 women with current AN (AN group), 18 women recovered from AN (ANRec group) and 28 age-matched healthy controls (HC group). Set-shifting was measured using the Wisconsin Card Sorting Test (WCST) and the Trail Making Task (TMT). Dimensional measures of psychopathology were used, including the Eating Disorder Examination Questionnaire (EDEQ), the Maudsley Obsessive-Compulsive Inventory (MOCI) and the Hospital Anxiety and Depression Scale (HADS).
Serum glutamine concentrations in the AN group (1,310.2 +/- 265.6 muM, mean +/- SD) were significantly higher (by approximately 20%) than those in the HC group (1,102.9 +/- 152.7 muM, mean +/- SD) (F(2, 70) = 6.3, P = 0.003, 95% CI 61.2 to 353.4). Concentrations of serum glutamine were positively associated with markers of the illness severity: a negative correlation was present between serum glutamine concentrations and body mass index (BMI) and lowest BMI and a positive correlation was found between duration of illness and EDEQ. The AN group showed significantly impaired set shifting in the WCST, both total errors, and perseverative errors. In the AN group, there were no correlations between serum glutamine concentrations and set shifting.
Serum concentrations of glutamine may be a biomarker of illness severity in people with AN. It does not appear to be directly associated with changes in executive function.
在神经性厌食症(AN)患者中,转换能力受损,但潜在的生理和生化过程尚不清楚。动物研究已经确定,前额叶皮层中的谷氨酸能途径在转换能力中起重要作用。然而,目前尚不清楚血清谷氨酸能氨基酸的水平是否与人类的转换表现相关。本研究旨在确定急性 AN 患者和恢复期 AN 患者的血清中与谷氨酸能神经传递有关的氨基酸(谷氨酰胺、谷氨酸、甘氨酸、l-丝氨酸、d-丝氨酸)浓度是否与转换能力相关。
测定 27 名当前患有 AN 的女性(AN 组)、18 名从 AN 中康复的女性(ANRec 组)和 28 名年龄匹配的健康对照者(HC 组)的血清谷氨酸能氨基酸浓度。使用威斯康星卡片分类测试(WCST)和 Trail Making Test(TMT)测量转换能力。使用多维精神病理学测量,包括饮食障碍检查问卷(EDEQ)、Maudsley 强迫量表(MOCI)和医院焦虑抑郁量表(HADS)。
AN 组血清谷氨酰胺浓度(1,310.2 +/- 265.6 muM,均值 +/- SD)明显高于 HC 组(1,102.9 +/- 152.7 muM,均值 +/- SD)(F(2, 70)= 6.3,P = 0.003,95%置信区间 61.2 至 353.4)。血清谷氨酰胺浓度与疾病严重程度的标志物呈正相关:血清谷氨酰胺浓度与体重指数(BMI)和最低 BMI 呈负相关,与疾病持续时间与 EDEQ 呈正相关。AN 组在 WCST 中的总错误和持续错误方面表现出明显的转换能力受损。在 AN 组中,血清谷氨酰胺浓度与转换能力之间无相关性。
血清谷氨酰胺浓度可能是 AN 患者疾病严重程度的生物标志物。它似乎与执行功能的变化没有直接关系。