Newcomer J W, Craft S, Askins K, Hershey T, Bardgett M E, Csernansky J G, Gagliardi A E, Vogler G
Department of Psychiatry, Washington University School of Medicine, St. Louis, MO 63110, USA.
Psychoneuroendocrinology. 1998 Jan;23(1):65-72. doi: 10.1016/s0306-4530(97)00081-4.
Glucocorticoid (GC) exposure can affect brain function, including potential adverse effects on hippocampal physiology and on specific elements of cognitive performance. In a prior study of healthy adult humans, decreased verbal memory performance was detected during four days of double-blind, placebo-controlled dexamethasone (DEX) treatment. Using an identical experimental design and sample size (n = 19), the cognitive effect of DEX treatment was studied in 11 subjects with schizophrenia, compared with 8 receiving placebo. In contrast to the effect in healthy adults, GC treatment with DEX at this dose (cumulative 3.5 mg) and duration did not decrease verbal memory performance or other measures of cognitive function in the patients with schizophrenia. When data from this experiment was compared with data from the previous study of healthy adults, covarying differences in baseline memory performance, a significant 3-way interaction was detected between subject group, treatment condition, and the repeated measurements of verbal memory performance across baseline, treatment and washout (F[3,87] = 4.84, p = .0066), suggesting differential cognitive effects of DEX in the patients versus the previously studied healthy subjects. Baseline plasma cortisol concentrations (0800 h) prior to DEX treatment were inversely correlated with baseline delayed (rs = -0.536, p = .03) verbal recall performance, supporting a previous report. The current results await replication using a larger sample size but provide preliminary evidence for an altered behavioral response to acute GC exposure in schizophrenic versus healthy subjects, and further evidence for a relationship between chronic changes in circulating cortisol and the memory impairments found in this disorder.
糖皮质激素(GC)暴露会影响脑功能,包括对海马生理以及认知表现的特定要素产生潜在的不利影响。在一项针对健康成年人的前期研究中,在为期四天的双盲、安慰剂对照的地塞米松(DEX)治疗期间,发现言语记忆表现有所下降。采用相同的实验设计和样本量(n = 19),对11名精神分裂症患者进行了DEX治疗的认知效果研究,并与8名接受安慰剂治疗的患者进行了比较。与健康成年人中的效果相反,以该剂量(累积3.5毫克)和疗程进行的DEX糖皮质激素治疗并未降低精神分裂症患者的言语记忆表现或其他认知功能指标。当将该实验的数据与先前针对健康成年人的研究数据进行比较时,考虑到基线记忆表现的协变差异,在受试者组、治疗条件以及跨基线、治疗和洗脱期的言语记忆表现重复测量之间检测到显著的三因素交互作用(F[3,87] = 4.84,p = .0066),这表明DEX对患者的认知影响与先前研究的健康受试者不同。DEX治疗前的基线血浆皮质醇浓度(0800时)与基线延迟言语回忆表现呈负相关(rs = -0.536,p = .03),支持了先前的一项报告。目前的结果有待使用更大的样本量进行重复验证,但为精神分裂症患者与健康受试者对急性GC暴露的行为反应改变提供了初步证据,并进一步证明了循环皮质醇的慢性变化与该疾病中发现的记忆损害之间的关系。