Peterson Carly K, James Lisa M, Anders Samantha L, Engdahl Brian E, Georgopoulos Apostolos P
From the Brain Sciences Center, Minneapolis Veterans Affairs Medical Center, Minneapolis, MN.
J Neuropsychiatry Clin Neurosci. 2015;27(2):157-61. doi: 10.1176/appi.neuropsych.13090205. Epub 2015 Mar 9.
Apolipoprotien E (ApoE) is involved in critical neural functions and is associated with various neuropsychiatric disorders. ApoE exists in three isoforms that differ in the number of cysteine residues per mole (CysR/mole). This study evaluated associations between this informative ordinal biochemical scale (CysR/mole) and symptom severity in veterans with posttraumatic stress disorder (PTSD) or subthreshold PTSD. Results demonstrated a significant negative relationship between the CysR/mole and severity of PTSD re-experiencing symptoms, adjusted for trauma. The findings suggest a genetic influence on PTSD symptomatology and dovetail with recent advances regarding the molecular mechanisms underlying the differential effects of ApoE in the brain.
载脂蛋白E(ApoE)参与关键的神经功能,并与多种神经精神疾病相关。ApoE存在三种异构体,它们每摩尔的半胱氨酸残基数量(每摩尔半胱氨酸残基数量,CysR/mole)不同。本研究评估了这种具有信息性的有序生化指标(CysR/mole)与创伤后应激障碍(PTSD)或亚阈值PTSD退伍军人症状严重程度之间的关联。结果表明,在对创伤进行校正后,CysR/mole与PTSD重新体验症状的严重程度之间存在显著负相关。这些发现表明基因对PTSD症状学有影响,并且与最近关于ApoE在大脑中产生不同作用的分子机制的进展相吻合。