Dysregulation of inflammation, neurobiology, and cognitive function in PTSD: an integrative review

被引:64
作者
Quinones, Maria M. [1 ]
Gallegos, Autumn M. [2 ]
Lin, Feng Vankee [1 ,2 ,3 ]
Heffner, Kathi [1 ,2 ,4 ]
机构
[1] Univ Rochester, Med Ctr, Sch Nursing, Elaine C Hubbard Ctr Nursing Res Aging, Rochester, NY 14642 USA
[2] Univ Rochester, Med Ctr, Dept Psychiat, Rochester, NY 14642 USA
[3] Univ Rochester, Med Ctr, Dept Neurosci, Rochester, NY 14642 USA
[4] Univ Rochester, Med Ctr, Dept Med, Div Geriatr & Aging, Rochester, NY 14642 USA
关键词
Posttraumatic stress disorder; Inflammation; Neurobiology; Cognition; Intervention; POSTTRAUMATIC-STRESS-DISORDER; HEART-RATE-VARIABILITY; MEDIAL PREFRONTAL CORTEX; AUTOBIOGRAPHICAL MEMORY SPECIFICITY; RANDOMIZED CONTROLLED-TRIAL; FEAR EXTINCTION MEMORY; TRAUMATIC BRAIN-INJURY; HIPPOCAMPAL VOLUME; EMOTION REGULATION; MINDFULNESS MEDITATION;
D O I
10.3758/s13415-020-00782-9
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Compelling evidence from animal and human research suggest a strong link between inflammation and posttraumatic stress disorder (PTSD). Furthermore, recent findings support compromised neurocognitive function as a key feature of PTSD, particularly with deficits in attention and processing speed, executive function, and memory. These cognitive domains are supported by brain structures and neural pathways that are disrupted in PTSD and which are implicated in fear learning and extinction processes. The disruption of these supporting structures potentially results from their interaction with inflammation. Thus, the converging evidence supports a model of inflammatory dysregulation and cognitive dysfunction as combined mechanisms underpinning PTSD symptomatology. In this review, we summarize evidence of dysregulated inflammation in PTSD and further explore how the neurobiological underpinnings of PTSD, in the context of fear learning and extinction acquisition and recall, may interact with inflammation. We then present evidence for cognitive dysfunction in PTSD, highlighting findings from human work. Potential therapeutic approaches utilizing novel pharmacological and behavioral interventions that target inflammation and cognition also are discussed.
引用
收藏
页码:455 / 480
页数:26
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