Association of baseline inflammatory markers and the development of negative symptoms in individuals at clinical high risk for psychosis

被引:54
作者
Goldsmith, David R. [1 ]
Haroon, Ebrahim [1 ]
Miller, Andrew H. [1 ]
Addington, Jean [2 ]
Bearden, Carrie [3 ,4 ]
Cadenhead, Kristin [5 ]
Cannon, Tyrone [6 ]
Cornblatt, Barbara [7 ]
Mathalon, Daniel [8 ]
McGlashan, Thomas [6 ]
Seidman, Larry [9 ]
Tsuang, Ming [5 ]
Woods, Scott W. [6 ]
Walker, Elaine F. [10 ]
Perkins, Diana O. [11 ]
机构
[1] Emory Univ, Sch Med, Dept Psychiat & Behav Sci, 10 Pk Pl South SE, Atlanta, GA 30303 USA
[2] Univ Calgary, Dept Psychiat, Calgary, AB, Canada
[3] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Los Angeles, CA USA
[4] Univ Calif Los Angeles, Dept Psychol, Los Angeles, CA USA
[5] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92103 USA
[6] Yale Univ, Dept Psychiat, New Haven, CT 06520 USA
[7] Zucker Hillside Hosp, Dept Psychiat, Long Isl City, NY USA
[8] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USA
[9] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Psychiat, Boston, MA USA
[10] Emory Univ, Dept Psychol, Atlanta, GA 30322 USA
[11] Univ N Carolina, Dept Psychiat, Chapel Hill, NC 27515 USA
基金
美国国家卫生研究院;
关键词
Clinical high risk; Negative symptoms; Inflammation; Cytokines; Schizophrenia; Psychosis; ULTRA-HIGH RISK; 1ST EPISODE PSYCHOSIS; INTERRATER RELIABILITY; CYTOKINE ALTERATIONS; PRODROMAL SYNDROMES; SERUM-LEVELS; SCHIZOPHRENIA; 1ST-EPISODE; DEPRESSION; STATE;
D O I
10.1016/j.bbi.2018.11.315
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Negative symptoms are common in individuals at clinical high-risk (CHR) for psychosis and are associated with worse functional outcomes. Inflammation may be one mechanism underlying negative symptoms. Inflammatory markers are altered in individuals at CHR and are associated with negative symptoms in patients with schizophrenia. We thus hypothesized that baseline inflammatory markers would predict the development of negative symptoms in individuals at CHR for psychosis. Thirty seven individuals from the North American Prodromal Longitudinal Study who met CHR criteria were included in the study. Inflammatory cytokines, including interferon (IFN)-X., Interleukin (IL)-1 beta, IL-1 receptor antagonist (IL-1RA), IL-4, IL-6, IL-8, IL-10, and tumor necrosis factor (TNF) were measured at baseline. Negative symptoms as measured by the Scale of Prodromal Symptoms, were measured at baseline and six and twelve months. Associations-between inflammatory markers arid- the trajectory of negative symptoms (slope) over the first year of follow-up, were assessed using linear regression models controlling for age, sex, race and depressive symptom severity (as assessed by the Calgary Depression Scale for Schizophrenia). Baseline TNF (beta = 0.361, p = 0.007) and IL-6 (beta = -0.306, p = 0.026) predicted negative symptoms slopes, along with depressive symptom severity at baseline (beta = -0.596, p = 0.000). These findings demonstrate that inflammatory cytokines may underlie the development of negative symptoms in some individuals at CHR for psychosis. TNF predicted the development of negative symptoms independent of baseline depression. Given the heterogeneity of the CHR population, the comorbidity of negative symptoms and depression in this population, and the particular challenges in treating negative symptoms, immune markers could represent potential biomarkers that underlie the development of negative symptoms, representing a potential treatment target.
引用
收藏
页码:268 / 274
页数:7
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