Increased peripheral inflammation in schizophrenia is associated with worse cognitive performance and related cortical thickness reductions

被引:60
作者
North, Hayley F. [1 ,2 ]
Bruggemann, Jason [1 ,2 ]
Cropley, Vanessa [3 ,4 ]
Swaminathan, Vaidy [5 ,6 ]
Sundram, Suresh [5 ,6 ,7 ,8 ]
Lenroot, Rhoshel [1 ,2 ,9 ]
Pereira, Avril M. [3 ,4 ,8 ]
Zalesky, Andrew [3 ,4 ]
Bousman, Chad [3 ,4 ,10 ]
Pantelis, Christos [3 ,4 ]
Weickert, Thomas W. [1 ,2 ,11 ]
Shannon Weickert, Cynthia [1 ,2 ,11 ]
机构
[1] Univ New South Wales, Sch Psychiat, Sydney, NSW, Australia
[2] Neurosci Res Australia, Sydney, NSW, Australia
[3] Univ Melbourne, Dept Psychiat, Melbourne Neuropsychiat Ctr, Parkville, Vic, Australia
[4] Melbourne Hlth, Parkville, Vic, Australia
[5] Monash Univ, Sch Clin Sci, Dept Psychiat, Clayton, Vic, Australia
[6] Monash Hlth, Mental Hlth Program, Clayton, Vic, Australia
[7] Melbourne Hlth, North Western Mental Hlth, Northern Psychiat Res Ctr, Melbourne, Vic, Australia
[8] Florey Inst Neurosci & Mental Hlth, Mol Psychopharmacol Lab, Parkville, Vic, Australia
[9] Univ New Mexico, Sch Med, Dept Psychiat & Behav Sci, Albuquerque, NM 87131 USA
[10] Univ Calgary, Dept Med Genet Psychiat & Physiol & Pharmacol, Calgary, AB, Canada
[11] SUNY Upstate Med Univ, Dept Neurosci & Physiol, Syracuse, NY 13210 USA
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
CRP; Immune system; RBANS; Biomarker; Neuropathology; MRI; C-REACTIVE PROTEIN; HUMAN CEREBRAL-CORTEX; BIPOLAR DISORDER; 1ST-EPISODE PSYCHOSIS; SYSTEMIC INFLAMMATION; CYTOKINE ALTERATIONS; PREFRONTAL CORTEX; IMMUNE ACTIVATION; IMPAIRS ATTENTION; MAJOR DEPRESSION;
D O I
10.1007/s00406-021-01237-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
While the biological substrates of brain and behavioural changes in persons with schizophrenia remain unclear, increasing evidence implicates that inflammation is involved. In schizophrenia, including first-episode psychosis and anti-psychotic naive patients, there are numerous reports of increased peripheral inflammation, cognitive deficits and neuropathologies such as cortical thinning. Research defining the relationship between inflammation and schizophrenia symptomatology and neuropathology is needed. Therefore, we analysed the level of C-reactive protein (CRP), a peripheral inflammation marker, and its relationship with cognitive functioning in a cohort of 644 controls and 499 schizophrenia patients. In a subset of individuals who underwent MRI scanning (99 controls and 194 schizophrenia cases), we tested if serum CRP was associated with cortical thickness. CRP was significantly increased in schizophrenia patients compared to controls, co-varying for age, sex, overweight/obesity and diabetes (p < 0.006E-10). In schizophrenia, increased CRP was mildly associated with worse performance in attention, controlling for age, sex and education (R =- 0.15, p = 0.001). Further, increased CRP was associated with reduced cortical thickness in three regions related to attention: the caudal middle frontal, the pars opercularis and the posterior cingulate cortices, which remained significant after controlling for multiple comparisons (all p < 0.05). Together, these findings indicate that increased peripheral inflammation is associated with deficits in cognitive function and brain structure in schizophrenia, especially reduced attention and reduced cortical thickness in associated brain regions. Using CRP as a biomarker of peripheral inflammation in persons with schizophrenia may help to identify vulnerable patients and those that may benefit from adjunctive anti-inflammatory treatments.
引用
收藏
页码:595 / 607
页数:13
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