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Decreased Plasma Levels of Growth Differentiation Factor 11 in Patients With Schizophrenia

Correlation With Psychopathology and Cognition

Bibliographic Data

ID15528176
AuthorsYang Zhao-xi (First Affiliated Hospital of Nanchang University), Zhao-xi Yang, Jin‐Qiong Zhan (Nanchang University), Jin-qiong Zhan, Jian Xiong (0000-0003-3820-8432, Nanchang University), Jian-wen Xiong, Bo Wei (0000-0002-1058-5888, Nanchang University), Yonghui Fu (Jiangxi Mental Health Center), Yong-hui Fu, Zhipeng Liu (0009-0005-7854-9284, Jiangxi Mental Health Center), Zhi-Peng Liu (0000-0001-7652-1783), Yating Tu (Jiangxi Mental Health Center), Ya-ting Tu, Yuan-Jian Yang (0000-0002-0175-5646, Jiangxi Mental Health Center, corresponding author), Ai-lan Wan (First Affiliated Hospital of Nanchang University, corresponding author)
Year2020
Volume11
Pages555133-555133
Publication date2020-12-07
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2020.555133
PMID33364986
OpenAlexW3112965873
LanguageEN
References cited43

Schizophrenia is linked with abnormal neurodevelopment, on which growth differentiation factor 11 (GDF-11) has a great impact. However, a direct evidence linking GDF-11 to the pathophysiology of schizophrenia is still lacking. The current study aimed to investigate the relationship between plasma GDF-11 levels and both psychopathological symptoms and cognitive function in schizophrenia. Eighty-seven schizophrenia patients and 76 healthy controls were enrolled in the present study. The symptomatology of schizophrenia was evaluated using the Positive and Negative Syndrome Scale (PANSS). Cognitive function was assessed by Repeatable Battery for the Assessment of Neuropsychological Status (RBANS) including twelve neurocognitive tests in five aspects of cognitive function. Plasma GDF-11 levels were determined by enzyme-linked immunosorbent assay (ELISA). We found that plasma levels of GDF-11 were significantly lower in schizophrenia patients relative to healthy controls. Correlation analysis showed significant negative correlations between the GDF-11 levels and the PANSS total score, the positive symptoms score, the negative symptoms score or the general score. Additionally, positive associations were observed between plasma GDF-11 levels and the visuospatial/constructional, attention, immediate memory, or delayed memory in patients. Partial correlation analysis showed that these correlations were still significant after adjusting for age, gender, education years, body mass index, duration of illness, and age of onset except for the visuospatial/constructional and attention index. Multiple regression analysis revealed that GDF-11 was an independent contributor to the immediate memory, delayed memory and RBANS total score in patients. Collectively, the correlations between plasma GDF-11 and psychopathological and cognitive symptoms suggest that abnormal GDF-11 signaling might contribute to schizophrenic psychopathology and cognitive impairments and GDF-11 could be a potential and promising biomarker for schizophrenia

Cognition · Correlation · Neurocognitive · Neuropsychology · Positive and Negative Syndrome Scale · Psychiatry · Psychopathology · Psychosis · Repeatable Battery for the Assessment of Neuropsychological Status · Schizophrenia (object-oriented programming · Clinical Psychology · Diet and metabolism studies · GDF15 and Related Biomarkers · Genetic Syndromes and Imprinting · Medicine · Psychology · Internal Medicine

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Highly citedNo

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