Relationship of Brain-Derived Neurotrophic Factor with Interleukin-23, Testosterone and Disease Severity in Schizophrenia

被引:0
作者
Priya Allimuthu
Hanumanthappa Nandeesha
Raghavi Chinniyappan
Balaji Bhardwaz
Jesudas Blessed raj
机构
[1] Jawaharlal Institute of Postgraduate Medical Education and Research,Department of Biochemistry and Psychiatry
[2] Jawaharlal Institute of Postgraduate Medical Education and Research,Department of Psychiatry
来源
Indian Journal of Clinical Biochemistry | 2021年 / 36卷
关键词
Schizophrenia; Brain derived neurotrophic factor; Inflammation; Testosterone; Positive and Negative symptom score;
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摘要
Hormonal imbalance, inflammation and alteration in synaptic plasticity are reported to play a crucial role in the pathogenesis of schizophrenia. The objective of the study was to assess the serum levels of brain derived neurotrophic factor (BDNF) and its association with interleukin-23 (IL-23), testosterone and disease severity in schizophrenia. 40 cases and 40 controls were included in the study. Serum levels of BDNF, IL-23 and testosterone were estimated in all the subjects. Disease severity was assessed using Positive and Negative Syndrome Scale (PANSS). The study was designed in Tertiary care hospital, South India. The results were compared between two groups using Mann–Whitney U test. Spearman Correlation analysis was used to assess the association between biochemical parameters and PANSS. Interleukin-23 and testosterone were significantly increased and BDNF was significantly reduced in schizophrenia cases when compared with controls. BDNF was negatively correlated with IL-23 (r = − 400, p = 0.011), positive symptom subscale (r = − 0.393, p = 0.012), general psychopathology score subscale (r = − 407, p = 0.009) and total symptom subscale (r = − 404, p = 0.010). There was no significant association of IL-23 and testosterone with disease severity in schizophrenia cases. BDNF was reduced in schizophrenia cases and negatively associated with interleukin-23 and disease severity scores.
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页码:365 / 369
页数:4
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  • [1] MacDonald AW(2009)What we know: findings that every theory of schizophrenia should explain Schizophr Bull 35 493-508
  • [2] Schulz SC(2017)The role of genes, stress, and dopamine in the development of schizophrenia Biol Psychiatry 81 9-20
  • [3] Howes OD(2006)Regulation of innate and adaptive immune responses by the related cytokines IL-12, IL-23, and IL-27 Arch Immunol Ther Exp Warsz 54 15-24
  • [4] McCutcheon R(2008)Inducible IL-23p19 expression in human microglia via p38 MAPK and NFkappaB signal pathways Exp Mol Pathol 84 1-8
  • [5] Owen MJ(2012)Interleukin-23: as a drug target for autoimmune inflammatory diseases Immunology 135 112-124
  • [6] Murray RM(2015)IL-23 and TGF-β1 levels as potential predictive biomarkers in treatment of bipolar I disorder with acute manic episode J Affect Disord 174 361-366
  • [7] Beadling C(2015)Increased interleukin 23 (IL23) levels in schizophrenia patients treated with depot antipsychotic medication Cytokine 73 196-198
  • [8] Slifka MK(2004)Neuroprotective role of testosterone in the nervous system Pol J Pharmacol 56 509-518
  • [9] Li Y(2016)Low testosterone level and risk of Alzheimer’s disease in the elderly men: a systematic review and meta-analysis Mol Neurobiol 53 2679-2684
  • [10] Chu N(2015)Effects of hormones on cognition in schizophrenic male patients—preliminary results Psychiatr Danub 27 S261-S265