Clinical Psychopharmacology and Neuroscience 2017; 15(3): 269-275  https://doi.org/10.9758/cpn.2017.15.3.269
Plasma Levels of Tumor Necrosis Factor Superfamily Molecules Are Increased in Bipolar Disorder
Izabela G. Barbosa1, Gabriela Neves Vaz1, Natalia Pessoa Rocha1,2, Rodrigo Machado-Vieira3, Marcio Rogerio Diniz Ventura1, Rodrigo B. Huguet1, Moises E. Bauer4, Michael Berk5,6, and Antônio L. Teixeira1,2
1Laboratório Interdisciplinar de Investigação Médica, Faculdade de Medicina, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Brazil, 2Neuropsychiatry Program, Department of Psychiatry and Behavioral Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA, 3Experimental Therapeutics and Pathophysiology Branch, National Institute of Mental Health, Bethesda, MD, USA, 4Laboratório de Imunologia do Envelhecimento, Instituto de Pesquisas Biomédicas, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Brazil, 5Deakin University, IMPACT Strategic Research Centre, School of Medicine, Geelong, Australia, 6Orygen, The National Centre of Excellence in Youth Mental Health, Department of Psychiatry and The Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Parkville, Australia
Correspondence to: Izabela G. Barbosa, MD, PhD, Antonio L. Teixeira, MD, PhD, Laboratório Interdisciplinar de Investigação Médica. Faculdade de Medicina, UFMG. Av. Alfredo Balena, 190, room 281, Santa Efigênia, Belo Horizonte 30130-100, Brazil, Tel: +55-31-3409-8073, E-mail: izabelagb@gmail.com (Izabela G. Barbosa), altexr@gmail.com (Antonio L. Teixeira)
Received: November 2, 2016; Revised: January 14, 2017; Accepted: April 9, 2017; Published online: August 31, 2017.
© The Korean College of Neuropsychopharmacology. All rights reserved.

This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract

Objective

Patients with bipolar disorder (BD) exhibit peripheral low-grade inflammation. The aim of the current study was to investigate the involvement of hitherto unexplored components of the tumor necrosis factor (TNF) superfamily in BD.

Methods

Eighty patients with type I BD and 50 healthy controls matched for age and gender were enrolled in this study. All subjects were assessed with the Mini-Plus to evaluate psychiatric comorbidities; the Young Mania Rating Scale and the Hamilton Depression Rating Scale to evaluate manic and depressive symptoms severity, respectively. TNF superfamily molecules (TNF, TNF-related weak inducer of apoptosis [TWEAK], TNF-related apoptosis-inducing ligand [TRAIL], soluble TNF receptor type 1 [sTNFR1], and soluble TNF receptor type 2 [sTNFR2]) levels were measured by ELISA.

Results

Patients with BD, regardless of mood state, presented increased plasma levels of sTNFR1 and TWEAK in comparison with controls.

Conclusion

These findings corroborate the view that TNF superfamily may play a role in BD pathophysiology.

Keywords: Bipolar disorder, TNF-α, TWEAK, TRAIL, sTNFR
INTRODUCTION

There is mounting evidence indicating that patients with bipolar disorder (BD) present peripheral low-grade inflammation. In this regard, one of the most consistently reported findings is tumor necrosis factor (TNF)-α activation represented by increased circulating levels of soluble TNF receptor type 1 (sTNFR1).14) TNF-α dysregulation was also evidenced in the central nervous system (CNS) of patients with BD. A postmortem study found increased levels of transmembrane TNF-α in the anterior cingulate area and decreased levels of TNF-α receptor 2 mRNA in the dorsolateral prefrontal cortex,5) regions implicated in executive functioning.6) Interestingly, we have previously shown that impairment in executive functioning was associated with increased plasma levels of TNF-α and decreased plasma levels of soluble TNF receptor type 2 (sTNFR2) in patients with BD.7)

TNF-α is a cytokine that plays a key role in inflammatory responses. TNF-α acts by regulating the activity of immune cells and promoting the secretion of pro-inflammatory cytokines. The TNF superfamily includes several receptors and ligands (most of them in a soluble form) that regulate immune responses and apoptosis. Two specific receptors, TNFR1 (p55) and TNFR2 (p75), bind to TNF-α with high affinity, being responsible for translating into intracellular pathways TNF-α signaling. The TNFR1 and TNFR2 transmembrane receptors can be cleaved, and the extracellular domains can be released in the form of soluble receptors: sTNFR1 and sTNFR2, respectively. Blood levels of these two receptors can vary during inflammatory responses. As mentioned above, higher circulating levels of sTNFR1 were reported in patients with BD, especially in mania, in comparison with controls.1,8)

Other components of the TNF superfamily include the TNF-related weak inducer of apoptosis (TWEAK) and the TNF-related apoptosis-inducing ligand (TRAIL). TWEAK attenuates the transition from innate to adaptive T helper 1 immune response, repressing pro-inflammatory cytokines like interferon-γ and interleukin (IL)-12 produced by natural killer cells and macrophages, and counterbalancing TNF-α activity.9,10) TRAIL induces extrinsic apoptotic pathway by interacting with its receptors TRAIL-R1 and TRAIL-R2, also known as ‘death receptors’.11) Accordingly, TRAIL is involved in immune homeostasis and tumor suppression.12) TNF-α, TRAIL, and TWEAK can also activate the NF-kappa B group of transcription factors which are implicated in the production of cytokines.13)

There is only one study that evaluated the involvement of TWEAK and TRAIL in psychiatric disorders. In this study, authors found decreased plasma levels of TWEAK in crack cocaine users in comparison with controls. In addition, TWEAK and TRAIL levels were associated with mood symptoms severity.12) Recently, TWEAK was found capable to induce depressive symptoms in mice, being implicated on mood disorder pathophysiology.14)

To date, no study has been conducted in order to evaluate the levels of the TNF superfamily molecules TWEAK and TRAIL in patients with BD. Therefore, the aim of the current study was to investigate the involvement of hitherto unexplored components of the TNF superfamily in BD. We hypothesize that the patients with BD present increased plasma levels of TNF superfamily components in comparison with controls.

METHODS

Eighty patients with type 1 BD and 50 aged-matched controls were enrolled in this study. Patients were consecutively recruited from the Mood Disorders Outpatient Clinic at Governador Israel Pinheiro Hospital, Belo Horizonte, Brazil. BD diagnosis was confirmed independently by two psychiatrists according to the Mini-International Neuro-psychiatric Interview (MINI-Plus).15) Psychiatric co-morbidities were also evaluated by the MINI-Plus15) interview and were not considered as exclusion criteria. All patients were assessed by the Young Mania Rating Scale (YMRS),16) and the Hamilton Depression Rating Scale (HDRS)17) in order to evaluate the severity of manic and depressive symptoms, respectively. Remission was defined by YMRS score <7 and HDRS score <7 points for at least eight consecutive weeks.

Control group was recruited from the local population and it was composed of subjects without any psychiatric comorbidity, family history of psychiatry disease, suicide behavior or cognitive deficit. Controls were subjected to MINI-Plus interview to exclude psychiatric disorders.

Subjects with dementia, infectious or autoimmune diseases, or who had used steroids, anti-inflammatory drugs, or antibiotics within four weeks previous to the evaluation were excluded from this research protocol. The study was approved by the local ethic committees (COEP of Univer-sidade Federal de Minas Gerais; CAAE.26363614.0. 0000.5149). All participants signed written informed consent prior to study participation.

Ten milliliters of blood were drawn by venipuncture into a vacuum tube containing heparin at the same day of the clinical assessment (between 8 to 10 a.m.). Blood was immediately centrifuged twice at 1,800 g for 10 minutes. Plasma was collected and stored at −70ºC until assayed. Plasma levels of TNF-α (catalog number: DY210), sTNFR1 (catalog number: DY225), sTNFR2 (catalog number: DY726), TWEAK (catalog number: DY1090), and TRAIL (catalog number: DY375) were measured by enzyme-linked immunosorbent assay (ELISA) according to the procedures supplied by the manufacturer (DuoSet; R&D Systems, Minneapolis, MN, USA). All molecules were measured in duplicate and experiments were performed blinded regarding the participants’ diagnosis. Concentrations are expressed as pg/ml.

Descriptive statistics were used to report socio-demographic and clinical features of the sample. All variables were tested for normal distribution by means of the Kolmogorov–Smirnov test. Differences between two groups (patients vs. controls or BD in remission vs. BD in mania) were assessed by Mann–Whitney or Student t tests when non-normally or normally distributed, respectively. Spearman’s correlation analyses were performed to evaluate the association between TWEAK, TRAIL, TNF-α, sTNFR1, and sTNFR2 levels and age, length of illness, YMRS, HDRS scores. All statistical tests were two tailed and used a significance level of p<0.05. Statistical analyses were performed using SPSS software version 17.0 (SPSS Inc., Chicago, IL, USA).

RESULTS

Demographic and clinical features of the study populations are shown in Table 1. Control subjects and patients with BD presented comparable age and gender. Among 80 patients with BD, 38 were in remission (11 male, 27 female; mean±standard deviation [SD] of age 46.37±11.15 years) and 42 in mania (17 male, 25 female; age 51.07±13.02 years). The mean (±SD) length of illness was 22.68 (±11.08) years in patients in remission and 23.19 (±14.26) years in patients in mania. There were no significant differences between patients in remission and mania regarding age, gender and disease length. Patients with BD in mania presented YMRS and HDRS of 25.36 (±7.48) and 5.09 (±5.49), respectively. Patients with BD in remission presented YMRS and HDRS of 1.00 (±1.97) and 2.16 (±2.82), respectively. Forty-five out of 80 patients with BD (56.3%) were in use of at least two different mood stabilizer drugs. The information about mood stabilizers in use is shown in Table 1.

We observed changes in plasma levels of TNF family molecules in BD. Patients with BD exhibited increased plasma levels of sTNFR1 (Fig. 1A) and TWEAK (Fig. 1C) in comparison with controls. We did not find differences between patients with BD and controls regarding plasma levels of sTNFR2, TRAIL and TNF (Fig. 1A, 1D, and 1E, respectively). We found no significant differences when comparing the levels of TNF family markers between patients with BD in remission and in mania (Fig. 2A–2F).

In patients with BD, TWEAK plasma levels positively correlated with TNF-α plasma levels (ρ=0.528, p< 0.001) and with TRAIL plasma levels (ρ=0.621, p< 0.001). TNF-α, TRAIL, and TWEAK plasma levels did not correlate with age, length of disease, YMRS and HDRS scores. TWEAK and TRAIL plasma levels were not associated with the presence of psychiatric and clinical co-morbidities, nicotine dependence, or the use of any mood-stabilizing drug (i.e., atypical antipsychotics, lithium or anticonvulsants). When considering controls, there was a positive correlation between TWEAK and Trail plasma levels (ρ=0.297, p=0.04).

DISCUSSION

This is the first study to evaluate the TNF superfamily molecules TWEAK and TRAIL in BD. Patients with BD presented increased plasma levels of TWEAK and sTNFR1 in comparison with controls. The changes in TWEAK and sTNFR1 levels might be a trait marker of BD, since patients in different mood states (i.e., patients in mania and patients in remission) did not present any difference in the levels of the evaluated markers. The current results corroborate the view of chronic low-grade inflammation in BD, indicating the involvement of the TNF superfamily. TWEAK plasma levels were increased in BD patients regardless their mood state.18)

TWEAK has the potential to promote tissue remodeling through its ability to orchestrate inflammatory, angiogenic and/or fibrogenic processes, and regulate parenchymal cell survival and growth.8,10) During acute mood episodes, like mania, in parallel with increase in pro-inflammatory stimuli,8,19) TWEAK levels may increase in order to control or even counterbalance this process. During remission, low grade inflammation might also lead to persistent TWEAK pathway activation. Theoretically, even this mild chronic inflammation may drive and/or be associated with progressive CNS damage and pathological tissue remodeling.20,21) It remains to be determined whether TWEAK increase is specific for patients with BD or this phenomenon is observed in other major psychiatric diseases.

We did not find any significant difference between patients with BD and controls regarding plasma levels of TRAIL. Similar to our study, a previous study involving patients with crack cocaine abstinence and controls did not report difference in TRAIL plasma levels between groups.12) TRAIL is not expressed under physiological conditions in the CNS, and its role in regulating inflammation and apoptosis in the CNS needs to be further explored.22)

TNF-α activation is consistently reported in BD. For instance, Fiedorowicz et al.23) showed increased circulating levels of TNF-α, as well as its soluble receptors— sTNFR1/sTNFR2—in mania. Similarly, Pandey et al.24) described high mRNA levels of TNF-α, TNFR1 and IL-1R1 in BD. TNF-α degrades soon after release, partly explaining the fact that this molecule is not necessarily found altered in BD case series.8) It is worth mentioning that inconsistencies in the literature might also arise from the heterogeneity of BD samples in terms of clinical features and immune profile. Anyway, TNF-α levels positively correlated with TWEAK and our results reinforce the hypothesis that the TNF system is activated in BD.

This study has strengths and limitations that must be considered when interpreting the results. The diagnostic interviews of patients and controls were performed using the same protocol. In addition, the exclusion of patients with medical conditions such as inflammatory diseases can be regarded as strength of the study. The lack of strict control for confounding factors, such as body mass index, medications in use, and tobacco use must be considered limitations, as well as the cross-sectional nature of the study. In-vitro studies have demonstrated that mood stabilizers, antipsychotics, and antiepileptic drugs influence the production of inflammatory markers by immune cells.25,26) Our results, however, were not influenced by medication in use. In addition, it would have been informative to evaluate the association between functionality and the TNF molecules’ levels and to have a bipolar depression only arm as well. The fact that other molecules from the TNF superfamily were not investigated is also a limitation of our study.

In conclusion, our findings reinforce the view that inflammatory dysfunction is present in BD and that the TNF superfamily, particularly TWEAK, may play a role in the pathophysiology of BD. Given the role of TWEAK as an apoptosis regulator, this study has implications for the understanding the pathways to progressive CNS structural changes in BD.

Acknowledgments

Authors would like to acknowledge the participation of volunteers in this study. We also appreciate the critical comments and expert technical assistance of members of our collaborative research groups. This work was funded by the Brazilian government agencies CAPES, CNPq and Fapemig. The funding sources had no influence on study design, data analysis, interpretation of results, writing of the manuscript, or the decision to submit the paper for publication.

Figures
Fig. 1. Plasma levels of TNF superfamily molecules in patients with bipolar disorder (BD) and controls. Patients with BD presented higher levels of sTNFR1 (A) and TWEAK (C) than controls. No differences between groups were observed regarding plasma levels of sTNFR2 (B), TRAIL (D), and TNF (E). Plasma levels (pg/ml) of all measured molecules (mean±standard deviation [median]) and statistics are provided in (F). TNF, tumor necrosis factor; sTNFR1, soluble TNF receptor type 1; sTNFR2, soluble TNF receptor type 2; TWEAK, TNF-related weak inducer of apoptosis; TRAIL, TNF-related apoptosis-inducing ligand.

*Student’s t-test, Mann-Whitney test. Horizontal bars represent the medians.

Fig. 2. Plasma levels of TNF superfamily molecules in patients with bipolar disorder (BD) in remission and in mania. Patients with BD in remission and in mania presented similar plasma levels of sTNFR1 (A), sTNFR2 (B), TWEAK (C), TRAIL (D), and TNF (E). Plasma levels (pg/ml) of all measured molecules (mean±standard deviation [median]) and statistics are provided in (F).

TNF, tumor necrosis factor; sTNFR1, soluble TNF receptor type 1; sTNFR2, soluble TNF receptor type 2; TWEAK, TNF-related weak inducer of apoptosis; TRAIL, TNF-related apoptosis-inducing ligand.

*Student’s t-test, Mann-Whitney test. Horizontal bars represent the medians.

Tables

Demographic and clinical features of controls and bipolar disorder (BD) patients

Feature Control (n=50)  BD patient (n=80) p value 
Age (yr)46.80±9.4746.09±12.320.38*
Sex, male/female15/3552/800.58
Length of illness (yr) -22.93±12.66-
YMRS score-13.78±13.44-
HDRS score-3.70±4.65-
Medications in use
 Lithium-43 (53.8)-
 Antipsychotics-49 (61.3)-
 Anticonvulsants-39 (48.8)-

Values are presented as mean±standard deviation, number only, or number (%).

YMRS, Young Mania Rating Scale; HDRS, Hamilton Depression Rating Scale.

Mann Whitney test.

References
  1. Modabbernia, A, Taslimi, S, Brietzke, E, and Ashrafi, M (2013). Cytokine alterations in bipolar disorder: a meta-analysis of 30 studies. Biol Psychiatry. 74, 15-25.
    Pubmed CrossRef
  2. Munkholm, K, Braüner, JV, Kessing, LV, and Vinberg, M (2013). Cytokines in bipolar disorder vs. healthy control subjects: a systematic review and meta-analysis. J Psychiatr Res. 47, 1119-1133.
    Pubmed CrossRef
  3. Munkholm, K, Vinberg, M, and Vedel Kessing, L (2013). Cytokines in bipolar disorder: a systematic review and meta-analysis. J Affect Disord. 144, 16-27.
    CrossRef
  4. Teixeira, AL, de Sousa, RT, Zanetti, MV, Brunoni, AR, Busatto, GF, and Zarate, CA (2015). Increased plasma levels of soluble TNF receptors 1 and 2 in bipolar depression and impact of lithium treatment. Hum Psychopharmacol. 30, 52-56.
    Pubmed CrossRef
  5. Dean, B, Gibbons, AS, Tawadros, N, Brooks, L, Everall, IP, and Scarr, E (2013). Different changes in cortical tumor necrosis factor- α-related pathways in schizophrenia and mood disorders. Mol Psychiatry. 18, 767-773.
    CrossRef
  6. Townsend, JD, Torrisi, SJ, Lieberman, MD, Sugar, CA, Bookheimer, SY, and Altshuler, LL (2013). Frontal-amygdala connectivity alterations during emotion downregulation in bipolar I disorder. Biol Psychiatry. 73, 127-135.
    CrossRef
  7. Barbosa, IG, Rocha, NP, Huguet, RB, Ferreira, RA, Salgado, JV, and Carvalho, LA (2012). Executive dysfunction in euthymic bipolar disorder patients and its association with plasma biomarkers. J Affect Disord. 137, 151-155.
    Pubmed CrossRef
  8. Barbosa, IG, Huguet, RB, Mendonça, VA, Sousa, LP, Neves, FS, and Bauer, ME (2011). Increased plasma levels of soluble TNF receptor I in patients with bipolar disorder. Eur Arch Psychiatry Clin Neurosci. 261, 139-143.
    CrossRef
  9. Maecker, H, Varfolomeev, E, Kischkel, F, Lawrence, D, LeBlanc, H, and Lee, W (2005). TWEAK attenuates the transition from innate to adaptive immunity. Cell. 123, 931-944.
    Pubmed CrossRef
  10. Croft, M (2014). The TNF family in T cell differentiation and function--unanswered questions and future directions. Semin Immunol. 26, 183-190.
    Pubmed KoreaMed CrossRef
  11. Cullen, SP, and Martin, SJ (2015). Fas and TRAIL ‘death receptors’ as initiators of inflammation: Implications for cancer. Semin Cell Dev Biol. 39, 26-34.
    Pubmed CrossRef
  12. Levandowski, ML, Viola, TW, Wearick-Silva, LE, Wieck, A, Tractenberg, SG, and Brietzke, E (2014). Early life stress and tumor necrosis factor superfamily in crack cocaine withdrawal. J Psychiatr Res. 53, 180-186.
    Pubmed CrossRef
  13. Mas, S, Martínez-Pinna, R, Martín-Ventura, JL, Pérez, R, Gomez-Garre, D, and Ortiz, A (2010). Local non-esterified fatty acids correlate with inflammation in atheroma plaques of patients with type 2 diabetes. Diabetes. 59, 1292-1301.
    Pubmed KoreaMed CrossRef
  14. Wen, J, Chen, CH, Stock, A, Doerner, J, Gulinello, M, and Putterman, C (2016). Intracerebroventricular administration of TNF-like weak inducer of apoptosis induces depression-like behavior and cognitive dysfunction in non-autoimmune mice. Brain Behav Immun. 54, 27-37.
    Pubmed KoreaMed CrossRef
  15. Sheehan, DV, Lecrubier, Y, Sheehan, KH, Amorim, P, Janavs, J, and Weiller, E (1998). The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry. 59, 22-33.
  16. Young, RC, Biggs, JT, Ziegler, VE, and Meyer, DA (1978). A rating scale for mania: reliability, validity and sensitivity. Br J Psychiatry. 133, 429-435.
    Pubmed CrossRef
  17. Hamilton, M (1967). Development of a rating scale for primary depressive illness. Br J Soc Clin Psychol. 6, 278-296.
    Pubmed CrossRef
  18. Davis, J, Maes, M, Andreazza, A, McGrath, JJ, Tye, SJ, and Berk, M (2015). Towards a classification of biomarkers of neuropsy-chiatric disease: from encompass to compass. Mol Psychiatry. 20, 152-153.
    CrossRef
  19. Kapczinski, F, Dal-Pizzol, F, Teixeira, AL, Magalhaes, PV, Kauer-Sant’Anna, M, and Klamt, F (2011). Peripheral biomarkers and illness activity in bipolar disorder. J Psychiatr Res. 45, 156-161.
    CrossRef
  20. Berk, M, Berk, L, Dodd, S, Cotton, S, Macneil, C, and Daglas, R (2014). Stage managing bipolar disorder. Bipolar Disord. 16, 471-477.
    CrossRef
  21. Barbosa, IG, Bauer, ME, Machado-Vieira, R, and Teixeira, AL (2014). Cytokines in bipolar disorder: paving the way for neuroprogression. Neural Plast. 2014, 360481.
    Pubmed KoreaMed CrossRef
  22. Griffiths, MR, Gasque, P, and Neal, JW (2009). The multiple roles of the innate immune system in the regulation of apoptosis and inflammation in the brain. J Neuropathol Exp Neurol. 68, 217-226.
    Pubmed CrossRef
  23. Fiedorowicz, JG, Prossin, AR, Johnson, CP, Christensen, GE, Magnotta, VA, and Wemmie, JA (2015). Peripheral inflammation during abnormal mood states in bipolar I disorder. J Affect Disord. 187, 172-178.
    Pubmed KoreaMed CrossRef
  24. Pandey, GN, Ren, X, Rizavi, HS, and Zhang, H (2015). Abnormal gene expression of proinflammatory cytokines and their receptors in the lymphocytes of patients with bipolar disorder. Bipolar Disord. 17, 636-644.
    Pubmed KoreaMed CrossRef
  25. Himmerich, H, Schönherr, J, Fulda, S, Sheldrick, AJ, Bauer, K, and Sack, U (2011). Impact of antipsychotics on cytokine production in-vitro. J Psychiatr Res. 45, 1358-1365.
    Pubmed CrossRef
  26. Himmerich, H, Bartsch, S, Hamer, H, Mergl, R, Schönherr, J, and Petersein, C (2013). Impact of mood stabilizers and anti-epileptic drugs on cytokine production in-vitro. J Psychiatr Res. 47, 1751-1759.
    Pubmed CrossRef


This Article


Cited By Articles
  • CrossRef (0)

Funding Information

Services
Social Network Service

e-submission

Archives