- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
Stroke Research and Treatment
Volume 2011 (2011), Article ID 920584, 5 pages
Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek Population
1Department of Neurology, School of Medicine, University of Ioannina, University Campus, 45110 Ioannina, Greece
2Laboratory of Medical Genetics, School of Medicine, University of Ioannina, University Campus, 45110 Ioannina, Greece
3Neurosurgical Research Institute, School of Medicine, University of Ioannina, 45110 Ioannina, Greece
4Department of Clinical Therapeutics, National and Kapodistrian, University of Athens, 11528 Athens, Greece
Received 17 November 2010; Revised 12 February 2011; Accepted 15 March 2011
Academic Editor: Stefan Engelter
Copyright © 2011 Sofia Markoula et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background. The role of genetic factors in the predisposition to develop ischemic stroke has been assessed by previous studies. The main goal of the current study was to determine any possible role of TNF-857C>T,TNFRSF1A36A>G, and TNFRSF1B676T>G polymorphisms in risk for stroke. Materials and Methods. One hundred seventy-three patients with first ever ischemic stroke of solely atherosclerotic etiology in Northwest Greece and a control group of 179 healthy unrelated subjects were evaluated. Results. TNFα-857TT, TNFR136AA, and TNFR2676TT genotypes were significantly increased in the patient group compared to controls (, OR = 2.47 (1.26–4.84), , OR = 1.97 (1.22–3.17), and , OR = 2.2 (1.43–3.37), resp.). In addition, the TNFR136A and the TNFR2676T alleles were found significantly increased in patients compared to controls (, OR = 1.48 (1.1–2) and , OR = 1.75 (1.25–2.46), resp.). Conclusion. The high incidence of these genotypes and alleles in patient group suggests that they are potentially predisposing factors for stroke in the Greek population studied. Large-scale multicenter controlled studies are needed to verify these polymorphisms effects on stroke susceptibility.
Ischemic stroke is a multifactorial disease, caused by the interactions of genetic and environmental factors, based on atherosclerosis and arterial thrombogenesis . Central nervous system (CNS) can mount a well-defined inflammatory response to a variety of insults including ischemia and atherosclerosis . Atherosclerosis has many inflammatory mediators contributing to atheroma formation, atheromatous injury, rupture of the plaque, and hence to intraluminal thrombosis [2, 3]. Tumor necrosis factor-(TNF-) alpha is involved in every step of inflammation, from initiation to downregulation, and elevated levels of TNF and other cytokines have been demonstrated in the cerebrospinal fluid (CSF) and the plasma of acute stroke and subarachnoid hemorrhage patients [4–6]. TNF exerts its biological effects via the two cell surface receptors that act as physiological attenuators, TNFRSF1A and TNFRSF1B.
Functional polymorphisms inside the TNF gene promoter and polymorphisms that could influence the function or the expression of TNFRSF1 and TNFRSF1B have been investigated in various immune, inflammatory, and neurodegenerative conditions [7–14] but only few genetic studies have focused on the association of these polymorphisms with stroke [15, 16].
Under the rationale that individuals with genetic variants might possibly be at greater risk for ischemic stroke, we analyzed the role of the TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G polymorphisms in ischemic stroke patients in Northwestern Greece, a rather restricted area with limited recent immigration.
2. Materials and Methods
2.1. Study Population
Cases eligible for recruitment were 173 patients hospitalized with first ever ischemic stroke in the Stroke Reference Center of Northwestern Greece in a period of 18 months, from May 2008 to November 2009, defined according to the WHO definition, and confirmed by brain imaging showing a recent brain infarct corresponding to the clinical presentation. As a control group, 179 age-matched unrelated subjects were recruited from the same medical center, among nonfamily visitors. Controls had no history of previous ischemic cerebrovascular event, established by the Questionnaire for Verifying Stroke-Free Status (QVSFS)  and normal neurological examination. The study protocol was in compliance with the Helsinki Declaration, approved by the Institutional Ethics Committee. An informed consent was signed by all eligible patients and controls.
In all subjects a detailed medical history was obtained and a thorough physical examination was performed. Demographic data, biochemical profile, and established risk factors for stroke were recorded. Arterial hypertension was documented when systolic blood pressure (BP) was ≥140 mmHg or diastolic BP ≥ 90 mmHg or when individuals were receiving antihypertensive drugs for previously established hypertension. Smoking, active or ceased within the last 3 months, was considered as current. Diabetes mellitus was considered as present if fasting glucose was >126 mg/dl or the individual was treated with antidiabetic medication. Dyslipidemia was defined as fasting cholesterol >220 mg/dl or the individual was on current treatment with specific antilipidemic agents. Further evaluation of the patients included triplex ultrasound imaging or CT angiography of extracranial or/and intracranial arteries, electrocardiogram (ECG), echocardiography (transthoracic or transesophageal), and clinical/laboratory assessment to rule out systemic thrombotic and autoimmune disorders.
Recruitment in the study was performed according to TOAST definitions and included patients with lacunars (small, subcortical, hypodense lesions with a diameter less than 15 mm and corresponding to lesion clinical lacunar syndrome) and patients with large artery atherosclerosis (hypodense lesions with a diameter >15 mm and >50% stenosis in the appropriate intracranial artery) .
Cardioembolic strokes were excluded since they could result from different etiology (e.g., atrial fibrillation). Strokes occurred in the course of systemic conditions such as coagulopathies or immunological disorders or of undetermined etiology were also excluded in order to assure the solely atherosclerotic etiology of the stroke.
2.2. Genetic Analysis
Genomic DNA was extracted from peripheral blood lymphocytes according to the standard salt extraction procedure. Polymorphisms TNF-857C>T (rs1799724), TNFRSF1A36A>G (rs767455), and TNFRSF1B676T>G (rs1061622) were amplified using the following primer pairs: 36F: 5′-GAG CCC AAA TGG GGG AGT GAG AGG-3′ 36R: 5′-ACC AGG CCC GGG CAG GAG AG-3′, 676F: 5′-ACT CTC CTA TCC TGC CTG CT-3′ 676R: 5′-TTC TGG AGT TGG CTG CGT GT-3′, and 857F: 5′-AAG TCG AGT ATG GGG ACC CCC CGT TAA-3′ 857R: 5′-CCC CAG TGT GTG GCC ATA TCT TCT T-3′. Subsequently, restriction assays were employed using the restriction endonucleases MspA1 I, Nla III, and Hinc II, respectively. All samples were run in duplicates with positive and negative for each genotype samples as controls and blanks.
2.3. Statistical Analysis
The Chi-square test was used to test the agreement of genotype frequencies with Hardy-Weinberg equilibrium expectations. Binary data were described as percentages, while continuous data were expressed as the mean ± standard deviation (SD). We calculated odds ratios and 95% confidence intervals (CIs) to compare allele and genotype distributions. All tests were two-sided with 95% significance level (). The statistical analysis was performed with the statistical package StatXact 3.0 (Cytel Inc., Cambridge, Mass, USA). Furthermore, a power analysis showed that at least 302 subjects should be recruited in each group (cases and controls) for TNF-857C>T, 272 subjects for TNFRSF1A36A>G, and 85 subjects in each group for TNFRSF1B676T>G polymorphism, if the study power required was 80 per cent with a significance level of 0.05.
Of 173 patients, 113 (65%) were men and 60 (35%) were women with a mean age of 58.6 (SD ± 7.2 years). Of 179 controls, 123 (69%) were men and 56 (31%) were women and mean age was 57.1 (SD ± 5.9 years). Patients and controls demographics are shown in Table 1. In terms of stroke subtype, 84 patients had lacunar strokes, whereas 89 patients had large artery strokes.
The genotype frequencies for all three polymorphisms were in Hardy-Weinberg equilibrium in healthy controls. The genotype frequencies for TNFRSF1A and TNFRSF1B polymorphisms were in Hardy-Weinberg equilibrium in patients. Regarding the TNF-857C>T polymorphism distribution, a high prevalence of TT genotype in patients (, OR = 2.47 (1.26–4.84)) was revealed, implying a TT selection in patients causing Hardy-Weinberg disequilibrium, despite equilibrium in the controls. No statistically significant difference was observed in the allele frequencies, to further establish the hypothesis of the TT selection in patients.
The distribution and frequencies of genotypes and alleles for TNF, TNFRSF1A, and TNFRSF1B are summarized in Table 2. Regarding TNFRSF1A36A>G, a statistically significant difference was observed between patients carrying the AA genotype and controls (, OR = 1.97 (1.22–3.17)). Significant differences were also noted in the allele frequencies, namely, A and G with 58.1% in patients versus 48.3% in controls for A allele and 41.9% in patients versus 51.7% in controls for G allele (, OR = 1.48 (1.1–2)). For the TNFRSF1B676T>G, the TT genotype was more frequent in the stroke group than in controls, with 61.9% versus 42.5%, respectively (, OR = 2.2 (1.43–3.37)). Similarly, statistically significant differences between the allele frequencies with 78.3% in patients versus 67.3% in controls for T allele and conversely 21.7% in patients versus 32.7% in controls for G allele (, OR = 1.75 (1.25–2.46)) (Table 2) were revealed.
In terms of stroke subtype, subgroups analysis did not disclose any statistically significant result when genotypes and alleles distribution in the lacunar stroke group was compared to the large artery atherosclerosis stroke group (data not shown).
In the present study, we investigated the association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G polymorphisms with ischemic stroke, under the rationale that, as the proinflammatory cytokines play an important role in cerebral ischemia [4, 5, 19, 20], certain TNF and TNF receptors polymorphisms may be implicated in stroke occurrence.
A gene located on chromosome 6p21 encodes TNF-α. The TNF-857C>T polymorphism is a functional polymorphism through binding to the transcription factor octamer transcription factor-1 (OCT-1) . No research group, working on stroke, has focused on this polymorphism. Most groups have worked on the TNF-308G>A polymorphism with Pereira et al. suggesting that the TNF-308G>A polymorphism may play a role in ischemic stroke  showing that young subjects of European ancestry carrying the A allele (AA + GA versus GG) were associated with a statistically significant increase in the risk of stroke compared with individuals homozygous for the G allele (OR = 2.04, ). In a cohort of young Italian stroke patients, the A allele of −308G>A polymorphism exerted an independent effect on predisposition to ischemic stroke in young stroke patients with AA + GA genotypes frequency being 25.2% + 1.7%, respectively, in the stroke group versus 15% + 0.6 5% in the control group . Dissimilar findings suggest that this polymorphism is clinically important in stroke in sickle cell anemia children  but shows protective effects of TNF(-308)A allele (OR = 0.39, ) with 18% carriers of the A allele in stroke group versus 38% in the control group.
In our healthy population in Northwest Greece, as recorded in a recent study conducted by our group , the TNF-308G>A polymorphism is not in Hardy-Weinberg equilibrium, and our study was designed on the specific characteristics of our population to exclude this polymorphism and focus on the TNF-857C>T polymorphism. Our study exerted that this other functional polymorphism plays a role in stroke development with the recessive genotype being more frequent in ischemic stroke patients.
TNFRSF1A is encoded by a gene located on chromosome 12p13.2. The TNFRSF1A36A>G polymorphism is a silent mutation in codon 12, and it although has no obvious functional influence on protein structure, many studies have tried to find any association of this polymorphism with specific inflammatory disease manifestations and response to treatment, such as Multiple Sclerosis (MS), Crohn's disease, and Rheumatoid Arthritis (RA) [10, 11, 14].
TNFRSF1B is encoded by a gene located on chromosome 1 p36.3 with a higher affinity for TNF than TNFRSF1, and polymorphisms in this receptor affect the binding of TNF and the pathway involved in inflammation; associations of TNFRSF1B polymorphisms with chronic inflammatory diseases such as RA and systemic lupus erythematosus have been reported [10, 12].
Our results indicate that the most studied, for many inflammatory diseases, polymorphisms of TNFRSF1A and TNFRSF1B are also associated with stroke, with the AA genotype of TNFRSF1A and the TT of TNFRSF1B being more frequent in stroke patients. The same applies for the A allele of TNFSF1A and the T allele of TNFSF1B.
Limitations of our study include the relatively small number of patients and the TNF-857TT Hardy-Weinberg disequilibrium in our cases. As a consequence of the small number of the cases the power of our study is limited regarding the TNF-857C>T and the TNFRSF1A36A>G polymorphism. Regarding the TNFRSF1B676T>G polymorphism, power analysis confirmed a sound power of this result. The strengths of the study were the solely atherosclerotic etiology of subjects and the prospective design with all ischemic stroke patients under certain inclusion criteria and the significant result for TNFRSF1B676T>G polymorphism.
Conclusively, our results indicate a possible association of −857C>T polymorphism of TNF with stroke and are in favor of a direct, contributory effect of the most studied polymorphisms of TNFRSF1A and TNFRSF1B on ischemic stroke predisposition, with TNFRSF1B676T>G polymorphism showing the closest association. Our assumption is that specific polymorphisms are involved in the process of inflammation, and thus they promote extra- and intracranial atherosclerosis and subsequently strokes. The genetically homogenous population allows the extractions of assumptions concerning our population, but no further conclusions should be reached without large-scale multicenter studies and a wider range of results. Any role for TNF and TNF receptor genes on stroke is far from being established with these genes being excellent candidates for further research on the genetics of stroke.
This paper is part of the 03ED research project, implemented within the framework of the Reinforcement Programme of Human Research Manpower and cofinanced by National and Community Funds (25% from the Greek Ministry of Development-General Secretariat of Research and Technology and 75% from European Union Social Fund).
- J. Y. Um, N. H. An, and H. M. Kim, “TNF-α and TNF-β gene polymorphisms in cerebral infarction,” Journal of Molecular Neuroscience, vol. 21, no. 2, pp. 167–171, 2003.
- B. Arvin, L. F. Neville, F. C. Barone, and G. Z. Feuerstein, “The role of inflammation and cytokines in brain injury,” Neuroscience and Biobehavioral Reviews, vol. 20, no. 3, pp. 445–452, 1996.
- R. Ross, “Atherosclerosis—an inflammatory disease,” The New England Journal of Medicine, vol. 340, pp. 115–126, 1999.
- A. J. Grau, M. Aulmann, C. Lichy et al., “Increased cytokine release by leucocytes in survivors of stroke at young age,” European Journal of Clinical Investigation, vol. 31, no. 11, pp. 999–1006, 2001.
- N. Vila, J. Castillo, A. Davalos, and A. Chamorro, “Proinflammatory cytokines and early neurological worsening in ischemic stroke,” Stroke, vol. 31, no. 10, pp. 2325–2329, 2000.
- K. A. Hanafy, B. Grobelny, L. Fernandez et al., “Brain interstitial fluid TNF-α after subarachnoid hemorrhage,” Journal of the Neurological Sciences, vol. 291, no. 1-2, pp. 69–73, 2010.
- D. A. Van Heel, I. A. Udalova, A. P. De Silva et al., “Inflammatory bowel disease is associated with a TNF polymorphism that affects an interaction between the OCT1 and NF(-kappa)B transcription factors,” Human Molecular Genetics, vol. 11, no. 11, pp. 1281–1289, 2002.
- C. Cipriano, C. Caruso, D. Lio et al., “The -308G/A polymorphism of TNF-α influences immunological parameters in old subjects affected by infectious diseases,” International Journal of Immunogenetics, vol. 32, no. 1, pp. 13–18, 2005.
- D. Lio, G. Candore, A. Colombo et al., “A genetically determined high setting of TNF-α influences immunologic parameters of HLA-B8,DR3 positive subjects: implications for autoimmunity,” Human Immunology, vol. 62, no. 7, pp. 705–713, 2001.
- A. Chatzikyriakidou, I. Georgiou, P. V. Voulgari, A. I. Venetsanopoulou, and A. A. Drosos, “Combined tumour necrosis factor-α and tumour necrosis factor receptor genotypes could predict rheumatoid arthritis patients' response to anti-TNF-α therapy and explain controversies of studies based on a single polymorphism,” Rheumatology, vol. 46, no. 6, pp. 1034–1035, 2007.
- P. L. De Jager, X. Jia, J. Wang et al., “Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci,” Nature Genetics, vol. 41, no. 7, pp. 776–782, 2009.
- C. Morita, T. Horiuchi, H. Tsukamoto et al., “Association of tumor necrosis factor receptor type II polymorphism 196R with systemic lupus erythematosus in the Japanese molecular and functional analysis,” Arthritis and Rheumatism, vol. 44, no. 12, pp. 2819–2827, 2001.
- B. Wang, S. Zhou, ZE. Yang et al., “Genetic analysis of tumor necrosis factor-α (TNF-α) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease,” Journal of the Neurological Sciences, vol. 270, no. 1-2, pp. 148–151, 2008.
- M. Fabris, B. Tolusso, E. Di Poi, R. Assaloni, L. Sinigaglia, and G. Ferraccioli, “Tumor necrosis factor-α receptor II polymorphism in patients from Southern Europe with mild-moderate and severe rheumatoid arthritis,” Journal of Rheumatology, vol. 29, no. 9, pp. 1847–1850, 2002.
- S. Rubattu, R. Speranza, M. Ferrari et al., “A role of TNF-α gene variant on juvenile ischemic stroke: a case-control study,” European Journal of Neurology, vol. 12, no. 12, pp. 989–993, 2005.
- W. Lalouschek, M. Schillinger, K. Hsieh et al., “Polymorphisms of the inflammatory system and risk of ischemic cerebrovascular events,” Clinical Chemistry and Laboratory Medicine, vol. 44, no. 8, pp. 918–923, 2006.
- W. J. Jones, L. S. Williams, and J. F. Meschia, “Validating the questionnaire for Verifying Stroke-Free Status (QVSFS) by neurological history and examination,” Stroke, vol. 32, no. 10, pp. 2232–2236, 2001.
- L. B. Goldstein, M. R. Jones, D. B. Matchar et al., “Improving the reliability of stroke subgroup classification using the Trial of ORG 10172 in Acute Stroke Treatment (TOAST) criteria,” Stroke, vol. 32, no. 5, pp. 1091–1096, 2001.
- L. S. Rallidis, M. Vikelis, D. B. Panagiotakos, G. K. Liakos, E. Krania, and D. T. Kremastinos, “Usefulness of inflammatory and haemostatic markers to predict short-term risk for death in middle-aged ischaemic stroke patients,” Acta Neurologica Scandinavica, vol. 117, no. 6, pp. 415–420, 2008.
- J. Zaremba and J. Losy, “Early TNF-α levels correlate with ischaemic stroke severity,” Acta Neurologica Scandinavica, vol. 104, no. 5, pp. 288–295, 2001.
- T. V. Pereira, M. Rudnicki, R. F. Franco, A. C. Pereira, and J. E. Krieger, “Effect of the G-308A polymorphism of the tumor necrosis factor α gene on the risk of ischemic heart disease and ischemic stroke: a meta-analysis,” American Heart Journal, vol. 153, no. 5, pp. 821–830, 2007.
- C. Hoppe, W. Klitz, K. D'Harlingue et al., “Confirmation of an association between the TNF(-308) promoter polymorphism and stroke risk in children with sickle cell anemia,” Stroke, vol. 38, no. 8, pp. 2241–2246, 2007.