Blood Levels of Tumor Necrosis Factor Alpha and Its Type 2 Receptor Are Elevated in Patients with Boston Type I Keratoprosthesis

ABSTRACT Purpose: Boston keratoprosthesis (KPro) patients are prone to glaucoma even with well-controlled intraocular pressure (IOP). Recent experimental data have shown that soluble tumor necrosis factor alpha (TNF-α) after ocular injury may contribute to progressive retinal damage and subsequent glaucoma. This study evaluates the blood plasma levels of soluble TNF-α, TNF receptors 1 (TNFR1) and 2 (TNFR2), and leptin in patients with Boston type I KPro. Methods: Venous blood samples were collected from KPro patients with glaucoma (KPro G, n = 19), KPro patients without glaucoma (KPro NoG, n = 12), primary angle closure glaucoma without KPro (PACG, n = 13), and narrow angles without glaucoma or KPro (NA, n = 21). TNF-α, TNFR1, TNFR2, and leptin levels were quantified using the enzyme-linked immunosorbent assay. Erythrocyte sedimentation rate (ESR) was assessed using the Westergren test. Patients with underlying autoimmune conditions or diabetes were excluded from the study. Results: All groups had similar age, body mass index (BMI), IOP, and ESR (p ≥ 0.11). The mean time from KPro surgery to blood draw was 5.3 ± 3.7 years. Compared to NA patients (0.72 ± 0.3 pg/ml), KPro G and KPro NoG patients had higher blood plasma levels of TNF-α (1.18 ± 0.58 pg/ml, p = 0.006; 1.16 ± 0.50 pg/ml, p = 0.04, respectively). Similarly, KPro G patients had higher blood plasma levels of TNFR2 (2768 ± 1368 pg/ml) than NA patients (2020 ± 435 pg/ml, p = 0.048). In multivariate analysis, KPro status remained positively associated with TNF-α levels (β = 0.36; 95% confidence intervals [CI]: 0.14–0.58; p = 0.002) and TNFR2 levels (β = 458.3; 95% CI: 32.8–883.7; p = 0.035) after adjusting for age, gender, BMI, glaucoma status, and ESR. TNFR1 and leptin levels were not significantly different in the study groups. Conclusions: We detected elevated serum levels of TNF-α and TNFR2 in KPro patients. Longitudinal studies are needed to establish TNF-α and TNFR2 as serum biomarkers related to KPro surgery. Abbreviations: BCVA: best corrected visual acuity; BMI: body mass index; CDR: cup-to-disc ratio; EDTA: ethylenediaminetetraacetic acid; ELISA: enzyme-linked immunosorbent assay; ESR: erythrocyte sedimentation rate; HVF: Humphrey visual field; IOP: intraocular pressure; KPro G: keratoprosthesis with glaucoma; KPro NoG: keratoprosthesis without glaucoma; KPro: keratoprosthesis; MD: mean deviation; NA: narrow angle; non-KPro: without keratoprosthesis; PACG: primary angle closure glaucoma; RNFL: retinal nerve fiber layer; TNF-α: tumor necrosis factor alpha; TNFR1: tumor necrosis factor receptor 1; TNFR2: tumor necrosis factor receptor 2

[1]  R. Dana,et al.  Microglia Regulate Neuroglia Remodeling in Various Ocular and Retinal Injuries , 2018, The Journal of Immunology.

[2]  R. Dana,et al.  Permanent neuroglial remodeling of the retina following infiltration of CSF1R inhibition-resistant peripheral monocytes , 2018, Proceedings of the National Academy of Sciences.

[3]  R. Dana,et al.  Neuroglial Remodeling After Various Ocular Injuries is Regulated by Microglia , 2018 .

[4]  K. Abu-Amero,et al.  Association of increased levels of plasma tumor necrosis factor alpha with primary open-angle glaucoma , 2018, Clinical ophthalmology.

[5]  R. Dana,et al.  The Role of Microglia and Peripheral Monocytes in Retinal Damage after Corneal Chemical Injury. , 2018, The American journal of pathology.

[6]  S. Mosaed,et al.  Vision retention in early versus delayed glaucoma surgical intervention in patients with Boston Keratoprosthesis type 1 , 2017, PloS one.

[7]  R. Dana,et al.  Mechanisms of Retinal Damage after Ocular Alkali Burns. , 2017, The American journal of pathology.

[8]  S. Ramamoorthy,et al.  Obesity in IBD: epidemiology, pathogenesis, disease course and treatment outcomes , 2017, Nature Reviews Gastroenterology &Hepatology.

[9]  R. Dana,et al.  Effect of Penetrating Keratoplasty and Keratoprosthesis Implantation on the Posterior Segment of the Eye , 2016, Investigative ophthalmology & visual science.

[10]  C. Malone,et al.  Long-term visual acuity, retention and complications observed with the type-I and type-II Boston keratoprostheses in an Irish population , 2015, British Journal of Ophthalmology.

[11]  Claude Burgoyne,et al.  The morphological difference between glaucoma and other optic neuropathies. , 2015, Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society.

[12]  J. Chodosh,et al.  Idiopathic Vitritis in the Setting of Boston Keratoprosthesis , 2015, Cornea.

[13]  K. Lekhanont,et al.  Medium-term Outcomes of Boston Type 1 Keratoprosthesis Implantation in Bangkok, Thailand , 2014, Cornea.

[14]  E. Naumova,et al.  Infectious endophthalmitis in Boston keratoprosthesis: incidence and prevention , 2014, Acta ophthalmologica.

[15]  C. Dohlman Alkali burn to the eye: Protection using TNF-a inhibition , 2014 .

[16]  R. Dana,et al.  Alkali Burn to the Eye: Protection Using TNF-&agr; Inhibition , 2014, Cornea.

[17]  Lucy Q. Shen,et al.  Glaucoma Progression and Role of Glaucoma Surgery in Patients With Boston Keratoprosthesis , 2014, Cornea.

[18]  R. Dana,et al.  Corneal inflammation after miniature keratoprosthesis implantation. , 2014, Investigative ophthalmology & visual science.

[19]  N. Allemann,et al.  Serial Analysis of Anterior Chamber Depth and Angle Status Using Anterior Segment Optical Coherence Tomography After Boston Keratoprosthesis , 2013, Cornea.

[20]  P. Bogdański,et al.  Evaluation of insulin resistance, tumor necrosis factor alpha, and total antioxidant status in obese patients smoking cigarettes. , 2013, European review for medical and pharmacological sciences.

[21]  Michael W. Belin,et al.  Retention of the Boston keratoprosthesis type 1: multicenter study results. , 2013, Ophthalmology.

[22]  L. Pasquale,et al.  A nested case control study of plasma ICAM-1, E-selectin and TNF receptor 2 levels, and incident primary open-angle glaucoma. , 2013, Investigative ophthalmology & visual science.

[23]  M. Harissi-Dagher,et al.  Complications associated with Boston keratoprosthesis type 1 and glaucoma drainage devices , 2013, British Journal of Ophthalmology.

[24]  F. Yu,et al.  International results with the Boston type I keratoprosthesis. , 2012, Ophthalmology.

[25]  M. Harissi-Dagher,et al.  Prevalence, progression, and impact of glaucoma on vision after Boston type 1 keratoprosthesis surgery. , 2012, American journal of ophthalmology.

[26]  M. Tanito,et al.  Multiplex cytokine analysis of aqueous humor in eyes with primary open-angle glaucoma, exfoliation glaucoma, and cataract. , 2012, Investigative ophthalmology & visual science.

[27]  C. Grosskreutz,et al.  Glaucoma in Eyes With Severe Chemical Burn, Before and After Keratoprosthesis , 2011, Cornea.

[28]  F. Yu,et al.  The Boston Keratoprosthesis in the Management of Corneal Limbal Stem Cell Deficiency , 2011, Cornea.

[29]  J. Chodosh,et al.  Titanium back plate for a PMMA keratoprosthesis: clinical outcomes , 2011, Graefe's Archive for Clinical and Experimental Ophthalmology.

[30]  A. Dick,et al.  Mechanisms of TNFα regulation in uveitis: Focus on RNA-binding proteins , 2010, Progress in Retinal and Eye Research.

[31]  D. Ritterband,et al.  Evaluation of the Stability of Boston Type I Keratoprosthesis–Donor Cornea Interface Using Anterior Segment Optical Coherence Tomography , 2010, Cornea.

[32]  Maren S Fragala,et al.  Conceptual and methodological issues relevant to cytokine and inflammatory marker measurements in clinical research , 2010, Current opinion in clinical nutrition and metabolic care.

[33]  Miriam Davis,et al.  TNF receptor 2 pathway: drug target for autoimmune diseases , 2010, Nature Reviews Drug Discovery.

[34]  Jun Chen,et al.  Leptin neuroprotection in the CNS: mechanisms and therapeutic potentials , 2008, Journal of neurochemistry.

[35]  M. Mattson,et al.  Leptin-mediated Cell Survival Signaling in Hippocampal Neurons Mediated by JAK STAT3 and Mitochondrial Stabilization* , 2008, Journal of Biological Chemistry.

[36]  M. Harissi-Dagher,et al.  The Boston Keratoprosthesis in severe ocular trauma. , 2007, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

[37]  Danish M. Khan,et al.  Advances in Boston Keratoprosthesis: Enhancing Retention and Prevention of Infection and Inflammation , 2007, International ophthalmology clinics.

[38]  E. Collantes Estévez,et al.  Aqueous Humor and Serum Tumor Necrosis Factor-α in Clinical Uveitis , 2001, Ophthalmic Research.

[39]  M. Wax,et al.  TNF-alpha and TNF-alpha receptor-1 in the retina of normal and glaucomatous eyes. , 2001, Investigative ophthalmology & visual science.

[40]  M. Durand,et al.  Endophthalmitis after keratoprosthesis: incidence, bacterial causes, and risk factors. , 2001, Archives of ophthalmology.

[41]  K. Flegal,et al.  Criteria for definition of overweight in transition: background and recommendations for the United States. , 2000, The American journal of clinical nutrition.

[42]  P. Ponikowski,et al.  The relationship of the erythrocyte sedimentation rate to inflammatory cytokines and survival in patients with chronic heart failure treated with angiotensin-converting enzyme inhibitors. , 2000, Journal of the American College of Cardiology.

[43]  A. Ruello,et al.  Relationship between plasma leptin levels and the tumor necrosis factor-α system in obese subjects , 1999, International Journal of Obesity.

[44]  H. Hauner,et al.  Plasma concentrations of soluble TNF-alpha receptors in obese subjects , 1998, International Journal of Obesity.

[45]  P. Netland,et al.  Glaucoma associated with keratoprosthesis. , 1998, Ophthalmology.

[46]  L. Owen-Schaub,et al.  Human Tumor Necrosis Factor Receptor p75/80 (CD120b) Gene Structure and Promoter Characterization* , 1996, The Journal of Biological Chemistry.

[47]  D. Heney,et al.  Factors Affecting the Measurement of Cytokines in Biological Fluids: Implications for Their Clinical Measurement , 1995, Annals of clinical biochemistry.

[48]  A. Cope,et al.  Correlation between serum levels of soluble tumor necrosis factor receptor and disease activity in systemic lupus erythematosus. , 1993, Arthritis and rheumatism.

[49]  L. Tartaglia,et al.  Two TNF receptors. , 1992, Immunology today.