Relationship between Vitreous IL-6 Levels, Gender Differences and C-Reactive Protein (CRP) in a Blood Sample of Posterior Uveitis
Abstract
:1. Introduction
2. Materials and Methods
Statistical Analysis
3. Results
4. Discussion
Supplementary Materials
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Coupland, S.E. The pathologist’s perspective on vitreous opacities. Eye 2008, 22, 1318–1329. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Wakefield, D.; Chang, J.H. Epidemiology of uveitis. Int. Ophthalmol. Clin. 2005, 45, 1–13. [Google Scholar] [CrossRef] [PubMed]
- Hsu, Y.R.; Huang, J.C.; Tao, Y.; Kaburaki, T.; Lee, C.S.; Lin, T.C.; Hsu, C.C.; Chiou, S.H.; Hwang, D.K. Noninfectious uveitis in the Asia-Pacific region. Eye 2019, 33, 66–77. [Google Scholar] [CrossRef]
- Tagami, M.; Misawa, N.; Sakai, A.; Honda, S. Two Cases of Extremely High-IL-6 Pan-uveitis with Subretinal Exudation and Cell Migration. Ocul. Immunol. Inflamm. 2022, 30, 1577–1581. [Google Scholar] [CrossRef]
- Goto, H.; Mochizuki, M.; Yamaki, K.; Kotake, S.; Usui, M.; Ohno, S. Epidemiological survey of intraocular inflammation in Japan. Jpn J. Ophthalmol. 2007, 51, 41–44. [Google Scholar] [CrossRef] [PubMed]
- Maleki, A.; Gomez, S.; Asgari, S.; Bosenberg, Z.; Manhapra, A.; Walsh, M.; Weng, A.; Tsang, C.; He, C.; Anesi, S.D.; et al. Diagnostic and Prognostic Roles of Serum Interleukin-6 Levels in Patients with Uveitis. Ocul. Immunol. Inflamm. 2022, 30, 457–462. [Google Scholar] [CrossRef]
- Kishimoto, T. The biology of interleukin-6. Blood 1989, 74, 1–10. [Google Scholar] [CrossRef] [Green Version]
- Hashizume, M.; Ohsugi, Y. IL-6 as a target in autoimmune disease and inflammation. Nihon Yakurigaku Zasshi 2014, 144, 172–177. [Google Scholar] [CrossRef] [Green Version]
- Romano, M.; Sironi, M.; Toniatti, C.; Polentarutti, N.; Fruscella, P.; Ghezzi, P.; Faggioni, R.; Luini, W.; van Hinsbergh, V.; Sozzani, S.; et al. Role of IL-6 and its soluble receptor in induction of chemokines and leukocyte recruitment. Immunity 1997, 6, 315–325. [Google Scholar] [CrossRef] [Green Version]
- Modur, V.; Li, Y.; Zimmerman, G.A.; Prescott, S.M.; McIntyre, T.M. Retrograde inflammatory signaling from neutrophils to endothelial cells by soluble interleukin-6 receptor alpha. J. Clin. Invest. 1997, 100, 2752–2756. [Google Scholar] [CrossRef] [Green Version]
- Suzuki, M.; Hashizume, M.; Yoshida, H.; Mihara, M. Anti-inflammatory mechanism of tocilizumab, a humanized anti-IL-6R antibody: Effect on the expression of chemokine and adhesion molecule. Rheumatol. Int. 2010, 30, 309–315. [Google Scholar] [CrossRef]
- Tanaka, T. IL-6 blockade therapy for inflammatory diseases: Current perspectives and future directions. Nihon Rinsho Meneki Gakkai Kaishi 2015, 38, 433–442. [Google Scholar] [CrossRef]
- Okada, Y.; Takahashi, A.; Ohmiya, H.; Kumasaka, N.; Kamatani, Y.; Hosono, N.; Tsunoda, T.; Matsuda, K.; Tanaka, T.; Kubo, M.; et al. Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. Hum. Mol. Genet. 2011, 20, 1224–1231. [Google Scholar] [CrossRef] [Green Version]
- Murray, P.I.; Hoekzema, R.; van Haren, M.A.; de Hon, F.D.; Kijlstra, A. Aqueous humor interleukin-6 levels in uveitis. Invest Ophthalmol. Vis. Sci. 1990, 31, 917–920. [Google Scholar] [PubMed]
- Sato, T.; Kusaka, S.; Shimojo, H.; Fujikado, T. Simultaneous analyses of vitreous levels of 27 cytokines in eyes with retinopathy of prematurity. Ophthalmology 2009, 116, 2165–2169. [Google Scholar] [CrossRef] [PubMed]
- Ghasemi, H. Roles of IL-6 in Ocular Inflammation: A Review. Ocul. Immunol. Inflamm. 2018, 26, 37–50. [Google Scholar] [CrossRef] [PubMed]
- Wang, Y.; Shen, D.; Wang, V.M.; Sen, H.N.; Chan, C.C. Molecular biomarkers for the diagnosis of primary vitreoretinal lymphoma. Int. J. Mol. Sci. 2011, 12, 5684–5697. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Nakano, S.; Sugita, S.; Tomaru, Y.; Hono, A.; Nakamuro, T.; Kubota, T.; Takase, H.; Mochizuki, M.; Takahashi, M.; Shimizu, N. Establishment of Multiplex Solid-Phase Strip PCR Test for Detection of 24 Ocular Infectious Disease Pathogens. Invest. Ophthalmol. Vis. Sci. 2017, 58, 1553–1559. [Google Scholar] [CrossRef]
- Yamamoto, S.; Sugita, S.; Sugamoto, Y.; Shimizu, N.; Morio, T.; Mochizuki, M. Quantitative PCR for the detection of genomic DNA of Epstein-Barr virus in ocular fluids of patients with uveitis. Jpn J. Ophthalmol. 2008, 52, 463–467. [Google Scholar] [CrossRef] [PubMed]
- Kimura, K.; Usui, Y.; Goto, H.; Group, J.I.L.S. Clinical features and diagnostic significance of the intraocular fluid of 217 patients with intraocular lymphoma. Jpn J. Ophthalmol. 2012, 56, 383–389. [Google Scholar] [CrossRef]
- Oberholzer, A.; Keel, M.; Zellweger, R.; Steckholzer, U.; Trentz, O.; Ertel, W. Incidence of septic complications and multiple organ failure in severely injured patients is sex specific. J. Trauma 2000, 48, 932–937. [Google Scholar] [CrossRef]
- Lau, E.S.; McNeill, J.N.; Paniagua, S.M.; Liu, E.E.; Wang, J.K.; Bassett, I.V.; Selvaggi, C.A.; Lubitz, S.A.; Foulkes, A.S.; Ho, J.E. Sex differences in inflammatory markers in patients hospitalized with COVID-19 infection: Insights from the MGH COVID-19 patient registry. PLoS ONE 2021, 16, e0250774. [Google Scholar] [CrossRef] [PubMed]
- Liu, W.C.; Liu, Q.Y. Molecular mechanisms of gender disparity in hepatitis B virus-associated hepatocellular carcinoma. World J. Gastroenterol. 2014, 20, 6252–6261. [Google Scholar] [CrossRef] [PubMed]
- Miyamoto, N.; Mandai, M.; Suzuma, I.; Suzuma, K.; Kobayashi, K.; Honda, Y. Estrogen protects against cellular infiltration by reducing the expressions of E-selectin and IL-6 in endotoxin-induced uveitis. J. Immunol. 1999, 163, 374–379. [Google Scholar] [CrossRef]
- Ogueta, S.B.; Schwartz, S.D.; Yamashita, C.K.; Farber, D.B. Estrogen receptor in the human eye: Influence of gender and age on gene expression. Invest. Ophthalmol. Vis. Sci. 1999, 40, 1906–1911. [Google Scholar]
- Sepah, Y.J.; Sadiq, M.A.; Chu, D.S.; Dacey, M.; Gallemore, R.; Dayani, P.; Hanout, M.; Hassan, M.; Afridi, R.; Agarwal, A.; et al. Primary (Month-6) Outcomes of the STOP-Uveitis Study: Evaluating the Safety, Tolerability, and Efficacy of Tocilizumab in Patients With Noninfectious Uveitis. Am. J. Ophthalmol. 2017, 183, 71–80. [Google Scholar] [CrossRef] [PubMed]
Male | Female | ||
---|---|---|---|
Patients | 33 | 44 | |
Eyes | 35 | 47 | |
Age | 63.0 ± 19.26 | 58.4 ± 16.60 | p = 0.677 |
IL-6 levels | 6255.0 ± 14,108.3 | 277.6 ± 746.3 | p = 0.005 |
Unilateral | 31 | 41 (1 case is recurrence) | |
Bilateral | 2 | 3 | |
Infectious uveitis | 9 | 6 | |
IL-6 levels | 9023.1 ± 12,792.8 | 87.55 ± 99.34 | p = 0.135 |
Non-infectious uveitis | 26 | 41 | |
IL-6 levels | 5296.8 ± 14,412.6 | 305.4 ± 794.4 | p = 0.03 |
Lab data | |||
WBC (/μL) | 6298.6 ± 2504.0 | 6338.1 ± 1868.5 | p = 0.231 |
CRP (mg/L) | 1.30 ± 3.72 | 0.23 ± 0.56 | p = 0.057 |
A. In All Cases (N = 82). | |||
---|---|---|---|
Variable | Regression Coefficient | 95% CI | p-Value |
Age | −24.07 | −128.16–80.00 | 0.65 |
Gender(male) | −3254.23 | −6473.73–−34.72 | 0.048 * |
WBC | 0.11 | −0.70–0.93 | 0.78 |
CRP | 2500.15 | 1794.47–3205.82 | <0.01 * |
B. In infectious uveitis cases (N = 15). | |||
Variable | Regression coefficient | 95% CI | p-value |
Age | 130.50 | −239.70–500.70 | 0.45 |
Gender | −10,253.93 | −24,931.07–4425.21 | 0.15 |
WBC | 0.53 | −2.63–3.71 | 0.71 |
CRP | −1006.21 | −14,127.39–12,114.98 | 0.87 |
C. In non-infectious uveitis cases (N = 67). | |||
Variable | regression coefficient | 95% CI | p-value |
Age | −48.38 | −145.47–48.71 | 0.32 |
Gender | −1565.76 | −4459.90–1328.38 | 0.28 |
WBC | −0.15 | −0.94–0.65 | 0.71 |
CRP | 2734.08 | 2127.56–3340.61 | <0.01 * |
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Sakai, A.; Tagami, M.; Katsuyama-Yoshikawa, A.; Misawa, N.; Haruna, Y.; Azumi, A.; Honda, S. Relationship between Vitreous IL-6 Levels, Gender Differences and C-Reactive Protein (CRP) in a Blood Sample of Posterior Uveitis. J. Clin. Med. 2023, 12, 1720. https://doi.org/10.3390/jcm12051720
Sakai A, Tagami M, Katsuyama-Yoshikawa A, Misawa N, Haruna Y, Azumi A, Honda S. Relationship between Vitreous IL-6 Levels, Gender Differences and C-Reactive Protein (CRP) in a Blood Sample of Posterior Uveitis. Journal of Clinical Medicine. 2023; 12(5):1720. https://doi.org/10.3390/jcm12051720
Chicago/Turabian StyleSakai, Atsushi, Mizuki Tagami, Atsuko Katsuyama-Yoshikawa, Norihiko Misawa, Yusuke Haruna, Atsushi Azumi, and Shigeru Honda. 2023. "Relationship between Vitreous IL-6 Levels, Gender Differences and C-Reactive Protein (CRP) in a Blood Sample of Posterior Uveitis" Journal of Clinical Medicine 12, no. 5: 1720. https://doi.org/10.3390/jcm12051720
APA StyleSakai, A., Tagami, M., Katsuyama-Yoshikawa, A., Misawa, N., Haruna, Y., Azumi, A., & Honda, S. (2023). Relationship between Vitreous IL-6 Levels, Gender Differences and C-Reactive Protein (CRP) in a Blood Sample of Posterior Uveitis. Journal of Clinical Medicine, 12(5), 1720. https://doi.org/10.3390/jcm12051720