Please ensure Javascript is enabled for purposes of website accessibility
ORIGINAL PAPER
Retinal thickness in patients with elevated D-dimer and interleukin-6 levels as a result of SARS-CoV-2 infection
 
More details
Hide details
1
Collegium Medicum, Jan Kochanowski University, Kielce, Poland
 
2
Ophthalmic Clinic, Voivodeship Hospital, Kielce, Poland
 
3
Department of Infectious Disease, Voivodeship Hospital, Kielce, Poland
 
4
Department of Vitreoretinal Surgery, Medical University of Lublin, Lublin, Poland
 
5
Institute of Medical Science, Jan Kochanowski University, Kielce, Poland
 
6
Ophthalmology Clinic Boni Fratres Lodziensis, Lodz, Poland.
 
 
Submission date: 2023-09-21
 
 
Final revision date: 2023-11-22
 
 
Acceptance date: 2023-12-05
 
 
Publication date: 2023-12-30
 
 
Corresponding author
Michał Brzdęk
Michał Brzdęk   Collegium Medicum Jan Kochanowski University Department of Infectious Disease Voivodeship Hospital Kielce, Poland
 
 
Medical Studies 2023;39(4):342-351
 
KEYWORDS
TOPICS
ABSTRACT
Introduction:
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) can lead to various health issues, including severe pneumonia, organ damage, as well as effects on the retina. Researchers have detected SARS-CoV-2 in the retinas of infected patients, and new imaging methods, such as optical coherence tomography (OCT), are being used to investigate its impact on the eye.

Aim of the research:
To document changes in retinal thickness (RT) and their association with saturation (SpO2), D-dimers, and interleukin-6 (IL-6) levels in coronavirus disease 2019 (COVID-19) patients hospitalized for bilateral pneumonia.

Material and methods:
This prospective study included COVID-19 patients assessed after 2 months (Group 1) and re-evaluated after 8 months from hospital discharge (Group 2). RT was automatically assessed with OCT. Group 2 RT measurements were compared with those of healthy subjects, and D-dimers, IL-6, and SpO2 levels on admission were correlated with RT in group 1.

Results:
Group 2 exhibited a significant decrease in RT compared to group 1 in specific macular regions, accompanied by an increase in certain areas. Moreover, Group 2 demonstrated increased RT compared to a control group in specific regions. A positive correlation was observed between SpO2 ≤ 90% and RT in Group 1 in specific macular regions.

Conclusions:
RT in patients after SARS-CoV-2 infection is altered at the 6-month follow-up. Hypoxia, hypercoagulability, and inflammation in COVID-19 can collectively influence RT.
REFERENCES (38)
1.
Lani-Louzada R, Ramos C do VF, Cordeiro RM, Sadun AA. Retinal changes in COVID-19 hospitalized cases. PLoS One 2020; 15: e0243346.
 
2.
Jevnikar K, Meglič A, Lapajne L, Logar M, Vidovič Valentinčič N, Globočnik Petrovič M, Mekjavic PJ. The comparison of retinal microvascular findings in acute COVID-19 and 1-year after hospital discharge assessed with multimodal imaging – a prospective longitudinal cohort study. Int J Mol Sci 2023; 24: 4032.
 
3.
Jevnikar K, Meglič A, Lapajne L, Logar M, Vidovič Valentinčič N, Globočnik Petrovič M, Mekjavic PJ. The impact of acute COVID-19 on the retinal microvasculature assessed with multimodal imaging. Graefes Arch Clin Exp Ophthalmol 2023; 261: 1115-1125.
 
4.
González-Zamora J, Bilbao-Malavé V, Gándara E, Casablanca-Piñera A, Boquera-Ventosa C, Landecho MF, Zarranz-Ventura J, García-Layana A. Retinal microvascular impairment in COVID-19 bilateral pneumonia assessed by optical coherence tomography angiography. Biomedicines 2021; 9: 247.
 
5.
Casagrande M, Fitzek A, Püschel K, Aleshcheva G, Schultheiss HP, Berneking L, Spitzer MS, Schultheiss M. Detection of SARS-CoV-2 in human retinal biopsies of deceased COVID-19 patients. Ocul Immunol Inflamm 2020; 28: 721-725.
 
6.
Giannis D, Ziogas IA, Gianni P. Coagulation disorders in coronavirus infected patients: COVID-19, SARS-CoV-1, MERS-CoV and lessons from the past. J Clin Virol 2020; 127: 104362.
 
7.
Rodriguez-Morales AJ, Cardona-Ospina JA, Gutiérrez-Ocampo E, Villamizar-Peña R, Holguin-Rivera Y, Escalera-Antezana JP, Alvarado-Arnez LE, Bonilla-Aldana DK, Franco-Paredes C, Henao-Martinez AF, Paniz-Mondolfi A, Lagos-Grisales GJ, Ramírez-Vallejo E, Suárez JA, Zambrano LI, Villamil-Gómez WE, Balbin-Ramon GJ, Rabaan AA, Harapan H, Dhama K, Nishiura H, Kataoka H, Ahmad T, Sah R; Latin American Network of Coronavirus Disease 2019-COVID-19 Research (LANCOVID-19). Electronic address: https://www.lancovid.org Clinical, laboratory and imaging features of COVID-19: a systematic review and meta-analysis. Travel Med Infect Dis 2020; 34: 101623.
 
8.
Grifoni E, Valoriani A, Cei F, Lamanna R, Gelli AMG, Ciambotti B, Vannucchi V, Moroni F, Pelagatti L, Tarquini R, Landini G, Vanni S, Masotti L. Interleukin-6 as prognosticator in patients with COVID-19. J Infect 2020; 81: 452-482.
 
9.
Kal M, Winiarczyk M, Mackiewicz J, Odrobina D, Cieśla E, Płatkowska-Adamska B, Biskup M, Pabjan P, Zarębska-Michaluk D. The effect of reduced oxygen saturation on retinal microvascularization in COVID-19 patients with bilateral pneumonia based on optical coherence tomography study. J Pers Med 2022; 12: 1824.
 
10.
Idell S. Coagulation, fibrinolysis, and fibrin deposition in acute lung injury. Crit Care Med 2003; 31: S213-S220.
 
11.
Welty-Wolf KE, Carraway MS, Ortel TL, Piantadosi CA. Coagulation and inflammation in acute lung injury. Thromb Haemost 2002; 88: 17-25.
 
12.
Terpos E, Ntanasis-Stathopoulos I, Elalamy I, Kastritis E, Sergentanis TN, Politou M, Psaltopoulou T, Gerotziafas G, Dimopoulos MA. Hematological findings and complications of COVID-19. Am J Hematol 2020; 95: 834-847.
 
13.
Panigada M, Bottino N, Tagliabue P, Grasselli G, Novembrino C, Chantarangkul V, Pesenti A, Peyvandi F, Tripodi A. Hypercoagulability of COVID-19 patients in intensive care unit: a report of thromboelastography findings and other parameters of hemostasis. J Thromb Haemost 2020; 18: 1738-1742.
 
14.
Han H, Yang L, Liu R, Liu F, Wu KL, Li J, Liu XH, Zhu CL. Prominent changes in blood coagulation of patients with SARS-CoV-2 infection. Clin Chem Lab Med 2020; 58: 1116-1120.
 
15.
Tang N, Li D, Wang X, Sun Z. Abnormal coagulation parameters are associated with poor prognosis in patients with novel coronavirus pneumonia. J Thromb Haemost 2020; 18: 844-847.
 
16.
Płatkowska B, Kal M, Biskup M. Optical coherence tomography angiography – use in ophthalmological practice. Med Stud 2020; 36: 195-205.
 
17.
Kal M, Winiarczyk M, Cieśla E, Płatkowska-Adamska B, Walczyk A, Biskup M, Pabjan P, Głuszek S, Odrobina D, Mackiewicz J, Zarębska-Michaluk D. Retinal microvascular changes in COVID-19 bilateral pneumonia based on optical coherence tomography angiography. J Clin Med 2022; 11: 3621.
 
18.
Huber R, Adler DC, Fujimoto JG. Buffered Fourier domain mode locking: unidirectional swept laser sources for optical coherence tomography imaging at 370,000 lines/s. Opt Lett 2006; 31: 2975.
 
19.
Waldstein SM, Faatz H, Szimacsek M, Glodan AM, Podkowinski D, Montuoro A, Simader C, Gerendas BS, Schmidt-Erfurth U. Comparison of penetration depth in choroidal imaging using swept source vs spectral domain optical coherence tomography. Eye 2015; 29: 409-415.
 
20.
Michalewska Z. Swept Source OCT (SS-OCT) – czyli jak zajrzeć głębiej?, Topcon News Magazyn Informacyjny Topcon Polska 3/2014.
 
21.
Pogrzebielski A. Medycyna Praktyczna dla lekarzy. Aktualne nazewnictwo warstw siatkówki i naczyniówki w OCT – konsensus panelu ekspertów International Nomenclature for Optical Coherence Tomography. 22.01.2016. Available: https://www.mp.pl/okulistyka/p....
 
22.
Flisiak R, Horban A, Jaroszewicz J, Kozielewicz D, Pawłowska M, Parczewski M, Piekarska A, Simon K, Tomasiewicz K, Zarębska-Michaluk D. Recommendations of management in SARS-CoV-2 infection of the Polish Association of Epidemiologists and Infectiologists. Pol Arch Med Wewn 2022; 132: 16230. 0.
 
23.
Flisiak R, Horban A, Jaroszewicz J, Kozielewicz D, Pawłowska M, Parczewski M, Piekarska A, Simon K, Tomasiewicz K, Zarębska-Michaluk D. Annex #1 as of 8 June 2020 to: Management of SARS-CoV-2 infection: recommendations of the Polish Association of Epidemiologists and Infectiologists as of March 31, 2020. Pol Arch Med Wewn 2020; 130: 352-357. doi:10.20452/pamw.15424.
 
24.
Flisiak R, Parczewski M, Horban A, Jaroszewicz J, Kozielewicz D, Pawłowska M, Piekarska A, Simon K, Tomasiewicz K, Zarębska-Michaluk D. Management of SARS-CoV-2 infection: recommendations of the Polish Association of Epidemiologists and Infectiologists. Annex no. 2 as of October 13, 2020. Pol Arch Med Wewn 2020; 130: 915-918.
 
25.
Kouhpayeh S, Shariati L, Boshtam M, Rahimmanesh I, Mirian M, Esmaeili Y, Najaflu M, Khanahmad N, Zeinalian M, Trovato M, Tay FR, Khanahmad H, Makvandi P. The molecular basis of COVID-19 pathogenesis, conventional and nanomedicine therapy. Int J Mol Sci 2021; 22: 5438.
 
26.
Orlewska K, Klusek J, Zarębska-Michaluk D, Kocańda K, Oblap R, Cedro A, Witczak B, Klusek J, Śliwczyński A, Orlewska E. Association between glutathione S-transferases gene variants and COVID-19 severity in previously vaccinated and unvaccinated Polish patients with confirmed SARS-CoV-2 infection. Int J Environ Res Public Health 2023; 20: 3752.
 
27.
Bilbao-Malavé V, González-Zamora J, Saenz de Viteri M, de la Puente M, Gándara E, Casablanca-Piñera A, Boquera-Ventosa C, Zarranz-Ventura J, Landecho M, García-Layana A. Persistent retinal microvascular impairment in COVID-19 bilateral pneumonia at 6-months follow-up assessed by optical coherence tomography angiography. Biomedicines 2021; 9: 502.
 
28.
Furashova O, Matthé E. Retinal changes in different grades of retinal artery occlusion: an optical coherence tomography study. Invest Ophthalmol Vis Sci 2017; 58: 5209.
 
29.
Mesentier-Louro LA, Shariati MA, Dalal R, Camargo A, Kumar V, Shamskhou EA, se Jesus Perez V, Liao YJ. Systemic hypoxia led to little retinal neuronal loss and dramatic optic nerve glial response. Exp Eye Res 2020; 193: 107957.
 
30.
Lam TT, Abler AS, Tso MO. Apoptosis and caspases after ischemia-reperfusion injury in rat retina. Invest Ophthalmol Vis Sci 1999; 40: 967-975.
 
31.
Mittag TW, Danias J, Pohorenec G, Yuan HM, Burakgazi E, Chalmers-Redman R, Podos SM, Tatton WG. Retinal damage after 3 to 4 months of elevated intraocular pressure in a rat glaucoma model. Invest Ophthalmol Vis Sci 2000; 41: 3451-3459.
 
32.
Paranjpe I, Fuster V, Lala A, Russak AJ, Glicksberg BS, Levin MA, Charney AW, Narula J, Fayad ZA, Bagiella E, Zhao S, Nadkarni GN. Association of treatment dose anticoagulation with in-hospital survival among hospitalized patients with COVID-19. J Am Coll Cardiol 2020; 76: 122-124.
 
33.
Lehmann A, Prosch H, Zehetmayer S, Gysan MR, Bernitzky D, Vonbank K, Idzko M, Gompelmann D. Impact of persistent D-dimer elevation following recovery from COVID-19. PLoS One 2021; 16: e0258351.
 
34.
Guemes-Villahoz N, Burgos-Blasco B, Vidal-Villegas B, Donate-López J, Martín-Sánchez FJ, Porta-Etessam J, López-Guajardo L, Martín JLR, González-Armengol JJ, García-Feijoó J. Reduced retinal vessel density in COVID-19 patients and elevated D-dimer levels during the acute phase of the infection. Med Clin (Barc) 2021; 156: 541-546.
 
35.
Chen G, Wu D, Guo W, Cao Y, Huang D, Wang H, Zhang X, Chen H, Yu H, Zhang X, Zhang M, Wu S, Song J, Chen T, Han M, Li S, Luo X, Zhao J, Ning Q. Clinical and immunological features of severe and moderate coronavirus disease 2019. J Clin Invest 2020; 130: 2620-2629.
 
36.
Chauhan AJ, Wiffen LJ, Brown TP. COVID-19: a collision of complement, coagulation and inflammatory pathways. J Thromb Haemost 2020; 18: 2110-2117.
 
37.
Fei Y, Tang N, Liu H, Cao W. Coagulation dysfunction. Arch Pathol Lab Me. 2020; 144: 1223-1229.
 
38.
Noma H, Mimura T, Eguchi S. Association of inflammatory factors with macular edema in branch retinal vein occlusion. JAMA Ophthalmol 2013; 131: 160.
 
eISSN:2300-6722
ISSN:1899-1874
Journals System - logo
Scroll to top