Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of its Relationship with Complete Blood Count Parameters

Mehmet Ramazan Şekeroğlu; Erdem Çokluk; Selcuk Yaylacı; Ali Fuat Erdem; Fatıma Betül Tuncer; Hamad Dheir; Ertuğrul Güçlü; Aziz Öğütlü; Deniz Çekiç; Abdülkadir Aydın; Fatma Behice Serinkan Cinemre

doi:10.18521/ktd.917364

Research Article

Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of its Relationship with Complete Blood Count Parameters

Year 2021, , 460 - 467, 30.08.2021

Mehmet Ramazan Şekeroğlu , Erdem Çokluk , Selcuk Yaylacı , Ali Fuat Erdem , Fatıma Betül Tuncer , Hamad Dheir , Ertuğrul Güçlü , Aziz Öğütlü , Deniz Çekiç , Abdülkadir Aydın , Fatma Behice Serinkan Cinemre

https://doi.org/10.18521/ktd.917364

Cited By: 2

Abstract

Objective: In this study, we aimed to evaluate the relationship between thiol-disulfide homoeostasis and hemogram parameters in COVID-19 patients.
Methods: Total thiol(TT), Native thiol(NT), dynamic disulfide status(DDS), DDS/NT, DDS/TT, NT/TT ratio and CBC parameters were analyzed in 68 patients with positive COVID-19 and 31 healthy individuals.
Results: TT, NT, DD, hemoglobin and hematocrit levels were higher in the control group than in patient groups. TT, NT, DD and lymphocyte levels of COVID-19 patients treated in medical floor were higher than those treated in intensive care unit; WBC, neutrophil and NLR were low(P<0.05).PLR was higher in intensive care patients compared with the control group(P<0.05).COVID-19 patients who did not need mechanical ventilation were retrospectively evaluated according to their mortality. TT, NT, DDS and lymphocyte levels were higher; WBC, Neutrophil, PLR and NLR were lower(P<0.05) in survivors. The diagnostic performance of TT, NT and DDS levels to define requirement of intensive care treatment in COVID-19 patients were evaluated by using Receiver Operating Characteristic (ROC) curve analysis. By using ROC analysis, the optimum cut-off points for of TT, NT and DDS levels showed high sensitivity and specificity for requirement of intensive care treatment(P<0.05).
Conclusions: According to our results, it has been observed that the thiol-disulfide balance is disrupted In COVID-19 patients. It may be beneficial to monitor the thiol-disulfide balance in the follow-up and treatment of the patients.

Keywords

COVID-19, Total Thiol, Native Thiol, Dynamic Disulfide Status, Complete Blood Count

References

1. Perlman S. Another decade, another coronavirus. N Engl J Med. 2020;382(8):760-62. doi: 10.1056/NEJMe2001126.
2. Shah SGS, Farrow A. A commentary on “World Health Organization declares global emergency: A review of the 2019 novel Coronavirus (COVID-19)”. Int J Surg. 2020; 76:128-9. doi: 10.1016/j.ijsu.2020.03.001.
3. Weiss SR, Leibowitz JL. Coronavirus pathogenesis, in Advances in virus research. Adv Virus Res. 2011;81:85-164. doi: 10.1016/B978-0-12-385885-6.00009-2.
4. Kerget B, Kerget F, Kocak AO, Kızıltunç A, Araz Ö, Uçar EY, et al. Are Serum Interleukin 6 and Surfactant Protein D Levels Associated with the Clinical Course of COVID-19? Lung. 2020;198(5):777-84. doi: 10.1007/s00408-020-00393-8.
5. Mathys L, Balzarini J. The role of cellular oxidoreductases in viral entry and virus infection-associated oxidative stress: potential therapeutic applications. Expert Opin Ther Targets.2016;20(1):123-43. doi: 10.1517/14728222.2015.1068760.
6. Pernice F, Floccori F, Nostro L, Caccamo C, Belghity N, Mantuano S, et al. Oxidative stress, sister chromatid exchanges and apoptosis in the pathogenesis of lymphocytopenia in ESRD patients. J Nephrol 2006;19(5):613-20. https://pubmed.ncbi.nlm.nih.gov/17136690/
7. Harrison SC Viral membrane fusion. Virology 479-480:498-507. doi: 10.1016/j.virol.2015.03.043.
8. Fenouillet E, Barbouche R, Jones IM. Cell entry by enveloped viruses: redox considerations for HIV and SARS-coronavirus. Antioxid Redox Signal 2007; 9(8):1009-34. doi: 10.1089/ars.2007.1639.
9. Ivanov AV, Eliiston VT, Ivanova ON, Kochetkov SN, Starodubova ES, Bartosch B, et al. Oxidative stress during HIV infection: mechanisms and consequences. Oxid Med Cell Longev. 2016:8910396. doi: 10.1155/2016/8910396.
10. Camini FC, Cameino CC, Almeida LT, de Brito Magalhães CL. Implications of oxidative stress on viral pathogenesis. Arch Virol. 2017;162(4):907-17. doi: 10.1007/s00705-016-3187-y.
11. Kayacan Y, Yazar H, Kısa EC, Ghojebeigloo BE. A novel biomarker explaining the role of oxidative stress in exercise and l-tyrosine supplementation: thiol/disulphide homeostasis. Arch Physiol Biochem. 2018;124(3):232-36. doi: 10.1080/13813455.2017.1388410.
12. Kayacan Y, Yazar H, Cerit G, Ghojebeigloo BE. A new oxidative stress indicator: Effect of 5-hydroxytryptophan on thiol-disulfide homeostasis in exercise. Nutrition.2019;63-64:114-19. doi: 10.1016/j.nut.2019.01.013.
13. Erenler AK,Yardan T. Clinical Utility of Thiol/Disulfide Homeostasis. Clin Lab. 2017;63(5):867-70. doi: 10.7754/Clin.Lab.2017.161117..
14. Erel O, Neselioglu S A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014;47(18):326-32. doi: 10.1016/j.clinbiochem.2014.09.026.
15. Ates I, Ozkayar N, Inan B, Yilmaz FM, Topcuoglu C, Neselioglu S, et al. Dynamic thiol/disulphide homeostasis in patients with newly diagnosed primary hypertension. J Am Soc Hypertens. 2016;10(2):159-66. doi: 10.1016/j.jash.2015.12.008.
16. Turell L, Rad, R, Alvarez B. The thiol pool in human plasma: the central contribution of albumin to redox processes. Free Radic Biol Med. 2013;65:244-253. doi: 10.1016/j.freeradbiomed.2013.05.050.
17. Kumar S, Gıpta E, Kaushik S. Evaluation of oxidative stress and antioxidant status: Correlation with the severity of sepsis. Scand J Immunol. 2018;87(4):e12653. doi: 10.1111/sji.12653.
18. Lorente L, Martín MM, Almeida T, Abreu-González P, Ferreres J, Solé-Violán J, et al. Association between serum total antioxidant capacity and mortality in severe septic patients. J Crit Care. 2015;30(1):217.e7-12. doi: 10.1016/j.jcrc.2014.09.012.
19. Esen R, Aslan M, Kücükoğlu ME, Cıkman A, Yakan U, Sunnetcioglu M, et al. Serum paraoxonase activity, total thiols levels, and oxidative status in patients with acute brucellosis. Wien Klin Wochenschr. 2015;127(11-12):427-33. doi: 10.1007/s00508-015-0720-z.
20. Checconi P, Angali MD, Marcocci ME, Fraternale A, Magnani M, Palamara AT, et al. Redox-Modulating Agents in the Treatment of Viral Infections. Int J Mol Sci. 2020;8;21(11):4084. doi: 10.3390/ijms21114084.
21. Galley HF, Lowes DA, Allen L, Cameron G, Aucott LS, Webster NR. Melatonin as a potential therapy for sepsis: a phase I dose escalation study and an ex vivo whole blood model under conditions of sepsis. J Pineal Res. 2014;56(4):427-38. doi: 10.1111/jpi.12134.
22. Ayara G, Sahin S,Atmaca YM, Uysal Yazici M, Neselioglu S, Erel O. Thiol-disulphide homeostasis is an oxidative stress indicator in critically ill children with sepsis. Arch Argent Pediatr. 2019;117(3):143-8. doi: 10.5546/aap.2019.eng.143.
23. Aydogan S, Akduman H, Dilli D, Koyuncu E, Çitli R, Erel Ö, Neselioglu S, et al. The role of thiol–disulfide homeostasis in neonatal sepsis. J Matern Fetal Neonatal Med. 2019;8;1-7. doi: 10.1080/14767058.2019.1638904.
24. Kara S, Erel O, Demirdağ TB, Yayla BC, Gulhan B, Neselioglu S, et al. Alteration of thiol-disulphide homeostasis in acute tonsillopharyngitis. Redox Rep. 2017; 22(5):205-209. doi: 10.1080/13510002.2016.1173328.
25. Liu W, Li H. COVID-19: attacks the 1-beta chain of hemoglobin and captures the porphyrin to inhibit human heme metabolism. Preprint revised.2020;10 (04).
26. Patruta SI, Hörl WH. Iron and infection. Kidney Int Suppl. 1999;69:S125-30. doi: 10.1046/j.1523-1755.1999.055suppl.69125.x.
27. Rudd MJ, Good MF, Chapman DE, Powell LW, Halliday JW. Clonal analysis of the effect of iron on human cytotoxic and proliferating T lymphocytes. Immunol Cell Biol. 1990;68 (5):317-24. doi: 10.1038/icb.1990.43.
28. Husain N, Mahmood R. Copper (II) generates ROS and RNS, impairs antioxidant system and damages membrane and DNA in human blood cells. Environ Sci Pollut Res Int. 2019; 26(20):20654-68. doi: 10.1007/s11356-019-05345-1.
29. Nazima B, Manoharan V, Miltonprabu S. Oxidative stress induced by cadmium in the plasma, erythrocytes and lymphocytes of rats: Attenuation by grape seed proanthocyanidins. Hum Exp Toxicol. 2016;35(4):428-47. doi: 10.1177/0960327115591376.
30. Diederich L, Suvorava T, Sansone R, Keller TCS, Barbarino F, Sutton TR, et al. On the effects of reactive oxygen species and nitric oxide on red blood cell deformability. Front Physiol. 2018;11;9:332. doi: 10.3389/fphys.2018.00332.
31. Liu Y, Du X, Chen J, Jin Y, Jin Y, Peng L, Wang HHX, et al. Neutrophil-to-lymphocyte ratio as an independent risk factor for mortality in hospitalized patients with COVID-19. J Infect. 2020;81(1):e6-e12. doi: 10.1016/j.jinf.2020.04.002.
32. Mo P, Xing Y, Xiao Y, Deng L, Zhao Q, Wang H, et al. Clinical characteristics of refractory COVID-19 pneumonia in Wuhan, China. Clin Infect Dis. 2020 Mar 16;ciaa270. doi: 10.1093/cid/ciaa270.
33. Lagunas‐Rangel FA. Neutrophil‐to‐lymphocyte ratio and lymphocyte‐to‐C‐reactive protein ratio in patients with severe coronavirus disease 2019 (COVID‐19): A meta‐analysis. J Med Virol. 2020; 92(10):1733-4. doi: 10.1002/jmv.25819.
34. Tatum D, Taghavi S, Houghton A, Stover J, Toraih E, Duchesne J. Neutrophil-to-lymphocyte ratio and outcomes in Louisiana COVID-19 patients. Shock. 2020;54(5):652-8. doi: 10.1097/SHK.0000000000001585.
35. Xia X, Wen M, Zhan S, He J, Chen W. An increased neutrophil/lymphocyte ratio is an early warning signal of severe COVID-19. 2020;40(3):333-336. doi: 10.12122/j.issn.1673-4254.2020.03.06.

COVID-19'da Tiyol-Disülfid Dengesi: Tam Kan Sayımı Parametreleri ile İlişkisinin Değerlendirilmesi

Year 2021, , 460 - 467, 30.08.2021

https://doi.org/10.18521/ktd.917364

Cited By: 2

Abstract

Amaç: Bu çalışmada, COVID-19 hastalarında tiyol-disülfid homoeostazı ile hemogram parametreleri arasındaki ilişkiyi değerlendirmeyi amaçladık.
Gereç Yöntem: Total tiyol (TT), Native tiyol (NT), dinamik disülfid durumu (DDS), DDS / NT, DDS / TT, NT / TT oranı ve CBC parametreleri COVID-19 pozitif 68 hasta ve 31 sağlıklı bireyde analiz edildi.
Bulgular: Kontrol grubunda TT, NT, DD, hemoglobin ve hematokrit düzeyleri hasta gruplarına göre daha yüksekti. Serviste tedavi gören COVID-19 hastalarının TT, NT, DD ve lenfosit seviyeleri yoğun bakım ünitesinde tedavi edilenlere göre daha yüksekti; WBC, nötrofil ve NLO düşüktü (P <0.05). Yoğun bakım hastalarında PLR, kontrol grubuna göre daha yüksekti (P <0.05). Mekanik ventilasyona ihtiyaç duymayan COVID-19 hastaları mortalitelerine göre geriye dönük olarak değerlendirildi. TT, NT, DDS ve lenfosit seviyeleri daha yüksekti; Hayatta kalanlarda WBC, Nötrofil, PLR ve NLR daha düşüktü (P <0.05). COVID-19 hastalarında yoğun bakım tedavisi gereksinimini tanımlamak için TT, NT ve DDS düzeylerinin tanısal performansı, ROC eğrisi analizi kullanılarak değerlendirildi. ROC analizine göre, yoğun bakım tedavisi gereksinimi için TT, NT ve DDS düzeyleri optimum kestirim değerlerinde, yüksek duyarlılık ve özgüllük göstermiştir (P <0.05).
Sonuç: Sonuçlarımıza göre COVID-19 hastalarında tiyol-disülfid dengesinin bozulduğu görüldü. Hastaların takip ve tedavisinde tiyol-disülfid dengesinin izlenmesi faydalı olabilir.

Keywords

COVID-19, toplam tiyol, doğal tiyol, Dinamik Disülfür Durumu, Tam Kan Sayımı

References

1. Perlman S. Another decade, another coronavirus. N Engl J Med. 2020;382(8):760-62. doi: 10.1056/NEJMe2001126.
2. Shah SGS, Farrow A. A commentary on “World Health Organization declares global emergency: A review of the 2019 novel Coronavirus (COVID-19)”. Int J Surg. 2020; 76:128-9. doi: 10.1016/j.ijsu.2020.03.001.
3. Weiss SR, Leibowitz JL. Coronavirus pathogenesis, in Advances in virus research. Adv Virus Res. 2011;81:85-164. doi: 10.1016/B978-0-12-385885-6.00009-2.
4. Kerget B, Kerget F, Kocak AO, Kızıltunç A, Araz Ö, Uçar EY, et al. Are Serum Interleukin 6 and Surfactant Protein D Levels Associated with the Clinical Course of COVID-19? Lung. 2020;198(5):777-84. doi: 10.1007/s00408-020-00393-8.
5. Mathys L, Balzarini J. The role of cellular oxidoreductases in viral entry and virus infection-associated oxidative stress: potential therapeutic applications. Expert Opin Ther Targets.2016;20(1):123-43. doi: 10.1517/14728222.2015.1068760.
6. Pernice F, Floccori F, Nostro L, Caccamo C, Belghity N, Mantuano S, et al. Oxidative stress, sister chromatid exchanges and apoptosis in the pathogenesis of lymphocytopenia in ESRD patients. J Nephrol 2006;19(5):613-20. https://pubmed.ncbi.nlm.nih.gov/17136690/
7. Harrison SC Viral membrane fusion. Virology 479-480:498-507. doi: 10.1016/j.virol.2015.03.043.
8. Fenouillet E, Barbouche R, Jones IM. Cell entry by enveloped viruses: redox considerations for HIV and SARS-coronavirus. Antioxid Redox Signal 2007; 9(8):1009-34. doi: 10.1089/ars.2007.1639.
9. Ivanov AV, Eliiston VT, Ivanova ON, Kochetkov SN, Starodubova ES, Bartosch B, et al. Oxidative stress during HIV infection: mechanisms and consequences. Oxid Med Cell Longev. 2016:8910396. doi: 10.1155/2016/8910396.
10. Camini FC, Cameino CC, Almeida LT, de Brito Magalhães CL. Implications of oxidative stress on viral pathogenesis. Arch Virol. 2017;162(4):907-17. doi: 10.1007/s00705-016-3187-y.
11. Kayacan Y, Yazar H, Kısa EC, Ghojebeigloo BE. A novel biomarker explaining the role of oxidative stress in exercise and l-tyrosine supplementation: thiol/disulphide homeostasis. Arch Physiol Biochem. 2018;124(3):232-36. doi: 10.1080/13813455.2017.1388410.
12. Kayacan Y, Yazar H, Cerit G, Ghojebeigloo BE. A new oxidative stress indicator: Effect of 5-hydroxytryptophan on thiol-disulfide homeostasis in exercise. Nutrition.2019;63-64:114-19. doi: 10.1016/j.nut.2019.01.013.
13. Erenler AK,Yardan T. Clinical Utility of Thiol/Disulfide Homeostasis. Clin Lab. 2017;63(5):867-70. doi: 10.7754/Clin.Lab.2017.161117..
14. Erel O, Neselioglu S A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014;47(18):326-32. doi: 10.1016/j.clinbiochem.2014.09.026.
15. Ates I, Ozkayar N, Inan B, Yilmaz FM, Topcuoglu C, Neselioglu S, et al. Dynamic thiol/disulphide homeostasis in patients with newly diagnosed primary hypertension. J Am Soc Hypertens. 2016;10(2):159-66. doi: 10.1016/j.jash.2015.12.008.
16. Turell L, Rad, R, Alvarez B. The thiol pool in human plasma: the central contribution of albumin to redox processes. Free Radic Biol Med. 2013;65:244-253. doi: 10.1016/j.freeradbiomed.2013.05.050.
17. Kumar S, Gıpta E, Kaushik S. Evaluation of oxidative stress and antioxidant status: Correlation with the severity of sepsis. Scand J Immunol. 2018;87(4):e12653. doi: 10.1111/sji.12653.
18. Lorente L, Martín MM, Almeida T, Abreu-González P, Ferreres J, Solé-Violán J, et al. Association between serum total antioxidant capacity and mortality in severe septic patients. J Crit Care. 2015;30(1):217.e7-12. doi: 10.1016/j.jcrc.2014.09.012.
19. Esen R, Aslan M, Kücükoğlu ME, Cıkman A, Yakan U, Sunnetcioglu M, et al. Serum paraoxonase activity, total thiols levels, and oxidative status in patients with acute brucellosis. Wien Klin Wochenschr. 2015;127(11-12):427-33. doi: 10.1007/s00508-015-0720-z.
20. Checconi P, Angali MD, Marcocci ME, Fraternale A, Magnani M, Palamara AT, et al. Redox-Modulating Agents in the Treatment of Viral Infections. Int J Mol Sci. 2020;8;21(11):4084. doi: 10.3390/ijms21114084.
21. Galley HF, Lowes DA, Allen L, Cameron G, Aucott LS, Webster NR. Melatonin as a potential therapy for sepsis: a phase I dose escalation study and an ex vivo whole blood model under conditions of sepsis. J Pineal Res. 2014;56(4):427-38. doi: 10.1111/jpi.12134.
22. Ayara G, Sahin S,Atmaca YM, Uysal Yazici M, Neselioglu S, Erel O. Thiol-disulphide homeostasis is an oxidative stress indicator in critically ill children with sepsis. Arch Argent Pediatr. 2019;117(3):143-8. doi: 10.5546/aap.2019.eng.143.
23. Aydogan S, Akduman H, Dilli D, Koyuncu E, Çitli R, Erel Ö, Neselioglu S, et al. The role of thiol–disulfide homeostasis in neonatal sepsis. J Matern Fetal Neonatal Med. 2019;8;1-7. doi: 10.1080/14767058.2019.1638904.
24. Kara S, Erel O, Demirdağ TB, Yayla BC, Gulhan B, Neselioglu S, et al. Alteration of thiol-disulphide homeostasis in acute tonsillopharyngitis. Redox Rep. 2017; 22(5):205-209. doi: 10.1080/13510002.2016.1173328.
25. Liu W, Li H. COVID-19: attacks the 1-beta chain of hemoglobin and captures the porphyrin to inhibit human heme metabolism. Preprint revised.2020;10 (04).
26. Patruta SI, Hörl WH. Iron and infection. Kidney Int Suppl. 1999;69:S125-30. doi: 10.1046/j.1523-1755.1999.055suppl.69125.x.
27. Rudd MJ, Good MF, Chapman DE, Powell LW, Halliday JW. Clonal analysis of the effect of iron on human cytotoxic and proliferating T lymphocytes. Immunol Cell Biol. 1990;68 (5):317-24. doi: 10.1038/icb.1990.43.
28. Husain N, Mahmood R. Copper (II) generates ROS and RNS, impairs antioxidant system and damages membrane and DNA in human blood cells. Environ Sci Pollut Res Int. 2019; 26(20):20654-68. doi: 10.1007/s11356-019-05345-1.
29. Nazima B, Manoharan V, Miltonprabu S. Oxidative stress induced by cadmium in the plasma, erythrocytes and lymphocytes of rats: Attenuation by grape seed proanthocyanidins. Hum Exp Toxicol. 2016;35(4):428-47. doi: 10.1177/0960327115591376.
30. Diederich L, Suvorava T, Sansone R, Keller TCS, Barbarino F, Sutton TR, et al. On the effects of reactive oxygen species and nitric oxide on red blood cell deformability. Front Physiol. 2018;11;9:332. doi: 10.3389/fphys.2018.00332.
31. Liu Y, Du X, Chen J, Jin Y, Jin Y, Peng L, Wang HHX, et al. Neutrophil-to-lymphocyte ratio as an independent risk factor for mortality in hospitalized patients with COVID-19. J Infect. 2020;81(1):e6-e12. doi: 10.1016/j.jinf.2020.04.002.
32. Mo P, Xing Y, Xiao Y, Deng L, Zhao Q, Wang H, et al. Clinical characteristics of refractory COVID-19 pneumonia in Wuhan, China. Clin Infect Dis. 2020 Mar 16;ciaa270. doi: 10.1093/cid/ciaa270.
33. Lagunas‐Rangel FA. Neutrophil‐to‐lymphocyte ratio and lymphocyte‐to‐C‐reactive protein ratio in patients with severe coronavirus disease 2019 (COVID‐19): A meta‐analysis. J Med Virol. 2020; 92(10):1733-4. doi: 10.1002/jmv.25819.
34. Tatum D, Taghavi S, Houghton A, Stover J, Toraih E, Duchesne J. Neutrophil-to-lymphocyte ratio and outcomes in Louisiana COVID-19 patients. Shock. 2020;54(5):652-8. doi: 10.1097/SHK.0000000000001585.
35. Xia X, Wen M, Zhan S, He J, Chen W. An increased neutrophil/lymphocyte ratio is an early warning signal of severe COVID-19. 2020;40(3):333-336. doi: 10.12122/j.issn.1673-4254.2020.03.06.

There are 35 citations in total.

Details

Primary Language	English
Subjects	Health Care Administration
Journal Section	Articles
Authors	Mehmet Ramazan Şekeroğlu 0000-0001-8383-6740 Erdem Çokluk 0000-0002-6205-5109 Selcuk Yaylacı 0000-0002-6768-7973 Ali Fuat Erdem 0000-0001-6994-397X Fatıma Betül Tuncer 0000-0002-4034-4188 Hamad Dheir 0000-0002-3569-6269 Ertuğrul Güçlü 0000-0003-2860-2831 Aziz Öğütlü 0000-0003-3840-4038 Deniz Çekiç 0000-0002-7114-9334 Abdülkadir Aydın 0000-0003-0663-586X Fatma Behice Serinkan Cinemre 0000-0002-1972-1575
Publication Date	August 30, 2021
Acceptance Date	July 14, 2021
Published in Issue	Year 2021

Cite

APA	Şekeroğlu, M. R., Çokluk, E., Yaylacı, S., Erdem, A. F., et al. (2021). Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of its Relationship with Complete Blood Count Parameters. Konuralp Medical Journal, 13(S1), 460-467. https://doi.org/10.18521/ktd.917364
AMA	Şekeroğlu MR, Çokluk E, Yaylacı S, Erdem AF, Tuncer FB, Dheir H, Güçlü E, Öğütlü A, Çekiç D, Aydın A, Serinkan Cinemre FB. Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of its Relationship with Complete Blood Count Parameters. Konuralp Medical Journal. August 2021;13(S1):460-467. doi:10.18521/ktd.917364
Chicago	Şekeroğlu, Mehmet Ramazan, Erdem Çokluk, Selcuk Yaylacı, Ali Fuat Erdem, Fatıma Betül Tuncer, Hamad Dheir, Ertuğrul Güçlü, Aziz Öğütlü, Deniz Çekiç, Abdülkadir Aydın, and Fatma Behice Serinkan Cinemre. “Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of Its Relationship With Complete Blood Count Parameters”. Konuralp Medical Journal 13, no. S1 (August 2021): 460-67. https://doi.org/10.18521/ktd.917364.
EndNote	Şekeroğlu MR, Çokluk E, Yaylacı S, Erdem AF, Tuncer FB, Dheir H, Güçlü E, Öğütlü A, Çekiç D, Aydın A, Serinkan Cinemre FB (August 1, 2021) Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of its Relationship with Complete Blood Count Parameters. Konuralp Medical Journal 13 S1 460–467.
IEEE	M. R. Şekeroğlu, “Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of its Relationship with Complete Blood Count Parameters”, Konuralp Medical Journal, vol. 13, no. S1, pp. 460–467, 2021, doi: 10.18521/ktd.917364.
ISNAD	Şekeroğlu, Mehmet Ramazan et al. “Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of Its Relationship With Complete Blood Count Parameters”. Konuralp Medical Journal 13/S1 (August 2021), 460-467. https://doi.org/10.18521/ktd.917364.
JAMA	Şekeroğlu MR, Çokluk E, Yaylacı S, Erdem AF, Tuncer FB, Dheir H, Güçlü E, Öğütlü A, Çekiç D, Aydın A, Serinkan Cinemre FB. Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of its Relationship with Complete Blood Count Parameters. Konuralp Medical Journal. 2021;13:460–467.
MLA	Şekeroğlu, Mehmet Ramazan et al. “Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of Its Relationship With Complete Blood Count Parameters”. Konuralp Medical Journal, vol. 13, no. S1, 2021, pp. 460-7, doi:10.18521/ktd.917364.
Vancouver	Şekeroğlu MR, Çokluk E, Yaylacı S, Erdem AF, Tuncer FB, Dheir H, Güçlü E, Öğütlü A, Çekiç D, Aydın A, Serinkan Cinemre FB. Thiol-Disulphide Homoeostasis in COVID-19: Evaluation of its Relationship with Complete Blood Count Parameters. Konuralp Medical Journal. 2021;13(S1):460-7.

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