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Nötrositik asitli siroz hastalarında serum ve asit sıvısı TNF-alfa, interlökin-6, nitrik oksit ve myeloperoksidaz seviyelerinin, asit enfeksiyonu açısından tanısal ve prediktif değeri

Yıl 2020, Cilt: 19 Sayı: 2, 75 - 82, 04.10.2020
https://doi.org/10.17941/agd.799360

Öz

Giriş ve Amaç: Asitli siroz hastalarında ortaya çıkan spontan asit enfeksiyonu, mortalitesi yüksek bir komplikasyondur. Çalışmamızda, spontan asit enfeksiyonu sırasında, proinflamatuvar sitokinler olan interlökin-6 ve tümör nekrozis faktör-alfanın asit sıvısı ve serumda, nitrik oksit ve myeloperoksidazın ise asit sıvısındaki düzeylerine bakıp, bu sonuçların asit enfeksiyonu açısından tanısal ve prediktif değeri olup olmadığını araştırdık. Gereç ve Yöntem: Çalışmaya alınan 40 hasta, steril asitli grup, kültür negatif nötrositik asitli grup ve spontan bakteriyel peritonitli grup olarak ayrıldı. Hastalardan başvuru anında asit sıvısı ve serum örnekleri alınarak saklandı. Daha sonra tüm olguların asit sıvısı ve serumunda immünoradyometrik yöntemle interlökin-6 ve tümör nekrozis faktör-alfa, asit sıvılarında ELISA ile myeloperoksidaz ve enzimatik yöntemle nitrik oksit düzeyleri çalışılarak üç grup birbiriyle ayrı ayrı karşılaştırıldı. Bulgular: Olguların asit sıvısı ve serum interlökin-6 düzeyi ortalaması kültür negatif nötrositik asit ve spontan bakteriyel peritonit grubunda steril asit grubundan anlamlı derecede yüksek bulunmuştur. Asit sıvısı tümör nekrozis faktör-alfa düzeyi ortalaması spontan bakteriyel peritonit grubunda steril asit grubuna kıyasla anlamlı derecede yüksek saptanırken, serum tümör nekrozis faktör-alfa düzeyi ortalamasında her üç grup arasında istatistiksel anlamlı fark saptanmamıştır. Asit sıvısı myeloperoksidaz düzeyi ortalaması kültür negatif nötrositik asit ve spontan bakteriyel peritonit grubunda steril asit grubundan anlamlı derecede yüksek bulunmuştur. Asit sıvısı nitrik oksit düzeyi ortalaması arasında ise her üç grup arasında istatistiksel anlamlı fark saptanmamıştır. Sonuç: Elde edilen bulgular, asitli siroz hastalarında, spontan asit enfeksiyonu tanısında, asit sıvısı ve serumdaki interlökin-6 ile asitteki myeloperoksidaz düzeylerinin, konvansiyonel yöntemlere yardımcı olabileceğini, nitrik oksit ve tümör nekrozis faktör-alfa değerlerinin ise tanısal açıdan uygun olmadığını düşündürmektedir.

Kaynakça

  • 1. Filik L, Unal S. Clinical and labaratory features of spontaneous bacterial peritonitis. East Afr Med J 2004;81:474-9.
  • 2. Such J, Runyon BA. Spontaneous bacterial peritonitis. Clin Infect Dis 1988;27:669-74.
  • 3. Tilg H, Diehl AM. Cytokines in alcholic and nonalcoholic steatohepatitis. N Engl J Med 2000;343:1467-76.
  • 4. Gabay C, Kushner I. Acute-phase proteins and other systemic responses to inflammation. N Engl J Med 1999;340:448-54.
  • 5. Cortas NK, Wakid NW. Determination of inorganic nitrate in serum and urine by a kinetic cadmium-reduction method. Clin Chem 1990;36:1440-3.
  • 6. Byl B, Roucloux I, Crusiaux A, Dupont E, Deviere J. Tumor necrosis factor  and interleukin 6 plasma levels in infected cirrhotic patients. Gastroenterelogy 1993;104:1492-7.
  • 7. Nussler AK, Di Silvio M, Billiar TR, et al. Stimulation of the nitirc oxide synthase pathway in human hepatocytes by cytokines and endotoxin. J Exp Med 1992;176:261-4.
  • 8. Tilg H, Wilmer A, Vogel W, et al. Serum levels of cytokines in chronic liver diseases. Gastroenterology 1992;103:264-74.
  • 9. Nakamuta M, Ohashi M, Tanabe Y, Hiroshige K, Nawata H. High plasma concentration of myelopeeroxidase in cirrhosis: a possible marker of hypersplenism. Hepatology 1993;18:1377-83.
  • 10. Gaut JP, Byun J, Tran HD, et al. Myeloperoxidase produces nitrating oxidants in vivo. J Clin Invest 2002;109:1311-9.
  • 11. Strassmann G, Jacob CO, Evans R, Beall D, Fonq M. Mechanisms of experimental cancer cachexia. Interaction between mononuclear phagocytes and colon-26 carcinoma and its relevance to IL-6 mediated cancer cachexia. J Immunol 1992;148:3674-8.
  • 12. Baykal Y. Antiinflamatuar sitokinler. GATA Bülteni 1998;40:113-7.
  • 13. Rodriguez-Ramos C, Galan F, Diaz F, et al. Expression of pro-inflammatory cytokines and their inhibitors during the course of spontaneous bacterial peritonitis. Dig Dis Sci 2001;46:1668-76.
  • 14. Navasa M, Follo A, Filella X, et al. Tumor necrosis factor and interleukin-6 in spontaneous bacterial peritonitis in cirrhosis: Relationship with the development of renal impairment and mortality. Hepatology 1998; 27:1227-32.
  • 15. Such J, Hillebrand DJ, Guarner C, et al. Tumor necrosis factor-, interleukin-6, and nitric oxide in sterile ascitic fluid and serum from patients with cirrhosis who subsequently develop ascitic fluid infection. Dig Dis Sci 2000;46:2360-6.
  • 16. Jimenez W, Ros J, Morales-Ruiz M, et al. Nitric oxide production and inducible nitric oxide synthase expression in peritoneal macrophages of cirrhotic patients. Hepatology 1999;30:670-6.
  • 17. Propst T, Propst A, Herold M, et al. Spontaneous bacterial peritonitis is associated with high levels of interleukin-6 and its secondary mediators in ascitic fluid. Eur J Clin Invest 1993;23:832-6.
  • 18. Zeni F, Tardy B, Vindimian M, et al. High levels of tumor necrosis factor- and interleukin-6 in the ascitic fluid of cirrhotic patients with spontaneous bacterial peritonitis. Clin Infect Dis 1993;17:218-23.
  • 19. Bac DJ, Pruimboom WM, Mulder PG, Zijlstra FJ, Wilson JH. High interleukin-6 production within the peritoneal cavity in decompensated cirrhosis and malignancy- related ascites. Liver 1995;15:265-70.
  • 20. Aggarval BB, Kohr WS, Hass PE. Human tumor necrosis factor. J Biol Chem 1992;260:2345-54.
  • 21. Arai K, Lee F, Miyajam A, Miyatake S, Arai N, Yokota T. Cytokines: Coordinators of immune and inflammatory responses. Ann Rev Biochem 1990;59:783-836.
  • 22. Dinarello CA, Moldawer LL. Proinflammatory and anti-inflammatory cytokines in rheumatoid arthritis. Amgen Inc, USA 2000;3-79.
  • 23. Schindler R, Mancilla J, Endres S, et al. Correlation and interactions in the production of interleukin-6 (IL-6), interleukin-1 (IL-1) and tumor necrosis factor (TNF) in human blood mononuclear cells: IL-6 suppresses IL-1 and TNF. Blood 1990;75:40-7.
  • 24. Vallance P, Moncada S. Hyperdynamic circulation in cirrhosis: a role for nitric oxide? Lancet 1991;337:776-8.
  • 25. Garcia-Tsao G, Angulo P, Garcia JC, Groszmann RJ, Cadelina G. The diagnostic and predictive value of ascites nitric oxide levels in patients with spontaneous bacterial peritonitis. Hepatology 1998;28:17-21.
  • 26. Bories PN, Campillo B, Azaou L, Scherman E. Long-lasting NO overproduction in cirrhotic patients with spontaneous bacterial peritonitis. Hepatology 1997;25:1328-33.
  • 27. Nathan C, Xie QW. Regulation of biosynthesis of nitric oxide. J Biol Ghem 1994; 269:13725-8.
  • 28. Guarner C, Soriano G, Tomas A, et al. Increased serum nitrite and nitrate levels in patients with cirrhosis: relationship to endotoxemia. Hepatology 1993;18:1139-43.
  • 29. Schultz J, Cortin R, Oddi F, Kaminker K, Jones W. Myeloperoxidase of the leukocyte of normal blood. Arch Biochem Biophys 1965;111:73-9.
  • 30. Krawisz JE, Sharon P, Stenson WF. Quantitative assay for acute intestinal inflammation based on myeloperoxidase activity. Gastroenterology 1984;87:1344-50.
  • 31. Yao V, McCauley R, Cooper D, Platell C, Hall JC. Myeloperoxidase response to peritonitis in an experimental model. ANZ J Surg 2003;73:1052-6.

Diagnostic and predictive values of serum and acid fluid TNF-alpha, interleukin-6, nitric oxide, and myeloperoxidase in patients with neutrocytic acid cirrhosis

Yıl 2020, Cilt: 19 Sayı: 2, 75 - 82, 04.10.2020
https://doi.org/10.17941/agd.799360

Öz

Bacground and Aims: Spontaneous acid infection in patients with acidic cirrhosis is a complication with a high mortality rate. This study aimed to investigate the acid fluid and serum levels of proinflammatory cytokines interleukin-6 and tumor necrosis factor-alpha and acid fluid levels of nitric oxide and myeloperoxidase during spontaneous acid infection and to identify their diagnostic and predictive applicability with regard to acid cirrhosis. Materials and methods: We included 40 patients and categorized them into the following three groups: sterile acid, culture-negative neutrocytic acid, and spontaneous bacterial peritonitis. Acid fluid and serum samples were collected from patients upon admission and then stored. In all cases, acid fluid and serum levels of interleukin-6 and tumor necrosis factor-alpha were investigated by immunoradiometric method, acid fluid levels of myeloperoxidase by ELISA method, and nitric oxide levels by enzymatic method. Subsequently, these three groups were compared with each other. Results: Serum and acid fluid levels of interleukin-6 were significantly lower in the sterile acid group than in the culture-negative neutrocytic acid and spontaneous bacterial peritonitis groups. Serum interleukin-6 levels in the culture-negative neutrocytic acid and spontaneous bacterial peritonitis groups were significantly higher than those in the sterile acid group. Moreover, the acid fluid and serum tumor necrosis factor-alpha levels in the culture-negative neutrocytic acid group were significantly higher than those in the sterile acid group; however, there was no statistical difference in the intergroup serum tumor necrosis factor-alpha levels. The acid fluid levels of myeloperoxidase were also significantly higher in the sterile acid group than in the culture-negative neutrocytic acid group and spontaneous bacterial peritonitis group. We observed no significant intergroup differences with regard to the nitric oxide levels in acid fluid. Conclusion: In chronic liver parenchyma patients with neutrocytic acid cirrhosis, acid fluid and serum levels of interleukin-6 and acid fluid levels of myeloperoxidase may help the conventional methods in diagnosing spontaneous acid infection; however, the serum levels of nitric oxide and tumor necrosis factor-alpha have no diagnostic value.

Key words: , , , , myeloperoxidase.

Kaynakça

  • 1. Filik L, Unal S. Clinical and labaratory features of spontaneous bacterial peritonitis. East Afr Med J 2004;81:474-9.
  • 2. Such J, Runyon BA. Spontaneous bacterial peritonitis. Clin Infect Dis 1988;27:669-74.
  • 3. Tilg H, Diehl AM. Cytokines in alcholic and nonalcoholic steatohepatitis. N Engl J Med 2000;343:1467-76.
  • 4. Gabay C, Kushner I. Acute-phase proteins and other systemic responses to inflammation. N Engl J Med 1999;340:448-54.
  • 5. Cortas NK, Wakid NW. Determination of inorganic nitrate in serum and urine by a kinetic cadmium-reduction method. Clin Chem 1990;36:1440-3.
  • 6. Byl B, Roucloux I, Crusiaux A, Dupont E, Deviere J. Tumor necrosis factor  and interleukin 6 plasma levels in infected cirrhotic patients. Gastroenterelogy 1993;104:1492-7.
  • 7. Nussler AK, Di Silvio M, Billiar TR, et al. Stimulation of the nitirc oxide synthase pathway in human hepatocytes by cytokines and endotoxin. J Exp Med 1992;176:261-4.
  • 8. Tilg H, Wilmer A, Vogel W, et al. Serum levels of cytokines in chronic liver diseases. Gastroenterology 1992;103:264-74.
  • 9. Nakamuta M, Ohashi M, Tanabe Y, Hiroshige K, Nawata H. High plasma concentration of myelopeeroxidase in cirrhosis: a possible marker of hypersplenism. Hepatology 1993;18:1377-83.
  • 10. Gaut JP, Byun J, Tran HD, et al. Myeloperoxidase produces nitrating oxidants in vivo. J Clin Invest 2002;109:1311-9.
  • 11. Strassmann G, Jacob CO, Evans R, Beall D, Fonq M. Mechanisms of experimental cancer cachexia. Interaction between mononuclear phagocytes and colon-26 carcinoma and its relevance to IL-6 mediated cancer cachexia. J Immunol 1992;148:3674-8.
  • 12. Baykal Y. Antiinflamatuar sitokinler. GATA Bülteni 1998;40:113-7.
  • 13. Rodriguez-Ramos C, Galan F, Diaz F, et al. Expression of pro-inflammatory cytokines and their inhibitors during the course of spontaneous bacterial peritonitis. Dig Dis Sci 2001;46:1668-76.
  • 14. Navasa M, Follo A, Filella X, et al. Tumor necrosis factor and interleukin-6 in spontaneous bacterial peritonitis in cirrhosis: Relationship with the development of renal impairment and mortality. Hepatology 1998; 27:1227-32.
  • 15. Such J, Hillebrand DJ, Guarner C, et al. Tumor necrosis factor-, interleukin-6, and nitric oxide in sterile ascitic fluid and serum from patients with cirrhosis who subsequently develop ascitic fluid infection. Dig Dis Sci 2000;46:2360-6.
  • 16. Jimenez W, Ros J, Morales-Ruiz M, et al. Nitric oxide production and inducible nitric oxide synthase expression in peritoneal macrophages of cirrhotic patients. Hepatology 1999;30:670-6.
  • 17. Propst T, Propst A, Herold M, et al. Spontaneous bacterial peritonitis is associated with high levels of interleukin-6 and its secondary mediators in ascitic fluid. Eur J Clin Invest 1993;23:832-6.
  • 18. Zeni F, Tardy B, Vindimian M, et al. High levels of tumor necrosis factor- and interleukin-6 in the ascitic fluid of cirrhotic patients with spontaneous bacterial peritonitis. Clin Infect Dis 1993;17:218-23.
  • 19. Bac DJ, Pruimboom WM, Mulder PG, Zijlstra FJ, Wilson JH. High interleukin-6 production within the peritoneal cavity in decompensated cirrhosis and malignancy- related ascites. Liver 1995;15:265-70.
  • 20. Aggarval BB, Kohr WS, Hass PE. Human tumor necrosis factor. J Biol Chem 1992;260:2345-54.
  • 21. Arai K, Lee F, Miyajam A, Miyatake S, Arai N, Yokota T. Cytokines: Coordinators of immune and inflammatory responses. Ann Rev Biochem 1990;59:783-836.
  • 22. Dinarello CA, Moldawer LL. Proinflammatory and anti-inflammatory cytokines in rheumatoid arthritis. Amgen Inc, USA 2000;3-79.
  • 23. Schindler R, Mancilla J, Endres S, et al. Correlation and interactions in the production of interleukin-6 (IL-6), interleukin-1 (IL-1) and tumor necrosis factor (TNF) in human blood mononuclear cells: IL-6 suppresses IL-1 and TNF. Blood 1990;75:40-7.
  • 24. Vallance P, Moncada S. Hyperdynamic circulation in cirrhosis: a role for nitric oxide? Lancet 1991;337:776-8.
  • 25. Garcia-Tsao G, Angulo P, Garcia JC, Groszmann RJ, Cadelina G. The diagnostic and predictive value of ascites nitric oxide levels in patients with spontaneous bacterial peritonitis. Hepatology 1998;28:17-21.
  • 26. Bories PN, Campillo B, Azaou L, Scherman E. Long-lasting NO overproduction in cirrhotic patients with spontaneous bacterial peritonitis. Hepatology 1997;25:1328-33.
  • 27. Nathan C, Xie QW. Regulation of biosynthesis of nitric oxide. J Biol Ghem 1994; 269:13725-8.
  • 28. Guarner C, Soriano G, Tomas A, et al. Increased serum nitrite and nitrate levels in patients with cirrhosis: relationship to endotoxemia. Hepatology 1993;18:1139-43.
  • 29. Schultz J, Cortin R, Oddi F, Kaminker K, Jones W. Myeloperoxidase of the leukocyte of normal blood. Arch Biochem Biophys 1965;111:73-9.
  • 30. Krawisz JE, Sharon P, Stenson WF. Quantitative assay for acute intestinal inflammation based on myeloperoxidase activity. Gastroenterology 1984;87:1344-50.
  • 31. Yao V, McCauley R, Cooper D, Platell C, Hall JC. Myeloperoxidase response to peritonitis in an experimental model. ANZ J Surg 2003;73:1052-6.
Toplam 31 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Sağlık Kurumları Yönetimi
Bölüm Makaleler
Yazarlar

Ferda Harmandar Bu kişi benim 0000-0002-7897-6658

Orbay Harmandar Bu kişi benim 0000-0003-3727-1667

Ahmet Tezel Bu kişi benim 0000-0002-3054-475X

Yayımlanma Tarihi 4 Ekim 2020
Yayımlandığı Sayı Yıl 2020 Cilt: 19 Sayı: 2

Kaynak Göster

APA Harmandar, F., Harmandar, O., & Tezel, A. (2020). Nötrositik asitli siroz hastalarında serum ve asit sıvısı TNF-alfa, interlökin-6, nitrik oksit ve myeloperoksidaz seviyelerinin, asit enfeksiyonu açısından tanısal ve prediktif değeri. Akademik Gastroenteroloji Dergisi, 19(2), 75-82. https://doi.org/10.17941/agd.799360

test-5