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Yenidoğan Dönemi Pnömoni Vakalarında Dinamik Tiyol/Disülfit Dengesi

Yıl 2021, Cilt: 15 Sayı: 1, 24 - 29, 22.01.2021
https://doi.org/10.12956/tchd.746085

Öz

Amaç: Yenidoğan döneminin önemli enfeksiyonlarından biri olan pnömoni akciğerlerin enflamasyonu ile giden bir klinik tablodur. Solunum sıkıntısı olan her yenidoğan pnömoni açısından dikkatli değerlendirilmelidir. Dinamik tiyol-disülfid homeostazı antioksidan koruma, apoptoz, enzim aktivitesinin düzenlenmesi ve detoksifikasyon gibi birçok mekanizmada rol almaktadır. Bu çalışma ile yenidoğan dönemi pnömoni hastalarında tiyol-disülfid dengesini belirlemeyi amaçladık.



Gereç ve Yöntemler:
Çalışmaya Ocak 2019- Ocak 2020 tarihleri arasında pnömoni tanısı ile yatırılan 40 olgu ve kontrol grubu olarak yenidoğan polikliniğinde değerlendirilen 40 sağlıklı yenidoğan bebek, toplam 80 olgu alındı. Hasta grubunda tüm olguların fizik muayene bulguları, tam kan sayımı ve biyokimya sonuçları, akciğer grafisi, kan kültürü ve viral PCR sonuçları kaydedildi. Tüm olguların disülfid, nativ tiyol ve total tiyol değerleri çalışıldı ve oranları hesaplandı. İstatistik metodu olarak Ki-Kare testi, Independent t-testi ve Mann-Whitney-U testi kullanıldı. Çalışmada p˂0,05 değeri anlamlı olarak kabul edildi.


Bulgular:
Gruplar arasında cinsiyet dağılımı, doğum şekli, gebelik haftası ve doğum ağırlığı ortalaması açısından anlamlı fark bulunmadı (p˃0,05). Pnömoni grubunda tedavi öncesi disülfid düzeyinin nativ ve total tiyol düzeylerine oranı yüksek iken tedavi sonrası düştüğü tespit edildi (p˂0,05). Pnömoni grubunda tedavi öncesi disülfid düzeyinin nativ ve total tiyol düzeylerine oranı kontrol grubuna göre yüksek iken(p˂0,05), tedavi sonrası oranların kontrol grubu ile benzer olduğu görüldü.


Sonuç:
Bu çalışmadaki pnömoni hastalarında tedavi öncesi disülfid düzeyindeki artış ile birlikte serum nativ tiyol ve total tiyol oranlarının düşüklüğü oksidatif stresi gösterirken, tedavi sonrası tiyol düzeylerinin kontrol grubundaki gibi yüksek bulunması oksidatif stresin gerilediğini göstermektedir. Çok düşük serum düzeyleri ile çalışılabilen tiyol-disülfid dengesi tanı ve tedavi takibinde destekleyici olacaktır. 

Destekleyen Kurum

yok

Proje Numarası

yok

Teşekkür

Çalışmanın biyoistatistiksel değerlendirmesi için istatistik uzmanı sayın Aslıhan Alhan'a teşekkür ederiz.

Kaynakça

  • 1) Nissen MD. Congenital and neonatal pneumonia. Paediatr Respir Rev. 2007 Sep;8(3):195-203.
  • 2) Yoder BA, Gordon MC, Barth WH Jr. Late-preterm birth: does the changing obstetric paradigm alter the epidemiology of respiratory complications? Obstet Gynecol. 2008 Apr;111(4):814-822.
  • 3) Rathore H, Rahman AJ, Salman M, Nasir M, Sherali S. Frequency of Early-onset Neonatal Sepsis Following Prolonged Rupture of Membranes. Cureus. 2020 Feb 4;12(2): e6864.
  • 4) Scamardo MS, Dolce P, Esposito EP, Raimondi F, Triassi M, Zarrilli R. Trends, risk factors and outcomes of healthcare-associated infections in a neonatal intensive care unit in Italy during 2013-2017. Ital J Pediatr. 2020 Mar 18;46(1):34.
  • 5) Sen CK, Packer L. Thiol homeostasis and supplements in physical exercise. Am J Clin Nutr. 2000;72: 653–669.
  • 6) Köseoğlu H, Alışık M, Başaran M, et al. Dynamic thiol/disulphide homeostasis in acute pancreatitis. Turk J Gastroenterol. 2018;29:348–353.
  • 7) Erel O, Neselioglu S. A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014;47: 326–332.
  • 8) Matteucci E, Giampietro O. Thiol signalling network with an eye to diabetes. Molecules. 2010;15: 8890–8903.
  • 9) Kundi H, Ates I, Kiziltunc E, et al. A novel oxidative stress marker in acute myocardial infarction; thiol/ disulphide homeostasis. Am J Emerg Med. 2015;33: 1567–1571.
  • 10) Ates I, Kaplan M, Yuksel M, et al. Determination of thiol/disulphide homeostasis in type 1 diabetes mellitus and the factors associated with thiol oxidation. Endocrine. 2016;51:47–51.
  • 11) Asci A, Surmeli-Onay O, Erkekoglu P, et al. Oxidant and antioxidant status in neonatal proven and clinical sepsis according to selenium status. Pediatr Int. 2015; 57:1131–1137.
  • 12) Hedstrom AB, Gove NE, Mayock DE, Batra M. Performance of the Silverman Andersen Respiratory Severity Score in predicting PCO2 and respiratory support in newborns: a prospective cohort study. J Perinatol. 2018;38(5):505‐511.
  • 13) Circu ML, Aw TY. Reactive oxygen species, cellular redox systems, and apoptosis. Free Radic Biol Med. 2010;48:749–762.
  • 14) Bhuiyan MU, Blyth CC, West R, et al. Combination of clinical symptoms and blood biomarkers can improve discrimination between bacterial or viral community-acquired pneumonia in children. BMC Pulm Med. 2019;19(1):71.
  • 15) Aydogan S, Akduman H, Dilli D, et al. The role of thiol-disulfide homeostasis in neonatal sepsis [published online ahead of print, 2019 Jul 8]. J Matern Fetal Neonatal Med. 2019;1‐7.
  • 16) Kara SS, Erel O, Demirdag TB, et al. Alteration of thiol– disulphide homeostasis in acute tonsillopharyngitis. Redox Rep. 2017;22: 205–209.
  • 17) Zhang Q, Ju Y, Ma Y, Wang T. N-acetylcysteine improves oxidative stress and inflammatory response in patients with community acquired pneumonia: A randomized controlled trial. Medicine (Baltimore). 2018;97(45).
  • 18) Hosakote YM, Jantzi PD, Esham DL, et al. Viral-mediated inhibition of antioxidant enzymes contributes to the pathogenesis of severe respiratory syncytial virus bronchiolitis. Am J Respir Crit Care Med 2011;183:1550–1560.
  • 19) Kratzer E, Tian Y, Sarich N, et al. Oxidative stress contributes to lung injury and barrier dysfunction via microtubule destabilization. Am J Respir Cell Mol Biol 2012;47:688–697. 20) Andrades M, Ritter C, de Oliveira MR, et al. Antioxidant treatment reverses organ failure in rat model of sepsis: role of antioxidant enzymes imbalance, neutrophil infiltration, and oxidative stress. J Surg Res 2011;167:307–313.
  • 21) Ginter E, Simko V, Panakova V. Antioxidants in health and disease. Bratisl Lek Listy. 2014;115:603–606.
  • 22) Tekin Koruk S, Aksoy N, Hamidanoglu M, et al. The activity of paraoxonase and arylesterase in patients with osteomyelitis. Scand J Clin Lab Invest. 2012;72: 513–517.
  • 23) Duygu F, Tekin Koruk S, Aksoy N. Serum paraoxonase and arylesterase activities in various forms of hepatitis B virus infection. J Clin Lab Anal. 2011;25:311–316.
  • 24) Esen R, Aslan M, Kucukoglu ME, et al. Serum paraoxonase activity, total thiols levels, and oxidative status in patients with acute brucellosis. Wien Klin Wochenschr. 2015;127:427–433.

Dynamic Thiol / Disulfide Homeostasis in Neonatal Pneumonia

Yıl 2021, Cilt: 15 Sayı: 1, 24 - 29, 22.01.2021
https://doi.org/10.12956/tchd.746085

Öz

Objective: Pneumonia, is an important infection of the newborn period and clinic status goes with inflammation of the lungs. Every newborn with respiratory distress should be carefully evaluated for pneumonia. Dynamic thiol-disulfide homeostasis is involved in many mechanisms such as antioxidant protection, apoptosis, regulation of enzyme activity and detoxification. The aim of this study is to determine the thiol-disulfide homeostasis in neonatal pneumonia.

Material and Methods: We included data of a total of 80 cases in study, 40 patients with neonatal pneumonia and 40 healthy cases in control group admitted to hospital between January 2019- January 2020. Physical examination findings, blood count and biochemistry results, chest radiography, blood culture and viral PCR results were recorded in the patient group. Disulfide, native thiol and total thiol levels of all cases were determined and their rates were calculated. Pearson’s chi-square test, Independent t-test and Mann-Whitney-U test were used for statistical analysis, and p<0.05 was considered significant.

Results: There was no significant difference between the groups in terms of gender distribution, type of delivery, gestational week and mean of birth weight (p>0.05). Before treatment disulfide levels were higher than native and total thiol levels in the patients with pneumonia and we have seen decreased disulfide levels after treatment (p<0.05). The ratio of pre-treatment disulfide level to native and total thiol levels in pneumonia group was higher than the control group (p<0.05). But the ratio of disulfide level to native and total thiol levels after treatment were similar to the control group.

Conclusion: High pre-treatment disulfide level and low serum native thiol and total thiol levels showed oxidative stress in patients with pneumonia, while the higher thiol levels after treatment as like control group showed that oxidative stress regressed. The thiol-disulfide homeostasis, which can be studied with very low serum levels, will be supportive in diagnosis and treatment follow-up.


Proje Numarası

yok

Kaynakça

  • 1) Nissen MD. Congenital and neonatal pneumonia. Paediatr Respir Rev. 2007 Sep;8(3):195-203.
  • 2) Yoder BA, Gordon MC, Barth WH Jr. Late-preterm birth: does the changing obstetric paradigm alter the epidemiology of respiratory complications? Obstet Gynecol. 2008 Apr;111(4):814-822.
  • 3) Rathore H, Rahman AJ, Salman M, Nasir M, Sherali S. Frequency of Early-onset Neonatal Sepsis Following Prolonged Rupture of Membranes. Cureus. 2020 Feb 4;12(2): e6864.
  • 4) Scamardo MS, Dolce P, Esposito EP, Raimondi F, Triassi M, Zarrilli R. Trends, risk factors and outcomes of healthcare-associated infections in a neonatal intensive care unit in Italy during 2013-2017. Ital J Pediatr. 2020 Mar 18;46(1):34.
  • 5) Sen CK, Packer L. Thiol homeostasis and supplements in physical exercise. Am J Clin Nutr. 2000;72: 653–669.
  • 6) Köseoğlu H, Alışık M, Başaran M, et al. Dynamic thiol/disulphide homeostasis in acute pancreatitis. Turk J Gastroenterol. 2018;29:348–353.
  • 7) Erel O, Neselioglu S. A novel and automated assay for thiol/disulphide homeostasis. Clin Biochem. 2014;47: 326–332.
  • 8) Matteucci E, Giampietro O. Thiol signalling network with an eye to diabetes. Molecules. 2010;15: 8890–8903.
  • 9) Kundi H, Ates I, Kiziltunc E, et al. A novel oxidative stress marker in acute myocardial infarction; thiol/ disulphide homeostasis. Am J Emerg Med. 2015;33: 1567–1571.
  • 10) Ates I, Kaplan M, Yuksel M, et al. Determination of thiol/disulphide homeostasis in type 1 diabetes mellitus and the factors associated with thiol oxidation. Endocrine. 2016;51:47–51.
  • 11) Asci A, Surmeli-Onay O, Erkekoglu P, et al. Oxidant and antioxidant status in neonatal proven and clinical sepsis according to selenium status. Pediatr Int. 2015; 57:1131–1137.
  • 12) Hedstrom AB, Gove NE, Mayock DE, Batra M. Performance of the Silverman Andersen Respiratory Severity Score in predicting PCO2 and respiratory support in newborns: a prospective cohort study. J Perinatol. 2018;38(5):505‐511.
  • 13) Circu ML, Aw TY. Reactive oxygen species, cellular redox systems, and apoptosis. Free Radic Biol Med. 2010;48:749–762.
  • 14) Bhuiyan MU, Blyth CC, West R, et al. Combination of clinical symptoms and blood biomarkers can improve discrimination between bacterial or viral community-acquired pneumonia in children. BMC Pulm Med. 2019;19(1):71.
  • 15) Aydogan S, Akduman H, Dilli D, et al. The role of thiol-disulfide homeostasis in neonatal sepsis [published online ahead of print, 2019 Jul 8]. J Matern Fetal Neonatal Med. 2019;1‐7.
  • 16) Kara SS, Erel O, Demirdag TB, et al. Alteration of thiol– disulphide homeostasis in acute tonsillopharyngitis. Redox Rep. 2017;22: 205–209.
  • 17) Zhang Q, Ju Y, Ma Y, Wang T. N-acetylcysteine improves oxidative stress and inflammatory response in patients with community acquired pneumonia: A randomized controlled trial. Medicine (Baltimore). 2018;97(45).
  • 18) Hosakote YM, Jantzi PD, Esham DL, et al. Viral-mediated inhibition of antioxidant enzymes contributes to the pathogenesis of severe respiratory syncytial virus bronchiolitis. Am J Respir Crit Care Med 2011;183:1550–1560.
  • 19) Kratzer E, Tian Y, Sarich N, et al. Oxidative stress contributes to lung injury and barrier dysfunction via microtubule destabilization. Am J Respir Cell Mol Biol 2012;47:688–697. 20) Andrades M, Ritter C, de Oliveira MR, et al. Antioxidant treatment reverses organ failure in rat model of sepsis: role of antioxidant enzymes imbalance, neutrophil infiltration, and oxidative stress. J Surg Res 2011;167:307–313.
  • 21) Ginter E, Simko V, Panakova V. Antioxidants in health and disease. Bratisl Lek Listy. 2014;115:603–606.
  • 22) Tekin Koruk S, Aksoy N, Hamidanoglu M, et al. The activity of paraoxonase and arylesterase in patients with osteomyelitis. Scand J Clin Lab Invest. 2012;72: 513–517.
  • 23) Duygu F, Tekin Koruk S, Aksoy N. Serum paraoxonase and arylesterase activities in various forms of hepatitis B virus infection. J Clin Lab Anal. 2011;25:311–316.
  • 24) Esen R, Aslan M, Kucukoglu ME, et al. Serum paraoxonase activity, total thiols levels, and oxidative status in patients with acute brucellosis. Wien Klin Wochenschr. 2015;127:427–433.
Toplam 23 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular İç Hastalıkları
Bölüm ORIGINAL ARTICLES
Yazarlar

Ahmet Öktem 0000-0001-7209-6732

Ayşegül Zenciroğlu 0000-0002-3488-4962

Ahmet Özyazıcı 0000-0002-1389-7799

Duygu Bidev 0000-0002-0145-0551

Emine Özçelik Bu kişi benim 0000-0003-4619-8342

Dilek Dilli 0000-0003-2634-2562

Özcan Erel 0000-0002-2996-3236

Proje Numarası yok
Yayımlanma Tarihi 22 Ocak 2021
Gönderilme Tarihi 31 Mayıs 2020
Yayımlandığı Sayı Yıl 2021 Cilt: 15 Sayı: 1

Kaynak Göster

Vancouver Öktem A, Zenciroğlu A, Özyazıcı A, Bidev D, Özçelik E, Dilli D, Erel Ö. Yenidoğan Dönemi Pnömoni Vakalarında Dinamik Tiyol/Disülfit Dengesi. Türkiye Çocuk Hast Derg. 2021;15(1):24-9.

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