ENDOGENOUS INTOXICATION AND BIOCHEMICAL PROTECTION IN CHILDREN WITH CELIAC DISEASE: STATE ASSESMENT AND CORRELATION-REGRESSION ANALYSIS

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Abstract

Aim: The purpose of the study was to determine the characteristics of endogenous intoxication parameters, biochemical protection and reveal their
interaction in children with celiac disease. Materials and methods: 81 children aged from 1 to 16 years with celiac disease were examined in acute and remission periods. In erythrocytes, blood serum and urine we determined low and moderate molecular weight substances (LMMWS), oligopeptides (OP); in erythrocytes — the value of erythrocyte mechanical hemolysis (MH), malondialdehyde (MDA) content, the activity of glutathione reductase (GR) and superoxide dismutase (SOD); in blood serum — ceruloplasmin (CP) level, alcohol dehydrogenase (ADH) activity; in erythrocytes and blood serum — glutathione transferase (GT), and calculated intoxication index (II). Results: In children with celiac disease in acute and remission periods LMMWS, OP, II levels in blood were statistically significantly high, while LMMWS level in urine was low. In both periods MH activity was high (p <0.001), and GSR (p <0.001) and SOD (p <0.01) levels were low. We revealed the correlation between MDA and II (r =0.67; p =0.006), erythrocyte LMMWS and SOD (r = -0.61; p =0.015), erythrocyte LMMWS and ADH (r =0.62; p =0.006), between GT and OP in urine (r = -0.31; p =0.026), GT and MDA (r =0.68; p =0.000), GT and MH (r = -0.46; p =0.004), between MDA and CP (r =0.57; p =0.002) that made it possible to develop the models of dependence of the parameters in relation to each other. Conclusion: In celiac disease there is endogenous intoxication. The changes of the first and the second phases of biotransformation, antioxidant protection is an essential factor of the disease pathogenesis, since they have an effect on endogenous intoxication formation that should be taken into consideration in therapy.

About the authors

I. D. Uspenskaya

Nizhny Novgorod Research Institute of Children Gastroenterology

Author for correspondence.
Email: iusp@mail.ru

PhD, Head of the Department of the Clinical picture of the small intestine pathology of Nizhny Novgorod Research Institute of Children Gastroenterology

Conflict of interests
The authors have indicated they have no financial relationships relevant to this article to disclose.

Russian Federation

E. I. Shabunina

Nizhny Novgorod Research Institute of Children Gastroenterology, Russian Federation

Email: niidg@mail.ru
доктор медицинских наук, профессор, директор ННИИДГ Адрес: 603950, Нижний Новгород, ул. Семашко, д. 22, тел.: +7 (831) 436-63-70 Russian Federation

E. A. Zhukova

Nizhny Novgorod Research Institute of Children Gastroenterology, Russian Federation

Email: zhulenn@mail.ru
доктор медицинских наук, профессор, заместитель директора по научной работе ННИИДГ Адрес: 603950, Нижний Новгород, ул. Семашко, д. 22, тел.: +7 (831) 436-62-46 Russian Federation

M. V. Erzutova

Nizhny Novgorod Research Institute of Children Gastroenterology, Russian Federation

Email: ermariva@mail.ru
кандидат медицинских наук, научный сотрудник отдела Клиники патологии тонкой кишки ННИИДГ Адрес: 603950, Нижний Новгород, ул. Семашко, д. 22, тел.: +7 (831) 436-01-13 Russian Federation

L. V. Korkotashvili

Nizhny Novgorod Research Institute of Children Gastroenterology, Russian Federation

Email: lvkor@inbox.ru
кандидат биологических наук, заведующая лабораторно-диагностическим отделом ННИИДГ Адрес: 603950, Нижний Новгород, ул. Семашко, д. 22, тел.: +7 (831) 436-54-60 Russian Federation

References

  1. Husby S., Koletzko S., Korponay-Szab I.R., Mearin M.L., Phillips A., Shamir R., Troncone R., Giersiepen K., Branski D., Catassi C., Lelgeman M., M ki M. European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease. J. Pediatr. Gastroenterol. Nutr. 2012; 1: 136–160.
  2. Lionetti E., Catassi C. New clues in celiac disease epidemiology, pathogenesis, clinical manifestations, and treatment. Int. Rev. Immunol. 2011; 4: 219–231.
  3. Gujral N. Celiac disease: Prevalence, diagnosis, pathogenesis and treatment. World J. of Gastroenteroly. 2012; 42: 6036–6059.
  4. Успенская И.Д. Эндогенная интоксикация и состояние биохимической защиты у детей с муковисцидозом. Детская больница. 2009; 2: 18–23.
  5. Келина Н.Ю., Безручко Н.В., Рубцов Г.К. Биохимические проявления эндотоксикоза: методические аспекты изучения и оценки, прогностическая значимость (аналитический обзор). Вестн. Тюменского гос. ун-та. 2012; 6: 143–147.
  6. Тиунов Л.А. Механизмы естественной детоксикации и антиоксидантной защиты. Вестник РАМН. 1995; 3: 9–13.
  7. Владимиров Ю.А. Свободные радикалы в биологи- ческих системах. Соросовский образоват. журн. 2000; 12: 13–19.
  8. Walker-Smith J.A., Guandalini S., Schmitz J., Shmerling D.H., Visakorpi J.K. Revised criteria for diagnosis of coeliac disease. Report of Working Group of European Society of Paediatric Gastroenterology and Nutrition. Arch. Dis. Child. 1990; 8: 909–911.
  9. Диагностика и биокоррекция нарушений антиинфек- ционного гомеостаза в системе «мать-дитя». Книга для практического врача. Под ред. Е.И. Ефимова. Н. Новгород: НГМА. 2004. 378 с.
  10. Ishihara M. Studies on lipoperoxide of normal pregnant women and of patients with toxemia of pregnancy. Clin. Chim. Acta. 1978; 1–2: 1–9.
  11. Pinto R.E., Bartley W. The effect of age and sex on glutathione reductase and glutathione peroxidase activities and on aerobic glutathione oxidation in rat liver homogenates. Biochem. J. 1969; 1: 109–115.
  12. Kakkar P., Das B., Viswanathan P.N. A modified spectrophotometric assay of superoxide dismutase. Indian J. Biochem. Biophys. 1984; 2: 130–132.
  13. Садовникова И.В. Клинические проявления эндо- генной интоксикации и механизмы метаболической защиты организма при хронических гепатитах у детей. Совр. технол. в медицине. 2011; 3: 168–170.
  14. Федорова О.В., Федулова Э.Н., Тутина О.А., Коркоташвили Л.В. Эндогенная интоксикация при воспалительных заболеваниях кишечника у детей: обосно- вание эфферентной терапии. Совр. технол. в медицине. 2011; 3: 94–97.
  15. Uspenskaya I.D., Shirokova N.Y. Duodenal mucosa in children with coeliac disease in catamnesis and varying compliance with the gluten-free diet. Bratisl. Lek. Listy. 2014; 3: 150–155.
  16. Жукова Е.А., Грошовкина М.В., Романова С.В., Каплина Л.В., Коркоташвили Л.В. Нарушения активности ферментов первой фазы биотрансформации у детей c хроническими вирусными гепатитами C и B. Медицинский альманах. 2011; 4: 217–220.
  17. Коркоташвили Л.В., Маткивский Е.А., Жукова Е.А., Колесов С.А., Федулова Э.Н. Ферменты немикросомальной биотрансформации у детей с заболеваниями органов пищеварения. Педиатрия. 2013; 6: 6–11.
  18. Калинина Е.В., Чернов Н.Н., Алеид Р., Новичкова М.Д., Саприн А.Н., Березов Т.Т. Современные представления об антиоксидантной роли глутатиона и глутатионзависимых ферментов. Вестник РАМН. 2010; 3: 46–54.
  19. Stojiljković V., Todorović A., Radlović N., Pejić S., Mladenović M., Kasapović J., Pajović S.B. Antioxidant enzymes, glutathione and lipid peroxidation in peripheral blood of children affected by coeliac disease. Ann. Clin. Biochem. 2007; 6: 537–543.

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