Preview

Nephrology (Saint-Petersburg)

Advanced search

DIAGNOSTIC VALUE OF BLOOD NGAL, COMPLEMENT PROTEINS C3 AND C4, IMMUNOGLOBULINS IN CHILDREN WITH HEMOLYTIC-UREMIC SYNDROME

https://doi.org/10.24884/1561-6274-2017-3-39-46

Abstract

The aim: to determine changes of levels of blood neutrophil gelatinase-associated lipocalin (NGAL), complement proteins C3 and C4, immunoglobulins in children with hemolytic-uremic syndrome (HUS) and to find the relationship between them and factors determining the severity of kidney injury. A prospective study included 159 children: 35 in the acute phase of HUS, 124 – after HUS, at least 6 months after discharge from the hospital and 28 healthy children. NGAL was elevated in all children with HUS more pronounced in those who required renal replacement therapy. Activation of the alternative pathway of the complement system in HUS D «+» due to reduced C3 and normal C4 levels was found. The degree of increasing NGAL and decreasing complement C3 has a close correlation with parameters reflecting the severity of renal damage. At the onset of HUS the decreasing of IgG and IgA with normal IgM levels was found, indicating inadequate humoral protection and the risks of infectious complications.

About the Authors

S. V. Baiko
Belarusian State Medical University
Belarus

Dr., MD, PhD, 1st Department of Pediatrics, 

220016, Minsk, Narochanskaya St., 17



A. V. Sukalo
Belarusian State Medical University; Belarusian National Academy of Sciences
Belarus

Prof., MD, PhD, DMedSci, Acad., 1st Department of Pediatrics, 

220016, Minsk, Narochanskaya St., 17



A. I. Burackovski
Institute of Bioorganic Chemistry, Belarusian National Academy of Sciences
Belarus

PhD,

220141, Minsk, Kuprevich Str. 5/2



References

1. Ruggenenti P, Noris M, Remuzzi G. Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura. Kidney Int 2001; 60(3): 831–846

2. Байко СВ. Гемолитико-уремический синдром: эпидемиология, классификация, клиника, диагностика, лечение (Часть 1). Нефрология и диализ 2007; 9(4): 370–377 [Bajko SV. Gemolitiko-uremicheskij sindrom: e'pidemiologiya, klassifikaciya, klinika, diagnostika, lechenie (Chast’ 1). Nefrologiya i dializ 2007; 9(4): 370-377]

3. Loirat C, Fakhouri F, Ariceta G et al. An international consensus approach to the management of atypical hemolytic uremic syndrome in children. Pediatr Nephrol 2016; 31(1): 15–39

4. Kidney Disease: Improving Global Outcomes (KDIGO) Acute Kidney Injury Work Group. KDIGO Clinical Practice Guideline for Acute Kidney Injury. Kidney Int Suppl 2012; 2(1): 1-138

5. Uchino S. Serum creatinine. Curr Opin Crit Care 2010; 16(6): 562-567

6. Kjeldsen L, Johnsen AH, Sengeløv H et al. Isolation and primary structure of NGAL, a novel protein associated with human neutrophil gelatinase. J Biol Chem 1993; 268(14): 10425-1032

7. Kjeidsen L, Cowland JB, Borregard N. Human neutrophil gelatinase-associated lipocalin and homologous proteins in rat and mouse. Biochim Biophys Acta 2000; 1482(1-2): 272-283

8. Haase-Fielitz A, Bellomo R, Devarjan P et al. The predictive performance of plasma neutrophil gelatinase-associated lipocalin (NGAL) increases with grade of acute kidney injury. Nephrol Dial Transplant 2009; 24(11): 3349-3354

9. Mishra J, Ma O, Prada A et al. Identification of neutrophil gelatinase-associated lipocalin as a novel early biomarker for ischemic renal injury. J Am Soc Nephrol 2003; 14(10): 2534-2543

10. Adachi T. Structures and functions of antibodies. Nihon Rinsho 2005; 63(Suppl 4): 237-242

11. Cho H. Complement regulation: physiology and disease relevance. Korean J Pediatr 2015; 58(7): 239-244

12. Trachtman H, Christen E, Cnaan A et al. Urinary neutrophil gelatinase-associated lipocalcin in D+HUS: a novel marker of renal injury. Pediatr Nephrol. 2006; 21(7): 989-994

13. Ohlsson S, Wieslander J, Segelmark M. Increased circulating levels of proteinase 3 in patients with anti-neutrophilic cytoplasmic autoantibodies-associated systemic vasculitis in remission. Clin Exp Immunol 2003; 131(3): 528-535

14. Monnens L, Molenaar J, Lambert PH et al. The complement system in hemolytic-uremic syndrome in childhood. N Engl J Med 1980; 13(4): 168-171

15. Robson WL, Leung AK, Fick GH et al. Hypocomplementemia and leukocytosis in diarrhea-associated hemolytic uremic syndrome. Nephron 1992; 62(3): 296-299

16. Keir LS, Saleem MA. Current evidence for the role of complement in the pathogenesis of Shiga toxin haemolytic uraemic syndrome. Pediatr Nephrol 2014; 29(10): 1895-1902

17. Thurman JM, Marians R, Emlen W et al. Alternative pathway of complement in children with diarrhea-associated hemolytic uremic syndrome. Clin J Am Soc Nephrol 2009; 4(12): 1920-1924

18. Angioi A, Fervenza FC, Sethi S et al. Diagnosis of complement alternative pathway disorders. Kidney Int 2016; 89(2): 278-288

19. Monnens L, Samwel M, Lestijo BJ et al. Serum immunoglobulin levels in the hemolytic-uremic syndrome in children. Acta Paediatr Belg 1980; 33(3): 157-161

20. Лора Ш, Фремю-Бачи B (Loirat C, Fremeaux-Bacchi V). Атипичный гемолитико-уремический синдром. Нефрология 2012; 16(2): 16-48 [Atipichnij Gemolitiko-uremicheskij sindrom. Nefrologiya. 2012; 16(2): 16-48]


Review

For citations:


Baiko S.V., Sukalo A.V., Burackovski A.I. DIAGNOSTIC VALUE OF BLOOD NGAL, COMPLEMENT PROTEINS C3 AND C4, IMMUNOGLOBULINS IN CHILDREN WITH HEMOLYTIC-UREMIC SYNDROME. Nephrology (Saint-Petersburg). 2017;21(3):39-46. (In Russ.) https://doi.org/10.24884/1561-6274-2017-3-39-46

Views: 26356


ISSN 1561-6274 (Print)
ISSN 2541-9439 (Online)