Evaluation of Lipid Profile changes in children with urinary tract infections
Main Article Content
Abstract
Back ground: many researches about urinary tract infection has been conducted on adults but very little has been done on children. Therefore, this research is novel in Salahaddin city-Iraq.
Urinary tract infection is a bacterial infection that affects part of the urinary tract. It affects the lower urinary tract as well as upper urinary tract. It is characterized by painful urination, urge to urinate or sometimes frequent urination. Other symptoms include fever in addition to flank pains.
Bacteria infections cause a variety of changes in lipid profile concentrations by generating free radicals. Free radicals are reactive species generated by biochemical redox interactions that occur as a part of normal cell metabolism. These free radicals may cause lipid peroxidation and damage cellular structures of organism particularly erythrocytes and endothelium. Lipid peroxidation are free radicals mediated chain of reaction that, once initiated, results in oxidative deterioration of polyunsaturated lipids. The most common goal are components of biological membrane. When propagated in biological membranes, these reaction can be initiated or enhanced by a number of toxic products, including endoperoxides and aldehydes.
Aim: The aims of this study were to evaluate the lipid profile of the children in acute phase of urinary tract infections.
Methodology: Case-control study was designed to evaluate the lipid profile change in children with lower UTI. The study was performed on 130 children with ages between (4 – 12) years, 90 children with lower UTI (34.4% male) and (65.6% female,) and 40 control (45.0% male) and (55.0% female) in pediatric department of Salahaddin Teaching hospital from May 2017 till October 2017. The data were analyzed through the SPSS V.23 application, descriptive data analysis was done through frequency, percentage, mean, standard deviation in addition to T-test to compare results.
Results: The results showed there was a significant decreased in the levels of Cholesterol, LDL, and HDL when compared to control group (144.02±17.69, 75.76±12.695, and 44.66±8.742 vs 167.65±13.13, 89.73±13.45, and 60.95±6.26 respectively), while there were a significant increase in triglycerides and VLDL in study group when compared to control group (118.03±18.66, and 23.56±3.76 vs 85.95±10.25, and 17.28±2.063 respectively).
Conclusion: These observation shows that low levels of lipid, particularly total cholesterol, low density lipoprotein (LDL), high density lipoprotein (HDL) and increased triglycerides (TG) probably be
Article Details

This work is licensed under a Creative Commons Attribution 4.0 International License.
Tikrit Journal of Pure Science is licensed under the Creative Commons Attribution 4.0 International License, which allows users to copy, create extracts, abstracts, and new works from the article, alter and revise the article, and make commercial use of the article (including reuse and/or resale of the article by commercial entities), provided the user gives appropriate credit (with a link to the formal publication through the relevant DOI), provides a link to the license, indicates if changes were made, and the licensor is not represented as endorsing the use made of the work. The authors hold the copyright for their published work on the Tikrit J. Pure Sci. website, while Tikrit J. Pure Sci. is responsible for appreciate citation of their work, which is released under CC-BY-4.0, enabling the unrestricted use, distribution, and reproduction of an article in any medium, provided that the original work is properly cited.
References
1. Nnodim J.K; Ihim A. and Uduji H. I. (2012). Attenuation of chloroquine - induced hepatoxicity and renal damage by Gnetum bucholzianum leaf extract. New Zealand Journal of medical Laboratory Science. 66:46-47.
2. Khovidhunkit, W., et al., (2004). Effects of infection and inflammation on lipid and lipoprotein metabolism: mechanisms and consequences to the host. J Lipid Res, 45(7): p. 1169-96.
3. Alvarez, C. and A. Ramos, (1986). Lipids, lipoproteins, and apoproteins in serum during infection. Clin Chem,. 32(1 Pt 1): p. 142-5.
4. Sammalkorpi, K., et al., (1988).Changes in serum lipoprotein pattern induced by acute infections. Metabolism, 37(9): p. 859-65.
5. Apostolou, F., et al., (2009). Persistence of an atherogenic lipid profile after treatment of acute infection with Brucella. J Lipid Res,50(12): p.2532-9.
6. Deniz, O., et al., (2007). Serum total cholesterol, HDL-C and LDL-C concentrations significantly correlate with the radiological extent of disease and the degree of smear positivity in patients with
pulmonary tuberculosis. Clin Biochem, 40(3-4): p. 162-6.
7. Deniz, O., et al., (2006). Serum HDL-C levels, log (TG/HDL-C) values and serum total cholesterol/ HDL-C ratios significantly correlate with radiological extent of disease in patients with community-acquired pneumonia. Clin Biochem, 39(3): p. 287-92.
8. Barlage, S., et al., (2009). Changes in HDL-associated apolipoproteins relate to mortality in human sepsis and correlate to monocyte and platelet activation. Intensive Care Med, 35(11): p. 1877-85.
9. Chien, J.Y., et al. (2005). Low serum level of high-density lipoprotein cholesterol is a poor prognostic factor for severe sepsis. Crit Care Med, 33(8): p. 1688-93.
10. Grion, C.M., et al., (2010). Lipoproteins and CETP levels as risk factors for severe sepsis in hospitalized patients. Eur J Clin Invest, 40(4): p. 330-8.
11. Patel, P.N., et al., (2015). Human experimental endotoxemia in modeling the pathophysiology, genomics, and therapeutics of innate immunity in
complex cardiometabolic diseases. Arterioscler Thromb Vasc Biol, 35(3): p. 525-34.
12. Missala, I., U. Kassner, and E. Steinhagen-Thiessen, (2012). A Systematic Literature Review of the Association of Lipoprotein(a) and Autoimmune Diseases and Atherosclerosis. Int J Rheumatol,: p. 480784.
13. Teeuw, W.J., et al., (2014). Treatment of periodontitis improves the atherosclerotic profile: a systematic review and meta-analysis. J Clin Periodontol, 41(1): p. 70-9.
14. Buhlin, K., et al., (2009). Periodontal treatment influences risk markers for atherosclerosis in patients with severe periodontitis. Atherosclerosis, 206(2): p. 518-22.
15. de Carvalho, J.F., et al.,(2004). Anti-lipoprotein lipase antibodies: a new player in the complex atherosclerotic process in systemic lupus erythematosus? Arthritis Rheum, 50(11): p. 3610-5.
16. Reichlin, M., et al., (2002). Autoantibodies to lipoprotein lipase and dyslipidemia in systemic lupus erythematosus. Arthritis Rheum, 46(11): p. 2957-63.
17. Friedewald WT, Levy RI, Fredrickson DS. (1972). Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem ;18:499-502.
18. Tershakovec AM, Daniel D J. (2004). Disorders of lipoprotein metabolism and transport .In: Behrman RE, Kliegman RM, Jenson HB, eds .Nelson textbook of pediatrics, 17th ed. Philadelphia, PA: Saunders; 445-59.
19. Azizi F, Rahmani M, Madjid M, Allahverdian S, Ghanbili J, Ghanbarian A, Hajipour R. (2001). Serum lipid levels in an Iranian population of children and adolescents: Tehran lipid and glucose study. European J Epidemiol,;17:281-8.
20. Mohammed A. Younis, Ahmed H. Alanee, Amina H. Alobaidy, Zaid Y. Radeef. (2016). The relationship between urinary tract infection and hyperuricemia among children In tikrit teaching hospital. Tikrit Journal of Pure Science. 21 (3).
21. Jack S. Elder. (2011). Urologic Disorders in Infants and Children. In: Robert M. Kliegman. Nelson Textbook Of Pediatrics. 19th edition. Saunders. 1829.
22. Vanleeuwen H J; Heezius E C; Dallinga G M; Vanstrijp J A; Verhoef J and Vankessel K P. (2003). Lipoprotein metabolism in patients with severe sepsis. Crit Care Med. 31:1359-1366.
23. Barcia, A.M. and H.W. Harris; (2005). Triglyceride - rich lipoproteins as agents of innate immunity. Clin Infect Dis, S498-503.
24. Pirillo, A.; A.L. Catapano; and G.D. Norata; (2015). HDL in infectious diseases and sepsis. Handb Exp Pharmacol, 224: p. 483-508.
25. Vermont C.L; Denbrinker M; Kakeci N; Dekleijn E.D; Derijke Y.B and Joosten K.F; (2005). Serum lipids and disease severity in children with severe meningococcalsepsis. Crit Care Med.;33:1610-1615.
26. Gordon B. R; Parker T. S; Levine D M; Saal S. D; Wang J. C and Sloan B. J. (2001). Relationship of hypolipidaemia to cytokine concentrations and out comes in critically ill patients. Crit Care Med. 29:1563-1568.