Assessment of the nephroprotective efficacy of steroid therapy by analyzing concentrations of new markers of the renal damage at the extracorporeal remote shock wave lithotripsy in children
- Authors: Zorkin S.N.1, Nikulin O.D.1, Semikina E.L.1, Tsygin A.N.1, Snowskaya M.A.1, Milovanova A.M.1, Shakhnovsky D.S.1, Bayazitov R.R.1
-
Affiliations:
- National Medical Research Center for Children’s Health
- Issue: Vol 28, No 2 (2024)
- Pages: 158-169
- Section: ORIGINAL STUDY
- Submitted: 08.02.2024
- Accepted: 03.04.2024
- Published: 30.05.2024
- URL: https://jps-nmp.ru/jour/article/view/790
- DOI: https://doi.org/10.17816/ps790
- ID: 790
Cite item
Abstract
BACKGROUND: for several decades, the remote shock wave lithotripsy was a leading technique for surgical management of concretions in the upper urinary tract. The key reason for its wide spread was minimal invasion combined with high efficiency. However, it has been proven that after each lithotripsy session the acute kidney injury develops. Currently, there is no any curative strategy aimed to protect the renal parenchyma from pathological impacts of shock wave energy.
AIM: to evaluate Prednisolone nephroprotective efficacy after analysing dynamic levels of biomarkers of kidney damage during the remote shock wave lithotripsy in children.
METHODS: 108 children with urolithiasis after a session of remote shock wave lithotripsy were enrolled in the study. All patients were divided into two groups of 54 participants in each. Participants from the control group were treated according to the standard protocol. Participants from the studied group, in addition to the traditional therapy, were prescribed Prednisolone orally at dosage 0.5 mg/kg once a day for 2 days before the session of external shock wave lithotripsy and 2 hours before the surgery. Urine and blood samples were taken from all patients: before surgery, 45 minutes and 24 hours after it. Biomarker concentration was assessed in all samples.
RESULTS: The biomarker concentration in the urine differed statistically significantly in patients of the studied group and of the control one. The most pronounced changes were noted 45 minutes after the surgery. A statistically significant concentration increase of all studied biomarkers was revealed in patients from the control group. In children from the studied group, concentration of kidney damage molecule 1 did not change, and lipocalin concentration associated with neutrophil gelatinase, tissue inhibitor of metalloproteinase 2 and hepatic forms of fatty acid binding protein increased statistically significantly less than in patients of the control group. Interleukin 18 concentration in the blood serum of patients from the control group increased statistically significantly, while in patients from the studied group - statistically insignificantly.
CONCLUSION: A statistically significant decrease in the concentration of studied biomarkers, and, consequently, less degree of renal damage in the studied group, can promote implementation of the glucocorticoid therapy as a medical support during the external shock wave lithotripsy in children.
Full Text
About the authors
Sergey N. Zorkin
National Medical Research Center for Children’s Health
Email: zorkin@nczd.ru
ORCID iD: 0000-0002-4038-1472
SPIN-code: 4762-8837
MD, Dr. Sci. (Medicine), Professor
Россия, 2 bldg 1 Lomonosovsky prospekt, 119991 MoscowOleg D. Nikulin
National Medical Research Center for Children’s Health
Author for correspondence.
Email: dr.nikulin.oleg@yandex.ru
ORCID iD: 0000-0003-3640-9994
SPIN-code: 9310-2660
MD
Россия, 2 bldg 1 Lomonosovsky prospekt, 119991 MoscowElena L. Semikina
National Medical Research Center for Children’s Health
Email: semikina@nczd.ru
ORCID iD: 0000-0001-8923-4652
SPIN-code: 3647-4967
MD, Dr. Sci. (Medicine), Professor
Россия, 2 bldg 1 Lomonosovsky prospekt, 119991 MoscowAkexey N. Tsygin
National Medical Research Center for Children’s Health
Email: tsygin@nczd.ru
ORCID iD: 0000-0001-6301-9313
SPIN-code: 7948-5065
MD, Dr. Sci. (Medicine), Professor
Россия, 2 bldg 1 Lomonosovsky prospekt, 119991 MoscowMarina A. Snowskaya
National Medical Research Center for Children’s Health
Email: snows@inbox.ru
ORCID iD: 0000-0002-5263-6743
SPIN-code: 9899-1095
MD, Cand. Sci. (Medicine)
Россия, 2 bldg 1 Lomonosovsky prospekt, 119991 MoscowAnastasia M. Milovanova
National Medical Research Center for Children’s Health
Email: milovanova@nczd.ru
ORCID iD: 0000-0003-1615-2044
SPIN-code: 8260-5227
MD, Cand. Sci. (Medicine)
Россия, 2 bldg 1 Lomonosovsky prospekt, 119991 MoscowDmitriy S. Shakhnovsky
National Medical Research Center for Children’s Health
Email: shakhnovski@nczd.ru
ORCID iD: 0000-0003-2883-2493
SPIN-code: 4946-0848
MD
Россия, 2 bldg 1 Lomonosovsky prospekt, 119991 MoscowRimir R. Bayazitov
National Medical Research Center for Children’s Health
Email: krasik17@yandex.ru
SPIN-code: 5506-6828
MD, Cand. Sci. (Medicine)
Россия, 2 bldg 1 Lomonosovsky prospekt, 119991 MoscowReferences
- Talso M, Tefik T, Mantica G, et al. Extracorporeal shockwave lithotripsy: Current knowledge and future perspectives. Minerva Urol Nefrol. 2019;71(4):365–372. doi: 10.23736/S0393-2249.19.03415-5
- Zorkin SN, Nikulin OD, Shahnovskiy DS. Remote shock wave lithotripsy in the treatment of urolithiasis in children: Types and possibilities. Detskaya khirurgiya (Russian Journal of Pediatric Surgery). 2022;26(6):321–326. EDN: IYZCXD doi: 10.55308/1560-9510-2022-26-6-321-326
- Hughes SF, Jones N, Thomas-Wright SJ, et al. Shock wave lithotripsy, for the treatment of kidney stones, results in changes to routine blood tests and novel biomarkers: A prospective clinical pilot-study. Eur J Med Res. 2020;25(1):18. doi: 10.1186/s40001-020-00417-2
- Milišić E, Alić J, Zvizdić Z, et al. Urinary neutrophil gelatinase-associated lipocalin level as a biomarker of acute kidney injury following extracorporeal shock wave lithotripsy. Cent Eur J Urol. 2021;74(4):579–587. EDN: DPGUHH doi: 10.5173/ceju.2021.0174
- Nazarov TK, Komyakov BK, Rychkov IV, et al. Role of biomarkers of acute kidney damage during lithotripsy of high-density stones. Urologiia. 2019. № 1. С. 23–27. EDN: FKKLMH doi: 10.18565/urology.2019.1.23-27
- Wołyniec W, Ratkowski W, Renke J, Renke M. Changes in novel AKI biomarkers after Exercise. A Systematic Review. Int J Mol Sci. 2020;21(16):5673. EDN: VGZRZK doi: 10.3390/ijms21165673
- Kazachenko AV, Voytko DA, Prosyannikov MY, et al. Modern markers for determining the functional ability of the kidneys in urological practice. Exp Clin Urol. 2023;16,(1):174–187. EDN: GPAHOJ doi: 10.29188/2222-8543-2023-16-1-174-187
- Clark DL, Connors BA, Evan AP, et al. Localization of renal oxidative stress and inflammatory response after lithotripsy. BJU Int. 2009;103(11):1562–1568. doi: 10.1111/j.1464-410X.2008.08260.x
- Leedahl DD, Frazee EN, Schramm GE, et al. Derivation of urine output thresholds that identify a very high risk of AKI in patients with septic shock. Clin J Am Soc Nephrol. 2014;9(7):1168–1174. doi: 10.2215/CJN.09360913
- Sharma A, Mucino MJ, Ronco C. Renal functional reserve and renal recovery after acute kidney injury. Nephron Clin Pract. 2014;127(1-4):94–100. doi: 10.1159/000363721
- Ronco C, Bellomo R, Kellum J. Understanding renal functional reserve. Intensive Care Med. 2017;43(6):917–920. EDN: NBAHCO doi: 10.1007/s00134-017-4691-6
- Szumilas D, Owczarek AJ, Brzozowska A, et al. The value of urinary NGAL, KIM-1, and IL-18 measurements in the early detection of kidney injury in oncologic patients treated with cisplatin-based chemotherapy. Int J Mol Sci. 2024;25(2):1074. doi: 10.3390/ijms25021074
- Spasojević-Dimitrijeva B, Kotur-Stevuljević J, Dukić M, et al. Serum neutrophil gelatinase-associated lipocalin and urinary kidney injury molecule-1 as potential biomarkers of subclinical nephrotoxicity after gadolinium-based and iodinated-based contrast media exposure in pediatric patients with normal kidney function. Med Sci Monit. 2017;(23):4299–4305. doi: 10.12659/msm.903255
- Breglia A, Godi I, Virzì GM, et al. Subclinical contrast-induced acute kidney injury in patients undergoing cerebral computed tomography. Cardiorenal Med. 2020;10(2):125–136. doi: 10.1159/000505422
- Scridon A, Somkereki C, Nicoară TR, et al. Neutrophil gelatinase-associated lipocalin monitoring reveals persistent subclinical kidney injury following intraarterial administration of iodinated contrast agents. Sci Rep. 2022;12(1):19464. EDN: UALKHC doi: 10.1038/s41598-022-24169-7
- Dalton RN. Serum creatinine and glomerular filtration rate: Perception and reality. Clin Chem. 2010;56(5):687–689. doi: 10.1373/clinchem.2010.144261
- Nikulin OD, Zorkin SN, Semikina EL, et al. Biomarkers of acute kidney injury in remote shock wave lithotripsy in children. Pediatria G.N. Speransky. 2023;102(5):181–190. doi: 10.24110/0031-403X-2023-102-5-181-190
- Yuan SM. Acute kidney injury after cardiac surgery: Risk factors and novel biomarkers. Braz J Cardiovasc Surg. 2019;34(3):352–360. doi: 10.21470/1678-9741-2018-0212
- Zhang YL, Qiao SK, Wang RY, Guo XN. NGAL attenuates renal ischemia/reperfusion injury through autophagy activation and apoptosis inhibition in rats. Chem Biol Interact. 2018;(289):40–46. doi: 10.1016/j.cbi.2018.04.018
- Kachko A, Costafreda MI, Zubkova I, et al. Determinants in the Ig variable domain of human HAVCR1 (TIM-1) are required to enhance hepatitis C virus entry. J Virol. 2018;92(6):e01742-17. EDN: YFLEPB doi: 10.1128/JVI.01742-17
- Miroshkina IV, Gritskevich AA, Baytman TP, et al. The role of markers of acute kidney damage in assessing kidney function with its ischemia. Exp Clin Urol. 2018;(4):114–121. EDN: VRTKPJ
- Yamamoto T, Noiri E, Ono Y, et al. Renal L-type fatty acid–binding protein in acute ischemic injury. J Am Society Nephrol. 2007;18(11):2894–2902. doi: 10.1681/ASN.2007010097
- Schrezenmeier EV, Barasch J, Budde K, et al. Biomarkers in acute kidney injury: Pathophysiological basis and clinical performance. Acta Physiologica. 2017;219(3):554–572. EDN: YVTLYF doi: 10.1111/apha.12764
- Lin X, Yuan J, Zhao Y, Zha Y. Urine interleukin-18 in prediction of acute kidney injury: A systemic review and meta-analysis. J Nephrol. 2015;28(1):7–16. EDN: YZOJLD doi: 10.1007/s40620-014-0113-9
- Wang S, Zhang Z, Wang J, Miao H. MiR-107 induces TNF-α secretion in endothelial cells causing tubular cell injury in patients with septic acute kidney injury. Biochem Biophys Res Commun. 2017;483(1):45–51. doi: 10.1016/j.bbrc.2017.01.013
- Fagerberg L, Hallström BM, Oksvold P, et al. Analysis of the human tissue-specific expression by genome-wide integration of transcriptomics and antibody-based proteomics. Mol Cell Proteomics. 2014;13(2):397–406. EDN: MTOMUS doi: 10.1074/mcp.M113.035600
- Ortega LM, Heung M. The use of cell cycle arrest biomarkers in the early detection of acute kidney injury. Is this the new renal troponin? Nefrología. 2018;38(4):361–367. doi: 10.1016/j.nefro.2017.11.013
- Emlet DR, Pastor-Soler N, Marciszyn A, et al. Insulin-like growth factor binding protein 7 and tissue inhibitor of metalloproteinases-2: Differential expression and secretion in human kidney tubule cells. Am J Physiol Renal Physiol. 2017;312(2):F284–296. EDN: YXCIST doi: 10.1152/ajprenal.00271.2016
- Johnson AC, Zager RA. Mechanisms underlying increased TIMP2 and IGFBP7 urinary excretion in experimental AKI. J Am Society Nephrol. 2018;29(8):2157–2167. doi: 10.1681/ASN.2018030265
- Guzeloglu M, Yalcinkaya F, Atmaca S, et al. The beneficial effects of tadalafil on renal ischemia-reperfusion injury in rats. Urol Int. 2011;86(2):197–203. doi: 10.1159/000321927
- Gasanov F, Aytac B, Vuruskan H. The effects of tadalafil on renal ischemia reperfusion injury: An experimental study. Bosn J Basic Med Sci. 2011;11(3):158–162. doi: 10.17305/bjbms.2011.2567
- Danisoglu ME, Aytac B, Kilicaslan H, et al. Reduction of shock wave lithotripsy-induced renal tubular injury by tadalafil. Bratislava Med J. 2013;114(11):616–620. doi: 10.4149/BLL_2013_131
- Ozmerdiven G, Vuruskan BA, Kaygisiz O, Vuruskan H. Protective effects of diltiazem and tadalafil on shock wave-induced kidney injury in rats. Bratislava Med J. 2017;118(4):228–232. doi: 10.4149/BLL_2017_045
- Park HK, Lee HW, Lee KS, et al. Preventive effects of COX-2 inhibitor, celecoxib on renal tubular injury induced by shock wave lithotriptor. Urol Res. 2010;38(4):223–228. doi: 10.1007/s00240-009-0243-z
- Al-Awadi KA, Kehinde EO, Loutfi I, et al. Treatment of renal calculi by lithotripsy: Minimizing short-term shock wave induced renal damage by using antioxidants. Urol Res. 2008;36(1):51–60. doi: 10.1007/s00240-007-0126-0
- Armaly Z, Artol S, Jabbour AR, et al. Impact of pretreatment with carnitine and tadalafil on contrast-induced nephropathy in CKD patients. Ren Fail. 2019;41(1):976–986. doi: 10.1080/0886022X.2019.1669459
- Heybeli C, Canaslan K, Oktan MA, et al. Acute kidney injury following colistin treatment in critically-ill patients: May glucocorticoids protect? J Chemotherapy. 2021;33(2):85–94. doi: 10.1080/1120009X.2020.1770027
- Ying P, Yang C, Wu X, et al. Effect of hydrocortisone on the 28-day mortality of patients with septic acute kidney injury. Ren Fail. 2019;41(1):794–799. doi: 10.1080/0886022X.2019.1658605
- González E, Gutiérrez E, Galeano C, et al. Early steroid treatment improves the recovery of renal function in patients with drug-induced acute interstitial nephritis. Kidney Int. 2008;73(8):940–946. doi: 10.1038/sj.ki.5002776
- Fontana J, Vogt A, Hohenstein A, et al. Impact of steroids on the inflammatory response after ischemic acute kidney injury in rats. Indian J Nephrol. 2017;27(5):365–371. doi: 10.4103/ijn.IJN_40_17
- Prendecki M, Tanna A, Salama AD, et al. Long-term outcome in biopsy-proven acute interstitial nephritis treated with steroids. Clin Kidney J. 2017;10(2):233–239. doi: 10.1093/ckj/sfw116
- Friedewald JJ, Rabb H. Inflammatory cells in ischemic acute renal failure. Kidney Int. 2004;66(2):486–491. doi: 10.1111/j.1523-1755.2004.761_3.x
- Choi HM, Jo SK, Kim SH, et al. Glucocorticoids attenuate septic acute kidney injury. Biochem Biophys Res Commun. 2013;435(4):678–684. EDN: YDKRCX doi: 10.1016/j.bbrc.2013.05.042
- Hall RI, Smith MS, Rocker G. The systemic inflammatory response to cardiopulmonary bypass: Pathophysiological, therapeutic, and pharmacological considerations. Anesth Analg. 1997;85(4):766–782. doi: 10.1097/00000539-199710000-00011
- Kawamura T, Inada K, Nara N, et al. Influence of methylprednisolone on cytokine balance during cardiac surgery. Crit Care Med. 1999;27(3):545–548. doi: 10.1097/00003246-199903000-00033
- Toledo-Pereyra LH, Lin CY, Kundler H, Replogle RL. Steroids in heart surgery: A clinical double-blind and randomized study. Am Surg. 1980;46(3):155–160.
- Whitlock RP, Young E, Noora J, et al. Pulse low dose steroids attenuate post-cardiopulmonary bypass SIRS; SIRS I. J Surg Res. 2006;132(2):188–194. doi: 10.1016/j.jss.2006.02.013
- Weis F, Beiras-Fernandez A, Schelling G, et al. Stress doses of hydrocortisone in high-risk patients undergoing cardiac surgery: Effects on interleukin-6 to interleukin-10 ratio and early outcome. Crit Care Med. 2009;37(5):1685–1690. doi: 10.1097/CCM.0b013e31819fca77
- Schurr UP, Zünd G, Hoerstrup SP, et al. Preoperative administration of steroids: Influence on adhesion molecules and cytokines after cardiopulmonary bypass. Ann Thorac Surg. 2001;72(4):1316–1320. doi: 10.1016/s0003-4975(01)03062-4
- Semedo P, Palasio CG, Oliveira CD, et al. Early modulation of inflammation by mesenchymal stem cell after acute kidney injury. Int Immunopharmacol. 2009;9(6):677–682. doi: 10.1016/j.intimp.2008.12.008
- Zhang J, Yao Y, Xiao F, et al. Administration of dexamethasone protects mice against ischemia/reperfusion induced renal injury by suppressing PI3K/AKT signaling. Int J Clin Exp Pathol. 2013;6(11):2366–2375.
- Acar G, Akcay A, Sayarlioglu M, et al. Assessment of atrial conduction time in patients with familial Mediterranean fever. Pacing Clin Electrophysiol. 2009;32(3):308–313. doi: 10.1111/j.1540-8159.2008.02237.x