Biomarcadores de estrés oxidativo e inflamación en lesión renal aguda postcontraste yodado

  1. Elisabeth Stoll 1
  2. Pablo Monedero 1
  3. Paloma L. Martin-Moreno 1
  4. Nuria Garcia-Fernandez 1
  1. 1 Clínica Universidad de Navarra. Pamplona
Journal:
Anales del sistema sanitario de Navarra

ISSN: 1137-6627

Year of publication: 2024

Volume: 47

Issue: 2

Pages: 47-58

Type: Article

DOI: 10.23938/ASSN.1081 DIALNET GOOGLE SCHOLAR lock_openOpen access editor

More publications in: Anales del sistema sanitario de Navarra

Abstract

Background. Iodinated contrast-induced acute kidney injury (CI-AKI) is a common cause of renal failure, especially in patients with risk factors. This study analyses different renal biomarkers in patients undergoing computed tomography scans with iodinated contrast to identify the molecular and cel-lular mechanisms involved in the pathogenesis of CI-AKI.Methodology. Prospective study that included patients with high risk of renal disease who received iodinated contrast (iohexol) for the computed tomography scans. Functional biomarkers (creati-nine and cystatin C), inflammatory and oxidative stress markers (neutrophil gelatinase-associated lipocalin [NGAL], interleukin-8 [IL-8], superoxide dismutase [SOD], F2-isoprostanes, and cardio-trophin-1), and cell cycle biomarkers (Nephrocheck®) were ana-lysed before the iodinated contrast and 4, 12, 24, and 48 hours post-contrast, in relation to the incidence of IC-AKI.Results. IC-AKI was observed in 30.6% of the 62 study partici-pants and in 57.1% of the patients with diabetes and renal dys-function. Factors associated with IC-AKI were a higher mean age (74.4 vs 64.9 years), pre-existing renal dysfunction (60 vs16.7%), and higher adjusted mean volume of iohexol (42.9 vs32.1%). As for non-functional biomarkers. No differences were found between patients with and without CI-AKI. The use of iodinated contrast was associated with a decrease in SOD anti-oxidant activity at 4 hours and an increase in IL-8 at 12 hours post-administration of the iodinated contrast.Conclusions. Administration of iohexol in computed tomog-raphy scans in patients with high risk of renal disease results in an elevated percentage of CI-AKI, attributable to ischemia/ reperfusion injury and/or direct toxicity of the iodinated contrast

Bibliographic References

  • CHAUDHARI H, MAHENDRAKAR S, BASKIN SE, REDDI AS. Contrast-induced acute kidney injury: evidence in support of its existence and a review of its pathogenesis and management. Int J Nephrol Renovasc Dis 2022;15:253-266. https://doi.org/10.2147/IJNRD.S371700
  • STANSKI NL, RODRIGUES CE, STRADER M, MURRAY PT, ENDRE ZH, BAGSHAW SM. Precision management of acute kidney injury in the intensive care unit: current state of the art. Intensive Care Med 2023; 49(9): 1049-1061. https://doi.org/10.1007/s00134-023-07171-z
  • CHENG W, ZHAO F, TANG CY, LI XW, LUO M, DUAN SB. Comparison of iohexol and iodixanol induced nephrotoxicity, mitochondrial damage and mitophagy in a new contrast-induced acute kidney injury rat model. Arch Toxicol 2018; 92: 2245-2257. https://doi.org/10.1007/s00204-018-2225-9
  • VLACHOPANOS G, SCHIZAS D, HASEMAKI N, GEORGALIS A. Pathophysiology of contrast-induced acute kidney injury (CIAKI). Curr Pharm Des 2019; 25(44): 4642-4647. https://doi.org/10.2174/1381612825666191210152944
  • CHO E, KO GJ. the pathophysiology and the management of radiocontrast-induced nephropathy. Diagnostics (Basel) 2022; 12(1): 180. https://doi.org/10.3390/diagnostics12010180
  • D'AMORE C, NUZZO S, BRIGUORI C. Biomarkers of contrast-induced nephropathy: Which ones are clinically important? Interv Cardiol Clin 2020; 9: 335-344. https://doi.org/10.1016/j.iccl.2020.02.004
  • SCHREZENMEIER EV, BARASCH J, BUDDE K, WESTHOFF T, SCHMIDT-OTT KM. Biomarkers in acute kidney injury - pathophysiological basis and clinical performance. Acta Physiol (Oxf) 2017; 219: 554-572. https://doi.org/10.1111/apha.12764
  • BIRKELO BC, PANNU N, SIEW ED. Overview of diagnostic criteria and epidemiology of acute kidney injury and acute kidney disease in the critically ill patient. Clin J Am Soc Nephrol 2022; 17:717-735. https://doi.org/10.2215/CJN.14181021
  • AOUN J, NICOLAS D, BROWN JR, JABER BL. Maximum allowable contrast dose and prevention of acute kidney injury following cardiovascular procedures. Curr Opin Nephrol Hypertens 2018; 27: 121-129. https://doi.org/10.1097/MNH.0000000000000389
  • FERNANDEZ-RUIZ V, KAWA M, BERASAIN C, IÑIGUEZ M, SCHMITZ V, MARTINEZ-ANSÓ E et al. Treatment of murine fulminant hepatitis with genetically engineered endothelial progenitor cells. J Hepatol 2011; 55: 828-837. https://doi.org/10.1016/j.jhep.2011.01.036
  • Kidney Disease: Improving Global Outcomes (KDIGO) Acute Kidney Injury work group. KDIGO clinical practice guideline for acute kidney injury. Kidney Inter Suppl 2012; 2 (Suppl 1): 1–138. https://doi.org/10.1038/kisup.2012.2
  • MARTIN-MORENO PL, VARO N, MARTÍNEZ-ANSÓ E, MARTIN-CALVO N, SAYÓN-OREA C, BILBAO JI, GARCIA-FERNANDEZ N. Comparison of intravenous and oral hydration in the prevention of contrast-induced acute kidney injury in low-risk patients: A randomized trial. Nephron 2015; 131(1): 51-58. https://doi.org/10.1159/000438907
  • MCDONALD JS, MCDONALD RJ. Risk of acute kidney injury following IV iodinated contrast media exposure: 2023 update, from the AJR special series on contrast media. AJR Am J Roentgenol 2024. https://doi.org/10.2214/AJR.23.30037
  • SŮVA M, KALA P, POLOCZEK M, KAŇOVSKÝ J, ŠTÍPAL R, RADVAN M et al. Contrast-induced acute kidney injury and its contemporary prevention. Front Cardiovasc Med 2022; 9: 1073072. https://doi.org/10.3389/fcvm.2022.1073072
  • WEISBORD SD, GALLAGHER M, JNEID H, GARCIA S, CASS A, THWIN SS et al. PRESERVE trial group. outcomes after angiography with sodium bicarbonate and acetylcysteine. N Engl J Med 2018; 378(7): 603-614. https://doi.org/10.1056/NEJMoa1710933
  • LIANGOS O, KOLYADA A, TIGHIOUART H, PERIANAYAGAM MC, WALD R, JABER BL. Interleukin-8 and acute kidney injury following cardiopulmonary bypass: a prospective cohort study. Nephron Clin Pract 2009 ;113(3): c148-c154. https://doi.org/10.1159/000232595
  • MARAKALA V. Neutrophil gelatinase-associated lipocalin (NGAL) in kidney injury - A systematic review. Clin Chim Acta 2022; 536: 135-141. https://doi.org/10.1016/j.cca.2022.08.029
  • FILIOPOULOS V, BIBLAKI D, VLASSOPOULOS D. Neutrophil gelatinase-associated lipocalin (NGAL): a promising biomarker of contrast-induced nephropathy after computed tomography. Ren Fail 2014; 36(6): 979-986. https://doi.org/10.3109/0886022X.2014.900429
  • MAGNO AL, HERAT LY, CARNAGARIN R, SCHLAICH MP, MATTHEWS VB. CURRENT knowledge of IL-6 cytokine family members in acute and chronic kidney disease. Biomedicines 2019; 7(1): 19. https://doi.org/10.3390/biomedicines7010019
  • QUIROS Y, SÁNCHEZ-GONZÁLEZ PD, LÓPEZ-HERNÁNDEZ FJ, MORALES AI, LÓPEZ-NOVOA JM. Cardiotrophin-1 administration prevents the renal toxicity of iodinated contrast media in rats. Toxicol Sci 2013; 132(2): 493-501. https://doi.org/10.1093/toxsci/kft007
  • NALESSO F, CATTARIN L, GOBBI L, FRAGASSO A, GARZOTTO F, CALÒ LA. Evaluating nephrocheck® as a predictive tool for acute kidney injury. Int J Nephrol Renovasc Dis 2020; 13: 85-96. https://doi.org/10.2147/IJNRD.S198222
  • ROUVE E, LAKHAL K, SALMON GANDONNIÈRE C, JOUAN Y, BODET-CONTENTIN L, EHRMANN S. Lack of impact of iodinated contrast media on kidney cell-cycle arrest biomarkers in critically ill patients. BMC Nephrol 2018; 19(1): 308. https://doi.org/10.1186/s12882-018-1091-2
  • PICKKERS P, DARMON M, HOSTE E, JOANNIDIS M, LEGRAND M, OSTERMANN M et al. Acute kidney injury in the critically ill: An updated review on pathophysiology and management. Intensive Care Med 2021; 47(8): 835-850. https://doi.org/10.1007/s00134-021-06454-7
  • MCCULLOUGH PA. Renal safety of iodixanol. Expert Rev Cardiovasc Ther 2006; 4: 655-661. https://doi.org/10.1586/14779072.4.5.655
Data source: Dialnet