HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Mechanisms underlying early rapid increases in creatinine in paraquat poisoning.

AbstractBACKGROUND:
Acute kidney injury (AKI) is common after severe paraquat poisoning and usually heralds a fatal outcome. The rapid large increases in serum creatinine (Cr) exceed that which can be explained by creatinine kinetics based on loss of glomerular filtration rate (GFR).
METHODS AND FINDINGS:
This prospective multi-centre study compared the kinetics of two surrogate markers of GFR, serum creatinine and serum cystatin C (CysC), following paraquat poisoning to understand and assess renal functional loss after paraquat poisoning. Sixty-six acute paraquat poisoning patients admitted to medical units of five hospitals were included. Relative changes in creatinine and CysC were monitored in serial blood and urine samples, and influences of non-renal factors were also studied.
RESULTS:
Forty-eight of 66 patients developed AKI (AKIN criteria), with 37 (56%) developing moderate to severe AKI (AKIN stage 2 or 3). The 37 patients showed rapid increases in creatinine of >100% within 24 hours, >200% within 48 hours and >300% by 72 hours and 17 of the 37 died. CysC concentration increased by 50% at 24 hours in the same 37 patients and then remained constant. The creatinine/CysC ratio increased 8 fold over 72 hours. There was a modest fall in urinary creatinine and serum/urine creatinine ratios and a moderate increase in urinary paraquat during first three days.
CONCLUSION:
Loss of renal function contributes modestly to the large increases in creatinine following paraquat poisoning. The rapid rise in serum creatinine most probably represents increased production of creatine and creatinine to meet the energy demand following severe oxidative stress. Minor contributions include increased cyclisation of creatine to creatinine because of acidosis and competitive or non-competitive inhibition of creatinine secretion. Creatinine is not a good marker of renal functional loss after paraquat poisoning and renal injury should be evaluated using more specific biomarkers of renal injury.
AuthorsFahim Mohamed, Zoltan Endre, Shaluka Jayamanne, Timothy Pianta, Philip Peake, Chathura Palangasinghe, Umesh Chathuranga, Kithsiri Jayasekera, Klintean Wunnapuk, Fathima Shihana, Seyed Shahmy, Nicholas Buckley
JournalPloS one (PLoS One) Vol. 10 Issue 3 Pg. e0122357 ( 2015) ISSN: 1932-6203 [Electronic] United States
PMID25815837 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers
  • Cystatin C
  • Creatinine
  • Paraquat
Topics
  • Acute Kidney Injury (blood, chemically induced, urine)
  • Adult
  • Biomarkers (blood, urine)
  • Creatinine (blood, urine)
  • Cystatin C (blood, urine)
  • Female
  • Glomerular Filtration Rate (drug effects)
  • Humans
  • Kidney (drug effects, pathology)
  • Male
  • Middle Aged
  • Paraquat (toxicity)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: