Ischemia-Modified Albumin, Creatinine, And Paraoxonase-1 Levels in Serum of Patients Undergoing Intravenous Contrast-Enhanced Computed Tomography and Its Association with Contrast-Induced Nephropathy.

Contrast media (CM) Contrast-enhanced computed tomography (CECT) Contrast-induced nephropathy (CIN) Creatinine Ischemia-modified albumin (IMA) Paraoxonase-1 (PON-1)

Journal

Reports of biochemistry & molecular biology
ISSN: 2322-3480
Titre abrégé: Rep Biochem Mol Biol
Pays: Iran
ID NLM: 101637937

Informations de publication

Date de publication:
Apr 2019
Historique:
entrez: 24 7 2019
pubmed: 25 7 2019
medline: 25 7 2019
Statut: ppublish

Résumé

Following contrast-enhanced computed tomography (CECT) contrast-induced nephropathy (CIN) may occur in patients with renal insufficiency or diabetes. Creatinine, the most common marker of CIN, may not be an accurate measure of damage and is affected by many non-renal factors. Our aim was to evaluate ischemia-modified albumin (IMA) as an early CIN marker and correlate it with paraoxonase-1 (PON-1) and creatinine before and after CECT. Forty-eight adult patients scheduled for intravenous CECT, regardless of indication or body region for CECT, were included in this prospective study. Venous blood samples were obtained 12-24 hours before and after contrast media (CM) administration. Ischemia-modified albumin and PON-1 were estimated using methods described by Bar-Or et al. and Dantoine et.al., respectively. Creatinine was estimated on an automated analyzer. Significant differences in IMA (P < 0.001) and PON-1 (P < 0.001) levels were found between pre- and post-CECT samples, while the difference for creatinine was not significant (p = 0.073). No correlation was found between IMA and PON-1 or IMA and creatinine in either the pre- or post-CECT samples. After CM administration patients are subjected to oxidative stress and/or ischemia, as revealed by elevated IMA and decreased PON-1 levels; however, creatinine levels, most commonly estimated to assess reduced renal function, did not reflect the condition accurately. IMA may be a sensitive marker for CIN but further studies are required to confirm its usefulness.

Sections du résumé

BACKGROUND BACKGROUND
Following contrast-enhanced computed tomography (CECT) contrast-induced nephropathy (CIN) may occur in patients with renal insufficiency or diabetes. Creatinine, the most common marker of CIN, may not be an accurate measure of damage and is affected by many non-renal factors. Our aim was to evaluate ischemia-modified albumin (IMA) as an early CIN marker and correlate it with paraoxonase-1 (PON-1) and creatinine before and after CECT.
METHODS METHODS
Forty-eight adult patients scheduled for intravenous CECT, regardless of indication or body region for CECT, were included in this prospective study. Venous blood samples were obtained 12-24 hours before and after contrast media (CM) administration. Ischemia-modified albumin and PON-1 were estimated using methods described by Bar-Or et al. and Dantoine et.al., respectively. Creatinine was estimated on an automated analyzer.
RESULTS RESULTS
Significant differences in IMA (P < 0.001) and PON-1 (P < 0.001) levels were found between pre- and post-CECT samples, while the difference for creatinine was not significant (p = 0.073). No correlation was found between IMA and PON-1 or IMA and creatinine in either the pre- or post-CECT samples.
CONCLUSION CONCLUSIONS
After CM administration patients are subjected to oxidative stress and/or ischemia, as revealed by elevated IMA and decreased PON-1 levels; however, creatinine levels, most commonly estimated to assess reduced renal function, did not reflect the condition accurately. IMA may be a sensitive marker for CIN but further studies are required to confirm its usefulness.

Identifiants

pubmed: 31334291
pmc: PMC6590936

Types de publication

Journal Article

Langues

eng

Pagination

72-78

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Auteurs

Chanda Jha (C)

Department of Biochemistry, Kasturba Medical College, Manipal University, Manipal, India.

Shobha Ullas Kamath (S)

Department of Biochemistry, Kasturba Medical College, Manipal University, Manipal, India.

Sambit Dash (S)

Department of Biochemistry, Melaka Manipal Medical College, Manipal University, Manipal, India.

Ravindra Prabhu Attur (R)

Department of Nephrology, Kasturba Hospital, Manipal, India.

Lingadakai Ramachandra (L)

Department of Surgery, Kasturba Hospital, Manipal, India.

Rajgopal Shenoy Kallya (R)

Department of Surgery, Kasturba Hospital, Manipal, India.

Classifications MeSH