Cargando…

NGAL as Biomarker of Clinical and Subclinical Damage of Kidney Function after Coronary Angiography

Contrast-induced acute kidney injury (CI-AKI) is a serious complication after angiographic examinations in cardiology. Diagnosis may be delayed based on standard serum creatinine, and subclinical forms of kidney damage may not be detected at all. In our study, we investigate the clinical use in thes...

Descripción completa

Detalles Bibliográficos
Autores principales: Petrova, Iliyana, Alexandrov, Alexander, Vladimirov, Georgi, Mateev, Hristo, Bogov, Ivaylo, Paskaleva, Iva, Gotcheva, Nina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047760/
https://www.ncbi.nlm.nih.gov/pubmed/36980488
http://dx.doi.org/10.3390/diagnostics13061180
_version_ 1785014006944104448
author Petrova, Iliyana
Alexandrov, Alexander
Vladimirov, Georgi
Mateev, Hristo
Bogov, Ivaylo
Paskaleva, Iva
Gotcheva, Nina
author_facet Petrova, Iliyana
Alexandrov, Alexander
Vladimirov, Georgi
Mateev, Hristo
Bogov, Ivaylo
Paskaleva, Iva
Gotcheva, Nina
author_sort Petrova, Iliyana
collection PubMed
description Contrast-induced acute kidney injury (CI-AKI) is a serious complication after angiographic examinations in cardiology. Diagnosis may be delayed based on standard serum creatinine, and subclinical forms of kidney damage may not be detected at all. In our study, we investigate the clinical use in these directions of a “damage”-type biomarker—neutrophil gelatinase-associated lipocalin (NGAL). Among patients with a high-risk profile undergoing scheduled coronary angiography and/or angioplasty, plasma NGAL was determined at baseline and at 4th and 24th h after contrast administration. In the CI-AKI group, NGAL increased significantly at the 4th hour (Me 109.3 (IQR 92.1–148.7) ng/mL versus 97.6 (IQR 69.4–127.0) ng/mL, p = 0.006) and at the 24th hour (Me 131.0 (IQR 81.1–240.8) ng/mL, p = 0.008). In patients with subclinical CI-AKI, NGAL also increased significantly at the 4th hour (Me 94.0 (IQR 75.5–148.2) ng/mL, p = 0.002) and reached levels close to those in patients with CI-AKI. Unlike the new biomarker, however, serum creatinine did not change significantly in this group. The diagnostic power of NGAL is extremely good—AUC 0.847 (95% CI: 0.677–1.000; p = 0.001) in CI-AKI and AUC 0.731 (95% CI: 0.539–0.924; p = 0.024) in subclinical CI-AKI. NGAL may be a reliable biomarker for the early diagnosis of clinical and subclinical forms of renal injury after contrast angiographic studies.
format Online
Article
Text
id pubmed-10047760
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-100477602023-03-29 NGAL as Biomarker of Clinical and Subclinical Damage of Kidney Function after Coronary Angiography Petrova, Iliyana Alexandrov, Alexander Vladimirov, Georgi Mateev, Hristo Bogov, Ivaylo Paskaleva, Iva Gotcheva, Nina Diagnostics (Basel) Article Contrast-induced acute kidney injury (CI-AKI) is a serious complication after angiographic examinations in cardiology. Diagnosis may be delayed based on standard serum creatinine, and subclinical forms of kidney damage may not be detected at all. In our study, we investigate the clinical use in these directions of a “damage”-type biomarker—neutrophil gelatinase-associated lipocalin (NGAL). Among patients with a high-risk profile undergoing scheduled coronary angiography and/or angioplasty, plasma NGAL was determined at baseline and at 4th and 24th h after contrast administration. In the CI-AKI group, NGAL increased significantly at the 4th hour (Me 109.3 (IQR 92.1–148.7) ng/mL versus 97.6 (IQR 69.4–127.0) ng/mL, p = 0.006) and at the 24th hour (Me 131.0 (IQR 81.1–240.8) ng/mL, p = 0.008). In patients with subclinical CI-AKI, NGAL also increased significantly at the 4th hour (Me 94.0 (IQR 75.5–148.2) ng/mL, p = 0.002) and reached levels close to those in patients with CI-AKI. Unlike the new biomarker, however, serum creatinine did not change significantly in this group. The diagnostic power of NGAL is extremely good—AUC 0.847 (95% CI: 0.677–1.000; p = 0.001) in CI-AKI and AUC 0.731 (95% CI: 0.539–0.924; p = 0.024) in subclinical CI-AKI. NGAL may be a reliable biomarker for the early diagnosis of clinical and subclinical forms of renal injury after contrast angiographic studies. MDPI 2023-03-20 /pmc/articles/PMC10047760/ /pubmed/36980488 http://dx.doi.org/10.3390/diagnostics13061180 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Petrova, Iliyana
Alexandrov, Alexander
Vladimirov, Georgi
Mateev, Hristo
Bogov, Ivaylo
Paskaleva, Iva
Gotcheva, Nina
NGAL as Biomarker of Clinical and Subclinical Damage of Kidney Function after Coronary Angiography
title NGAL as Biomarker of Clinical and Subclinical Damage of Kidney Function after Coronary Angiography
title_full NGAL as Biomarker of Clinical and Subclinical Damage of Kidney Function after Coronary Angiography
title_fullStr NGAL as Biomarker of Clinical and Subclinical Damage of Kidney Function after Coronary Angiography
title_full_unstemmed NGAL as Biomarker of Clinical and Subclinical Damage of Kidney Function after Coronary Angiography
title_short NGAL as Biomarker of Clinical and Subclinical Damage of Kidney Function after Coronary Angiography
title_sort ngal as biomarker of clinical and subclinical damage of kidney function after coronary angiography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10047760/
https://www.ncbi.nlm.nih.gov/pubmed/36980488
http://dx.doi.org/10.3390/diagnostics13061180
work_keys_str_mv AT petrovailiyana ngalasbiomarkerofclinicalandsubclinicaldamageofkidneyfunctionaftercoronaryangiography
AT alexandrovalexander ngalasbiomarkerofclinicalandsubclinicaldamageofkidneyfunctionaftercoronaryangiography
AT vladimirovgeorgi ngalasbiomarkerofclinicalandsubclinicaldamageofkidneyfunctionaftercoronaryangiography
AT mateevhristo ngalasbiomarkerofclinicalandsubclinicaldamageofkidneyfunctionaftercoronaryangiography
AT bogovivaylo ngalasbiomarkerofclinicalandsubclinicaldamageofkidneyfunctionaftercoronaryangiography
AT paskalevaiva ngalasbiomarkerofclinicalandsubclinicaldamageofkidneyfunctionaftercoronaryangiography
AT gotchevanina ngalasbiomarkerofclinicalandsubclinicaldamageofkidneyfunctionaftercoronaryangiography