New early non-invasive biomarkers for acute kidney injury in critically ill full-term neonatal infants

Critically ill neonates are at high risk for acute kidney injury (AKI). Objective: to estimate the clinical and diagnostic value of urinary neutrophil gelatinase-associated lipocalin (NGAL) 2, interleukin-18 (IL-18), and kidney injury molecule-1 (KIM-1) levels in diagnosing AKI in critically ill ful...

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Main Authors: M. A. Daminova, A. I. Safina, M. O. Koporulina
Format: Article
Language:Russian
Published: Ltd. “The National Academy of Pediatric Science and Innovation” 2016-03-01
Series:Rossijskij Vestnik Perinatologii i Pediatrii
Subjects:
Online Access:https://www.ped-perinatology.ru/jour/article/view/180
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author M. A. Daminova
A. I. Safina
M. O. Koporulina
author_facet M. A. Daminova
A. I. Safina
M. O. Koporulina
author_sort M. A. Daminova
collection DOAJ
description Critically ill neonates are at high risk for acute kidney injury (AKI). Objective: to estimate the clinical and diagnostic value of urinary neutrophil gelatinase-associated lipocalin (NGAL) 2, interleukin-18 (IL-18), and kidney injury molecule-1 (KIM-1) levels in diagnosing AKI in critically ill full-term newborn infants. Subjects and methods. A study group consisted of 86 critically ill full-term neonates who were divided into 2 subgroups according to their blood creatinine levels at the age of less than 2 days of life: 1) creati-nine >1,5 mg/dl (и=12) and 2) creatinine <1,5 mg/dl (и=74). A control group included 26 healthy full-term newborns. Results. The incidence of AKI was 14%. Its clinical sign was urine output less thanl, 5 ml/kg/h(/K0,001). On days 3—5 of life, Subgroup 1 showed urinary NGAL values that were twice higher than those in Subgroup 2; on days 10-14, there was a 1,5-fold decrease in this indicator, but it remained at a rather high level in the control group. On days 3-5 of life, the levels of urinary KIM-1 were thrice higher in Subgroup 1 than those in Subgroup 2; on days 18—21, the difference between them was almost 7 times higher (/K0,01). On days 3—5 of life, Subgroup 1 displayed urinary IL-18 values that were twice higher than those in Subgroup 2; on days 18—21, the difference remained at the same level (/K0,05). Conclusion. Determination of urinary NGAL, IL-18, and KIM-1 levels is recommended for the early non-invasive diagnosis of AKI in critically ill full-term neonates. Urinary NGAL and KIM-1 are markers of poor outcomes; IL-18 is a marker of the aggressive nephrotoxicity of the therapy performed.
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spelling doaj.art-cf6a6b4d4b894cdb82a3dd253a343b9d2023-03-13T09:12:41ZrusLtd. “The National Academy of Pediatric Science and Innovation”Rossijskij Vestnik Perinatologii i Pediatrii1027-40652500-22282016-03-01605198205173New early non-invasive biomarkers for acute kidney injury in critically ill full-term neonatal infantsM. A. Daminova0A. I. Safina1M. O. Koporulina2Казанская государственная медицинская академияКазанская государственная медицинская академияКазанская государственная медицинская академияCritically ill neonates are at high risk for acute kidney injury (AKI). Objective: to estimate the clinical and diagnostic value of urinary neutrophil gelatinase-associated lipocalin (NGAL) 2, interleukin-18 (IL-18), and kidney injury molecule-1 (KIM-1) levels in diagnosing AKI in critically ill full-term newborn infants. Subjects and methods. A study group consisted of 86 critically ill full-term neonates who were divided into 2 subgroups according to their blood creatinine levels at the age of less than 2 days of life: 1) creati-nine >1,5 mg/dl (и=12) and 2) creatinine <1,5 mg/dl (и=74). A control group included 26 healthy full-term newborns. Results. The incidence of AKI was 14%. Its clinical sign was urine output less thanl, 5 ml/kg/h(/K0,001). On days 3—5 of life, Subgroup 1 showed urinary NGAL values that were twice higher than those in Subgroup 2; on days 10-14, there was a 1,5-fold decrease in this indicator, but it remained at a rather high level in the control group. On days 3-5 of life, the levels of urinary KIM-1 were thrice higher in Subgroup 1 than those in Subgroup 2; on days 18—21, the difference between them was almost 7 times higher (/K0,01). On days 3—5 of life, Subgroup 1 displayed urinary IL-18 values that were twice higher than those in Subgroup 2; on days 18—21, the difference remained at the same level (/K0,05). Conclusion. Determination of urinary NGAL, IL-18, and KIM-1 levels is recommended for the early non-invasive diagnosis of AKI in critically ill full-term neonates. Urinary NGAL and KIM-1 are markers of poor outcomes; IL-18 is a marker of the aggressive nephrotoxicity of the therapy performed.https://www.ped-perinatology.ru/jour/article/view/180новорожденныекритическое состояниеострое повреждение почекассоциированный с нейтрофильной желатиназой липокалин-2 (нгал)интерлейкин-18 (ил-18)молекулы повреждения почки-1 (ким-1).
spellingShingle M. A. Daminova
A. I. Safina
M. O. Koporulina
New early non-invasive biomarkers for acute kidney injury in critically ill full-term neonatal infants
Rossijskij Vestnik Perinatologii i Pediatrii
новорожденные
критическое состояние
острое повреждение почек
ассоциированный с нейтрофильной желатиназой липокалин-2 (нгал)
интерлейкин-18 (ил-18)
молекулы повреждения почки-1 (ким-1).
title New early non-invasive biomarkers for acute kidney injury in critically ill full-term neonatal infants
title_full New early non-invasive biomarkers for acute kidney injury in critically ill full-term neonatal infants
title_fullStr New early non-invasive biomarkers for acute kidney injury in critically ill full-term neonatal infants
title_full_unstemmed New early non-invasive biomarkers for acute kidney injury in critically ill full-term neonatal infants
title_short New early non-invasive biomarkers for acute kidney injury in critically ill full-term neonatal infants
title_sort new early non invasive biomarkers for acute kidney injury in critically ill full term neonatal infants
topic новорожденные
критическое состояние
острое повреждение почек
ассоциированный с нейтрофильной желатиназой липокалин-2 (нгал)
интерлейкин-18 (ил-18)
молекулы повреждения почки-1 (ким-1).
url https://www.ped-perinatology.ru/jour/article/view/180
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AT aisafina newearlynoninvasivebiomarkersforacutekidneyinjuryincriticallyillfulltermneonatalinfants
AT mokoporulina newearlynoninvasivebiomarkersforacutekidneyinjuryincriticallyillfulltermneonatalinfants