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The Role of Biomarkers in Acute Kidney Injury
Nattachai Srisawat1, John A Kellum2
1Division of Nephrology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand 3rd floor, Anantamahidol Building, Henri Dunant Road, Pathumwan, Bangkok 10330, Thailand; Department of Critical Care Medicine, Center for Critical Care Nephrology, The CRISMA Center, University of Pittsburgh School of Medicine, 3347 Forbes Avenue, Suite 220, Pittsburgh, PA 15213, USA; Excellence Center for Critical Care Nephrology, King Chulalongkorn Memorial Hospital, 1873 Rama IV Road, Khwaeng Pathum Wan, Khet Pathum Wan, Krung Thep Maha Nakhon 10330, Thailand; Critical Care Nephrology Research Unit, Chulalongkorn University, 3rd floor, Anantamahidol Building, Henri Dunant Road, Pathumwan, Bangkok 10330, Thailand; Academic of Science, Royal Society of Thailand, 197 Rama 5 Road Khwaeng Dusit, Khet Dusit, Bangkok 10300, Thailand; Tropical Medicine Cluster, Chulalongkorn University, 3rd floor, Anantamahidol Building, Henri Dunant Road, Pathumwan, Bangkok 10330, Thailand.
New biomarkers for acute kidney injury (AKI), such as tissue inhibitor of metalloproteinases-2 (TIMP-2) and insulinlike growth factor-binding protein 7 (IGFBP7), show promise for early detection and outcome prediction.
Area of Science:
- Biomarkers and diagnostics
- Nephrology
- Critical care medicine
Background:
- Acute kidney injury (AKI) detection and outcome prediction remain challenging.
- Existing biomarkers often lag behind clinical indicators like serum creatinine and urine output.
- Limited research exists on the clinical impact of implementing novel AKI biomarkers.
Purpose of the Study:
- To review the development and clinical utility of a second generation of AKI biomarkers.
- To highlight the potential of tissue inhibitor of metalloproteinases-2 (TIMP-2) and insulinlike growth factor-binding protein 7 (IGFBP7) in AKI management.
Main Methods:
- Review of existing literature on AKI biomarkers.
- Analysis of clinical studies supporting the approval and utility of new biomarkers.
- Focus on tissue inhibitor of metalloproteinases-2 (TIMP-2) and insulinlike growth factor-binding protein 7 (IGFBP7).
Main Results:
- Second-generation AKI biomarkers, including TIMP-2 and IGFBP7, demonstrate improved sensitivity and specificity over traditional markers.
- These biomarkers are often expressed earlier than serum creatinine.
- Regulatory approval in numerous countries suggests established clinical utility based on rigorous studies.
Conclusions:
- Tissue inhibitor of metalloproteinases-2 (TIMP-2) and insulinlike growth factor-binding protein 7 (IGFBP7) represent significant advancements in AKI diagnostics.
- These biomarkers offer potential for earlier and more accurate detection and outcome prediction in AKI.
- Further studies on implementation are needed to fully realize their clinical impact.
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