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Value of [68Ga]Ga-FAPI-04 imaging in the diagnosis of renal fibrosis
Purpose Renal fibrosis is a pathological state in the progression of chronic kidney disease. Early detection and treatment are vital to prolonging patient survival. Renal puncture examination is the gold standard for renal fibrosis, but it has several limitations. This study aims to evaluate the dia...
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Published in: | European journal of nuclear medicine and molecular imaging 2021-10, Vol.48 (11), p.3493-3501 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Purpose
Renal fibrosis is a pathological state in the progression of chronic kidney disease. Early detection and treatment are vital to prolonging patient survival. Renal puncture examination is the gold standard for renal fibrosis, but it has several limitations. This study aims to evaluate the diagnostic performance of a novel PET radiotracer, [
68
Ga]Ga-fibroblast activation protein inhibitor (FAPI)-04, which specifically images fibroblast activation protein (FAP) expression for renal fibrosis.
Methods
All patients underwent renal puncture before receiving [
68
Ga]Ga-FAPI-04 PET/CT imaging. They then underwent [
68
Ga]Ga-FAPI-04 PET/CT and immunochemistry examinations. The data obtained were analyzed.
Results
The [
68
Ga]Ga-FAPI-04 PET/CT examination results demonstrated that almost all patients (12/13) exhibited increased radiotracer uptake. The maximum standardized uptake value (SUVmax) in patients with mild, moderate, and severe fibrosis was 3.92 ± 1.50, 5.98 ± 1.6, and 7.67 ± 2.23, respectively.
Conclusion
Compared with renal puncture examination, non-invasive imaging of FAP expression through [
68
Ga]Ga-FAPI-04 PET/CT quickly demonstrates bilateral kidney conditions with high sensitivity. [
68
Ga]Ga-FAPI-04 PET/CT can facilitate the evaluation of disease progression, diagnosis, and the development of a treatment plan. |
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ISSN: | 1619-7070 1619-7089 |
DOI: | 10.1007/s00259-021-05343-x |