2020
DOI: 10.6061/clinics/2020/e1809
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Pentraxin-2 is Associated with Renal Fibrosis in Patients Undergoing Renal Biopsy

Abstract: OBJECTIVES: Progressive renal disease is characterized by histological changes in the kidney and fibrosis is a common outcome. Renal biopsy is the only diagnostic tool to evaluate these histopathological changes. Pentraxin-2 (PTX-2) is an anti-inflammatory constitutive plasma protein associated with the innate immune system. Recently, as a biomarker, the circulating level of PTX-2 is shown to be decreased in chronic fibrotic diseases. In this study, we aimed to investigate the relationship between… Show more

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Cited by 7 publications
(3 citation statements)
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“…Blood lysyl oxidase (LOX), human epididymis protein 4 (HE4), and pentraxin-2, have the potential to assess renal brosis, but they are easily affected by other brotic diseases (liver brosis, pulmonary brosis, etc.) [15][16][17]. Non-invasive imaging examinations such as B-ultrasound can only indirectly re ect renal brosis through renal anatomical changes, making it di cult to determine the degree of renal brosis early and accurately.…”
Section: Discussionmentioning
confidence: 99%
“…Blood lysyl oxidase (LOX), human epididymis protein 4 (HE4), and pentraxin-2, have the potential to assess renal brosis, but they are easily affected by other brotic diseases (liver brosis, pulmonary brosis, etc.) [15][16][17]. Non-invasive imaging examinations such as B-ultrasound can only indirectly re ect renal brosis through renal anatomical changes, making it di cult to determine the degree of renal brosis early and accurately.…”
Section: Discussionmentioning
confidence: 99%
“…PRM-151 is a recombinant human pentraxin 2/serum amyloid P protein. Serum pentraxin 2 levels are low in fibrotic conditions, including kidney fibrosis, and recombinant human pentraxin 2 delays CKD progression in Alport mice, enhancing lifespan and decreasing kidney inflammation and fibrosis (51,52). Reduced activator protein 1 (AP-1)-driven inflammation is a key mechanism of action.…”
Section: Prm-151mentioning
confidence: 99%
“…Therefore, this non-specific LC-MS approach is not applicable to measure zinpentraxin alfa in human samples. ELISA was also reported to quantify zinpentraxin alfa in nonclinical and clinical studies (1,2,9,10,18,19). It is worth noting that the ELISA reported was incapable of distinguishing zinpentraxin alfa from SAP because neither the capture reagent nor the detection reagent was sufficiently selective.…”
Section: Introductionmentioning
confidence: 99%