2019
DOI: 10.1097/meg.0000000000001291
|View full text |Cite
|
Sign up to set email alerts
|

Comparison of chitinase-3-like protein 1, aspartate aminotransferase-to-platelet ratio index, and fibrosis-4 index with shear-wave elastography

Abstract: Background In the past, there has been an exponential increase in the potential biomarkers that can be used for staging of liver fibrosis. In light of intraobserver and intralobular variations, criticism has been directed at liver biopsy, and its efficacy has been challenged. Shear-wave elastography (SWE) has become a routine method for pre-assessment of liver fibrosis. Serum markers such as chitinase-3-like protein 1 (CHI3L1) also known as YKL-40, aspartate aminotransferase-to-platelet ratio index… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
4
0

Year Published

2019
2019
2022
2022

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 7 publications
(5 citation statements)
references
References 35 publications
1
4
0
Order By: Relevance
“…In our study, we did not find significant elevations of Bl (µmol/L), cholesterol (mmol/L), β-lipoproteins (g/L), AST (U/L), ALT (U/L) in all groups of patients. The use of indexes is a more convenient, cheap and non-invasive method to identify possible fibrotic changes, as also reported by other authors (10,(14)(15)(16)(17)(18) . Liver damage can significantly complicate JIA treatment with MTX; therefore, studies on non-invasive methods for the diagnosis and assessment of liver steatosis and fibrosis as prognostic factors seem to be promising.…”
Section: Discussionsupporting
confidence: 58%
See 1 more Smart Citation
“…In our study, we did not find significant elevations of Bl (µmol/L), cholesterol (mmol/L), β-lipoproteins (g/L), AST (U/L), ALT (U/L) in all groups of patients. The use of indexes is a more convenient, cheap and non-invasive method to identify possible fibrotic changes, as also reported by other authors (10,(14)(15)(16)(17)(18) . Liver damage can significantly complicate JIA treatment with MTX; therefore, studies on non-invasive methods for the diagnosis and assessment of liver steatosis and fibrosis as prognostic factors seem to be promising.…”
Section: Discussionsupporting
confidence: 58%
“…Liver fibrosis and steatosis indexes can be used to identify a group of children who need careful monitoring of the liver. However, the criteria for the appropriateness of using these indexes with JIA are still to be studied (14)(15)(16)(17)(18) . The use of fibrosis and steatosis indexes has been repeatedly studied.…”
Section: Introductionmentioning
confidence: 99%
“…Conversely, no relationship is found between CHI3L1 overexpression and survival in patients with cervical squamous cell carcinoma and liver cancer, while a negative correlation was observed between among patients bearing sarcoma. (from https://kmplot.com, http://www.cgga.org.cn) [177][178][179][180] Serum CHI3L1↑ → liver fibrosis Alcoholic liver disease 181,182 CHI3L1↑ → liver fibrosis Non-alcoholic fatty liver disease 183 CHI3L1↑ → liver fibrosis Bowel diseases IBD Fecal CHI3L1 → mucosal inflammation 184 and endoscopic activity 185 Colitis CHI3L1 binds to bacterial chitin-binding protein, 186,187 enhances bacterial adhesion and invasion, 60 activates Akt signaling 145 and IL-6-mediated STAT3 Phosphorylation 188 Cardiovascular Atherosclerosis CHI3L1↑ → coronary 189,190 and carotid 191 atherosclerosis severity↑, risk↑, 193 exacerbates atherosclerosis 192 Coronary artery disease Type 1 194 and type 2 195 diabetes CHI3L1↑…”
Section: Respiratory Diseases Inflammationmentioning
confidence: 99%
“… 176 For hepatitis B virus (HBV) infection, serum ChI3L1 level is a feasible biomarker to identify advanced liver fibrosis in patients with HBV-related liver fibrosis. 177 179 Moreover, CHI3L1 is regarded as a potential useful marker for monitoring the change of liver fibrosis in patients with chronic HBV infection during therapy. 180 For alcohol-induced fibrosis, increased serum CHI3L1 in patients with liver disease of various degree and etiology seems to reflect fibrosis and fibrogenesis.…”
Section: Chi3l1 In Digestive Diseasesmentioning
confidence: 99%
“…Until now, a series of clinical diagnostic techniques such as liver biopsy, B-mode ultrasonography, TE, and conventional serum markers (type III procollagen, type IV collagen, laminin, and hyaluronidase) have been devised for liver fibrosis diagnosis and assessment [ 65 , 66 ]. However, these methods have disadvantages that include invasiveness, high cost burden, and a lack of specificity.…”
Section: Discussionmentioning
confidence: 99%