Evidence map›Paper›PMID 39311786›Full record

ArticleZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences2024

Expression and predictive value of serum core fucosylated low molecular weight kininogen and alpha-galactosylated antibodies in patients with hepatic fibrosis.

Xiangling Zhang, Zhongshang Dai, Xinqiang Xiao, Zhihao Zeng, Yao Yang, Zhi Gao, Yongfang Jiang, Guozhong Gong, Min Zhang

Abstract read
In one paragraph

Article in Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

9 authors.

Xiangling ZhangDepartment of Infectious Diseases, Second Xiangya Hospital, Central South University, Changsha 410011, China. zxl18153824044@163.com.
Zhongshang DaiDepartment of Infectious Diseases, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Xinqiang XiaoDepartment of Infectious Diseases, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhihao ZengDepartment of Infectious Diseases, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Yao YangDepartment of Infectious Diseases, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhi GaoDepartment of Infectious Diseases, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Yongfang JiangDepartment of Infectious Diseases, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Guozhong GongDepartment of Infectious Diseases, Second Xiangya Hospital, Central South University, Changsha 410011, China.
Min ZhangDepartment of Infectious Diseases, Second Xiangya Hospital, Central South University, Changsha 410011, China. zhangmin001@csu.edu.cn.

Funding

the Changsha Natural Science Foundation kq2202397the Natural Science Foundation of Hunan Province Department Joint Fund 2023JJ60440
6 · The paper itself

Abstract

objectivesHepatic fibrosis is a common pathological basis for many chronic liver diseases and can progress to cirrhosis, a leading cause of mortality in liver diseases. Early identification and reversal of hepatic fibrosis are key in the treatment of chronic liver disease. This study aims to compare the expression levels of serum core fucosylated low molecular weight kininogen (LMWK-Fc) and alpha-galactosylated (α-Gal) antibodies in patients with hepatic fibrosis at different stages, and to evaluate their diagnostic efficacy for hepatic fibrosis.

methodsA retrospective analysis was conducted on 275 patients with chronic liver disease who visited the Department of Infectious Diseases at the Second Xiangya Hospital of Central South University between June 2022 and March 2023. Among these, 115 patients underwent liver biopsy. Based on the extent of collagen deposition and its impact on liver structure and microcirculation, patients were staged from 0 to 4: S0 (no significant collagen deposition in liver tissues; liver structure and microcirculation are normal), S1 (mild collagen deposition in liver tissues, with partial disruption of lobule structure, but microcirculation remains largely normal), S2 (moderate collagen deposition in liver tissues, with partial disruption of lobule structure and microcirculation), S3 (extensive collagen deposition in liver tissues, with substantial disruption of lobule structure and microcirculation), and S4 (development of cirrhosis, with heavy collagen deposition, complete disruption of lobule structure, and severe impairment of microcirculation). Patients were grouped as no fibrosis (S0), fibrosis (S1-S2), and significant fibrosis (S3-S4). For the 160 patients without liver biopsy, they were categorized based on liver stiffness measurement (LSM) value: no fibrosis (F0: LSM<7.3 kPa), fibrosis (F1-F2: LSM 7.3-12.4 kPa), and significant fibrosis (F3-F4: LSM>12.4 kPa). Demographic data (age, gender) and laboratory indicators (alanine transaminase, aspartate transaminase, gamma-glutamyl transferase, alkaline phosphatase, alpha-fetoprotein, platelet count) were collected to calculate the fibrosis-4 index (FIB-4) and aspartate aminotransferase-to-platelet ratio index (APRI). Serum LMWK-Fc and α-Gal antibodies were measured and compared across the groups, and their correlation with fibrosis severity was analyzed. The receiver operating characteristic (ROC) curve was used to assess the predictive value of serum LMWK-Fc and α-Gal antibody levels for hepatic fibrosis.

resultsAmong the 160 patients without complete liver biopsy, serum α-Gal antibody and LMWK-Fc levels increased progressively from the no fibrosis group to the significant fibrosis group, with statistically significant differences (

conclusionsThe expression levels of serum LMWK-Fc and α-Gal antibodies vary across different stages of hepatic fibrosis, suggesting a potential association with fibrosis progression. LMWK-Fc levels have a certain predictive value for the diagnosis of hepatic fibrosis.

Indexed as

Liver CirrhosisAdultAntibodiesFemaleFucoseGalactoseHumansKininogensLiverMaleMiddle AgedPredictive Value of TestsRetrospective StudiesAntibodiesFucoseGalactoseKininogensKNG1 protein, humanalpha-galactosylated antibodiescore fucosylationhepatic fibrosislow molecular weight kininogenserum biomarkers

Identifiers

PMID39311786
PMCPMC11420974

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.