Evidence map›Paper›PMID 38244124›Full record

ArticleDigestive diseases and sciences2024

VWF/ADAMTS13 Ratio as a Potential Predictive Biomarker for Acute Kidney Injury Onset in Cirrhosis.

Shohei Asada, Tadashi Namisaki, Kosuke Kaji, Hiroaki Takaya, Takahiro Kubo, Takemi Akahane, Hideto Kawaratani, Norihisa Nishimura, Soichi Takeda, Hiroyuki Masuda and 11 more

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Article in Digestive diseases and 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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0cells of the map it votes in
0citing papers in PubMed
0.7field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed, 2 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

21 authors at 1 institution in 1 country.

Shohei AsadaDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Tadashi NamisakiDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan. tadashin@naramed-u.ac.jp.ORCID http://orcid.org/0000-0002-3158-5318
Kosuke KajiDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Hiroaki TakayaDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Takahiro KuboDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Takemi AkahaneDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Hideto KawarataniDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Norihisa NishimuraDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Soichi TakedaDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Hiroyuki MasudaDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Akihiko ShibamotoDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Takashi InoueDepartment of Evidence-Based Medicine, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Satoshi IwaiDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Fumimasa TomookaDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Yuki TsujiDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Yukihisa FujinagaDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Koh KitagawaDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Akira MitoroDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Shinya SatoDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Masanori MatsumotoDepartment of Hematology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Hitoshi YoshijiDepartment of Gastroenterology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara, Japan.
Nara Medical University · JP

Funding

Japan Agency for Medical Research and Development 22fk0210097h0002
6 · The paper itself

Abstract

aimWe investigated the von Willebrand factor to ADAMTS13 ratio (von Willebrand factor [VWF]:Ag/ADAMTS13:AC) as a potential biomarker for the outcomes of acute kidney injury (AKI) in liver cirrhosis (LC).

methodsThis retrospective cross-sectional study included patients with LC who developed AKI (AKI group: n = 91) and patients with LC who did not develop AKI [non-AKI (NAKI) group, n = 91] as a control group. Plasma levels of the von Willebrand factor antigen (Ag) and ADAMTS13 activity (AC) were measured in patients with AKI or NAKI. Moreover, risk factors for onset of AKI, AKI-associated 90-day mortality, and poor AKI treatment response were identified.

resultsThe AKI group had a significantly higher VWF:Ag/ADAMTS13:AC than the NAKI group. Values of VWF:Ag/ADAMTS13:AC ≥ 5.7 were identified as risk factors for AKI onset in patients with LC (odds ratio [OR] 2.56; 95% CI 1.26-4.99; p < 0.001). Among patients with AKI, values of VWF:Ag/ADAMTS13:AC ≥ 9.0 were identified as risk factors for 90-day mortality (OR 6.83; 95% CI 2.32-20.10; p < 0.001). Cumulative survival was significantly lower in those with high (≥ 9.0) than in those with low (< 9.0) VWF:Ag/ADAMTS13:AC. Furthermore, values of VWF:Ag/ADAMTS13:AC ≥ 7.4 were identified as risk factors for poor treatment response (OR 4.2; 95% CI 1.39-12.70; p < 0.001). The treatment response rates were significantly higher in those with low (< 7.4) VWF:Ag/ADAMTS13:AC than in those with high (≥ 7.4) VWF:Ag/ADAMTS13:AC.

conclusionVWF:Ag/ADAMTS13:AC potentially predicts the onset, prognosis, and treatment response of AKI in patients with LC.

Indexed as

Acute Kidney Injuryvon Willebrand FactorADAMTS13 ProteinBiomarkersCross-Sectional StudiesHumansLiver CirrhosisRetrospective StudiesADAMTS13 ProteinADAMTS13 protein, humanBiomarkersvon Willebrand FactorADAMTS13:ACAKI outcomesPredictionVWF:Ag

Identifiers

PMID38244124
OpenAlexW4391046316

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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.