High presepsin concentrations in bile and its marked elevation in biliary tract diseases: A retrospective analysis
•Presepsin elevated without apparent infection in TAFRO syndrome and malignant lymphoma.•Presepsin is correlated with elevated biliary enzymes without renal dysfunction or sepsis.•Bile presepsin is high in cases of dilated intrahepatic or extrahepatic bile ducts. Presepsin is a diagnostic and progno...
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| Veröffentlicht in: | Clinica chimica acta 2021-10, Vol.521, p.278-284 |
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| creator | Yamaguchi, Takashi Ohira, Masahiro Kawagoe, Naoyuki Nakamura, Shoko Tanaka, Sho Oka, Rena Watanabe, Yasuhiro Sato, Yuta Nagayama, Daiji Saiki, Atsuhito Matsuzawa, Yasuo Bujo, Hideaki Terai, Kensuke Hiruta, Nobuyuki Tatsuno, Ichiro Nakaseko, Chiaki Kikuchi, Hidemasa Matsuoka, Katsuyoshi Yokota, Hiromitsu Shimizu, Naomi |
| description | •Presepsin elevated without apparent infection in TAFRO syndrome and malignant lymphoma.•Presepsin is correlated with elevated biliary enzymes without renal dysfunction or sepsis.•Bile presepsin is high in cases of dilated intrahepatic or extrahepatic bile ducts.
Presepsin is a diagnostic and prognostic biomarker of both bacterial infection and sepsis; however, elevated presepsin levels have also been observed without sepsis. We conducted several analyses to evaluate the clinical laboratory parameters affecting presepsin levels.
We analyzed the association between sequential organ failure assessment (SOFA) scores and plasma presepsin levels and then analyzed clinical laboratory parameters in 567 patients with univariate and multivariate regression analysis and analysis of covariance (ANCOVA). We also determined presepsin in the bile of 11 patients and examined the presepsin immunostaining in liver.
Spearman’s rank correlation analysis with loge change revealed that presepsin levels were closely associated with loge-transformed SOFA score (ρ = 0.541), alkaline phosphatase (ALP); (ρ = 0.454) and gamma-glutamyl transferase; (ρ = 0.505). Multivariate regression analysis revealed that loge-transformed SOFA score (β-coefficient = 0.316), ALP level (β-coefficient = 0.380), and creatinine level (β-coefficient = 0.290) independently and significantly affected loge presepsin levels. ANCOVA revealed that presepsin levels were significantly higher in patients with hepatobiliary disease. Patients who presented with dilatation of the bile ducts and elevated ALP levels or total bilirubin levels exhibited high presepsin levels in the bile. Presepsin production in liver Kupffer cells was also confirmed by immunostaining.
Presepsin levels is correlated with the elevation of biliary enzymes in patients without renal dysfunction or sepsis. Additionally, presepsin exists with high concentrations in the bile and is positive in Kupffer cells. |
| doi_str_mv | 10.1016/j.cca.2021.07.025 |
| format | Article |
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Presepsin is a diagnostic and prognostic biomarker of both bacterial infection and sepsis; however, elevated presepsin levels have also been observed without sepsis. We conducted several analyses to evaluate the clinical laboratory parameters affecting presepsin levels.
We analyzed the association between sequential organ failure assessment (SOFA) scores and plasma presepsin levels and then analyzed clinical laboratory parameters in 567 patients with univariate and multivariate regression analysis and analysis of covariance (ANCOVA). We also determined presepsin in the bile of 11 patients and examined the presepsin immunostaining in liver.
Spearman’s rank correlation analysis with loge change revealed that presepsin levels were closely associated with loge-transformed SOFA score (ρ = 0.541), alkaline phosphatase (ALP); (ρ = 0.454) and gamma-glutamyl transferase; (ρ = 0.505). Multivariate regression analysis revealed that loge-transformed SOFA score (β-coefficient = 0.316), ALP level (β-coefficient = 0.380), and creatinine level (β-coefficient = 0.290) independently and significantly affected loge presepsin levels. ANCOVA revealed that presepsin levels were significantly higher in patients with hepatobiliary disease. Patients who presented with dilatation of the bile ducts and elevated ALP levels or total bilirubin levels exhibited high presepsin levels in the bile. Presepsin production in liver Kupffer cells was also confirmed by immunostaining.
Presepsin levels is correlated with the elevation of biliary enzymes in patients without renal dysfunction or sepsis. Additionally, presepsin exists with high concentrations in the bile and is positive in Kupffer cells.</description><identifier>ISSN: 0009-8981</identifier><identifier>EISSN: 1873-3492</identifier><identifier>DOI: 10.1016/j.cca.2021.07.025</identifier><identifier>PMID: 34331951</identifier><language>eng</language><publisher>AMSTERDAM: Elsevier B.V</publisher><subject>Alkaline phosphatase ; Bile ; Life Sciences & Biomedicine ; Medical Laboratory Technology ; Presepsin ; Science & Technology ; Sepsis ; Sequential organ failure assessment (SOFA) score</subject><ispartof>Clinica chimica acta, 2021-10, Vol.521, p.278-284</ispartof><rights>2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>2</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000685288700022</woscitedreferencesoriginalsourcerecordid><cites>FETCH-LOGICAL-c348t-be6ea47b4f945812c31dd11322539a862af5dd4e42e4b92e6e2af15e8aae275b3</cites><orcidid>0000-0003-1175-226X ; 0000-0001-7470-6303 ; 0000-0002-2950-7660 ; 0000-0003-0464-4674 ; 0000-0001-6119-8012</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cca.2021.07.025$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27928,27929,45999</link.rule.ids></links><search><creatorcontrib>Yamaguchi, Takashi</creatorcontrib><creatorcontrib>Ohira, Masahiro</creatorcontrib><creatorcontrib>Kawagoe, Naoyuki</creatorcontrib><creatorcontrib>Nakamura, Shoko</creatorcontrib><creatorcontrib>Tanaka, Sho</creatorcontrib><creatorcontrib>Oka, Rena</creatorcontrib><creatorcontrib>Watanabe, Yasuhiro</creatorcontrib><creatorcontrib>Sato, Yuta</creatorcontrib><creatorcontrib>Nagayama, Daiji</creatorcontrib><creatorcontrib>Saiki, Atsuhito</creatorcontrib><creatorcontrib>Matsuzawa, Yasuo</creatorcontrib><creatorcontrib>Bujo, Hideaki</creatorcontrib><creatorcontrib>Terai, Kensuke</creatorcontrib><creatorcontrib>Hiruta, Nobuyuki</creatorcontrib><creatorcontrib>Tatsuno, Ichiro</creatorcontrib><creatorcontrib>Nakaseko, Chiaki</creatorcontrib><creatorcontrib>Kikuchi, Hidemasa</creatorcontrib><creatorcontrib>Matsuoka, Katsuyoshi</creatorcontrib><creatorcontrib>Yokota, Hiromitsu</creatorcontrib><creatorcontrib>Shimizu, Naomi</creatorcontrib><title>High presepsin concentrations in bile and its marked elevation in biliary tract diseases: A retrospective analysis</title><title>Clinica chimica acta</title><addtitle>CLIN CHIM ACTA</addtitle><description>•Presepsin elevated without apparent infection in TAFRO syndrome and malignant lymphoma.•Presepsin is correlated with elevated biliary enzymes without renal dysfunction or sepsis.•Bile presepsin is high in cases of dilated intrahepatic or extrahepatic bile ducts.
Presepsin is a diagnostic and prognostic biomarker of both bacterial infection and sepsis; however, elevated presepsin levels have also been observed without sepsis. We conducted several analyses to evaluate the clinical laboratory parameters affecting presepsin levels.
We analyzed the association between sequential organ failure assessment (SOFA) scores and plasma presepsin levels and then analyzed clinical laboratory parameters in 567 patients with univariate and multivariate regression analysis and analysis of covariance (ANCOVA). We also determined presepsin in the bile of 11 patients and examined the presepsin immunostaining in liver.
Spearman’s rank correlation analysis with loge change revealed that presepsin levels were closely associated with loge-transformed SOFA score (ρ = 0.541), alkaline phosphatase (ALP); (ρ = 0.454) and gamma-glutamyl transferase; (ρ = 0.505). Multivariate regression analysis revealed that loge-transformed SOFA score (β-coefficient = 0.316), ALP level (β-coefficient = 0.380), and creatinine level (β-coefficient = 0.290) independently and significantly affected loge presepsin levels. ANCOVA revealed that presepsin levels were significantly higher in patients with hepatobiliary disease. Patients who presented with dilatation of the bile ducts and elevated ALP levels or total bilirubin levels exhibited high presepsin levels in the bile. Presepsin production in liver Kupffer cells was also confirmed by immunostaining.
Presepsin levels is correlated with the elevation of biliary enzymes in patients without renal dysfunction or sepsis. Additionally, presepsin exists with high concentrations in the bile and is positive in Kupffer cells.</description><subject>Alkaline phosphatase</subject><subject>Bile</subject><subject>Life Sciences & Biomedicine</subject><subject>Medical Laboratory Technology</subject><subject>Presepsin</subject><subject>Science & Technology</subject><subject>Sepsis</subject><subject>Sequential organ failure assessment (SOFA) score</subject><issn>0009-8981</issn><issn>1873-3492</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>HGBXW</sourceid><recordid>eNqNkE2P0zAQhi0EYsvCD-DmIxJK8GfiwGlVAYu0Ehc4W44zAZdsEjxuV_33TLcVR8TJ9uh9Xo0fxl5LUUshm3e7OsZQK6FkLdpaKPuEbaRrdaVNp56yjRCiq1zn5BV7gbijpxGNfM6utNFadlZuWL5NP37yNQPCimnmcZkjzCWHkpYZOU36NAEP88BTQX4f8i8YOExweExcAinkIycoFj4khICA7_kNz1DygivEkg6njjAdMeFL9mwME8Kry3nNvn_6-G17W919_fxle3NXRW1cqXpoIJi2N2NnrJMqajkMUmqlrO6Ca1QY7TAYMApM3ylK00RacCGAam2vr9mbc--al997wOLvE0aYpjDDskevrG2prFUdReU5GmlfzDD6NSf669FL4U-q_c6Tan9S7UXrSTUxb8_MA_TLiDEBmfvLkevGWeVcSzelKO3-P71N5dHudtnPhdAPZxRI1iFB9hd8SJnU-mFJ_1jzD3szp3I</recordid><startdate>202110</startdate><enddate>202110</enddate><creator>Yamaguchi, Takashi</creator><creator>Ohira, Masahiro</creator><creator>Kawagoe, Naoyuki</creator><creator>Nakamura, Shoko</creator><creator>Tanaka, Sho</creator><creator>Oka, Rena</creator><creator>Watanabe, Yasuhiro</creator><creator>Sato, Yuta</creator><creator>Nagayama, Daiji</creator><creator>Saiki, Atsuhito</creator><creator>Matsuzawa, Yasuo</creator><creator>Bujo, Hideaki</creator><creator>Terai, Kensuke</creator><creator>Hiruta, Nobuyuki</creator><creator>Tatsuno, Ichiro</creator><creator>Nakaseko, Chiaki</creator><creator>Kikuchi, Hidemasa</creator><creator>Matsuoka, Katsuyoshi</creator><creator>Yokota, Hiromitsu</creator><creator>Shimizu, Naomi</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>BLEPL</scope><scope>DTL</scope><scope>HGBXW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1175-226X</orcidid><orcidid>https://orcid.org/0000-0001-7470-6303</orcidid><orcidid>https://orcid.org/0000-0002-2950-7660</orcidid><orcidid>https://orcid.org/0000-0003-0464-4674</orcidid><orcidid>https://orcid.org/0000-0001-6119-8012</orcidid></search><sort><creationdate>202110</creationdate><title>High presepsin concentrations in bile and its marked elevation in biliary tract diseases: A retrospective analysis</title><author>Yamaguchi, Takashi ; 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Presepsin is a diagnostic and prognostic biomarker of both bacterial infection and sepsis; however, elevated presepsin levels have also been observed without sepsis. We conducted several analyses to evaluate the clinical laboratory parameters affecting presepsin levels.
We analyzed the association between sequential organ failure assessment (SOFA) scores and plasma presepsin levels and then analyzed clinical laboratory parameters in 567 patients with univariate and multivariate regression analysis and analysis of covariance (ANCOVA). We also determined presepsin in the bile of 11 patients and examined the presepsin immunostaining in liver.
Spearman’s rank correlation analysis with loge change revealed that presepsin levels were closely associated with loge-transformed SOFA score (ρ = 0.541), alkaline phosphatase (ALP); (ρ = 0.454) and gamma-glutamyl transferase; (ρ = 0.505). Multivariate regression analysis revealed that loge-transformed SOFA score (β-coefficient = 0.316), ALP level (β-coefficient = 0.380), and creatinine level (β-coefficient = 0.290) independently and significantly affected loge presepsin levels. ANCOVA revealed that presepsin levels were significantly higher in patients with hepatobiliary disease. Patients who presented with dilatation of the bile ducts and elevated ALP levels or total bilirubin levels exhibited high presepsin levels in the bile. Presepsin production in liver Kupffer cells was also confirmed by immunostaining.
Presepsin levels is correlated with the elevation of biliary enzymes in patients without renal dysfunction or sepsis. Additionally, presepsin exists with high concentrations in the bile and is positive in Kupffer cells.</abstract><cop>AMSTERDAM</cop><pub>Elsevier B.V</pub><pmid>34331951</pmid><doi>10.1016/j.cca.2021.07.025</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-1175-226X</orcidid><orcidid>https://orcid.org/0000-0001-7470-6303</orcidid><orcidid>https://orcid.org/0000-0002-2950-7660</orcidid><orcidid>https://orcid.org/0000-0003-0464-4674</orcidid><orcidid>https://orcid.org/0000-0001-6119-8012</orcidid></addata></record> |
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| subjects | Alkaline phosphatase Bile Life Sciences & Biomedicine Medical Laboratory Technology Presepsin Science & Technology Sepsis Sequential organ failure assessment (SOFA) score |
| title | High presepsin concentrations in bile and its marked elevation in biliary tract diseases: A retrospective analysis |
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