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Soluble LR11 as a Novel Biomarker in Acute Kawasaki Disease

Background: Intimal smooth muscle cells (SMCs) play an important role in the vasculitis caused by Kawasaki disease (KD). Lipoprotein receptor 11 (LR11) is a member of the low-density lipoprotein receptor family, which is expressed markedly in intimal vascular SMCs and secreted in a soluble form (sLR...

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Published in:Circulation Journal 2022/05/25, Vol.86(6), pp.977-983
Main Authors: Watanabe, Kenichi, Suzuki, Hiroshi, Jiang, Meizi, Tsukano, Shinya, Kataoka, Satoshi, Ito, Sueshi, Sakai, Takatsugu, Hirokawa, Toru, Haniu, Hisanori, Numano, Fujito, Hoshina, Satoshi, Hasegawa, Satoshi, Matsunaga, Masamichi, Chiba, Kousei, Saito, Naka, Yoshida, Hiroshi, Takami, Satoru, Okubo, Soichiro, Hirano, Harunobu, Saitoh, Akihiko, Bujo, Hideaki
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cited_by cdi_FETCH-LOGICAL-c551t-23aa7e0ce0b79cf44b8343faed2c85f6c5761c684626381e2c4c537cfdd11d33
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container_end_page 983
container_issue 6
container_start_page 977
container_title Circulation Journal
container_volume 86
creator Watanabe, Kenichi
Suzuki, Hiroshi
Jiang, Meizi
Tsukano, Shinya
Kataoka, Satoshi
Ito, Sueshi
Sakai, Takatsugu
Hirokawa, Toru
Haniu, Hisanori
Numano, Fujito
Hoshina, Satoshi
Hasegawa, Satoshi
Matsunaga, Masamichi
Chiba, Kousei
Saito, Naka
Yoshida, Hiroshi
Takami, Satoru
Okubo, Soichiro
Hirano, Harunobu
Saitoh, Akihiko
Bujo, Hideaki
description Background: Intimal smooth muscle cells (SMCs) play an important role in the vasculitis caused by Kawasaki disease (KD). Lipoprotein receptor 11 (LR11) is a member of the low-density lipoprotein receptor family, which is expressed markedly in intimal vascular SMCs and secreted in a soluble form (sLR11). sLR11 has been recently identified as a potential vascular lesion biomarker. sLR11 is reportedly elevated in patients with coronary artery lesions long after KD, but there is no description of sLR11 in acute KD. Our aim was to determine the sLR11 dynamics in acute KD and to assess its usefulness as a biomarker.Methods and Results: 106 acute KD patients and 18 age-matched afebrile controls were enrolled. KD patients were classified into the following subgroups: intravenous immunoglobulin (IVIG) responders (n=85) and non-responders (n=21). Serum sLR11 levels before IVIG therapy were higher in non-responders (median, 19.6 ng/mL; interquartile range [IQR], 13.0–24.9 ng/mL) than in controls (11.9 ng/mL, 10.4–14.9 ng/mL, P
doi_str_mv 10.1253/circj.CJ-20-1271
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Lipoprotein receptor 11 (LR11) is a member of the low-density lipoprotein receptor family, which is expressed markedly in intimal vascular SMCs and secreted in a soluble form (sLR11). sLR11 has been recently identified as a potential vascular lesion biomarker. sLR11 is reportedly elevated in patients with coronary artery lesions long after KD, but there is no description of sLR11 in acute KD. Our aim was to determine the sLR11 dynamics in acute KD and to assess its usefulness as a biomarker.Methods and Results: 106 acute KD patients and 18 age-matched afebrile controls were enrolled. KD patients were classified into the following subgroups: intravenous immunoglobulin (IVIG) responders (n=85) and non-responders (n=21). Serum sLR11 levels before IVIG therapy were higher in non-responders (median, 19.6 ng/mL; interquartile range [IQR], 13.0–24.9 ng/mL) than in controls (11.9 ng/mL, 10.4–14.9 ng/mL, P&lt;0.01) or responders (14.3 ng/mL, 11.7–16.5 ng/mL, P&lt;0.01). Using a cutoff of &gt;17.5 ng/mL, non-responders to initial IVIG therapy were identified with 66.7% sensitivity and 78.8% specificity.Conclusions: sLR11 can reflect the state of acute KD and might be a biomarker for patient response to IVIG therapy.</description><identifier>ISSN: 1346-9843</identifier><identifier>ISSN: 1347-4820</identifier><identifier>EISSN: 1347-4820</identifier><identifier>DOI: 10.1253/circj.CJ-20-1271</identifier><identifier>PMID: 34526431</identifier><language>eng</language><publisher>Japan: The Japanese Circulation Society</publisher><subject>Biomarkers ; Humans ; Immunoglobulins, Intravenous - therapeutic use ; Intravenous immunoglobulins ; Kawasaki disease ; LDL-Receptor Related Proteins ; LR11 ; Membrane Transport Proteins ; Mucocutaneous Lymph Node Syndrome - diagnosis ; Mucocutaneous Lymph Node Syndrome - drug therapy</subject><ispartof>Circulation Journal, 2022/05/25, Vol.86(6), pp.977-983</ispartof><rights>2022, THE JAPANESE CIRCULATION SOCIETY</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c551t-23aa7e0ce0b79cf44b8343faed2c85f6c5761c684626381e2c4c537cfdd11d33</citedby><cites>FETCH-LOGICAL-c551t-23aa7e0ce0b79cf44b8343faed2c85f6c5761c684626381e2c4c537cfdd11d33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34526431$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Watanabe, Kenichi</creatorcontrib><creatorcontrib>Suzuki, Hiroshi</creatorcontrib><creatorcontrib>Jiang, Meizi</creatorcontrib><creatorcontrib>Tsukano, Shinya</creatorcontrib><creatorcontrib>Kataoka, Satoshi</creatorcontrib><creatorcontrib>Ito, Sueshi</creatorcontrib><creatorcontrib>Sakai, Takatsugu</creatorcontrib><creatorcontrib>Hirokawa, Toru</creatorcontrib><creatorcontrib>Haniu, Hisanori</creatorcontrib><creatorcontrib>Numano, Fujito</creatorcontrib><creatorcontrib>Hoshina, Satoshi</creatorcontrib><creatorcontrib>Hasegawa, Satoshi</creatorcontrib><creatorcontrib>Matsunaga, Masamichi</creatorcontrib><creatorcontrib>Chiba, Kousei</creatorcontrib><creatorcontrib>Saito, Naka</creatorcontrib><creatorcontrib>Yoshida, Hiroshi</creatorcontrib><creatorcontrib>Takami, Satoru</creatorcontrib><creatorcontrib>Okubo, Soichiro</creatorcontrib><creatorcontrib>Hirano, Harunobu</creatorcontrib><creatorcontrib>Saitoh, Akihiko</creatorcontrib><creatorcontrib>Bujo, Hideaki</creatorcontrib><title>Soluble LR11 as a Novel Biomarker in Acute Kawasaki Disease</title><title>Circulation Journal</title><addtitle>Circ J</addtitle><description>Background: Intimal smooth muscle cells (SMCs) play an important role in the vasculitis caused by Kawasaki disease (KD). Lipoprotein receptor 11 (LR11) is a member of the low-density lipoprotein receptor family, which is expressed markedly in intimal vascular SMCs and secreted in a soluble form (sLR11). sLR11 has been recently identified as a potential vascular lesion biomarker. sLR11 is reportedly elevated in patients with coronary artery lesions long after KD, but there is no description of sLR11 in acute KD. Our aim was to determine the sLR11 dynamics in acute KD and to assess its usefulness as a biomarker.Methods and Results: 106 acute KD patients and 18 age-matched afebrile controls were enrolled. KD patients were classified into the following subgroups: intravenous immunoglobulin (IVIG) responders (n=85) and non-responders (n=21). Serum sLR11 levels before IVIG therapy were higher in non-responders (median, 19.6 ng/mL; interquartile range [IQR], 13.0–24.9 ng/mL) than in controls (11.9 ng/mL, 10.4–14.9 ng/mL, P&lt;0.01) or responders (14.3 ng/mL, 11.7–16.5 ng/mL, P&lt;0.01). 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Lipoprotein receptor 11 (LR11) is a member of the low-density lipoprotein receptor family, which is expressed markedly in intimal vascular SMCs and secreted in a soluble form (sLR11). sLR11 has been recently identified as a potential vascular lesion biomarker. sLR11 is reportedly elevated in patients with coronary artery lesions long after KD, but there is no description of sLR11 in acute KD. Our aim was to determine the sLR11 dynamics in acute KD and to assess its usefulness as a biomarker.Methods and Results: 106 acute KD patients and 18 age-matched afebrile controls were enrolled. KD patients were classified into the following subgroups: intravenous immunoglobulin (IVIG) responders (n=85) and non-responders (n=21). Serum sLR11 levels before IVIG therapy were higher in non-responders (median, 19.6 ng/mL; interquartile range [IQR], 13.0–24.9 ng/mL) than in controls (11.9 ng/mL, 10.4–14.9 ng/mL, P&lt;0.01) or responders (14.3 ng/mL, 11.7–16.5 ng/mL, P&lt;0.01). Using a cutoff of &gt;17.5 ng/mL, non-responders to initial IVIG therapy were identified with 66.7% sensitivity and 78.8% specificity.Conclusions: sLR11 can reflect the state of acute KD and might be a biomarker for patient response to IVIG therapy.</abstract><cop>Japan</cop><pub>The Japanese Circulation Society</pub><pmid>34526431</pmid><doi>10.1253/circj.CJ-20-1271</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source Freely Accessible Journals
subjects Biomarkers
Humans
Immunoglobulins, Intravenous - therapeutic use
Intravenous immunoglobulins
Kawasaki disease
LDL-Receptor Related Proteins
LR11
Membrane Transport Proteins
Mucocutaneous Lymph Node Syndrome - diagnosis
Mucocutaneous Lymph Node Syndrome - drug therapy
title Soluble LR11 as a Novel Biomarker in Acute Kawasaki Disease
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