Soluble LR11 as a Novel Biomarker in Acute Kawasaki Disease.


Journal

Circulation journal : official journal of the Japanese Circulation Society
ISSN: 1347-4820
Titre abrégé: Circ J
Pays: Japan
ID NLM: 101137683

Informations de publication

Date de publication:
25 05 2022
Historique:
pubmed: 17 9 2021
medline: 28 5 2022
entrez: 16 9 2021
Statut: ppublish

Résumé

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<0.01) or responders (14.3 ng/mL, 11.7-16.5 ng/mL, P<0.01). Using a cutoff of >17.5 ng/mL, non-responders to initial IVIG therapy were identified with 66.7% sensitivity and 78.8% specificity. sLR11 can reflect the state of acute KD and might be a biomarker for patient response to IVIG therapy.

Sections du résumé

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<0.01) or responders (14.3 ng/mL, 11.7-16.5 ng/mL, P<0.01). Using a cutoff of >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.

Identifiants

pubmed: 34526431
doi: 10.1253/circj.CJ-20-1271
doi:

Substances chimiques

Biomarkers 0
Immunoglobulins, Intravenous 0
LDL-Receptor Related Proteins 0
Membrane Transport Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

977-983

Commentaires et corrections

Type : CommentIn

Auteurs

Kenichi Watanabe (K)

Department of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences.

Hiroshi Suzuki (H)

Department of Pediatrics, Uonuma Institute of Community Medicine, Niigata University Medical and Dental Hospital.

Meizi Jiang (M)

Department of Clinical-laboratory and Experimental-Research Medicine, Toho University Sakura Medical Center.

Shinya Tsukano (S)

Department of Pediatrics, Niigata Prefectural Shibata Hospital.

Satoshi Kataoka (S)

Department of Pediatrics, Saiseikai Sanjo Hospital.

Sueshi Ito (S)

Department of Pediatrics, Tsuruoka Municipal Shonai Hospital.

Takatsugu Sakai (T)

Department of Pediatrics, Niigata Medical Center.

Toru Hirokawa (T)

Department of Pediatrics, Saiseikai Niigata Hospital.

Hisanori Haniu (H)

Department of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences.

Fujito Numano (F)

Department of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences.

Satoshi Hoshina (S)

Department of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences.

Satoshi Hasegawa (S)

Department of Pediatrics, Niigata Prefectural Shibata Hospital.

Masamichi Matsunaga (M)

Department of Pediatrics, Niigata Prefectural Shibata Hospital.

Kousei Chiba (K)

Department of Pediatrics, Saiseikai Sanjo Hospital.

Naka Saito (N)

Department of Pediatrics, Tsuruoka Municipal Shonai Hospital.

Hiroshi Yoshida (H)

Department of Pediatrics, Tsuruoka Municipal Shonai Hospital.

Satoru Takami (S)

Department of Pediatrics, Niigata Medical Center.

Soichiro Okubo (S)

Department of Pediatrics, Saiseikai Niigata Hospital.

Harunobu Hirano (H)

Department of Pediatrics, Saiseikai Niigata Hospital.

Akihiko Saitoh (A)

Department of Pediatrics, Niigata University Graduate School of Medical and Dental Sciences.

Hideaki Bujo (H)

Department of Clinical-laboratory and Experimental-Research Medicine, Toho University Sakura Medical Center.

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