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Further evidence for association of YKL-40 with severe asthma airway remodeling.
Kimura, Hirokazu; Shimizu, Kaoruko; Tanabe, Naoya; Makita, Hironi; Taniguchi, Natsuko; Kimura, Hiroki; Suzuki, Masaru; Abe, Yuki; Matsumoto-Sasaki, Machiko; Oguma, Akira; Takimoto-Sato, Michiko; Takei, Nozomu; Matsumoto, Munehiro; Goudarzi, Houman; Sato, Susumu; Ono, Junya; Izuhara, Kenji; Hirai, Toyohiro; Nishimura, Masaharu; Konno, Satoshi.
Afiliação
  • Kimura H; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan. Electronic address: hikimura@pop.med.hokudai.ac.jp.
  • Shimizu K; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Tanabe N; Graduate School of Medicine, Department of Respiratory Medicine, Kyoto University, Kyoto, Japan.
  • Makita H; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Taniguchi N; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Kimura H; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Suzuki M; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Abe Y; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Matsumoto-Sasaki M; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Oguma A; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Takimoto-Sato M; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Takei N; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Matsumoto M; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Goudarzi H; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
  • Sato S; Graduate School of Medicine, Department of Respiratory Medicine, Kyoto University, Kyoto, Japan.
  • Ono J; R&D Center, Shino-Test Corporation, Kanagawa, Japan.
  • Izuhara K; Division of Medical Biochemistry, Department of Biomolecular Sciences, Saga Medical School, Saga, Japan.
  • Hirai T; Graduate School of Medicine, Department of Respiratory Medicine, Kyoto University, Kyoto, Japan.
  • Nishimura M; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan; Hokkaido Medical Research Institute for Respiratory Diseases, Sapporo, Japan.
  • Konno S; Faculty of Medicine, Department of Respiratory Medicine, Hokkaido University, Sapporo, Japan.
Ann Allergy Asthma Immunol ; 128(6): 682-688.e5, 2022 06.
Article em En | MEDLINE | ID: mdl-35342020
BACKGROUND: The chitinase-like protein YKL-40 is associated with airflow limitation on spirometry and airway remodeling in patients with asthma. It remains unclear whether YKL-40 is associated with morphologic changes in the airways and parenchyma or with future progression of airflow limitation in severe asthma. OBJECTIVE: To evaluate the association of circulating YKL-40 levels with morphologic changes in the airways and parenchyma and with longitudinal progression of airflow limitation. METHODS: The patients were participants in the Hokkaido Severe Asthma Cohort Study (n = 127), including smokers. This study consisted of 2 parts. In analysis 1, we analyzed associations between circulating YKL-40 levels and several asthma-related indices, including computed tomography-derived indices of proximal wall area percentage, the complexity of the airways (airway fractal dimension), and the parenchyma (exponent D) cross-sectionally (n = 97). In analysis 2, we evaluated the impact of circulating YKL-40 levels on forced expiratory volume in 1 second (FEV1) decline longitudinally for a 5-year follow-up (n = 103). RESULTS: Circulating YKL-40 levels were significantly associated with proximal wall area percentage and airway fractal dimension (r = 0.25, P = .01; r = -0.22, P = .04, respectively), but not with exponent D. The mean annual change in FEV1 was -33.7 (± 23.3) mL/y, and the circulating YKL-40 level was a significant independent factor associated with annual FEV1 decline (ß = -0.24, P = .02), even after controlling for exponent D (ß = -0.26, P = .01). CONCLUSION: These results provide further evidence for the association of YKL-40 with the pathogenesis of airway remodeling in severe asthma.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Remodelação das Vias Aéreas / Proteína 1 Semelhante à Quitinase-3 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Ann Allergy Asthma Immunol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Asma / Remodelação das Vias Aéreas / Proteína 1 Semelhante à Quitinase-3 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Ann Allergy Asthma Immunol Ano de publicação: 2022 Tipo de documento: Article