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Baseline serum syndecan-4 predicts prognosis after the onset of acute exacerbation of idiopathic interstitial pneumonia.
Sato, Yuki; Tanino, Yoshinori; Wang, Xintao; Nikaido, Takefumi; Sato, Suguru; Misa, Kenichi; Togawa, Ryuichi; Frevert, Charles W; Munakata, Mitsuru.
Affiliation
  • Sato Y; Department of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
  • Tanino Y; Department of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
  • Wang X; Department of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
  • Nikaido T; Department of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
  • Sato S; Department of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
  • Misa K; Department of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
  • Togawa R; Department of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushima, Fukushima, Japan.
  • Frevert CW; Division of Pulmonary/Critical Care Medicine, Department of Comparative Medicine, University of Washington, Seattle, Washington, United States of America.
  • Munakata M; The Comparative Pathology Program in the Department of Comparative Medicine, University of Washington, Seattle, Washington, United States of America.
PLoS One ; 12(5): e0176789, 2017.
Article in En | MEDLINE | ID: mdl-28467516
ABSTRACT

BACKGROUND:

Patients with idiopathic interstitial pneumonia can experience acute respiratory worsening, also known as acute exacerbation, with a large deterioration on prognosis. The precise mechanism remains unclear; however, syndecan-4 may be involved. Syndecan-4, a transmembrane heparan sulfate proteoglycan expressed in a variety of cells (e.g., epithelial cells, macrophages, fibroblasts, etc.), performs various biological roles by binding to several proteins through its heparan sulfate glycosaminoglycan side chains. The goal of this study was to clarify the role of syndecan-4 in acute exacerbation of idiopathic interstitial pneumonia.

METHODS:

Patients with idiopathic interstitial pneumonia who had been sequentially admitted to our hospital due to acute exacerbation were retrospectively analyzed. First, serum syndecan-4 levels in the acute exacerbation and clinically stable phases were compared. Second, the relationship between serum syndecan-4 levels and clinical parameters was analyzed. Third, the relationship between serum syndecan-4 levels and prognosis was evaluated.

RESULTS:

Serum syndecan-4 levels were significantly lower in patients with acute exacerbation of idiopathic interstitial pneumonia than in patients in the clinically stable phase. Serum syndecan-4 levels also showed a significant positive correlation with white blood cell count and a weak positive tendency with KL-6 and baseline %VC. Prognosis was significantly worse in patients with idiopathic interstitial pneumonia with high baseline serum syndecan-4 levels than with low baseline levels. Multiple logistic analysis indicated baseline serum syndecan-4 level as the only prognostic predictor following acute exacerbation.

CONCLUSIONS:

Baseline serum syndecan-4 is a possible prognostic biomarker after the onset of acute exacerbation of idiopathic interstitial pneumonia.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Syndecan-4 / Idiopathic Interstitial Pneumonias Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Document type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Syndecan-4 / Idiopathic Interstitial Pneumonias Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male Language: En Journal: PLoS One Journal subject: CIENCIA / MEDICINA Year: 2017 Document type: Article Affiliation country: Japan