Increased red blood cell distribution width in the first year after diagnosis predicts worsening of systemic sclerosis-associated interstitial lung disease at 5 years: A pilot study

Satoshi Ebata, Ayumi Yoshizaki, Takemichi Fukasawa, Asako Yoshizaki-Ogawa, Yoshihide Asano, Kosuke Kashiwabara, Koji Oba, Shinichi Sato

Research output: Contribution to journalArticlepeer-review

Abstract

The course of systemic sclerosis-associated interstitial lung disease (SSc-ILD) varies among individuals. Red blood cell distribution width (RDW) has been reported to be a predictor of idiopathic pulmonary fibrosis. However, there are no studies on the relationship between RDW and SSc-ILD. We conducted a retrospective study of 28 patients who were diagnosed with SSc-ILD on their first visit to our hospital and were followed-up for 5 years. The correlation between the changes in RDW, KL-6, and SP-D (∆RDW, ∆KL-6, ∆SP-D) and the changes in percent-predicted forced lung volume and % carbon monoxide diffusion (∆%FVC, ∆%DLco) was investigated. ∆RDW at 1 year after diagnosis was significantly inversely correlated with ∆%FVC at 5 years after diagnosis (r = −0.51, p < 0.001) and ∆%DLco at 5 years after diagnosis (r = −0.47, p < 0.001), whereas ∆KL-6 and ∆SP-D at 1 year were not correlated with ∆%FVC or ∆%DLco at 5 years. In the group of SSc-ILD patients with RDW increase in the first year after diagnosis, %FVC and %DLco were significantly lower than baseline at 3-, 4-, and 5-year assessments. In the group of patients without RDW increase in the first year, %FVC and %DLco did not decrease during the follow-up period. In conclusion, the changes in RDW in the first year after diagnosis may be useful surrogate markers to predict the long-term course of SSc-ILD.

Original languageEnglish
Article number2274
JournalDiagnostics
Volume11
Issue number12
DOIs
Publication statusPublished - 2021 Dec

Keywords

  • Forced vital capacity
  • Peripheral blood marker
  • Red blood cell distribution width
  • Systemic sclerosis
  • Systemic sclerosis-associated interstitial lung disease

ASJC Scopus subject areas

  • Clinical Biochemistry

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