Geriatric nutritional risk index in antifibrotic therapy can predict tolerability and mortality risk

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Authors: Takuya Masuda, Yasutaka Mochizuka, Yuzo Suzuki, Masato Kono, Sayomi Matsushima, Shinpei Kato, Kosuke Suzuki, Kazuki Tanaka, Keigo Koda, Toshihiro Masuda, Miho Kanai, Masaki Ikeda
+17 more Mitsuru Niwa, Yusuke Kaida, Hiroyuki Matsuda, Masanori Harada, Dai Hashimoto, Kazuhiro Asada, Koshi Yokomura, Mikio Toyoshima, Yusuke Inoue, Hideki Yasui, Hironao Hozumi, Masato Karayama, Kazuki Furuhashi, Noriyuki Enomoto, Tomoyuki Fujisawa, Naoki Inui, Takafumi Suda
Cited by: 1
References: 41

Abstract

No prospective studies have investigated the relationship between nutritional status, tolerability to antifibrotic therapy, and mortality in patients with fibrotic interstitial lung diseases (ILDs). This prospective longitudinal study enrolled 290 consecutive patients with fibrotic ILDs who initiated antifibrotic therapy, including 164 with idiopathic pulmonary fibrosis (IPF) and 126 with non-IPF. Nutritional status was assessed using the Geriatric Nutritional Risk Index (GNRI). Overall, 106 patients (36.6%) were classified as having malnutrition-related risk (GNRI < 98) at baseline. The prevalence of malnutrition-related risk was comparable between patients with IPF and non-IPF, although it tended to be higher in the non-IPF group than in the IPF group. Patients with malnutrition-related risk showed higher cumulative incidence of antifibrotic therapy discontinuation. Importantly, in both IPF and non-IPF groups, the mortality risk was significantly higher in patients with malnutrition-related risk than in those without. Longitudinally, a lower GNRI at 1 year was associated with shorter survival. In multivariable analyses, baseline malnutrition-related risk was independently associated with increased risk of therapy discontinuation and mortality, even after adjusting for the ILD-gender-age-physiology index. These findings indicate that assessment of nutritional status helps predict antifibrotic therapy tolerability and mortality risk in patients with fibrotic ILD.

Fields of Study & Subjects

Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis Inflammatory Myopathies and Dermatomyositis Cystic Fibrosis Research Advances

Publication details

Journal / source
Scientific Reports
Publisher
Springer Science and Business Media LLC
Volume
16
Issue
1
Publication date
1 April 2026
Language
EN