Nutritional assessment in idiopathic pulmonary fibrosis: a prospective multicentre study.
Journal
ERJ open research
ISSN: 2312-0541
Titre abrégé: ERJ Open Res
Pays: England
ID NLM: 101671641
Informations de publication
Date de publication:
Jan 2022
Jan 2022
Historique:
received:
05
07
2021
accepted:
27
09
2021
entrez:
10
3
2022
pubmed:
11
3
2022
medline:
11
3
2022
Statut:
epublish
Résumé
Nutritional status impacts quality of life and prognosis of patients with respiratory diseases, including idiopathic pulmonary fibrosis (IPF). However, there is a lack of studies performing an extensive nutritional assessment of IPF patients. This study aimed to investigate the nutritional status and to identify nutritional phenotypes in a cohort of IPF patients at diagnosis. Patients underwent a thorough pulmonary and nutritional evaluation including questionnaires on nutritional status, and physical activity, anthropometry, body impedance, dynamometry, 4-m gait speed and blood tests. 90 IPF patients (78.9% males, mean age 72.7 years) were enrolled. The majority of patients were classified as Gender-Age-Physiology Index stage 2 (47, 52.2%) with an inactive lifestyle according to International Physical Activity Questionnaire score (39, 43.3%), and had mean forced vital capacity and diffusing capacity for carbon monoxide 86.5% and 54.2%, respectively. In regards to nutritional phenotypes, the majority of patients were normally nourished (67.8%, 95% CI 58.6-77.7%), followed by non-sarcopenic obese (25.3%, 95% CI 16.1-35.2%), sarcopenic (4.6%, 95% CI 0.0-14.5%) and sarcopenic obese (2.3%, 95% CI 0.0-12.2%). Among the normally nourished, 49.2% showed early signs of nutritional and physical performance alterations, including body mass index ≥30 kg·m IPF patients at diagnosis are mainly normally nourished and obese, but early signs of nutritional and physical performance impairment can already be identified at this stage.
Sections du résumé
Background
UNASSIGNED
Nutritional status impacts quality of life and prognosis of patients with respiratory diseases, including idiopathic pulmonary fibrosis (IPF). However, there is a lack of studies performing an extensive nutritional assessment of IPF patients. This study aimed to investigate the nutritional status and to identify nutritional phenotypes in a cohort of IPF patients at diagnosis.
Methods
UNASSIGNED
Patients underwent a thorough pulmonary and nutritional evaluation including questionnaires on nutritional status, and physical activity, anthropometry, body impedance, dynamometry, 4-m gait speed and blood tests.
Results
UNASSIGNED
90 IPF patients (78.9% males, mean age 72.7 years) were enrolled. The majority of patients were classified as Gender-Age-Physiology Index stage 2 (47, 52.2%) with an inactive lifestyle according to International Physical Activity Questionnaire score (39, 43.3%), and had mean forced vital capacity and diffusing capacity for carbon monoxide 86.5% and 54.2%, respectively. In regards to nutritional phenotypes, the majority of patients were normally nourished (67.8%, 95% CI 58.6-77.7%), followed by non-sarcopenic obese (25.3%, 95% CI 16.1-35.2%), sarcopenic (4.6%, 95% CI 0.0-14.5%) and sarcopenic obese (2.3%, 95% CI 0.0-12.2%). Among the normally nourished, 49.2% showed early signs of nutritional and physical performance alterations, including body mass index ≥30 kg·m
Conclusions
UNASSIGNED
IPF patients at diagnosis are mainly normally nourished and obese, but early signs of nutritional and physical performance impairment can already be identified at this stage.
Identifiants
pubmed: 35265706
doi: 10.1183/23120541.00443-2021
pii: 00443-2021
pmc: PMC8899499
pii:
doi:
Types de publication
Journal Article
Langues
eng
Informations de copyright
Copyright ©The authors 2022.
Déclaration de conflit d'intérêts
Conflict of interest: P. Faverio reports personal fees from Boehringer Ingelheim and grants from Roche, outside the submitted work. Conflict of interest: A. Fumagalli has nothing to disclose. Conflict of interest: S. Conti has nothing to disclose. Conflict of interest: F. Madotto has nothing to disclose. Conflict of interest: F. Bini has nothing to disclose. Conflict of interest: S. Harari reports personal fees from Actelion, Roche and Boehringer Ingelheim, outside the submitted work. Conflict of interest: M. Mondoni has nothing to disclose. Conflict of interest: T. Oggionni has nothing to disclose. Conflict of interest: E. Barisione reports personal fees from Chiesi Farmaceutici, Boehringer Ingelheim and GlaxoSmithKline, outside the submitted work. Conflict of interest: P. Ceruti has nothing to disclose. Conflict of interest: M.C. Papetti has nothing to disclose. Conflict of interest: B.D. Bodini has nothing to disclose. Conflict of interest: A. Caminati reports personal fees from Roche and Boehringer Ingelheim, outside the submitted work. Conflict of interest: A. Valentino has nothing to disclose. Conflict of interest: S. Centanni has nothing to disclose. Conflict of interest: D. Noè has nothing to disclose. Conflict of interest: M. Della Zoppa has nothing to disclose. Conflict of interest: S. Crotti has nothing to disclose. Conflict of interest: M. Grosso reports personal fees from Chiesi Farmaceutici and Johnson & Johnson, outside the submitted work. Conflict of interest: S.G. Sukkar has nothing to disclose. Conflict of interest: D. Modina has nothing to disclose. Conflict of interest: M. Andreoli has nothing to disclose. Conflict of interest: R. Nicali has nothing to disclose. Conflict of interest: G. Suigo has nothing to disclose. Conflict of interest: F. De Giacomi has nothing to disclose. Conflict of interest: S. Busnelli has nothing to disclose. Conflict of interest: E. Cattaneo has nothing to disclose. Conflict of interest: L.G. Mantovani has nothing to disclose. Conflict of interest: G. Cesana has nothing to disclose. Conflict of interest: A. Pesci has nothing to disclose. Conflict of interest: F. Luppi reports lectures fee from Roche and from Boehringer Ingelheim.
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