Evidence map›Paper›PMID 42215926›Full record

ArticleBMC pulmonary medicine2026

Relationship of prognostic nutritional index with clinical outcomes and survival in idiopathic pulmonary fibrosis.

Nurcan Guler, Aylin Ozgen Alpaydin, Kemal Can Tertemiz, Can Sevinc, Hulya Ellidokuz, Gokçen Omeroğlu Simsek, Eyup Sabri Ucan

Abstract read
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Article in BMC pulmonary medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Nurcan GulerDepartment of Respiratory Diseases, Bucak State Hospital, Burdur, Turkey.ORCID http://orcid.org/0000-0002-6991-8181
Aylin Ozgen AlpaydinDepartment of Respiratory Diseases, Faculty of Medicine, Dokuz Eylul University, İzmir, Turkey. aylin.alpaydin@deu.edu.tr.ORCID http://orcid.org/0000-0002-5711-1372
Kemal Can TertemizDepartment of Respiratory Diseases, Faculty of Medicine, Dokuz Eylul University, İzmir, Turkey.ORCID http://orcid.org/0000-0002-1141-5637
Can SevincDepartment of Respiratory Diseases, Faculty of Medicine, Dokuz Eylul University, İzmir, Turkey.ORCID http://orcid.org/0000-0003-3691-9150
Hulya EllidokuzDepartment of Preventive Oncology, Institute of Oncology, Dokuz Eylul University, İzmir, Türkiye.ORCID http://orcid.org/0000-0001-8503-061X
Gokçen Omeroğlu SimsekDepartment of Respiratory Diseases, Faculty of Medicine, Dokuz Eylul University, İzmir, Turkey.ORCID http://orcid.org/0000-0002-2724-0616
Eyup Sabri UcanDepartment of Respiratory Diseases, Faculty of Medicine, Dokuz Eylul University, İzmir, Turkey.ORCID http://orcid.org/0000-0001-7341-654X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIdiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease. Nutritional indices have been reported as significant prognostic factors in IPF. This study aimed to evaluate the relationship between the prognostic nutritional index (PNI) and clinical findings, functional parameters, prognosis, and mortality in patients with IPF followed in our clinic.

methodsThis retrospective study reviewed the medical records of patients diagnosed with IPF between 2014 and 2021. The GAP (Gender, Age, Physiology) score, pulmonary function tests, and laboratory results were recorded at the time of diagnosis and at the initiation of antifibrotic treatment. PNI was calculated using serum albumin and lymphocyte counts according to a previously defined formula. Patients were followed from the start of antifibrotic therapy to their final visit within the sixth month. All baseline data were reassessed at the six-month follow-up. Survival time was defined as the period from the initiation of follow-up to the date of death. For patients who were still alive, survival was calculated up to the end of the final data collection, which concluded in December 2024.

resultsA total of 120 patients (86 males; mean age: 69.2 ± 8.5 years) diagnosed with IPF were included. The most common symptoms were dyspnea (87.5%) and cough (82.5%). Forty-eight patients died during the study period. The modified Medical Research Council (mMRC) dyspnea scores and GAP scores were significantly lower in survivors (p = 0.016 and p < 0.001, respectively), whereas PNI levels were significantly higher in this group (p = 0.004). Baseline PNI levels showed weak negative correlations with both the mMRC score (r = - 0.308, p < 0.001) and the GAP score (r = - 0.358, p < 0.001). PNI levels at baseline and at 6 months were significantly higher in patients with stable parenchymal findings than in those with progressive fibrosis (p < 0.001).

conclusionsThese findings suggest that PNI, which reflects both nutritional and inflammatory status, may serve as a useful prognostic marker for predicting disease progression and mortality in patients with IPF.

Indexed as

Idiopathic Pulmonary FibrosisNutritional StatusNutrition AssessmentAgedDyspneaFemaleHumansLymphocyte CountMaleMiddle AgedPrognosisRespiratory Function TestsRetrospective StudiesIdiopathic pulmonary fibrosisMortalityPrognostic nutritional index

Identifiers

PMID42215926
PMCPMC13417851

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.