# Analysis of body composition with bioelectrical impedance analysis in different subtypes of pulmonary fibrosis

**Authors:** Katharina Buschulte, Ben Ehrhart, Bernhard Kötter, Katharina Abbasi Dezfouli, Oliver Weinheimer, Katharina Cremer, Christoph Lederer, Philipp Höger, Markus Polke, Felix F. J. Herth, Judith Brock

PMC · DOI: 10.1038/s41598-026-39350-5 · Scientific Reports · 2026-03-06

## TL;DR

This study uses bioelectrical impedance analysis to find that patients with different types of pulmonary fibrosis have poor body composition and lower cell health indicators.

## Contribution

The study is the first to analyze body composition in various subtypes of pulmonary fibrosis using bioelectrical impedance analysis.

## Key findings

- Patients with pulmonary fibrosis showed reduced phase angle and cell percentage compared to healthy controls.
- Those with acute exacerbations and women had significantly lower phase angle values.
- No strong correlations were found between BIA parameters and lung function or quality of life.

## Abstract

Patients with Idiopathic Pulmonary Fibrosis (IPF) often have an unfavourable body composition, characterized by a reduced phase angle (PhA) as an index of cellular health and associated with increased mortality. Little is known about body composition in other subtypes of pulmonary fibrosis (PF). In this single-centre, prospective study, bioelectrical impedance analysis (BIA) was used to assess body composition in patients with PF. In addition, metabolic parameters, lung function, exercise capacity and quality of life (QoL) questionnaires were collected. The fibrosis index (FIBI) was calculated by quantitative computed tomography. A total of 90 patients (57.8% male, mean age 70.8 ± 8.9 years) was analysed. Lung function was mildly impaired with a mean forced vital capacity (FVC) of 76.8 ± 21.4% predicted and mean diffusion capacity for carbon monoxide single breath (DLCO-SB) of 49.5 ± 16.0% predicted. The mean FIBI was 22.5% (SD 10.2). Main diagnoses were systemic autoimmune rheumatic diseases-associated ILD (n = 26, 29.9%), unclassified ILD (n = 19, 21.1%) and fibrosing hypersensitivity pneumonitis (n = 14, 15.6%). 22 patients (24.4%) received steroids and 26 (28.9%) other immunosuppressants. 22 patients (24.4%) experienced ≥ 1 acute exacerbation (AE). The mean body weight was 84.5 ± 18.2 kg with a mean body mass index (BMI) of 28.6 ± 5.7 kg/m2. One patient was underweight, and 31 patients (34.4%) had lost weight during the previous 6 months. BIA showed unfavourable values compared to healthy controls: body fat ↑ (28.9 ± 8.0%), extracellular mass/ body cell mass (ECM/BCM) index ↑ (1.2; IQR 1.0, 1.4), PhA ↓ (4.9 ± 1.0°), cell percentage ↓ (45.4 ± 6.3%) and fat-free mass index ↑ (19.9 ± 2.7 kg/m2). Correlation analyses showed a moderate correlation between PhA and FVC (p < 0.001). No relevant correlations were found between DLCO-SB, walking distance, FIBI, QoL and BIA parameters. Patients with ≥ 1 AE had a significantly worse PhA (p = 0.030). In addition, a sex difference was observed with significantly worse values of PhA for women compared to men (p = 0.036). Patients with PF had an unfavourable body composition with reduced PhA, reduced cell percentage and elevated ECM/BCM index. Significantly lower PhA values were found in patients with ≥ 1 AE and in women. Following longitudinal and interventional confirmation of our results, future research aimed at improving body composition and patient outcomes for those with PF could be conducted.

## Linked entities

- **Diseases:** Idiopathic Pulmonary Fibrosis (MONDO:0800029), pulmonary fibrosis (MONDO:0002771)

## Full-text entities

- **Genes:** TNFRSF17 (TNF receptor superfamily member 17) [NCBI Gene 608] {aka BCM, BCMA, CD269, TNFRSF13A}, MMRN1 (multimerin 1) [NCBI Gene 22915] {aka ECM, EMILIN4, GPIa*, MMRN}
- **Diseases:** Fibrosis (MESH:D005355), amyotrophic lateral sclerosis (MESH:D000690), neurodegenerative disorder (MESH:D019636), sarcopenia (MESH:D055948), inflammation (MESH:D007249), CL (MESH:D002971), Respiratory bronchiolitis-ILD (MESH:D012140), malnutrition (MESH:D044342), hypothyroidism (MESH:D007037), Diabetes mellitus (MESH:D003920), cancer (MESH:D009369), impairment of FVC (MESH:D060825), IPF (MESH:D054990), Dyspnea (MESH:D004417), osteoporosis (MESH:D010024), DM (MESH:D009223), autoimmune rheumatic diseases (MESH:D012216), idiopathic non-specific interstitial pneumonia (MESH:D054988), dry cough (MESH:D003371), weight loss (MESH:D015431), obese (MESH:D009765), idiopathic haemorrhagic syndrome (MESH:D006470), inflammatory bowel disease (MESH:D015212), Fibrosing hypersensitivity pneumonitis (MESH:D000542), YACTA (MESH:C000719218), thyroid disease (MESH:D013959), LBM (MESH:D013851), motor neuron disease (MESH:D016472), overweight (MESH:D050177), PF (MESH:D011658), hyperthyroidism (MESH:D006980), tuberculosis (MESH:D014376), fatigue (MESH:D005221), COPD (MESH:D029424), non-pulmonary wasting disease (MESH:D019282), ILA (MESH:D017563), muscle diseases (MESH:D009135), AE (MESH:D000208), SARD (MESH:C537236), muscular dystrophy (MESH:D009136), systemic sclerosis (MESH:D012595), FH (OMIM:143890), impaired lung function (MESH:D003072), PhA (MESH:D000210), Fat-free mass (MESH:C536030)
- **Chemicals:** MDT (-), oxygen (MESH:D010100), zinc (MESH:D015032), CO (MESH:D002248), carbon (MESH:D002244), triglycerides (MESH:D014280), steroid (MESH:D013256), water (MESH:D014867), lipid (MESH:D008055), iron (MESH:D007501), alcohol (MESH:D000438), cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12972317/full.md

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Source: https://tomesphere.com/paper/PMC12972317