# Clinical, Functional, and Psychosocial Profiles of Chronic Obstructive Pulmonary Disease (COPD) Etiotypes: A Taxonomy-Based Analysis

**Authors:** Irem Altan, Fatih Alasan, Ozlem Sengoren Dikis, Fulden Cantas Turkis

PMC · DOI: 10.3390/medicina62020348 · 2026-02-09

## TL;DR

This study identifies distinct clinical and functional profiles among different types of COPD based on their underlying causes, helping guide personalized treatment.

## Contribution

The study provides detailed clinical, functional, and psychosocial profiles for each GOLD 2023 COPD etiotype.

## Key findings

- COPD due to environmental exposure was the most common type (98.7%).
- COPD-A patients were younger, had less tobacco exposure, and less emphysema on CT scans.
- COPD-G showed more severe airflow obstruction and higher symptom burden.

## Abstract

Background and Objectives: The 2023 GOLD report introduced seven etiological categories, known as etiotypes, to better reflect the heterogeneity of chronic obstructive pulmonary disease (COPD). However, the clinical, functional, radiological, and psychosocial characteristics associated with these etiologies remain insufficiently defined. This study aimed to explore the differences among GOLD 2023 etiotypes in a stable COPD cohort. Materials and Methods: This prospective, observational, cross-sectional study included 315 stable outpatients with COPD from a tertiary clinic between June and July 2025. Etiological classification was based on predefined criteria, including genetic predisposition, impaired lung development, exposure-related mechanisms, infection-related mechanisms, and asthma-like characteristics. Patients were evaluated using clinical instruments (mMRC and CAT), psychological assessments (LCQ, BDI, BAI, and CAFS), pulmonary function tests, and thoracic CT scans. Results: COPD due to environmental exposure (COPD-E) was the most common type (98.7%), followed by infection-related (COPD-I, 13.3%), asthma-related (COPD-A, 9.8%), and combined forms (COPD-D and COPD-G, each 2.5%). Participants with COPD-A were younger (median 54 vs. 66 years; p < 0.001), reported less tobacco exposure (36 vs. 50 pack-years; p < 0.001), and showed less CT-detected emphysema (31.6% vs. 78.3%; p < 0.001). COPD-G exhibited more severe airflow obstruction (FEV1 25.5% predicted; p < 0.001), higher symptom burden (CAT score 21 vs. 6; p < 0.001), and lower oxygen saturation (p = 0.001). Eosinophil counts and psychosocial measures did not significantly differ by etiology. Conclusions: The GOLD 2023 COPD etiotypes demonstrated distinct clinical and functional profiles, reflecting diverse underlying mechanisms of the disease. Recognizing these etiological differences can help clinicians tailor diagnostic evaluations, guide individualized treatment strategies, and ultimately improve patient outcomes. Understanding disease etiology remains a cornerstone for accurate diagnosis, personalized management and optimized therapeutic decisions in COPD.

## Linked entities

- **Diseases:** chronic obstructive pulmonary disease (MONDO:0005002), COPD (MONDO:0005002), asthma (MONDO:0004979)

## Full-text entities

- **Genes:** CAT (catalase) [NCBI Gene 847], SERPINA1 (serpin family A member 1) [NCBI Gene 5265] {aka A1A, A1AT, AAT, PI, PI1, PRO2275}
- **Diseases:** cardiac/hepatic/renal disease (MESH:D006331), tuberculosis (MESH:D014376), Depression (MESH:D003866), GOLD IV (MESH:D006011), cognitive impairment (MESH:D003072), lung development (MESH:D002658), limitation (MESH:D045745), sputum purulence (MESH:D003234), Bronchiectasis (MESH:D001987), Symptom (MESH:D012816), cough (MESH:D003371), AAT deficiency (MESH:D019896), post (MESH:D000094025), Infection (MESH:D007239), pneumonia (MESH:D011014), COPD-A (MESH:D029424), Fatigue (MESH:D005221), Chest Diseases (MESH:D002637), Hypoxemia (MESH:D000860), psychological distress (MESH:D012128), genetic diseases (MESH:D030342), airway and/or alveolar abnormalities (MESH:D000402), respiratory diseases (MESH:D012140), inflammation (MESH:D007249), airway remodelling (MESH:D056151), injury to (MESH:D014947), E (MESH:D016751), pulmonary infections (MESH:D012141), Anxiety (MESH:D001007), lung injury (MESH:D055370), emphysema (MESH:D004646), Asthma (MESH:D001249), malignancy (MESH:D009369), Thoracic CT abnormalities (MESH:D013896), HIV-associated lung disease (MESH:D008171), Dyspnea (MESH:D004417)
- **Chemicals:** oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12941940/full.md

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Source: https://tomesphere.com/paper/PMC12941940