# Clinical and Functional Heterogeneity of COPD Phenotypes: A Multicenter Study from Turkey (DIPTUR Study)

**Authors:** Tevfik Ozlu, Ozlem Sengoren Dikis, Fulden Cantas Turkis, Ceren Degirmenci, Ahmet Ilgazlı, Inci Gülmez, Burcu Yalcin, Gulistan Karadeniz, Yasemin Soyler, Hatice Selimoglu Sen, Aysel Sunnetcioglu, Nimet Aksel, Sibel Boga, Nurhan Sarioglu, Haci Ahmet Bircan, Aylin Capraz, Serap Argun Baris, Aycan Yuksel, Umut Sabri Kasapoglu, Sibel Arınc, Esra Yarar, Nur Aleyna Yetkin, Fusun Sahin, Ali Tabaru, Dildar Duman, Gunhan Yavasoglu, Dursun Tatar, Mehmet Karadag, Kadir Coban, Ersin Alkilinc, Ebru Tas, Taha Tahir Bekci, Derya Kizilgoz, Buket Mermit, Murat Kavas, Hakan Alp Yilmazli, Ilknur Basyigit, Esen Sayin Gulensoy, Meltem Agca, Filiz Alkan Baylan, Canan Bol, Berat Uslu, Gamze Celik

PMC · DOI: 10.3390/medicina62020402 · 2026-02-19

## TL;DR

This study identifies distinct COPD phenotypes in Turkey and shows that exacerbator types have worse clinical outcomes and higher healthcare use.

## Contribution

The study provides a detailed characterization of GesEPOC COPD phenotypes in a Turkish population, highlighting their clinical and functional differences.

## Key findings

- Exacerbator with emphysema (EE) and exacerbator with chronic bronchitis (ECB) phenotypes had higher healthcare utilization and worse outcomes.
- Non-exacerbator (NE) and asthma-COPD overlap (ACO) phenotypes showed lower disease burden and better clinical profiles.
- Phenotype-based classification reveals heterogeneity beyond standard GOLD categories in COPD management.

## Abstract

Background and Objectives: Chronic obstructive pulmonary disease (COPD) is heterogeneous, and phenotype-based classification may better capture differences in clinical burden and healthcare needs beyond standard GOLD categories. We aimed to describe the distribution of GesEPOC COPD phenotypes in Turkey and compare their demographic, clinical, functional, radiological, treatment, and healthcare utilization profiles. Materials and Methods: DIPTUR was a multicenter, observational, cross-sectional study conducted prospectively in 26 centers across 17 Turkish cities (October 2019–June 2021). Stable COPD patients (≥40 years; post-bronchodilator FEV1/FVC < 0.7) without exacerbation or major treatment modification within the previous four weeks were enrolled consecutively. Phenotypes were assigned per GesEPOC: exacerbator with emphysema (EE), exacerbator with chronic bronchitis (ECB), asthma–COPD overlap (ACO), and non-exacerbator (NE). Frequent exacerbators were defined as patients who experienced two or more exacerbations during the 12 months preceding enrollment, based on medical records and patient reports. Results: Among 894 patients, phenotype distribution was NE 44.1%, ECB 26.2%, EE 20.5%, and ACO 9.3%. Male predominance was observed across groups (80–89%; p = 0.006). Active smoking was most frequent in ECB (37.6%; p < 0.001), and BMI was lowest in EE (p < 0.001). Comorbidity patterns differed, with hypertension (p < 0.001), diabetes mellitus (p = 0.029), and heart failure (p < 0.001) most prevalent in ECB. Pulmonary function (FEV1 and FVC) was lowest in EE (both p < 0.001), and severe airflow limitation (GOLD III–IV) was most common in EE and ECB (p < 0.001). Dyspnea (mMRC ≥ 2) was more frequent in EE/ECB than in ACO/NE (p < 0.001). Emphysematous changes on thoracic CT predominated in EE (91.7%; p < 0.001). Long-term oxygen therapy was most common in EE (32.4%; p < 0.001). Emergency admissions, hospitalizations, and total length of stay were markedly higher in EE and ECB than in ACO and NE (all p < 0.001). Conclusions: COPD phenotypes in Turkey show substantial heterogeneity in clinical, functional, radiological, and utilization domains. Exacerbator phenotypes—particularly EE and ECB—represent higher-burden groups, supporting phenotype-oriented management and closer monitoring beyond GOLD classification.

## Linked entities

- **Diseases:** Chronic obstructive pulmonary disease (MONDO:0005002), diabetes mellitus (MONDO:0005015), heart failure (MONDO:0005252)

## Full-text entities

- **Diseases:** limitation (MESH:D045745), chronic bronchitisappears (MESH:D002908), pleuropulmonary disease (MESH:C537516), exchange (MESH:D001816), emphysematous (MESH:D041882), GOLD III-IV (MESH:D006011), Heart failure (MESH:D006333), Obstructive sleep apnea (MESH:D020181), coronary artery disease (MESH:D003324), tuberculosis (MESH:D014376), COVID-19 (MESH:D000086382), chronic renal failure (MESH:D007676), pulmonary tuberculosis (MESH:D014397), infection (MESH:D007239), alpha-1 antitrypsin deficiency (MESH:D019896), bronchiectasis (MESH:D001987), Hypertension (MESH:D006973), hematological malignancy (MESH:D019337), GOLD I-II (MESH:D056829), chronic neurological disorders (MESH:D009461), Arrhythmia (MESH:D001145), ACO (MESH:D000080445), obese (MESH:D009765), pulmonary function impairment (OMIM:608852), granulomatous diseases (MESH:D006105), overweight (MESH:D050177), COPD (MESH:D029424), lung damage (MESH:D008171), diabetes mellitus (MESH:D003920), ECB (MESH:D029481), solid organ malignancy (MESH:D009369), impaired (MESH:D060825), Dyspnea (MESH:D004417), asthma (MESH:D001249), EE (MESH:D004646), Medical Research Council (MESH:D014947), airway inflammation (MESH:D007249), chronic liver disease (MESH:D008107), respiratory disease (MESH:D012140)
- **Chemicals:** - and long-acting bronchodilators (-), SABA (MESH:C046122), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606], Meleagris gallopavo (common turkey, species) [taxon 9103], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12942314/full.md

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Source: https://tomesphere.com/paper/PMC12942314