Chronic obstructive pulmonary disease (COPD) is a common disease that severely threatens human health. As World Health Organization (WHO) has predicted, social and economic burden of COPD will rise to the fifth and COPD will become the third leading cause of death worldwide by 2030.1 COPD is a complex syndrome with pulmonary and extra-pulmonary manifestations. In the recent years, clinicians also proved that the heterogeneity of COPD is associated with different clinical outcomes including symptoms, exacerbations, responses to recommended therapy, decline of lung function and death.2

Generally, phenotype is any observed quality of an organism, like its morphology, development or behavior, as opposed to its genotype, which is the inherited instructions it carries, which may or may not be expressed.3However, only phenotypes associatedwith symptoms, prognosis, progressionand response to therapy are relevant in clinical practice. So, the term clinical phenotype in the field of COPD is defined as “a single or combination of disease attributes that describe differences between individuals with COPD as they relate to clinically meaningful outcomes symptoms, exacerbations, response to treatment, speed of progression of the disease or death.3

Adding to lung involvement, a lot of “co-morbidities” may present in patients with COPD such as cardiovascular disease, metabolic dysfunctions, and depressive disorders are more commonly present. A number of potential mechanisms linking COPD and co-morbidities have been hypothesis: The pro-inflammatory cascade,4,5,6 increased oxidative stress,7 increased arterial stiffness,8,9 catabolic state,10 and sedentary lifestyle.11 Patients with COPD are often “multi-system diseased patients,” presenting with different clinical pictures, with a poorer quality of life and outcomes,12 and a high disease-related burden.13,14 Therefore, the phenotype should be able to classify the patients into subgroups with a prognostic value that allow for determining the best therapy in order to achieve better clinical results.

This prospective study of phenotypes of chronic obstructive pulmonary disease and its co-morbidities was carried out on 110 patients (74 males and 36 females) with mean age (59.8±11.3), they were admitted to chest department of Qena university hospital from our outpatient clinic and emergency room during the period from January 2016 to December 2016.

In our study 110 COPD patients (74 males and 36 females), with mean age 59.8±11.3 divided into 5 different COPD phenotypes; (ACOS) were 12%, (Chronic bronchitis) 18%, (COPD with bronchiectasis) 19%, (Emphysema) 31% and (Frequent exacerbator) phenotype 18%. There was significant difference in age and sex between different phenotypes. The frequent exacerbator and ACOS were older than other phenotypes. Most of COPD phenotypes were prevalent in male but only (COPD with bronchiectasis) phenotype was prevalent more in female. There was significance difference in smoking status between COPD phenotypes. Current smokers were prevalent in Chronic bronchitis phenotype as shown in Table 1.

As regards pulmonary function tests of different COPD phenotypes, there was significance difference in all values except in FEF 25-75. The lowest parameters were recorded in frequent exacerbator followed by COPD with Bronchiectasis phenotypes as shown in Table 2.

There was significance difference in all items of St. George’s Respiratory Questionnaire of different COPD phenotypes. Symptoms score it was highest in (ACOS) followed by (Frequent exacerbator). Activity score, impact and total scores were highest in (Frequent exacerbator) then (COPD with bronchiectasis ) as shown in Table 3.

There was significance difference in BODEx index (BMI, FEV1,dyspnea and exacerbations) and CAT score of different COPD phenotypes P-value 0.020 and <0.001 respectively. As shown in Figure 1, Figure 2

The most common co-morbidities in all studied subjects was gastritis 58.2% of studied subjects, followed by cor-pulmonale 41.8%, Systemic hypertension 40.0 %, depression 25.5%, pulmonary hypertension 28.2%, and Diabetes Mellitus 19.1% as shown in Figure 3.

More cases developed exacerbation in the last years, sever form of excerbation and ICU admission was related to frequent exacerbator phenotype with significant difference between phenotypes as regards one or two previous hospitalization and sever excerbation as shown in Table 4.

As regards evaluation of co-morbidities in different COPD phenotypes, there was significance difference in IHD (ischemic heart disease) it was more present in (Emphysema) 22.9 %, but less in other phenotypes. .Also there was significance difference in Cor-pulmonale, founded more in (Frequent exacerbator) 65.0 %, less in (ACOS) 4.3%. There was significance difference in diabeties mellitus, it was present in 50% of (ACOS), and 5.7 % in (Emphysema) cases.

There was significance difference in Osteoporosis co-morbidity, presented more in (Emphysema) 11.4 %, it was rare in (ACOS) and (Chronic bronchitis) There was significance difference in anemia, it was more in (COPD with Bronchiectasis) 23.8 %, and it was rare in (ACOS), (Chronic bronchitis) and (Frequent exacerbator). There was significance difference in depression co-morbidity, it was more in (Frequent exacerbator) 45.0%, less in both (Chronic bronchitis) and (ACOS). There was no significance difference in Arrhythmia, Pulmonary HTN, systemic hypertension, Obesity hypoventilation syndrome, Liver disease, Renal disease, pulmonary co-morbidities (Pneumonia, Pleural effusion, Pneumothorax, Pulmonary embolism, Lung cancer), Polythesthemia, Anxiety, Stroke and gastritis co-morbidities between phenotypes as shown in Table 5.

As regards discharge from hospital with domcilliary oxygen was more in frequent excerbator phenotype and four cases died in emphysema phenotypes denoting the more severe form of phenotypes and more responsive phenotypes related to ACOS and chronic bronchitis as shown in Table 6.

COPD is a major cause of chronic morbidity and mortality throughout the world; many people suffer from this disease for years, and die prematurely from it or its complications. Globally, the COPD burden is projected to increase in coming decades because of continued exposure to COPD risk factors and aging of the population.18 The classical COPD classification has been based on Forced Expiratory Volume in the first second (FEV1), but this alone is no longer accepted as a single parameter to define severity or to guide treatment (GOLD 2015) The updated Global Initiative for Chronic Obstructive Lung Disease (GOLD) recommendations proposed treatment approach based on two additional parameters symptoms and exacerbations.1 So it is important to identify specific attributes in order to group the heterogeneous COPD into different phenotypes and guide treatment a patient therapeutic approach.

Several phenotypes have already been proposed but the understanding of which attributes define which groups of patient's remains challenges.19 Our study included 110 COPD patients (74 males and 36 females), with mean age 59.8±11.3 divided into 5 different COPD phenotypes 14 patients (ACOS) phenotype, 20 patients (Chronic bronchitis) phenotype, 21 patients (COPD with bronchiectasis) phenotype, 35 patients (Emphysema) phenotype and 20 patients (Frequent excerbator), it was compared with the study of (Jose´Luis et al.,)20 the authors studied 331 patients with mean age 66.3± 2.5 and were divided into 3 different COPD phenotypes only, 143 patients (Emphysema), 148 (Chronic bronchitis), 40 patients (ACOS).

In our study there was significant difference in sex between different COPD phenotypes with more prevalent in males except (COPD with bronchiectasis) phenotype was more prevalent in female this was in agreement with ( Jose´ Luis et al.,)20 stated that all phenotypes more prevalent in male. Also there was significance difference in smoking status between different COPD phenotypes. current smokers were more prevalent in (Chronic bronchitis) and (ACOS) phenotype, less prevalent in (COPD with bronchiectasis ) phenotype compared with same study there was no significance difference in smoking status among three different phenotypes this may be due to different study groups and numbers.

In our study there was significant difference in dypsnea (MMRC score) between different COPD phenotypes, most (ACOS) phenotype had Grade3 and Grade 4 50.0% , most (Chronic bronchitis) phenotype had Grade2 50.0%, most (COPD with bronchiectasis) phenotype had Grade4 47.6 % , most (Emphysema) phenotype had Grade3 48.6%, most (Frequent excerbator) phenotype had Grade4 75% and this is consistent with (Jose´ Luis et al.,) study who stated that there was significance difference in dypsnea (MMRC score), most phenotypes had Grade 2, (Emphysema) phenotype 37.8%,(Chronic bronchitis) phenotype 48% and (ACOS) phenotype 47.5% .

The most common co-morbidity present in our studied cases was gastritis followed by cor-pulmonale and hypertension and this is inconsistent with (Gianna et al.,).21 In our study there was no significance difference in number of exacerbation in last year of different COPD phenotypes, this was in agreement with ( Jose´ Luis et al.,)20

In our study there was significance difference between number of hospitalization in last year between different COPD phenotypes compared with (Jose´Luis et al.,) study there was no significance difference between number of hospitalization in last year. In our study there was no significance difference in number of ICU admission between phenotype, this was agreed with Beeh, Glaab et al., 2013)22 and ( Jose´Luis et al.,)20.

In our study there was significance difference in FEV1, FVC, FEV1\FVC ratio, FEV1, FVC values showed the lower value in (Frequent excerbator), and (COPD with Bronchiectasis) phenotype, FEVI/FVC ratio values showed the lower value in (COPD with Bronchiectasis), then (ACOS) phenotype. This in agreement with (Jose´Luis et al.,) study there was significance difference in FEV1 values, the (Emphysema) phenotype showed lower FEV1 values, in (Chronic bronchitis) and in (ACOS) phenotype. There was also significance difference in FEVI/FVC ratio, in (Emphysema) phenotype showed lower FEVI/FVC ratio value, in (Chronic bronchitis) phenotype, in (ACOS) phenotype, there was no significance difference in FVC.

In our study there was no significance difference in systemic hypertension between different COPD phenotypes. But there was significance difference in (Jose´Luis et al.,), it was more prevalent in (chronic bronchitis) phenotype 60.8%. In our study there was significance difference in diabeties mellitus, it was more common in (ACOS) phenotype. This was in agreement with (Jose´Luis et al.,) study there was also significance difference but it was more common in (chronic bronchitis). In our study there was significance difference in IHD (ischemic heart disease) co-morbidity between different COPD phenotypes, it was more common in (Emphysema) phenotype, Also there was significance difference in Cor-pulmonale co-morbidity, it was more common in (Frequent excerbator) phenotype 65.0 %. But in (Jose´Luis et al.,) study there was no significance difference, and it was more common in (ACOS) phenotype.

In our study there was no significance difference in (Obesity hypoventilation syndrome) co-morbidity between different COPD phenotypes. This was inconsistent with (Jose´Luis et al.,), as it was more present in (chronic bronchitis) phenotype. Our study and (Jose´Luis et al.,) study was consistent as regards no significance difference in arrhythmia and cerebrovascular disorder.

Osteoporosis was founded more in COPD with bronchiactasis, Emphysema and Frequent excerbator phenotypes with significant difference and this was in agreement with Gianna et al. 21

Our results showed that the highest association of co-morbidities is seen mostly in patients with severe COPD phenotypes. These findings were in agreement with Mahboub et al.,23 and Dal Negro et al.,24 who reported an association between the prevalence of comorbidity and COPD severity measured by a COPD assessment test score >10 or by Global Initiative on Obstructive Lung Disease stages, respectively, and disagreement with with findings of Watz et al.25

The co-morbidity related to heart dysfunction in frequent excerbator and emphysema phenotypes are particularly important predictors of increased risk of death in patients with COPD and indicate the importance of cardiovascular disease as a factor contributing to COPD mortality and this was consistent with Zielinski et al.,26

The presence of significant co-morbidities is one of the most important modifying risk factors for severity in COPD. They contribute to the overall severity in individual patients, have a major impact on quality of life, increase the risk of certain causes of mortality and of all-cause mortality and are major causes of hospitalization , Co-morbidities can be associated with any clinical phenotype. But we found that distribution of Co morbidities not much different between these phenotypes, gastritis was the most frequent co-morbidity in all phenotypes, then systemic hypertension and cor-pulmonale. But diabetes mellitus was more common in ACOS phenotypes, depression was more common in frequent excerbator phenotype.