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Journal of Clinical and Diagnostic Research. 2017 May, Vol-11(5): CC11-CC13 1111
DOI: 10.7860/JCDR/2017/25643.9841
Original Article
PhysiologySection
Occurrence of COPD in Patients with
Respiratory Allergy: A Clinico-Spirometric
Evaluation in a Tertiary Hospital, Kolkata
INTRODUCTION
Chronic lung disease is a rapidly emerging pandemic. Volcano is
a more appropriate word to depict the situation rather than the
traditional iceberg phenomenon [1]. Intergovernmental Panel on
Climate Change (IPCC) and WHO concluded that overall incidences
of obstructive lung diseases, upper respiratory tract allergy and
respiratory tract infection are rapidly rising as a result of global
warming.
Till date smoking is the most important causative factor for COPD.
Dyspnoea, wheeze & wet cough are the major symptoms [2,3].
Sinonasal inflammation in COPD may be produced as a result
of inflammation, pathological neurogenic reflexes or directly by
products of smoking [4]. Allergens, dust, microbes and nonspecific
respiratory irritants typically narrow the airways by excessive mucus
production thereby exacerbating COPD symptoms [5,6]. On the
other hand, till recently American Thoracic Society did not include
strategies for the management of respiratory allergies in routine
treatment protocol of COPD [6]. The principal focus of the present
study was to evaluate the coexistence of COPD with respiratory
allergy so that the treatment of respiratory allergy may accelerate
the recovery from acute exacerbation of COPD. The combination of
clinical examination followed by spirometry can significantly increase
the sensitivity of detection of lung diseases [7]. Reversibility testing
with bronchodilators reduces the overall prevalence of airway
obstruction significantly and post bronchodilatation obstruction is
more specific for COPD [8].
The aim of the present study was to evaluate the occurrence of
COPD in respiratory allergy among subjects presenting with chronic
respiratory symptoms.
MATERIALS AND METHODS
An observational cross-sectional study was conducted between
November 2015 and April 2016. Male and female subjects aged 18
to 60 years presenting with chronic respiratory symptoms like cough,
wheeze and SOB for more than three months duration were included
in the study. All patients were Bengali speaking and belonged to
urban areas of North 24–Parganas district, West Bengal, India. They
were referred from different outpatient departments of a tertiary
hospital, Kolkata for routine spirometric screening at the spirometry
laboratory in Department of Physiology.
Asymptomatic patients coming for pre-anaesthetic checkup,
Paediatric and Geriatric patients, patients suffering from acute illness
and debilitation of any origin, patients with third trimester pregnancy,
active haemoptysis, tuberculosis, sub diaphragmatic and known
cardiovascular diseases associated with SOB were summarily
excluded from the present study. On an average in our department we
perform routine spirometry in 160 patients per month. In six months
from about 950 patients we selected 550 patients maintaining
appropriate inclusion and exclusion criteria. The sampling technique
was complete enumeration. Ethical permission was obtained from
Institutional Ethics Committee, prior to study and written consent
was taken from each of the subject prior to examination.
At first all patients were asked to respond to a standardized
respiratory symptoms questionnaire (ATS/DLD-78 A questionnaire)
[9]. After obtaining detailed clinical profile, patients with respiratory
symptoms were divided in two groups: subjects suffering from
clinical symptoms suggestive of respiratory allergy (n=260) like nasal
catarrh, nasal stuffiness and sneezing all together as written on
OPD card and subjects with no symptoms suggestive of respiratory
allergy (n=290).
SUJOY MUKHERJEE1
, GOUTAM BANERJEE2
, DEBAJYOTI DAS3
, ANIL BARAN SINGHA MAHAPATRA4
Keywords:	Acute exacerbation, Pandemic, Spirometry
ABSTRACT
Introduction: Smoking is established as the most important
causative factor responsible for Chronic Obstructive Pulmonary
Disease (COPD). Occurrence of allergy in COPD patients
causes acute exacerbation of this disease, but role of allergy is
not established in aetiopathogenesis of COPD.
Aim: The present study was aimed at evaluation of occurrence
of COPD in patients having symptoms suggestive of respiratory
allergy.
Materials and Methods: An observational cross-sectional study
was conducted to evaluate occurrence of COPD in patients
having respiratory allergic symptoms by routine spirometric
screening. Five hundred and fifty urban patients aged 18-60
years (both gender) ailing from chronic respiratory symptoms
like cough, wheeze and Shortness Of Breath (SOB), who were
referred from OPDs of RGKMCH, Kolkata, were included in this
study. After obtaining detailed clinical profile, patients were
divided into two groups: subjects having additional clinical
symptoms suggestive of respiratory allergy (n=260) like nasal
catarrh, nasal stuffiness and sneezing and subjects with no
symptoms suggestive of respiratory allergy (n=290). Thereafter,
routine spirometry was carried out following recommendations
of ATS/ERS (2005). Patients were then categorized based on
FVC, FEV1
, FEV1
/FVC, FEF25-75
and PEFR percent predicted
values.
Results: Study revealed that 18.97% of non-allergic population
was suffering from COPD whereas only 7.69% of allergic
subjects had COPD. This difference was statistically highly
significant (p=0.0001). Although there was no significant
difference in prevalence of respiratory symptoms between
these two groups.
Conclusion: Present study concludes that patients with
respiratory allergy may have coexistent COPD but occurrence
of COPD is much less than that in patients with no respiratory
allergy.
Sujoy Mukherjee et al., Occurrence of COPD in Patients with Respiratory Allergy	 www.jcdr.net
Journal of Clinical and Diagnostic Research. 2017 May, Vol-11(5): CC11-CC131212
We did not perform any laboratory test for allergy as clinical symp­
tomatology is established as the most reliable factor in detection of
allergy [10,11]. Smoking history was obtained and subjects were
categorized as per US Centers for Disease Control and Prevention
definition of “Never Smokers” – adults who have never smoked a
cigarette or who smoked fewer than 100 cigarettes in their entire
lifetime. Rest of the subjects was marked as smokers. All the patients
had received one or more bronchodilators and anti-inflammatory
agents for treatment of their respiratory symptoms.
As all the data was collected at a point of time (cross-sectional data)
with no known confounding variable so unpaired t-test was applied
to compare these two populations. After calibration, spirometry was
carried out by using a non-heated spirometer (RMS HELIOS 702)
following current guidelines of the American Thoracic Society [12].
The largest observed values of FEV1
and FVC available from among
at least three acceptable and reproducible tests were taken as the
key parameters for interpretation. Then, the subject was asked to
inhale short acting bronchodilator in the pre-prescribed doses. After
ten minutes of taking the inhaler the subject was asked to perform
the spirometry once again and thus the reversibility test done
[12]. The highest values of FVC and FEV1
were selected. Periodic
calibrations were done as per protocol.
In absence of normative spirometric data of Indian population the
data obtained was interpreted as per directions furnished in the
user manual of RMS HELIOS 702 along with given ethnic correction
[13]. As the study populace seemed to be ethnically homogenous
predictive equation was not obtained.
We categorized all the patients as per pre-set criteria: i) Normal
Spirometric Finding; ii) Small Airway Obstruction (SAO); iii) COPD;
iv) Mixed Ventilatory Defect; & v) Restrictive Pattern [13].
Statistical Analysis
Descriptive analyses were performed using Fisher’s-Exact Test (for
categorical variables) and two-sided unpaired t-tests (for continuous
variables). All spirometric variables were expressed in percent
predicted (%) form. Statistical analyses was done by using Microsoft
excel sheet and GraphPad Quickcalcs Software, California, USA. A
p-value of <0.05 was considered significant.
RESULTS
Non allergic patients were significantly more likely to be older (mean
age was 44 years), percentage of smokers were also higher in the
older population. There was no significant difference regarding
prevalence of respiratory symptoms like SOB, dry cough, wet cough
between allergic and non-allergic populations except wheeze which
was more significant finding in allergic population. Furthermore,
bronchodilator reversibility (BDR) data had shown that mean values
of FEV1
/FVC, FEF25-75
and PEFR were significantly lower in non-
allergic subjects as compared to allergic group [Table/Fig-1].
Occurrence of COPD in BDR analysis was significantly more in non-
allergic group rather than allergic population [Table/Fig-2].
Non allergic patients with spirometry diagnosed COPD were
significantly more likely to be older (mean age was 52 years). More
than half of the non-allergic patients had smoking history. Non-
allergic patients had a lesser mean body weight. Persistence of
lower respiratory symptom like wet cough was more in the non-
allergic population compared to allergic population. Furthermore
mean values of FEV1
& FEV1
/FVC were significantly less in non allergic
COPD population compared to allergic patients [Table/Fig-3].
DISCUSSION
In the present study, we divided the whole population based only
on prior clinical diagnosis and allergy testing was not performed.
As drug/treatment history of patients was not supposed to alter
our study outcome so we had not included drug history as a study
variable. As the present study was of observational and cross-
Variables
Allergic Patients
(N=260)
Non-Allergic Patients
(N=290)
p-value
Gender
{N (%)}
Male: 110 (42.30)
Female:150 (57.70)
Male: 145 (50.00)
Female:145 (50.00) 0.0729
Age (Years)
(Mean ±SD) 35.07±13.02 43.89±11.33 <0.0001*
Weight (Kg)
(Mean ±SD) 55.34±13.05 54.89±11.47 0.6671
Height (Cm)
(Mean ±SD) 155.88±9.23 156.53±8.78 0.3979
BMI (Kg/M2
)
(Mean ±SD) 22.92±5.01 22.45±4.4 0.242
Smoking Statusa
{N (%)}
Ever Smoker: 40
(15.38)
Never Smoker: 220
(84.62)
Ever Smoker: 100
(34.48)
Never Smoker: 190
(65.52)
<0.0001*
SOBb
{N (%)}
Yes: 260 (100.00)
No: 00 (0.00)
Yes: 290 (100.00)
No: 00 (0.00) 1.000
Dry Cough c
{N (%)}
Yes: 100 (38.46)
No: 160 (61.54)
Yes: 105 (36.20)
No: 185 (63.80) 0.5972
Wet Cough c
{N (%)}
Yes: 70 (26.92)
No: 190 (73.08)
Yes: 75 (25.86)
No:215 (74.14) 0.8464
Wheeze
{N (%)}
Yes: 40 (15.38)
No: 220 (84.62)
Yes: 00 (0.00)
No: 290 (100.00) <0.0001*
FVCd
(Mean ±SD) 112.75±26.42 113.2±37.19 0.8715
FEV1
e
(Mean ±SD) 99.05±44.58 96.01±53.78 0.4737
FEV1
/FVC
(Mean ±SD) 92.63±29.18 81.51±30.14 <0.0001*
FEF25-75
f
(Mean ±SD) 72.88±34.61 66.62±37.58 0.0434*
PEFRg
(Mean ±SD) 69.61±32.49 63.27±35.43 0.0298*
[Table/Fig-1]: Overall profile of the study population.
(SD: Standard Deviation, BMI: Body Mass Index: a. Smoking status defined as
ever/never smoker of cigarette, beerie or huqqa; b. Shortness of breath: to evaluate
SOB NYHA standard guidelines were followed*; c. Dry and wet cough defined as
cough on most days of month, for three consecutive months or more in a year; d.
(FVC) Forced Vital Capacity. e. (FEV) Forced Expiratory Volume in one second; f.
(FEF) Forced Expiratory Flow 25-75%; g. (PEFR) Peak Expiratory Flow Rate.)
(*All of the patients belonged to NYHA Class I or Class II grade of dyspnoea.)
Spirometric Finding
Allergic patients
(n=260)
Non-Allergic
patients (n=290)
p-value
Normal Patternh
{n (%)}
Yes: 150 (57.69)
No: 110 (42.31)
Yes: 145 (50.00)
No: 145 (50.00) 0.0729
Small airways obstructioni
{n (%)}
Yes: 75 (28.85)
No:185 (71.15)
Yes: 65 (22.41)
No:225 (77.59) 0.0956
COPDj
{n(%)}
Yes: 20 (7.69)
No: 240 (92.31)
Yes: 55 (18.97)
No: 235 (81.03) 0.0001*
Mixed Ventilatory Defectk
{n(%)}
Yes: 15 (5.77)
No: 245 (94.23)
Yes: 20 (6.90)
No:270 (93.10) 0.6052
Restrictive Patternl
{n(%)}
Yes: 00 (0.00)
No: 260 (100.00)
Yes: 5 (1.72)
No: 285 (98.28) 0.0632
[Table/Fig-2]: Categorization of BDR test results.
(h.FVC:80%-120%pred; FEV1: 80%-120% pred.; FEV1/FVC:70%-85%; FEF25-75
:
Values ranging from 50%-60% & up to 130% of the average, PEFR : >60% pred.
value. i. FEF25-75
<50% pred. mainly. j. FEV1/FVC <70% & FEV1 value <100% pred.:
Mild COPD or higher. k. FEV1/FVC <0.7 and FVC <80% of predicted. l. FVC <80%,
FEV1 ≤ 80% (normal /decreased) & FEV1/FVC ≥0.7.)
sectional nature so no confounding variable like age and smoking
could be ascertained. However, these were important variables
which influenced the overall outcome. Therefore, we categorized
the study subjects based on these parameters and compared the
different groups to deduce the study results.
In the present study, we did not categorize patients based on
grade of SOB as all of the patients fell in NYHA grade I or grade II.
This is most probably because spirometry is very difficult or rather
impracticable in the management of NYHA grade III or grade IV
SOB.
In this study we found that respiratory allergic group was significantly
younger and had lesser percentage of smokers compared to
nonallergic group. This finding was in accordance with the study
www.jcdr.net	 Sujoy Mukherjee et al., Occurrence of COPD in Patients with Respiratory Allergy
Journal of Clinical and Diagnostic Research. 2017 May, Vol-11(5): CC11-CC13 1313
result of Eder W et al., [14]. They also documented that allergic
hypersensitivity due to plant pollens was more commonly found in
younger age group and in older people, the cause was almost always
hypersensitivity to nonallergenic types of irritants in the air, such as
irritants in smog.
The present study had shown that post BDR parameters were
significantly lower in non allergic patients compared to allergic patients
and smokers were at a significantly higher number in non allergic group.
Detection of COPD by spirometry screening was much higher in the
samegroup.SimilarlySichletidisLetal.,foundthatprevalenceofCOPD
was not significantly high among individuals having respiratory allergy
[11]. As smoking causes COPD which showed poor BDR response
in this study, the hypothesis that can be drawn from the constellation
of these findings was that presence of respiratory allergy might refrain
the affected subjects from smoking. This was in accordance with
the findings of Shargorodsky J et al., that the relationship between
tobacco smoke exposure and sinonasal pathology in adults might
be independent of allergic sensitization [15]. Therefore, smoking may
cause symptoms of respiratory allergy. Our study further indicates that
smoking was probably a stronger causative factor for development
of COPD than allergy. This was in accordance with the findings of
Sichletidis et al., who had shown that prevalence of COPD was not
significantly high among allergic subjects [11].
The mean age was significantly higher with greater percentage of
smokers and more persistence of wet cough in non-allergic COPD
population compared with allergic COPD patients. This was in
accordance with the findings of Eisner et al., Jarad et al., & Smith
et al., [16-18]. This further asserts that smoking was much stronger
aetiological factor for COPD than respiratory allergy.
There were no significant differences in BMI, chronic respiratory
symptoms like SOB, dry and wet cough and also FEV1
reversibility
between these two populations again most possibly because smokers
were present in both in allergic and non-allergic patients with COPD
and as because of stronger aetiopathogenic effect of smoking on
COPD effect of allergy on symptoms was blurred.
All the subjects were residents of urban downtown areas. High degree
of air pollution might also contribute to higher prevalence of symptoms
in COPD besides smoking in non-allergic populace as shown by Ko
FW et al., [19].
LIMITATION
Due to cross-sectional nature of this study, it was difficult to
establish causal association between impaired lung function and
the chronic respiratory symptoms. Furthermore air pollution as
a contributing factor cannot be quantified. These might act as
important confounding variables influencing the study result.
CONCLUSION
This present study concludes that COPD may coexist with respiratory
allergy but overall occurrence of COPD was significantly much
more in non-allergic population presenting with chronic respiratory
symptoms. However to establish this finding large scale follow up
investigations should be performed in future.
ACKNOWLEDGEMENTs
The authors are thankful to all faculty members and staff of
Department of Physiology of a medical college, Kolkata and also
our study subjects who gave consent for the research work.
REFERENCES
	[1] Bhome AB. COPD in India: Iceberg or volcano. J Thorac Dis. 2012;4(3):298–309.
	 World Meteorological Organization, United Nations Environment Programme.[2]
Intergovernmental Panel on Climate Change. Available from: http://www.unep.
org/climatechange/
	 Matthies F, Bickler G, Cardenosa Marin N, Hales S. Heat–Health Action Plans.[3]
Guidance. Copenhagen, World Health Organization Regional Office for Europe,
2008.http://www.euro.who.int/__data/assets/pdf_file/0006/95919/E91347.pdf
	 Hakansson K, Konge L, Thomsen SF, Backer V, Buchwald CV. Sinonasal[4]
inflammation in COPD: a systematic review. Eur Respir J. 2013;42:1402–11.
	 Jovinelly J. COPD and Allergies: Avoiding Pollutants and Allergens. Healthline.[5]
August 31,2016. http://www.healthline.com/health/copd/allergies#Overview1
	 Hansel NN. Allergic Disease Worsens Respiratory Symptoms and Exacerbations[6]
in COPD. American Thoracic Society.May 2013 press releases. http://www.
atsjournals.org/doi/abs/10.1164/rccm.201211-2103OC
	 Gavriely N, Nissan M[7] , Cugell DW, Rubin AHE. Respiratory health screening using
pulmonary function tests and lung sound analysis. Eur Respir J. 1994;(7):35–42.
	 P´erez-padilla R, Hallal PC, V´azquez-garc´ıa JC, Mui˜no A, M´aque M, L´opez MV,[8]
et al. Impact of bronchodilator use on the prevalence of COPD in population-based
samples. Journal of Chronic Obstructive Pulmonary Disease. 2007;4(2):113-20.
	 Ferris BG. Epidemiology standardization project (American thoracic society). Am[9]
Rev Respir Dis.1978;118:1-120.
	 Turkeltaub PC, Gergen PJ. Prevalence of upper and lower respiratory conditions[10]
in the US population by social and environmental factors: data from the second
National Health and Nutrition Examination Survey, 1976 to 1980 (NHANES II).
Ann Allergy. 1991;67:147–54.
	 Sichletidis L, Tsiotsios I, Gavriilidis A,[11] Chloros D,  Kottakis I,  Daskalopoulou E,
et al. Prevalence of chronic obstructive pulmonary disease and rhinitis in northern
Greece. Respiration. 2005;72:270–77.
	 Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates RA, et al.[12]
Standardisation of spirometry. Eur Respir J. 2005;26:319-38.
	 HELIOS 702 (Portable Spirometer) Evaluation of 51 vital parameters with[13]
interpretation. Copy writes 2010-2013 Accurate. Available from: http://www.
surgicalmall.com/product/1024.
	 Eder W, Ege MJ, Von-mutius E. The asthma epidemic. N Eng J Med.[14]
2006;355:2226.
	 Shargorodsky J, Garcia-esquinas E, Galán I, Navas-acien A, Lin SY. Allergic[15]
sensitization, rhinitis and tobacco smoke exposure in US adults. PLoS ONE.
2015;10(7):e0131957.
	 Eisner MD, Anthonisen N, Coultas D, Kuenzli N, Perez-padilla R, Postma D, et al.[16]
An official American thoracic society public policy statement: novel risk factors
and the global burden of chronic obstructive pulmonary disease. Am J Respir
Crit Care Med. 2010;182:693–718.
	 Jarad N. Chronic obstructive pulmonary disease (COPD) and old age? Chron[17]
Respir Dis. 2011;8(2):143-51.
	 Smith J, Woodcock A. Cough and its importance in COPD. Int J Chron Obstruct[18]
Pulmon Dis. 2006;1(3):305–14.
	 Ko FW, Hui DS. Air pollution and chronic obstructive pulmonary disease.[19]
Respirology. 2012;17(3):395-401.
PARTICULARS OF CONTRIBUTORS:
1.	 Junior Resident, Department of Physiology, R G Kar Medical College and Hospital, Kolkata, West Bengal, India.
2.	 Professor, Department of Physiology, R G Kar Medical College and Hospital, Kolkata, West Bengal, India.
3.	 Assistant Professor, Department of Physiology, R G Kar Medical College and Hospital, Kolkata, West Bengal, India.
4.	 Professor and Head, Department of Physiology, R G Kar Medical College and Hospital, Kolkata, West Bengal, India.
NAME, ADDRESS, E-MAIL ID OF THE CORRESPONDING AUTHOR:
Dr. Sujoy Mukherjee,
253/1, Ground Floor, Block-B, Bangur Avenue, PS-Laketown, Kolkata-700055, West Bengal, India.
E-mail: dr.sujoymukherjee@rediffmail.com
Financial OR OTHER COMPETING INTERESTS: None.
Date of Submission: Nov 25, 2016
Date of Peer Review: Jan 23, 2017
Date of Acceptance: Feb 23, 2017
Date of Publishing: May 01, 2017
Parameter
Allergic Patients
having COPD
(n=20)
Non-Allergic
Patients having
COPD (n=55)
p-value
Age (Years)
{Mean ±SD}
40.25±11.24 51.63±9.60 <0.0001*
Weight (Kg)
{Mean ±SD}
57.75±8.47 50.09±10.45 0.0044*
Smoking Status
{N (%)}
Ever Smoker:
00 (00.00)
Never Smoker:
20 (100.00)
Ever Smoker:
35 (63.63)
Never Smoker:
20 (36.37)
<0.0001*
Wet Cough
{N (%)}
Yes:00 (00.00)
No:20 (100.00)
Yes:20 (36.37)
No: 35 (63.63)
0.0008*
FEV1
{Mean ±SD}
79.5±21.15 44.00±22.39 <0.0001*
FEV1
/FVC
{Mean ±SD}
57.75±3.99 45.54±12.97 <0.0001*
[Table/Fig-3]: Comparison of COPD Patients with and without Allergy.

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Occurrence of COPD in Patients with Respiratory Allergy: A Clinico-Spirometric Evaluation in a Tertiary Hospital, Kolkata

  • 1. Journal of Clinical and Diagnostic Research. 2017 May, Vol-11(5): CC11-CC13 1111 DOI: 10.7860/JCDR/2017/25643.9841 Original Article PhysiologySection Occurrence of COPD in Patients with Respiratory Allergy: A Clinico-Spirometric Evaluation in a Tertiary Hospital, Kolkata INTRODUCTION Chronic lung disease is a rapidly emerging pandemic. Volcano is a more appropriate word to depict the situation rather than the traditional iceberg phenomenon [1]. Intergovernmental Panel on Climate Change (IPCC) and WHO concluded that overall incidences of obstructive lung diseases, upper respiratory tract allergy and respiratory tract infection are rapidly rising as a result of global warming. Till date smoking is the most important causative factor for COPD. Dyspnoea, wheeze & wet cough are the major symptoms [2,3]. Sinonasal inflammation in COPD may be produced as a result of inflammation, pathological neurogenic reflexes or directly by products of smoking [4]. Allergens, dust, microbes and nonspecific respiratory irritants typically narrow the airways by excessive mucus production thereby exacerbating COPD symptoms [5,6]. On the other hand, till recently American Thoracic Society did not include strategies for the management of respiratory allergies in routine treatment protocol of COPD [6]. The principal focus of the present study was to evaluate the coexistence of COPD with respiratory allergy so that the treatment of respiratory allergy may accelerate the recovery from acute exacerbation of COPD. The combination of clinical examination followed by spirometry can significantly increase the sensitivity of detection of lung diseases [7]. Reversibility testing with bronchodilators reduces the overall prevalence of airway obstruction significantly and post bronchodilatation obstruction is more specific for COPD [8]. The aim of the present study was to evaluate the occurrence of COPD in respiratory allergy among subjects presenting with chronic respiratory symptoms. MATERIALS AND METHODS An observational cross-sectional study was conducted between November 2015 and April 2016. Male and female subjects aged 18 to 60 years presenting with chronic respiratory symptoms like cough, wheeze and SOB for more than three months duration were included in the study. All patients were Bengali speaking and belonged to urban areas of North 24–Parganas district, West Bengal, India. They were referred from different outpatient departments of a tertiary hospital, Kolkata for routine spirometric screening at the spirometry laboratory in Department of Physiology. Asymptomatic patients coming for pre-anaesthetic checkup, Paediatric and Geriatric patients, patients suffering from acute illness and debilitation of any origin, patients with third trimester pregnancy, active haemoptysis, tuberculosis, sub diaphragmatic and known cardiovascular diseases associated with SOB were summarily excluded from the present study. On an average in our department we perform routine spirometry in 160 patients per month. In six months from about 950 patients we selected 550 patients maintaining appropriate inclusion and exclusion criteria. The sampling technique was complete enumeration. Ethical permission was obtained from Institutional Ethics Committee, prior to study and written consent was taken from each of the subject prior to examination. At first all patients were asked to respond to a standardized respiratory symptoms questionnaire (ATS/DLD-78 A questionnaire) [9]. After obtaining detailed clinical profile, patients with respiratory symptoms were divided in two groups: subjects suffering from clinical symptoms suggestive of respiratory allergy (n=260) like nasal catarrh, nasal stuffiness and sneezing all together as written on OPD card and subjects with no symptoms suggestive of respiratory allergy (n=290). SUJOY MUKHERJEE1 , GOUTAM BANERJEE2 , DEBAJYOTI DAS3 , ANIL BARAN SINGHA MAHAPATRA4 Keywords: Acute exacerbation, Pandemic, Spirometry ABSTRACT Introduction: Smoking is established as the most important causative factor responsible for Chronic Obstructive Pulmonary Disease (COPD). Occurrence of allergy in COPD patients causes acute exacerbation of this disease, but role of allergy is not established in aetiopathogenesis of COPD. Aim: The present study was aimed at evaluation of occurrence of COPD in patients having symptoms suggestive of respiratory allergy. Materials and Methods: An observational cross-sectional study was conducted to evaluate occurrence of COPD in patients having respiratory allergic symptoms by routine spirometric screening. Five hundred and fifty urban patients aged 18-60 years (both gender) ailing from chronic respiratory symptoms like cough, wheeze and Shortness Of Breath (SOB), who were referred from OPDs of RGKMCH, Kolkata, were included in this study. After obtaining detailed clinical profile, patients were divided into two groups: subjects having additional clinical symptoms suggestive of respiratory allergy (n=260) like nasal catarrh, nasal stuffiness and sneezing and subjects with no symptoms suggestive of respiratory allergy (n=290). Thereafter, routine spirometry was carried out following recommendations of ATS/ERS (2005). Patients were then categorized based on FVC, FEV1 , FEV1 /FVC, FEF25-75 and PEFR percent predicted values. Results: Study revealed that 18.97% of non-allergic population was suffering from COPD whereas only 7.69% of allergic subjects had COPD. This difference was statistically highly significant (p=0.0001). Although there was no significant difference in prevalence of respiratory symptoms between these two groups. Conclusion: Present study concludes that patients with respiratory allergy may have coexistent COPD but occurrence of COPD is much less than that in patients with no respiratory allergy.
  • 2. Sujoy Mukherjee et al., Occurrence of COPD in Patients with Respiratory Allergy www.jcdr.net Journal of Clinical and Diagnostic Research. 2017 May, Vol-11(5): CC11-CC131212 We did not perform any laboratory test for allergy as clinical symp­ tomatology is established as the most reliable factor in detection of allergy [10,11]. Smoking history was obtained and subjects were categorized as per US Centers for Disease Control and Prevention definition of “Never Smokers” – adults who have never smoked a cigarette or who smoked fewer than 100 cigarettes in their entire lifetime. Rest of the subjects was marked as smokers. All the patients had received one or more bronchodilators and anti-inflammatory agents for treatment of their respiratory symptoms. As all the data was collected at a point of time (cross-sectional data) with no known confounding variable so unpaired t-test was applied to compare these two populations. After calibration, spirometry was carried out by using a non-heated spirometer (RMS HELIOS 702) following current guidelines of the American Thoracic Society [12]. The largest observed values of FEV1 and FVC available from among at least three acceptable and reproducible tests were taken as the key parameters for interpretation. Then, the subject was asked to inhale short acting bronchodilator in the pre-prescribed doses. After ten minutes of taking the inhaler the subject was asked to perform the spirometry once again and thus the reversibility test done [12]. The highest values of FVC and FEV1 were selected. Periodic calibrations were done as per protocol. In absence of normative spirometric data of Indian population the data obtained was interpreted as per directions furnished in the user manual of RMS HELIOS 702 along with given ethnic correction [13]. As the study populace seemed to be ethnically homogenous predictive equation was not obtained. We categorized all the patients as per pre-set criteria: i) Normal Spirometric Finding; ii) Small Airway Obstruction (SAO); iii) COPD; iv) Mixed Ventilatory Defect; & v) Restrictive Pattern [13]. Statistical Analysis Descriptive analyses were performed using Fisher’s-Exact Test (for categorical variables) and two-sided unpaired t-tests (for continuous variables). All spirometric variables were expressed in percent predicted (%) form. Statistical analyses was done by using Microsoft excel sheet and GraphPad Quickcalcs Software, California, USA. A p-value of <0.05 was considered significant. RESULTS Non allergic patients were significantly more likely to be older (mean age was 44 years), percentage of smokers were also higher in the older population. There was no significant difference regarding prevalence of respiratory symptoms like SOB, dry cough, wet cough between allergic and non-allergic populations except wheeze which was more significant finding in allergic population. Furthermore, bronchodilator reversibility (BDR) data had shown that mean values of FEV1 /FVC, FEF25-75 and PEFR were significantly lower in non- allergic subjects as compared to allergic group [Table/Fig-1]. Occurrence of COPD in BDR analysis was significantly more in non- allergic group rather than allergic population [Table/Fig-2]. Non allergic patients with spirometry diagnosed COPD were significantly more likely to be older (mean age was 52 years). More than half of the non-allergic patients had smoking history. Non- allergic patients had a lesser mean body weight. Persistence of lower respiratory symptom like wet cough was more in the non- allergic population compared to allergic population. Furthermore mean values of FEV1 & FEV1 /FVC were significantly less in non allergic COPD population compared to allergic patients [Table/Fig-3]. DISCUSSION In the present study, we divided the whole population based only on prior clinical diagnosis and allergy testing was not performed. As drug/treatment history of patients was not supposed to alter our study outcome so we had not included drug history as a study variable. As the present study was of observational and cross- Variables Allergic Patients (N=260) Non-Allergic Patients (N=290) p-value Gender {N (%)} Male: 110 (42.30) Female:150 (57.70) Male: 145 (50.00) Female:145 (50.00) 0.0729 Age (Years) (Mean ±SD) 35.07±13.02 43.89±11.33 <0.0001* Weight (Kg) (Mean ±SD) 55.34±13.05 54.89±11.47 0.6671 Height (Cm) (Mean ±SD) 155.88±9.23 156.53±8.78 0.3979 BMI (Kg/M2 ) (Mean ±SD) 22.92±5.01 22.45±4.4 0.242 Smoking Statusa {N (%)} Ever Smoker: 40 (15.38) Never Smoker: 220 (84.62) Ever Smoker: 100 (34.48) Never Smoker: 190 (65.52) <0.0001* SOBb {N (%)} Yes: 260 (100.00) No: 00 (0.00) Yes: 290 (100.00) No: 00 (0.00) 1.000 Dry Cough c {N (%)} Yes: 100 (38.46) No: 160 (61.54) Yes: 105 (36.20) No: 185 (63.80) 0.5972 Wet Cough c {N (%)} Yes: 70 (26.92) No: 190 (73.08) Yes: 75 (25.86) No:215 (74.14) 0.8464 Wheeze {N (%)} Yes: 40 (15.38) No: 220 (84.62) Yes: 00 (0.00) No: 290 (100.00) <0.0001* FVCd (Mean ±SD) 112.75±26.42 113.2±37.19 0.8715 FEV1 e (Mean ±SD) 99.05±44.58 96.01±53.78 0.4737 FEV1 /FVC (Mean ±SD) 92.63±29.18 81.51±30.14 <0.0001* FEF25-75 f (Mean ±SD) 72.88±34.61 66.62±37.58 0.0434* PEFRg (Mean ±SD) 69.61±32.49 63.27±35.43 0.0298* [Table/Fig-1]: Overall profile of the study population. (SD: Standard Deviation, BMI: Body Mass Index: a. Smoking status defined as ever/never smoker of cigarette, beerie or huqqa; b. Shortness of breath: to evaluate SOB NYHA standard guidelines were followed*; c. Dry and wet cough defined as cough on most days of month, for three consecutive months or more in a year; d. (FVC) Forced Vital Capacity. e. (FEV) Forced Expiratory Volume in one second; f. (FEF) Forced Expiratory Flow 25-75%; g. (PEFR) Peak Expiratory Flow Rate.) (*All of the patients belonged to NYHA Class I or Class II grade of dyspnoea.) Spirometric Finding Allergic patients (n=260) Non-Allergic patients (n=290) p-value Normal Patternh {n (%)} Yes: 150 (57.69) No: 110 (42.31) Yes: 145 (50.00) No: 145 (50.00) 0.0729 Small airways obstructioni {n (%)} Yes: 75 (28.85) No:185 (71.15) Yes: 65 (22.41) No:225 (77.59) 0.0956 COPDj {n(%)} Yes: 20 (7.69) No: 240 (92.31) Yes: 55 (18.97) No: 235 (81.03) 0.0001* Mixed Ventilatory Defectk {n(%)} Yes: 15 (5.77) No: 245 (94.23) Yes: 20 (6.90) No:270 (93.10) 0.6052 Restrictive Patternl {n(%)} Yes: 00 (0.00) No: 260 (100.00) Yes: 5 (1.72) No: 285 (98.28) 0.0632 [Table/Fig-2]: Categorization of BDR test results. (h.FVC:80%-120%pred; FEV1: 80%-120% pred.; FEV1/FVC:70%-85%; FEF25-75 : Values ranging from 50%-60% & up to 130% of the average, PEFR : >60% pred. value. i. FEF25-75 <50% pred. mainly. j. FEV1/FVC <70% & FEV1 value <100% pred.: Mild COPD or higher. k. FEV1/FVC <0.7 and FVC <80% of predicted. l. FVC <80%, FEV1 ≤ 80% (normal /decreased) & FEV1/FVC ≥0.7.) sectional nature so no confounding variable like age and smoking could be ascertained. However, these were important variables which influenced the overall outcome. Therefore, we categorized the study subjects based on these parameters and compared the different groups to deduce the study results. In the present study, we did not categorize patients based on grade of SOB as all of the patients fell in NYHA grade I or grade II. This is most probably because spirometry is very difficult or rather impracticable in the management of NYHA grade III or grade IV SOB. In this study we found that respiratory allergic group was significantly younger and had lesser percentage of smokers compared to nonallergic group. This finding was in accordance with the study
  • 3. www.jcdr.net Sujoy Mukherjee et al., Occurrence of COPD in Patients with Respiratory Allergy Journal of Clinical and Diagnostic Research. 2017 May, Vol-11(5): CC11-CC13 1313 result of Eder W et al., [14]. They also documented that allergic hypersensitivity due to plant pollens was more commonly found in younger age group and in older people, the cause was almost always hypersensitivity to nonallergenic types of irritants in the air, such as irritants in smog. The present study had shown that post BDR parameters were significantly lower in non allergic patients compared to allergic patients and smokers were at a significantly higher number in non allergic group. Detection of COPD by spirometry screening was much higher in the samegroup.SimilarlySichletidisLetal.,foundthatprevalenceofCOPD was not significantly high among individuals having respiratory allergy [11]. As smoking causes COPD which showed poor BDR response in this study, the hypothesis that can be drawn from the constellation of these findings was that presence of respiratory allergy might refrain the affected subjects from smoking. This was in accordance with the findings of Shargorodsky J et al., that the relationship between tobacco smoke exposure and sinonasal pathology in adults might be independent of allergic sensitization [15]. Therefore, smoking may cause symptoms of respiratory allergy. Our study further indicates that smoking was probably a stronger causative factor for development of COPD than allergy. This was in accordance with the findings of Sichletidis et al., who had shown that prevalence of COPD was not significantly high among allergic subjects [11]. The mean age was significantly higher with greater percentage of smokers and more persistence of wet cough in non-allergic COPD population compared with allergic COPD patients. This was in accordance with the findings of Eisner et al., Jarad et al., & Smith et al., [16-18]. This further asserts that smoking was much stronger aetiological factor for COPD than respiratory allergy. There were no significant differences in BMI, chronic respiratory symptoms like SOB, dry and wet cough and also FEV1 reversibility between these two populations again most possibly because smokers were present in both in allergic and non-allergic patients with COPD and as because of stronger aetiopathogenic effect of smoking on COPD effect of allergy on symptoms was blurred. All the subjects were residents of urban downtown areas. High degree of air pollution might also contribute to higher prevalence of symptoms in COPD besides smoking in non-allergic populace as shown by Ko FW et al., [19]. LIMITATION Due to cross-sectional nature of this study, it was difficult to establish causal association between impaired lung function and the chronic respiratory symptoms. Furthermore air pollution as a contributing factor cannot be quantified. These might act as important confounding variables influencing the study result. CONCLUSION This present study concludes that COPD may coexist with respiratory allergy but overall occurrence of COPD was significantly much more in non-allergic population presenting with chronic respiratory symptoms. However to establish this finding large scale follow up investigations should be performed in future. ACKNOWLEDGEMENTs The authors are thankful to all faculty members and staff of Department of Physiology of a medical college, Kolkata and also our study subjects who gave consent for the research work. REFERENCES [1] Bhome AB. COPD in India: Iceberg or volcano. J Thorac Dis. 2012;4(3):298–309. World Meteorological Organization, United Nations Environment Programme.[2] Intergovernmental Panel on Climate Change. Available from: http://www.unep. org/climatechange/ Matthies F, Bickler G, Cardenosa Marin N, Hales S. Heat–Health Action Plans.[3] Guidance. Copenhagen, World Health Organization Regional Office for Europe, 2008.http://www.euro.who.int/__data/assets/pdf_file/0006/95919/E91347.pdf Hakansson K, Konge L, Thomsen SF, Backer V, Buchwald CV. Sinonasal[4] inflammation in COPD: a systematic review. Eur Respir J. 2013;42:1402–11. Jovinelly J. COPD and Allergies: Avoiding Pollutants and Allergens. Healthline.[5] August 31,2016. http://www.healthline.com/health/copd/allergies#Overview1 Hansel NN. Allergic Disease Worsens Respiratory Symptoms and Exacerbations[6] in COPD. American Thoracic Society.May 2013 press releases. http://www. atsjournals.org/doi/abs/10.1164/rccm.201211-2103OC Gavriely N, Nissan M[7] , Cugell DW, Rubin AHE. Respiratory health screening using pulmonary function tests and lung sound analysis. Eur Respir J. 1994;(7):35–42. P´erez-padilla R, Hallal PC, V´azquez-garc´ıa JC, Mui˜no A, M´aque M, L´opez MV,[8] et al. Impact of bronchodilator use on the prevalence of COPD in population-based samples. Journal of Chronic Obstructive Pulmonary Disease. 2007;4(2):113-20. Ferris BG. Epidemiology standardization project (American thoracic society). Am[9] Rev Respir Dis.1978;118:1-120. Turkeltaub PC, Gergen PJ. Prevalence of upper and lower respiratory conditions[10] in the US population by social and environmental factors: data from the second National Health and Nutrition Examination Survey, 1976 to 1980 (NHANES II). Ann Allergy. 1991;67:147–54. Sichletidis L, Tsiotsios I, Gavriilidis A,[11] Chloros D,  Kottakis I,  Daskalopoulou E, et al. Prevalence of chronic obstructive pulmonary disease and rhinitis in northern Greece. Respiration. 2005;72:270–77. Miller MR, Hankinson J, Brusasco V, Burgos F, Casaburi R, Coates RA, et al.[12] Standardisation of spirometry. Eur Respir J. 2005;26:319-38. HELIOS 702 (Portable Spirometer) Evaluation of 51 vital parameters with[13] interpretation. Copy writes 2010-2013 Accurate. Available from: http://www. surgicalmall.com/product/1024. Eder W, Ege MJ, Von-mutius E. The asthma epidemic. N Eng J Med.[14] 2006;355:2226. Shargorodsky J, Garcia-esquinas E, Galán I, Navas-acien A, Lin SY. Allergic[15] sensitization, rhinitis and tobacco smoke exposure in US adults. PLoS ONE. 2015;10(7):e0131957. Eisner MD, Anthonisen N, Coultas D, Kuenzli N, Perez-padilla R, Postma D, et al.[16] An official American thoracic society public policy statement: novel risk factors and the global burden of chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2010;182:693–718. Jarad N. Chronic obstructive pulmonary disease (COPD) and old age? Chron[17] Respir Dis. 2011;8(2):143-51. Smith J, Woodcock A. Cough and its importance in COPD. Int J Chron Obstruct[18] Pulmon Dis. 2006;1(3):305–14. Ko FW, Hui DS. Air pollution and chronic obstructive pulmonary disease.[19] Respirology. 2012;17(3):395-401. PARTICULARS OF CONTRIBUTORS: 1. Junior Resident, Department of Physiology, R G Kar Medical College and Hospital, Kolkata, West Bengal, India. 2. Professor, Department of Physiology, R G Kar Medical College and Hospital, Kolkata, West Bengal, India. 3. Assistant Professor, Department of Physiology, R G Kar Medical College and Hospital, Kolkata, West Bengal, India. 4. Professor and Head, Department of Physiology, R G Kar Medical College and Hospital, Kolkata, West Bengal, India. NAME, ADDRESS, E-MAIL ID OF THE CORRESPONDING AUTHOR: Dr. Sujoy Mukherjee, 253/1, Ground Floor, Block-B, Bangur Avenue, PS-Laketown, Kolkata-700055, West Bengal, India. E-mail: dr.sujoymukherjee@rediffmail.com Financial OR OTHER COMPETING INTERESTS: None. Date of Submission: Nov 25, 2016 Date of Peer Review: Jan 23, 2017 Date of Acceptance: Feb 23, 2017 Date of Publishing: May 01, 2017 Parameter Allergic Patients having COPD (n=20) Non-Allergic Patients having COPD (n=55) p-value Age (Years) {Mean ±SD} 40.25±11.24 51.63±9.60 <0.0001* Weight (Kg) {Mean ±SD} 57.75±8.47 50.09±10.45 0.0044* Smoking Status {N (%)} Ever Smoker: 00 (00.00) Never Smoker: 20 (100.00) Ever Smoker: 35 (63.63) Never Smoker: 20 (36.37) <0.0001* Wet Cough {N (%)} Yes:00 (00.00) No:20 (100.00) Yes:20 (36.37) No: 35 (63.63) 0.0008* FEV1 {Mean ±SD} 79.5±21.15 44.00±22.39 <0.0001* FEV1 /FVC {Mean ±SD} 57.75±3.99 45.54±12.97 <0.0001* [Table/Fig-3]: Comparison of COPD Patients with and without Allergy.