Background
According to available global estimates, around 300 million people currently suffer from asthma, which has become more common in adults in recent decades [
1]. One in every 250 deaths worldwide has been attributed to asthma, which was found to rank 26th among causes associated with years of life lost in South Asia [
1,
2]. The increase in the prevalence of asthma has been associated with an increase in atopic sensitization, and is paralleled by similar increases in other allergic disorders such as eczema and rhinitis [
1]. The rate of asthma increases as communities become more urbanized; with the projected increase in the proportion of the world’s population that is urban from 45 to 59% in 2025, there is likely to be a marked increase in the number of asthmatics worldwide [
1].
The known risk factors for developing asthma include a combination of genetic predisposition and environmental exposure to various substances that may provoke allergic reactions or irritate the airways. Such environmental exposures may include house dust mites in bedding, carpets and stuffed furniture, pet dander, pollens and molds, tobacco smoke and chemical irritants [
3,
4]. Some additional factors which may exacerbate or cause asthma include work related stress, sedentary lifestyle and indoor air pollutants [
5].
Globally, there is a lack of standardized data regarding prevalence of asthma due to variations in the operational definition and assessment techniques [
6]. There is a lack of community based studies identifying burden of asthma through spirometry, while most of the studies rely on questionnaires [
5,
7,
8]. The question regarding self-reported physician diagnosed asthma has been shown to have high specificity for assessing asthma in several epidemiological surveys worldwide, however, sizeable proportion of asthma may still remain undiagnosed [
9]. In order to address this concern, the recent guidelines recommend a combination of questionnaire and spirometry based information as the best method for determining asthma in epidemiological surveys [
6,
10].
According to India’s National Family Health Survey, prevalence of adult self-reported asthma was around 1.8% [
11]. Asthma prevalence has been found to vary from 0.7 to 11.9% across Asia, but the definitions used to identify asthma also varied extensively [
5]. The report on global burden of asthma estimated the prevalence of asthma, in Pakistan to be 4.3% [
1]. Employing a robust methodology and using comprehensive set of definitions, this study was conducted in order to determine the prevalence of asthma and associated risk factors in the adult population of Karachi, Pakistan.
Results
Approximately 3000 adults aged 18 years and above were contacted to participate in the study in the selected households, out of which 1629 agreed to participate; giving a response rate of around 55%. Most of the non-responses were due to permanent relocation, or untraceable addresses and contact details. Participants who completed post-bronchodilator spirometry were 1054 and for those 930 spirograms were found to be acceptable according to standard guidelines. Majority (43%) of the participants belonged to the age group ≥38 years. Most common ethnicity among study participants was Urdu (44.6%) and majority of the participants were females (60%). Most of the study participants were currently unemployed (includes students, housewives, those currently not working anywhere or retired) (61%), while 20% were blue collar workers and 18.5% were white collar workers according to ISCO categories and 27% reported exposure to a dusty job. Ever smokers in our study were 13.5% while 28% reported exposure to environmental tobacco smoke. History of any allergy was reported by 28% while 12% reported positive family history of asthma (Table
1).
Table 1
Socio-demographic, anthropometric, household, lifestyle and occupational factors among adults ≥18 years, Karachi, Pakistan (n = 1629)
Age |
18 to 27 years | 531 (32.6) |
28 to 37 years | 399 (24.5) |
≥ 38 years | 699 (42.9) |
Gender |
Male | 658 (40.4) |
Female | 971 (59.6) |
Birth Order |
1st | 394 (24.2) |
2nd | 310 (19.0) |
3rd | 295 (18.1) |
≥ 4th | 630 (38.7) |
Total number of children in household |
1 to 3 | 232 (14.3) |
4 to 5 | 442 (27.1) |
≥ 6 | 955 (58.6) |
Ethnicity |
Urdu | 715 (43.9) |
Punjabi | 469 (28.8) |
Sindhi | 295 (18.1) |
Pushto | 90 (5.5) |
Baluchi | 60 (3.7) |
Educational levela (n = 1626) |
Literate | 1109 (68.2) |
Illiterate | 517 (31.8) |
Socio-economic statusb (n = 1621) |
High-income | 537 (33.0) |
Middle-income | 544 (33.4) |
Low-income | 540 (33.1) |
Number of rooms in house |
1 room | 293 (18.0) |
≥ 2 rooms | 1336 (82.0) |
House ownership status |
Own | 1223 (75.1) |
Rented | 407 (24.9) |
Type of household |
Pakka | 1579 (97.0) |
Kacha-Pakka | 50 (3.0) |
Type of clusterc |
Planned | 855 (52.5) |
Unplanned | 774 (47.5) |
Wet spots inside house | 844 (51.8) |
Mold Inside house | 81 (5.0) |
Animal or birds inside housed | 474 (29.0) |
Carpeting inside house | 528 (32.4) |
Incense burning in house | 767 (47.1) |
Mosquito coil burning in house | 739 (45.4) |
Painted home in last 6 months | 204 (12.5) |
Cook food | 894 (54.9) |
Frequency of cooking food |
No cooking at all | 735 (45.1) |
Occasionally | 143 (8.8) |
Daily | 751 (46.1) |
Presence of window in kitchen | 491 (30.1) |
Presence of exhaust fan in kitchen | 227 (13.9) |
Type of kitchen |
Outdoor | 632 (38.7) |
Indoor separate | 268 (16.5) |
Indoor non-separate | 729 (44.8) |
Smoking statuse |
Never | 1409 (86.5) |
Ever | 220 (13.5) |
Pack years of smokingf |
Non smoker | 1409 (86.5) |
≤ 10 | 132 (8.1) |
10–20 | 31 (1.9) |
> 20 | 57 (3.5) |
Exposure to environmental tobacco smokeg | 452 (28.1) |
Body Mass Indexh (n = 1611) |
Underweight | 673 (41.8) |
Normal weight | 575 (35.7) |
Overweight and obese | 363 (22.5) |
History of any allergy | 451 (27.7) |
Family history of asthma | 192 (11.8) |
Family History of tuberculosis | 44 (2.7) |
Exposure to any dusty job |
Never worked | 899 (55.2) |
Working and no dust exposure | 293 (18.0) |
Working and dust exposure | 437 (26.8) |
Exposure to gas or fumes at work |
Never worked | 899 (55.2) |
Working and no gas exposure | 592 (36.3) |
Working and gas exposure | 138 (8.5) |
Current employment statusi |
Unemployed | 1000 (61.4) |
Employed | 629 (38.6) |
ISCO Categoriesj |
Not working | 1000 (61.4) |
White collar worker | 301 (18.5) |
Blue collar worker | 328 (20.1) |
The prevalence of self-reported asthma was 1.8% (95% CI: 1.0–2.6), while prevalence according to reversibility in FEV
1 was 11.3% (95% CI: 9.4–13.3) and symptoms and reversibility in FEV
1 was 6.6% (95% CI: 5.1–8.1) (Table
2). The break-up by sex (female/male) was: self-reported asthma: 1.6% /2.0%, reversibility in FEV
1: 10.8% /11.7% and symptoms and reversibility in FEV
1: 6.9% /6.2%.
Table 2
Prevalence of asthma and respiratory symptoms among adults ≥18 years, Karachi, Pakistan, 2015 (n = 1629)
Self-reported asthmaa | 29 (1.8) | 1.0–2.6 |
Reversibility ≥200 ml in FEV1b d | 105 (11.3) | 9.4–13.3 |
Respiratory symptoms and reversibility ≥200 ml in FEV1C d | 61 (6.6) | 5.1–8.1 |
SOB grade I | 410 (25.2) | 22.5–27.9 |
SOB grade II | 359 (22.0) | 19.5–24.6 |
Acute cough | 72 (4.4) | 3.1–5.7 |
Chronic cough | 49 (3.0) | 1.9–4.1 |
Acute wheeze | 164 (10.1) | 8.2–11.9 |
Chronic wheeze | 130 (8.0) | 6.3–9.7 |
Acute phlegm | 107 (6.6) | 5.1–8.1 |
Chronic phlegm | 60 (3.7) | 2.5–4.9 |
Among those with self-reported asthma (n = 29), common triggering factors for aggravation of asthma included; exposure to smoke (83%), strong smell (53%) and dust (83%). Participants currently on prescribed medications for asthma were 80% and out of these 71% participants were taking inhaled bronchodilators whereas 42% were on oral medications.
The prevalence of respiratory symptoms identified in this study was: acute cough, 4.4% (95% CI: 3.1–5.7); acute wheeze, 10.1% (95% CI: 8.2–11.9); and shortness of breath (Grade I), 25.2% (95% CI: 22.5–27.9) (Table
2).
Various factors found to be associated with self-reported asthma include: age ≥ 38 years; presence of two or more rooms in house; living in a
Kacha-Pakka house; pack years of smoking for ≥20 years; history of any allergy and family history of asthma (see Additional file
1).
Univariate logistic regression analysis found that asthmatics based on reversibility in FEV
1 were more likely to belong to the age group ≥38 years (OR 1.9, 95% CI: 1.1 to 3.2), low socio-economic status (OR 1.8, 95% CI: 1.1 to 3.1), were ever smokers (OR 1.6, 95% CI: 1.1 to 2.6), and those with pack years of smoking of 5 years or more (OR 2.2, 95% CI: 1.2 to 4.1) and those with history of any allergy (OR 1.7, 95% CI: 1.1 to 2.6). Asthmatics according to respiratory symptoms and reversibility in FEV
1 were more likely to belong to the age group ≥38 years (OR 2.2, 95% CI: 1.1 to 4.2), were illiterate (OR 1.9, 95% CI: 1.1 to 3.2), were among those with pack years of smoking of 5 years or more (OR 3.2, 95% CI: 1.7 to 6.3), had exposure to environmental tobacco smoke (OR 1.8, 95% CI: 1.1 to 3.1), had history of allergies (OR 2.7, 95% CI: 1.6 to 4.5) and had family history of asthma (OR 2.0, 95% CI: 1.1 to 3.9) (Table
3).
Table 3
Univariate logistic regression analysis for factors associated with asthma among adults ≥18 years, Karachi, Pakistan (n = 930)
Age |
18 to 27 years | 1 | 0.02 | 1 | 0.01 |
28 to 37 years | 0.9 (0.5–1.8) | 0.51 | 0.7 (0.3–1.8) | 0.47 |
≥ 38 years | 1.9 (1.1–3.2) | 0.03 | 2.2 (1.1–4.2) | 0.02 |
Gender |
Male | 1 | | 1 | |
Female | 0.9 (0.6–1.4) | 0.40 | 1.1 (0.7–1.9) | 0.64 |
Birth Order |
1st | 0.8 (0.5–1.5) | 0.51 | 0.8 (0.4–1.6) | 0.48 |
2nd | 0.9 (0.6–1.7) | 0.61 | 0.8 (0.4–1.8) | 0.67 |
3rd | 1.0 (0.6–1.8) | 0.31 | 1.4 (0.7–2.7) | 0.37 |
≥ 4th | 1 | | 1 | |
Total number of Children |
1 to 3 | 0.9 (0.5–1.6) | 0.22 | 0.9 (0.5–1.7) | 0.21 |
4 to 5 | 0.9 (0.5–1.4) | 0.81 | 0.5 (0.2–1.4) | 0.82 |
≥ 6 | 1 | | 1 | 0.44 |
Educationa |
Literate | 1 | | 1 | |
Illiterate | 1.4 (0.9–2.1) | 0.05 | 1.9 (1.1–3.2) | 0.02 |
Socio-economic statusb | | | | |
High income | 1 | 0.21 | 1 | 0.13 |
Middle income | 1.6 (0.9–2.6) | 0.10 | 0.9 (0.5–1.7) | 0.22 |
Low income | 1.8(1.1–3.1) | 0.03 | 1.2 (0.6–2.2) | 0.24 |
Number of rooms |
≥ 2 rooms | 1 | | 1 | |
1 room | 1.1 (0.7–1.8) | 0.75 | 1.1 (0.6–2.2) | 0.71 |
Ownership status |
Own | 1 | | 1 | |
Rented | 0.9 (0.6–1.5) | 0.31 | 1.3 (0.7–2.2) | 0.44 |
Type of clusterc |
Planned | 1 | | 1 | |
Unplanned | 1.0 (0.7–1.6) | 0.29 | 0.9 (0.5–1.5) | 0.73 |
Wet spots inside house |
No | 1 | | 1 | |
Yes | 1.1 (0.7–1.6) | 0.28 | 0.9 (0.6–1.7) | 0.99 |
Animal or birds inside housed |
No | 1 | | 1 | |
Yes | 0.7 (0.4–1.2) | 0.19 | 0.6 (0.3–1.1) | 0.10 |
Carpeting inside house |
No | 1 | | 1 | |
Yes | 0.9 (0.6–1.4) | 0.81 | 0.9 (0.6–1.7) | 0.88 |
Incense burning in home |
Never | 1 | | 1 | |
Ever | 1.0 (0.7–1.5) | 0.96 | 1.0 (0.6–1.7) | 0.97 |
Mosquito coil |
Never | 1 | | 1 | |
Ever | 0.7 (0.5–1.1) | 0.85 | 0.9 (0.6–1.6) | 0.91 |
Cooking food |
No | 1 | | 1 | |
Yes | 1.0 (0.7–1.5) | 0.41 | 0.5 (0.3–1.1) | 0.47 |
Window in Kitchen |
Yes | 1 | | 1 | |
No | 0.9 (0.6–1.3) | 0.08 | 0.6 (0.4–1.0) | 0.05 |
Exhaust in kitchen |
Yes | 1 | | 1 | |
No | 0.8 (0.5–1.5) | 0.51 | 0.5 (0.3–0.9) | 0.04 |
Type of kitchen |
Outdoor | 1 | | 1 | 0.401 |
Indoor separate | 1.5 (0.8–2.6) | 0.15 | 1.6 (0.8–3.4) | 0.17 |
Indoor non separate | 1.2 (0.7–1.9) | 0.21 | 1.3 (0.7–2.4) | 0.41 |
Smoking statuse |
Never | 1 | | 1 | |
Ever | 1.6 (1.1–2.6) | 0.03 | 1.7 (0.9–3.1) | 0.07 |
Pack years of smokingf |
Non smoker | 1 | 0.00 | 1 | 0.001 |
< 5 years | 1.1 (0.5–2.4) | 0.39 | 0.6 (0.2–2.1) | 0.47 |
≥ 5 years | 2.2 (1.2–4.1) | 0.001 | 3.2 (1.7–6.3) | 0.001 |
Exposure to environmental tobacco smokeg |
No | 1 | | 1 | |
Yes | 1.5 (0.9–2.3) | 0.05 | 1.8 (1.1–3.1) | 0.03 |
Body Mass Indexh |
Underweight | 1 | 0.490 | 1 | 0.410 |
Normal | 1.4 (0.9–2.2) | 0.100 | 1.4 (0.8–2.6) | 0.287 |
Overweight and obese | 1.3 (0.8–2.3) | 0.101 | 1.6 (0.8–3.1) | 0.208 |
History of any allergy |
No | 1 | | 1 | |
Yes | 1.7 (1.1–2.6) | 0.02 | 2.7 (1.6–4.5) | 0.001 |
Family history of asthma |
No | 1 | | 1 | |
Yes | 1.0 (0.5–1.9) | 0.41 | 2.0 (1.1–3.9) | 0.00 |
Exposure of dusty job |
Not working | 1 | 0.81 | 1 | 0.82 |
Working and no dust exposure | 0.9 (0.5–1.5) | 0.42 | 0.4 (0.1–0.9) | 0.04 |
Working and dust exposure | 1.4 (0.9–2.1) | 0.39 | 1.2 (0.7–2.2) | 0.42 |
Exposure of gas or fumes at work |
Not working | 1 | 0.10 | 1 | 0.91 |
Working and no gas exposure | 1.1 (0.7–1.7) | 0.41 | 0.9 (0.5–1.6) | 0.68 |
Working and gas exposure | 1.5 (0.8–2.8) | 0.35 | 0.9 (0.4–2.3) | 0.97 |
Current employment statusi |
Unemployed | 1 | | 1 | |
Employed | 1.1 (0.7–1.7) | 0.51 | 0.9 (0.5–1.5) | 0.701 |
ISCO Categories j |
Not working | 1 | 0.78 | 1 | 0.88 |
White collar worker | 0.9 (0.5–1.5) | 0.59 | 0.8 (0.4–1.7) | 0.62 |
Blue collar worker | 1.3 (0.8–2.1) | 0.34 | 0.95 (0.5–1.8) | 0.87 |
Multivariate logistic regression models found that participants categorized as asthmatics on reversibility in FEV
1 were more likely to belong to the age group ≥38 years (AOR 1.9, 95% CI: 1.2 to 3.3), low socioeconomic group (AOR 1.9, 95% CI: 1.2 to 3.4), to have history of allergies (AOR 1.9, 95% CI: 1.2 to 2.9), exposure to environmental tobacco smoke (AOR 1.6, 95% CI: 1.1 to 2.5). While asthmatics based on respiratory symptoms and reversibility in FEV
1 were more likely belong to age group ≥38 years (AOR 2.1, 95% CI: 1.1 to 4.2), reported 5 or more pack years of smoking (AOR 2.3, 95% CI: 1.1 to 4.7), reported exposure to environmental tobacco smoke (AOR 1.9, 95% CI: 1.1 to 3.3) and had history of any allergy (AOR 2.8, 95% CI: 1.7 to 4.8) (Table
4).
Table 4
Multivariate logistic regression analysis for factors associated with asthma among adults ≥18 years, Karachi, Pakistan (n = 930)
| AOR (95% CI) | AOR (95% CI) |
Age |
18 to 27 years | 1 | 1 |
28 to 37 years | 0.9 (0.5–1.7) | 0.7 (0.3–1.8) |
≥ 38 years | 1.9 (1.2–3.3) | 2.1 (1.1–4.2) |
Socio-economic statusa |
High income | 1 | – |
Middle income | 1.7 (0.9–2.8) | – |
Low income | 1.9 (1.2–3.4) | – |
History of any allergy |
No | 1 | 1 |
Yes | 1.9 (1.2–2.9) | 2.8 (1.7–4.8) |
Pack years of smokingb |
Non smoker | – | 1 |
< 5 years | – | 0.6 (0.2–1.9) |
≥ 5 years | – | 2.3 (1.1–4.7) |
Exposure to environmental tobacco smokec |
No | 1 | 1 |
Yes | 1.6 (1.1–2.5) | 1.9 (1.1–3.3) |
Discussion
To the best of our knowledge, this is the first community-based epidemiological assessment identifying prevalence of adult asthma in Pakistan. Globally, there is a lack of reliable estimates for asthma and a lack of agreement on standardized criteria for epidemiological assessment of asthma and therefore we believe that this study fills an important gap in knowledge by providing reliable estimates on adult asthma using a combination of respiratory symptoms and objective assessment. This study found significant unreported asthma with the use of spirometry in the city of Karachi, Pakistan; 11.3 and 6.6% for ‘reversibility in FEV1’ and ‘respiratory symptoms and reversibility in FEV1’ respectively; while reporting comparatively lower prevalence (1.8%) for self-reported asthma.
Prevalence of self-reported asthma (1.8%) in this study was comparable to regional estimates; approximately 2% in India and Thailand [
7,
14]. In the Indian INSEARCH survey, self-reported asthma was diagnosed based on asthma symptoms, previous diagnosis of asthma or medication use [
7]. Whereas, the survey from Thailand also identified asthma based on self-reported physician diagnosed asthma accompanied by any asthma symptoms or use of medications [
14]. However, our study estimate was lower than that reported by a national survey in Iran, using symptoms of wheezing with dyspnea, as 9.4%; and also somewhat lower when using their definition of ‘current asthma’ which included asthma attack or use of asthma medications i.e. 4.7% [
8]. Obel et al. reported asthma burden to be 6.9% in a population based survey from sub-Saharan Africa using self-reported asthma-ever and and/or receiving asthma medications, which is higher than in our study [
25]. Furthermore, South Asian women including those of Pakistani origin living in the United Kingdom were found to have a self-reported asthma prevalence of 10.9% [
15]. Some of these differences are due to the use of varying definitions for asthma while the study from the UK may reflect an additional risk of asthma among migrants from South Asian countries. The use of the variable physician-diagnosed asthma may also be unreliable due to the varying capacity of general practitioners to identify asthma in different countries [
6].
Prevalence of asthma based on reversibility in FEV
1 was 11.3% in this study, which is comparable to prevalence reported from Iran of 9.4% [
26]. We believe that our study identified a previously unreported burden of asthma through spirometry. Though this is a robust and objective assessment, spirometry may still underestimate the actual prevalence of asthma due to the less sensitive nature of the reversibility test as compared to physicians’ assessment [
27]. There is a probability of people who fail to accomplish the reversibility criteria significantly on a single occasion but who actually have asthma [
27].
Lower prevalence rates of 2.9 and 2.3% have been reported from Thailand and South Australia [
14,
27], respectively. Whereas, prevalence found in our study was 6.6%, comparatively higher based on respiratory symptoms and reversibility in FEV
1. The study by Dejsomritrutai et al. among Thai adults was a community based survey which identified asthma on reversibility in spirometry or having any respiratory symptoms, in addition to bronchial hyper-responsiveness on broncho-provocation test [
14]. Furthermore, Amiri et al. reported 9% prevalence from a cross-sectional survey from Iran where asthma assessed through spirometry [
26]. De Marco et al. reported that asthma prevalence may be overestimated if assessed through self-reported wheezing but might be underestimated if assessed through self-reported asthma and clinical judgment [
28]. Our study also supports the use of a combination of lung function and respiratory symptoms data for assessing asthma and identified a wide gap between self-reported asthma and substantial unidentified burden of asthma in the community.
Prevalence of acute and chronic wheeze reported in this study was 10 and 8% respectively, while prevalence of wheeze in past 12 months reported in a study from India was 2.6% [
7]. Prevalence for shortness of breath (Grade I) found in this study was 25%, while prevalence of breathlessness on exertion was reported by 5% in India, which might be due to over-reporting in our study [
7].
The prevalence of acute and chronic cough reported in our study was 4.4 and 3%, respectively, which is comparable to the prevalence of chronic cough found in India, i.e. 4.6% [
7]. Prevalence of acute and chronic phlegm was found to be 6.6 and 3.7% respectively in this study which is also similar to 3.8% prevalence of chronic phlegm reported from India [
7].
A study conducted in Mashhad, Iran, found that history of allergy was an important risk factor for asthma, a finding which is similar to our study which found history of allergy to be associated with asthma according to both definitions ‘reversibility in FEV
1’ and ‘respiratory symptoms and reversibility in FEV
1’ with odds ratio of AOR (95% CI): 1.9 (1.2–2.9) and 2.8 (1.7–4.8) respectively. [
29]. Allergy has been commonly reported risk factor across many studies and established associations have also been found for high Serum IgE level, a substitute for allergic sensitization, and for common allergens identified by skin prick tests with asthma [
3,
30]. A nationally representative survey among Iranian adults showed that prevalence of asthma was significantly higher among the older age group [
8]. This finding is comparable to the INSEARCH survey from India which determined significant relationship with advancing age, highlighting a possible “cumulative effect” of age, including asthma diagnosed in past, besides late onset of the disease [
7]. New onset asthma may also occur in adulthood because of prolonged environmental or occupational exposures to respiratory irritants [
3]. High asthma prevalence has been observed progressively with increasing age in Asia [
5]. Likewise, evidence suggests that older people with a history of smoking may develop asthma-COPD overlap syndrome (ACOS) [
31]. People with COPD might have airway responsiveness, have shown reversibility in FEV
1 and therefore may be categorized as ACOS. Such cases may have overestimated the prevalence in our study however, symptoms suggestive of asthma were also taken into account in one of the definitions in order to overcome such over-reporting [
32].
Tobacco smoking is known to cause inflammatory changes of the airway tract, resulting in developing or worsening of pre-existing asthma symptoms; however, there is inconsistency of evidence regarding association of tobacco smoking and adult asthma [
2,
33]. An Indian survey found smoking to be an important risk factor for asthma [
11]. Further, Swedish studies reported population attributable risk for asthma symptoms attributed to smoking between 9.8 to 25.5% [
33]. Recently, a follow up study suggested that smokers with asthma tend to have more complaint of chronic cough and phlegm as compared to non-smokers [
34]. These findings are consistent with our study where we found an association between tobacco smoking and asthma according to “respiratory symptoms and reversibility in FEV
1” AOR (95% CI): 2.3 (1.1–4.7).
Previous studies found that environmental tobacco smoke exposure, one of the consistent modifiable risk factor, played a strong role in developing and aggravating asthma [
3,
35]. Our finding for environmental tobacco smoke AOR (95% CI): 1.6 (1.1–2.5) and 1.9 (1.1–3.3) respectively for definitions based on ‘reversibility in FEV
1’ and ‘respiratory symptoms and reversibility in FEV
1’ was consistent with other studies [
3]. European Community Respiratory Health Survey (ECRHS) findings suggest that maternal smoking during pregnancy or post-natal period as well as paternal smoking is associated with development of symptoms suggestive of asthma and had detrimental effect on lung function of children later in the adulthood [
36]. Socioeconomic position has an important role to be identified for preventing inequalities and overall decreasing disease burden [
37]. In our study, significant association of lower socioeconomic status has been found with asthma AOR (95% CI): 1.9 (1.2–2.9). This finding was consistent with a multicenter study which found low socio-economic position as a consistent risk factor for asthma [
37]. Another cohort study reported association of lower socioeconomic position with the asthma onset in adulthood [
38]. Our study could not find any significant association of asthma with gender, which is similar to findings of a population based study from Iran [
8]. There is some inconsistent evidence suggesting possible role of hormonal changes during puberty for greater likelihood of asthma among women [
39].
Some limitations need to be considered for this study. We had a relatively high non-response rate of 45% which may be attributed to a generally poor security situation in the city at the time of data collection, resulting in limited access for study teams. However, spirometry based surveys have been found to report low response rates, such as studies conducted in Thailand, Tanzania and Sweden [
14,
40,
41]. Probable reasons for low participation in spirometry based surveys may include apprehensions for the spirometry procedure, which requires physical exertion. Since the study was conducted in urban setting, hence, generalizability may be limited to similar urban population in Pakistan. However, we believe that the population in Karachi represents common ethnic groups of the country; therefore our findings are applicable for various ethno-linguistic groups from urban areas of the country.
There are several strengths which need to be considered for this study as well. This was the first community based respiratory health survey conducted in Pakistan employing robust methodology and objective lung function assessment. This study used standard ATS guidelines and protocols for conducting spirometry for asthma assessment, along with WHO Global Health Survey based standard definitions of physician-diagnosed asthma [
19,
20]. American Thoracic Society respiratory questionnaire (ATS-DLD-78A) was used in this study for assessment of respiratory symptoms, which has been validated both internationally and locally in Pakistan [
17]. In addition, a sampling frame was developed prior to data collection for purpose of random selection of households which adds to the strengths of this study. We believe that this study would have a substantial research impact in terms of providing much needed empirical evidence related to respiratory epidemiology on prevalence of asthma in Pakistan via three different definitions. The information obtained from this study may be utilized for priority-setting and developing strategic public health plans for the optimal resource allocation for preventive and curative programs.