Printer Friendly

Frequency of allergic asthma and common aeroallergens sensitization in Pakistani patients of bronchial asthma.

Byline: Sara Waqar Khan, Ali Hamid, Fuad Ahmad Siddiqi and Mehroo Bakhtawar

Abstract

Objective: To determine the frequency of allergic asthma and 18common causative aeroallergens sensitisation among patients of bronchial asthma.

Methods: This descriptive cross-sectional study was conducted at the Armed Forces Institute of Pathology, Rawalpindi, Pakistan, from March 2014 to March 2016, and comprised clinically-diagnosed adult patients of bronchial asthma referred from various hospitals of Rawalpindi and Islamabad. Detailed history of each patient was recorded. Serum total immunoglobulin E level was determined using enzyme-linked immunosorbent assay. Skin prick test for 18 common aeroallergens was performed. SPSS 20 was used for data analysis.

Results: Of the 105 patients, 62 (59.05%) were males and 43(40.95%) were females. The overall mean age for males and females was 29.9+-10.2 years and 28.7+-7.0 years respectively. Overall mean serum total immunoglobulin E was 285.01+-241.39IU/ml. Frequency of atopy/allergic asthma was 59(56.2%) and patients with raised total immunoglobulin E had more chance of developing allergic asthma than those having normal immunoglobulin E(p <0.05). Frequency of allergen sensitisation was the highest with house dust mite 35(33.3%), followed by paper mulberry 33(31.4%) and grass 28(26.7%) cases.

Conclusion: Prevalence of allergic asthma was high and the most common allergen causing highest sensitisation was house dust mite.

Keywords: Aeroallergens, Allergic asthma, Bronchial asthma, Atopy, Allergen sensitisation.

Introduction

Bronchial asthma is an inflammatory disease of the airways causing reversible airflow obstruction, airway hyper responsiveness, mucous hyper secretion and airway wall remodelling. Incidence of allergic asthma has increased in the past few years due to urbanisation. The disease has affected more than 300 million people worldwide with around 250,000 annual deaths.1 Worldwide prevalence is 1-6%.2 Prevalence in the United States of America (USA) is 8%.3 and in Pakistan it is around 5%.4

The strongest risk factor for asthma is atopy which is the genetic propensity to develop IgE antibodies in response to exposure to allergen. Allergens and allergen-specific IgE antibody assays are assessed by skin prick test (SPT). Prevalence of asthma among atopic subjects is 12.9%.5

There is an increase in the global prevalence and economic burden of allergic diseases.6 Population based studies have shown a definitive relationship between serum total immunoglobulin E (IgE) and asthma.7-11

Bronchial hyper responsiveness is a fundamental feature of asthma and thought to have a heritable component.12 Studies in both humans and animals have revealed a genetic propensity to bronchial hyper responsiveness.13 A greater concordance for this trait among monozygotic twins than among dizygotic twins has been observed.14

In children with no history or symptoms of atopy or asthma, bronchial hyper responsiveness is strongly associated with elevated serum IgE levels.8 Population studies clearly reveal a very strong association between atopy and bronchial hyper responsiveness.8,9

Major locus regulating serum IgE levels is on chromosomes 5q31-q33.15-17

This chromosomal region is rich in candidate genes, and many of them regulate IgE production either directly or indirectly and affect the activation and proliferation of cells involved in inflammatory processes associated with bronchial hyper responsiveness, allergy and asthma.15

It has been reported that IgE production is tightly controlled by a balance between T helper type1 (Th1) and T helper type2 (Th2) cytokines, interleukin (IL) 4 and 13 being involved in the immunological switching towards IgE production. Th17 and Th9 cell subtypes are known to contribute to the inflammation or enhancing smooth muscle contraction or stimulating mast cells.1

Published studies have revealed the association between airway hyper responsiveness and the number of allergen sensitisations.4,7

A study reported that the development of sensitisation to perennial allergens early in life (3mm at the SPT.9 Allergen extracts for SPT were procured from abroad (Greerlabs, USA) and included allergens of HDMs, paper mulberry, grass, mixed pollen, neem and eucalyptus, cannabis, dandelion, ragweed, bottle brush, cockroach, cat and dog hair, wasp and pigeon feathers, Candida albicans, Alternariaalternata and Aspergillus fumigatus.

Frequency and percentages were calculated for gender, atopic asthma and allergen sensitisation. Mean and Standard Deviation (SD) were calculated for numerical data like age and serum total IgE using SPSS 20. Significance of association of raised serum total IgE with development of allergic asthma was calculated using Chi square test. Level of significance was set at 0.05. Odds ratio (OR) was calculated at 95% confidence interval (CI) for which upper limit was set at 15.7 and the lower limit at 2.81.

Results

Of the 105 patients, 62(59.05%) were males and 43(40.95%) were females. The mean age was 29.9+-10.2 years (range: 18-53 years) for males, and 28.7+-7.0 (range: 19-43 years) for females.

Overall mean serum total IgE of the patients was 285.01+-241.39IU/ml (Table-1) which was compared with the cut-off value for adult patients which is 150 IU/L. SPT (SPT) was performed on all the patients (Table-2).

Table-1: Serum total IgE.

Range (IU/L)###Mean (IU/L)###SD###Patients with raised total IgE###Patients with normal total IgE

25-860###285.01###+-241.39###60 (57.14%)###45 (42.86%)

Table-2: Skin prick test, frequency of atopy/allergic asthma in patients with normal and raised serum total IgE levels.

No. of tests###Positive to one or more###Negative to###SPT+ patients with###SPT+ patients with###p-value###Odd's ratio

performed###allergens (Atopic asthma)###all allergens###raised total IgE n= 60###normal total IgE n= 45###(95% CI)###(95%CI)

105###59 (56.2%)###46 (43.8%)###45 (75%)###14 (31.1%)###<0.01###6.64

The frequency of atopy/allergic asthma was 59(56.2%) (p<0,05). SPT was performed using commercially available allergen extracts of 18 common aeroallergens and the frequency of each of them was noted ((Table-3).

Table-3: Frequency of different aeroallergens sensitization.

Sr. No.###Name of allergen###Result

1.###House dust mite mix###35 (33.3%)

2.###Paper mulberry###33 (31.4%)

3.###Grass###28 (26.7%)

4.###Mixed pollen###20 (19.0%)

5.###Cannabis###18 (17.1%)

6.###Cat hair###12 (11.4%)

7.###Aspergillusfumigatus###8 (7.6%)

8.###Dandelion###8 (7.6%)

9.###Dog hair###8 (7.6%)

10.###Ragweed###7 (6.7%)

11.###Pigeon feathers###5 (4.8%)

12.###Bottle brush###5 (4.8%)

13.###Cockroach###5 (4.8%)

14.###Wasp###3 (2.9%)

15.###Candida albicans###3 (2.9%)

16.###Alternariaalternata###3 (2.9%)

17.###Neem###3 (2.9%)

18.###Eucalyptus###3 (2.9%)

HDM was the main inhalant allergen causing the highest sensitisation in 35(33.1%) patients, followed by paper mulberry 33(31.4%), grass 28(26.7%), mixed pollen 20(19%), cannabis 18(17.1%), cat hair 12(11.4%), aspergillus fumigatus, dandelion and dog hair 8 (7.6%) each, ragweed 7(6.7%), pigeon feathers, bottle brush and cockroach 5 (4.8%) each, wasp, Candida albicans, Alternariaalternata, neem and eucalyptus 3 (2.9%) each.

Discussion

There is an increase in the global prevalence and economic burden of allergic diseases.6 Environmental factors are considered to play more important role than genetic factors for the recent increment in the prevalence of allergic diseases.16 Environmental factors such as smoking, lifestyle, obesity, pets, diet, and air pollution are considered causative or aggravating factors for allergic diseases.17 Therefore it is very important to accurately investigate the prevalence of allergic diseases and the level of exposure to indoor and outdoor allergens.

IgE-mediated allergic reactions to environmental allergens play a very significant role in the pathophysiology of asthma. Atopic persons have high levels of IgE which is reactive against one or more specific environmental allergens and they also often have increased plasma total IgE concentrations.10 Also, the prevalence of asthma is quite closely related to serum IgE levels standardised for age and gender.11 Our results indicated that patients with raised total IgE have 6.6 times more chance of developing asthma which is in accordance with international data.10,11

Frequency of allergic asthma in our patients was 57.2% and HDM was the main inhalant allergen causing the highest sensitisation in 35(33.1%) patients, which is in accordance with other regional and international studies.

One study revealed that prevalence of asthma and atopy were 25.5% and 56% respectively in Korean population. HDM was the most common aeroallergen in 60% population followed by cockroach (23.6%), mugwort (22.9%), oak (22.9%), ragweed (10%), Japenese hop (9.1%), dog dander (8.2%), and cat dander, birch, rye grass and Alternaria (5.5%).18

A study conducted on Pakistani population revealed that the prevalence of allergic asthma was 19.36%. Sensitisation of various inhalant allergens was: pollen 20.3%, HDM 20.3%, paper mulberry 20.3%, thresher 20.2% and raw cotton 17%.22

Sensitisation to animal allergens is a very important risk factor for developing allergic diseases like asthma, rhinitis, and atopic dermatitis, especially in occupationally exposed workers.23 Our results revealed that frequency of sensitisation to cat and dog allergens was 20(19%) and 15(14.3%) respectively.

An American study reported the prevalence of atopic/allergic asthma to be 56.3% with highest sensitisation to cat allergen (29.3%), followed by positive responses to Alternaria (21.1%), white oak (20.9%), dust mite (10.1%), and cockroach (7.6%).24

A pan European study revealed that 27% of patients referred to an allergy centre were sensitised to cat and/or dog related allergens.25 Another study reported that among asthma patients 43.9% were sensitised to dog allergens, 41.7% to cat allergens and 38.9% to rabbit allergens.20

A study reported that sensitisation to cat allergens was a more potent risk factor in adults for developing asthma than was cat ownership, suggesting that sensitisation to cat allergens can develop regardless of cat ownership.26

One study reported that the prevalence of atopic asthma in Indian asthmatics was 55.6% with highest sensitisation to housefly antigen in 31.1% patients and lowest to HDM which was only in 7.8% patients.27 This difference in sensitisation of aeroallergens can be due to regional and environmental differences in indoor and outdoor settings.

The most important implication of diagnosing allergen sensitisation in patients with asthma or other allergic diseases is the treatment modification in these patients. Specific allergen immunotherapy (SIT) is a unique therapy with an ability to change the natural evolution of allergic diseases.28 In this treatment modality, allergens are given to patients in repeated and gradually increasing doses to provide immune tolerance. The efficacy of both subcutaneous (SCIT) and sublingual (SLIT) immunotherapy is documented for perennial and seasonal allergic respiratory diseases by systematic reviews and meta-analyses.29 SIT should be considered in the management of asthmatic patients who experience adverse effects of medications, to reduce or avoid long-term pharmacotherapy and the increasing economic burden of medications and in the presence of allergic rhinitis or other comorbid allergic conditions.30

Avoidance of allergens is another important tool in the prevention of allergic asthma and asthma-like symptoms.31

The patients included in the study were from almost all parts of Pakistan and they were selected according to a well-defined inclusion and exclusion criteria, adding to the strength of the study. However, most patients belonged to Rawalpindi and Islamabad only which means there was a relatively uneven area representation from different parts of Pakistan, which is a limitation of the study.

Conclusion

The prevalence of allergic asthma was high at 56.2% and the most common allergen causing highest sensitisation was HDM. Identifying causative allergen can be very helpful in the management of patients. Environmental control of allergens, their avoidance and use of SIT are important management tools.

Disclaimer: None.

Conflict of Interest: None.

Funding Sources: Immunology Department, AFIP, Rawalpindi.

References

1. Kudo M, Ishigatsubo Y, Aoki I. Pathology of Asthma. Front Microbiol 2013; 4: 263.

2. Sala-Cunill A, Bartra J, Dalmau G, Tella R, Botey E, Raga E, et al. Prevalence of Asthma and Severity of Allergic Rhinitis Comparing 2 Perennial Allergens: House Dust Mites and Parietariajudaica Pollen. J Investig Allergol ClinImmunol 2013; 23:145-51.

3. Rotsides DZ, Goldstein IF, Canfield SM, Perzanowski M, Mellins RB, Hoepner L, et al. Asthma, allergy, and IgE levels in NYC head start children. Respir Med 2010; 104: 345-55.

4. Craig TJ. Aeroallergen sensitization in asthma: prevalence and correlation with severity. Allergy Asthma Proc 2010; 31: 96-102.

5. Gergen PJ, Arbes SJ, Calatroni A, Mitchell HE, Zeldin DC. Total IgE levels and asthma prevalence in the US population: results from the National health and nutrition examination survey 2005-2006. J Allergy Clinimmunol 2009; 124: 447-53.

6. Suh M, Kim HH, Sohn MH, Kim KE, Kim C, Shin DC. Prevalence of allergic diseases among Korean school-age children: a nationwide cross-sectional questionnaire study. J Korean Med Sci 2011; 26:332-8.

7. Kim BS, Jin HS, Kim HB, Lee SY, Kim JH, Kwon JW, et al. Airway hyper responsiveness is associated with total serum immunoglobulin E and sensitization to aeroallergens in Korean adolescents. Allergy 2009; 64:1083-92.

8. Sears MR, Burrows B, Flannery EM, Herbison GP, Hewitt CJ, Holdaway MD. Relation between airway responsiveness and serum IgE in children with asthma and in apparently normal children. N Engl J Med 1991; 325: 1067-71.

9. Burrows B, Sears MR, Flannery EM, Herbison GP, Holdaway MD. Relationships of bronchial responsiveness assessed by methacholine to serum IgE, lung function, symptoms, and diagnoses in 11-year-old New Zealand children. J Allergy Clin Immunol 1992; 90: 376-85.

10. Gould HJ, Sutton BJ, Beavil AJ, Beavil RL, McCloskey N, Coker HA, et al. The biology of IGE and the basis of allergic disease. Annu Rev Immunol 2003; 21: 579-628.

11. Burrows B, Martinez FD, Halonen M, Barbee RA, Cline MG. Association of asthma with serum IgE levels and skin-test reactivity to allergens. N Engl J Med 1989; 320: 271-7.

12. Orie NGM, Sluiter HJ, De Vries K, Tammeling GJ, Witkop J. The host factors in bronchitis. In: Orie NGM, Sluiter HJ, Eds. Bronchitis. Assen: Royal van Gorcum 1961.

13. Hopp RJ, Townley RG, Biven RE, Bewtra AK, Nair NM. The presence of airway reactivity before the development of asthma. Am Rev Respir Dis 1990; 141: 2-8.

14. Townley RG, Guirgis H, Bewtra A, Watt G, Burke K, Carney K. IgE levels and methacholine inhalation responses in monozygous and dizygous twins. J Allergy Clin Immunol 1976; 57: 277.

15. Postma DS, Bleecker ER, Amelung PJ, Holroyd KJ, Xu J, Panhuysen CI, et al. Genetic susceptibility to asthma - bronchial hyper responsiveness coinherited with a major gene for atopy. The N Engl J Med 1995; 333: 894-900.

16. Strachan DP. The role of environmental factors in asthma. Br Med Bull 2000; 56: 865-82.

17. Ellwood P, Asher MI, Beasley R, Clayton TO, Stewart AW; ISAAC Steering Committee. The international study of asthma and allergies in childhood (ISAAC): phase three rationale and methods. Int J Tuberc Lung Dis 2005; 9:10-6.

18. Park HJ, Lee JH, Park KH, Ann H W, Jin MN, Choi SY, et al. A nationwide survey of inhalant allergens sensitization and levels of indoor major allergens in Korea. Allergy Asthma Immunol Res 2014; 6: 222-7.

19. Li J, Sun B, Huang Y, Lin X, Zhao D, Tan G, et al. A multicentre study assessing the prevalence of sensitizations in patients with asthma and/or rhinitis in China. Allergy 2009; 64: 1083-92.

20. Park YB, Mo EK, Lee JY, Kim JH, Kim CH, Hyun IG, et al. Association between pet ownership and the sensitization to pet allergens in adults with various allergic diseases. Allergy Asthma Immunol Res 2013; 5: 295-300.

21. Lawanga SK, Lemeshow S. Sample size determination in health studies. World Health Organization 1991; 1.

22. Ahmad F, Yousaf F, Asif S. Prevalence of allergic disease and related allergens in Pakistan in 2007. JPMI 2011; 25: 14-23.

23. Bush RK, Wood RA, Eggleston PA. Laboratory animal allergy. J Allergy Clin Immunol 1998; 102: 99-112.

24. Arbes SJ, Gergen PJ, Vaughn B, Zeldin DC. Asthma cases attributable to atopy: results from the Third National Health and Nutrition Examination Survey. J Allergy Clin Immunol 2007; 120: 1139-45.

25. Heinzerling LM, Burbach GJ, Edenharter G, Bachert C, Bindslev-Jensen C, Bonini S, et al. GA (2) LEN skin test study I: GA (2) LEN harmonization of skin prick testing: novel sensitization patterns for inhalant allergens in Europe. Allergy 2009; 64: 1498-506.

26. Noertjojo K, Dimich-Ward H, Obata H, Manfreda J, Chan-Yeung M. Exposure and sensitization to cat dander: asthma and asthma-like symptoms among adults. J Allergy Clin Immunol 1999; 103: 60-5.

27. Raj D, Lodha R, Pandey A, Mukherjee A, Agrawal A, Kabra SK. Aeroallergen Sensitization in Childhood Asthmatics in North India. Indian Pediatr.2013 Jul 5.pii: S097475591300141.

28. Akdis CA, Akdis M. Mechanisms of allergen-specific immunotherapy. J Allergy Clin Immunol 2011; 127: 18-27.

29. Akdis CA. Therapies for allergic inflammation: refining strategies to induce tolerance. Nat Med 2012; 18: 736-49.

30. Dahl R, Stender A, Rak S. Specific immunotherapy with SQ standardized grass allergen tablets in asthmatics with rhinoconjunctivitis. Allergy 2006; 61: 185-90.

31. National Heart, Lung, and Blood Institute. Education for a partnership in asthma care. Expert panel report 3: guidelines for the diagnosis and management of asthma. National Asthma Education and Prevention Program (NAEPP). Aug 2007.
COPYRIGHT 2018 Asianet-Pakistan
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2018 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Publication:Journal of Pakistan Medical Association
Geographic Code:9PAKI
Date:Aug 31, 2018
Words:3118
Previous Article:Radiographic analysis of the lumbar and sacral region angles in young Turkish adults.
Next Article:T cell reactivity to Collagen II as a possible prognostic marker in patients with rheumatoid arthritis.
Topics:

Terms of use | Privacy policy | Copyright © 2020 Farlex, Inc. | Feedback | For webmasters