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Iranian Journal of Medical Sciences logoLink to Iranian Journal of Medical Sciences
. 2014 Jan;39(1):29–35.

Skin Prick Test Reactivity to Common Aero and Food Allergens among Children with Allergy

Safoora Hosseini 1, Raheleh Shokouhi Shoormasti 1, Rozita Akramian 1, Masoud Movahedi 2, Mohammad Gharagozlou 2, Negar Foroughi 1, Babak Saboury 1, Anoushiravan Kazemnejad 3, Maryam Mahlooji Rad 2, Alireza Mahdaviani 2, Zahra Pourpak 1,2, Mostafa Moin 1,2
PMCID: PMC3895892  PMID: 24453391

Abstract

Background: The prevalence of allergic diseases has risen in the last decades. The objective of this study was to determine the common allergens in children via the skin prick test.

Methods: This cross-sectional study recruited 313 allergic children (4 months to 18 years old) referred to the Asthma and Allergy Clinic of Children’s Medical Center in Tehran. A questionnaire containing demographic data and patient history was completed. The Skin Prick Test (SPT) was selected according to the patients’ history of food and/or aeroallergen sensitivity.

Results: Patients (62.4% male, 37.6% female) with symptoms of asthma (n=141, 57.1%), allergic rhinitis (n=50, 20.4%), atopic dermatitis (n=29, 11.7%), and urticaria (n=20, 8.1%) were studied. Positive skin prick test to at least one allergen was 58.1%. The most prevalent allergens were tree mix (26%), Alternaria alternata (26%), weed mix (23.6%), Dermatophagoides farinae (22.9%), Dermatophagoides pteronyssinus (22.9%), milk (21.7%), eggs (20%), and wheat flour (18.3%). Also, common allergens in the patients with different symptoms of allergic disorders were as follows: asthma (tree mix, weed mix, and Dermatophagoides farinae); allergic rhinitis (Dermatophagoides farinae, tree mix, and Dermatophagoides pteronyssinus); and atopic dermatitis (Alternaria alternata, Dermatophagoides pteronyssinus, and cockroaches).

Conclusion: Identifying allergens in each area is necessary and has an important role in the diagnosis and management of allergic disorders and possibility of performing immunotherapy. In this study, the most common aeroallergens were tree mix, Alternaria alternata, and weed mix and also the most common food allergens were milk, eggs, and wheat. Considering these data, appropriate preventive strategies can decrease the cost and morbidity of therapeutic actions.

Keywords: Allergens, Children, Skin test

Introduction

The prevalence of allergic disorders such as atopic dermatitis, allergic respiratory diseases, and food allergy has increased in the last decades and become a major medical concern.1-4 To understand the cause of this trend, researchers have studied such environmental factors as air pollution,2,3,5 decrease in exposure to microbiologic stimuli,6 and changes in dietary habits.7

Allergy is an overreaction (immune-mediated reaction) to various proteins (allergens),8 first and foremost among which are aeroallergens (e.g. trees, grasses, weeds, moulds, house dust mites, and animal dander).9 In addition, other factors known to be responsible for the development of atopy include genetic factors, age of exposure to allergens,9 and number of siblings.10

For the confirmation of the presence of allergy, the most common diagnostic procedures available are the IgE specific test, food challenge test, and skin prick test (SPT).8,11 The relationship between the results of the SPT and the allergic disease is interpreted by the patient’s clinical history. Allergen selection should be on the basis of the patient’s symptoms, environmental exposures, occupational situation, age, and hobbies and the clinical history of the patient must be considered in the interpretation of the allergy test.12 In fact, the SPT is utilized to verify or leave out sensitization to allergens.13

The aim of this study was to determine the common allergens in children by means of the SPT results.

Patients and Methods

The study was performed cross-sectionally on a population of 313 patients with symptoms of allergic disorders who were referred to the Asthma and Allergy Clinic of Children’s Medical Center in Tehran between December 2006 and December 2009 for the confirmation of allergy and appropriate treatment. Adults and patients without clear symptoms were excluded. This study was approved by the Ethics Committee of the Immunology, Asthma, and Allergy Research Institute, Tehran University of Medical Sciences. There is no conflict of interest in this study.

An interview-administered questionnaire containing demographic information, patient history, and family history of allergic diseases was completed. The seasons during which the patients were symptomatic were recorded (4 groups). Consent was verbally obtained from the patients and/or their guardians before the performance of the SPT. The SPT results were later added to the main questionnaire.

The SPT was selected according to the patients’ history of food and/or aeroallergen sensitivity. The SPT was conducted using a standard allergen extract panel (Stallergenes, France) and comprised histamine and saline respectively as positive and negative controls, 9 aeroallergens (tree mix [maples, horse chestnuts, planes, false acacias, and limes], weed mix [golden rod, dandelion, ox-eye-daisy, and cocklebur], grass mix [cocksfoot, sweet vernal-grass, rye-grass, meadow grass, and timothy], Dermatophagoides farinae [DF], Dermatophagoides pteronyssinus [DP], cockroaches (Blatella germanica), Alternaria alternata, cats, and feather mix [ducks, geese, and hens]), and 6 common food allergens (cow’s milk, eggs, walnuts, hazelnuts, peanuts, and wheat flour).

In the SPT, a small drop of each allergen and control solution is placed on the volar surface of the forearm. In order to avoid false-positive results, the drops must be placed at least 2 cm apart from each other. A needle (25 or 26 gauge) must touch each drop and be penetrated into the epidermal surface at a low angle. The tip of the needle must then be gently lifted up to raise the epidermis, while no bleeding is induced. After about one minute, the solution is wiped away with a cotton tissue. Each test must be performed with separate needles. The SPT shows a reaction which reaches the peak in 15 to 20 minutes for allergens. By means of a millimeter ruler, the largest and smallest diameters of each complete reaction are measured; the result is summed and then divided by 2 (mean diameter). A wheal diameter >3 mm and a flare diameter >10 mm are considered positive results and indicative of clinical allergy.14

Statistics

The statistical analyses were performed using SPSS (version 15) as well as descriptive statistics and the chi-squared test. A P<0.05 was considered statistically significant.

Results

A total of 313 subjects, comprised of 118 female (37.6%) and 195 male patients (62.4%) aged between 4 months and 18 years (mean=5.7 years), with asthma symptoms (n=141, 57.1%), allergic rhinitis (n=50, 20.4%), atopic dermatitis (n=29, 11.7%), and urticaria (n=20, 8.1%) were studied. 73 subjects had no definitive diagnosis and were, therefore, considered as missing value. Among them, 58.1% had a positive SPT to at least one allergen. As regards history, 39.1% of the study population had a previous history of allergy and 67% had a positive previous family history of allergy. Most of the subjects were from Tehran (71.6%), Alborz (9.3%), and Mazandaran (2.6%) provinces, and 16.5% were from the other regions of Iran. The most prevalent allergens among the patients were tree mix (26%), Alternaria alternata (26%), weed mix (23.6%), DF (22.9%), DP (22.9%), grass mix (21.7%), milk (21.7%), eggs (20%), wheat (18.3%), walnuts (17.1%), hazelnuts (14.9%), and peanuts (14.3%), respectively. Table 1 shows the prevalence of sensitivity to allergens in the different seasons. The patients were divided into 4 groups: 0-3 years (n=111, 35.5%), 4-6 years (n=80, 25.6%), 7-12 years (n=102, 32.6%), and 13-18 years (n=20, 6.4%) (figure 1).

Table 1.

Prevalence of sensitivity to allergens in different seasons

Allergens % (N) Spring % (N) Summer % (N) Autumn % (N) Winter % (N)
Tree mix 26 (43) 34.9 (15) 14 (6) 18.6 (8) 32.6 (14)
Weed mix 23.6 (38) 36.8 (14) 10.5 (4) 18.4 (7) 34.2 (13)
Grass mix 21.7 (38) 39.5 (15) 21.1 (8) 13.2 (5) 26.3 (10)
Dermatophagoides pteronyssinus 22.9 (43) 30.2 (13) 32.6 (14) 16.3 (7) 20.9 (9)
Dermatophagoides farinae 22.9 (43) 34.9 (15) 23.3 (10) 4.7 (2) 37.2 (16)
Cockroaches 18 (25) 44 (11) 24 (6) 16 (4) 16 (4)
Alternaria alternata 26 (34) 32.4 (11) 29.4 (10) 14.7 (5) 23.5 (8)
Feather mix 8.4 (10) 20 (2) 0 10 (1) 70 (7)
Cats 15.5 (18) 22.2 (4) 22.2 (4) 22.2 (4) 33.3 (6)
Wheat flour 18.3 (11) 18.2 (2) 0 18.2 (2) 63.6 (7)
Milk 21.7 (20) 15 (3) 25 (5) 15 (3) 45 (9)
Eggs 20 (14) 7.1 (1) 21.4 (3) 21.4 (3) 50 (7)
Walnuts 17.1 (13) 30.8 (4) 7.7 (1) 15.4 (2) 46.2 (6)
Hazelnuts 14.9 (7) 14.3 (1) 28.6 (2) 0 57.1 (4)
Peanuts 14.3 (13) 23.1 (3) 23.1 (3) 15.4 (2) 38.5 (5)

Figure 1.

Figure 1

Comparison of sensitivity to aeroallergens and food allergens between different age groups.

In the spring, the most prevalent allergens were cockroaches (44%), grass mix (39.5%), weed mix (36.8%), and tree mix (34.9%). In the summer, DP (32.6%) and Alternaria alternata (29.4%) accounted for the most prevalent allergens. During the autumn, tree mix and weed mix had a prevalence rate of 18.6%, while in the winter, DF (37.2%), weed mix (34.2%), tree mix (32.6%), and feather mix (70%) comprised the most common allergens.

Prevalence of sensitivity to allergens with respect to the clinical symptoms is depicted in table 2 and figure 2. Tree mix, weed mix, and DF, respectively, were the most common allergens in the patients with asthma symptoms, whereas DF, tree mix, and DP, respectively, constituted the most common allergens in the patients with allergic rhinitis. Statistically, there was a significant relationship between sensitivity to food allergens (especially milk and eggs) and aeroallergens in the children <3 and >3 years of age (P<0.01). Among the age groups, the most common allergens were as follows: <3 years (cow’s milk, eggs, hazelnuts, and wheat flour); 4-6 years (Alternaria alternata, DF, cat fur, and DP); 7-12 years (grass mix, tree mix, Alternaria alternata, and cockroaches); and 13-18 years (weed mix, walnuts, cat fur, and feather mix).

Table 2.

Prevalence of sensitivity to allergens regarding clinical symptoms

Clinical symptoms Tree mix % (N) Grass mix % (N) Weed mix % (N) DP % (N) DF % (N) Alternaria alternate % (N)
Allergic rhinitis 35 (13) 32 (14) 24.1 (10) 33 (13) 36 (12) 28 (8)
Asthma 30 (29) 23 (23) 25 (23) 21 (19) 25 (24) 23 (17)

DP: Dermatophagoides pteronyssinus; DF: Dermatophagoides farinae

Figure 2.

Figure 2

Sensitivity to different allergens according to clinical symptoms. Others: urticaria, and atopic dermatitis

Discussion

In this study, 58.1% of a total of 313 subjects showed a positive SPT to at least one allergen. Among them, 57.1% and 20.4% had asthma and allergic rhinitis, respectively. Pollens of trees, grasses, and weeds are the most common allergens that trigger asthma.15

In patients with perennial rhinitis and asthma, in whom an extended approach is needed, it is proper to use a chosen panel of outdoor and indoor allergens. These allergens are selected according to both the geographic features and the tree, grass, and weed types as well as the kinds of molds (e.g. Alternaria alternate, Penicillium notatum, Aspergillus fumigatus, and Cladosporium), dust mites, cockroaches, and animal dander.11

The considerable role of aeroallergens as risk factors for allergic disorders was shown in 141 asthmatic patients in our study, which is in accordance with a similar study on 151 asthmatic patients in Saudi Arabia.16 Also, 23.6% of our allergic patients had sensitivity to weeds, which is comparable to a prevalence rate of 21% reported by a study in Zanjan (Iran).17 Among our asthmatic patients, positive SPT results for trees, weeds, and grasses were closely similar to the results reported by Farhoudi et al.18 and Movahedi and Moin19 in Iran. Fereidouni et al.20 reported that weeds (81%) and grasses (62%) were the most prevalent allergens in 311 patients with allergic rhinitis. In our asthmatic patients, sensitivity to house dust mites (DP and DF) was 21% and 25%, respectively, which is parallel to the findings by Ceylan et al.15 This resemblance could be due to the similar geographical characteristics of the two countries. Our results on the sensitivity to mites and trees are highly in agreement with the findings of Safari et al.21 insofar as they reported prevalence rates of 27.3% and 27.2% among patients sensitive to mites and trees respectively; nevertheless, the findings of our two studies are not consistent vis-à-vis the percentages of patients sensitive to grasses (9%) and cockroaches (27.2%).

As was confirmed in our study, pollen levels are usually higher in spring and lower in autumn.22 Accordingly, there are various manifestations of allergic symptoms in different seasons. Sensitization to the pollens of trees, grasses, and weeds is higher in spring, and sensitization to house dust mites is elevated in winter for DF and in summer for DP. In contrast, Akarcay et al.23 revealed a significant prevalence of sensitization to pollens and house dust mites, both in spring. Overall, the highest prevalence of asthmatic and allergic rhinitis patients suffering from all allergens (aero and food allergens) is seen in winter. It is thought that DF is more frequent in dry climates, whereas DP is more prevalent in humid climates.23

Cat fur allergen induces rapid respiratory symptoms in individuals sensitized to cats.16 Sensitivity to cat fur allergen was found in 13% of our asthmatic patients. Studies in Iran18 and Spain24 have reported the prevalence rates of 15% and 15.5%, respectively, but studies in Baltimore25and Saudi Arabia16 have reported much higher frequencies. It seems that this difference is due to the genetic factors or lower exposure to cats in the Iranian population. Sensitivity to cat fur was found in 23% of our patients with allergic rhinitis, which is comparable to a study from South Africa.26

The present study demonstrated a 33% prevalence rate of positive SPT to DP and 36% to DF in patients with allergic rhinitis. The Mesdaghi et al.27 study showed a 25% prevalence rate of sensitivity to DP, and Dowaisan et al.28 and Seedat et al.26 reported sensitivity of 32.4% and 34% to DF among the same type of patients.

In allergic rhinitis patients, a 32.8% rate of positive SPT to Alternaria alternata was reported in the Iranian city of Mashhad,29 which chimes in with our study (28%).

Cockroach sensitivity among all the patients in our study was estimated at 18%. Approximately similar results were reported in two of Iran’s Arab neighboring countries: 19.2% in the city of Riyadh (139 patients with airway allergy)30 and 22.7% in Oman (689 patients).31 In contrast, a prevalence rate of 2.8% sensitivity to cockroaches was reported from Turkey;32 this finding is different from the rate reported in our country (2.8% versus 18%). These discrepancies require further research.

In our patients with allergic rhinitis, 8.4% had a positive SPT to feather mix. This finding is in accordance with studies conducted in Iran27 and South Africa,26 whose results revealed 9.5% and 10% prevalence rates of sensitivity to feather allergen.

A positive SPT to cow’s milk was seen in 21.7% of our patients. This finding is in agreement with that (21.46%) of the Khazaei et al.33study, which was done in the Iranian city of Zahedan.

In this study, walnuts were a common food allergen with a prevalence rate of 17.1%, which is similar to the rate reported by another study34 in Iran. Such similarity regarding a positive SPT to hazelnuts is seen between our study (14.9%) and another study33 carried out in Iran (15.32%). It is probable that the consumption of nuts is high in Iran.

In concordance with some previous studies,35-37 sensitivity to allergens in our patients with a positive family history (59.3%) was higher than that in those without a family history.

Conclusion

Determination of the most common allergens and the relationship between the results of the SPT and allergic diseases in each area plays an important role in the diagnosis and management of allergic disorders and possibility of performing immunotherapy. In this study, tree mix, Alternaria alternate, and weed mix comprised the most common aeroallergens and milk, eggs, and wheat constituted the most common food allergens. In light of the findings of the present study, it can be concluded that appropriate preventive strategies can decrease the cost and morbidity of therapeutic measures.

Conflict of Interest: None declared.

References

  • 1.Compalati E, Penagos M, Henley K, Canonica GW. Allergy prevalence survey by the World Allergy Organization. Allergy Clin Immunol Int- J World Allergy Org. 2007;19:82–90. [Google Scholar]
  • 2.Ridolo E, Albertini R, Giordano D, Soliani L, Usberti I, Dall'Aglio PP. Airborne pollen concentrations and the incidence of allergic asthma and rhinoconjunctivitis in northern Italy from 1992 to 2003. Int Arch Allergy Immunol. 2007;142:151–7. doi: 10.1159/000096441. doi: 10.1159/000096441. PubMed PMID: 17057413. [DOI] [PubMed] [Google Scholar]
  • 3.Senol M, Ozcan A, Kandi B, Karaca S, Aki T, Bayram N. Incidence of atopic stigmata and prick test results in patients with asthma, allergic rhinitis and conjunctivitis. Asian Pac J Allergy Immunol. 2006;24:105–9. PubMed PMID: 17136874. [PubMed] [Google Scholar]
  • 4.Arshad SH. Primary prevention of asthma and allergy. J Allergy Clin Immunol. 2005;116:3–14. doi: 10.1016/j.jaci.2005.03.043. doi: 10.1016/j.jaci.2005.03.043. PubMed PMID: 15990764. [DOI] [PubMed] [Google Scholar]
  • 5.D'Amato G, Liccardi G, D'Amato M. Environmental risk factors (outdoor air pollution and climatic changes) and increased trend of respiratory allergy. J Investig Allergol Clin Immunol. 2000;10:123–8. PubMed PMID: 10923585. [PubMed] [Google Scholar]
  • 6.von Mutius. Pro: the increase in asthma can be ascribed to cleanliness. Am J Respir Crit Care Med. 2001;164:1106–7. doi: 10.1164/ajrccm.164.7.2107130a. PubMed PMID: 11673189. [DOI] [PubMed] [Google Scholar]
  • 7.Black PN, Sharpe S. Dietary fat and asthma: is there a connection? Eur Respir J. 1997;10:6–12. doi: 10.1183/09031936.97.10010006. doi: 10.1183/09031936.97.10010006. PubMed PMID: 9032484. [DOI] [PubMed] [Google Scholar]
  • 8.Arshad SH, Tariq SM, Matthews S, Hakim E. Sensitization to common allergens and its association with allergic disorders at age 4 years: a whole population birth cohort study. Pediatrics. 2001;108:E33. doi: 10.1542/peds.108.2.e33. doi: 10.1542/peds.108.2.e33. PubMed PMID: 11483843. [DOI] [PubMed] [Google Scholar]
  • 9.Boulet LP, Turcotte H, Laprise C, Lavertu C, Bédard PM, Lavoie A, et al. Comparative degree and type of sensitization to common indoor and outdoor allergens in subjects with allergic rhinitis and/or asthma. Clin Exp Allergy. 1997;27:52–9. doi: 10.1111/j.1365-2222.1997.tb00672.x. PubMed PMID: 9117881. [PubMed] [Google Scholar]
  • 10.von Mutius. The environmental predictors of allergic disease. J Allergy Clin Immunol. 2000;105:9–19. doi: 10.1016/s0091-6749(00)90171-4. doi: 10.1016/S0091-6749(00)90171-4. PubMed PMID: 10629447. [DOI] [PubMed] [Google Scholar]
  • 11.Nolte H, Kowal K, Du Buske L. Overview of skin testing for allergic disease: [Internet]: http://www.uptodate.com/contents/overview-of-skin-testing-for-allergic-disease?detectedLanguage=en&source=search_result&search=overview+of+skin+testing+for+allergic+disease&selectedTitle=1%7E150&provider=noProvider. [Google Scholar]
  • 12.Cox L, Williams B, Sicherer S, Oppenheimer J, Sher L, Hamilton R, et al. Pearls and pitfalls of allergy diagnostic testing: report from the American College of Allergy, Asthma and Immunology/American Academy of Allergy, Asthma and Immunology Specific IgE Test Task Force. Ann Allergy Asthma Immunol. 2008;101:580–92. doi: 10.1016/S1081-1206(10)60220-7. PubMed PMID: 19119701. [PubMed] [Google Scholar]
  • 13.Mehl A, Rolinck-Werninghaus C, Staden U, Verstege A, Wahn U, Beyer K, et al. The atopy patch test in the diagnostic workup of suspected food-related symptoms in children. J Allergy Clin Immunol. 2006;118:923–9. doi: 10.1016/j.jaci.2006.07.003. doi: 10.1016/j.jaci.2006.07.003. PubMed PMID: 17030247. [DOI] [PubMed] [Google Scholar]
  • 14.Demoly P, Bousquet J, Romano A. In vivo Methods for the study of Allergy. In: Adkinson NF, Bochner BS, editors. Middleton's Allergy Principles & Practice. Philadelphia: Mosby; 2009. pp. 1267–79. [Google Scholar]
  • 15.Ceylan E, Gencer M. The Aeroallergen Sensitivity of Asthmatic Patients in Şanlıurfa. Turkish Respiratory Journal. 2006;7:48–51. [Google Scholar]
  • 16.Koshak EA. Skin test reactivity to indoor allergens correlates with asthma severity in jeddah, saudi arabia. Allergy Asthma Clin Immunol. 2006;2:11–9. doi: 10.1186/1710-1492-2-1-11. doi: 10.1186/1710-1492-2-1-11. PubMed PMID: 20529215; PubMed Central PMCID: PMC3231646. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Ahmadiafshar A, Sepehri S, Moosavinasab SN, Torabi SZ. Recognition and Frequency Determination of Common Allergens in Allergic Patients of Zanjan City by Skin Prick Test. Journal of Zanjan University of Medical Sciences and Health Services. 2008;16:45–53. [Google Scholar]
  • 18.Farhoudi A, Pourpak Z, Mesdaghi M, Chavoshzadeh Z, Kazemnejad A. The study of cockroach allergy in Iranian children with asthma. Iran J Med Sci. 2002;27:156–60. [Google Scholar]
  • 19.Movahedi M, Moin M, Farhoudi A. A comparison between diagnostic clinical tests and herbal geography in allergic patients in Tehran and Karaj cities. Iranian Journal of Allergy, Asthma and Immunology. 2000;1:29–31. [Google Scholar]
  • 20.Fereidouni M, Hossini RF, Azad FJ, Assarehzadegan MA, Varasteh A. Skin prick test reactivity to common aeroallergens among allergic rhinitis patients in Iran. Allergol Immunopathol. 2009;37:73–9. doi: 10.1016/s0301-0546(09)71108-5. doi: 10.1016/S0301-0546(09)71108-5. PubMed PMID: 19445863. [DOI] [PubMed] [Google Scholar]
  • 21.Safari M, Amin R, Kashef S, Aleyasin S, Ayatollahi M. Cockroach sensitivity in Iranian asthmatic children under the age of five years. Turk Toraks Der. 2009;10:26–30. [Google Scholar]
  • 22.D'Amato G, Spieksma FT, Liccardi G, Jäger S, Russo M, Kontou-Fili K, et al. Pollen-related allergy in Europe. Allergy. 1998;53:567–78. doi: 10.1111/j.1398-9995.1998.tb03932.x. doi: 10.1111/j.1398-9995.1998.tb03932.x. PubMed PMID: 9689338. [DOI] [PubMed] [Google Scholar]
  • 23.Akarcay M, Miman MC, Miman O, Kelles M, Ekici N. Does dermatophagoides cause different allergic rhinitis clinic than pollens? African Journal of Microbiology Research. 2010;4:2094–7. [Google Scholar]
  • 24.Sastre J, Ibañez MD, Lombardero M, Laso MT, Lehrer S. Allergy to cockroaches in patients with asthma and rhinitis in an urban area (Madrid) Allergy. 1996;51:582–6. doi: 10.1111/j.1398-9995.1996.tb04672.x. doi: 10.1111/j.1398-9995.1996.tb00116.x. PubMed PMID: 8874663. [DOI] [PubMed] [Google Scholar]
  • 25.Matsui EC, Wood RA, Rand C, Kanchanaraksa S, Swartz L, Curtin-Brosnan J, et al. Cockroach allergen exposure and sensitization in suburban middle-class children with asthma. J Allergy Clin Immunol. 2003;112:87–92. doi: 10.1067/mai.2003.1588. doi: 10.1067/mai.2003.1588. PubMed PMID: 12847484. [DOI] [PubMed] [Google Scholar]
  • 26.Seedat RY, Claassen J, Claassen AJ, Joubert G. Mite and cockroach sensitisation in patients with allergic rhinitis in the Free State. S Afr Med J. 2010;100:160–3. doi: 10.7196/samj.3669. PubMed PMID: 20459939. [DOI] [PubMed] [Google Scholar]
  • 27.Mesdaghi M, Pourpak Z, Moein M, Heidarzadeh M, Bemanian MH, Fazlollahi M, et al. The state of cockroach allergy among patients with cockroach allergy in Iran. Tehran University Medical Journal. 2005;63:667–73. Persian. [Google Scholar]
  • 28.Dowaisan A, Al-Ali S, Khan M, Hijazi Z, Thomson MS, Ezeamuzie CI. Sensitization to aeroallergens among patients with allergic rhinitis in a desert environment. Ann Allergy Asthma Immunol. 2000;84:433–8. doi: 10.1016/s1081-1206(10)62277-6. doi: 10.1016/S1081-1206(10)62277-6. PubMed PMID: 10795652. [DOI] [PubMed] [Google Scholar]
  • 29.Mokhtari Amirmajdi, Mokhtari Amirmajdi, Eftekharzadeh Mashhadi, Jabari Azad, Tavakol Afshari, Shakeri MT. Alternaria in patients with allergic rhinitis. Iran J Allergy Asthma Immunol. 2011;10:221–6. doi: 010.03/ijaai.221226. PubMed PMID: 21891828. [PubMed] [Google Scholar]
  • 30.Almogren A. Airway allergy and skin reactivity to aeroallergens in Riyadh. Saudi Med J. 2009;30:392–6. PubMed PMID: 19271069. [PubMed] [Google Scholar]
  • 31.Al-Tamemi SH, Al-Shidhani AN, Al-Abri RK, Jothi B, Al-Rawas OA, Al-Riyami BM. The pattern of sensitisation to inhalant allergens in omani patients with asthma, allergic rhinitis and rhinoconjunctivitis. Sultan Qaboos Univ Med J. 2008;8:319–24. PubMed PMID: 21748078; PubMed Central PMCID: PMC3074841. [PMC free article] [PubMed] [Google Scholar]
  • 32.Harmancı K, Bakırtaş A, Türktaş İ. Sensitization to Aeroallergens in Preschool Children with Respiratory Problems in Ankara, Turkey. Turkish Respiratory Journal. 2006;7:10–4. [Google Scholar]
  • 33.Khazaei HA, Hashemi SR, Aghamohammadi A, Farhoudi F, Rezaei N. The study of type 1 allergy prevalence among people of South-East of iran by skin prick test using common allergens. Iran J Allergy Asthma Immunol. 2003;2:165–8. PubMed PMID: 17301375. [PubMed] [Google Scholar]
  • 34.Pourpak Z, Farhoudi A, Arshi S, Movahedi M, Gharegozlou M, Yazdani F, et al. Common Food Allergens in Iranian Children. Iran J Med Sci. 2003;28:17–22. [Google Scholar]
  • 35.Govaere E, Van Gysel, Verhamme KM, Doli E, De Baets. The association of allergic symptoms with sensitization to inhalant allergens in childhood. Pediatr Allergy Immunol. 2009;20:448–57. doi: 10.1111/j.1399-3038.2008.00805.x. doi: 10.1111/j.1399-3038.2008.00805.x. PubMed PMID: 19175888. [DOI] [PubMed] [Google Scholar]
  • 36.Schäfer T, Ring J. Epidemiology of allergic diseases. Allergy. 1997;52:14–22. doi: 10.1111/j.1398-9995.1997.tb04864.x. doi: 10.1111/j.1398-9995.1997.tb04864.x. [DOI] [PubMed] [Google Scholar]
  • 37.Rönmark E, Bjerg A, Perzanowski M, Platts-Mills T, Lundbäck B. Major increase in allergic sensitization in schoolchildren from 1996 to 2006 in northern Sweden. J Allergy Clin Immunol. 2009;124:357–63. doi: 10.1016/j.jaci.2009.05.011. doi: 10.1016/j.jaci.2009.05.011. PubMed PMID: 19577282; PubMed Central PMCID: PMC2747664. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Kjaer HF, Eller E, Andersen KE, Høst A, Bindslev-Jensen C. The association between early sensitization patterns and subsequent allergic disease. The DARC birth cohort study. Pediatr Allergy Immunol. 2009;20:726–34. doi: 10.1111/j.1399-3038.2009.00862.x. doi: 10.1111/j.1399-3038.2009.00862.x. PubMed PMID: 19744222. [DOI] [PubMed] [Google Scholar]

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