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Kim, Ahn, Yoo, Kim, Yang, Park, Lee, Kim, Jeong, Kim, Bae, Jang, Park, Koh, Lee, Lim, Kim, Lee, Kim, Jun, Kim, Kim, Choi, and Work Group for Rhinitis, the Korean Academy of Asthma, Allergy and Clinical Immunology: Clinical Manifestations and Risk Factors of Anaphylaxis in Pollen-Food Allergy Syndrome
Original Article
Allergy

Yonsei Medical Journal 2019; 60(10): 960-968.

Published online: 16 September 2019

DOI: https://doi.org/10.3349/ymj.2019.60.10.960

Clinical Manifestations and Risk Factors of Anaphylaxis in Pollen-Food Allergy Syndrome

Minji Kim1, 2, *, Youngmin Ahn3, *, Young Yoo4, Dong-Kyu Kim5, Hyeon-Jong Yang6, Hae-Sim Park7, Hyun Jong Lee8, Mi-Ae Kim9, Yi Yeong Jeong10, Bong-Seong Kim11, Woo Yong Bae12, An-Soo Jang13, Yang Park14, Young-Il Koh15, Jaechun Lee16, Dae Hyun Lim17, Jeong Hee Kim17, Sang Min Lee18, Yong Min Kim19, Young Joon Jun20, Hyo Yeol Kim21, Yunsun Kim22, Jeong-Hee Choi2, 23; Work Group for Rhinitis, the Korean Academy of Asthma, Allergy and Clinical Immunology

1Department of Pediatrics, Hallym University Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Korea.

2Allergy and Clinical Immunology Research Center, Hallym University College of Medicine, Chuncheon, Korea.

3Department of Pediatrics, Eulji Hospital, Eulji University, Seoul, Korea.

4Department of Pediatrics, Korea University Anam Hospital, Korea University College of Medicine, Seoul, Korea.

5Department of Otorhinolaryngology-Head and Neck Surgery, Hallym University Chuncheon Sacred Heart Hospital and Nano-Bio Regenerative Medical Institute, Hallym University College of Medicine, Chuncheon, Korea.

6Department of Pediatrics, Pediatric Allergy and Respiratory Center, Soonchunhyang University Seoul Hospital, Soonchunhyang University College of Medicine, Seoul, Korea.

7Department of Allergy and Clinical Immunology, Ajou University School of Medicine, Suwon, Korea.

8Lee & Hong ENT, Sleep and Cosmetic Center, Seongnam, Korea.

9Department of Pulmonology, Allergy and Critical Care Medicine, CHA Bundang Medical Center, CHA University, Seongnam, Korea.

10Department of Internal Medicine, Gyeongsang National University College of Medicine, Jinju, Korea.

11Department of Pediatrics, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Korea.

12Department of Otorhinolaryngology, Head and Neck Surgery, Dong-A University College of Medicine, Busan, Korea.

13Department of Internal Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, Korea.

14Department of Pediatrics, Wonkwang University Sanbon Hospital, Wonkwang University College of Medicine, Gunpo, Korea.

15Department of Internal Medicine, Chonnam National University Hospital, Chonnam National University Medical School, Gwangju, Korea.

16Department of Internal Medicine, Jeju National University School of Medicine, Jeju, Korea.

17Department of Pediatrics, Inha University Hospital, Inha University College of Medicine, Incheon, Korea.

18Division of Pulmonology and Allergy, Department of Internal Medicine, Gil Medical Center, Gachon University College of Medicine, Incheon, Korea.

19Department of Otorhinolaryngology-Head and Neck Surgery, Chungnam National University College of Medicine, Daejeon, Korea.

20Department of Otorhinolaryngology-Head & Neck Surgery, Soonchunhyang University Gumi Hospital, Soonchunhyang University College of Medicine, Gumi, Korea.

21Department of Otorhinolaryngology-Head and Neck Surgery, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul, Korea.

22SCH Biomedical Informatics Research Unit, Soonchunhyang University Seoul Hospital, Seoul, Korea.

23Department of Pulmonology, Allergy and Critical Care Medicine, Hallym University Dongtan Sacred Heart Hospital, Hallym University College of Medicine, Hwaseong, Korea.

Co-corresponding author: Jeong-Hee Choi, MD, PhD, Department of Pulmonology, Allergy and Critical Care Medicine, Hallym University Dongtan Sacred Heart Hospital, Hallym University College of Medicine, 7 Keunjaebong-gil, Hwaseong 18450, Korea. Tel: 82-31-8086-2928, Fax: 82-31-8086-2482, mdqueen@hallym.or.kr

Co-corresponding author: Young Yoo, MD, PhD, Department of Pediatrics, Korea University Anam Hospital, Korea University College of Medicine, 73 Goryeodae-ro, Seongbuk-gu, Seoul 02841, Korea. Tel: 82-2-920-5090, Fax: 82-2-922-7476, yoolina@korea.ac.kr

Equal contributor:

*Minji Kim and Youngmin Ahn contributed equally to this work.

Received 21 May 2019       Revised 27 July 2019       Accepted 9 August 2019

© Copyright: Yonsei University College of Medicine 2019

Yonsei University College of Medicine

(open-access, https://creativecommons.org/licenses/by-nc/4.0/):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Purpose

Many studies have reported that pollen-food allergy syndrome (PFAS) can cause anaphylaxis. No comprehensive investigations into anaphylaxis in PFAS have been conducted, however. In this study, we investigated the clinical manifestations and risk factors for anaphylaxis in PFAS in Korean patients with pollinosis.

Materials and Methods

Data were obtained from a nationwide cross-sectional study that previously reported on PFAS in Korean patients with pollinosis. Data from 273 patients with PFAS were collected, including demographics, list of culprit fruits and vegetables, and clinical manifestations of food allergy. We analyzed 27 anaphylaxis patients and compared them with patients with PFAS with oropharyngeal symptoms only (n=130).

Results

The most common cause of anaphylaxis in PFAS was peanut (33.3%), apple (22.2%), walnut (22.2%), pine nut (18.5%), peach (14.8%), and ginseng (14.8%). Anaphylaxis was significantly associated with the strength of sensitization to alder, hazel, willow, poplar, timothy, and ragweed (p<0.05, respectively). Multivariable analysis revealed that the presence of atopic dermatitis [odds ratio (OR), 3.58; 95% confidence interval (CI), 1.25–10.23; p=0.017]; sensitization to hazel (OR, 5.27; 95% CI, 1.79–15.53; p=0.003), timothy (OR, 11.8; 95% CI, 2.70–51.64; p=0.001), or ragweed (OR, 3.18; 95% CI, 1.03–9.87; p=0.045); and the number of culprit foods (OR, 1.25; 95% CI, 1.15–1.37; p<0.001) were related to the development of anaphylaxis in PFAS.

Conclusion

The most common culprit foods causing anaphylaxis in PFAS were peanut and apple. The presence of atopic dermatitis; sensitization to hazel, timothy, or ragweed; and a greater number of culprit foods were risk factors for anaphylaxis in PFAS.

Keywords: Pollen-food allergy syndrome, pollen, food allergy, anaphylaxis

INTRODUCTION

Pollen-food allergy syndrome (PFAS) is an immunoglobulin E (IgE)-mediated allergic manifestation to fruits and vegetables due to cross-reactivity with prior sensitization to plant inhalant allergens. PFAS is an emerging public health issue, with a number of studies reporting an increased prevalence of pollen allergies over the last decade due to changes in atmospheric CO2, climate, and pollen counts.123 PFAS is the most common food allergy in adults, and the prevalence of PFAS varies in the literature from 5–8%.45
PFAS, called oral allergy syndrome previously, was thought to be restricted to oropharyngeal symptoms; however, extr-aoral symptoms and systemic symptoms in PFAS have been reported.678 Moreover, one study reported that 3% of patients experienced systemic reactions without oral symptoms, and 1.7% experienced anaphylaxis.69 Because the systemic symptoms reported by researchers have increased and because symptoms are not limited to the oral cavity, the use of the term PFAS is more relevant than oral allergy syndrome:10 This historical background has led to confusion among allergists concerning the diagnosis of PFAS. In a US study investigating the perception of PFAS, allergists estimated that 5–8% of patients with pollinosis had PFAS.4 However, PFAS has been reported in 20–70% of patients with a pollen allergy, and anaphylaxis was reported in 1–2%, which is more prevalent than what allergists had estimated.7811
Although the importance of PFAS is increasing and triggering foods differ from geographic regions and dietary habits, there are only a few studies on PFAS in Korea.1213 The first nationwide study of PFAS in Korea recently reported that the prevalence of PFAS is 41.7% in Korean patients with pollinosis and that 8.9% of patients with PFAS manifest with anaphylaxis, which is a substantial proportion among patients with PFAS.14
Several allergen components from plant foods are known to contribute to the development of anaphylaxis. Lipid transfer protein and cross-reactive carbohydrate determinants are known as pan-allergens of the plant, and they exhibit thermostability and resistance to proteolysis, which enables the food allergen to reach intestinal absorption in its intact form.15 Although several studies on anaphylaxis-inducing allergenic components have been investigated, studies on detailed clinical manifestations and risk factor analysis of anaphylaxis in PFAS have been rarely conducted worldwide. Therefore, in this study, we investigated the clinical characteristics and risk factors of anaphylaxis in PFAS among Korean patients with pollinosis using data from a previous nationwide survey of PFAS in 2016.14

MATERIALS AND METHODS

Study design and participants

The nationwide, cross-sectional study on PFAS was conducted in South Korea between March and December 2016.14 Data were collected from patients diagnosed with pollinosis at 21 institutes (19 university hospitals and two allergy clinics). The protocol was reviewed and approved by the institutional review boards of each institute (Hallym University Dongtan Sacred Heart Hospital, HDT-2016-04-155-003, etc.). Written informed consent was obtained from each patient or their parents.
Pollinosis was diagnosed according to 1) one or more allergic disease, including allergic rhinitis, allergic conjunctivitis, and/or bronchial asthma; 2) sensitization to the pollen of ≥one tree, grass, and/or weed; and 3) aggravated allergic symptoms when exposed to sensitized pollens. Sensitization to pollen was diagnosed by positive results to allergy skin tests and/or high serum-specific IgE levels using multiple allergen simultaneous tests [class ≥2+, Polycheck Allergy (Biocheck Co., Munster, Germany), AdvanSure Allergy Screen (LG Life Science, Seoul, Korea), AllergyScreen (Mediwiss Analytic GmbH, Moers, Germany)] or the ImmunoCAP® system (≥0.35 kU/L, ThermoFisher Scientific, Uppsala, Sweden). A positive skin prick test was defined as wheal size equal or greater to that of histamine [allergen/histamine (A/H) ratio ≥3+, Allergopharma (Reinbek, Germany), Lofarma (Milan, Italy), Bencard (Brefod, UK)] or a mean allergen wheal diameter of at least 3 mm.16 The investigated pollens included tree pollens (birch, alder, hazel, beech, oak, willow, poplar, pine, and tree mix), grass pollens (bermuda, meadow, orchard, rye, timothy, and grass mix), and weed pollens (mugwort, ragweed, and Hop Japanicus). Data were collected using a questionnaire and medical record review, including demographic characteristics, underlying allergic diseases, and allergy test results. For further analysis, we categorized subjects according to the number of systemic symptoms: 1) group 0 (G0), only oropharyngeal symptoms; 2) group 1 (G1), patients with any one systemic symptom; and 3) group 2 (G2) patients with more than two systemic symptoms, that is anaphylaxis.

Questionnaires about PFAS

The list of culprit foods included apple, pear, peach, apricot, plum, cherry, watermelon, melon, Korean melon, banana, kiwi, orange, mandarin, pineapple, strawberry, mango, avocado, grape, carrot, potato, sweet potato, celery, crown daisy, perilla leaf, lettuce, kale, chicory, taro/taro stem, ginseng, deodeok (Codonopsis lanceolata), bellflower root, kudzu, lotus root, Chinese yam, eggplant, zucchini, cucumber, tomato, jujube, chestnut, peanut, walnut, pine nut, and soy.
In addition to oropharyngeal symptoms (tingling/itching sense or edema of the lips, oral cavity, and/or throat), systemic symptoms were categorized according to the organ in which the symptoms developed: dermatologic symptoms (itching, urticaria, or angioedema), respiratory symptoms (rhinorrhea, cough, dyspnea, wheezing, cyanosis, or hypoxia), cardiovascular symptoms (chest pain, hypotension, pale, sweating, or cardiac arrest), gastrointestinal symptoms (nausea or vomiting, diarrhea, or abdominal pain), neurologic and systemic symptoms (dizziness, unconsciousness, anxiety, change of sense, or death), and anaphylaxis. The diagnosis of anaphylaxis was confirmed by a physician using the criteria proposed in the second symposium on the definition and management of anaphylaxis by the National Institute of Allergy and Infectious Disease/Food Allergy and Anaphylaxis Network.17 Anaphylaxis was defined by two or more of the following symptoms occur after exposure to a likely allergen, including involvement of skin tissue, respiratory compromise, cardiovascular symptoms, gastrointestinal symptoms, and neurologic symptoms.

Statistical analysis

All statistical analyses were performed using R version 3.4.0 (R Foundation, Vienna, Austria). Comparison between groups was performed using chi-squared analysis and Kruskal-Wallis test (>two independent groups) for discrete and continuous variables, respectively. Because the use of separate univariate tests leads to an inflated type 1 error, Bonferroni correction was applied to each pollen analysis. Multivariate logistic regression was utilized to determine potential predictors of anaphylaxis in PFAS. p<0.05 was considered statistically significant.

RESULTS

Baseline characteristics of the study subjects

Of 273 patients with PFAS, 130 (47.6%) reported oropharyngeal symptoms only, 88 (32.2%) showed oropharyngeal symptoms and one systemic symptom, and 27 (9.9%) showed anaphylaxis. Of 27 patients with anaphylaxis, 21 (77.8%) had oropharyngeal symptoms, and 6 (22.2%) experienced systemic reactions without oral symptoms. The patients showed cutaneous manifestations (84.0%), such as pruritus, urticaria and angioedema; respiratory (84.0%); gastrointestinal (48.0%); neurologic (36.0%); and cardiovascular (36.0%) symptoms. Twelve patients (44.4%) were younger than 18 years, and 15 were older than 18 years (Supplementary Table 1, only online).

Clinical characteristics of anaphylaxis patients with PFAS

The clinical characteristics of the patients with anaphylaxis in PFAS are described in Table 1. No differences were found between PFAS with anaphylaxis and only oropharyngeal symptoms groups in terms of sex and age (p>0.05, respectively). The anaphylaxis group had a higher prevalence of developing chronic urticaria than those in the only oropharyngeal symptom group (18.5% vs. 4.6%, p=0.023), as well as a higher prevalence of atopic dermatitis (AD) (48.1% vs. 26.2%, p=0.041). Patients with PFAS with anaphylaxis showed no significant differences in the presence of other allergic diseases, such as bronchial asthma, allergic rhinitis, allergic conjunctivitis, or drug allergy, and family history of allergic diseases, compared with only oropharyngeal symptoms (p>0.05, respectively). The severity and duration of allergic rhinitis symptoms were also not significantly different between the anaphylaxis and only oropharyngeal symptom groups. The patients with PFAS with anaphylaxis had significantly higher sensitization rates to hazel (66.7% vs. 41.5%, p=0.030) and willow (29.6% vs. 11.5%, p=0.031) than those with only oropharyngeal symptoms (Fig. 1).

Causative foods of anaphylaxis in PFAS

Twenty-seven anaphylaxis patients had 84 cases with 44 culprit foods (Table 2). Peanut (33.3%) was the most common offending food, followed by apple (22.2%), walnut (22.2%), pine nut (18.5%), peach (14.8%), ginseng (14.8%), soy (11.1%), etc. Most of the anaphylaxis patients (n=18, 66.7%) developed anaphylaxis to one food item. Two patients (7.4%) experienced anaphylactic reactions to two food items, three patients to three (11.1%), one patient to four (3.7%), and three patients to more than five food items (11.1%).

Risk factors for the development of anaphylaxis in PFAS

After analysis of the association of systemic symptoms in PFAS with the strength of sensitization to pollen (A/H ratio by skin prick test), a significant association was found between anaphylaxis (G2) and strength of sensitization to alder, birch, hazel, beech, oak, willow, poplar, timothy, ragweed, and Hop Japanicus (Fig. 2). Moreover, the anaphylaxis patients (G2) had a significantly higher number of causative foods (p<0.05), whereas the number of sensitized pollens was not associated with anaphylaxis in PFAS (Fig. 3).
Multivariate regression analysis revealed that the presence of AD [odds ratio (OR), 3.58; 95% confidence interval (CI), 1.25–10.23; p=0.017], sensitization to hazel (OR, 5.27; 95% CI, 1.79–15.53; p=0.002), sensitization to timothy (OR, 11.8; 95% CI, 2.70–51.64; p=0.001), sensitization to ragweed (OR, 3.18; 95% CI, 1.03–9.87; p=0.045), and number of culprit foods of PFAS (OR, 1.25; 95% CI, 1.15–1.37; p<0.001) were potential risk factors for the development of anaphylaxis in PFAS (Table 3).

DISCUSSION

In this study, the most commonly offending foods of anaphylaxis in PFAS were peanut, followed by apple, walnut, pine nut, peach, ginseng, and soy in order of frequency. Anaphylaxis was significantly associated with the strength of sensitization to alder, birch, hazel, willow, timothy, and ragweed pollen. Presence of AD; sensitization to hazel, timothy, and ragweed; and the increased number of culprit foods for PFAS would more likely lead to the development of anaphylaxis in PFAS.
Approximately 20% to 70% of patients with pollinosis reported symptoms of PFAS after ingesting causative foods,7811 and the prevalence of anaphylaxis in patients with PFAS is estimated to be 1–2%.6 In our previous reports, the prevalences of PFAS and anaphylaxis in PFAS were 41.7% and 8.9% in Korea, respectively.14 The prevalence of PFAS in our country was similar to that in previous reports for other countries, while the prevalence of anaphylaxis was much higher. This might be due to several reasons, such as 1) anaphylaxis in PFAS might be overlooked as class I food allergy by physicians; 2) the definition of anaphylaxis was broadly defined, including more than two organ involvements; and 3) the number of patients with PFAS might be increased when considering the increasing pollen allergic populations due to global climate changes and increases in pollen counts.1718
In the present study, the most common anaphylaxis-triggering foods in PFAS were peanut, followed by apple, walnut, pine nut, peach, ginseng, and soy, whereas the most common causative foods of PFAS in Korea were peach, apple, kiwi, peanut, and plum.14 Although common foods that are causative of anaphylaxis in PFAS have not been reported in other countries, apple and hazelnut are the most common causative foods of PFAS because of the high rate of birch sensitization in Europe, and apple and peach are known as the most common causative foods in relation to oak sensitization in Japan.192021 In Korea, the most important sensitized pollens are oak, followed by birch and alder, which have cross-allergenicity with the Rosaceae family (apple, peach, plum, pear, cherry, apricot, almond, etc.), Apiaceae family (cantaloupe, honeydew, watermelon, zucchini, and cucumber), Fabaceae family (soybean and peanut), Juglans family (walnut), and Betulaceae family (hazelnut).9182223 Accordingly, cross-reactivity patterns between pollens and foods vary depending on regional distribution of inhaled pollens and dietary habits. Relatedly, hazelnut anaphylaxis has not been reported in Korea, potentially in reflection of dietary customs of not consuming hazelnut, whereas ginseng is a frequently consumed herbal medication in Far-East Asia. Lim, et al.24 reported a case of anaphylaxis after ingestion of fresh ginseng, wherein they found 17-kDa common allergens between birch pollen and ginseng using immunoblot analysis. Furthermore, Kim, et al.25 reported that 45% of birch pollen-sensitized patients with allergic rhinitis show positive responses to skin tests with raw Korean ginseng extracts, suggesting cross-allergenicity between birch and ginseng. Interestingly, all of the anaphylaxis cases to ginseng were sensitized to birch pollen in our study. However, there has been no study about cross-allergenicity between pollens and other local foods, such as jujube, lotus root, crown daisy, yacon, and mulberry. Further research will be needed.
In this study, the most frequent causative food of anaphylaxis in PFAS was peanut. Sensitization to seed storage allergenic components (Ara h 1, 2, 3, and 6) in peanut suggests the possibility of class I food allergy, whereas isolated specific IgE to pathogenesis-related protein PR-10 family members, such as Bet v1 (birch), Mal d 1 (apple), Cor a 1 (hazelnut), Gly m 1(soybean), or Ara h 8 (peanut), usually causes PFAS without systemic symptoms.26 Lipid transfer proteins, including Art v 3 (mugwort), Ara h 9 (peanut), Pru p 3 (peach), Mal d 3 (apple), and Gly m 1 (soybean), frequently are attributed to the development of anaphylaxis in PFAS.27 However, this was a questionnaire-based epidemiological study, and allergenic components analysis was not performed. Ara h 9 (peanut) or other unknown allergenic components might contribute to the development of anaphylaxis in our study subjects. Further studies will be needed to elucidate which allergenic components of pollens and foods are related to the development of anaphylaxis in PFAS in these study subjects.
The risk factors of anaphylactic reactions in PFAS have been previously reported, such as systemic reactions to one of the associated foods and positive skin test results with commercial extracts.28 In our study, the strength of sensitization to skin tests to alder, birch, hazel, willow, timothy, and ragweed was associated with development of anaphylaxis in PFAS. Furthermore, the sensitization to specific pollens, such as hazel, timothy, and ragweed, was an independent risk factor of anaphylaxis in PFAS. Eriksson, et al.29 have reported a positive correlation between the size of the skin reaction to birch pollen and the incidence of hypersensitivity to PFAS; however, the association between the strength of pollen sensitization and anaphylaxis in PFAS has not been reported to date. In this study, the presence of AD and a higher number of culprit foods were also important risk factors for anaphylaxis in PFAS. AD has been reported as an important risk factor in a study with recurrent anaphylaxis patients.30 Although the exact mechanism has not been elucidated, researchers have suggested that patients with AD have more activated mast cells and basophil cells.31
Currently, many clinicians maintain that PFAS does not cause anaphylaxis.4 Considering our study results with a higher prevalence of anaphylaxis in PFAS than that which has been reported, clinicians must be aware of the potential risks generated by PFAS and consider this when making a decision for risk management. If pollinosis patients have multiple pollen-related food allergies and strong positive responses on skin tests to hazel, timothy, or ragweed, the culprit foods may be related to the development of anaphylaxis. In addition, if patients have systemic symptoms or an anaphylactic reaction, allergists should educate the patients to avoid potential culprit foods, and they should not hesitate to prescribe self-injectable epinephrine.
This study has several limitations. First, this study was conducted as a questionnaire-based study depending on the patient's recollection and clinical history. Double-blind, placebo-controlled food challenge (DBPCFC), a gold standard for the diagnosis of food allergy, was not performed for diagnosis of PFAS in this study. Although DBPCFC is the gold standard for diagnosis of food allergy, careful clinical history in patients with pollinosis could replace provocation tests for diagnosis of PFAS because the excipient and taste covering for DBPCFC may cause the loss of the allergenic properties. Moreover, component-resolved diagnosis has yet to be prevalent for the diagnosis of PFAS. Therefore, in this study, PFAS was defined by typical oropharyngeal symptoms, including systemic symptoms, with raw fruits and/or vegetables and positive results of allergy tests to pollens. Second, this study was conducted by voluntarily participating hospitals, and the possibility of selection bias cannot be excluded. Because most of the contributing hospitals are referral hospitals, the prevalence of PFAS and anaphylaxis was possibly higher due to the involvement of more severe pollinosis cases. Third, all investigators did not use same allergy skin test solutions for diagnosis of pollen allergy, which are not standardized between manufacturers. This might affect the results of strength of pollen sensitization. Fourth, the relationship between specific allergenic components and the risk of anaphylaxis has not been studied. Component-resolved diagnosis could also help differentiating class I food allergy and PFAS, especially in case of peanut allergy. Further studies are needed.
In conclusion, the most frequently associated foods with anaphylaxis in PFAS were peanut, apple, walnut, pine nut, peach, ginseng, and soy in Korea. The presence of AD, strong sensitization to specific pollens, such as hazel, timothy, and ragweed, and a higher number of pollen-related foods significantly increased the risk of anaphylaxis in patients with PFAS, compared to patients with only oropharyngeal symptoms. Allergists should inform their patients that pollen-related foods can cause anaphylaxis and prescribe self-injectable epinephrine to high-risk patients.

ACKNOWLEDGEMENTS

This study was supported by a grant from the Korean Academy of Asthma, Allergy, and Clinical Immunology (2016).

Notes

The authors have no potential conflicts of interest to disclose.

AUTHOR CONTRIBUTIONS:

  • Conceptualization: Jeong-Hee Choi and Dae Hyun Lim.

  • Data curation: Dong-Kyu Kim, Young-Il Koh, Jaechun Lee, Sang Min Lee, and Yang Park, Work Group for Rhinitis, the Korean Academy of Asthma, Allergy and Clinical Immunology.

  • Formal analysis: Dong-Kyu Kim, Hyo Yeol Kim, and Hyun Jong Lee.

  • Funding acquisition: Mi-Ae Kim, Young Joon Jun, and Bong-Seong Kim.

  • Investigation: Hyun Jong Lee, Bong-Seong Kim, Yong Min Kim, and Woo Yong Bae.

  • Methodology: Dong-Kyu Kim, Woo Yong Bae, Yunsun Kim, Jeong Hee Kim, and Yang Park.

  • Project administration: Dong-Kyu Kim and Jaechun Lee.

  • Resources: Young-Il Koh, Dae Hyun Lim, and Hyo Yeol Kim.

  • Software: Hae-Sim Park, Mi-Ae Kim, and An-Soo Jang.

  • Supervision: Hae-Sim Park, Young Yoo, and An-Soo Jang.

  • Validation: Hyeon-Jong Yang and Yi Yeong Jeong.

  • Visualization: Hyeon-Jong Yang, Yunsun Kim, and Yi Yeong Jeong.

  • Writing—original draft: Minji Kim and Youngmin Ahn.

  • Writing—review & editing: Young Yoo and Jeong-Hee Choi.

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SUPPLEMENTARY MATERIAL

Supplementary Table 1

Causative Foods and Sensitized Pollens in Pollen-Food Allergy Syndrome Patients with Anaphylaxis
ymj-60-960-s001.pdf
Fig. 1

Comparison of allergen sensitization profiles between anaphylaxis (n=27) and only oropharyngeal symptom patients (n=130) with pollen-food allergy syndrome (PFAS). More patients with anaphylaxis were sensitized to hazel and willow than patients with only oropharyngeal symptoms. *p<0.05. D, Dermatophagoides.

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Fig. 2

Associations between the number of systemic symptoms other than oral symptoms in pollen-food allergy syndrome and the strength of sensitization to pollen by allergy skin tests. Significant association was found between anaphylaxis and strength of pollen sensitization (A, C, D, E, F, G, H, J: p<0.05 in G2 vs. G0, G1) (B, I: p<0.05 in G2 vs. G1). X-axis, number of systemic symptoms other than oropharyngeal symptoms, G0: only oropharyngeal symptoms, G1: one systemic symptom, G2: anaphylaxis, Y-axis, strength of sensitization (A/H ratio: Allergen/Histamine ratio). *p<0.05 in G2 vs. G0, G1, respectively; †p<0.05 in G2 vs. G1. Neg, negative skin prick test.

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Fig. 3

Associations between the number of systemic symptoms other than oropharyngeal symptoms in pollen-food allergy syndrome (PFAS) and the number of causative pollen-related foods (A) and between the number of systemic symptoms other than oropharyngeal symptoms and the number of sensitized pollen (B). Anaphylaxis (G2) was significantly associated with a higher number of pollen-related foods (p<0.05), but was not associated with the number of sensitized pollens (p>0.05). X-axis, number of systemic symptoms other than oropharyngeal symptoms, G0: only oropharyngeal symptom, G1: one systemic symptom, G2: anaphylaxis. *p<0.05 in G2 vs. G0, G1, respectively.

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Table 1

Clinical Characteristics of the Study Subjects with Anaphylaxis in PFAS

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PFAS with anaphylaxis (n=27) PFAS with only oropharyngeal symptoms (n=130) p value
Sex (male) 14 (51.9) 69 (53.1) 1.000
Age (yr) 27.2±18.7 26.2±16.7 0.767
Allergic diseases
 Bronchial asthma 9 (33.3) 52 (40) 0.667
 Allergic rhinitis 27 (100) 126 (96.9) 1.000
 Allergic conjunctivitis 17 (63.0) 75 (57.7) 0.770
 Atopic dermatitis 13 (48.1) 34 (26.2) 0.041
 Chronic urticaria 5 (18.5) 6 (4.6) 0.023
 Drug allergy 3 (11.1) 11 (8.5) 0.710
Family history of allergic diseases 21 (77.8) 98 (75.4) 0.986
Severity of allergic rhinitis 0.613
 Mild 13 (48.1) 52 (40.6)
 Moderate/severe 14 (51.9) 76 (59.4)
Duration of allergic rhinitis 0.723
 Intermittent 13 (48.1) 54 (42.2)
 Persistent 14 (51.9) 74 (57.8)

PFAS, pollen-food allergy syndrome.

Data are presented as mean±standard deviation or number (%) unless otherwise indicated.

Table 2

Causative Foods of Anaphylaxis in Pollen-Food Allergy Syndrome (n=27)

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Foods No. (%)
Peanut 9 (33.3)
Apple 6 (22.2)
Walnut 6 (22.2)
Pine nut 5 (18.5)
Peach 4 (14.8)
Ginseng 4 (14.8)
Soy 3 (11.1)
Eggplant 2 (7.4)
Jujube 2 (7.4)
Chinese yam 2 (7.4)
Buckwheat 2 (7.4)
Chestnut 2 (7.4)
Lotus root 2 (7.4)
Plum 2 (7.4)
Kiwi 2 (7.4)
Taro/Taro stem 2 (7.4)
Pineapple 2 (7.4)
Potato 1 (3.7)
Sweet potato 1 (3.7)
Mandarin 1 (3.7)
Perilla leaf 1 (3.7)
Carrot 1 (3.7)
Deodeok (Codonopsis lanceolata) 1 (3.7)
Bellflower root 1 (3.7)
Perilla 1 (3.7)
Strawberry 1 (3.7)
Garlic 1 (3.7)
Melon 1 (3.7)
Fig 1 (3.7)
Banana 1 (3.7)
Pear 1 (3.7)
Apricot 1 (3.7)
Celery 1 (3.7)
Watermelon 1 (3.7)
Crown daisy 1 (3.7)
Yacon 1 (3.7)
Mulberry 1 (3.7)
Grape fruit 1 (3.7)
Korean melon 1 (3.7)
Cherry 1 (3.7)
Tomato 1 (3.7)
Grape fruit 1 (3.7)
Pistachio 1 (3.7)
Rye 1 (3.7)

Data are presented as number (%).

Table 3

Multivariate Analysis of Risk Factors for the Development of Anaphylaxis in Pollen-Food Allergy Syndrome

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Predictor OR 95% CI p value
Presence of atopic dermatitis 3.58 1.25–10.23 0.017
Sensitization to hazel 5.27 1.79–15.53 0.002
Sensitization to timothy 11.8 2.70–51.64 0.001
Sensitization to ragweed 3.18 1.03–9.87 0.045
The number of culprit foods 1.25 1.15–1.37 <0.001

OR, odds ratio; CI, confidence interval.

Sensitization was diagnosed by allergy skin tests.

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