Allergic respiratory diseases in children mainly include allergic rhinitis (AR) and asthma, which are noninfectious inflammatory diseases mediated by silicon-germanium (sIgE) in the respiratory mucosa after children with allergic constitutions have been exposed to allergens (1). In recent years, the incidence of respiratory allergic diseases in children has been increasing. The third epidemiological survey of childhood asthma in 2013 showed that the 2-year prevalence rate of asthma in urban children aged 0–14 years was 2.32% on average, and the cumulative prevalence rate was 3.02% on average. In all, 50.1% of these children were also accompanied by AR (2). Compared with the results of the national epidemiological survey of childhood asthma in 2000, the current incidence of asthma increased by 50.6% and the cumulative prevalence increased by 53.3%. In China, the survey data of AR in different regions fluctuates greatly. Zhao et al. (3) conducted an epidemiological survey on children’s AR in Beijing, Chongqing, and Guangzhou by using a multi-order sampling method, and found that the prevalence rate was 14.46%, 20.42%, and 7.83%, respectively, with the prevalence level gradually increasing.
Allergen immunotherapy (AIT) has been recommended to treat AR and asthma. AIT mainly includes sublingual-specific immunotherapy (SLIT) and subcutaneous-specific immunotherapy (SCIT), both of which can alleviate patients’ respiratory symptoms, reduce the use of appropriate drugs, and improve patients’ quality of life (4). Both of the above approaches have been proved effective in treating children with respiratory irritability. The results of meta-analysis showed that both SCIT and SLIT were safe and effective in treating dust mite allergic rhinitis. However, no unanimous conclusion has been reached on the merits of the two methods in treating children with asthma (5), at present, only a few literatures have been reported. Miao et al. (6) found that different immunotherapy approaches had time differences in the intrinsic immunological response of asthmatic children, among which SCIT immunotherapy children showed earlier immune response. However, because of the limited delivery method of SCIT and the high requirement of patient compliance, its clinical application was greatly limited, while SLIT was more easily accepted by patients and their families. The World Allergy Organization (WAO) indicated that although the clinical efficacy of SLIT is limited by the dose, course, and patient selection, the effectiveness of SLIT in adult rhinitis and conjunctivitis and in asthma and rhinitis in children is worth promoting (7). SLIT in children with allergic asthma or AR has been studied in China (8,9), but there are few comprehensive studies on the improvement of lung function, and changes of exhaled nitric oxide (FeNO) after SLIT treatment in children with allergic asthma and rhinitis. Therefore, dust mite drops were used in this study to treat children with asthma and rhinitis, and the clinical efficacy, pulmonary function level, and the changes of FeNO indexes were observed. We present the following article in accordance with the STROBE reporting checklist (available at http://dx.doi.org/10.21037/tp-20-322).
SLIT treatment of asthma with rhinitis was randomly selected from February 2016 to February 2018 in 48 cases of children admitted to our hospital with asthma and rhinitis. After a year of follow-up, 8 cases were lost to follow-up. For acute asthma attacks [less than 70% of the expected forced expiratory volume in one second (FEV1)], termination of desensitization therapy occurred in 5 cases, and 4 cases were out on their own research. Ultimately, 31 cases completed the follow-up.
SLIT treatment of asthma without allergic rhinitis in our hospital in the same time was selected as the asthma group. Fifty-six children were placed into the group. After 1 year of follow-up, 5 cases were lost to follow-up for acute asthma attacks in the process of follow-up (less than 70% of the expected FEV1), termination of desensitization therapy occurred in 5 cases, and 6 cases withdrew from the study by themselves. Finally 40 cases completed the follow-up.
The inclusion criteria: (I) the diagnosis and treatment of patients were based on The Guidelines for Diagnosis and Treatment of Allergic Rhinitis in Children (2010, Chongqing) and the Guidelines for Prevention and Treatment of Bronchial Asthma in Children (2016). Accordingly, the inclusion criteria were the following: (II) children with asthma in remission stage; (III) tested for allergen skin puncturing before treatment, with the results showing dust mites and/or household dust mite were positive; meanwhile, the exclusion criteria were the following: (I) acute asthma attack with FEV1 less than 70% of the expected value; (II) loss to follow-up or withdrawal from the study due to various reasons; (III) occurrence of a severe allergic reaction.
In this study, sublingual desensitization treatment was performed with sublingual dust mite drops (national drug approval No. S20060012) produced by Zhejiang Wolwo Biotechnology Co., Ltd (Zhejiang, China), which were divided into 1–4 bottles, with corresponding total protein concentrations of 1, 10, 100, and 333 µg/mL. The drug was placed under the tongue for 1–3 minutes before swallowing. The treatment process includes the increment phase and the maintenance phase. During the increment phase, bottles 1, 2, and 3 were used in order for 1 week each, and 1, 2, 3, 4, 6, 8, and 10 drops of duster were administered from day 1 to day 7 of each week. Dust mite drop no. 4 was administered at 3 drops/time/day, until the end of the treatment period. SLIT therapy was adopted, and other corresponding drugs were used to treat asthma and rhinitis according to the clinical symptoms.
Lung function tests
Lung function was determined by the Master Screen lung function instrument (Jaeger GmbH, Cologne, Germany). The parameters include forced vital capacity (FVC), forced expiratory volume in one second (FEV1), FEV1/FVC, maximum forced peak flow expiratory (PEF), forced expiratory flow (FEF25, FEF50, FEF75), and maximum mid-expiratory flow (MMEF) (10).
Determination of exhaled nitric oxide
AN exhaled nitric oxide (FeNO) tester (NIOX VERO, Sollentuna, Sweden) was used to measure the exhaled nitric oxide index of children. FeNO levels were measured in accordance with the standardized FeNO assay guidelines recommended by the American Thoracic Society/European Respiratory Society (ATS/ESR) (11).
All procedures performed in this study involving human participants were in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by ethics board of Chengdu Women and Children Center Hospital and informed consent was taken from all the patients.
The severity of the main symptoms of rhinitis was assessed by the “four-point method” (Table 1) (12). The symptom score of asthma included daytime symptom score, nighttime symptom score, and visual analog scale (VAS) score, which depended on the severity of the symptoms and their impact on life (Table 2) (13).
A quantitative index of the application of symptomatic drugs was used to record the use of symptomatic drugs in the children, so as to evaluate the clinical efficacy of immunotherapy. Our study adopted the “three-step” scoring method (Table 3) (14).
SPSS 17.0 software (IBM, Armonk, NY, USA) was used for statistical analysis of the data. If the quantitative data were normally distributed, the mean ± standard deviation (SD) was used for description, and two independents sample t-test (Student’s t-test) was used for comparison between the groups. The quantitative data are described by median, upper, and lower quartile (M, P25-P75) for non-normal distribution, and the rank-sum test of the two independent samples was used for intergroup comparison (Mann-Whitney U test). Qualitative data are described by percentage, and comparisons between groups were performed by chi-square test. The cut-off value of P was 0.05.
There were 31 patients in the asthmatic rhinitis group, including 24 males (77.4%) and 7 females (22.6%), and 40 patients in the asthma-alone group, including 23 (57.5%) males and 17 (42.5%) females. There was no significant difference in gender composition between the two groups (χ2=3.097, P=0.078). The mean age of the asthmatic rhinitis group was 6.6±2.5 years old, and that of the asthmatic group was 7.6±3.2 years old. There was no significant difference in age between the two groups (χ2=1.567, P=0.122).
After treatment, the scores of daytime symptoms, VAS scores, and drug scores in the asthma group were lower than those before treatment, and the differences were statistically significant. There was no statistically significant difference in the scores of night symptoms before and after treatment (Table 4). The scores of rhinitis, daytime symptom scores, nighttime symptom scores, VAS scores, and drug scores of patients with asthma combined with rhinitis were all significantly lower after treatment than before treatment (P<0.05) (Table 5).
For both the asthma-alone group alone and the asthmatic rhinitis group, the pulmonary function index of the children after treatment was significantly improved compared with that before treatment, while the FeNO level after treatment was significantly decreased compared with that before treatment (P<0.05) (Tables 6,7).
The VAS score of patients with asthma combined with rhinitis was higher than that of patients with asthma alone, and the difference was statistically significant. There was no significant difference in the other scores between the two groups (Table 8). There was no significant difference in lung function and FeNO between the two groups (Table 9).
The natural process of allergic diseases means that their occurrence and development follow certain patterns (15); that is, the onset of allergic diseases begins in infancy and generally manifests as a food allergy or skin eczema. Most of these symptoms resolve automatically by the age of 3, but children in this group have a significantly increased risk of developing respiratory allergic diseases in their teens, especially asthma with/without AR. Allergic asthma and variant rhinitis are the most common respiratory allergic diseases that seriously affect the quality of life of children. Allergens are common factors that induce allergic asthma and variant rhinitis, while dust mites are the main allergens that cause asthma (16).
Children’s respiratory allergic diseases are chronic non-communicable diseases, and the management of diseases refers to the “four-in-one” treatment principle, which includes avoiding allergens, drug therapy, immunotherapy, and patient education (7). Although drug therapy can control allergic symptoms, it cannot affect the natural process of allergic diseases. Currently, AIT is considered as the only treatment method that can change the natural process of allergic diseases. In 2013, WAO confirmed SLIT’s therapeutic effect on disease and its reliable safety in the World Allergy Organization position paper 2013 update (17). Its adverse reactions were mild and limited, mainly manifested as tongue itching, swelling, pain, ulcer, taste change, ear itching, sore throat, uvula edema and gastrointestinal symptoms, which could be alleviated by themselves or reduced by drug dosage, and soon alleviated after the administration of symptomatic drugs. It also made it clear that SLIT's application does not need to be conditional on drug treatment failure, and SLIT can be applied in the initial clinical stage and early stage of allergic diseases. In the past 20 years, SLIT has been increasingly recognized as a safe and effective treatment for allergic diseases, especially AR and asthma (18). International studies have reported that SLIT can reduce the symptom scores of children with allergic asthma (19), while research in China shows that specific immunotherapy with dust mite drops can significantly improve the clinical symptoms of asthma and significantly reduce FeNO levels (20). The results of one meta-analysis showed that SLIT brought significant relief of symptoms and reduced medication demand in children with AR (21). Another recent meta-analysis found that SLIT applied to allergy to dust mites could significantly improve allergic symptoms, reduce long-term medication, and improve FEV1 (22). Furthermore, a study in Japan showed that sublingual immunotherapy with house dust mites could significantly improve airflow limitation in patients with allergic asthma complicated with rhinitis (FEV1 was significantly improved), significantly reduce FeNO level, and reduce airway eosinophilic inflammation (23). Another Chinese study retrospectively analyzed the data of 124 children with asthma and rhinitis treated with sublingual dust mite drops for 3 years, showing that this treatment had a significant effect on children with allergic asthma and rhinitis (24).
A domestic study retrospectively analyzed the data of 124 children with asthma and rhinitis. These children were treated with sublingual dust mite drops for 3 years. The results showed that the treatment was effective in children with allergic asthma and rhinitis. This study is based on the expert consensus (16) on mite specific immunotherapy for airway allergic diseases in children, using the symptom drug score as the main therapeutic effect evaluation index. The results showed that the symptom drug score in each group decreased significantly after treatment (P<0.05), which is consistent with the conclusions of domestic and foreign reports. However, in the asthma-alone group of our study, the improvement of nighttime symptoms after SLIT treatment was not significant compared with that before treatment, which was inconsistent with the above conclusions, and larger-sample-size studies are perhaps needed to produce more conclusive results.
In this study, the pulmonary function and exhaled nitric oxide of the children showed significant improvement in both asthma group and asthmatic group with rhinitis compared with those before treatment. In addition, the present study found that after SLIT treatment, the small airway parameters of lung function (FEF25-75, FEF75/FEF25) in the two groups were significantly improved compared with those before treatment. Thus far, few studies have been conducted on the effect of SLIT on FeNO level and lung function in children with asthma and rhinitis, especially using the indexes of small airway ventilation. Huang et al. (25) found no significant improvement in lung function after SLIT treatment and a follow-up of 3 years in 26 children with asthma complicated with rhinitis. However, Ma et al. (26) found significant improvement in FEF 25–75% in 32 asthmatic children after SLIT treatment, but no significant difference in FEV1. Another study by Li et al. (27) showed that SLIT treatment could significantly improve the symptoms of children with asthma complicated with rhinitis, reduce FeNO level, reduce airway inflammation, and improve the ventilation indexes of large and small airway lung function, which was consistent with our study. However, related research from outside China does not seem to be available.
Due the reported advantages of SLIT, which include its reliability and practicality, SLIT has been more commonly used in treating allergic respiratory diseases in China in recent years. However, there are still some unresolved issues related to this therapy. The inflammatory reactions of the upper and lower airways are similar and affect each other, so allergic asthma and rhinitis are described as “the same airway, the same disease” (28), with AR often inducing the attack and deterioration of asthma (29). Our study also found that the VAS score of patients with asthma combined with rhinitis was higher than that of those with asthma alone, which may be related to this phenomenon. Thus far, few studies have compared the effectiveness of SLIT therapy in children with allergic asthma combined with rhinitis to those with allergic asthma alone. The only relevant Chinese study by Li et al. (27) showed that SLIT treatment also improved the small pulmonary function airway index, FEF25, in children with asthma at 3, 6, 9, and 12 months compared with treatment in children with asthma combined with rhinitis in the same period; however, other pulmonary function ventilation indexes showed no significant differences. In this study, SLIT significantly improved the clinical symptoms, drug scores, lung function, and FeNO in children with asthma and rhinitis. This could be a result of the children’s mild illness and tendency of the disease to be in remission before immunotherapy, and thus our results require confirmation by a larger-sample-size study in the future.
Funding: Health and Family Planning research project in Sichuan Province.
Reporting Checklist: The authors have completed the STROBE reporting checklist. Available at http://dx.doi.org/10.21037/tp-20-322
Data Sharing Statement: Available at http://dx.doi.org/10.21037/tp-20-322
Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tp-20-322). The authors have no conflicts of interest to declare.
Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All procedures performed in this study involving human participants were in accordance with the Declaration of Helsinki (as revised in 2013). The study was approved by ethics board of Chengdu Women and Children Center Hospital and informed consent was taken from all the patients.
Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
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(English Language Editor: J. Gray)