Montelukast use over the past 20 years: monitoring of its effects and safety issues

Article information

Clin Exp Pediatr. 2020;63(10):376-381
Publication date (electronic) : 2020 February 5
doi : https://doi.org/10.3345/cep.2019.00325
1Department of Pediatrics, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin, Korea
2Asthma and Allergy Center, Department of Pediatrics, Inje University Sanggye Paik Hospital, Seoul, Korea
Corresponding author: Chang-Keun Kim, MD. Asthma and Allergy Center, Department of Pediatrics, Inje University Sanggye Paik Hospital, 1342 Dongil-ro, Nowon-gu, Seoul 01757, Korea E-mail: kimck@paik.ac.kr
Received 2019 April 7; Revised 2019 November 19; Accepted 2019 December 3.

Abstract

Montelukast, a leukotriene receptor antagonist, was launched 20 years ago in Korea. It is recommended as an alternative treatment for asthma in children with mild persistent symptoms or as an add-on treatment to existing low-dose inhaled corticosteroids (ICSs) in children who require additional treatment. However, in the real-world setting, many doctors and patients prefer montelukast over ICSs despite their lower efficacy. Although montelukast is considered to be a safe drug, there are concerns regarding adverse drug reactions, including the rare occurrence of Churg-Strauss syndrome and, despite insufficient data, the possibility of neuropsychiatric events such as anxiety, depression, sleep disturbance, and suicidality. This review identified that montelukast has significantly contributed to asthma control over the past 20 years in Korea and has been critical for reducing asthma severity, especially early wheezing and disease control. Our findings suggest that the effects of montelukast treatment can be monitored by measuring serum eosinophilderived neurotoxin levels.

Key message

Although the efficacy of montelukast is inferior to that of ICS, both physicians and parents prefer montelukast to ICSs.

EDN may be a useful biomarker for the treatment and monitoring of preschool children with asthma.

The US FDA requires boxed warning about serious neuropsychiatric events of montelukast, therefore, physicians should consider the benefits and risks of montelukast before prescribing it.

Introduction

Leukotrienes (LTs) are substances secreted by leukocytes that have three conjugated double bonds. Researchers have known since 1930 that the sputum of asthmatic patients contains a substance that causes smooth muscle constriction [1]. This substance was termed slow-reacting substance of anaphylaxis (SRS-A) since it causes slow contractions of the smooth muscle after being released from sensitized lungs during an anaphylactic reaction [2]. In the late 1970s, SRS-A was shown to be part of the LT family [3]. In 1980, the LTs C4 and D4 (LTC4 and LTD4, respectively) reportedly showed remarkable contractile activity on isolated human bronchi [4]. Thereafter, the number of studies on LTs as candidate asthma treatments increased. LT modifiers include LT receptor antagonists (LTRAs) and 5-lipoxygenase (5-LO) inhibitors. LTRAs include zafirlukast, montelukast, and pranlukast, while 5-LO inhibitors include zileuton. Of these, montelukast is the most widely prescribed and studied worldwide. This review describes the synthesis and function of LTs and the effects and safety of montelukast, a representative LTRA.

Biosynthesis of LTs

The biosynthesis of LTs begins in the cell membrane. When a variety of biological stimuli occur, phospholipids in the cell membrane are metabolized to arachidonic acid (AA) by phospholipase A2. AA is converted to prostaglandin (PG) or thromboxane by cyclooxygenase or to 5-hydroperoxyeicosatetraenoic acid (5-HPETE) by 5-LO and 5-LO-activating protein (FLAP). Next, 5-HPETE is transformed into 5-hydroxyeicosatetraenoic acid (5-HETE) or LTA4. LTA4 is then converted to LTB4 by LTA4 hydrolase or binds to reduced glutathione using LTC4 synthase to form LTC4. LTC4 is converted to LTD4 by the removal of glutamic acid by α-glutamyl transpeptidase, while LTD4 is converted to LTE4 by the removal of glycine by dipeptidase. LTC4, LTD4, and LTE4 are called cysteinyl LTs (cysLTs) because they contain cysteine.

Role of LTs in the airway

CysLTs have several effects that contribute to the pathogenesis of asthma. First, they act as potent bronchoconstrictors in humans. When the lung tissues of asthmatic patients were stimulated with specific allergens, cysLT secretions increased and the cysLT amounts released were correlated with bronchial smooth muscle contractions [5]. When LTD4 was inhaled in vivo, the bronchial smooth muscle contracted and lung function was decreased regardless of asthma status [6]. CysLTs up-regulate the expression of endothelial adhesion molecules, act as a powerful chemoattractant for eosinophils, and reduce eosinophil apoptosis, thus leading to eosinophilic inflammation [7]. CysLTs also increase vascular leakage, which in turn exacerbates mucosal edema, increases mucus production and secretion by goblet cells, and decreases mucociliary clearance [8-10]. Furthermore, cysLTs con tribute to airway remodeling, promote smooth muscle cell proliferation, and increase collagen deposition in the airways (Fig. 1) [11,12].

Fig. 1.

Biosynthesis and role of leukotrienes. 5-LO, 5-lipoxygenase; FLAP, 5-LO-activating protein; 5-HPETE, 5-hydroperoxyeicosatetraenoic acid; 5-HETE, 5-hydroxyeicosatetraenoic acid; LT, leukotriene; GTP, glutamyl transpeptidase.

CysLT receptors are classified as cysLT1 and cysLT2. Montelukast, zafirlukast, and pranlukast are selective cysLT1 antagonists. CysLT1 is expressed by macrophages, dendritic cells, eosinophils, basophils, mast cells, B cells, CD4+ T cells, hematopoietic progenitor cells, epithelial cells, airway smooth muscle cells, fibroblasts, fibrocytes, and endothelial cells. CysLT2 is expressed by macrophages, eosinophils, basophils, mast cells, epithelial cells, fibrocytes, and endothelial cells [13]. The binding affinity for cysLT1 among cysLTs is the highest in LTD4, followed by LTC4 and LTE, which shows very weak binding affinity. The binding affinity for cysLT2 is similar in LTD4 and LTC4, while that of LTE4 is weak [13-15]. There is no currently available selective cysLT2 antagonist. Commercialized LTRAs, such as montelukast, pranlukast, and zafirlukast, act selectively on cysLT1 but not cysLT2. Therefore, asthma-associated cysLT activity is thought to involve cysLT1.

Clinical use of montelukast in children with asthma

1. Current pediatric asthma management guidelines

The current guidelines state that low-dose inhaled corticosteroids (ICS) may be used primarily in children of all ages when maintenance therapy is needed and that LTRAs should be administered as an alternative treatment. If step-up treatment is required, the prescription of moderate-dose ICS or LTRAs in combination with low-dose ICS is recommended for children aged <6 years. For children aged ≥6 years, the use of low-dose ICS in combination with long-acting beta-2 agonists is recommended, while high- or low-dose ICS with LTRAs are recommended as alternative treatments [16,17].

2. Comparison with ICSs

A Cochrane review that analyzed 19 pediatric randomized controlled trials (RCTs) to compare the efficacy of montelukast to that of ICS revealed the superior efficacy of the latter [18]. A meta-analysis of RCTs in preschoolers with asthma or recurrent wheezing also reported that daily ICS use was more effective than montelukast treatment [19]. However, several studies showed different outcomes in real-life environments since the actual effects of a medication are determined by both medication efficacy and patient compliance. Ducharme et al. [20] examined the real-life effectiveness of montelukast versus ICS in children with mild or moderate asthma. Physicians prescribed medication for 62% of the follow-up period when prescribing ICS versus 97% of follow-up when prescribing montelukast. Patients purchased 51% versus 74% of the prescribed ICS and montelukast at pharmacies, respectively. As a result, children who were prescribed ICS used the medication for 24% of the follow-up period, while those who were prescribed montelukast used the medication for 38% of the follow-up period. There was no intergroup difference in the rates of oral corticosteroid use or emergency room visits, but the ICS prescription groups were the more frequently admitted and more frequently required rescue beta-2 agonists [20]. According to a study analyzing the Korean National Health Insurance claim database from 2010 to 2014, LTRAs including montelukast were the most prescribed in children of all ages with asthma. The rate of ICS prescriptions for asthmatic patients aged ≥6 years was <15% [21]. These results suggest that Korean pediatricians prefer to prescribe montelukast rather than ICS. In a recent survey of 1,838 pediatric patients currently receiving treatment for asthma in Korea and their parents, 38% of patients receiving inhaled treatment and 50% of those receiving LTRAs were taking the treatment as prescribed. Furthermore, 70% of LTRA users versus only 34% of inhaler users felt that their treatment modality was easy to use [22].

A randomized study comparing responses to fluticasone inhaler and montelukast treatment in school-aged children with mild to moderate asthma defined a response as a ≥7.5% improvement in forced expiratory volume in 1 second (FEV1), and showed that 5% of the children responded to montelukast only, 23% responded to fluticasone only, 17% responded to both medications, and 55% responded to neither medication. Predictors of good response to fluticasone only were lower pulmonary function and provocative concentration causing a 20% drop in FEV1, and higher FeNO levels, total eosinophil counts, serum eosinophil cationic protein (ECP), and total immunoglobulin E. Conversely, predictors of good response to montelukast were lower age and short duration of asthma [23].

In summary, although the efficacy of montelukast is inferior to that of ICSs and asthma management guidelines recommend that ICSs be prescribed primarily when starting maintenance therapy, both physicians and patients prefer montelukast to ICSs. In addition, some patients respond better to montelukast than to ICS, but additional studies are needed to determine which patients will respond better.

3. Preschool children with asthma or recurrent wheezing

There are currently no specific tools or biomarkers available to diagnose asthma in preschool children. Therefore, it is important for physicians to recognize the various patterns of recurrent wheez ing in this population. The proposed phenotypes of recurrent wheezing in early childhood are as follows: transient wheezing, nonatopic wheezing, persistent asthma, and severe intermittent wheezing [24,25]. This classification is helpful in under standing childhood wheezing but is difficult to use clinically. Wheezing may be classified as an “episodic (viral) wheeze” (EVW) or “multipletrigger wheeze” (MTW) [26]. An EVW is defined as wheezing during discrete time periods, often in association with the clinical evidence of a viral cold, with an absence of wheezing between episodes. An MTW is defined as wheezing that shows discrete exacerbations but also symptoms between episodes.

A recent meta-analysis reported on the effects of montelukast treatment for the prevention of post-bronchiolitis wheezing [27]. The authors concluded that montelukast reduced the frequency of recurrent wheezing but did not reduce the incidence of recurrent wheezing, corticosteroid use, or number of symptom-free days in post-bronchiolitis infants; therefore, it was not appropriate for clinical use. However, in an RCT of post-bronchiolitis patients treated with montelukast for 3 months and followed up for 12 months, the serum eosinophil-derived neurotoxin (EDN) levels were significantly decreased and cumulative recurrent wheezing episodes were significantly decreased in the montelukast-treated group [28].

A Cochrane review of the effects of LTRA against EVW in preschool children reported that LTRA maintenance or intermittent therapy did not reduce the number of children experi encing one or more episodes requiring rescue medicine, emergency room visits, or hospital admissions [29,30]. However, the authors suggested that certain subgroups may respond to LTRA since children with EVW did not show homogeneous phenotypes and that they should be prescribed montelukast as a therapeutic trial and continue maintenance therapy if they respond well. The European Respiratory Society (ERS) recommended that, montelukast should be the first choice for daily maintenance therapy in children with EVW, while ICSs should be the first choice of maintenance therapy in children with MTW. However, the ERS highlighted that it is difficult to distinguish EVW from MTW in some children [31]. A recent meta-analysis of the effects of montelukast against both EVW and MTW in preschool children reported that montelukast was ineffective in preschool children with recurrent wheezing. The authors suggested that further studies should be conducted to investigate how to easily identify montelukast responders in clinical settings [32].

EDN may be a useful biomarker for the treatment and monitoring of preschool children with asthma or recurrent wheezing [33,34]. EDN is one of four major proteins secreted by activated eosinophils together with ECP, major basic protein, and eosinophil peroxidase. Unlike the other three, EDN has an isoelectronic point of 8.3, which is close to neutral; therefore, it is possible to measure accurately and reproducibly in the blood [35]. In a previous study, we compared the concentrations of serum EDN to asthma symptom scores in preschool children [36]. Serum EDN levels were the highest in children with acute asthma, followed by those with stable asthma and those in the control group, and the differences among the three groups were significant. Another study suggested that serum EDN levels 3 months after respiratory syncytial virus bronchiolitis were predictive of recurrent wheezing within 12 months. The serum EDN concentration cutoff value for predicting wheezing recurrence was 53 ng/mL (positive predictive value, 57%; negative predictive value, 76%; sensitivity, 72%; and specificity, 62%). The normal range of serum EDN concentration was 13–45 ng/mL [28]. Predictive value of EDN levels for asthma was based on clinical performance result. Using 44.2 ng/mL (median+1SD) as the cut off for an elevated EDN level compared to those found in Controls, the sensitivity was 81.3%, the specificity was 87.1%, the positive predictive value (PPV) of EDN level for asthma 90.7 %, and the negative predictive value (NPV) was 75.0% [35]. Another recent study compared the effects of montelukast and 0.5-mg budesonide inhalation suspension therapy for 12 weeks in symptomatic preschool children with asthma and serum EDN levels ≥53 ng/mL [37]. During the study period, asthma control days increased in both groups and there was no significant intergroup difference. However, serum EDN levels were significantly decreased only in the montelukast group. Therefore, based on several years of EDN-related research, we recommend starting maintenance therapy with montelukast when the EDN concentration is ≥53 ng/mL (1 SD of normal) and stopping when it decreases to <45 ng/mL (Fig. 2).

Fig. 2.

Monitoring of leukotriene receptor antagonist effects. EDN, eosinophil-derived neurotoxin.

Current clinical practice guidelines recommended controller therapy for children experiencing daytime asthma symptoms more than once a week, with activity limitations, who require the use of a reliever more than once a week, or who have any nighttime symptoms [16]. However, a recent study compared the efficacy of montelukast maintenance therapy and as-needed β2-agonist therapy for 48 weeks in preschool children experiencing asthma symptoms more than once a month but less than once a week [38]. During the study, 28% of the montelukast group and 50% of the no-controller group experienced asthma exacerbations; 21% and 41% of the children, respectively, required increased treatment. Therefore, montelukast use should be considered as maintenance therapy in preschool children with intermittent asthma (Table 1).

Clinical effects of montelukast in preschool children

The efficacy of LTRAs combined with antihistamines is often mentioned in clinical journals and guidelines. The combination of montelukast and 2nd-generation antihistamines may protect against seasonal decreases in lung function in patients with allergic rhinitis. Furthermore, LTRAs may be more effective at treating allergic rhinitis when combined with antihistamines since the agents have different efficacies. Recently, one such compound was developed and marketed for children in Korea [39].

Safety profile

The most commonly reported clinical adverse events of montelukast treatment were fever, upper respiratory infection, and asthma exacerbation. However, montelukast is considered a safe drug because its reported incidence of adverse drug reactions (ADRs) was similar to that of the control group [40].

Major concerns related to montelukast-associated ADRs included the occurrence of Churg-Strauss syndrome (CSS) and the possible association between LTRA and suicidality. A case-crossover study of 78 patients with CSS reported that the use of montelukast was associated with a 4.5-fold increased risk of CSS onset within 3 months [41]. CSS, also known as eosinophilic granulomatosis with polyangiitis, is a rare autoimmune disorder that causes vasculitis in patients with a history of asthma or allergic rhinitis. Treatment for CSS includes glucocorticoids (such as prednisolone) and other immunosuppressive drugs. Therefore, montelukast is simply a confounding factor, and the withdrawal of steroid use may be associated with the development of CSS symptoms.

The United States Food and Drug Administration issued a warning in 2008 regarding the possible association between montelukast use and suicidality; moreover, in 2020, it announced that the drug requires a boxed warning about mental health side effects because many other antiallergy medicines can be prescribed instead and many health care professionals and patients/caregivers are not aware of the risk of mental health side effects. Many studies that have analyzed published case reports or databases of adverse drug response reporting systems suggested that montelukast use is associated with neuropsychiatric events such as anxiety, sleep disturbance, depression, and suicidality [42-44]. A recent nested case-control study of 898 cases and 3,497 con trols from a cohort of children with asthma aged 5–18 years in 2004–2015 reported that children who were prescribed montelukast had increased odds (2 times) of experiencing a neuropsychiatric event [45]. However, 2 recent systematic reviews on this issue reported that the association between neuropsychiatric events and montelukast use was reported by studies using pharmacovigilance databases and not by observational or cohort studies [46,47]. A study assessing a cohort of 670 adults with allergic rhinitis in Spain reported that the severity of allergic rhinitis was related to a worse quality of life, sleep disturbances, depression, and anxiety [48]. One study investigated the association between montelukast and antidepressant use and reported that montelukast initiation was weakly associated with antidepressant prescription. However, the study concluded that antidepressant use, not montelukast use, may be correlated with asthma severity [49]. A study using an animal allergic rhinitis model reported that allergic rhinitis was associated with the induction of an inflammatory response in the hippocampus and that it may trigger associated neuropsychiatric events [50]. These findings do not guarantee the safety of montelukast; therefore, clinicians should consider the benefits and risks of montelukast before prescribing it.

Conclusion

The efficacy of montelukast for pediatric asthma is inferior to that of ICSs. Nonetheless, montelukast has several advantages. First, patients using ICS must use the correct inhalation technique, whereas no special skills are required to administer montelukast. Second, both patients and prescribing physicians prefer to use a drug that is administered only once a day. Third, there is no impact on growth, unlike the use of ICSs, which can potentially impair a child’s growth [51].

Montelukast maintenance therapy is primarily recommended for asthmatic children who experience symptoms more than once a month but less than once a week and is recommended as an alternative method for children with step 2 asthma.

Serum EDN can be used as a biomarker to monitor the effectiveness of pediatric asthma treatment. We recommend starting maintenance therapy with montelukast when the EDN level is ≥53 ng/mL and stopping when the EDN level decreases to <45 ng/mL. However, additional studies are needed to determine the validity of these recommendations.

Notes

No potential conflict of interest relevant to this article was reported.

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Article information Continued

Fig. 1.

Biosynthesis and role of leukotrienes. 5-LO, 5-lipoxygenase; FLAP, 5-LO-activating protein; 5-HPETE, 5-hydroperoxyeicosatetraenoic acid; 5-HETE, 5-hydroxyeicosatetraenoic acid; LT, leukotriene; GTP, glutamyl transpeptidase.

Fig. 2.

Monitoring of leukotriene receptor antagonist effects. EDN, eosinophil-derived neurotoxin.

Table 1.

Clinical effects of montelukast in preschool children

Phenotype Clinical effects of montelukast
Wheeze
Episodic viral wheeze Decrease in wheezing frequency after RSV infection. No short-acting effects on reducing wheezing episodes requiring rescue medicine, ER visit, and hospital admission
Recommended as a therapeutic trial
Multiple-trigger wheeze Montelukast responder’ phenotype exists. Studying how to easily identify these phenotypes
Recommended as an alternative treatment of low-dose ICS
Asthma
Intermittent Effective on reducing asthma exacerbation
Recommended as an additional treatment of short-acting beta agonist
Persistent Effective on reducing serum EDN concentrations.
Less effective than daily ICS for improving asthma symptoms and preventing exacerbation
Recommended as an alternative treatment of low-dose ICS

RSV. respiratory syncytial virus; ER, emergency room; ICS, inhalation corticosteroids; EDN, eosinophil-derived neurotoxin.