# Effectiveness of adjunctive Xiao-er Kechuanling to terbutaline and montelukast in children with uncontrolled asthma: a prospective observational cohort study

**Authors:** Shutao Luo, Cuiyuan Li, Shaojin Huo

PMC · DOI: 10.3389/fped.2025.1617547 · Frontiers in Pediatrics · 2025-10-16

## TL;DR

Adding Xiao-er Kechuanling to standard asthma medications improved asthma control and lung function in children over six months, with no significant safety issues.

## Contribution

Demonstrates that Xiao-er Kechuanling, a traditional Chinese medicine, may enhance asthma treatment outcomes when added to standard therapies.

## Key findings

- Triple Therapy (XKL + terbutaline + montelukast) significantly improved asthma control scores compared to Dual Therapy.
- Triple Therapy reduced inflammation markers and airway remodeling indicators more effectively than Dual Therapy.
- Lung function and variability improved significantly in the Triple Therapy group.

## Abstract

Achieving optimal control in childhood asthma remains challenging, particularly with therapies like short-acting beta2-agonists (SABA) plus leukotriene receptor antagonists (LTRA). Xiao-er Kechuanling (XKL), a traditional Chinese medicine formula with demonstrated anti-inflammatory and bronchodilatory effects, presents a potential adjunctive therapy. This study aimed to compare the clinical effectiveness and safety of adjunctive XKL added to terbutaline (SABA) and montelukast (LTRA) (Triple Therapy) vs. terbutaline plus montelukast alone (Dual Therapy) in children with uncontrolled asthma.

This single-center, prospective observational cohort study enrolled children aged 6–14 years with uncontrolled asthma (ACT ≤ 19) receiving either Dual or Triple Therapy based on physician prescription, with no inhaled corticosteroid use for ≥3 months prior. Participants were followed for 6 months. Primary outcomes included the proportion achieving ≥3-point ACT score increase, severe exacerbation frequency, and changes in serum (TGF-β1, MMP-9/TIMP-1 ratio) and HRCT (WT/D ratio) remodeling markers. Secondary outcomes included lung function (FEV1/FVC, PEF variability), inflammatory markers (IL-4, IL-13, ECP), and safety.

199 children were enrolled (95 Dual, 104 Triple); 94 Dual and 88 Triple completed the 6-month follow-up. Baseline characteristics were comparable between groups (P > 0.05). At Month 6, a significantly higher proportion in the Triple Therapy cohort achieved ≥3-point ACT increase (85.2% vs. 61.7%, P = 0.002). Triple Therapy was associated with significantly greater reductions in serum TGF-β1 (P = 0.017), MMP-9/TIMP-1 ratio (P < 0.001), and HRCT WT/D ratio (P = 0.017). Significantly greater improvements in FEV1/FVC (P = 0.002) and PEF variability (P < 0.001), and greater reductions in IL-4 (P = 0.015), IL-13 (P = 0.032), and ECP (P = 0.011) were also observed in the Triple Therapy group at Month 6. Exacerbation frequency was numerically lower but not significantly different (P = 0.125). Safety profiles, including adverse event rates, were comparable (P > 0.05).

In this observational study, adding XKL to terbutaline and montelukast was associated with significant improvements in asthma control, lung function, and markers of inflammation and airway remodeling in children with uncontrolled asthma over 6 months, with a comparable safety profile. However, due to the observational design and lack of confounder adjustment, these findings indicate association, not causality. Randomized controlled trials are needed to confirm the effectiveness of this adjunctive therapy.

## Linked entities

- **Proteins:** TGFB1 (transforming growth factor beta 1), MMP9 (matrix metallopeptidase 9), TIMP1 (TIMP metallopeptidase inhibitor 1), IL4 (interleukin 4), IL13 (interleukin 13), RNASE3 (ribonuclease A family member 3)
- **Chemicals:** terbutaline (PubChem CID 5403), montelukast (PubChem CID 5281040)
- **Diseases:** asthma (MONDO:0004979)

## Full-text entities

- **Genes:** TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, TIMP1 (TIMP metallopeptidase inhibitor 1) [NCBI Gene 7076] {aka CLGI, EPA, EPO, HCI, TIMP, TIMP-1}
- **Diseases:** asthma (MESH:D001249), inflammation (MESH:D007249)
- **Chemicals:** ECP (-), terbutaline (MESH:D013726), montelukast (MESH:C093875)

## Full text

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## Figures

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## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12571650/full.md

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Source: https://tomesphere.com/paper/PMC12571650