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| Name | Class |
|---|---|
| Academia Sinica, Taiwan | OTHER |
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Inhaled corticosteroid (ICS) is considered the first line medication for asthma, however, the therapeutic effect is markedly different even in patients with almost similar clinical manifestations. Our study was designed to explore the clinical and genetic factors that may influence the effectiveness of ICS in asthmatic children.
The three major common classes of asthma controller medications include inhaled corticosteroids (ICS), beta-2-agonists and leukotriene antagonists. Among them, ICS was now suggested as the first-line therapy demonstrated in Global Initiative for Asthma guideline updated in 2017.
The response to asthma medication is markedly different even in patients with almost similar clinical manifestations. Despite the wide availability of therapeutic asthma medications and large studies supporting their efficacy, there is significant inter-personal variability in the response to each of the three major classes of asthma medications with a subgroup of patients that have limited disease control, persistent symptoms and exacerbations even under controller medications use. For example, inter-individual variability in therapeutic effectiveness to ICS in both asthma children and adults is significant, with 22 to 60% of patients being classified as non-responders.
Although many factors can contribute to variation in response to therapy effectiveness, such as higher exhaled nitric oxide, higher total eosinophil counts, higher immunoglobulin E, lower forced expiratory volume at one second (FEV1) predicted. and lower concentration of methacholine needed to produce a 20% fall in FEV1 from baseline (PC20), it is still believed that genetic variability can also play an important role. Hence asthma represents a major burden with respect to mortality, morbidity and National Health Insurance costs, searching for appropriate mediations for asthma control is imperative and investigating the effect of genetic variability on therapy response is an important step to develop personalized prescription.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NTUH | National Taiwan University Hospital, all participants receive Duasma (budesonide, 200mcg/puff) |
| |
| FJUH | Fu Jen University Hospital, all participants receive Duasma (budesonide, 200mcg/puff) |
| |
| CGH | Cathay General Hospital, all participants receive Alvesco (Ciclesonide, 160mcg/puff) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Budesonide/Cisclesonide | Drug | One arm observation study: Duasma 1 puff bid (Budesonide 200mcg bid) or Alvesco 1 puff qd (Ciclesonide 160mcg qd) for participants aged 11 years and younger, Duasma 2 puffs bid (Budesonide 400mcg bid) or Alvesco 1 puff bid(Ciclesonide 160mcg bid) for participants aged 12 years and older |
| Measure | Description | Time Frame |
|---|---|---|
| FEV1 | change of forced expiratory volume at one second (FEV1) from baseline | 1 month |
| Measure | Description | Time Frame |
|---|---|---|
| PEF | change of peak expiratory flow (PEF) from baseline | 1 month |
| Asthma control test | change of subjective symptoms of asthma | 1 month |
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Inclusion Criteria:
Exclusion Criteria:
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Asthmatic children with mild to moderate severity, tolerable with inhaled corticosteroid device, can receive blood check.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Yungling Lee, Professor | Contact | 886-2-26523013 | leolee@ibms.sinica.edu.tw |
| Name | Affiliation | Role |
|---|---|---|
| Yungling Lee, Professor | NTUH | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| NTUH | Recruiting | Taipei | Taiwan |
Share with other researchers majored in asthma pharmacogenetic study
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| ID | Term |
|---|---|
| D001249 | Asthma |
| ID | Term |
|---|---|
| D001982 | Bronchial Diseases |
| D012140 | Respiratory Tract Diseases |
| D008173 | Lung Diseases, Obstructive |
| D008171 | Lung Diseases |
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| ID | Term |
|---|---|
| D019819 | Budesonide |
| ID | Term |
|---|---|
| D011282 | Pregnenediones |
| D011283 | Pregnenes |
| D011278 | Pregnanes |
| D013256 | Steroids |
| D000072473 |
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Blood, peripheral blood mononuclear cell (PBMC), DNA, RNA
|
| Serum biomarkers | change of ICS response related serum biomarkers (S100 calcium binding protein A12, eosinophil-derived neurotoxin, signal-regulatory protein alpha ..) | 3 months |
| exhaled nitric oxide (eNO) | change of exhaled nitric oxide | 1 month |
| exhaled nitric oxide (eNO) | change of exhaled nitric oxide | 3 months |
| D012130 |
| Respiratory Hypersensitivity |
| D006969 | Hypersensitivity, Immediate |
| D006967 | Hypersensitivity |
| D007154 | Immune System Diseases |
| Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |