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Asthma GLCCI1 gene polymorphisms on glucocorticoid therapeutic effect andits mechanism

GLCCI1 response effect of glucocorticoid regulation asthmatic mice adrenal medulla chromaffin cell transdifferentiation epigenetic mechanisms

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-RCC-13003634
Enrollment
Unknown
Registered
2013-09-26
Start date
2013-03-01
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

bronchial asthma

Interventions

asthma patients:no intervention
Wild type of GLCCI1:treatment with Flixotide
Heterozygous of GLCCI1:treatment with Flixotide

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. mild to moderate persistent asthma that meet the 2008 diagnostic criteria established by Chinese Medical Association Respiratory Diseases Asthma Study Group; 2. Age 18-70 years old , male or female; 3. Bronchial provocation test or Bronchodilation test positive; 4. No use of systemic or inhaled corticosteroids during the last 4 weeks; 5. No use of leukotriene receptor modulators, theophylline derivatives andmast cell stabilizers Within 2 weeks before the test; 6. No use of long-acting ß2 agonists, oral ß2 agonists or inhaled anti- cholinergic receptor 1 week before the test; 7.Abscent of without respiratory infections andsystemic infections, particularly acute respiratory infections , tuberculosis, fungal infections 4 weeks before the test; 8. Abscent of acute asthma exacerbations andhospitalizations 4 weeks before the test; 9. Did not receive any study medication 4 weeks before the test; 10. No inhaled corticosteroids, ß2 agonists allergies; 11. No serious heart, liver, kidney andother systemic disorders; 12. Agreed to join the study andsigned a written informed consent

Exclusion criteria

Exclusion criteria: 1. Intermittent status asthma, severe asthma andacute exacerbation of asthma; 2. Occupational asthma or aspirin or non- steroidal anti-inflammatory drugs -related asthma; 3. Life-threatening acute asthma exacerbations occurred within one year before the test; 4. Using of monoclonal anti-IgE Within 6 months prior to the test; 5. Recent drug use that can lead to bronchospasm or affect the Forced lung function; 6. Allergic to inhaled corticosteroids, ß2 agonists allergy, antibiotics or a history of food or drug -related serious allergic reactions; 7. Have serious disease of heart, liver, kidneys, lungs, gastrointestinal tract, endocrine andblood system diseases. Treated or untreated malignancies of any organ; 8. Obvious potential medical conditions( such as infection, blood diseases, kidney disease, liver disease, coronary heart disease or other cardiovascular diseases , cerebrovascular diseases, endocrine or gastrointestinal disease. ) that may affect the interpretation of the results 1 year before the test. 9. Other history of active lung diseases except asthma such as chronic bronchitis , chronic obstructive pulmonary disease, allergic granulomatous vasculitis, allergic bronchopulmonary aspergillosis; 10. Before the test, an average annual smoking. Former smokers should quit smoking in the 12 months prior to trial; 11. History of alcoholism anddrug abuse; 12. Pregnant andlactating women; 13. With psychiatric disorders; 14. had a hospitalization due to asthma exacerbations or failed to complete the whole process of determination during the study; 15. Not expected to complete the study or unable to continue to participate in planned visits; 16. Unable or unwilling to comply with research operations or study visits.

Design outcomes

Primary

MeasureTime frame
genotype of GLCCI1;expression level of GLCCI1;forced pulmonary function test;blood routine examination;

Secondary

MeasureTime frame
ACT score;AQLQ score;NGF expression;expression level of Epinephrine;expression level of Norepinephrin;

Countries

China

Contacts

Public ContactJuntao Feng

Xiangya Hospital, Central South University

Jtfeng1976@hotmail.com+86 13786145799

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 3, 2026