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GLCCI1 and STIP1 variants are associated with asthma susceptibility and inhaled corticosteroid response in a Tunisian population

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单位: [1]Univ Tunis El Manar, Fac Sci, Tunis, Tunisia [2]Abderrahman Mami Hosp, Unit Res Homeostasis & Mol Dysfunct Lung 12SP15, Pavillon B, Ariana, Tunisia [3]Univ Tunis El Manar, Med Fac Tunis, Tunis, Tunisia [4]Srebrnjak Childrens Hosp, Dept Translat Med, Zagreb, Croatia [5]Huazhong Univ Sci & Technol, Coll Life Sci & Technol, Ctr Human Genome Res, Wuhan, Hubei, Peoples R China [6]Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Resp & Crit Care Med,Natl Clin Res Ctr Resp, Wuhan, Hubei, Peoples R China [7]A Mami Hosp, Div Pediat Resp Dis, Pavil B, Ariana, Tunisia [8]Srebrnjak Childrens Hosp, Dept Pulmonol & Allergol, Zagreb, Croatia [9]JJ Strossmayer Univ Osijek, Fac Med, Osijek, Croatia
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关键词: Asthma risk glucocorticoid lung function SNPs association

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Objective: Pharmacogenetic studies have recognized specific genes that highly correlate with response to inhaled corticosteroids (ICS) treatment in asthma patients. Among the genes identified, we selected glucocorticoid-induced transcript 1 (GLCCI1) and stress-induced phosphoprotein 1 (STIP1) to evaluate the impact of these gene polymorphisms on ICS treatment response in Tunisian asthmatics. Methods: We analyzed four single nucleotide polymorphisms (SNPs): two in GLCCI1 (rs37972 and rs37973), and two in STIP1 (rs2236647 and rs2236648), which are genes associated with susceptibility to asthma and response to ICS in a Tunisian cohort. The SNPs were genotyped using reverse transcriptase polymerase chain reaction (RT-PCR) techniques. Results: This case-control study consisted of 230 adult asthmatic patients and 236 healthy subjects. Seventy-five asthmatics were selected and followed through 12 weeks of routine treatment. The T allele rs2236648 in STIP1 was associated with allergic asthma (OR = 0.38, 95%CI = 0.20-0.69, p = 0.001). The rs37972 and rs37973 of GLCCI1 were associated with a higher risk of asthma (p < 0.001). The T allele rs37972 and G allele rs37973 were correlated with a strong risk for developing severe asthma (p < 0.001). Asthma patients carrying the rs37973 GG genotype had less improvement in the forced expiratory volume in one second (FEV1) than those with the AA or AG genotypes after 12 weeks of treatment (p < 0.001). Also, the G allele of rs37973 was associated with worse response to ICS after 12 weeks of treatment (p < 0.001). Conclusion: The rs37972 and rs37973 polymorphisms can serve as potential asthma risk biomarkers in a Tunisian population.

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出版当年[2020]版:
大类 | 4 区 医学
小类 | 4 区 过敏 4 区 呼吸系统
最新[2025]版:
大类 | 4 区 医学
小类 | 4 区 过敏 4 区 呼吸系统
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出版当年[2019]版:
Q3 ALLERGY Q4 RESPIRATORY SYSTEM
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Q3 ALLERGY Q3 RESPIRATORY SYSTEM

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第一作者单位: [1]Univ Tunis El Manar, Fac Sci, Tunis, Tunisia [2]Abderrahman Mami Hosp, Unit Res Homeostasis & Mol Dysfunct Lung 12SP15, Pavillon B, Ariana, Tunisia [3]Univ Tunis El Manar, Med Fac Tunis, Tunis, Tunisia
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通讯机构: [1]Univ Tunis El Manar, Fac Sci, Tunis, Tunisia [2]Abderrahman Mami Hosp, Unit Res Homeostasis & Mol Dysfunct Lung 12SP15, Pavillon B, Ariana, Tunisia [3]Univ Tunis El Manar, Med Fac Tunis, Tunis, Tunisia
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