Association of genetic variants with level of asthma control in the Arab population

被引:12
作者
Almomani, Basima A. [1 ]
Al-Eitan, Laith N. [2 ,3 ]
Al-Sawalha, Nour A. [1 ]
Samrah, Shaher M. [4 ,5 ]
Al-Quasmi, Mohammed N. [6 ]
机构
[1] Jordan Univ Sci & Technol, Fac Pharm, Dept Clin Pharm, POB 3030, Irbid 22110, Jordan
[2] Jordan Univ Sci & Technol, Dept Appl Biol Sci, Irbid, Jordan
[3] Jordan Univ Sci & Technol, Dept Biotechnol & Genet Engn, Irbid, Jordan
[4] Jordan Univ Sci & Technol, Fac Med, Irbid, Jordan
[5] King Abdullah Univ Hosp, Dept Internal Med, Irbid, Jordan
[6] King Abdullah Univ Hosp, Dept Med Lab, Hematol Lab, Irbid, Jordan
来源
JOURNAL OF ASTHMA AND ALLERGY | 2019年 / 12卷
关键词
ADRB2; Arab; asthma control; genetic association; Jordan; SNPs; BETA-2-ADRENERGIC RECEPTOR GENE; IMPROVED LUNG-FUNCTION; BETA(2) AGONIST; POLYMORPHISMS; GENOTYPE; ADRB2; PHARMACOGENETICS; EXACERBATIONS; ALBUTEROL; RISK;
D O I
10.2147/JAA.S186252
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Rates of asthma in Jordan have been doubled in the past decade, but this increased prevalence was not met with improved asthma control protocols. The aim of the present study was to assess whether there was any significant association between the level of asthma control and certain single-nucleotide polymorphisms (SNPs) in five genes: (ADRB2; rs1042713 and rs1042714), (CRHR1; rs1876828, rs242939, and rs242941), (STIP1; rs2236647), (ADH5, rs1154400), and (ARG1; rs2781659). These SNPs were selected based on their involvement in enzymes and receptors that are related to asthma pathways and subsequent response to medication and based on a high degree of linkage disequilibrium. Patients and methods: A cross-sectional genetic association study was conducted from June 2016 to June 2017 in the two major hospitals in Jordan. The present study involved sampling from adult asthmatic patients of Arab descent who were selected from two phenotypic groups, ie, controlled and uncontrolled asthma. The blood samples and medical data were collected from the participants. DNA samples were extracted, quantified, and genotyped according to standard operating procedure. Allelic and haplotypic analyses were performed using the Haploview (R). Results: A total of 245 Arab asthmatic patients were enrolled in this study. Genotyping analysis revealed that the two SNPs (rs1042713 and rs1042714) in ADRB2 gene, along with their related haplotypes, were nominally significantly associated with asthma control in the Jordanian population. The A-allele of rs1042713 and the C-allele of rs1042714 were more common in the uncontrolled asthma group than in the controlled asthma group (P=0.048 and P=0.017, respectively). Conclusion: This was the first study that identified the nominal significant association between the level of asthma control and genetic variants in ADRB2 gene in Arab population. Further studies in other Arab region with larger sample size are recommended to confirm the relationship.
引用
收藏
页码:35 / 42
页数:8
相关论文
共 50 条
  • [41] Association Between MTHFR Genetic Variants and Multiple Sclerosis in a Southern Iranian Population
    Naghibalhossaini, Fakhraddin
    Ehyakonandeh, Hesam
    Nikseresht, Alireza
    Kamali, Eskandar
    INTERNATIONAL JOURNAL OF MOLECULAR AND CELLULAR MEDICINE, 2015, 4 (02) : 87 - 93
  • [42] Association of common genetic variants with risperidone adverse events in a Spanish schizophrenic population
    B Almoguera
    R Riveiro-Alvarez
    J Lopez-Castroman
    P Dorado
    C Vaquero-Lorenzo
    J Fernandez-Piqueras
    A Llerena
    F Abad-Santos
    E Baca-García
    R Dal-Ré
    C Ayuso
    The Pharmacogenomics Journal, 2013, 13 : 197 - 204
  • [43] Association of CASZ1 genetic variants with stroke risk in the Chinese population
    Zhang, Fan
    Fu, Chuanyi
    Deng, Yidong
    Zhang, Mao
    Peng, Hao
    Li, Wenan
    Zhong, Jian
    Zhou, Qing
    Huang, Li
    Xiao, Shuli
    Zhao, Jiannong
    JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 2023, 32 (08)
  • [44] Association between microRNA genetic variants and susceptibility to colorectal cancer in Chinese population
    Hu, Xuejiao
    Li, Lixin
    Shang, Mengqiao
    Zhou, Juan
    Song, Xingbo
    Lu, Xiaojun
    Wang, Jun
    Ying, Binwu
    Wang, Lanlan
    TUMOR BIOLOGY, 2014, 35 (03) : 2151 - 2156
  • [45] Genetic Variants of MicroRNA and DROSHA Genes in Association With the Risk of Tuberculosis in the Amazon Population
    Leal, Diana Feio da Veiga Borges
    Santana da Silva, Mayara Natalia
    Pastana, Lucas Favacho
    Fernandes, Marianne Rodrigues
    Costa de Athayde, Aidalucy do Socorro
    Fernandes Porchera, Debora Christina Ricardo
    Silva, Cleonardo Augusto da
    Modesto, Antonio Andre Conde
    De Assumpcao, Paulo Pimentel
    Santos, Sidney Emanuel Batista dos
    Santos, Ney Pereira Carneiro dos
    FRONTIERS IN GENETICS, 2022, 13
  • [46] Association of liver X receptors (LXRs) genetic variants to gallbladder cancer susceptibility
    Sharma, Kiran Lata
    Misra, Sanjeev
    Kumar, Ashok
    Mittal, Balraj
    TUMOR BIOLOGY, 2013, 34 (06) : 3959 - 3966
  • [47] Effect of genetic variants of chemokine receptors on the development of myocardial infarction in Turkish population
    Karaali, Zeynep Ermis
    Sozen, Seyma
    Yurdum, Melis
    Cacina, Canan
    Toptas, Bahar
    Gok, Ozlem
    Agachan, Bedia
    MOLECULAR BIOLOGY REPORTS, 2010, 37 (07) : 3615 - 3619
  • [48] Association of JAK/STAT genetic variants with cutaneous melanoma
    Boas Gomez, Gabriela Vilas
    Lourenco, Gustavo Jacob
    Oliveira Monteiro, Lummy Maria
    Rocha, Rafael Silva
    McGrail Fernandez, Kimberly Anne
    Recio, Juan Angel
    Torricelli, Caroline
    Coser, Lilian Oliveira
    Rodrigues Oliveira, Alexandre Leite
    Carron, Juliana
    Moraes, Aparecida Machado
    Passos Lima, Carmen Silvia
    FRONTIERS IN ONCOLOGY, 2022, 12
  • [49] An Association Study of 13 SNPs from Seven Candidate Genes with Pediatric Asthma and a Preliminary Study for Genetic Testing by Multiple Variants in Taiwanese Population
    Wang, Jiu-Yao
    Liou, Ya-Huei
    Wu, Ying-Jye
    Hsiao, Ya-Hsin
    Wu, Lawrence Shih-Hsin
    JOURNAL OF CLINICAL IMMUNOLOGY, 2009, 29 (02) : 205 - 209
  • [50] Identifying novel genetic variants for brain amyloid deposition: a genome-wide association study in the Korean population
    Kim, Hang-Rai
    Jung, Sang-Hyuk
    Kim, Jaeho
    Jang, Hyemin
    Kang, Sung Hoon
    Hwangbo, Song
    Kim, Jun Pyo
    Kim, So Yeon
    Kim, Beomsu
    Kim, Soyeon
    Jeong, Jee Hyang
    Yoon, Soo Jin
    Park, Kyung Won
    Kim, Eun-Joo
    Yoon, Bora
    Jang, Jae-Won
    Hong, Jin Yong
    Choi, Seong Hye
    Noh, Young
    Kim, Ko Woon
    Kim, Si Eun
    Lee, Jin San
    Jung, Na-Yeon
    Lee, Juyoun
    Kim, Byeong C.
    Son, Sang Joon
    Hong, Chang Hyung
    Na, Duk L.
    Seo, Sang Won
    Won, Hong-Hee
    Kim, Hee Jin
    ALZHEIMERS RESEARCH & THERAPY, 2021, 13 (01)