Association of IL4 rs2070874, FoxP3 rs3761548 Polymorphisms with Keratoconus in Algeria

被引:3
|
作者
Meteoukki, Wafaa [1 ,2 ]
Fodil, Mostefa [2 ,3 ]
Negaz, Nawel Adda [2 ,4 ]
Rahmoun, Nesrine [1 ]
Hetraf, Sarah Lardjam [1 ]
Djellouli, Hadjira Ouhaibi [1 ]
Messal, Ahlem Djelti [1 ]
Abdi, Meriem [1 ]
Aberkane, Meriem Samia [1 ]
Chiali, Abdelillah [4 ]
Derdour, Amine [5 ]
Idder, Aicha [2 ,5 ]
Zemani-Fodil, Faouzia [1 ,2 ]
机构
[1] Univ Sci & Technol Oran Mohamed BOUDIAF USTO MB, Lab Genet Mol & Cellulaire LGMC, BP 1505, El Mnaouer 31000, Oran, Algeria
[2] Agence Themat Rech Sci Sante ATRSS, Oran, Algeria
[3] Ecole Super Sci Biol Oran ESSBO, Oran, Algeria
[4] Clin Chiali, Oran, Algeria
[5] Clin Hammou Boutlelis Oran, Lab Genet Med Appl Ophtalmol, Oran, Algeria
关键词
Case-Control Study; FOXP3; Gene; IL4; Keratoconus; Polymorphisms; Western Algeria; ALLERGIC RHINITIS; INTERLEUKIN-4; PROMOTER; GENE POLYMORPHISMS; ATOPIC DISEASE; ETHNIC-ORIGIN; ASTHMA; RISK; IL4;
D O I
10.18502/jovr.v16i4.9745
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: The aim of this case-control study was to determine the impact of environmental factors on the predisposition to develop keratoconus in a sample of Western Algerian population. Subsequently, we were interested in the implication of two single nucleotide polymorphisms (SNPs) IL4 rs2070874 and FOXP3 rs3761548, previously described as contributing to the occurrence of allergy, in the development of keratoconus. Methods: The study included 70 unrelated KC cases and 70 controls originating from Western Algeria. DNA genotyping was done using predesigned probe-based allelic discrimination TaqMan (R) assays. Allele and genotype frequencies were compared between the cases and controls by Chi-square test and odds ratios with 95% confidence intervals. Results: A significant association between risk factors such as family history, atopy, eye rubbing, and the development of keratoconus was found in our sample. Smoking would provide a protective effect against the pathology. No statistically significant differences were found in the allele and genotype frequencies between cases and controls neither for IL4 rs2070874 nor for FOXP3 rs3761548. Conclusion: Our study provides, for the first time, a clear demonstration of the absence of association of the allergy-associated IL4 and FOXP3 polymorphisms with KC in a sample from Western Algerian population.
引用
收藏
页码:558 / 565
页数:8
相关论文
共 50 条
  • [1] Association of Foxp3 rs3761548 polymorphism with cytokines concentration in gastric adenocarcinoma patients
    Ezzeddini, Rana
    Somi, Mohammad Hossein
    Taghikhani, Mohammad
    Moaddab, Seyyed-Yaghoub
    Shirazi, Kourosh Masnadi
    Shirmohammadi, Masoud
    Eftekharsadat, Amir Taher
    Moghaddam, Bizhan Sadighi
    Farrokhi, Amir Salek
    CYTOKINE, 2021, 138
  • [2] Association of FoxP3 rs3761548 polymorphism with susceptibility to colorectal cancer in the Chinese population
    Chen, Lei
    Yu, Qiming
    Liu, Bixia
    Zhu, Liming
    MEDICAL ONCOLOGY, 2014, 31 (12) : 1 - 4
  • [3] rs3761548 (C/A) and rs5902434 (del/ATT) polymorphisms of Foxp3 gene in Iranian patients with migraine
    Faraji, Fardin
    Mosayebi, Ghasem
    Bahrami, Maryam
    Shojapour, Mana
    EGYPTIAN JOURNAL OF MEDICAL HUMAN GENETICS, 2023, 24 (01)
  • [4] The role of FOXP3 rs3761548 and rs2294021 polymorphisms in pediatrics acute lymphoblastic leukemia: association with risk and response to therapy
    Zahra Ghasemi
    Kurosh Kalantar
    Zahra Amirghofran
    Molecular Biology Reports, 2021, 48 : 1139 - 1150
  • [5] Association of FoxP3 rs3761548 polymorphism with susceptibility to colorectal cancer in the Chinese population
    Lei Chen
    Qiming Yu
    Bixia Liu
    Liming Zhu
    Medical Oncology, 2014, 31
  • [6] The role of FOXP3 rs3761548 and rs2294021 polymorphisms in pediatrics acute lymphoblastic leukemia: association with risk and response to therapy
    Ghasemi, Zahra
    Kalantar, Kurosh
    Amirghofran, Zahra
    MOLECULAR BIOLOGY REPORTS, 2021, 48 (02) : 1139 - 1150
  • [7] Comments on: rs3761548 (C/A) and rs5902434 (del/ATT) polymorphisms of Foxp3 gene in Iranian patients with migraine
    Mostafa Saadat
    Egyptian Journal of Medical Human Genetics, 24
  • [8] rs3761548 (C/A) and rs5902434 (del/ATT) polymorphisms of Foxp3 gene in Iranian patients with migraine
    Fardin Faraji
    Ghasem Mosayebi
    Maryam Bahrami
    Mana Shojapour
    Egyptian Journal of Medical Human Genetics, 24
  • [9] Association of FOXP3 (rs3761548) promoter polymorphism with nondermatomal vitiligo: A study from India
    Jahan, Parveen
    Cheruvu, Rajeshwari
    Tippisetty, Surekha
    Komaravalli, Prasanna Latha
    Valluri, Vijayalakshmi
    Ishaq, Mohammed
    JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2013, 69 (02) : 262 - 266
  • [10] FOXP3 rs3761548 polymorphism is associated with knee osteoarthritis in a Turkish population
    Cekin, Nilgun
    Pinarbasi, Ergun
    Bildirici, Aslihan Esra
    Donmez, Gonca
    Oztemur, Zekeriya
    Bulut, Okay
    Arslan, Serdal
    INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES, 2018, 21 (10) : 1779 - 1786