Association of Thyroid Peroxidase Gene Polymorphisms and Serum Anti-TPO Levels in Egyptian Patients with Autoimmune Hypothyroidism

被引:5
作者
Ahmed, Hanan S. [1 ]
Nsrallah, Ayman A. M. [2 ]
Abdel-Fatah, Azza H. [2 ]
Mahmoud, Amira A. [2 ]
Fikry, Abeer A. [1 ]
机构
[1] Zagazig Univ, Fac Med, Clin Pathol Dept, Zagazig, Egypt
[2] Zagazig Univ, Fac Med, Internal Med Dept, Zagazig, Egypt
关键词
Autoimmune; hypothyroidism; thyroid peroxidase; HD; TPO; polymorphism; ANTIBODIES; MUTATIONS; DISEASE; SCORE;
D O I
10.2174/1871530320666200715101907
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Thyroid peroxidase (TPO) gene mutation leads to a change in enzyme built structure resulting in the anti-TPO autoantibodies production that may cause thyroid destruction. Aim: To evaluate the association of three single nucleotide polymorphisms (SNPs) of the TPO gene and anti-TPO levels in Egyptian patients with autoimmune hypothyroidism and correlate them with the disease severity. Methods: Two hundred patients with newly discovered autoimmune hypothyroidism were included in the study (100 with subclinical hypothyroidism and 100 of them with overt hypothyroidism) and 100 healthy individuals as a control group were genotyped by PCR-REFLP. Results: The TT genotype of rs2071400 C/T and the T allele were significantly more frequent in patients with subclinical hypothyroidism and overt hypothyroidism than in the control group. But there were no significant differences in the TT genotype and T allele between subclinical and overt hypothyroidism patients. As regards TPO rs732609 A/C polymorphism, the CC genotype of rs732609 A/C and the C allele were significantly increased in patients with subclinical hypothyroidism and overt hypothyroidism than in controls. There was a significant difference in the CC genotype and C allele between subclinical and overt hypothyroidism patients. Concerning TPO rs1126797 C/T polymorphism, there were no significant differences of genotype or allele frequencies between patients groups and control group. Conclusion: We found an association of rs2071400 C/T and rs732609A/C polymorphisms with autoimmune hypothyroidism and correlated anti-TPO levels with different genotypes in hypothyroid patients. Also, we found an association of rs732609A/C polymorphism with the disease severity.
引用
收藏
页码:734 / 742
页数:9
相关论文
共 25 条
  • [1] AN ANALYSIS OF THE STRUCTURE AND ANTIGENICITY OF DIFFERENT FORMS OF HUMAN THYROID PEROXIDASE
    BAKER, JR
    ARSCOTT, P
    JOHNSON, J
    [J]. THYROID, 1994, 4 (02) : 173 - 178
  • [2] Genetic analysis of thyroid peroxidase (TPO) gene in patients whose hypothyroidism was found in adulthood in West Bengal, India
    Balmiki, Nisha
    Bankura, Biswabandhu
    Guria, Srikanta
    Das, Tapas Kumar
    Pattanayak, Arup Kumar
    Sinha, Anirban
    Chakrabarti, Sudipta
    Chowdhury, Subhankar
    Das, Madhusudan
    [J]. ENDOCRINE JOURNAL, 2014, 61 (03) : 289 - 296
  • [3] Thyroid Autoantibodies in Pregnancy: Their Role, Regulation and Clinical Relevance
    Balucan, Francis S.
    Morshed, Syed A.
    Davies, Terry F.
    [J]. JOURNAL OF THYROID RESEARCH, 2013, 2013
  • [4] Berg M.J., 2012, PROTEIN COMPOSITION, P368
  • [5] Molecules important for thyroid hormone synthesis and action - Known facts and future perspectives
    Brix K.
    Führer D.
    Biebermann H.
    [J]. Thyroid Research, 4 (Suppl 1)
  • [6] Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community
    Cangul, Hakan
    Aycan, Zehra
    Olivera-Nappa, Alvaro
    Saglam, Halil
    Schoenmakers, Nadia A.
    Boelaert, Kristien
    Cetinkaya, Semra
    Tarim, Omer
    Bober, Ece
    Darendeliler, Feyza
    Bas, Veysel
    Demir, Korcan
    Aydin, Banu K.
    Kendall, Michaela
    Cole, Trevor
    Hoegler, Wolfgang
    Chatterjee, V. Krishna K.
    Barrett, Timothy G.
    Maher, Eamonn R.
    [J]. CLINICAL ENDOCRINOLOGY, 2013, 79 (02) : 275 - 281
  • [7] The human anti-thyroid peroxidase autoantibody repertoire in Graves' and Hashimoto's autoimmune thyroid diseases
    Chardès, T
    Chapal, N
    Bresson, D
    Bès, C
    Giudicelli, V
    Lefranc, MP
    Péraldi-Roux, S
    [J]. IMMUNOGENETICS, 2002, 54 (03) : 141 - 157
  • [8] Pseudodominant inheritance of goitrous congenital hypothyroidism caused by TPO mutations:: Molecular and in silico studies
    Deladoeey, Johnny
    Pfarr, Nicole
    Vuissoz, Jean-Marc
    Parma, Jasmine
    Vassart, Gilbert
    Biesterfeld, Stefan
    Pohlenz, Joachim
    Van Vliet, Guy
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (02) : 627 - 633
  • [9] Subclinical Hypothyroidism: An Update for Primary Care Physicians
    Fatourechi, Vahab
    [J]. MAYO CLINIC PROCEEDINGS, 2009, 84 (01) : 65 - 71
  • [10] Total iodide organification defect: Clinical and molecular characterization of an Italian family
    Fugazzola, L
    Mannavola, D
    Vigone, MC
    Cirello, V
    Weber, G
    Beck-Peccoz, P
    Persani, L
    [J]. THYROID, 2005, 15 (09) : 1085 - 1088