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

被引:7
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 [J].
BAKER, JR ;
ARSCOTT, P ;
JOHNSON, 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 [J].
Balmiki, Nisha ;
Bankura, Biswabandhu ;
Guria, Srikanta ;
Das, Tapas Kumar ;
Pattanayak, Arup Kumar ;
Sinha, Anirban ;
Chakrabarti, Sudipta ;
Chowdhury, Subhankar ;
Das, Madhusudan .
ENDOCRINE JOURNAL, 2014, 61 (03) :289-296
[3]   Thyroid Autoantibodies in Pregnancy: Their Role, Regulation and Clinical Relevance [J].
Balucan, Francis S. ;
Morshed, Syed A. ;
Davies, Terry F. .
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 [J].
Brix K. ;
Führer D. ;
Biebermann H. .
Thyroid Research, 4 (Suppl 1)
[6]   Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community [J].
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. .
CLINICAL ENDOCRINOLOGY, 2013, 79 (02) :275-281
[7]   The human anti-thyroid peroxidase autoantibody repertoire in Graves' and Hashimoto's autoimmune thyroid diseases [J].
Chardès, T ;
Chapal, N ;
Bresson, D ;
Bès, C ;
Giudicelli, V ;
Lefranc, MP ;
Péraldi-Roux, S .
IMMUNOGENETICS, 2002, 54 (03) :141-157
[8]   Pseudodominant inheritance of goitrous congenital hypothyroidism caused by TPO mutations:: Molecular and in silico studies [J].
Deladoeey, Johnny ;
Pfarr, Nicole ;
Vuissoz, Jean-Marc ;
Parma, Jasmine ;
Vassart, Gilbert ;
Biesterfeld, Stefan ;
Pohlenz, Joachim ;
Van Vliet, Guy .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (02) :627-633
[9]   Subclinical Hypothyroidism: An Update for Primary Care Physicians [J].
Fatourechi, Vahab .
MAYO CLINIC PROCEEDINGS, 2009, 84 (01) :65-71
[10]   Total iodide organification defect: Clinical and molecular characterization of an Italian family [J].
Fugazzola, L ;
Mannavola, D ;
Vigone, MC ;
Cirello, V ;
Weber, G ;
Beck-Peccoz, P ;
Persani, L .
THYROID, 2005, 15 (09) :1085-1088