Association between FokI, ApaI and TaqI RFLP polymorphisms in VDR gene and Hashimoto's thyroiditis: preliminary data from female patients in Serbia.

Abstract:

:Hashimoto's thyroiditis (HT) is the most prevalent autoimmune thyroid disorder caused by an interaction between genes and environmental triggers. Intrathyroid lymphocytic infiltration may lead to progressive destruction of thyroid tissue and consequently to hypothyroidism. Many studies in different populations have shown association between vitamin D receptor (VDR) gene polymorphisms and various autoimmune diseases, including HT. The study included 44 female patients (mean age ± standard deviation 38 ± 5.4) with Hashimoto's thyroiditis and 32 healthy age-matched, sex-matched and geographically matched controls without personal history of autoimmune and endocrine diseases. Genomic DNA was isolated from peripheral blood-EDTA, and the target VDR gene was genotyped by PCR-RFLP technique after VDR-FokI (rs2228570), VDR-ApaI (rs7975232) and VDR-TaqI (rs731236) restriction enzymes digestion. We used spss 20.0 integrated software for data analysis and found a significant difference in the genotype distribution of VDR-FokI polymorphism between patients with HT and controls (P = 0.009). For ApaI and TaqI, we observed a higher frequency of variant allele in patients with HT, which was not significantly different compared to control women (P > 0.05). The current first and preliminary results identified the association between VDR-FokI gene polymorphism and Hashimoto's thyroiditis in Serbian population. Results need to be supported by further investigations that define haplotype patterns for VDR gene polymorphisms in a larger group of HT patients of both sexes.

journal_name

Int J Immunogenet

authors

Djurovic J,Stojkovic O,Ozdemir O,Silan F,Akurut C,Todorovic J,Savic K,Stamenkovic G

doi

10.1111/iji.12199

subject

Has Abstract

pub_date

2015-06-01 00:00:00

pages

190-4

issue

3

eissn

1744-3121

issn

1744-313X

journal_volume

42

pub_type

杂志文章
  • Genetic variants of the inflammatory C-reactive protein and schizophrenia in Armenian population: a pilot study.

    abstract::C-reactive protein (CRP) is an inflammation marker implicated in the pathogenesis of schizophrenia. To investigate association of the CRP rs1417938, rs1800947, rs1205 variants with susceptibility to schizophrenia 208 unrelated Armenians (103 patients and 105 healthy controls) were genotyped. In this pilot study, none ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2010.00942.x

    authors: Zakharyan R,Chavushyan A,Khoyetsyan A,Stahelova A,Arakelyan A,Boyajyan A,Mrazek F,Petrek M

    更新日期:2010-10-01 00:00:00

  • Mannose-binding lectin and MBL-associated serine protease-2 gene polymorphisms in a Brazilian population from Rio de Janeiro.

    abstract::Mannose-binding lectin (MBL) is a protein able to bind to carbohydrate patterns on pathogen membranes; upon MBL binding, its' associated serine protease MBL-associated serine protease type 2 (MASP2) is autoactivated, promoting the activation of complement via the lectin pathway. For both MBL2 and MASP2 genes, the freq...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.01052.x

    authors: Ferraroni NR,Segat L,Guimarães RL,Brandão LA,Crovella S,Constantino-Silva RN,Loja C,da Silva Duarte AJ,Grumach AS

    更新日期:2012-02-01 00:00:00

  • The first report of the human platelet alloantigen 4b allele in a Brazilian.

    abstract::The human platelet alloantigen (HPA) 4b allele is rarely observed in Caucasians and the observed incidence in Asians is usually lower than 1.0%. We report the first Brazilian with the allele HPA-4b, and were able to determined that he inherited it from his father. ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2005.00511.x

    authors: Toralles-Pereira C,de M C Pardini MI,Deffune E,Machado PE

    更新日期:2005-06-01 00:00:00

  • The association between BANK1 and TNFAIP3 gene polymorphisms and systemic lupus erythematosus: a meta-analysis.

    abstract::The past decade has witnessed hundreds of reports declaring or not being able to replicable genetic association with systemic lupus erythematosus (SLE) susceptibility. BANK1 is a gene that encodes a B-cell-specific scaffold protein and its activation can affect B-cell-receptor-induced calcium mobilization from intrace...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,meta分析

    doi:10.1111/j.1744-313X.2010.00990.x

    authors: Fan Y,Tao JH,Zhang LP,Li LH,Ye DQ

    更新日期:2011-04-01 00:00:00

  • The Pekin duck programmed death-ligand 1: cDNA cloning, genomic structure, molecular characterization and mRNA expression analysis.

    abstract::Programmed death ligand-1 (PD-L1) plays an important role in the attenuation of adaptive immune responses in higher vertebrates. Here, we describe the identification of the Pekin duck PD-L1 orthologue (duPD-L1) and its gene structure. The duPD-L1 cDNA encodes a 311-amino acid protein that has an amino acid identity of...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12175

    authors: Yao Q,Fischer KP,Tyrrell DL,Gutfreund KS

    更新日期:2015-04-01 00:00:00

  • HLA-DPB1, -DRB1, and -DQB1 polymorphism defined in Ewenki ethnic minority of China Inner Mongolia Autonomous Region.

    abstract::In the present study, DNA typing for human leucocyte antigen (HLA)-DPB1, -DRB1, and -DQB1 was performed using polymerase chain reaction-sequence-based-typing (PCR-SBT) method on 94 randomly selected, healthy, unrelated individuals from the Ewenki ethnic population in Inner Mongolia Autonomous Region of China. A total ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2007.00718.x

    authors: Su X,Bi L,Hai R,Qimuge S,Ying M,Bahring S,Gong M

    更新日期:2007-12-01 00:00:00

  • Using ESTs database to predict and validate single polymorphisms at the HLA system.

    abstract::We propose a bioinformatics pipeline in which we use an ESTs database to predict and validate single-nucleotide polymorphisms (SNPs) directly linked to gene-coding regions at the HLA class I genes (HLA-A, HLA-B and HLA-C). Annotation originated from our analysis revealed various classes of possible new variations that...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.01076.x

    authors: Figueiredo TC,de Oliveira JR

    更新日期:2012-06-01 00:00:00

  • Molecular approaches to transfusion medicine in Polynesians and Maori in New Zealand.

    abstract::In recent years, with the application of genotyping technology, there has been a substantial increase in the number of reported blood group alleles. This survey was designed to evaluate new molecular blood group genotyping methods and compile reference blood group data sets for Polynesian and Maori subjects. Subsequen...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12073

    authors: Edinur HA,Dunn PP,Lea RA,Chambers GK

    更新日期:2013-12-01 00:00:00

  • Vascular endothelial growth factor +405 G/C,-460 T/C and -2578 A/C polymorphisms are not associated with insulin resistance in polycystic ovary syndrome.

    abstract::Insulin resistance (IR) and pancreatic beta-cell dysfunction are usual comorbidities in polycystic ovary syndrome (PCOS). Vascular endothelial growth factor (VEGF) is known to play an important role in the pathogenesis of PCOS. This study examined firstly the possible association of common +405 G/C,-460 T/C and -2578 ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2010.00915.x

    authors: Vural P,Küskü-Kiraz Z,Doğru-Abbasoğlu S,Cil E,Karadağ B,Uysal M

    更新日期:2010-08-01 00:00:00

  • Solid phase testing in the HLA laboratory: implications for organ allocation.

    abstract::This piece was originally requested as a white paper from the Scientific and Clinical Affairs Committee of the American Society for Histocompatibility and Immunogenetics (ASHI), of which the author was then Chairman. Upon review by the ASHI Board of Directors and the Editors of their journal, it was considered too con...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,评审

    doi:10.1111/j.1744-313X.2008.00768.x

    authors: Eckels DD

    更新日期:2008-08-01 00:00:00

  • The dichotomy between disease phenotype databases and the implications for understanding complex diseases involving the major histocompatibility complex.

    abstract::Many genes related to innate and adaptive immunity reside within the major histocompatibility complex (MHC) and have been associated with a multitude of complex, immune-related disorders. Despite years of genetic study, this region has seen few causative determinants discovered for immune-mediated diseases. Reported a...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,评审

    doi:10.1111/iji.12236

    authors: Clark PM,Kunkel M,Monos DS

    更新日期:2015-12-01 00:00:00

  • The distributions of HLA-A, HLA-B, HLA-C, HLA-DRB1 and HLA-DQB1 allele and haplotype at high-resolution level in Zhejiang Han population of China.

    abstract::The distributions of HLA allele and haplotype are variable in different ethnic populations and the data for some populations have been published. However, the data on HLA-C and HLA-DQB1 loci and the haplotype of HLA-A, HLA-B, HLA-C, HLA-DRB1 and HLA-DQB1 loci at a high-resolution level are limited in Zhejiang Han popu...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12411

    authors: Chen N,Wang W,Wang F,Dong L,Zhao S,Zhang W,He J,Huang H,Zhu F

    更新日期:2019-02-01 00:00:00

  • The influence of glucocorticoid receptor single nucleotide polymorphisms on outcome after haematopoietic stem cell transplantation.

    abstract::Haematopoietic stem cell transplantation (HSCT) remains the only cure for most haematological malignancies, however, the mortality rate remains high. Complications after HSCT include relapse, graft versus host disease (GvHD), graft rejection and infection. Over the last few years several groups, have demonstrated that...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12380

    authors: Norden J,Pearce KF,Irving JAE,Collin MP,Wang XN,Wolff D,Kolb HJ,Socie G,Kuzmina Z,Greinix H,Holler E,Rocha V,Gluckman E,Hromadnikova I,Dickinson AM

    更新日期:2018-07-25 00:00:00

  • A chromosomal event resulting in possession and expression of multiple HLA-B and Cw genes in a renal patient.

    abstract::Routine HLA typing of a renal patient for purposes of registration for transplantation revealed an unusual human leucocyte antigen (HLA)-B and Cw genotype, with three specificities detected. Results were confirmed in a second sample, and in a second laboratory. The possibility of these results reflecting a chimaeric s...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2006.00610.x

    authors: Poole K,Montague B,Roberts R,Stoves J,Bendukidze N,Clark B

    更新日期:2006-08-01 00:00:00

  • HLA class II eplet mismatch load improves prediction of dnDSA development after living donor kidney transplantation.

    abstract::HLA donor-specific antibodies developed de novo after transplant remain a major cause of chronic allograft dysfunction. Our study main purpose was to determine whether HLA MM, assessed traditionally and by HLA total and AbVer eplet mismatch load (EptMM and EpvMM) assessed with HLAMatchMaker, had impact on dnDSA develo...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12519

    authors: Tafulo S,Malheiro J,Santos S,Dias L,Almeida M,Martins S,Pedroso S,Mendes C,Lobato L,Castro-Henriques A

    更新日期:2021-02-01 00:00:00

  • Cytokine typing: SNP allele frequencies in the Iranian population.

    abstract::Single nucleotide polymorphisms within the promoter or other regulatory sequences of cytokine genes were evaluated and compared between an Iranian population and populations of different ethnic/geographical background. In 40 healthy Iranian subjects, cytokine typing was performed by polymerase chain reaction-sequence-...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,收录出版

    doi:10.1111/j.1744-313X.2006.00595.x

    authors: Bagheri M,Abdi-Rad I,Omrani D,Khalkhali HR

    更新日期:2006-06-01 00:00:00

  • Immunophenotyping in peripheral blood mononuclear cells, aqueous humour and vitreous in a Blau syndrome patient caused by a novel NOD2 mutation.

    abstract::The genetic and immunophenotypic characteristics of a 3-year-old patient with Blau syndrome (BS), an early onset sarcoidosis caused by mutations in NOD2, were investigated. Molecular analysis of NOD2 gene was achieved by PCR and direct nucleotide sequencing. Immunophenotyping included cytometric analysis of memory-eff...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.00998.x

    authors: Jimenez-Martinez MC,Cruz F,Groman-Lupa S,Zenteno JC

    更新日期:2011-06-01 00:00:00

  • Association of tumour necrosis factor-alpha -308 G/A promoter polymorphism with susceptibility and disease profile of rheumatoid arthritis.

    abstract::The objective was to analyze the possible involvement of tumour necrosis factor-alpha (TNF-α) -308 G/A promoter polymorphism in the susceptibility and/or the disease profile of rheumatoid arthritis (RA) in Egyptian patients. TNF-α-308 G/promoter polymorphism detection by amplification refractory mutation system (ARMS)...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.01028.x

    authors: Mosaad YM,Abdelsalam A,El-Bassiony SR

    更新日期:2011-10-01 00:00:00

  • Coenzyme Q plays opposing roles on bacteria/fungi and viruses in Drosophila innate immunity.

    abstract::Coenzyme Q (CoQ or ubiquinone) is a lipid-soluble component of virtually all types of cell membranes and has been shown to play multiple metabolic functions. Several clinical diseases including encephalomyopathy, cerebellar ataxia and isolated myopathy were shown to be associated with CoQ deficiency. However, the role...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.01012.x

    authors: Cheng W,Song C,Anjum KM,Chen M,Li D,Zhou H,Wang W,Chen J

    更新日期:2011-08-01 00:00:00

  • HLA-A*11:53 is shown to be identical to the corrected A*11:02:01 allele sequence.

    abstract::According to the IMGT/HLA Database, the DNA sequence of A*11:53 is identical to A*11:02:01 in exons 2, 3, 4 and 5 except at codon 276. A*11:53 was reported as a rare variant of A*11, while A*11:02:01 was understood to be the second most frequently observed variant of A*11 after A*11:01:01 in Taiwanese. We sequenced HL...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01121.x

    authors: Yang KL,Chu CC,Marsh SG,Lin PY

    更新日期:2012-12-01 00:00:00

  • A clinical case-control study on the association between mannose-binding lectin and susceptibility to HIV-1 infection among northern Han Chinese population.

    abstract::Mannose-binding lectin (MBL) is a key molecule of the innate immune system and a competent to bind carbohydrates of a variety of microorganisms, resulting in complement activation and opsonophagocytosis against various pathogens. However, there is no systemic investigation on the MBL's role in innate immune responses ...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2010.00946.x

    authors: Sheng A,Lan J,Wu H,Lu J,Wang Y,Chu Q,Jia Z,Song M,Liu L,Wang W

    更新日期:2010-12-01 00:00:00

  • Th-1 cytokines gene polymorphism in human brucellosis.

    abstract::Brucellosis is a worldwide zoonosis. Infection with Brucella species results in the activation of cell-mediated immune response. The interaction between Th1and Th2 cytokines determines the outcome of disease. Production of each cytokine is in turn affected by genetic factors. In this study, we investigated the possibl...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2006.00626.x

    authors: Davoudi S,Amirzargar AA,Hajiabdolbaghi M,Rasoolinejad M,Soodbakhsh A,Jafari S,Piri H,Maleknejad P,Bagherian H,Madadi N,Nikbin B

    更新日期:2006-10-01 00:00:00

  • Association study of polymorphisms within matrix metalloproteinase 9 with bronchial asthma.

    abstract::Matrix metalloproteinase 9 plays an important role in the development of bronchial asthma. We were interested in whether the polymorphisms -T1702A, -C1562T, R279Q and +C6T within the matrix metalloproteinase 9 (MMP-9) gene were associated with asthma in a population of 231 asthmatic children. However, we found no asso...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2005.00516.x

    authors: Ganter K,Deichmann KA,Heinzmann A

    更新日期:2005-08-01 00:00:00

  • Molecular cloning and characterization of Th1 and Th2 cytokines of African buffalo (Syncerus caffer).

    abstract::The African buffalo (Syncerus caffer) has been implicated as the reservoir of several bovine infectious agents. However, there is insufficient information on the protective immune responses in the African buffalo, particularly in infected animals. In this study, we analysed Th1 cytokines IL-2 and IFN-γ, and Th2 cytoki...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2011.01062.x

    authors: Suzuki S,Konnai S,Okagawa T,Githaka NW,Kariuki E,Gakuya F,Kanduma E,Shirai T,Ikebuchi R,Ikenaka Y,Ishizuka M,Murata S,Ohashi K

    更新日期:2012-04-01 00:00:00

  • Genetic polymorphisms of tumour necrosis factor alpha (TNF-α) promoter gene and response to TNF-α inhibitors in Spanish patients with inflammatory bowel disease.

    abstract::Tumour necrosis factor alpha (TNF-α) has an important role in inflammatory response. Alterations in the regulation of TNF-α have been implicated in a variety of inflammatory disorders, including Inflammatory bowel disease (IBD). Indeed, a common treatment for IBD is the use of TNF-α inhibitors. Polymorphisms in the TN...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12059

    authors: López-Hernández R,Valdés M,Campillo JA,Martínez-Garcia P,Salama H,Salgado G,Boix F,Moya-Quiles MR,Minguela A,Sánchez-Torres A,Miras M,Garcia A,Carballo F,Álvarez-López MR,Muro M

    更新日期:2014-02-01 00:00:00

  • Investigation of JAK2, STAT3 and CCR6 polymorphisms and their gene-gene interactions in inflammatory bowel disease.

    abstract::Genome-wide association studies identified many loci associated with the two forms of inflammatory bowel disease (IBD), Crohn's disease (CD) and ulcerative colitis (UC). Components of the interleukin-23 signalling pathway, such as IL23R, JAK2 and STAT3, have been implicated in both diseases. In addition, emerging evid...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01084.x

    authors: Polgar N,Csongei V,Szabo M,Zambo V,Melegh BI,Sumegi K,Nagy G,Tulassay Z,Melegh B

    更新日期:2012-06-01 00:00:00

  • MHC class I polymorphic Alu insertion (POALIN) allele and haplotype frequencies in the Arabs of the United Arab Emirates and other world populations.

    abstract::Polymorphic Alu insertions (POALINs) are found throughout the human genome and have been used in various studies to infer geographic origin of human populations. The main aim of this study was to determine the allele and haplotype frequencies of five POALINs, AluHF, AluHG, AluHJ, AluTF and AluMICB, within the major hi...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/iji.12426

    authors: Kulski JK,Mawart A,Marie K,Tay GK,AlSafar HS

    更新日期:2019-08-01 00:00:00

  • No evidence for association of the TP53 12139 and the BAX-248 polymorphisms with endemic pemphigus foliaceus (fogo selvagem).

    abstract::Pemphigus foliaceus (PF) is an autoimmune bullous epidermal disease, characterized by autoantibodies specific to the desmosomal protein desmoglein 1 (dsg1) and by acantholysis, the rupture of the cellular junctions among keratinocytes. Known also as fogo selvagem (wild fire) in Brazil, the disease has distinct epidemi...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2006.00585.x

    authors: Köhler KF,Petzl-Erler ML

    更新日期:2006-04-01 00:00:00

  • HLA gene and haplotype frequencies in Russians, Bashkirs and Tatars, living in the Chelyabinsk Region (Russian South Urals).

    abstract::We have characterized the HLA-A, -B, -DRB1, -DQA1 and -DQB1 profiles of three major ethnic groups living in Chelyabinsk Region of Russian South Urals, viz., Russians (n = 207), Bashkirs (n = 146) and Tatars (n = 135). First field level typing was performed by PCR using sequence-specific primers. Estimates included car...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章

    doi:10.1111/j.1744-313X.2012.01117.x

    authors: Suslova TA,Burmistrova AL,Chernova MS,Khromova EB,Lupar EI,Timofeeva SV,Devald IV,Vavilov MN,Darke C

    更新日期:2012-10-01 00:00:00

  • HLA and disease: guilt by association.

    abstract::It is now over forty years since the first associations between particular HLA antigens and disease susceptibility were described, and the identification of large numbers HLA-associated diseases parallels our increased understanding of the genetic complexity of the HLA system and its extensive polymorphism. However, s...

    journal_title:International journal of immunogenetics

    pub_type: 杂志文章,评审

    doi:10.1111/iji.12088

    authors: Howell WM

    更新日期:2014-02-01 00:00:00