CTLA-4+49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients

被引:8
|
作者
Cizmarevic, N. Starcevic [1 ]
Gasparovic, I. [2 ]
Peterlin, B. [3 ]
Sepcic, J. [4 ]
Rudolf, G. [3 ]
Kapovic, M. [1 ]
Lavtar, P. [3 ]
Ristic, S. [1 ]
机构
[1] Univ Rijeka, Sch Med, Dept Biol & Med Genet, Rijeka 51000, Croatia
[2] Clin Hosp Ctr Rijeka, Dept Neurol, Rijeka, Croatia
[3] Univ Med Ctr Ljubljana, Inst Med Genet, Ljubljana, Slovenia
[4] Univ Rijeka, Sch Med, Postgrad Study, Rijeka 51000, Croatia
关键词
TYPE-1; DIABETES-MELLITUS; NO EVIDENCE; CLINICAL-COURSE; CTLA4; SUSCEPTIBILITY; ASSOCIATION; RISK; METAANALYSIS; DIMORPHISMS; PROGRESSION;
D O I
10.1111/j.1744-313X.2011.01027.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Polymorphisms in the CTLA-4 gene are known to be important in several autoimmune diseases, including multiple sclerosis (MS). Previous studies on the impact of CTLA-4 +49 A/G gene polymorphism have given contradictory results. We investigated the possible influence of this polymorphism on MS susceptibility and disease behaviour in Croatian and Slovenian populations. Genotyping was performed in 367 patients with MS and 480 control subjects using PCR-RFLP method. The G allele was present in 216 (58.9%) patients with MS vs. 282 (58.7%) healthy controls (P = 0.975, OR = 1.01, 95% CI = 0.76-1.32). No significant differences were observed in CTLA-4 +49 A or G allele distribution between patients and controls, indicating that this polymorphism does not influence susceptibility to MS in the surveyed populations. No correlation was observed between G allele carrier status and age at disease onset, disease course or severity.
引用
收藏
页码:419 / 426
页数:8
相关论文
共 50 条
  • [31] No association of CCR5Δ32 gene mutation with multiple sclerosis in Croatian and Slovenian patients
    Ristic, S
    Lovrecic, L
    Starcevic-Cizmarevic, N
    Brajenovic-Milic, B
    Jazbec, SS
    Barac-Latas, V
    Vejnovic, D
    Sepcic, J
    Kapovic, M
    Peterlin, B
    MULTIPLE SCLEROSIS, 2006, 12 (03): : 360 - 362
  • [32] CTLA4+49 A/G POLYMORPHISM IN TUNISIAN BEHCET'S DISEASE PATIENTS
    Ben Dhifallah, I.
    Smiti-Khanfir, M.
    Braham-Sfaxi, A.
    Hamzaoui, A.
    Houman, M. H.
    CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 2008, 26 (04) : S10 - S10
  • [33] A49G polymorphism in exon 1 of the CTLA-4 gene in Slovene patients with autoimmune thyroid disease
    Krhin, B
    Zaletel, K
    Gaberscek, S
    Hojker, S
    CLINICAL CHEMISTRY, 2005, 51 : A241 - A241
  • [34] Recipient CTLA-4+49 G/G genotype is associated with reduced incidence of acute rejection after liver transplantation
    de Reuver, P
    Pravica, V
    Hop, W
    Boor, P
    Metselaar, HJ
    Hutchinson, IV
    Tilanus, HW
    Kwekkeboom, J
    AMERICAN JOURNAL OF TRANSPLANTATION, 2003, 3 (12) : 1587 - 1594
  • [35] Progression of multiple sclerosis is associated with exon 1 CTLA-4 gene polymorphism
    Bilinska, M
    Frydecka, I
    Noga, L
    Dobosz, T
    Zoledziewska, M
    Suwalska, K
    Tutak, A
    Pokryszko-Dragan, A
    ACTA NEUROLOGICA SCANDINAVICA, 2004, 110 (01): : 67 - 71
  • [36] Lack of association of CTLA-4 polymorphism 49 (A→G) with migraine
    Trabace, S
    Morellini, M
    Lulli, P
    Cicciarelli, G
    Coloprisco, G
    De Filippis, S
    Santi, PG
    Rodio, A
    Fiore, G
    Martelletti, P
    CEPHALALGIA, 2003, 23 (07) : 663 - 663
  • [37] Association of CTLA-4 exon 1+49 gene polymorphism with treatment response on betaferon therapy in population of multiple sclerosis patients in Serbia and Montenegro
    Dincic, E.
    Zivkovic, M.
    Toncev, G.
    Vujisic, S.
    Popovic, S.
    Stankovic, A.
    Rakovic, A.
    Alavantic, D.
    Raicevic, R.
    MULTIPLE SCLEROSIS JOURNAL, 2006, 12 : S190 - S190
  • [38] Analysis of CTLA4 gene 49A/G polymorphism association with development of allergic rhinitis
    Alieva, V. Sh.
    Karimov, Kh. Ya.
    Nazarov, A. A.
    Arifov, S. S.
    Boboev, K. T.
    CYTOLOGY AND GENETICS, 2010, 44 (03) : 140 - 143
  • [39] Analysis of CTLA4 gene 49A/G polymorphism association with development of allergic rhinitis
    V. Sh. Alieva
    Kh. Ya. Karimov
    A. A. Nazarov
    S. S. Arifov
    K. T. Boboev
    Cytology and Genetics, 2010, 44 : 140 - 143
  • [40] Analysis of CTLA-4+49A/G gene polymorphism in cases with leprosy of Azerbaijan, Northwest Iran
    Almasi, Shohreh
    Aliparasti, Mohammad Reza
    Naghili, Behrouz
    Yeganeh, Khalil
    Rahnama, Badrossadat
    Tavanafar, Fatemeh
    Karzar, Bita Hazhir
    Khiabani, Syamak Amini
    Naghili, Arman
    Babaloo, Zohreh
    INFECTION GENETICS AND EVOLUTION, 2018, 57 : 121 - 127