Association of the HLA-DRB1 alleles with characteristic MRI features of Asian multiple sclerosis

被引:26
|
作者
Matsuoka, T. [1 ]
Matsushita, T. [1 ]
Osoegawa, M. [1 ]
Kawano, Y. [1 ]
Minohara, M. [1 ]
Mihara, F. [2 ]
Nishimura, Y. [3 ]
Ohyagi, Y. [1 ]
Kira, J. [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Neurol Inst, Dept Neurol,Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Radiol, Div Neuroradiol, Fukuoka 8128582, Japan
[3] Kumamoto Univ, Grad Sch Med Sci, Dept Neurosci & Immunol, Div Immunogenet, Kumamoto, Japan
关键词
aquaporin-4; genetics; human leukocyte antigen; MRI; multiple sclerosis;
D O I
10.1177/1352458508097818
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background In Asian patients with multiple sclerosis ( MS), a paucity of brain lesions and longitudinally extensive spinal cord lesions (LESCLs) extending three or more vertebral segments are characteristic findings on magnetic resonance imaging (MRI). We aimed to disclose possible factors contributing to the development of such MRI features. Method Genotyping of HLA-DRB1 and -DPB1 alleles was performed in 121 consecutive Japanese patients with clinically definite MS based on the Poser criteria and 125 healthy controls. Possible factors associated with MRI features were determined by multiple logistic analysis. Patients with MS were classified based on the presence or absence of brain lesions fulfilling the Barkhof criteria (Barkhof brain lesions) and LESCLs. Barkhof brain lesion-negative (-) patients had a markedly lower frequency of HLA-DRB1*0901 than controls (P-corr < 0.05), whereas the frequency of DRB1*1501 was increased in the Barkhof brain lesion-positive (+) group, although this increase was not significant after correction. No Barkhof(-)LESCL(+) patients carried DRB1*0901 (P-corr < 0.05), despite this being the most common allele in Japanese. The Barkhof(-) LESCL(-) group showed a significant increase in the frequency of DRB1*0405 compared with controls (P-corr < 0.05). None of the DPB1 alleles were significantly different among the groups. Using multiple logistic analysis, the absence of oligoclonal bands was positively associated with an absence of Barkhof brain lesions, whereas a higher EDSS score was positively associated with the presence of LESCLs; however, the presence of anti-aquaporin-4 antibodies was not associated with either feature. Conclusion The characteristic MRI features in Asians are partly related to distinct HLA-DRB1 gene alleles and an absence of oligoclonal bands. Multiple Sclerosis 2008; 14: 1181-1190. http://msj.sagepub.com
引用
收藏
页码:1181 / 1190
页数:10
相关论文
共 50 条
  • [41] Association of HLA-DRB1, DQB1 Alleles with Chronic Urticaria
    陈静
    谭志建
    李家文
    熊平
    华中科技大学学报(医学英德文版), 2005, (03) : 354 - 356
  • [42] Association of HLA-DRB1, DQB1 alleles with chronic urticaria
    Chen Jing
    Tan Zhijian
    Li Liawen
    Xiong Ping
    Current Medical Science, 2005, 25 (3) : 354 - 356
  • [43] An extremes of outcome strategy provides evidence that multiple sclerosis is determined by alleles at the HLA-DRB1 locus
    DeLuca, G. C.
    Ramagopalan, S. V.
    Herrera, B. M.
    Dymentt, D. A.
    Lincoln, M. R.
    Montpetit, A.
    Pugliattill, M.
    Barnardo, M. C. N.
    Risch, N. J.
    Sadovnick, A. D.
    Chao, M.
    Sotgiu, S.
    Hudson, T. J.
    Ebers, G. C.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (52) : 20896 - 20901
  • [44] The influence of HLA-DRB1 alleles on the susceptibility and resistance to multiple sclerosis with respect to the criteria of neuromyelitis optica
    Isobe, N.
    Matsushita, T.
    Yamasaki, R.
    Ramagopalan, S. V.
    Kawano, Y.
    Nishimura, Y.
    Ebers, G. C.
    Kira, J.
    MULTIPLE SCLEROSIS, 2010, 16 (02): : 270 - 270
  • [45] Multiple sclerosis, vitamin D, and HLA-DRB1*15
    Handunnetthi, Lahiru
    Ramagopalan, Sreeram V.
    Ebers, George C.
    NEUROLOGY, 2010, 74 (23) : 1905 - 1910
  • [46] Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis
    Barcellos, Lisa F.
    Sawcer, Stephen
    Ramsay, Patricia P.
    Baranzini, Sergio E.
    Thomson, Glenys
    Briggs, Farren
    Cree, Bruce C. A.
    Begovich, Ann B.
    Villoslada, Pablo
    Montalban, Xavier
    Uccelli, Antonio
    Savettieri, Giovanni
    Lincoln, Robin R.
    DeLoa, Carolyn
    Haines, Jonathan L.
    Pericak-Vance, Margaret A.
    Compston, Alastair
    Hauser, Stephen L.
    Oksenberg, Jorge R.
    HUMAN MOLECULAR GENETICS, 2006, 15 (18) : 2813 - 2824
  • [47] Parental transmission of HLA-DRB1*15 in multiple sclerosis
    Ramagopalan, Sreeram V.
    Herrera, Blanca M.
    Bell, Jordana T.
    Dyment, David A.
    DeLuca, Gabriele C.
    Lincoln, Matthew R.
    Orton, Sarah M.
    Chao, Michael J.
    Sadovnick, A. Dessa
    Ebers, George C.
    HUMAN GENETICS, 2008, 122 (06) : 661 - 663
  • [48] HLA-DRB1 susceptibility in multiple sclerosis Algerian patients
    Hecham, N.
    Tazir, M.
    Boudjella, M. L.
    Benhalima, M.
    Pacha, L. Ali
    MULTIPLE SCLEROSIS JOURNAL, 2021, 27 (2_SUPPL) : 360 - 361
  • [49] Parental transmission of HLA-DRB1*15 in multiple sclerosis
    Sreeram V. Ramagopalan
    Blanca M. Herrera
    Jordana T. Bell
    David A. Dyment
    Gabriele C. DeLuca
    Matthew R. Lincoln
    Sarah M. Orton
    Michael J. Chao
    A. Dessa Sadovnick
    George C. Ebers
    Human Genetics, 2008, 122 : 661 - 663
  • [50] HLA-DRB1 and Month-of-Birth in Multiple Sclerosis
    Ebers, George C.
    Ramagopalan, Sreeram V.
    Link, Jenny
    Sadovnick, Dessa
    Harbo, Hanne
    Hillert, Jan
    ANNALS OF NEUROLOGY, 2009, 66 : S66 - S66