Cocco Eleonora, Murru Maria Rita, Melis Cristina, Schirru Lucia, Solla Elisabetta, Lai Marina, Rolesu Marcella, Marrosu Maria Giovanna
Dipartimento di Neuroscienze, Centro Sclerosi Multipla, Ospedale Binaghi, Via Is Guadazzonis, 2, 09126, Cagliari, Italy.
J Neurol. 2004 Sep;251(9):1085-8. doi: 10.1007/s00415-004-0485-1.
A linkage and association of the CD45 (protein-tyrosine phosphatase, receptor-type C) C77G polymorphism and multiple sclerosis (MS) has been found in some studies but not in others. We analysed the C77G polymorphism in MS patients from the genetically homogeneous population of Sardinia. Using the transmission disequilibrium test, the mutation has been sought in 241 patients and 217 healthy sibs (HS) from singleton MS families and it was found in 5 (2.07 %) affected and 3 (1.38%) HS from 7 heterozygous parents (1.45 %). Transmission of the G77 allele was 71.4 % (TDT = 1.3, P = 0.26) in patients and 50% (TDT = 0, P = 1) in HS. Stratifying families according to carriage of MS-predisposing (DR+) or not-predisposing (DR-) HLA-DR-DQ genotype in patients, percentage of G77 transmission to DR+ patients was 33 (TDT = 0.33, P = 0.56, Pc = 1.12), while it was 100 (TDT = 4, P = 0.045, Pc = 0.09) in the DR-patients. We concluded that, despite the presence of CD45 G77 polymorphism in a few patients who did not carry the HLADR- DQ MS-predisposing molecules, CD45 did not contribute to development of the disease in Sardinian MS.
一些研究发现CD45(蛋白酪氨酸磷酸酶,C型受体)C77G多态性与多发性硬化症(MS)之间存在连锁和关联,但其他研究未发现。我们分析了来自撒丁岛基因同质人群的MS患者的C77G多态性。使用传递不平衡检验,在来自单胎MS家庭的241例患者和217名健康同胞(HS)中寻找该突变,在7名杂合子父母的5例(2.07%)患者和3例(1.38%)HS中发现了该突变(1.45%)。患者中G77等位基因的传递率为71.4%(TDT = 1.3,P = 0.26),HS中为50%(TDT = 0,P = 1)。根据患者中携带MS易感(DR+)或非易感(DR-)HLA-DR-DQ基因型对家庭进行分层,DR+患者中G77传递的百分比为33(TDT = 0.33,P = 0.56,Pc = 1.12),而DR-患者中为100(TDT = 4,P = 0.045,Pc = 0.09)。我们得出结论,尽管在一些未携带HLA-DR-DQ MS易感分子的患者中存在CD45 G77多态性,但CD45对撒丁岛MS患者的疾病发展没有影响。