Lane N E, Lian K, Nevitt M C, Zmuda J M, Lui L, Li J, Wang J, Fontecha M, Umblas N, Rosenbach M, de Leon P, Corr M
University of California at San Francisco, USA.
Arthritis Rheum. 2006 Apr;54(4):1246-54. doi: 10.1002/art.21673.
To examine the association of the Arg200Trp and Arg324Gly variants of FRZB with the risk and phenotype of radiographic osteoarthritis (OA) of the hip and serum levels of Frizzled-related protein (FRP) in a prospective cohort of elderly Caucasian women.
Radiographic hip OA status of patients was defined by the presence of severe joint space narrowing (JSN) (feature grade>or=3), a summary grade>or=3, or definite osteophytes (grade>or=2) and JSN (grade>or=2) in the same hip. Genotypes were obtained in 569 patients with radiographic OA of the hip and in 1,317 and 4,136 controls for the Arg200Trp and Arg324Gly variants, respectively. Serum FRP levels were measured by enzyme-linked immunosorbent assay. Multivariate logistic regression was performed.
The minor allele frequency for the Arg200Trp polymorphism was 0.12 in the control group compared with 0.14 in the group with radiographic OA of the hip (P=0.12), and the minor allele frequency for the Arg324Gly variant was 0.083 in the control group compared with 0.088 in the group with radiographic OA of the hip (P=0.63). The multilocus genotypes available in 1,886 subjects suggested that inheritance of both minor alleles was a risk factor for developing OA characterized by JSN (P<0.01). Patients with radiographic OA of the hip who were homozygous for the Arg200Trp minor allele had higher serum FRP levels than controls who were homozygous for the major allele.
Our data confirm findings of another study, that a rare haplotype with both Arg200Trp and Arg324Gly FRZB variants contributes to the genetic susceptibility to hip OA among Caucasian women, and that these polymorphisms may contribute to increased serum levels of proteins as biomarkers of OA.
在一个老年白种女性前瞻性队列中,研究FRZB基因的Arg200Trp和Arg324Gly变异与髋关节放射学骨关节炎(OA)风险、表型以及卷曲相关蛋白(FRP)血清水平之间的关联。
患者的髋关节放射学OA状态通过同一髋关节存在严重关节间隙狭窄(JSN)(特征分级≥3级)、综合分级≥3级或明确骨赘(分级≥2级)且伴有JSN(分级≥2级)来定义。分别在569例髋关节放射学OA患者以及1317例和4136例对照中获取Arg200Trp和Arg324Gly变异的基因型。通过酶联免疫吸附测定法测量血清FRP水平。进行多因素逻辑回归分析。
对照组中Arg200Trp多态性的次要等位基因频率为0.12,而髋关节放射学OA组为0.14(P = 0.12);对照组中Arg324Gly变异的次要等位基因频率为0.083,髋关节放射学OA组为0.088(P = 0.63)。1886名受试者的多位点基因型表明,两个次要等位基因的遗传是发生以JSN为特征的OA的危险因素(P < 0.01)。髋关节放射学OA患者中,Arg200Trp次要等位基因纯合子的血清FRP水平高于主要等位基因纯合子的对照组。
我们的数据证实了另一项研究的结果,即同时具有Arg200Trp和Arg324Gly FRZB变异的罕见单倍型会导致白种女性对髋关节OA的遗传易感性,并且这些多态性可能导致作为OA生物标志物的蛋白质血清水平升高。