Chen Z Y, Fedrick J A, Pandey J P, Silver R, Maricq H R, Fudenberg H H, Dobson R L, Ainsworth S K
Arch Dermatol. 1985 Mar;121(3):339-44.
Fifty-five unrelated whites with disorders in the scleroderma spectrum who had both antinuclear antibodies and Raynaud's phenomenon (RP) were studied. Of the 22 patients with anticentromere antibody (ACA), three had diffuse scleroderma; 16 had the complete or incomplete syndrome of calcinosis, RP, esophageal dysmotility, sclerodactyly, and telangiectasia (CREST syndrome); and three had RP only. Thirty-three patients with other nuclear patterns all had systemic scleroderma (28 diffuse scleroderma, five CREST syndrome). Patients with ACA had less organ system involvement, and lower frequencies of anemia and elevation of sedimentation rate than ACA-negative patients, but these differences were not statistically significant. They also had fewer manifestations of CREST syndrome. All 55 patients were studied for the Gm and Km allotypic markers. No association was found between Gm or Km allotypic markers and scleroderma or between the allotypic markers and the presence of ACA.
对55名患有硬皮病谱系疾病的无血缘关系的白人进行了研究,这些患者均有抗核抗体和雷诺现象(RP)。在22名抗着丝点抗体(ACA)阳性患者中,3例患有弥漫性硬皮病;16例患有钙质沉着、雷诺现象、食管动力障碍、指端硬化和毛细血管扩张的完全或不完全综合征(CREST综合征);3例仅有雷诺现象。33例具有其他核型的患者均患有系统性硬皮病(28例弥漫性硬皮病,5例CREST综合征)。ACA阳性患者的器官系统受累较少,贫血和血沉升高的频率低于ACA阴性患者,但这些差异无统计学意义。他们的CREST综合征表现也较少。对所有55例患者进行了Gm和Km同种异型标记物研究。未发现Gm或Km同种异型标记物与硬皮病之间或同种异型标记物与ACA存在之间有相关性。