实用肝脏病杂志 ›› 2014, Vol. 17 ›› Issue (4): 392-396.doi: 10.3969/j.issn.1672-5069.2014.04.015

• 肝豆状核变性 • 上一篇    下一篇

不同临床分型的Wilson’s病临床特点分析

陈宇宁, 王锦辉, 薛立峰, 林述洲, 林耿鹏, 陈旻湖   

  1. 510080广州市 中山大学附属第一医院消化内科(陈宇宁); 惠州市第三人民医院消化内科(王锦辉,薛立峰,林耿鹏,陈旻湖)
  • 收稿日期:2014-01-03 出版日期:2014-08-30 发布日期:2016-04-11
  • 通讯作者: 王锦辉,E-mail:jinhuiwang2009@163.com
  • 作者简介:陈宇宁,进修医生,原单位为惠州市第三人民医院

Clinical features of patients with Wilson's disease in different clinical classification

Chen Yuning, Wang Jinhui, Xue Lifeng   

  1. Department of Gastroenterology and Hepatology,First Affiliated Hospital, Sun Yetsen University,Guangzhou 510080,Guangdong Province,China
  • Received:2014-01-03 Online:2014-08-30 Published:2016-04-11

摘要: 目的探讨不同亚型Wilson’s病(WD)的临床特点及肝型患者预后转归。方法收集256例WD患者的临床资料并随访,根据临床表现将患者分为不同的临床亚型,进一步分析比较肝型、脑型和混合型WD患者的临床特点差异和随访追踪肝型WD患者的预后。结果在256例WD患者中,以混合型(152例,59.4%)和肝型(74例,28.9%)患者常见,而脑型(27例,10.5%)和其他亚型(3例,1.2%)较少;肝型WD患者失代偿期肝硬化比例(78.4%)高于混合型患者(22.0%,P<0.001);肝型WD患者肝脏血清生化学指标(转氨酶、ALP、GGT、胆红素以及球蛋白水平)高于混合型WD患者(P<0.05);肝型WD患者血清铜[(1.04±1.50) mg/L]水平明显低于脑型WD患者[(2.96±2.88) mg/L]和混合型WD患者[(2.34±2.68) mg/L,P<0.001],但两者铜蓝蛋白和尿铜水平无统计学差异(P>0.05);肝型WD患者K-F环检出率(64.9%)低于脑型WD患者(92.6%)和混合型WD患者(90.1%,P<0.05);经Logistic回归分析显示角膜K-F的有无与年龄(OR=0.922,P=0.014)、血清铜蓝蛋白 (OR=35902.1,P=0.015)相关;平均随访31例肝型WD患者(8.3±5.8)年,3例(9.7%)进展为混合型WD患者。结论WD以混合型和肝型最多见,肝型患者肝脏损害比混合型更为严重,提示肝脏是WD最主要的靶器官。

关键词: 肝豆状核变性, 铜代谢, 临床分型, 临床特点

Abstract: Objective To investigate the clinical features of patients with Wilson’s disease(WD) in different clinical classification. Methods Clinical data of 256 inpatients with WD were collected retrospectively. The patients were then divided into liver type,cerebral type and mixed type according to their major clinical presentations and the differences in clinical features of patients in each group were further analyzed. Results Among 256 patients with WD,patients with mixed type (152 cases,59.4%) and liver type(74cases,28.9%)were the common type as compared to cerebral type (27cases,10.5%) or other subtypes(3 cases,1.2%). The ratio of patients with decompensated cirrhosis and the levels of various liver serum biochemical parameters (ALT,AST,ALP,GGT,BIL and GLB) in patients with liver type (78.4%) were higher than in patient with mixed type (22.0%,P<0.05). Serum copper in patients with liver type [(1.04±1.50)mg/L] were lower than patients with cerebra type [(2.96±2.88) mg/L] and mixed type [(2.34±2.68)mg/L,P<0.001],but no difference in serum ceruloplasmin level and 24-h urinary copper excretion between the two groups(P>0.05). The positive ratio of Kayser-Fleischer rings in patients with liver type (64.9%) was lower than in patients with cerebral type (92.6%) and mixed type (90.1%,P<0.05). A logistic regression analysis showed that age (OR 0.922,P=0.014) and serum ceruloplasmin level (OR=35902.1,P=0.015) were related to the presence of Kayser-Fleischer rings. Only 3(9.7%) out of 31 patients with WD with liver type developed into mixed type during the average follow-up of(8.3±5.8) years. Conclusions Mixed and liver type are more common in patients with WD,and liver dysfunction is more severe in patients with liver type than in mixed type,suggesting that the liver is the most common target in WD.

Key words: Wilson’, s disease, Copper metabolism, Clinical classification, Clinical features