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[肝豆状核变性携带者的临床特征]

[Clinical characteristics of the Wilson disease carrier].

作者信息

Zhou X X, He R X, Pu X Y, Li X H, Qin H L, Huang H W, Liang X L

机构信息

Department of Neurology, Huangpu Area, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510700, China.

Department of Image, Huangpu Area, the First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2019 Mar 19;99(11):806-811. doi: 10.3760/cma.j.issn.0376-2491.2019.11.002.

Abstract

To study the clinical symptoms, copper metabolism and imaging characteristics of Wilson disease (WD) carriers and to explore the treatment strategy of WD carriers. Forty WD carriers, 40 WD patients and 20 normal controls from the First Affiliated Hospital of Sun Yat-sen University from July 2007 to May 2018 were included. The modified Young scale was used for neural symptom scoring, and Child grading of liver function, mental symptoms rating scale, magnetic resonance imaging (MRI) scan, susceptibility weighted imaging (SWI) inspection, metal metabolism tests were also applied to all the included subjects. Corrected phase (CP) was measured by SWI. WD carriers were divided into symptomatic group and asymptomatic group. Symptomatic WD carriers were treated with penicillamine for 2 weeks and zinc gluconate for 3 months, then their neurological symptoms, liver function grade, metal metabolism index were rechecked. Six WD carriers presented with some clinical symptoms, including 5 with neurological symptoms and 4 with liver dysfunction. The score of Hamilton anxiety (HAMA) scale of symptomatic WD carriers was higher than that of normal control group (=0.021). 85% of carriers had ceruloplasmin level less than 0.26 g/L. 80% of carriers had serum copper between normal controls and WD patients. The free copper level of WD carriers was lower than that of WD patients (=0.012, 0.019). Urinary copper in symptomatic WD carriers was higher than normal controls (=0.047). The CP values of thalamus, globus pallidus and putamen in symptomatic WD carriers were lower than those in normal control group. After treatment with penicillamine in symptomatic WD carriers, urinary copper was higher than that before treatment (=0.036). After treatment, the liver enzymes of symptomatic WD carriers returned to normal, and the score of modified Young scale was lower than before treatment (=0.031). Mild copper metabolism abnormality is seen in WD carriers. A few carriers have neurological symptoms such as limb tremors, or liver symptoms such as abnormal liver enzymes. Abnormal copper metabolism is more serious in symptomatic WD carriers than in asymptomatic WD carriers. Symptomatic WD carriers can be treated with zinc gluconate.

摘要

研究肝豆状核变性(WD)携带者的临床症状、铜代谢及影像学特征,并探讨WD携带者的治疗策略。纳入2007年7月至2018年5月中山大学附属第一医院的40例WD携带者、40例WD患者及20例正常对照者。采用改良Young量表进行神经症状评分,同时对所有纳入对象应用肝功能Child分级、精神症状评定量表、磁共振成像(MRI)扫描、磁敏感加权成像(SWI)检查及金属代谢检测。通过SWI测量校正相位(CP)。将WD携带者分为有症状组和无症状组。对有症状的WD携带者给予青霉胺治疗2周,葡萄糖酸锌治疗3个月,然后复查其神经症状、肝功能分级、金属代谢指标。6例WD携带者出现一些临床症状,其中5例有神经症状,4例有肝功能异常。有症状的WD携带者汉密尔顿焦虑(HAMA)量表评分高于正常对照组(P=0.021)。85%的携带者血浆铜蓝蛋白水平低于0.26g/L。80%的携带者血清铜水平介于正常对照者与WD患者之间。WD携带者的游离铜水平低于WD患者(P=0.012,0.019)。有症状的WD携带者尿铜高于正常对照者(P=0.047)。有症状的WD携带者丘脑、苍白球及壳核的CP值低于正常对照组。有症状的WD携带者经青霉胺治疗后,尿铜高于治疗前(P=0.036)。治疗后,有症状的WD携带者肝酶恢复正常,改良Young量表评分低于治疗前(P=0.031)。WD携带者存在轻度铜代谢异常。少数携带者有肢体震颤等神经症状或肝酶异常等肝脏症状。有症状的WD携带者铜代谢异常比无症状的WD携带者更严重。有症状的WD携带者可采用葡萄糖酸锌治疗。

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