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眼咽型肌营养不良症在中国是一种被低估的疾病吗?报告一例中国出生的携 PABPN1 突变的患者,并对文献进行流行病学回顾。

Oculopharyngeal muscular dystrophy --an under-diagnosed disease in China? Report a China-born Chinese with PABPN1 mutation and epidemiology review of the literature.

机构信息

Department of Neurology Keelung Chang Gung Memorial Hospital, Keelung, Taiwan.

出版信息

J Formos Med Assoc. 2012 Jul;111(7):397-402. doi: 10.1016/j.jfma.2011.06.017. Epub 2012 May 3.

Abstract

BACKGROUND/PURPOSE: Most reports about oculopharyngeal muscular dystrophy (OPMD) have been contributed by occidental countries, and most of the victims of this disease are racially white. In contrast, this disorder is rarely seen in Asians and has only one African report. Consequently, OPMD has been regarded as a disease of the Western world. The purpose of this paper is to challenge the accuracy of this concept.

METHODS

In a Chinese immigrant family, 3 patients manifesting signs related to OPMD were examined. Electromyography, nerve conduction studies, muscle biopsy and genetic analysis were performed on the proband. All the 322 papers about OPMD were reviewed and their country of origin was labeled to perceive the approximate prevalence of OPMD. Countries were categorized into groups according to the continents to which they belonged.

RESULTS

The proband's muscle histopathology showed small angulated fiber with rimmed vacuoles, ultrastructural pathology exposed filamentous intranuclear inclusions, and genetic analysis of the polyadenylate binding protein nuclear 1(PABPN1) gene revealed 13 GCG trinucleotide repeats in one allele (GCG)13 while being normal in the other. The survey of the country of origin of OPMD reports showed that 80% of these papers were contributed by occidental countries and that the number of publications of OPMD among countries of Americas and Asia were unequal, when compared to those of European countries, which were fairly proportioned. An epidemiologic review of the literature is presented and the prevalence of OPMD is discussed.

CONCLUSION

This is a China-born Chinese patient with both morphologically and genetically proven of OPMD. The very low OPMD report rate in developing countries of East Asia is due to the unfamiliarity of medical workers to OPMD and the unavailability of medical supplies to confirm the diagnosis. In addition, the present and previous reports provide clear evidence that OPMD in these areas is underdiagnosed.

摘要

背景/目的:大多数关于眼咽型肌营养不良症(OPMD)的报告都来自西方国家,而且这种疾病的大多数患者都是白种人。相比之下,亚洲很少见到这种疾病,只有一例来自非洲。因此,OPMD 被认为是一种西方世界的疾病。本文的目的是对这一概念的准确性提出挑战。

方法

对一个表现出与 OPMD 相关体征的华裔移民家庭的 3 名患者进行了检查。对先证者进行了肌电图、神经传导研究、肌肉活检和基因分析。回顾了所有 322 篇关于 OPMD 的论文,并对其来源国进行了标记,以了解 OPMD 的大致流行情况。根据所属大陆将国家分为不同的组。

结果

先证者的肌肉组织病理学显示出小角纤维和边缘空泡,超微结构病理学显示出细丝状核内包涵体,多聚腺苷酸结合蛋白核 1(PABPN1)基因的分析显示,一个等位基因中存在 13 个 GCG 三核苷酸重复(GCG)13,而另一个等位基因正常。对 OPMD 报告来源国的调查显示,80%的论文来自西方国家,与欧洲国家相比,美洲和亚洲国家的 OPMD 出版物数量不均等。本文还对文献进行了流行病学综述,并讨论了 OPMD 的流行情况。

结论

这是一个中国出生的中国患者,其形态学和遗传学均证实患有 OPMD。东亚发展中国家 OPMD 报告率很低,这是由于医务人员对 OPMD 不熟悉,也无法获得医疗用品来确诊。此外,目前和以前的报告提供了明确的证据,表明这些地区的 OPMD 诊断不足。

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