Chen Hsin-Hung, Hu Chaur-Jong
Department of Neurology, Taiwan Miners General Hospital.
Acta Neurol Taiwan. 2006 Sep;15(3):161-9.
The most common causes of dementia in Taiwan are Alzheimer's disease (AD) followed by vascular dementia (VaD). Several genetic studies have documented an increased risk of AD among apolipoprotein E gene allele 4 (ApoE4) carriers in Taiwanese (ethnic Chinese). Although ApoE4 is considered the most important risk factor for AD, the ApoE4 allele frequency is lower in Taiwanese (around 7%), than that in most Caucasian populations (over 10%). This phenomenon raises the hypothesis that low ApoE4 allele frequency contributes to the low prevalence of AD in Taiwanese. Other studies of the genetic impacts on modulation or regulation of manifestations, progression, and treatment response of AD in Taiwan have been inconclusive. Familial AD, which is conferred by PS1 gene mutation has been identified. There were very few studies of fronto-temporal dementia (FTD) or dementia with Lewy body (DLB) in Taiwan. Genetic studies of VaD remain limited and only NOTCH3 gene mutation has been detected in a Taiwanese cerebral autosomal dominant arteriopathy with subcortical infarct and leukoencephalopathy (CADASIL) family. Limited data indicated that non- ApoE4-associated AD may represent a larger proportion of AD in Taiwanese, suggesting the existence of novel genetic factors which remain to be identified.
台湾痴呆症最常见的病因是阿尔茨海默病(AD),其次是血管性痴呆(VaD)。多项基因研究表明,台湾汉族人群中载脂蛋白E基因等位基因4(ApoE4)携带者患AD的风险增加。尽管ApoE4被认为是AD最重要的风险因素,但台湾人群中ApoE4等位基因频率(约7%)低于大多数白种人群(超过10%)。这一现象引发了一种假说,即低ApoE4等位基因频率导致了台湾人群中AD的低患病率。台湾其他关于基因对AD表现、进展和治疗反应的调节或调控影响的研究尚无定论。已发现由PS1基因突变导致的家族性AD。台湾关于额颞叶痴呆(FTD)或路易体痴呆(DLB)的研究很少。VaD的基因研究仍然有限,仅在一个患有大脑常染色体显性动脉病伴皮质下梗死和白质脑病(CADASIL)的台湾家族中检测到NOTCH3基因突变。有限的数据表明,非ApoE4相关的AD在台湾人群中可能占更大比例,这表明存在有待确定的新基因因素。