Ju Xiao-Dong, Liu Tao, Chen Jing, Li Xiao-Gang, Liu Xin-Xiu, Liu Wen-Chao, Wang Kai, Deng Min
Medical Research Center, Peking University Third Hospital, Beijing 100191, China.
Chin Med J (Engl). 2015 Dec 20;128(24):3305-9. doi: 10.4103/0366-6999.171421.
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that primarily affects motor neurons and has no effective treatment. Recently, Iida et al. identified a single-nucleotide polymorphism (SNP) rs2275294 in the ZNF512B gene that is significantly associated with susceptibility to ALS in the Japanese population. Here, we performed a case-control study examining the possible association of rs2275294 with risk of sporadic ALS (SALS) in a large Chinese cohort.
To assess this association, we performed a replication study in 953 SALS patients and 1039 age- and gender-matched healthy control subjects, who were recruited from Peking University Third Hospital and the First Affiliated Hospital of Anhui Medical University from January 2004 to December 2013 throughout China. We genotyped the rs2275294 SNP using polymerase chain reaction and direct sequencing.
The allele frequency of rs2275294 in ZNF512B was different between Japanese and Chinese. The association in Chinese between ALS patients and controls did not reach statistical significance (P = 0.54; odds ratio = 0.94; 95% confidence interval = 0.76-1.15).
The SNP rs2275294 in ZNF512B is not considered to be associated with ALS susceptibility in the Chinese population. Our study highlights genetic heterogeneity in ALS susceptibility in different population. Given our negative results, further replication study involving larger and more homogeneous samples in different ethnicities should be performed in the future.
肌萎缩侧索硬化症(ALS)是一种致命的神经退行性疾病,主要影响运动神经元,且尚无有效治疗方法。最近,饭田等人在ZNF512B基因中鉴定出一个单核苷酸多态性(SNP)rs2275294,该多态性与日本人群中ALS易感性显著相关。在此,我们进行了一项病例对照研究,以检验rs2275294与中国一大群散发型ALS(SALS)患者风险之间的可能关联。
为评估这种关联,我们在953例SALS患者和1039例年龄及性别匹配的健康对照者中进行了一项重复研究,这些患者和对照者于2004年1月至2013年12月期间在中国各地从北京大学第三医院和安徽医科大学第一附属医院招募。我们使用聚合酶链反应和直接测序对rs2275294 SNP进行基因分型。
ZNF512B中rs2275294的等位基因频率在日本人和中国人之间存在差异。在中国,ALS患者与对照者之间的关联未达到统计学显著性(P = 0.54;优势比 = 0.94;95%置信区间 = 0.76 - 1.15)。
ZNF512B中的SNP rs2275294不被认为与中国人群中ALS易感性相关。我们的研究突出了不同人群中ALS易感性的遗传异质性。鉴于我们的阴性结果,未来应进行涉及不同种族更大且更同质样本的进一步重复研究。