Zhang Jing, Li Xingwang, Wang Yang, Ji Jue, Yang Fengping, Feng Guoyin, Wan Peng, Lindpaintner Klaus, He Lin, He Guang
Bio-X Center, Shanghai Jiao Tong University, Haoran Building, 1954 Huashan Road, 200030, Shanghai, People's Republic of China.
J Neural Transm (Vienna). 2009 Mar;116(3):357-61. doi: 10.1007/s00702-009-0185-1. Epub 2009 Feb 5.
Bipolar disorder is known to be subject to maternal transmission. Mitochondrial DNA has been suggested as playing a role in the illness. NDUFV2, located on 18p11.31-p11.2, encodes an important subunit of mitochondrial NADH (complex I). Previous studies have reported the association of NDUFV2 with bipolar disorder in the Japanese and Caucasian populations. Whether it is also a susceptible gene in the Chinese population is unknown. To study the role of NDUFV2 in bipolar disorder in the Chinese population, 506 unrelated bipolar patients and 507 unrelated controls of Chinese Han origin were recruited. Six SNPs (rs11661859, rs6506640, rs1156044, rs4148965, rs906807, rs977581) were genotyped using either TaqMan technology or direct sequencing. The haplotype consisting of rs6506640 (-342G > A) and rs906807 (86C > T) was found to be associated with bipolar disorder (global p = 0.012 before corrected, p = 0.030 after 10,000 permutations; individual p (A-T of rs6506640-rs906807) = 0.014 after 100,000 permutations (p = 0.0065 before corrected). The genotype frequency of rs906807 differed between bipolar female patients and female controls (p = 0.012, uncorrected). No other individual associations of SNPs with bipolar were detected. Our study indicated that the regions spanning from the promoter to the exon 2 may contain susceptible polymorphisms which predispose to bipolar disorder.
已知双相情感障碍会通过母体遗传。有研究表明线粒体DNA在该疾病中发挥作用。位于18p11.31 - p11.2的NDUFV2编码线粒体NADH(复合体I)的一个重要亚基。先前的研究已报道NDUFV2与日本人和高加索人群中的双相情感障碍有关联。它在中国人群中是否也是一个易感基因尚不清楚。为了研究NDUFV2在中国人群双相情感障碍中的作用,招募了506名无亲缘关系的中国汉族双相情感障碍患者和507名无亲缘关系的对照。使用TaqMan技术或直接测序对六个单核苷酸多态性(SNP,rs11661859、rs6506640、rs1156044、rs4148965、rs906807、rs977581)进行基因分型。发现由rs6506640(-342G>A)和rs906807(86C>T)组成的单倍型与双相情感障碍相关(校正前总体p = 0.012,经10000次置换后p = 0.030;经100000次置换后rs6506640 - rs906807的A - T个体p = 0.014(校正前p = 0.0065)。rs906807的基因型频率在双相情感障碍女性患者和女性对照之间存在差异(未校正p = 0.012)。未检测到其他SNP与双相情感障碍的个体关联。我们的研究表明,从启动子到外显子2的区域可能包含易患双相情感障碍 的易感多态性。