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生存运动神经元基因2和神经元凋亡抑制蛋白基因拷贝数与中国脊髓性肌萎缩队列自然史的关联

Association of copy numbers of survival motor neuron gene 2 and neuronal apoptosis inhibitory protein gene with the natural history in a Chinese spinal muscular atrophy cohort.

作者信息

Qu Yu-jin, Ge Xiu-shan, Bai Jin-li, Wang Li-wen, Cao Yan-yan, Lu Yan-yu, Jin Yu-wei, Wang Hong, Song Fang

机构信息

Department of Medical Genetics, Capital Institute of Pediatrics, Beijing, P. R. China.

Department of Neurology, Children's Hospital Affiliated Capital Institute of Pediatrics, Beijing, P. R. China.

出版信息

J Child Neurol. 2015 Mar;30(4):429-36. doi: 10.1177/0883073814553271. Epub 2014 Oct 20.

Abstract

We evaluated survival motor neuron 2 (SMN2) and neuronal apoptosis inhibitory protein (NAIP) gene copy distribution and the association of copy number with survival in 232 Chinese spinal muscular atrophy (SMA) patients. The SMN2 and NAIP copy numbers correlated positively with the median onset age (r = 0.72 and 0.377). The risk of death for patients with fewer copies of SMN2 or NAIP was much higher than for those with more copies (P < .01). The survival probabilities at 5 years were 5.1%, 90.7%, and 100% for 2, 3, and 4 SMN2 copies and 27.9%, 66.7%, and 87.2% for 0, 1, and 2 NAIP copies, respectively. Our results indicated that combined SMN1-SMN2-NAIP genotypes with fewer copies were associated with earlier onset age and poorer survival probability. Better survival status for Chinese type I SMA might due to a higher proportion of 3 SMN2 and a lower rate of zero NAIP.

摘要

我们评估了232例中国脊髓性肌萎缩症(SMA)患者的生存运动神经元2(SMN2)和神经元凋亡抑制蛋白(NAIP)基因拷贝数分布以及拷贝数与生存的相关性。SMN2和NAIP拷贝数与中位发病年龄呈正相关(r = 0.72和0.377)。SMN2或NAIP拷贝数较少的患者死亡风险远高于拷贝数较多的患者(P <.01)。对于2、3和4个SMN2拷贝,5年时的生存概率分别为5.1%、90.7%和100%;对于0、1和2个NAIP拷贝,5年时的生存概率分别为27.9%、66.7%和87.2%。我们的结果表明,拷贝数较少的SMN1-SMN2-NAIP联合基因型与发病年龄较早和生存概率较差相关。中国I型SMA患者较好的生存状况可能归因于3个SMN2拷贝的比例较高和NAIP为零的比例较低。

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