Ar Rochmah Mawaddah, Shima Ai, Harahap Nur Imma Fatimah, Niba Emma Tabe Eko, Morisada Naoya, Yanagisawa Shinichiro, Saito Toshio, Kaneko Kaori, Saito Kayoko, Morioka Ichiro, Iijima Kazumoto, Lai Poh San, Bouike Yoshihiro, Nishio Hisahide, Shinohara Masakazu
Department of Community Medicine and Social Health Care, Kobe University Graduate School of Medicine, Kobe, Japan.
Institute of Industrial Science, University of Tokyo, Tokyo, Japan.
Kobe J Med Sci. 2017 Oct 16;63(2):E41-E44.
Spinal muscular atrophy (SMA) is a neuromuscular disease caused by a mutation in SMN1. SMA is classified into three subtypes (types 1, 2, 3) based on achieved motor milestones. Although NAIP and SMN2 are widely accepted as SMA-modifying factors, gender-related modifying factors or gender effects on the clinical phenotype are still controversial.
A total of 122 Japanese patients with SMA, of which SMN1 was homozygously deleted, were analyzed from the perspective of the achieved motor milestone, NAIP status and SMN2 copy number.
A predominance of male patients was observed in SMA type 3 (the walker group) without NAIP-deletion or with high SMN2 copy number (3 or 4 copies).
We suggest the presence of gender-related modifiers on disease severity in SMA patients. The modifiers may contribute only in the presence of NAIP and a high copy number of SMN2.
脊髓性肌萎缩症(SMA)是一种由SMN1基因突变引起的神经肌肉疾病。根据所达到的运动里程碑,SMA被分为三种亚型(1型、2型、3型)。尽管NAIP和SMN2被广泛认为是SMA修饰因子,但性别相关修饰因子或性别对临床表型的影响仍存在争议。
从所达到的运动里程碑、NAIP状态和SMN2拷贝数的角度,对122例SMN1纯合缺失的日本SMA患者进行了分析。
在3型SMA(行走者组)中,未发生NAIP缺失或SMN2拷贝数高(3或4拷贝)的情况下,观察到男性患者占优势。
我们认为SMA患者疾病严重程度存在性别相关修饰因子。这些修饰因子可能仅在存在NAIP和高拷贝数SMN2的情况下起作用。