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Neurology:Nusinersen颈椎穿刺鞘内注射治疗脊髓性肌萎缩症

2018-07-14 zhangfan MedSci原创

研究认为Nusinersen颈椎穿刺鞘内注射是无法接受腰椎注射脊髓性肌萎缩症患者的一种可行的替代途径

近日研究人员考察了颈椎穿刺神经鞘内Nusinersen注射治疗对脊髓性肌萎缩症(SMA)的治疗效果。

SMA是一种神经肌肉疾病,其特征是由于前角细胞退化而导致严重的肌肉无力、萎缩和瘫痪。Nusinersen是首个FDA批准的SMA治疗药物,通过腰椎穿刺给药,但许多SMA患者由于脊柱侧凸或硬脊椎骨融合术,无法接受腰椎穿刺。灵长类动物模型研究表明,鞘内注射可实现药物在脊髓组织富集,故研究人员拟采用颈椎C1/C2穿刺作为Nusinersen可选给药手段。

3例胸腰骶段脊柱融合术患者接受颈穿刺鞘内Nusinersen注射,其中1名为12岁的I型SMA女童,2名为17岁的II型SMA女童。在透视及脑脊液流动可视化设备引导下,在颈椎C1-C2间隙后侧,使用Whitacre针进行全剂量Nusinersen(12 mg/5ml)注射。患者完成了4次负荷剂量以及1次维持剂量的Nusinersen治疗,总计15次,注射过程全部成功并且耐受性良好。

研究认为Nusinersen颈椎穿刺鞘内注射是无法接受腰椎注射脊髓性肌萎缩症患者的一种可行的替代途径。

原始出处:

Aravindhan Veerapandiyan et al. Cervical puncture to deliver nusinersen in patients with spinal muscular atrophy. Neurology. July 13,2018.

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    2019-03-10 chendoc252
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2018, time=2018-07-15, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1503096, encodeId=20ef1503096ac, content=<a href='/topic/show?id=a71481058ca' target=_blank style='color:#2F92EE;'>#肌萎缩#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=62, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=81058, encryptionId=a71481058ca, topicName=肌萎缩)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=eebd9606217, createdName=neizongke, createdTime=Sun Jul 15 23:43:00 CST 2018, time=2018-07-15, status=1, ipAttribution=)]
    2018-11-01 yinhl1978
  5. 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2018, time=2018-07-15, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1503096, encodeId=20ef1503096ac, content=<a href='/topic/show?id=a71481058ca' target=_blank style='color:#2F92EE;'>#肌萎缩#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=62, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=81058, encryptionId=a71481058ca, topicName=肌萎缩)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=eebd9606217, createdName=neizongke, createdTime=Sun Jul 15 23:43:00 CST 2018, time=2018-07-15, status=1, ipAttribution=)]
    2018-07-15 anminleiryan
  6. 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content=<a href='/topic/show?id=c75c9998e5d' target=_blank style='color:#2F92EE;'>#鞘内注射#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=72, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=99987, encryptionId=c75c9998e5d, topicName=鞘内注射)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=c3bb19663119, createdName=zywlvao, createdTime=Sun Jul 15 23:43:00 CST 2018, time=2018-07-15, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1514437, encodeId=69b6151443ee6, content=<a href='/topic/show?id=1ae010211143' target=_blank style='color:#2F92EE;'>#髓性#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=82, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=102111, encryptionId=1ae010211143, topicName=髓性)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=ae8810654266, createdName=more is better!, createdTime=Sun Jul 15 23:43:00 CST 2018, time=2018-07-15, status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1503096, encodeId=20ef1503096ac, content=<a href='/topic/show?id=a71481058ca' target=_blank style='color:#2F92EE;'>#肌萎缩#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=62, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=81058, encryptionId=a71481058ca, topicName=肌萎缩)], attachment=null, authenticateStatus=null, createdAvatar=null, createdBy=eebd9606217, createdName=neizongke, createdTime=Sun Jul 15 23:43:00 CST 2018, time=2018-07-15, status=1, ipAttribution=)]
    2018-07-21 zwjnj2

    好好学习天天向上

    0

  7. 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    2018-07-15 rgjl
  8. 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奥利索西可与其他靶向药物联用用于脊髓性肌萎缩症患者的治疗

NEJM:基因治疗将脊髓性肌萎缩症获重大突破

脊髓性肌萎缩症是致命的遗传性疾病,即使进行治疗,绝大多数患儿也活不过20个月。SMA此前被视为无药可医的遗传病,虽然发病率约为万分之一,但以中国每年出生1500万新生儿计算,国内目前的SMA患儿预计有3-5万名。 SMA患者体内,一种名为SMN的蛋白质因编码基因SMN-1的功能缺失而异常,而SMN蛋白对运动神经元的存活至关重要。没了这种蛋白,神经元无法正常工作,就导致了肌无力,肌肉迟缓、

NEJM:Nusinersen治疗婴儿脊髓性肌萎缩症III期临床结果

研究认为,Nusinersen治疗可改善脊髓性肌萎缩症,患儿生存期和运动功能,早期治疗有助于药物效应的最大化

基因治疗药物Spinraza可改II型SMA

日前,基因疗法药物Spinraza被证明可以显著改善神经肌肉疾病,脊髓性肌萎缩症(SMA)的严重形式,这种病症通常会影响6至18个月的儿童。由百健(Biogen)与Ionis制药公司合作开发的一款罕见病治疗药物Spinraza(nusinersen)已获得美国食品和药物管理局(FDA)的批准用于脊髓性肌萎缩症(SMA)儿科患者和成人患者的治疗。Spinraza是一种反义寡核苷酸(ASO),旨在改变

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