Spinal muscular atrophy: Diagnosis and management in a new therapeutic era

作者：William David Arnold, Darine Kassar, John T. Kissel · 发表于：Muscle & Nerve · 年份：2014 · DOI：10.1002/mus.24497 · 被引用次数：447 · 研究领域：Neurogenetic and Muscular Disorders Research、Congenital Anomalies and Fetal Surgery、RNA modifications and cancer

Spinal muscular atrophy (SMA) describes a group of disorders associated with spinal motor neuron loss. In this review we provide an update regarding the most common form of SMA, proximal or 5q-SMA, and discuss the contemporary approach to diagnosis and treatment. Electromyography and muscle biopsy features of denervation were once the basis for diagnosis, but molecular testing for homozygous deletion or mutation of the SMN1 gene allows efficient and specific diagnosis. In combination with loss of SMN1, patients retain variable numbers of copies of a second similar gene, SMN2, which produces reduced levels of the survival motor neuron (SMN) protein that are insufficient for normal motor neuron function. Despite the fact that understanding of how ubiquitous reduction of SMN protein leads to motor neuron loss remains incomplete, several promising therapeutics are now being tested in early-phase clinical trials.