Department of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390, USA.
J Peripher Nerv Syst. 2012 May;17 Suppl 2:43-9. doi: 10.1111/j.1529-8027.2012.00395.x.
Idiopathic neuropathy, now designated as chronic idiopathic axonal polyneuropathy (CIAP), is a major public health problem in the United States. The disorder affects an estimated 5-8 million Americans, comprising about one-third of patients with neuropathy, based on data from referral centers. Typically, patients develop symptoms in the sixth decade or older. The onset is insidious, with numbness, paresthesias, and pain appearing over months to years. Although strength is generally preserved, the sensory loss and pain can be disabling. The clinical approach to this condition has evolved in important ways over the years, enabling improved diagnosis and characterization of this population. Current work has focused on identifying modifiable risk factors that may be associated with idiopathic neuropathy. The results may suggest that an underlying mechanism such as oxidative stress contributes to the development of CIAP.
特发性神经病,现被指定为慢性特发性轴索性多发性神经病(CIAP),是美国的一个主要公共卫生问题。根据转诊中心的数据,这种疾病估计影响了 500 万至 800 万美国人,占神经病患者的三分之一左右。通常,患者在 60 岁或以上出现症状。发病隐匿,数月至数年内出现麻木、感觉异常和疼痛。尽管通常保留了力量,但感觉丧失和疼痛可能会导致残疾。近年来,这种疾病的临床治疗方法发生了重要变化,从而改善了对这种人群的诊断和特征描述。目前的工作重点是确定可能与特发性神经病相关的可改变的危险因素。结果可能表明,潜在的机制,如氧化应激,导致 CIAP 的发展。