Mitchell Cassie S, Hollinger Sabrina K, Goswami Shivani D, Polak Meraida A, Lee Robert H, Glass Jonathan D
Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Ga., USA.
Neurodegener Dis. 2015;15(2):109-13. doi: 10.1159/000369812. Epub 2015 Feb 20.
BACKGROUND/AIMS: Recent studies suggest that antecedent disease could impact the pathophysiology of the motoneuron disease Amyotrophic Lateral Sclerosis (ALS). We performed a case-control study to examine the prevalence of 11 antecedent diseases in ALS.
Prevalence of antecedent disease in a 1,288 patient ALS population (Emory University ALS Clinic, Atlanta, Ga., USA) is compared to an age, gender, and geography-matched 7,561 subject control population using a statistical odds ratio (OR) with 95% confidence interval.
Association of ALS with odds of arthritis (OR = 0.14); non-ALS neurological disease (OR = 0.14); liver disease (OR = 0.19); chronic obstructive pulmonary disorder or COPD (OR = 0.23); kidney disease (OR = 0.32); adult asthma (OR = 0.39); diabetes (OR = 0.47); hypertension (OR = 0.56); obesity (OR = 0.6); hyperlipidemia or hypercholesterolemia (OR = 0.62); and thyroid disease (OR = 0.78).
The prevalence of antecedent disease was overall less in the ALS population. We present two potential lines of inquiry to explain these results: (1) 'Other disease as ALS protection'--antecedent diseases infer biochemical neuroprotection to ALS; (2) 'ALS as other disease protection'--the underpinnings of ALS could infer protection to other diseases, possibly via the mechanism hypervigilant regulation or 'too-high' regulatory feedback gains.
背景/目的:近期研究表明,既往疾病可能会影响运动神经元疾病肌萎缩侧索硬化症(ALS)的病理生理学。我们进行了一项病例对照研究,以调查ALS患者中11种既往疾病的患病率。
将1288例ALS患者(美国佐治亚州亚特兰大市埃默里大学ALS诊所)的既往疾病患病率与7561例年龄、性别和地理位置匹配的对照人群进行比较,采用统计学优势比(OR)及95%置信区间。
ALS与关节炎(OR = 0.14)、非ALS神经系统疾病(OR = 0.14)、肝脏疾病(OR = 0.19)、慢性阻塞性肺疾病或COPD(OR = 0.23)、肾脏疾病(OR = 0.32)、成人哮喘(OR = 0.39)、糖尿病(OR = 0.47)、高血压(OR = 0.56)、肥胖(OR = 0.6)、高脂血症或高胆固醇血症(OR = 0.62)以及甲状腺疾病(OR = 0.78)的患病几率相关。
ALS人群中既往疾病的总体患病率较低。我们提出两条潜在的研究方向来解释这些结果:(1)“其他疾病对ALS具有保护作用”——既往疾病对ALS具有生化神经保护作用;(2)“ALS对其他疾病具有保护作用”——ALS的发病机制可能通过过度警惕调节或“过高”的调节反馈增益机制对其他疾病具有保护作用。