Akmatov Manas K, Graf Jonas, Kohring Claudia, Ellenberger David, Bätzing Jörg, Tremlett Helen, Holstiege Jakob
Department of Epidemiology and Health Care Atlas, Central Research Institute of Ambulatory Health Care, Berlin, Germany.
Department of Neurology, Medical Faculty and University Hospital Düsseldorf, Heinrich-Heine-University Düsseldorf, Germany.
JAMA Netw Open. 2024 Dec 2;7(12):e2452652. doi: 10.1001/jamanetworkopen.2024.52652.
A growing body of literature suggests the presence of a prodromal period with nonspecific signs and symptoms before onset of multiple sclerosis (MS).
To systematically assess diseases and symptoms diagnosed in the 5 years before a first MS- or central nervous system (CNS) demyelinating disease-related diagnostic code in pediatric patients compared with controls without MS and controls with another immune-mediated disorder, juvenile idiopathic arthritis (JIA).
DESIGN, SETTING, AND PARTICIPANTS: This population-based, matched case-control study included children and adolescents (aged <18 years) in Germany with statutory health insurance from January 2010 to December 2020. The study population consisted of 3 groups: case individuals with MS, control individuals without MS, and control individuals with JIA. Data were analyzed from November 2023 to April 2024.
Diagnoses coded according to the International Statistical Classification of Diseases and Related Health Problems, 10th Revision, German Modification (ICD-10-GM).
The main outcome was incident cases of MS, defined as the first confirmed diagnosis of MS (ICD-10-GM code G35) in 1 quarter between 2013 and 2020 and at least 1 additional diagnosis in the following quarters. In total, 163 ICD-10-GM codes before a first MS diagnosis were assessed using univariable and multivariable logistic regression analyses.
The study population consisted of 1091 children and adolescents with MS, 10 910 without MS, and 1068 with JIA. Of the children and adolescents with MS, 788 (72.2%) were female. Mean (SD) age at disease diagnosis was 15.7 (1.7) years. Nine ICD-10-GM codes were present more frequently among children and adolescents with MS in the 5 years before their first MS diagnosis than among controls without MS: obesity (adjusted odds ratio [AOR], 1.70; 95% CI, 1.42-2.02), disorders of eye refraction and accommodation (AOR, 1.26; 95% CI, 1.09-1.47), visual disturbances (AOR, 1.31; 95% CI, 1.10-1.55), gastritis and duodenitis (AOR, 1.35; 95% CI, 1.08-1.70), patella disorders (AOR, 1.47; 95% CI, 1.13-1.90), heartbeat abnormalities (AOR, 1.94; 95% CI, 1.27-2.96), flatulence (AOR, 1.43; 95% CI, 1.01-2.01), skin sensation disturbances (AOR, 12.93; 95% CI, 8.98-18.62), as well as dizziness and giddiness (AOR, 1.52; 95% CI, 1.22-1.89). Four of these ICD-10-GM codes were significantly more prevalent in children and adolescents with MS than in controls with JIA: obesity (AOR, 3.19; 95% CI, 2.03-5.02), refraction and accommodation disorders (AOR, 3.08; 95% CI, 2.33-4.08), visual disturbances (AOR, 1.62; 95% CI, 1.13-2.33), and skin sensation disturbances (AOR, 27.70; 95% CI, 6.52-117.64).
In this population-based, matched case-control study, children and adolescents with MS had diverse metabolic, ocular, musculoskeletal, gastrointestinal, and cardiovascular symptoms, signs, or diagnoses within 5 years before their first MS diagnosis. Better characterization of early symptoms and/or risk factors, comorbid disorders, and possible prodromal features of MS may have considerable implications for early recognition and subsequent progression of the disease.
越来越多的文献表明,在多发性硬化症(MS)发病前存在一个具有非特异性体征和症状的前驱期。
与无MS的对照组和患有另一种免疫介导疾病——幼年特发性关节炎(JIA)的对照组相比,系统评估儿科患者在首次出现MS或中枢神经系统(CNS)脱髓鞘疾病相关诊断代码前5年被诊断出的疾病和症状。
设计、背景和参与者:这项基于人群的配对病例对照研究纳入了2010年1月至2020年12月在德国参加法定医疗保险的儿童和青少年(年龄<18岁)。研究人群包括3组:患有MS的病例个体、无MS的对照个体和患有JIA的对照个体。数据于2023年11月至2024年4月进行分析。
根据《疾病和相关健康问题国际统计分类》第10次修订版德国修改版(ICD-10-GM)编码的诊断。
主要结局是MS的发病病例,定义为2013年至2020年期间某一季度首次确诊的MS(ICD-10-GM编码G35),且在随后几个季度至少有1次额外诊断。在首次MS诊断前,共评估了163个ICD-10-GM编码,采用单变量和多变量逻辑回归分析。
研究人群包括1091名患有MS的儿童和青少年、10910名无MS的儿童和青少年以及1068名患有JIA的儿童和青少年。在患有MS的儿童和青少年中,788名(72.2%)为女性。疾病诊断时的平均(标准差)年龄为15.7(1.7)岁。在首次MS诊断前5年,9个ICD-10-GM编码在患有MS的儿童和青少年中比在无MS的对照组中更频繁出现:肥胖(调整优势比[AOR],1.70;95%置信区间[CI],1.42 - 2.02)、眼屈光和调节障碍(AOR,1.26;95%CI,1.09 - 1.47)、视觉障碍(AOR,1.31;95%CI,1.10 - 1.55)、胃炎和十二指肠炎(AOR,1.35;95%CI,1.08 - 1.70)、髌骨疾病(AOR,1.47;95%CI,1.13 - 1.90)、心跳异常(AOR,1.94;95%CI,1.27 - 2.96)、肠胃胀气(AOR,1.43;95%CI,1.01 - 2.01)、皮肤感觉障碍(AOR,12.93;95%CI,8.98 - 18.62)以及头晕目眩(AOR,1.52;95%CI,1.22 - 1.89)。其中4个ICD-10-GM编码在患有MS的儿童和青少年中比在患有JIA的对照组中显著更普遍:肥胖(AOR,3.19;95%CI,2.03 - 5.02)、屈光和调节障碍(AOR,3.08;95%CI,2.33 - 4.08)、视觉障碍(AOR,1.62;95%CI,1.13 - 2.33)以及皮肤感觉障碍(AOR,27.70;95%CI,6.52 - 117.64)。
在这项基于人群的配对病例对照研究中,患有MS的儿童和青少年在首次MS诊断前5年内有多种代谢、眼部、肌肉骨骼、胃肠道和心血管症状、体征或诊断。更好地描述MS的早期症状和/或危险因素、共病以及可能的前驱特征可能对疾病的早期识别和后续进展具有重要意义。