Marin Benoît, Boumédiene Farid, Logroscino Giancarlo, Couratier Philippe, Babron Marie-Claude, Leutenegger Anne Louise, Copetti Massimilano, Preux Pierre-Marie, Beghi Ettore
INSERM, U1094, Tropical Neuroepidemiology, Limoges, France.
Univ. Limoges, UMR_S 1094, Tropical Neuroepidemiology, Institute of Neuroepidemiology and Tropical Neurology, CNRS FR 3503 GEIST, F-87000 Limoges, France.
Int J Epidemiol. 2017 Feb 1;46(1):57-74. doi: 10.1093/ije/dyw061.
To assess the worldwide variation of amyotrophic lateral sclerosis (ALS) incidence, we performed a systematic review and meta-analysis of population-based data published to date.
We reviewed Medline and Embase up to June 2015 and included all population-based studies of newly diagnosed ALS cases, using multiple sources for case ascertainment. ALS crude and standardized incidence (on age and sex using the US 2010 population) were calculated. Random effect meta-analysis and meta-regression were performed using the subcontinent as the main study level covariate. Sources of heterogeneity related to the characteristics of the study population and the study methodology were investigated.
Among 3216 records, 44 studies were selected, covering 45 geographical areas in 11 sub-continents. A total of 13 146 ALS cases and 825 million person-years of follow-up (PYFU) were co-nsidered. The overall pooled worldwide crude ALS incidence was at 1.75 (1.55-1.96)/100 000 PYFU; 1.68 (1.50-1.85)/100 000 PYFU after standardization. Heterogeneity was identified in ALS standardized incidence between North Europe [1.89 (1.46-2.32)/100 000 PYFU] and East Asia [0.83 (0.42-1.24)/100 000 PYFU, China and Japan P = 0.001] or South Asia [0.73 (0.58-0.89)/100 000/PYFU Iran, P = 0.02]. Conversely, homogeneous rates have been reported in populations from Europe, North America and New Zealand [pooled ALS standardized incidence of 1.81 (1.66-1.97)/100 000 PYFU for those areas].
This review confirms a heterogeneous distribution worldwide of ALS, and sets the scene to sustain a collaborative study involving a wide international consortium to investigate the link between ancestry, environment and ALS incidence.
为评估肌萎缩侧索硬化症(ALS)发病率的全球差异,我们对迄今发表的基于人群的数据进行了系统评价和荟萃分析。
我们检索了截至2015年6月的Medline和Embase数据库,纳入所有基于人群的新诊断ALS病例研究,并使用多种来源确定病例。计算ALS的粗发病率和标准化发病率(采用美国2010年人口年龄和性别标准)。以次大陆作为主要研究水平协变量进行随机效应荟萃分析和荟萃回归。调查了与研究人群特征和研究方法相关的异质性来源。
在3216条记录中,选取了44项研究,涵盖11个次大陆的45个地理区域。共纳入13146例ALS病例和8.25亿人年的随访(PYFU)。全球总体汇总的ALS粗发病率为1.75(1.55 - 1.96)/10万PYFU;标准化后为1.68(1.50 - 1.85)/10万PYFU。在北欧[1.89(1.46 - 2.32)/10万PYFU]与东亚[0.83(0.42 - 1.24)/10万PYFU,中国和日本P = 0.001]或南亚[0.73(0.58 - 0.89)/10万/PYFU,伊朗,P = 0.02]之间的ALS标准化发病率存在异质性。相反,欧洲、北美和新西兰人群的发病率报告为同质[这些地区汇总的ALS标准化发病率为1.81(1.66 - 1.97)/10万PYFU]。
本综述证实了ALS在全球分布的异质性,并为开展一项涉及广泛国际联盟的合作研究奠定了基础,以调查血统、环境与ALS发病率之间的联系。