Orioli Iêda M, Dolk Helen, Lopez-Camelo Jorge S, Mattos Daniel, Poletta Fernando A, Dutra Maria G, Carvalho Flavia M, Castilla Eduardo E
Latin American Collaborative Study of Congenital Malformations (ECLAMC) at Department of Genetics, Institute of Biology, Federal University of Rio de Janeiro, 21944-001, Rio de Janeiro, Brazil.
National Institute of Population Medical Genetics (INAGEMP), Porto Alegre, Brazil.
BMJ. 2017 Nov 21;359:j5018. doi: 10.1136/bmj.j5018.
To describe the prevalence and clinical spectrum of microcephaly in South America for the period 2005-14, before the start of the Zika epidemic in 2015, as a baseline for future surveillance as the Zika epidemic spreads and as other infectious causes may emerge in future. Prevalence and case-control study. ECLAMC (Latin American Collaborative Study of Congenital Malformations) database derived from 107 hospitals in 10 South American countries, 2005 to 2014. Data on microcephaly cases, four non-malformed controls per case, and all hospital births (all births for hospital based prevalence, resident within municipality for population based prevalence). For 2010-14, head circumference data were available and compared with Intergrowth charts. 552 microcephaly cases were registered, giving a hospital based prevalence of 4.4 (95% confidence interval 4.1 to 4.9) per 10 000 births and a population based prevalence of 3.0 (2.7 to 3.4) per 10 000. Prevalence varied significantly between countries and between regions and hospitals within countries. Thirty two per cent (n=175) of cases were prenatally diagnosed; 29% (n=159) were perinatal deaths. Twenty three per cent (n=128) were associated with a diagnosed genetic syndrome, 34% (n=189) polymalformed without a syndrome diagnosis, 12% (n=65) with associated neural malformations, and 26% (n=145) microcephaly only. In addition, 3.8% (n=21) had a STORCH (syphilis, toxoplasmosis, other including HIV, rubella, cytomegalovirus, and herpes simplex) infection diagnosis and 2.0% (n=11) had consanguineous parents. Head circumference measurements available for 184/235 cases in 2010-14 showed 45% (n=82) more than 3 SD below the mean, 24% (n=44) between 3 SD and 2 SD below the mean, and 32% (n=58) larger than -2 SD. Extrapolated to the nearly 7 million annual births in South America, an estimated 2000-2500 microcephaly cases were diagnosed among births each year before the Zika epidemic began in 2015. Clinicians are using more than simple metrics to make microcephaly diagnoses. Endemic infections are important enduring causes of microcephaly.
描述2005 - 2014年期间,即2015年寨卡疫情开始前,南美洲小头畸形的患病率及临床谱,作为未来寨卡疫情蔓延以及未来可能出现其他感染病因时监测的基线。患病率及病例对照研究。数据来源于拉丁美洲先天性畸形协作研究(ECLAMC)数据库,该数据库涵盖了2005年至2014年期间南美洲10个国家的107家医院。记录小头畸形病例数据、每个病例的4名非畸形对照数据以及所有医院分娩情况(基于医院的患病率采用所有医院分娩数据,基于人群的患病率采用市镇内居民的分娩数据)。对于2010 - 2014年的数据,可获取头围数据并与国际生长图表进行比较。共登记了552例小头畸形病例,基于医院的患病率为每10000例分娩中有4.4例(95%置信区间4.1至4.9),基于人群的患病率为每10000例中有3.0例(2.7至3.4)。患病率在不同国家之间以及国家内不同地区和医院之间存在显著差异。32%(n = 175)的病例在产前被诊断出;29%(n = 159)为围产期死亡。23%(n = 128)与已诊断的遗传综合征相关,34%(n = 189)为多发畸形但无综合征诊断,12%(n = 65)与相关神经畸形有关,26%(n = 145)仅为小头畸形。此外,3.8%(n = 21)有TORCH(梅毒、弓形虫病、其他包括HIV、风疹、巨细胞病毒和单纯疱疹病毒)感染诊断,2.0%(n = 11)父母为近亲结婚。2010 - 2014年期间,235例病例中有184例可获取头围测量数据,结果显示45%(n = 82)超过均值以下3个标准差,24%(n = 44)在均值以下3个标准差至2个标准差之间,32%(n = 58)大于 - 2个标准差。推算至南美洲每年近700万例分娩,在2015年寨卡疫情开始前,估计每年出生的婴儿中有2000 - 2500例被诊断为小头畸形。临床医生在进行小头畸形诊断时使用的不止是简单指标。地方性感染是小头畸形的重要持续性病因。