Christian Parul, Lee Sun Eun, Donahue Angel Moira, Adair Linda S, Arifeen Shams E, Ashorn Per, Barros Fernando C, Fall Caroline H D, Fawzi Wafaie W, Hao Wei, Hu Gang, Humphrey Jean H, Huybregts Lieven, Joglekar Charu V, Kariuki Simon K, Kolsteren Patrick, Krishnaveni Ghattu V, Liu Enqing, Martorell Reynaldo, Osrin David, Persson Lars-Ake, Ramakrishnan Usha, Richter Linda, Roberfroid Dominique, Sania Ayesha, Ter Kuile Feiko O, Tielsch James, Victora Cesar G, Yajnik Chittaranjan S, Yan Hong, Zeng Lingxia, Black Robert E
Department of International Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA, Department of Nutrition, University of North Carolina, Chapel Hill, NC, USA, International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh, Department of International Health, University of Tampere, School of Medicine, Tampere, Finland, Programa de Pós-graduação em Saúde e Comportamento, Universidade Católica de Pelotas, Pelotas, Brazil, MRC Lifecourse Epidemiology Unit, Southampton General Hospital, Southampton, UK, Departments of Global Health and Population, Nutrition, and Epidemiology, Harvard School of Public Health, Boston, MA, USA, Hubert Department of Global Health, Rollins School of Public Health, Emory University, Atlanta, GA, USA, Pennington Biomedical Research Center, Baton Rouge, LA, USA, Woman and Child Health Research Center, Department of Public Health, Institute of Tropical Medicine, Nationalestraat 155, 2000 Antwerpen, Belgium, Department of Food Safety and Food Quality, Ghent University, Sint-Pietersnieuwstraat 25, B 9000 Ghent, Belgium, Diabetes Unit, King Edward Memorial Hospital and Research Centre, Pune, India, Center for Global Health Research, KEMRI, Kisumu, Kenya, KEMRI/CDC Research and Public Health Collaboration, Kisumu, Kenya, Epidemiology Research Unit, CSI Holdsworth Memorial Hospital, Mysore, India, Tianjin Women's and Children's Health Center, Tianjin, China, Institute for Global Health, UCL Institute of Child Health, London, UK, International Maternal and Child Health, Uppsala University, Uppsala, Sweden, Human Sciences Research Council and the Developmental Pathways for Health Research Programme, University of the Witwatersrand, Johannesburg, South Africa, Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA, Child and Reproductive Health Group, Liverpool School of Tropical Medicine, Liverpool UK, Centers for Disease Control and Prevention, Kenya, Department of Global Health, Ge
Int J Epidemiol. 2013 Oct;42(5):1340-55. doi: 10.1093/ije/dyt109. Epub 2013 Aug 6.
Low- and middle-income countries continue to experience a large burden of stunting; 148 million children were estimated to be stunted, around 30-40% of all children in 2011. In many of these countries, foetal growth restriction (FGR) is common, as is subsequent growth faltering in the first 2 years. Although there is agreement that stunting involves both prenatal and postnatal growth failure, the extent to which FGR contributes to stunting and other indicators of nutritional status is uncertain.
Using extant longitudinal birth cohorts (n=19) with data on birthweight, gestational age and child anthropometry (12-60 months), we estimated study-specific and pooled risk estimates of stunting, wasting and underweight by small-for-gestational age (SGA) and preterm birth.
We grouped children according to four combinations of SGA and gestational age: adequate size-for-gestational age (AGA) and preterm; SGA and term; SGA and preterm; and AGA and term (the reference group). Relative to AGA and term, the OR (95% confidence interval) for stunting associated with AGA and preterm, SGA and term, and SGA and preterm was 1.93 (1.71, 2.18), 2.43 (2.22, 2.66) and 4.51 (3.42, 5.93), respectively. A similar magnitude of risk was also observed for wasting and underweight. Low birthweight was associated with 2.5-3.5-fold higher odds of wasting, stunting and underweight. The population attributable risk for overall SGA for outcomes of childhood stunting and wasting was 20% and 30%, respectively.
This analysis estimates that childhood undernutrition may have its origins in the foetal period, suggesting a need to intervene early, ideally during pregnancy, with interventions known to reduce FGR and preterm birth.
低收入和中等收入国家仍然承受着巨大的发育迟缓负担;据估计,2011年有1.48亿儿童发育迟缓,约占所有儿童的30%-40%。在许多这些国家,胎儿生长受限(FGR)很常见,随后在出生后的头两年生长发育迟缓也很常见。虽然人们一致认为发育迟缓涉及产前和产后生长失败,但FGR对发育迟缓及其他营养状况指标的影响程度尚不确定。
利用现有的纵向出生队列(n=19),这些队列包含出生体重、孕周和儿童人体测量数据(12-60个月),我们通过小于胎龄儿(SGA)和早产估计了发育迟缓、消瘦和体重不足的研究特定风险估计值和合并风险估计值。
我们根据SGA和孕周的四种组合对儿童进行分组:适于胎龄(AGA)和早产;SGA和足月;SGA和早产;以及AGA和足月(参照组)。相对于AGA和足月,与AGA和早产、SGA和足月、SGA和早产相关的发育迟缓的比值比(95%置信区间)分别为1.93(1.71, 2.18)、2.43(2.22, 2.66)和4.51(3.42, 5.93)。消瘦和体重不足也观察到类似程度的风险。低出生体重与消瘦、发育迟缓和体重不足的几率高2.5-3.5倍相关。儿童发育迟缓和消瘦结局的总体SGA人群归因风险分别为20%和30%。
该分析估计儿童期营养不良可能起源于胎儿期,这表明需要尽早干预,理想情况下是在孕期进行干预,采用已知可降低FGR和早产的干预措施。