Zemel Babette S, Kawchak Deborah A, Ohene-Frempong Kwaku, Schall Joan I, Stallings Virginia A
Division of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia, Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Pediatr Res. 2007 May;61(5 Pt 1):607-13. doi: 10.1203/pdr.0b013e318045bdca.
Previous studies of children with sickle cell disease (SCD) reported poor growth and delayed maturation. However, the prevalence, magnitude, and correlates of suboptimal growth remain poorly understood. A prospective longitudinal study was undertaken to determine the effects of disease severity and nutritional status on growth, an indicator of childhood well-being. Children, birth to 18 y of age, with SCD-SS were evaluated annually for 4 y. Growth, nutritional status, skeletal and sexual maturation, disease severity, dietary intake, and maternal education were assessed. In this sample of 148 children (78 females), growth in height, weight, or body mass index declined in 84% of subjects; 38% fell below the 5th percentile in one or more measures. Puberty was delayed 1 to 2 y, and median age at menarche was 13.2 y. Skeletal age was delayed by 0.7 +/- 1.4 y overall and by 1.3 +/- 1.5 y in children 10 to 15 y old. Height status declined over time and was positively associated with advancing puberty and hematological measures in girls, and nutritional status in girls and boys. Growth failure and maturational delay remain significant chronic problems in children with SCD-SS and are related to potentially modifiable factors such as nutritional status.
先前针对镰状细胞病(SCD)患儿的研究报告称,这些患儿生长发育不良且成熟延迟。然而,对于生长发育欠佳的患病率、程度及其相关因素,人们仍知之甚少。为此开展了一项前瞻性纵向研究,以确定疾病严重程度和营养状况对生长发育(儿童健康状况的一项指标)的影响。对年龄在出生至18岁的SCD-SS患儿进行了为期4年的年度评估。评估内容包括生长发育、营养状况、骨骼和性成熟情况、疾病严重程度、饮食摄入量以及母亲的受教育程度。在这个由148名儿童(78名女性)组成的样本中,84%的受试者身高、体重或体重指数增长出现下降;38%的受试者在一项或多项指标上低于第5百分位数。青春期延迟1至2年,月经初潮的中位年龄为13.2岁。总体骨骼年龄延迟0.7±1.4岁,10至15岁儿童的骨骼年龄延迟1.3±1.5岁。身高状况随时间下降,并且在女孩中与青春期进展和血液学指标呈正相关,在女孩和男孩中与营养状况呈正相关。生长发育迟缓与成熟延迟在SCD-SS患儿中仍然是严重的慢性问题,并且与营养状况等潜在可改变因素有关。