Kelly Andrea, Winer Karen K, Kalkwarf Heidi, Oberfield Sharon E, Lappe Joan, Gilsanz Vicente, Zemel Babette S
Department of Pediatrics (A.K., B.S.Z.), Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104; Eunice Kennedy Shriver National Institute of Child Health and Human Development (K.K.W.), Bethesda, Maryland 20892; Department of Pediatrics (H.K.), Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229; Department of Pediatrics (S.E.O.), Columbia University Medical Center, New York, New York 10032; Department of Medicine (J.L.), Creighton University, Omaha, Nebraska 68102; and Departments of Orthopaedic Surgery and Radiology (V.G.), Children's Hospital Los Angeles, Los Angeles, California 90027.
J Clin Endocrinol Metab. 2014 Jun;99(6):2104-12. doi: 10.1210/jc.2013-4455. Epub 2014 Mar 6.
Clinicians caring for children rely on measures of linear growth as a biomarker of development and overall health. Current reference ranges for height velocity (HV) for US children are unable to provide HV percentiles or Z-scores for early maturing and late maturing children at ages other than age at peak velocity. We present empirically acquired, age-specific reference ranges for HV from a contemporary sample of US youth.
Subjects were enrolled in the Bone Mineral Density in Childhood Study, a large, multicenter, multiethnic, contemporary cohort of children (aged 5-19 y at enrollment) from the United States followed for up to 7 years. More than 4000 annual (12 ± 1 mo) HV measurements from approximately 1500 children were available. Pubertal status was determined by breast stage or testicular volume assessed by experienced health providers. Age-specific reference ranges were determined using the LMS method.
Reference ranges (third to 97th percentiles) were generated for the entire cohort and for subgroups whose pubertal timing was defined as "earlier," "average," or "later." African American girls experienced earlier pubertal onset and had greater HV at younger ages and lower HV at older ages, compared to non-African American girls; differences did not persist after adjustment for pubertal timing. These differences were not observed for males.
These reference ranges for annual HV can be used to assess growth relative to peers of the same age and sex, with consideration of pubertal timing. Z-scores and exact percentiles for HV can also be determined for population studies.
照顾儿童的临床医生依赖线性生长指标作为发育和整体健康的生物标志物。美国儿童当前的身高增长速度(HV)参考范围无法为早熟和晚熟儿童在峰值速度年龄以外的其他年龄提供HV百分位数或Z分数。我们展示了从美国青少年当代样本中通过实证获得的特定年龄HV参考范围。
研究对象参加了儿童骨密度研究,这是一个来自美国的大型、多中心、多民族当代队列儿童(入组时年龄为5 - 19岁),随访长达7年。可获得来自约1500名儿童的4000多次年度(12 ± 1个月)HV测量值。青春期状态由经验丰富的医疗人员通过乳房分期或睾丸体积来确定。使用LMS方法确定特定年龄参考范围。
为整个队列以及青春期时间定义为“较早”、“平均”或“较晚”的亚组生成了参考范围(第3至97百分位数)。与非非裔美国女孩相比,非裔美国女孩青春期开始更早,在较年轻时HV更高,在较年长时HV更低;在调整青春期时间后差异不再存在。男性未观察到这些差异。
这些年度HV参考范围可用于评估相对于同年龄和性别的同龄人以及青春期时间的生长情况。对于人群研究也可以确定HV的Z分数和确切百分位数。