Crowne E C, Shalet S M, Wallace W H, Eminson D M, Price D A
Royal Manchester Children's Hospital.
Arch Dis Child. 1990 Oct;65(10):1109-12. doi: 10.1136/adc.65.10.1109.
To determine the natural history and psychological impact of the growth pattern in boys with constitutional delay in growth and puberty (CDGP), 43 boys presenting with short stature due to CDGP were followed up to final height. At presentation mean (SD) chronological age was 14.0 (1.9) years, bone age delay 2.7 (1.0) years, standing height standard deviation score (SDS) -3.4 (0.6), and predicted adult height SDS -1.3 (0.7). Final adult height SDS was -1.6 (0.9), measured at 21.2 (2.6) years. There was no significant difference between final height and predicted adult height, but there was a significant difference between final height and measured mid-parental height. Psychological questionnaires showed no significant difference in self esteem, marital, or employment state between the CDGP group and a control group. There was no correlation between self esteem and final height, but 25 felt their growth delay had affected their success either at school, work, or socially and 20 would rather have had treatment to advance their growth spurt. This study supports the more frequent use of active medical treatment to advance growth in boys with CDGP, and shows that although boys with CDGP reach their predicted heights, this is short for their families.
为了确定体质性生长和青春期延迟(CDGP)男孩生长模式的自然史及心理影响,对43名因CDGP导致身材矮小的男孩进行随访直至达到最终身高。就诊时,平均(标准差)实足年龄为14.0(1.9)岁,骨龄延迟2.7(1.0)岁,站立身高标准差评分(SDS)为 -3.4(0.6),预测成人身高SDS为 -1.3(0.7)。最终成人身高SDS为 -1.6(0.9),在21.2(2.6)岁时测量。最终身高与预测成人身高之间无显著差异,但最终身高与实测父母平均身高之间存在显著差异。心理问卷显示,CDGP组与对照组在自尊、婚姻或就业状况方面无显著差异。自尊与最终身高之间无相关性,但25人认为他们的生长延迟在学业、工作或社交方面影响了他们的成功,20人宁愿接受治疗以提前进入生长突增期。本研究支持更频繁地对CDGP男孩采用积极的医学治疗来促进生长,并表明尽管CDGP男孩达到了他们的预测身高,但对其家庭而言这个身高仍偏矮。