Moreira-Andrés M N, Cañizo F J, de la Cruz F J, Gómez-de la Cámara A, Hawkins F G
Servicio de Endocrinología, Hospital Universitario 12 de Octubre, Madrid, Spain.
Eur J Endocrinol. 1998 Sep;139(3):271-5. doi: 10.1530/eje.0.1390271.
We wished to clarify whether the osteopenia reported in adult men with a history of constitutional delay of growth and puberty (CDGP) could be due to the delayed puberty or an independent predisposition to osteoporosis in this condition.
Short prepubertal children with CDGP and children with familial short stature (FSS) were matched for height and other auxological variables. The FSS children served as a control group.
We measured spinal (L1-L4) bone mineral content (BMC) and bone mineral density (BMD) by dual energy X-ray absorptiometry (Hologic QDR 1000/w) in 56 children aged 5-11 years. All children had height below the 10th percentile for chronological age (CA), and bone age (BA) less than 10 years, 29 of them with clinical diagnosis of possible CDGP and 27 of them with FSS. The BMD standard deviation scores (SDS) relative to the values for normal height children were obtained.
The mean (+/-S.D.) spinal BMD was significantly lower in the children with CDGP than in the FSS group (0.534+/-0.059 vs 0.623+/-0.060 g/cm2, P< 0.001). Both groups had negative mean lumbar BMD SDS, but in the CDGP group it was significantly lower than in the FSS group as well when the SDS was based on the CA (-1.41+/-0.61 vs -0.38+/-0.51, P< 0.001) and when it was related to BA (-0.78+/-0.64 vs -0.17+/-0.52, P< 0.01). BMC was significantly lower in the CDGP than in the FSS group, when multiple regression analysis was performed by using scanned bone area, body weight and height, sex and BA as independent variables (P = 0.0005).
The finding of decreased mineralization in prepubertal children with CDGP before the age of puberty suggests that they may have an inherent predisposition to osteopenia.
我们希望阐明,有体质性生长和青春期延迟(CDGP)病史的成年男性中报告的骨质减少是否可能归因于青春期延迟,或者是这种情况下骨质疏松的独立易患因素。
对青春期前患有CDGP的儿童和家族性身材矮小(FSS)的儿童按身高和其他体格变量进行匹配。FSS儿童作为对照组。
我们用双能X线吸收法(Hologic QDR 1000/w)测量了56名5至11岁儿童的脊柱(L1-L4)骨矿物质含量(BMC)和骨矿物质密度(BMD)。所有儿童的身高低于按实足年龄(CA)计算的第10百分位数,骨龄(BA)小于10岁,其中29例临床诊断为可能的CDGP,27例为FSS。获得相对于正常身高儿童值的BMD标准差评分(SDS)。
CDGP儿童的平均(±标准差)脊柱BMD显著低于FSS组(0.534±0.059 vs 0.623±0.060 g/cm2,P<0.001)。两组的腰椎BMD SDS均值均为负值,但当SDS基于CA时,CDGP组也显著低于FSS组(-1.41±0.61 vs -0.38±0.51, P<0.001),当与BA相关时也是如此(-0.78±0.64 vs -0.17±0.52, P<0.01)。当以扫描骨面积、体重和身高、性别和BA作为自变量进行多元回归分析时,CDGP组的BMC显著低于FSS组(P = 0.0005)。
青春期前患有CDGP的儿童在青春期前矿化减少的发现表明,他们可能存在骨质减少的内在易患因素。