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小于胎龄儿早产出生的儿童存在成年后低骨量风险。

Preterm Children Born Small for Gestational Age are at Risk for Low Adult Bone Mass.

作者信息

Buttazzoni Christian, Rosengren Björn, Tveit Magnus, Landin Lennart, Nilsson Jan-Åke, Karlsson Magnus

机构信息

Clinical and Molecular Osteoporosis Research Unit, Department of Clinical Sciences and Orthopedics, Lund University, Skåne University Hospital, 205 02, Malmō, Sweden.

出版信息

Calcif Tissue Int. 2016 Feb;98(2):105-13. doi: 10.1007/s00223-015-0069-3. Epub 2015 Oct 15.

Abstract

Cross-sectional studies suggest that premature birth and low birth weight may both be associated with low peak bone mass. We followed bone traits in preterm individuals and controls for 27 years and examined the effects of birth weight relative to gestational age [stratified as small for gestational age (SGA) or appropriate for gestational (AGA)] on adult bone mineral density (BMD). We measured distal forearm BMC (g/cm) and BMD (g/cm(2)) with single-photon absorptiometry (SPA) in 46 preterm children (31 AGA and 15 SGA) at mean age 10.1 years (range 4-16) and in 84 healthy age-matched children. The measurements were repeated 27 years later with the same SPA apparatus but then also with dual energy absorptiometry and peripheral computed tomography (pQCT). Preterm individuals were shorter (p = 0.03) in adulthood than controls. Preterm AGA individuals had similar BMC and BMD height-adjusted Z-scores in adulthood compared to controls. Preterm SGA individuals had lower distal forearm BMC and BMD height-adjusted Z-scores in adulthood than both controls and preterm AGA individuals. Preterm SGA individuals had lower gain from childhood to adulthood in distal forearm BMC height-adjusted Z-scores than controls (p = 0.03). The deficits in preterm SGA individuals in adulthood were also captured by DEXA in height-adjusted femoral neck (FN) BMC Z-score and height-adjusted FN BMD Z-score and by pQCT in tibial cross-sectional area (CSA) Z-score and stress strain index (SSI) Z-score, where all measurements were lower than controls (all p values <0.05). Preterm SGA individuals are at increased risk of reaching low adult bone mass, at least partly due to a deficit in the accrual of bone mineral during growth. In our cohort, we were unable to find a similar risk in preterm AGA individuals.

摘要

横断面研究表明,早产和低出生体重可能都与低骨峰值有关。我们对早产个体和对照组的骨骼特征进行了27年的跟踪,并研究了相对于胎龄的出生体重(分为小于胎龄儿[SGA]或适于胎龄儿[AGA])对成人骨矿物质密度(BMD)的影响。我们使用单光子吸收法(SPA)测量了46名平均年龄为10.1岁(范围4 - 16岁)的早产儿童(31名AGA和15名SGA)以及84名年龄匹配的健康儿童的远端前臂骨矿物质含量(BMC,g/cm)和骨密度(BMD,g/cm²)。27年后,使用相同的SPA设备重复测量,同时还使用双能吸收法和外周计算机断层扫描(pQCT)进行测量。早产个体成年后比对照组更矮(p = 0.03)。早产AGA个体成年后经身高调整的BMC和BMD Z值与对照组相似。早产SGA个体成年后远端前臂的BMC和经身高调整的BMD Z值低于对照组和早产AGA个体。早产SGA个体从儿童期到成年期远端前臂BMC经身高调整的Z值增加幅度低于对照组(p = 0.03)。早产SGA个体成年后的缺陷在经身高调整的股骨颈(FN)BMC Z值和经身高调整的FN BMD Z值的双能X线吸收法(DEXA)测量中以及胫骨横截面积(CSA)Z值和应力应变指数(SSI)Z值的pQCT测量中也有所体现,所有测量值均低于对照组(所有p值<0.05)。早产SGA个体达到低成人骨量的风险增加,至少部分原因是生长过程中骨矿物质积累不足。在我们的队列中,我们未在早产AGA个体中发现类似风险。

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