Romano Tania, Wark John D, Owens Julie A, Wlodek Mary E
Department of Physiology, The University of Melbourne, Parkville, Victoria, Australia.
Bone. 2009 Jul;45(1):132-41. doi: 10.1016/j.bone.2009.03.661. Epub 2009 Mar 28.
Low birth weight increases the risk of developing adult onset cardiovascular and metabolic diseases. Recently being born small has also been identified as a risk factor for adverse bone growth, development and adult fracture risk. Evidence also suggests that accelerated growth in offspring of normal birth weight, following periods of slowed growth, can also independently program adult diseases. The aim of this study was to determine the relative roles of prenatal and postnatal growth restriction on adult bone characteristics and strength. Bilateral uterine vessel ligation (Restricted) or sham surgery (Control) was performed on gestational day 18 in WKY rats to induce fetal growth restriction. Control, Reduced (reduced Control litter size to match Restricted) and Restricted pups were cross-fostered onto different Control (normal lactation) or Restricted (impaired lactation) mothers 1 day after birth. Femur length, dimensions, strength, mineral content and density were quantified using DXA and pQCT analysis. Markers of bone turnover were measured in offspring at 6 months. Restricted pups were born lighter than Controls with males, not females, remaining smaller than Control-on-Control at 6 months (P<0.05). Pups born of normal weight from a reduced litter suckling on a Restricted mother (Reduced-on-Restricted) grew slowly during lactation then quicker after weaning compared to Controls (P<0.05). Cortical bone mineral content, dimensions and strength were lower in Restricted-on-Restricted and Reduced-on-Restricted offspring compared to Controls with lower density in Reduced-on-Restricted females (P<0.05). The stress strain index of bone bending strength remained lower in the Restricted male offspring when body weight adjustments were made. Cross-fostering Restricted females, but not males, onto mothers with normal lactation (Restricted-on-Control) restored growth and bone parameters to Controls (P<0.05). Being born small, or postnatal growth restriction for normal birth weight offspring followed by accelerated growth, programs bone content and strength deficits. Deficits were corrected by improving postnatal nutrition for females born small, highlighting sex specific programming outcomes and impact of postnatal nutrition. These findings suggest a link between growth restriction and adult bone health with additional studies needed to further explore this link in humans.
低出生体重会增加成年后患心血管疾病和代谢疾病的风险。最近,出生时体重过小也被确定为骨骼生长发育不良以及成年后骨折风险增加的一个危险因素。有证据还表明,出生体重正常的后代在经历生长缓慢期后加速生长,也会独立地引发成年疾病。本研究的目的是确定产前和产后生长受限对成年骨骼特征和强度的相对作用。在妊娠第18天对WKY大鼠进行双侧子宫血管结扎(受限组)或假手术(对照组),以诱导胎儿生长受限。出生1天后,将对照组、减少组(将对照组窝仔数减少以匹配受限组)和受限组幼崽交叉寄养到不同的对照组(正常哺乳)或受限组(哺乳受损)母亲处。使用双能X线吸收法(DXA)和外周定量CT(pQCT)分析对股骨长度、尺寸、强度、矿物质含量和密度进行量化。在6个月时测量后代的骨转换标志物。受限组幼崽出生时比对照组轻,6个月时雄性(而非雌性)仍比对照组-对照组小(P<0.05)。与对照组相比,出生体重正常但窝仔数减少且由受限组母亲哺乳的幼崽(减少组-受限组)在哺乳期生长缓慢,断奶后生长加快(P<0.05)。与对照组相比,减少组-受限组和受限组-受限组后代的皮质骨矿物质含量、尺寸和强度较低,减少组-受限组雌性的骨密度较低(P<0.05)。在进行体重调整后,受限组雄性后代的骨弯曲强度应力应变指数仍然较低。将受限组雌性(而非雄性)交叉寄养到正常哺乳的母亲处(受限组-对照组)可使生长和骨骼参数恢复到对照组水平(P<0.05)。出生时体重过小,或出生体重正常的后代产后生长受限随后加速生长,会导致骨含量和强度不足。对于出生时体重过小的雌性,通过改善产后营养可纠正这些不足,这突出了性别特异性编程结果以及产后营养的影响。这些发现表明生长受限与成年骨骼健康之间存在联系,需要进一步开展研究以在人类中进一步探索这种联系。